HOXA3
| Gene Description: |
similar to homeobox-containing transcription factor; homeobox A3 |
| Synonyms: |
MGC10155, HOXA3, Hoxa3, HOX1E, Mo-10, HOX1, Hox-1.5, RGD1561431 |
| Orthologs: |
Human HOXA3 (protein-coding), Mouse Hoxa3 (protein-coding), Rat RGD1561431 (protein-coding)
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Sources
Sources
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Human-Mouse:
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HomoloGene, MGD, OrthoMCL
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Human-Rat:
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OrthoMCL
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Mouse-Rat:
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Inparanoid, OrthoMCL
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Possible sources:
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HomoloGene, MGD, RGD, Ensembl, Inparanoid, OrthoMCL, KEGG
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Regions of Interest Overlapping this feature from T1DBase
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Regions Overlapping this Feature:
Human: 1
Mouse: 1
Rat: 2
Associated Regions: Available
Regions were calculated based on variants available for a large study with a convincing p-value (P < 5 x 10-8) +/- 0.1cM, and then these regions were examined for genes based on the current set of T1DBase gene spans.
Other Regions: Available
Gene Overview from T1DBase
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Beta Cell Gene Atlas from T1DBase
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| Users should be aware that the scale represents a rank within an experiment rather than a normalized expression signal.
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Expression Legend
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The Beta Cell Gene Atlas is a collection of almost all available public microarray
data generated with pancreatic beta cells and related cell lines and types. The
expression data comes from 131 array analyses derived from 28 experiments
(open details in a new window).
The basal (untreated cell) expression signal intensity values in each array
were converted to ranks within the experiments; the highest value was used for
genes represented by more than one probe. The rank values of genes in a given cell
type were averaged with other calculated values from experiments performed with the
same cell type. The rank transformation of the expression values enable comparison
of gene expression across different organisms and tissues.
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A red border around a cell indicates greater certainty in the data;
specifically, the gene has >0.95 probability of being expressed in the tissue.
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| Users should be aware that the scale represents a rank within an experiment rather than a normalized expression signal.
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Expression Legend
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Signal intensity values were converted to ranks within the experiments.
For genes represented by more than one probeset, we averaged the intensity
signals for each probeset across all tissues and chose the probeset with the
highest average value. The rank transformation of the expression values enables
comparison of gene expression across different organisms and tissues.
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Interactions Table for HOXA3:
The HOXA3 interactions are shown below. Each row lists the two interactors, the sources which document this as an interaction, a classification of the interaction as empirical or predicted, and Pubmed IDs (if any) for the interaction.
The table of interactions is downloadable as a text file. Please note that the text file will not include data from HPRD due to restrictions imposed by the HPRD funding sources.
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Cross-Reference to Pathways and GO Terms
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KEGG Network: None available
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Biocarta: None available
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Reactome: None available
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NCI-Nature Pathway Interaction Database: None available
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Gene Ontology: 15
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KEGG Network: None available
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NCI-Nature Pathway Interaction Database: None available
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Publications: 146
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Plasticity of neural crest-placode interaction in the developing visceral nervous system.
Chen Y, Takano-Maruyama M, Gaufo GO
Dev Dyn. 2011
PubMed ID: 21674689
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HOX genes are expressed in bovine and mouse oocytes and early embryos.
Paul D, Bridoux L, Rezsöhazy R, Donnay I
Mol Reprod Dev. 2011
PubMed ID: 21567651
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Hox genes define distinct progenitor sub-domains within the second heart field.
Bertrand N, Roux M, Ryckebüsch L, Niederreither K, Dollé P, Moon A, Capecchi M, Zaffran S
Dev Biol. 2011
PubMed ID: 21385575
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HBO1 is required for H3K14 acetylation and normal transcriptional activity during embryonic development.
Kueh AJ, Dixon MP, Voss AK, Thomas T
Mol Cell Biol. 2011
PubMed ID: 21149574
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Hoxa3 promotes the differentiation of hematopoietic progenitor cells into proangiogenic Gr-1+CD11b+ myeloid cells.
Mahdipour E, Charnock JC, Mace KA
Blood. 2011
PubMed ID: 20974673
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A high-resolution anatomical atlas of the transcriptome in the mouse embryo.
Diez-Roux G, Banfi S, Sultan M, Geffers L, Anand S, Rozado D, Magen A, Canidio E, Pagani M, Peluso I, Lin-Marq N, Koch M, Bilio M, Cantiello I, Verde R, De Masi C, Bianchi SA, Cicchini J, Perroud E, Mehmeti S, Dagand E, Schrinner S, Nürnberger A, Schmidt K, Metz K, Zwingmann C, Brieske N, Springer C, Hernandez AM, Herzog S, Grabbe F, Sieverding C, Fischer B, Schrader K, Brockmeyer M, Dettmer S, Helbig C, Alunni V, Battaini MA, Mura C, Henrichsen CN, Garcia-Lopez R, Echevarria D, Puelles E, Garcia-Calero E, Kruse S, Uhr M, Kauck C, Feng G, Milyaev N, Ong CK, Kumar L, Lam M, Semple CA, Gyenesei A, Mundlos S, Radelof U, Lehrach H, Sarmientos P, Reymond A, Davidson DR, Dollé P, Antonarakis SE, Yaspo ML, Martinez S, Baldock RA, Eichele G, Ballabio A
PLoS Biol. 2011
PubMed ID: 21267068
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HoxA3 is an apical regulator of haemogenic endothelium.
Iacovino M, Chong D, Szatmari I, Hartweck L, Rux D, Caprioli A, Cleaver O, Kyba M
Nat Cell Biol. 2011
PubMed ID: 21170035
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Screening large numbers of expression patterns of transcription factors in late stages of the mouse thymus.
Chung YC, Tsai YJ, Shiu TY, Sun YY, Wang PF, Chen CL
Gene Expr Patterns. 2011
PubMed ID: 20932939
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EphB-ephrin-B2 interactions are required for thymus migration during organogenesis.
Foster KE, Gordon J, Cardenas K, Veiga-Fernandes H, Makinen T, Grigorieva E, Wilkinson DG, Blackburn CC, Richie E, Manley NR, Adams RH, Kioussis D, Coles MC
Proc Natl Acad Sci U S A. 2010
PubMed ID: 20616004
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Mouse and zebrafish Hoxa3 orthologues have nonequivalent in vivo protein function.
Chen L, Zhao P, Wells L, Amemiya CT, Condie BG, Manley NR
Proc Natl Acad Sci U S A. 2010
PubMed ID: 20498049
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Placodal sensory ganglia coordinate the formation of the cranial visceral motor pathway.
Takano-Maruyama M, Chen Y, Gaufo GO
Dev Dyn. 2010
PubMed ID: 20235227
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Dysregulation of the PDGFRA gene causes inflow tract anomalies including TAPVR: integrating evidence from human genetics and model organisms.
Bleyl SB, Saijoh Y, Bax NA, Gittenberger-de Groot AC, Wisse LJ, Chapman SC, Hunter J, Shiratori H, Hamada H, Yamada S, Shiota K, Klewer SE, Leppert MF, Schoenwolf GC
Hum Mol Genet. 2010
PubMed ID: 20071345
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An atlas of combinatorial transcriptional regulation in mouse and man.
Ravasi T, Suzuki H, Cannistraci CV, Katayama S, Bajic VB, Tan K, Akalin A, Schmeier S, Kanamori-Katayama M, Bertin N, Carninci P, Daub CO, Forrest AR, Gough J, Grimmond S, Han JH, Hashimoto T, Hide W, Hofmann O, Kamburov A, Kaur M, Kawaji H, Kubosaki A, Lassmann T, van Nimwegen E, MacPherson CR, Ogawa C, Radovanovic A, Schwartz A, Teasdale RD, Tegnér J, Lenhard B, Teichmann SA, Arakawa T, Ninomiya N, Murakami K, Tagami M, Fukuda S, Imamura K, Kai C, Ishihara R, Kitazume Y, Kawai J, Hume DA, Ideker T, Hayashizaki Y
Cell. 2010
PubMed ID: 20211142
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Nav2 is necessary for cranial nerve development and blood pressure regulation.
McNeill EM, Roos KP, Moechars D, Clagett-Dame M
Neural Dev. 2010
PubMed ID: 20184720
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Dosage-dependent hedgehog signals integrated with Wnt/beta-catenin signaling regulate external genitalia formation as an appendicular program.
Miyagawa S, Moon A, Haraguchi R, Inoue C, Harada M, Nakahara C, Suzuki K, Matsumaru D, Kaneko T, Matsuo I, Yang L, Taketo MM, Iguchi T, Evans SM, Yamada G
Development. 2009
PubMed ID: 19906864
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Moz and retinoic acid coordinately regulate H3K9 acetylation, Hox gene expression, and segment identity.
Voss AK, Collin C, Dixon MP, Thomas T
Dev Cell. 2009
PubMed ID: 19922872
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HOXA3 modulates injury-induced mobilization and recruitment of bone marrow-derived cells.
Mace KA, Restivo TE, Rinn JL, Paquet AC, Chang HY, Young DM, Boudreau NJ
Stem Cells. 2009
PubMed ID: 19544454
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A High-Density Association Study of 383 Candidate Genes for Volumetric Bone Density at the Femoral Neck and Lumbar Spine among Older Men.
Yerges LM, Klei L, Cauley JA, Roeder K, Kammerer CM, Moffett SP, Ensrud KE, Nestlerode CS, Marshall LM, Hoffman AR, Lewis C, Lang TF, Barrett-Connor E, Ferrell RE, Orwoll ES, Zmuda JM, for the MrOS Research Group
J Bone Miner Res. 2009
PubMed ID: 19453261
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Brpf1, a subunit of the MOZ histone acetyl transferase complex, maintains expression of anterior and posterior Hox genes for proper patterning of craniofacial and caudal skeletons.
Hibiya K, Katsumoto T, Kondo T, Kitabayashi I, Kudo A
Dev Biol. 2009
PubMed ID: 19254709
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Lineage-specific biology revealed by a finished genome assembly of the mouse.
Church DM, Goodstadt L, Hillier LW, Zody MC, Goldstein S, She X, Bult CJ, Agarwala R, Cherry JL, DiCuccio M, Hlavina W, Kapustin Y, Meric P, Maglott D, Birtle Z, Marques AC, Graves T, Zhou S, Teague B, Potamousis K, Churas C, Place M, Herschleb J, Runnheim R, Forrest D, Amos-Landgraf J, Schwartz DC, Cheng Z, Lindblad-Toh K, Eichler EE, Ponting CP, Mouse Genome Sequencing Consortium
PLoS Biol. 2009
PubMed ID: 19468303
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Ethanol exposure induces differential microRNA and target gene expression and teratogenic effects which can be suppressed by folic acid supplementation.
Wang LL, Zhang Z, Li Q, Yang R, Pei X, Xu Y, Wang J, Zhou SF, Li Y
Hum Reprod. 2009
PubMed ID: 19091803
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Rostral and caudal pharyngeal arches share a common neural crest ground pattern.
Minoux M, Antonarakis GS, Kmita M, Duboule D, Rijli FM
Development. 2009
PubMed ID: 19168678
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HOX gene analysis of endothelial cell differentiation in human bone marrow-derived mesenchymal stem cells.
Chung N, Jee BK, Chae SW, Jeon YW, Lee KH, Rha HK
Mol Biol Rep. 2009
PubMed ID: 17972163
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Quantification of Hox and surfactant protein-B transcription during murine lung development.
Grier DG, Thompson A, Lappin TR, Halliday HL
Neonatology. 2009
PubMed ID: 19204410
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Large-scale gene trapping in C57BL/6N mouse embryonic stem cells.
Hansen GM, Markesich DC, Burnett MB, Zhu Q, Dionne KM, Richter LJ, Finnell RH, Sands AT, Zambrowicz BP, Abuin A
Genome Res. 2008
PubMed ID: 18799693
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TGF-beta signaling in thymic epithelial cells regulates thymic involution and postirradiation reconstitution.
Hauri-Hohl MM, Zuklys S, Keller MP, Jeker LT, Barthlott T, Moon AM, Roes J, Holländer GA
Blood. 2008
PubMed ID: 18474727
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Hox paralog group 2 genes control the migration of mouse pontine neurons through slit-robo signaling.
Geisen MJ, Di Meglio T, Pasqualetti M, Ducret S, Brunet JF, Chedotal A, Rijli FM
PLoS Biol. 2008
PubMed ID: 18547144
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GUDMAP: the genitourinary developmental molecular anatomy project.
McMahon AP, Aronow BJ, Davidson DR, Davies JA, Gaido KW, Grimmond S, Lessard JL, Little MH, Potter SS, Wilder EL, Zhang P, GUDMAP project
J Am Soc Nephrol. 2008
PubMed ID: 18287559
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Toward a confocal subcellular atlas of the human proteome.
Barbe L, Lundberg E, Oksvold P, Stenius A, Lewin E, Björling E, Asplund A, Pontén F, Brismar H, Uhlén M, Andersson-Svahn H
Mol Cell Proteomics. 2008
PubMed ID: 18029348
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Tshz1 is required for axial skeleton, soft palate and middle ear development in mice.
Coré N, Caubit X, Metchat A, Boned A, Djabali M, Fasano L
Dev Biol. 2007
PubMed ID: 17586487
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Wnt signaling is a key mediator of Cdx1 expression in vivo.
Pilon N, Oh K, Sylvestre JR, Savory JG, Lohnes D
Development. 2007
PubMed ID: 17537796
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Gcm2 is required for the differentiation and survival of parathyroid precursor cells in the parathyroid/thymus primordia.
Liu Z, Yu S, Manley NR
Dev Biol. 2007
PubMed ID: 17382312
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The consensus coding sequences of human breast and colorectal cancers.
Sjöblom T, Jones S, Wood LD, Parsons DW, Lin J, Barber TD, Mandelker D, Leary RJ, Ptak J, Silliman N, Szabo S, Buckhaults P, Farrell C, Meeh P, Markowitz SD, Willis J, Dawson D, Willson JK, Gazdar AF, Hartigan J, Wu L, Liu C, Parmigiani G, Park BH, Bachman KE, Papadopoulos N, Vogelstein B, Kinzler KW, Velculescu VE
Science. 2006
PubMed ID: 16959974
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A dynamic expression survey identifies transcription factors relevant in mouse digestive tract development.
Choi MY, Romer AI, Hu M, Lepourcelet M, Mechoor A, Yesilaltay A, Krieger M, Gray PA, Shivdasani RA
Development. 2006
PubMed ID: 16971476
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Fgf8 expression in the Tbx1 domain causes skeletal abnormalities and modifies the aortic arch but not the outflow tract phenotype of Tbx1 mutants.
Vitelli F, Zhang Z, Huynh T, Sobotka A, Mupo A, Baldini A
Dev Biol. 2006
PubMed ID: 16696966
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Patterning of the third pharyngeal pouch into thymus/parathyroid by Six and Eya1.
Zou D, Silvius D, Davenport J, Grifone R, Maire P, Xu PX
Dev Biol. 2006
PubMed ID: 16530750
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Homeotic transformations of the axial skeleton of YY1 mutant mice and genetic interaction with the Polycomb group gene Ring1/Ring1A.
Lorente M, Pérez C, Sánchez C, Donohoe M, Shi Y, Vidal M
Mech Dev. 2006
PubMed ID: 16624538
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Hox cofactors in vertebrate development.
Moens CB, Selleri L
Dev Biol. 2006
PubMed ID: 16515781
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Dual origins of the mouse carotid body revealed by targeted disruption of Hoxa3 and Mash1.
Kameda Y
Adv Exp Med Biol. 2006
PubMed ID: 16683703
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The high-mobility-group domain of Sox proteins interacts with DNA-binding domains of many transcription factors.
Wissmüller S, Kosian T, Wolf M, Finzsch M, Wegner M
Nucleic Acids Res. 2006
PubMed ID: 16582099
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Tbx1 expression in pharyngeal epithelia is necessary for pharyngeal arch artery development.
Zhang Z, Cerrato F, Xu H, Vitelli F, Morishima M, Vincentz J, Furuta Y, Ma L, Martin JF, Baldini A, Lindsay E
Development. 2005
PubMed ID: 16284121
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BMP signaling is required for normal thymus development.
Bleul CC, Boehm T
J Immunol. 2005
PubMed ID: 16210626
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Microarray analysis detects differentially expressed genes in the pharyngeal region of mice lacking Tbx1.
Ivins S, Lammerts van Beuren K, Roberts C, James C, Lindsay E, Baldini A, Ataliotis P, Scambler PJ
Dev Biol. 2005
PubMed ID: 16109395
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Antisense transcription in the mammalian transcriptome.
Katayama S, Tomaru Y, Kasukawa T, Waki K, Nakanishi M, Nakamura M, Nishida H, Yap CC, Suzuki M, Kawai J, Suzuki H, Carninci P, Hayashizaki Y, Wells C, Frith M, Ravasi T, Pang KC, Hallinan J, Mattick J, Hume DA, Lipovich L, Batalov S, Engström PG, Mizuno Y, Faghihi MA, Sandelin A, Chalk AM, Mottagui-Tabar S, Liang Z, Lenhard B, Wahlestedt C, RIKEN Genome Exploration Research Group, Genome Science Group (Genome Network Project Core Group), FANTOM Consortium
Science. 2005
PubMed ID: 16141073
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The transcriptional landscape of the mammalian genome.
Carninci P, Kasukawa T, Katayama S, Gough J, Frith MC, Maeda N, Oyama R, Ravasi T, Lenhard B, Wells C, Kodzius R, Shimokawa K, Bajic VB, Brenner SE, Batalov S, Forrest AR, Zavolan M, Davis MJ, Wilming LG, Aidinis V, Allen JE, Ambesi-Impiombato A, Apweiler R, Aturaliya RN, Bailey TL, Bansal M, Baxter L, Beisel KW, Bersano T, Bono H, Chalk AM, Chiu KP, Choudhary V, Christoffels A, Clutterbuck DR, Crowe ML, Dalla E, Dalrymple BP, de Bono B, Della Gatta G, di Bernardo D, Down T, Engstrom P, Fagiolini M, Faulkner G, Fletcher CF, Fukushima T, Furuno M, Futaki S, Gariboldi M, Georgii-Hemming P, Gingeras TR, Gojobori T, Green RE, Gustincich S, Harbers M, Hayashi Y, Hensch TK, Hirokawa N, Hill D, Huminiecki L, Iacono M, Ikeo K, Iwama A, Ishikawa T, Jakt M, Kanapin A, Katoh M, Kawasawa Y, Kelso J, Kitamura H, Kitano H, Kollias G, Krishnan SP, Kruger A, Kummerfeld SK, Kurochkin IV, Lareau LF, Lazarevic D, Lipovich L, Liu J, Liuni S, McWilliam S, Madan Babu M, Madera M, Marchionni L, Matsuda H, Matsuzawa S, Miki H, Mignone F, Miyake S, Morris K, Mottagui-Tabar S, Mulder N, Nakano N, Nakauchi H, Ng P, Nilsson R, Nishiguchi S, Nishikawa S, Nori F, Ohara O, Okazaki Y, Orlando V, Pang KC, Pavan WJ, Pavesi G, Pesole G, Petrovsky N, Piazza S, Reed J, Reid JF, Ring BZ, Ringwald M, Rost B, Ruan Y, Salzberg SL, Sandelin A, Schneider C, Schönbach C, Sekiguchi K, Semple CA, Seno S, Sessa L, Sheng Y, Shibata Y, Shimada H, Shimada K, Silva D, Sinclair B, Sperling S, Stupka E, Sugiura K, Sultana R, Takenaka Y, Taki K, Tammoja K, Tan SL, Tang S, Taylor MS, Tegner J, Teichmann SA, Ueda HR, van Nimwegen E, Verardo R, Wei CL, Yagi K, Yamanishi H, Zabarovsky E, Zhu S, Zimmer A, Hide W, Bult C, Grimmond SM, Teasdale RD, Liu ET, Brusic V, Quackenbush J, Wahlestedt C, Mattick JS, Hume DA, Kai C, Sasaki D, Tomaru Y, Fukuda S, Kanamori-Katayama M, Suzuki M, Aoki J, Arakawa T, Iida J, Imamura K, Itoh M, Kato T, Kawaji H, Kawagashira N, Kawashima T, Kojima M, Kondo S, Konno H, Nakano K, Ninomiya N, Nishio T, Okada M, Plessy C, Shibata K, Shiraki T, Suzuki S, Tagami M, Waki K, Watahiki A, Okamura-Oho Y, Suzuki H, Kawai J, Hayashizaki Y, FANTOM Consortium, RIKEN Genome Exploration Research Group and Genome Science Group (Genome Network Project Core Group)
Science. 2005
PubMed ID: 16141072
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HOXA3 induces cell migration in endothelial and epithelial cells promoting angiogenesis and wound repair.
Mace KA, Hansen SL, Myers C, Young DM, Boudreau N
J Cell Sci. 2005
PubMed ID: 15914537
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Hoxa3 regulates the proliferation and differentiation of the third pharyngeal arch mesenchyme in mice.
Chisaka O, Kameda Y
Cell Tissue Res. 2005
PubMed ID: 15714286
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Differential expression of Sonic hedgehog along the anterior-posterior axis regulates patterning of pharyngeal pouch endoderm and pharyngeal endoderm-derived organs.
Moore-Scott BA, Manley NR
Dev Biol. 2005
PubMed ID: 15680353
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Genomic maps and comparative analysis of histone modifications in human and mouse.
Bernstein BE, Kamal M, Lindblad-Toh K, Bekiranov S, Bailey DK, Huebert DJ, McMahon S, Karlsson EK, Kulbokas EJ, Gingeras TR, Schreiber SL, Lander ES
Cell. 2005
PubMed ID: 15680324
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Mapping DNA-protein interactions in large genomes by sequence tag analysis of genomic enrichment.
Kim J, Bhinge AA, Morgan XC, Iyer VR
Nat Methods. 2005
PubMed ID: 15782160
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Gene and alternative splicing annotation with AIR.
Florea L, Di Francesco V, Miller J, Turner R, Yao A, Harris M, Walenz B, Mobarry C, Merkulov GV, Charlab R, Dew I, Deng Z, Istrail S, Li P, Sutton G
Genome Res. 2005
PubMed ID: 15632090
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Mouse brain organization revealed through direct genome-scale TF expression analysis.
Gray PA, Fu H, Luo P, Zhao Q, Yu J, Ferrari A, Tenzen T, Yuk DI, Tsung EF, Cai Z, Alberta JA, Cheng LP, Liu Y, Stenman JM, Valerius MT, Billings N, Kim HA, Greenberg ME, McMahon AP, Rowitch DH, Stiles CD, Ma Q
Science. 2004
PubMed ID: 15618518
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Abnormalities of caudal pharyngeal pouch development in Pbx1 knockout mice mimic loss of Hox3 paralogs.
Manley NR, Selleri L, Brendolan A, Gordon J, Cleary ML
Dev Biol. 2004
PubMed ID: 15581866
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The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC).
Gerhard DS, Wagner L, Feingold EA, Shenmen CM, Grouse LH, Schuler G, Klein SL, Old S, Rasooly R, Good P, Guyer M, Peck AM, Derge JG, Lipman D, Collins FS, Jang W, Sherry S, Feolo M, Misquitta L, Lee E, Rotmistrovsky K, Greenhut SF, Schaefer CF, Buetow K, Bonner TI, Haussler D, Kent J, Kiekhaus M, Furey T, Brent M, Prange C, Schreiber K, Shapiro N, Bhat NK, Hopkins RF, Hsie F, Driscoll T, Soares MB, Casavant TL, Scheetz TE, Brown-stein MJ, Usdin TB, Toshiyuki S, Carninci P, Piao Y, Dudekula DB, Ko MS, Kawakami K, Suzuki Y, Sugano S, Gruber CE, Smith MR, Simmons B, Moore T, Waterman R, Johnson SL, Ruan Y, Wei CL, Mathavan S, Gunaratne PH, Wu J, Garcia AM, Hulyk SW, Fuh E, Yuan Y, Sneed A, Kowis C, Hodgson A, Muzny DM, McPherson J, Gibbs RA, Fahey J, Helton E, Ketteman M, Madan A, Rodrigues S, Sanchez A, Whiting M, Madari A, Young AC, Wetherby KD, Granite SJ, Kwong PN, Brinkley CP, Pearson RL, Bouffard GG, Blakesly RW, Green ED, Dickson MC, Rodriguez AC, Grimwood J, Schmutz J, Myers RM, Butterfield YS, Griffith M, Griffith OL, Krzywinski MI, Liao N, Morin R, Morrin R, Palmquist D, Petrescu AS, Skalska U, Smailus DE, Stott JM, Schnerch A, Schein JE, Jones SJ, Holt RA, Baross A, Marra MA, Clifton S, Makowski KA, Bosak S, Malek J, MGC Project Team
Genome Res. 2004
PubMed ID: 15489334
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The proximal 2-kb of the Hoxa3 promoter directs gene expression in distinct branchial compartments and cranial ganglia.
Diman NY, Chauvier E, Pacico N, Picard JJ, Rezsohazy R
Brain Res Dev Brain Res. 2004
PubMed ID: 15158084
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The role of Hoxa3 gene in parathyroid gland organogenesis of the mouse.
Kameda Y, Arai Y, Nishimaki T, Chisaka O
J Histochem Cytochem. 2004
PubMed ID: 15100241
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Genome sequence of the Brown Norway rat yields insights into mammalian evolution.
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Nature. 2004
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Atlas of Hox gene expression in the developing kidney.
Patterson LT, Potter SS
Dev Dyn. 2004
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Gaufo GO, Wu S, Capecchi MR
Development. 2004
PubMed ID: 14960494
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Nat Genet. 2004
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Houle M, Sylvestre JR, Lohnes D
Development. 2003
PubMed ID: 14660544
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Ablation of specific expression domains reveals discrete functions of ectoderm- and endoderm-derived FGF8 during cardiovascular and pharyngeal development.
Macatee TL, Hammond BP, Arenkiel BR, Francis L, Frank DU, Moon AM
Development. 2003
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Hox3 genes coordinate mechanisms of genetic suppression and activation in the generation of branchial and somatic motoneurons.
Gaufo GO, Thomas KR, Capecchi MR
Development. 2003
PubMed ID: 12954718
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The DNA sequence of human chromosome 7.
Hillier LW, Fulton RS, Fulton LA, Graves TA, Pepin KH, Wagner-McPherson C, Layman D, Maas J, Jaeger S, Walker R, Wylie K, Sekhon M, Becker MC, O'Laughlin MD, Schaller ME, Fewell GA, Delehaunty KD, Miner TL, Nash WE, Cordes M, Du H, Sun H, Edwards J, Bradshaw-Cordum H, Ali J, Andrews S, Isak A, Vanbrunt A, Nguyen C, Du F, Lamar B, Courtney L, Kalicki J, Ozersky P, Bielicki L, Scott K, Holmes A, Harkins R, Harris A, Strong CM, Hou S, Tomlinson C, Dauphin-Kohlberg S, Kozlowicz-Reilly A, Leonard S, Rohlfing T, Rock SM, Tin-Wollam AM, Abbott A, Minx P, Maupin R, Strowmatt C, Latreille P, Miller N, Johnson D, Murray J, Woessner JP, Wendl MC, Yang SP, Schultz BR, Wallis JW, Spieth J, Bieri TA, Nelson JO, Berkowicz N, Wohldmann PE, Cook LL, Hickenbotham MT, Eldred J, Williams D, Bedell JA, Mardis ER, Clifton SW, Chissoe SL, Marra MA, Raymond C, Haugen E, Gillett W, Zhou Y, James R, Phelps K, Iadanoto S, Bubb K, Simms E, Levy R, Clendenning J, Kaul R, Kent WJ, Furey TS, Baertsch RA, Brent MR, Keibler E, Flicek P, Bork P, Suyama M, Bailey JA, Portnoy ME, Torrents D, Chinwalla AT, Gish WR, Eddy SR, McPherson JD, Olson MV, Eichler EE, Green ED, Waterston RH, Wilson RK
Nature. 2003
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Meunier D, Aubin J, Jeannotte L
Dev Dyn. 2003
PubMed ID: 12815622
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c-jun regulation and function in the developing hindbrain.
Mechta-Grigoriou F, Giudicelli F, Pujades C, Charnay P, Yaniv M
Dev Biol. 2003
PubMed ID: 12798298
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Human chromosome 7: DNA sequence and biology.
Scherer SW, Cheung J, MacDonald JR, Osborne LR, Nakabayashi K, Herbrick JA, Carson AR, Parker-Katiraee L, Skaug J, Khaja R, Zhang J, Hudek AK, Li M, Haddad M, Duggan GE, Fernandez BA, Kanematsu E, Gentles S, Christopoulos CC, Choufani S, Kwasnicka D, Zheng XH, Lai Z, Nusskern D, Zhang Q, Gu Z, Lu F, Zeesman S, Nowaczyk MJ, Teshima I, Chitayat D, Shuman C, Weksberg R, Zackai EH, Grebe TA, Cox SR, Kirkpatrick SJ, Rahman N, Friedman JM, Heng HH, Pelicci PG, Lo-Coco F, Belloni E, Shaffer LG, Pober B, Morton CC, Gusella JF, Bruns GA, Korf BR, Quade BJ, Ligon AH, Ferguson H, Higgins AW, Leach NT, Herrick SR, Lemyre E, Farra CG, Kim HG, Summers AM, Gripp KW, Roberts W, Szatmari P, Winsor EJ, Grzeschik KH, Teebi A, Minassian BA, Kere J, Armengol L, Pujana MA, Estivill X, Wilson MD, Koop BF, Tosi S, Moore GE, Boright AP, Zlotorynski E, Kerem B, Kroisel PM, Petek E, Oscier DG, Mould SJ, Döhner H, Döhner K, Rommens JM, Vincent JB, Venter JC, Li PW, Mural RJ, Adams MD, Tsui LC
Science. 2003
PubMed ID: 12690205
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Reversible gene inactivation in the mouse.
Mallo M, Kanzler B, Ohnemus S
Genomics. 2003
PubMed ID: 12676559
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Disruption of the Hoxa3 homeobox gene results in anomalies of the carotid artery system and the arterial baroreceptors.
Kameda Y, Watari-Goshima N, Nishimaki T, Chisaka O
Cell Tissue Res. 2003
PubMed ID: 12658442
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Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences.
Strausberg RL, Feingold EA, Grouse LH, Derge JG, Klausner RD, Collins FS, Wagner L, Shenmen CM, Schuler GD, Altschul SF, Zeeberg B, Buetow KH, Schaefer CF, Bhat NK, Hopkins RF, Jordan H, Moore T, Max SI, Wang J, Hsieh F, Diatchenko L, Marusina K, Farmer AA, Rubin GM, Hong L, Stapleton M, Soares MB, Bonaldo MF, Casavant TL, Scheetz TE, Brownstein MJ, Usdin TB, Toshiyuki S, Carninci P, Prange C, Raha SS, Loquellano NA, Peters GJ, Abramson RD, Mullahy SJ, Bosak SA, McEwan PJ, McKernan KJ, Malek JA, Gunaratne PH, Richards S, Worley KC, Hale S, Garcia AM, Gay LJ, Hulyk SW, Villalon DK, Muzny DM, Sodergren EJ, Lu X, Gibbs RA, Fahey J, Helton E, Ketteman M, Madan A, Rodrigues S, Sanchez A, Whiting M, Madan A, Young AC, Shevchenko Y, Bouffard GG, Blakesley RW, Touchman JW, Green ED, Dickson MC, Rodriguez AC, Grimwood J, Schmutz J, Myers RM, Butterfield YS, Krzywinski MI, Skalska U, Smailus DE, Schnerch A, Schein JE, Jones SJ, Marra MA, Mammalian Gene Collection Program Team
Proc Natl Acad Sci U S A. 2002
PubMed ID: 12477932
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Analysis of the mouse transcriptome based on functional annotation of 60,770 full-length cDNAs.
Okazaki Y, Furuno M, Kasukawa T, Adachi J, Bono H, Kondo S, Nikaido I, Osato N, Saito R, Suzuki H, Yamanaka I, Kiyosawa H, Yagi K, Tomaru Y, Hasegawa Y, Nogami A, Schönbach C, Gojobori T, Baldarelli R, Hill DP, Bult C, Hume DA, Quackenbush J, Schriml LM, Kanapin A, Matsuda H, Batalov S, Beisel KW, Blake JA, Bradt D, Brusic V, Chothia C, Corbani LE, Cousins S, Dalla E, Dragani TA, Fletcher CF, Forrest A, Frazer KS, Gaasterland T, Gariboldi M, Gissi C, Godzik A, Gough J, Grimmond S, Gustincich S, Hirokawa N, Jackson IJ, Jarvis ED, Kanai A, Kawaji H, Kawasawa Y, Kedzierski RM, King BL, Konagaya A, Kurochkin IV, Lee Y, Lenhard B, Lyons PA, Maglott DR, Maltais L, Marchionni L, McKenzie L, Miki H, Nagashima T, Numata K, Okido T, Pavan WJ, Pertea G, Pesole G, Petrovsky N, Pillai R, Pontius JU, Qi D, Ramachandran S, Ravasi T, Reed JC, Reed DJ, Reid J, Ring BZ, Ringwald M, Sandelin A, Schneider C, Semple CA, Setou M, Shimada K, Sultana R, Takenaka Y, Taylor MS, Teasdale RD, Tomita M, Verardo R, Wagner L, Wahlestedt C, Wang Y, Watanabe Y, Wells C, Wilming LG, Wynshaw-Boris A, Yanagisawa M, Yang I, Yang L, Yuan Z, Zavolan M, Zhu Y, Zimmer A, Carninci P, Hayatsu N, Hirozane-Kishikawa T, Konno H, Nakamura M, Sakazume N, Sato K, Shiraki T, Waki K, Kawai J, Aizawa K, Arakawa T, Fukuda S, Hara A, Hashizume W, Imotani K, Ishii Y, Itoh M, Kagawa I, Miyazaki A, Sakai K, Sasaki D, Shibata K, Shinagawa A, Yasunishi A, Yoshino M, Waterston R, Lander ES, Rogers J, Birney E, Hayashizaki Y, FANTOM Consortium, RIKEN Genome Exploration Research Group Phase I & II Team
Nature. 2002
PubMed ID: 12466851
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Aortic arch and pharyngeal phenotype in the absence of BMP-dependent neural crest in the mouse.
Ohnemus S, Kanzler B, Jerome-Majewska LA, Papaioannou VE, Boehm T, Mallo M
Mech Dev. 2002
PubMed ID: 12464426
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Mouse Af9 is a controller of embryo patterning, like Mll, whose human homologue fuses with Af9 after chromosomal translocation in leukemia.
Collins EC, Appert A, Ariza-McNaughton L, Pannell R, Yamada Y, Rabbitts TH
Mol Cell Biol. 2002
PubMed ID: 12242306
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Homeobox gene hoxa3 is essential for the formation of the carotid body in the mouse embryos.
Kameda Y, Nishimaki T, Takeichi M, Chisaka O
Dev Biol. 2002
PubMed ID: 12074562
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Eya1 is required for the morphogenesis of mammalian thymus, parathyroid and thyroid.
Xu PX, Zheng W, Laclef C, Maire P, Maas RL, Peters H, Xu X
Development. 2002
PubMed ID: 12070080
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Requirement for downregulation of kreisler during late patterning of the hindbrain.
Theil T, Ariza-McNaughton L, Manzanares M, Brodie J, Krumlauf R, Wilkinson DG
Development. 2002
PubMed ID: 11880356
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Complete mutation analysis panel of the 39 human HOX genes.
Kosaki K, Kosaki R, Suzuki T, Yoshihashi H, Takahashi T, Sasaki K, Tomita M, McGinnis W, Matsuo N
Teratology. 2002
PubMed ID: 11857506
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Krox20 and kreisler co-operate in the transcriptional control of segmental expression of Hoxb3 in the developing hindbrain.
Manzanares M, Nardelli J, Gilardi-Hebenstreit P, Marshall H, Giudicelli F, Martínez-Pastor MT, Krumlauf R, Charnay P
EMBO J. 2002
PubMed ID: 11823429
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Hoxa3 regulates integration of glossopharyngeal nerve precursor cells.
Watari N, Kameda Y, Takeichi M, Chisaka O
Dev Biol. 2001
PubMed ID: 11784044
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PTH regulates fetal blood calcium and skeletal mineralization independently of PTHrP.
Kovacs CS, Chafe LL, Fudge NJ, Friel JK, Manley NR
Endocrinology. 2001
PubMed ID: 11606467
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Independent regulation of initiation and maintenance phases of Hoxa3 expression in the vertebrate hindbrain involve auto- and cross-regulatory mechanisms.
Manzanares M, Bel-Vialar S, Ariza-McNaughton L, Ferretti E, Marshall H, Maconochie MM, Blasi F, Krumlauf R
Development. 2001
PubMed ID: 11566863
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Hoxa3 and pax1 regulate epithelial cell death and proliferation during thymus and parathyroid organogenesis.
Su D, Ellis S, Napier A, Lee K, Manley NR
Dev Biol. 2001
PubMed ID: 11476574
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Fetal parathyroids are not required to maintain placental calcium transport.
Kovacs CS, Manley NR, Moseley JM, Martin TJ, Kronenberg HM
J Clin Invest. 2001
PubMed ID: 11306604
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Functional annotation of a full-length mouse cDNA collection.
Kawai J, Shinagawa A, Shibata K, Yoshino M, Itoh M, Ishii Y, Arakawa T, Hara A, Fukunishi Y, Konno H, Adachi J, Fukuda S, Aizawa K, Izawa M, Nishi K, Kiyosawa H, Kondo S, Yamanaka I, Saito T, Okazaki Y, Gojobori T, Bono H, Kasukawa T, Saito R, Kadota K, Matsuda H, Ashburner M, Batalov S, Casavant T, Fleischmann W, Gaasterland T, Gissi C, King B, Kochiwa H, Kuehl P, Lewis S, Matsuo Y, Nikaido I, Pesole G, Quackenbush J, Schriml LM, Staubli F, Suzuki R, Tomita M, Wagner L, Washio T, Sakai K, Okido T, Furuno M, Aono H, Baldarelli R, Barsh G, Blake J, Boffelli D, Bojunga N, Carninci P, de Bonaldo MF, Brownstein MJ, Bult C, Fletcher C, Fujita M, Gariboldi M, Gustincich S, Hill D, Hofmann M, Hume DA, Kamiya M, Lee NH, Lyons P, Marchionni L, Mashima J, Mazzarelli J, Mombaerts P, Nordone P, Ring B, Ringwald M, Rodriguez I, Sakamoto N, Sasaki H, Sato K, Schönbach C, Seya T, Shibata Y, Storch KF, Suzuki H, Toyo-oka K, Wang KH, Weitz C, Whittaker C, Wilming L, Wynshaw-Boris A, Yoshida K, Hasegawa Y, Kawaji H, Kohtsuki S, Hayashizaki Y, RIKEN Genome Exploration Research Group Phase II Team and the FANTOM Consortium
Nature. 2001
PubMed ID: 11217851
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RIKEN integrated sequence analysis (RISA) system--384-format sequencing pipeline with 384 multicapillary sequencer.
Shibata K, Itoh M, Aizawa K, Nagaoka S, Sasaki N, Carninci P, Konno H, Akiyama J, Nishi K, Kitsunai T, Tashiro H, Itoh M, Sumi N, Ishii Y, Nakamura S, Hazama M, Nishine T, Harada A, Yamamoto R, Matsumoto H, Sakaguchi S, Ikegami T, Kashiwagi K, Fujiwake S, Inoue K, Togawa Y
Genome Res. 2000
PubMed ID: 11076861
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Normalization and subtraction of cap-trapper-selected cDNAs to prepare full-length cDNA libraries for rapid discovery of new genes.
Carninci P, Shibata Y, Hayatsu N, Sugahara Y, Shibata K, Itoh M, Konno H, Okazaki Y, Muramatsu M, Hayashizaki Y
Genome Res. 2000
PubMed ID: 11042159
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Effects of excess vitamin A on development of cranial neural crest-derived structures: a neonatal and embryologic study.
Mulder GB, Manley N, Grant J, Schmidt K, Zeng W, Eckhoff C, Maggio-Price L
Teratology. 2000
PubMed ID: 10992263
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Hoxa3 and pax1 transcription factors regulate the ability of fetal thymic epithelial cells to promote thymocyte development.
Su DM, Manley NR
J Immunol. 2000
PubMed ID: 10820253
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Maintenance of functional equivalence during paralogous Hox gene evolution.
Greer JM, Puetz J, Thomas KR, Capecchi MR
Nature. 2000
PubMed ID: 10688203
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Retinoic acid synthesis and hindbrain patterning in the mouse embryo.
Niederreither K, Vermot J, Schuhbaur B, Chambon P, Dollé P
Development. 2000
PubMed ID: 10654602
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Targeting genes for self-excision in the germ line.
Bunting M, Bernstein KE, Greer JM, Capecchi MR, Thomas KR
Genes Dev. 1999
PubMed ID: 10385621
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Conserved and distinct roles of kreisler in regulation of the paralogous Hoxa3 and Hoxb3 genes.
Manzanares M, Cordes S, Ariza-McNaughton L, Sadl V, Maruthainar K, Barsh G, Krumlauf R
Development. 1999
PubMed ID: 9895323
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High-efficiency full-length cDNA cloning.
Carninci P, Hayashizaki Y
Methods Enzymol. 1999
PubMed ID: 10349636
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Retinoic acid-induced thymic abnormalities in the mouse are associated with altered pharyngeal morphology, thymocyte maturation defects, and altered expression of Hoxa3 and Pax1.
Mulder GB, Manley N, Maggio-Price L
Teratology. 1998
PubMed ID: 9894676
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Toward a complete human genome sequence.
Genome Res. 1998
PubMed ID: 9847074
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Retardation of skeletal development and cervical abnormalities in transgenic mice expressing a dominant-negative retinoic acid receptor in chondrogenic cells.
Yamaguchi M, Nakamoto M, Honda H, Nakagawa T, Fujita H, Nakamura T, Hirai H, Narumiya S, Kakizuka A
Proc Natl Acad Sci U S A. 1998
PubMed ID: 9636177
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Molecular cloning of human and bovine LECT2 having a neutrophil chemotactic activity and its specific expression in the liver.
Yamagoe S, Mizuno S, Suzuki K
Biochim Biophys Acta. 1998
PubMed ID: 9524238
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Hox group 3 paralogs regulate the development and migration of the thymus, thyroid, and parathyroid glands.
Manley NR, Capecchi MR
Dev Biol. 1998
PubMed ID: 9520319
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Genetic mapping of mouse centromere protein (Incenp and Cenpe) genes.
Fowler KJ, Saffery R, Kile BT, Irvine DV, Hudson DF, Trowell HE, Choo KH
Cytogenet Cell Genet. 1998
PubMed ID: 9763662
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Hox group 3 paralogous genes act synergistically in the formation of somitic and neural crest-derived structures.
Manley NR, Capecchi MR
Dev Biol. 1997
PubMed ID: 9441667
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Homeobox genes from clusters A and B demonstrate characteristics of temporal colinearity and differential restrictions in spatial expression domains in the branching mouse lung.
Mollard R, Dziadek M
Int J Dev Biol. 1997
PubMed ID: 9415485
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Targeted disruption of the mouse homologue of the Drosophila polyhomeotic gene leads to altered anteroposterior patterning and neural crest defects.
Takihara Y, Tomotsune D, Shirai M, Katoh-Fukui Y, Nishii K, Motaleb MA, Nomura M, Tsuchiya R, Fujita Y, Shibata Y, Higashinakagawa T, Shimada K
Development. 1997
PubMed ID: 9367423
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Altered cellular proliferation and mesoderm patterning in Polycomb-M33-deficient mice.
Coré N, Bel S, Gaunt SJ, Aurrand-Lions M, Pearce J, Fisher A, Djabali M
Development. 1997
PubMed ID: 9043087
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Pax3 is required for cardiac neural crest migration in the mouse: evidence from the splotch (Sp2H) mutant.
Conway SJ, Henderson DJ, Copp AJ
Development. 1997
PubMed ID: 9053326
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In vivo functional analysis of the Hoxa-1 3' retinoic acid response element (3'RARE).
Dupé V, Davenne M, Brocard J, Dollé P, Mark M, Dierich A, Chambon P, Rijli FM
Development. 1997
PubMed ID: 9053316
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Normalization and subtraction: two approaches to facilitate gene discovery.
Bonaldo MF, Lennon G, Soares MB
Genome Res. 1996
PubMed ID: 8889548
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Sequence and expression of the murine Hoxd-3 homeobox gene.
Tan DP, Shao X, Pu L, Guo V, Nirenberg M
Proc Natl Acad Sci U S A. 1996
PubMed ID: 8710855
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Orientation of the Hoxa complex and placement of the Hd locus distal to Hoxa2 on mouse chromosome 6.
Innis JW, Darling SM, Kazen-Gillespie K, Post LC, Mortlock DP, Yang T
Mamm Genome. 1996
PubMed ID: 8833244
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Genetic composition of the recombinant congenic strains.
Stassen AP, Groot PC, Eppig JT, Demant P
Mamm Genome. 1996
PubMed ID: 8903730
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Fine mapping of human HOX gene clusters.
Apiou F, Flagiello D, Cillo C, Malfoy B, Poupon MF, Dutrillaux B
Cytogenet Cell Genet. 1996
PubMed ID: 8646877
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The role of Hoxa-3 in mouse thymus and thyroid development.
Manley NR, Capecchi MR
Development. 1995
PubMed ID: 7635047
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Ectopic Hoxa-1 induces rhombomere transformation in mouse hindbrain.
Zhang M, Kim HJ, Marshall H, Gendron-Maguire M, Lucas DA, Baron A, Gudas LJ, Gridley T, Krumlauf R, Grippo JF
Development. 1994
PubMed ID: 7956823
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The kreisler mouse: a hindbrain segmentation mutant that lacks two rhombomeres.
McKay IJ, Muchamore I, Krumlauf R, Maden M, Lumsden A, Lewis J
Development. 1994
PubMed ID: 7925021
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Mice with targeted disruptions in the paralogous genes hoxa-3 and hoxd-3 reveal synergistic interactions.
Condie BG, Capecchi MR
Nature. 1994
PubMed ID: 7913519
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Forward spreading in the establishment of a vertebrate Hox expression boundary: the expression domain separates into anterior and posterior zones, and the spread occurs across implanted glass barriers.
Gaunt SJ, Strachan L
Dev Dyn. 1994
PubMed ID: 7912569
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A homeotic transformation is generated in the rostral branchial region of the head by disruption of Hoxa-2, which acts as a selector gene.
Rijli FM, Mark M, Lakkaraju S, Dierich A, Dollé P, Chambon P
Cell. 1993
PubMed ID: 7903601
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Hoxa-2 mutant mice exhibit homeotic transformation of skeletal elements derived from cranial neural crest.
Gendron-Maguire M, Mallo M, Zhang M, Gridley T
Cell. 1993
PubMed ID: 7903600
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Mice homozygous for a targeted disruption of Hoxd-3 (Hox-4.1) exhibit anterior transformations of the first and second cervical vertebrae, the atlas and the axis.
Condie BG, Capecchi MR
Development. 1993
PubMed ID: 7910549
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Local alterations of Krox-20 and Hox gene expression in the hindbrain suggest lack of rhombomeres 4 and 5 in homozygote null Hoxa-1 (Hox-1.6) mutant embryos.
Dollé P, Lufkin T, Krumlauf R, Mark M, Duboule D, Chambon P
Proc Natl Acad Sci U S A. 1993
PubMed ID: 8102800
-
Nucleotides flanking a conserved TAAT core dictate the DNA binding specificity of three murine homeodomain proteins.
Catron KM, Iler N, Abate C
Mol Cell Biol. 1993
PubMed ID: 8096059
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Reversal of axonal pathways from rhombomere 3 correlates with extra Hox expression domains.
Kessel M
Neuron. 1993
PubMed ID: 8096385
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Conservation and divergence of patterns of expression and lineage-specific transcripts in orthologues and paralogues of the mouse Hox-1.4 gene.
Watrin F, Wolgemuth DJ
Dev Biol. 1993
PubMed ID: 7680626
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Expression of the mouse goosecoid gene during mid-embryogenesis may mark mesenchymal cell lineages in the developing head, limbs and body wall.
Gaunt SJ, Blum M, De Robertis EM
Development. 1993
PubMed ID: 8101169
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Vertebrate homeobox gene nomenclature.
Scott MP
Cell. 1992
PubMed ID: 1358459
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Hox-1.11 and Hox-4.9 homeobox genes.
Nazarali A, Kim Y, Nirenberg M
Proc Natl Acad Sci U S A. 1992
PubMed ID: 1348361
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Multilocus markers for mouse genome analysis: PCR amplification based on single primers of arbitrary nucleotide sequence.
Nadeau JH, Bedigian HG, Bouchard G, Denial T, Kosowsky M, Norberg R, Pugh S, Sargeant E, Turner R, Paigen B
Mamm Genome. 1992
PubMed ID: 1617215
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A distinct Hox code for the branchial region of the vertebrate head.
Hunt P, Gulisano M, Cook M, Sham MH, Faiella A, Wilkinson D, Boncinelli E, Krumlauf R
Nature. 1991
PubMed ID: 1682814
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Homeotic transformations of murine vertebrae and concomitant alteration of Hox codes induced by retinoic acid.
Kessel M, Gruss P
Cell. 1991
PubMed ID: 1680565
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Disruption of the Hox-1.6 homeobox gene results in defects in a region corresponding to its rostral domain of expression.
Lufkin T, Dierich A, LeMeur M, Mark M, Chambon P
Cell. 1991
PubMed ID: 1680563
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Regionally restricted developmental defects resulting from targeted disruption of the mouse homeobox gene hox-1.5.
Chisaka O, Capecchi MR
Nature. 1991
PubMed ID: 1673020
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The branchial Hox code and its implications for gene regulation, patterning of the nervous system and head evolution.
Hunt P, Whiting J, Nonchev S, Sham MH, Marshall H, Graham A, Cook M, Allemann R, Rigby PW, Gulisano M
Development. 1991
PubMed ID: 1688181
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The recombinant congenic strains--a novel genetic tool applied to the study of colon tumor development in the mouse.
Moen CJ, van der Valk MA, Snoek M, van Zutphen BF, von Deimling O, Hart AA, Demant P
Mamm Genome. 1991
PubMed ID: 1686571
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Nomenclature for human homeobox genes.
McAlpine PJ, Shows TB
Genomics. 1990
PubMed ID: 1973146
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Mouse Hox-3.4: homeobox sequence and embryonic expression patterns compared with other members of the Hox gene network.
Gaunt SJ, Coletta PL, Pravtcheva D, Sharpe PT
Development. 1990
PubMed ID: 1976088
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Mouse homeo-genes within a subfamily, Hox-1.4, -2.6 and -5.1, display similar anteroposterior domains of expression in the embryo, but show stage- and tissue-dependent differences in their regulation.
Gaunt SJ, Krumlauf R, Duboule D
Development. 1989
PubMed ID: 2576400
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Mouse homeobox gene transcripts occupy different but overlapping domains in embryonic germ layers and organs: a comparison of Hox-3.1 and Hox-1.5.
Gaunt SJ
Development. 1988
PubMed ID: 2904354
-
Expression of the murine homeo box gene Hox 1.5 during embryogenesis.
Fainsod A, Awgulewitsch A, Ruddle FH
Dev Biol. 1987
PubMed ID: 2444477
-
Hox-1.6: a mouse homeo-box-containing gene member of the Hox-1 complex.
Baron A, Featherstone MS, Hill RE, Hall A, Galliot B, Duboule D
EMBO J. 1987
PubMed ID: 2891503
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Homoeobox gene Hox-1.5 expression in mouse embryos: earliest detection by in situ hybridization is during gastrulation.
Gaunt SJ
Development. 1987
PubMed ID: 2452725
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A mouse homeo box gene, Hox-1.5, and the morphological locus, Hd, map to within 1 cM on chromosome 6.
Mock BA, D'Hoostelaere LA, Matthai R, Huppi K
Genetics. 1987
PubMed ID: 2887485
-
Homoeobox gene expression in mouse embryos varies with position by the primitive streak stage.
Gaunt SJ, Miller JR, Powell DJ, Duboule D
Nature. 1986
PubMed ID: 2879244
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The homeo domain of a murine protein binds 5' to its own homeo box.
Fainsod A, Bogarad LD, Ruusala T, Lubin M, Crothers DM, Ruddle FH
Proc Natl Acad Sci U S A. 1986
PubMed ID: 2879282
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Cognate homeo-box loci mapped on homologous human and mouse chromosomes.
Rabin M, Ferguson-Smith A, Hart CP, Ruddle FH
Proc Natl Acad Sci U S A. 1986
PubMed ID: 2878432
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A new homeo-box is present in overlapping cosmid clones which define the mouse Hox-1 locus.
Duboule D, Baron A, Mähl P, Galliot B
EMBO J. 1986
PubMed ID: 3019676
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Mammalian homeo box genes.
Ruddle FH, Hart CP, Awgulewitsch A, Fainsod A, Utset M, Dalton D, Kerk N, Rabin M, Ferguson-Smith A, Fienberg A
Cold Spring Harb Symp Quant Biol. 1985
PubMed ID: 2420513
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Molecular cloning and chromosome mapping of a mouse DNA sequence homologous to homeotic genes of Drosophila.
McGinnis W, Hart CP, Gehring WJ, Ruddle FH
Cell. 1984
PubMed ID: 6091896
Model Organism Phenotype Links
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This section provides links to model organism phenotype resources. Currently only to mouse phenotypes.
External resources (dkCOIN) from NIDDK Consortium Interconnectivity Network
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