HOXA7
| Gene Description: |
homeobox A7 |
| Synonyms: |
HOX1, Hoxa7, HOX1.1, HOXA7, AV118143, HOX1A, Hox-1.1, ANTP |
| Orthologs: |
Human HOXA7 (protein-coding), Mouse Hoxa7 (protein-coding)
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Sources
Sources
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Human-Mouse:
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HomoloGene, MGD
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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
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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no data |
no data |
no data |
no data |
no data |
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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 HOXA7:
The HOXA7 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.
| Interactor |
Interactor |
Sources |
Classification |
Pubmed IDs |
| HOXA7 |
MEIS1 |
HPRD |
empirical |
9405651
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| HOXA7 |
GMNN |
HPRD, MINT, IntAct |
empirical |
14973489
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Cross-Reference to Pathways and GO Terms
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View all
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KEGG Network: None available
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Biocarta: 1
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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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| Negative regulation of transcription from RNA polymerase II promoter |
GO:0000122 |
| Angiogenesis |
GO:0001525 |
| Negative regulation of cell-matrix adhesion |
GO:0001953 |
| Negative regulation of leukocyte migration |
GO:0002686 |
| Sequence-specific DNA binding transcription factor activity |
GO:0003700 |
| Nucleus |
GO:0005634 |
| Multicellular organismal development |
GO:0007275 |
| Transcription factor binding |
GO:0008134 |
| Anterior/posterior pattern specification |
GO:0009952 |
| Sequence-specific DNA binding |
GO:0043565 |
| Negative regulation of keratinocyte differentiation |
GO:0045617 |
| Negative regulation of monocyte differentiation |
GO:0045656 |
| Negative regulation of transcription, DNA-dependent |
GO:0045892 |
| Positive regulation of transcription from RNA polymerase II promoter |
GO:0045944 |
| Embryonic skeletal system morphogenesis |
GO:0048704 |
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KEGG Network: None available
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Biocarta: 1 |
| Keratinocyte Differentiation |
Human |
Mouse |
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NCI-Nature Pathway Interaction Database: None available
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Gene Ontology: 15 |
| Negative regulation of transcription from RNA polymerase II promoter |
GO:0000122 |
| Angiogenesis |
GO:0001525 |
| Negative regulation of cell-matrix adhesion |
GO:0001953 |
| Negative regulation of leukocyte migration |
GO:0002686 |
| Sequence-specific DNA binding transcription factor activity |
GO:0003700 |
| Nucleus |
GO:0005634 |
| Multicellular organismal development |
GO:0007275 |
| Transcription factor binding |
GO:0008134 |
| Anterior/posterior pattern specification |
GO:0009952 |
| Sequence-specific DNA binding |
GO:0043565 |
| Negative regulation of keratinocyte differentiation |
GO:0045617 |
| Negative regulation of monocyte differentiation |
GO:0045656 |
| Negative regulation of transcription, DNA-dependent |
GO:0045892 |
| Positive regulation of transcription from RNA polymerase II promoter |
GO:0045944 |
| Embryonic skeletal system morphogenesis |
GO:0048704 |
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Publications: 114
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Down-regulation of homeobox genes MEIS1 and HOXA in MLL-rearranged acute leukemia impairs engraftment and reduces proliferation.
Orlovsky K, Kalinkovich A, Rozovskaia T, Shezen E, Itkin T, Alder H, Ozer HG, Carramusa L, Avigdor A, Volinia S, Buchberg A, Mazo A, Kollet O, Largman C, Croce CM, Nakamura T, Lapidot T, Canaani E
Proc Natl Acad Sci U S A. 2011
PubMed ID: 21518888
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Ribosome-mediated specificity in Hox mRNA translation and vertebrate tissue patterning.
Kondrashov N, Pusic A, Stumpf CR, Shimizu K, Hsieh AC, Xue S, Ishijima J, Shiroishi T, Barna M
Cell. 2011
PubMed ID: 21529712
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In situ hybridization detection of homeobox genes reveals distinct expression patterns in oral squamous cell carcinomas.
Libório TN, Acquafreda T, Matizonkas-Antonio LF, Silva-Valenzuela MG, Ferraz AR, Nunes FD
Histopathology. 2011
PubMed ID: 21323949
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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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Hoxa9 regulates Flt3 in lymphohematopoietic progenitors.
Gwin K, Frank E, Bossou A, Medina KL
J Immunol. 2010
PubMed ID: 20971928
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Global control of motor neuron topography mediated by the repressive actions of a single hox gene.
Jung H, Lacombe J, Mazzoni EO, Liem KF, Grinstein J, Mahony S, Mukhopadhyay D, Gifford DK, Young RA, Anderson KV, Wichterle H, Dasen JS
Neuron. 2010
PubMed ID: 20826310
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Ring1B and Suv39h1 delineate distinct chromatin states at bivalent genes during early mouse lineage commitment.
Alder O, Lavial F, Helness A, Brookes E, Pinho S, Chandrashekran A, Arnaud P, Pombo A, O'Neill L, Azuara V
Development. 2010
PubMed ID: 20573702
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Pentapeptide insertion mutagenesis of the Hoxa1 protein: mapping of transcription activation and DNA-binding regulatory domains.
Lambert B, Vandeputte J, Desmet PM, Hallet B, Remacle S, Rezsohazy R
J Cell Biochem. 2010
PubMed ID: 20336696
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SUMO-specific protease 2 is essential for suppression of polycomb group protein-mediated gene silencing during embryonic development.
Kang X, Qi Y, Zuo Y, Wang Q, Zou Y, Schwartz RJ, Cheng J, Yeh ET
Mol Cell. 2010
PubMed ID: 20417598
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Maternal genes and facial clefts in offspring: a comprehensive search for genetic associations in two population-based cleft studies from Scandinavia.
Jugessur A, Shi M, Gjessing HK, Lie RT, Wilcox AJ, Weinberg CR, Christensen K, Boyles AL, Daack-Hirsch S, Nguyen TT, Christiansen L, Lidral AC, Murray JC
PLoS One. 2010
PubMed ID: 20634891
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Homeobox A7 increases cell proliferation by up-regulation of epidermal growth factor receptor expression in human granulosa cells.
Zhang Y, Huang Q, Cheng JC, Nishi Y, Yanase T, Huang HF, Leung PC
Reprod Biol Endocrinol. 2010
PubMed ID: 20540809
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Additional sex combs-like 1 belongs to the enhancer of trithorax and polycomb group and genetically interacts with Cbx2 in mice.
Fisher CL, Lee I, Bloyer S, Bozza S, Chevalier J, Dahl A, Bodner C, Helgason CD, Hess JL, Humphries RK, Brock HW
Dev Biol. 2010
PubMed ID: 19833123
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A systems approach reveals that the myogenesis genome network is regulated by the transcriptional repressor RP58.
Yokoyama S, Ito Y, Ueno-Kudoh H, Shimizu H, Uchibe K, Albini S, Mitsuoka K, Miyaki S, Kiso M, Nagai A, Hikata T, Osada T, Fukuda N, Yamashita S, Harada D, Mezzano V, Kasai M, Puri PL, Hayashizaki Y, Okado H, Hashimoto M, Asahara H
Dev Cell. 2009
PubMed ID: 20059953
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Uncovering early response of gene regulatory networks in ESCs by systematic induction of transcription factors.
Nishiyama A, Xin L, Sharov AA, Thomas M, Mowrer G, Meyers E, Piao Y, Mehta S, Yee S, Nakatake Y, Stagg C, Sharova L, Correa-Cerro LS, Bassey U, Hoang H, Kim E, Tapnio R, Qian Y, Dudekula D, Zalzman M, Li M, Falco G, Yang HT, Lee SL, Monti M, Stanghellini I, Islam MN, Nagaraja R, Goldberg I, Wang W, Longo DL, Schlessinger D, Ko MS
Cell Stem Cell. 2009
PubMed ID: 19796622
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Gfi1 integrates progenitor versus granulocytic transcriptional programming.
Horman SR, Velu CS, Chaubey A, Bourdeau T, Zhu J, Paul WE, Gebelein B, Grimes HL
Blood. 2009
PubMed ID: 19346496
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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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Impaired function of primitive hematopoietic cells in mice lacking the Mixed-Lineage-Leukemia homolog MLL5.
Madan V, Madan B, Brykczynska U, Zilbermann F, Hogeveen K, Döhner K, Döhner H, Weber O, Blum C, Rodewald HR, Sassone-Corsi P, Peters AH, Fehling HJ
Blood. 2009
PubMed ID: 18952892
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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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The Mll partial tandem duplication: differential, tissue-specific activity in the presence or absence of the wild-type allele.
Dorrance AM, Liu S, Chong A, Pulley B, Nemer D, Guimond M, Yuan W, Chang D, Whitman SP, Marcucci G, Caligiuri MA
Blood. 2008
PubMed ID: 18617636
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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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HOX cofactors expression and regulation in the human ovary.
Ota T, Asahina H, Park SH, Huang Q, Minegishi T, Auersperg N, Leung PC
Reprod Biol Endocrinol. 2008
PubMed ID: 18973687
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HOXA7 in epithelial ovarian cancer: interrelationships between differentiation and clinical features.
Ota T, Gilks CB, Longacre T, Leung PC, Auersperg N
Reprod Sci. 2007
PubMed ID: 17959889
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Critical role of the p400/mDomino chromatin-remodeling ATPase in embryonic hematopoiesis.
Ueda T, Watanabe-Fukunaga R, Ogawa H, Fukuyama H, Higashi Y, Nagata S, Fukunaga R
Genes Cells. 2007
PubMed ID: 17535249
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Mll partial tandem duplication induces aberrant Hox expression in vivo via specific epigenetic alterations.
Dorrance AM, Liu S, Yuan W, Becknell B, Arnoczky KJ, Guimond M, Strout MP, Feng L, Nakamura T, Yu L, Rush LJ, Weinstein M, Leone G, Wu L, Ferketich A, Whitman SP, Marcucci G, Caligiuri MA
J Clin Invest. 2006
PubMed ID: 16981007
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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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The Mll-Een knockin fusion gene enhances proliferation of myeloid progenitors derived from mouse embryonic stem cells and causes myeloid leukaemia in chimeric mice.
Kong CT, Sham MH, So CW, Cheah KS, Chen SJ, Chan LC
Leukemia. 2006
PubMed ID: 16888613
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cDNA cloning and expression of the human NOBOX gene in oocytes and ovarian follicles.
Huntriss J, Hinkins M, Picton HM
Mol Hum Reprod. 2006
PubMed ID: 16597639
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Histone and DNA methylation defects at Hox genes in mice expressing a SET domain-truncated form of Mll.
Terranova R, Agherbi H, Boned A, Meresse S, Djabali M
Proc Natl Acad Sci U S A. 2006
PubMed ID: 16618927
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BGEM: an in situ hybridization database of gene expression in the embryonic and adult mouse nervous system.
Magdaleno S, Jensen P, Brumwell CL, Seal A, Lehman K, Asbury A, Cheung T, Cornelius T, Batten DM, Eden C, Norland SM, Rice DS, Dosooye N, Shakya S, Mehta P, Curran T
PLoS Biol. 2006
PubMed ID: 16602821
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Sfrp1 and Sfrp2 regulate anteroposterior axis elongation and somite segmentation during mouse embryogenesis.
Satoh W, Gotoh T, Tsunematsu Y, Aizawa S, Shimono A
Development. 2006
PubMed ID: 16467359
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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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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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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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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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Additional enhancer copies, with intact cdx binding sites, anteriorize Hoxa-7/lacZ expression in mouse embryos: evidence in keeping with an instructional cdx gradient.
Gaunt SJ, Cockley A, Drage D
Int J Dev Biol. 2004
PubMed ID: 15470633
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Leukemic transformation of hematopoietic progenitors by MLL-GAS7 in the absence of Hoxa7 or Hoxa9.
So CW, Karsunky H, Wong P, Weissman IL, Cleary ML
Blood. 2004
PubMed ID: 15070702
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Atlas of Hox gene expression in the developing kidney.
Patterson LT, Potter SS
Dev Dyn. 2004
PubMed ID: 15042701
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Down-regulation of Hox A7 is required for cell adhesion and migration on fibronectin during early HL-60 monocytic differentiation.
Leroy P, Berto F, Bourget I, Rossi B
J Leukoc Biol. 2004
PubMed ID: 14704364
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The cell-cycle regulator geminin inhibits Hox function through direct and polycomb-mediated interactions.
Luo L, Yang X, Takihara Y, Knoetgen H, Kessel M
Nature. 2004
PubMed ID: 14973489
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Complete sequencing and characterization of 21,243 full-length human cDNAs.
Ota T, Suzuki Y, Nishikawa T, Otsuki T, Sugiyama T, Irie R, Wakamatsu A, Hayashi K, Sato H, Nagai K, Kimura K, Makita H, Sekine M, Obayashi M, Nishi T, Shibahara T, Tanaka T, Ishii S, Yamamoto J, Saito K, Kawai Y, Isono Y, Nakamura Y, Nagahari K, Murakami K, Yasuda T, Iwayanagi T, Wagatsuma M, Shiratori A, Sudo H, Hosoiri T, Kaku Y, Kodaira H, Kondo H, Sugawara M, Takahashi M, Kanda K, Yokoi T, Furuya T, Kikkawa E, Omura Y, Abe K, Kamihara K, Katsuta N, Sato K, Tanikawa M, Yamazaki M, Ninomiya K, Ishibashi T, Yamashita H, Murakawa K, Fujimori K, Tanai H, Kimata M, Watanabe M, Hiraoka S, Chiba Y, Ishida S, Ono Y, Takiguchi S, Watanabe S, Yosida M, Hotuta T, Kusano J, Kanehori K, Takahashi-Fujii A, Hara H, Tanase TO, Nomura Y, Togiya S, Komai F, Hara R, Takeuchi K, Arita M, Imose N, Musashino K, Yuuki H, Oshima A, Sasaki N, Aotsuka S, Yoshikawa Y, Matsunawa H, Ichihara T, Shiohata N, Sano S, Moriya S, Momiyama H, Satoh N, Takami S, Terashima Y, Suzuki O, Nakagawa S, Senoh A, Mizoguchi H, Goto Y, Shimizu F, Wakebe H, Hishigaki H, Watanabe T, Sugiyama A, Takemoto M, Kawakami B, Yamazaki M, Watanabe K, Kumagai A, Itakura S, Fukuzumi Y, Fujimori Y, Komiyama M, Tashiro H, Tanigami A, Fujiwara T, Ono T, Yamada K, Fujii Y, Ozaki K, Hirao M, Ohmori Y, Kawabata A, Hikiji T, Kobatake N, Inagaki H, Ikema Y, Okamoto S, Okitani R, Kawakami T, Noguchi S, Itoh T, Shigeta K, Senba T, Matsumura K, Nakajima Y, Mizuno T, Morinaga M, Sasaki M, Togashi T, Oyama M, Hata H, Watanabe M, Komatsu T, Mizushima-Sugano J, Satoh T, Shirai Y, Takahashi Y, Nakagawa K, Okumura K, Nagase T, Nomura N, Kikuchi H, Masuho Y, Yamashita R, Nakai K, Yada T, Nakamura Y, Ohara O, Isogai T, Sugano S
Nat Genet. 2004
PubMed ID: 14702039
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B-cell development in the presence of the MLL/AF4 oncoprotein proceeds in the absence of HOX A7 and HOX A9 expression.
Bertrand FE, Spengeman JD, Shah N, LeBien TW
Leukemia. 2003
PubMed ID: 14562113
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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
PubMed ID: 12853948
-
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
-
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
-
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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A novel factor associating with the upstream regulatory element of murine Hoxa-7 induces bacterial cell death.
Park S, Park HW, Kim MH
Mol Biol Rep. 2002
PubMed ID: 12549822
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The mouse PcG gene eed is required for Hox gene repression and extraembryonic development.
Wang J, Mager J, Schnedier E, Magnuson T
Mamm Genome. 2002
PubMed ID: 12370779
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Nup98-HoxA9 immortalizes myeloid progenitors, enforces expression of Hoxa9, Hoxa7 and Meis1, and alters cytokine-specific responses in a manner similar to that induced by retroviral co-expression of Hoxa9 and Meis1.
Calvo KR, Sykes DB, Pasillas MP, Kamps MP
Oncogene. 2002
PubMed ID: 12082612
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Directed differentiation of pluripotent cells to neural lineages: homogeneous formation and differentiation of a neurectoderm population.
Rathjen J, Haines BP, Hudson KM, Nesci A, Dunn S, Rathjen PD
Development. 2002
PubMed ID: 12015293
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Retinoic acid response element in HOXA-7 regulatory region affects the rate, not the formation of anterior boundary expression.
Kim MH, Shin JS, Park S, Hur MW, Lee MO, Park H, Lee CS
Int J Dev Biol. 2002
PubMed ID: 12068955
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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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Human homeobox HOXA7 regulates keratinocyte transglutaminase type 1 and inhibits differentiation.
La Celle PT, Polakowska RR
J Biol Chem. 2001
PubMed ID: 11435435
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Gradients and forward spreading of vertebrate Hox gene expression detected by using a Hox/lacZ transgene.
Gaunt SJ
Dev Dyn. 2001
PubMed ID: 11357191
-
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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Shotgun sequencing of the human transcriptome with ORF expressed sequence tags.
Dias Neto E, Correa RG, Verjovski-Almeida S, Briones MR, Nagai MA, da Silva W, Zago MA, Bordin S, Costa FF, Goldman GH, Carvalho AF, Matsukuma A, Baia GS, Simpson DH, Brunstein A, de Oliveira PS, Bucher P, Jongeneel CV, O'Hare MJ, Soares F, Brentani RR, Reis LF, de Souza SJ, Simpson AJ
Proc Natl Acad Sci U S A. 2000
PubMed ID: 10737800
-
Sequence analysis and tissue specific expression of human HOXA7.
Kim MH, Jin H, Seol EY, Yoo M, Park HW
Mol Biotechnol. 2000
PubMed ID: 10911612
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Stage-specific homeotic vertebral transformations in mouse fetuses induced by maternal hyperthermia during somitogenesis.
Li ZL, Shiota K
Dev Dyn. 1999
PubMed ID: 10633854
-
Evidence that Hoxa expression domains are evolutionarily transposed in spinal ganglia, and are established by forward spreading in paraxial mesoderm.
Gaunt SJ, Dean W, Sang H, Burton RD
Mech Dev. 1999
PubMed ID: 10354475
-
High-efficiency full-length cDNA cloning.
Carninci P, Hayashizaki Y
Methods Enzymol. 1999
PubMed ID: 10349636
-
Sequence characterisation and expression of homeobox HOX A7 in the multi-potential erythroleukaemic cell line TF-1.
McIlhatton MA, Bremner P, McMullin MF, Maxwell AP, Winter PC, Lappin TR
Biochim Biophys Acta. 1998
PubMed ID: 9804983
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Toward a complete human genome sequence.
Genome Res. 1998
PubMed ID: 9847074
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Analysis of Hoxa7/Hoxb7 mutants suggests periodicity in the generation of the different sets of vertebrae.
Chen F, Greer J, Capecchi MR
Mech Dev. 1998
PubMed ID: 9784603
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MLL, a mammalian trithorax-group gene, functions as a transcriptional maintenance factor in morphogenesis.
Yu BD, Hanson RD, Hess JL, Horning SE, Korsmeyer SJ
Proc Natl Acad Sci U S A. 1998
PubMed ID: 9724755
-
Growth disturbance in fetal liver hematopoiesis of Mll-mutant mice.
Yagi H, Deguchi K, Aono A, Tani Y, Kishimoto T, Komori T
Blood. 1998
PubMed ID: 9639506
-
307-bp fragment in HOXA7 upstream sequence is sufficient for anterior boundary formation.
Min W, Woo HJ, Lee CS, Lee KK, Yoon WK, Park HW, Kim MH
DNA Cell Biol. 1998
PubMed ID: 9539109
-
Meis1 and pKnox1 bind DNA cooperatively with Pbx1 utilizing an interaction surface disrupted in oncoprotein E2a-Pbx1.
Knoepfler PS, Calvo KR, Chen H, Antonarakis SE, Kamps MP
Proc Natl Acad Sci U S A. 1997
PubMed ID: 9405651
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Heat shock-induced homeotic transformations of the axial skeleton and associated shifts of Hox gene expression domains in mouse embryos.
Li ZL, Chisaka O, Koseki H, Akasaka T, Ishibashi M, Shiota K
Reprod Toxicol. 1997
PubMed ID: 9407586
-
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
-
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
-
Expression of homeobox genes, including an insulin promoting factor, in the murine yolk sac at the time of hematopoietic initiation.
McGrath KE, Palis J
Mol Reprod Dev. 1997
PubMed ID: 9291463
-
Sequence and functional analysis of an upstream regulatory region of human HOXA7 gene.
Min W, Cho M, Jang SI, Chang HH, Lee CS, Jun MH, Kim MH
Gene. 1996
PubMed ID: 8982060
-
The Polycomb-group homolog Bmi-1 is a regulator of murine Hox gene expression.
van der Lugt NM, Alkema M, Berns A, Deschamps J
Mech Dev. 1996
PubMed ID: 8887324
-
Repression by HoxA7 is mediated by the homeodomain and the modulatory action of its N-terminal-arm residues.
Schnabel CA, Abate-Shen C
Mol Cell Biol. 1996
PubMed ID: 8649375
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A role for mel-18, a Polycomb group-related vertebrate gene, during theanteroposterior specification of the axial skeleton.
Akasaka T, Kanno M, Balling R, Mieza MA, Taniguchi M, Koseki H
Development. 1996
PubMed ID: 8625838
-
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
-
Cooperative activation of Hoxa and Pbx1-related genes in murine myeloid leukaemias.
Nakamura T, Largaespada DA, Shaughnessy JD, Jenkins NA, Copeland NG
Nat Genet. 1996
PubMed ID: 8563752
-
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
-
Alterations in somite patterning of Myf-5-deficient mice: a possible role for FGF-4 and FGF-6.
Grass S, Arnold HH, Braun T
Development. 1996
PubMed ID: 8565825
-
Altered Hox expression and segmental identity in Mll-mutant mice.
Yu BD, Hess JL, Horning SE, Brown GA, Korsmeyer SJ
Nature. 1995
PubMed ID: 7477409
-
Disruption of the murine homeobox gene Cdx1 affects axial skeletal identities by altering the mesodermal expression domains of Hox genes.
Subramanian V, Meyer BI, Gruss P
Cell. 1995
PubMed ID: 7585967
-
Homeobox gene expression in human oocytes and preembryos.
Verlinsky Y, Morozov G, Gindilis V, Strom CM, Freidin M, Rechitsky S, Verlinsky O, Ivakhnenko V, Zdanovsky V, Kuliev A
Mol Reprod Dev. 1995
PubMed ID: 7654365
-
A conserved enhancer of the human and murine Hoxa-7 gene specifies the anterior boundary of expression during embryonal development.
Knittel T, Kessel M, Kim MH, Gruss P
Development. 1995
PubMed ID: 7538068
-
Organization, sequence and regulation of expression of the murine Hoxa-7 gene.
Parikh H, Shah S, Hilt D, Peterkofsky A
Gene. 1995
PubMed ID: 7890170
-
Hox genes in normal and neoplastic mouse mammary gland.
Friedmann Y, Daniel CA, Strickland P, Daniel CW
Cancer Res. 1994
PubMed ID: 7954431
-
Hox proteins have different affinities for a consensus DNA site that correlate with the positions of their genes on the hox cluster.
Pellerin I, Schnabel C, Catron KM, Abate C
Mol Cell Biol. 1994
PubMed ID: 7911971
-
Functional analysis of mouse Hoxa-7 in Saccharomyces cerevisiae: sequences outside the homeodomain base contact zone influence binding and activation.
Gross MK, Gruss P
Mol Cell Biol. 1994
PubMed ID: 8264592
-
Chromosomal mapping in the mouse of eight K(+)-channel genes representing the four Shaker-like subfamilies Shaker, Shab, Shaw, and Shal.
Klocke R, Roberds SL, Tamkun MM, Gronemeier M, Augustin A, Albrecht B, Pongs O, Jockusch H
Genomics. 1993
PubMed ID: 7905852
-
Macrophage-mediated enterocyte damage in BALB/c mice infected with different strains of Giardia lamblia.
Goyal R, Mahajan RC, Ganguly NK, Sehgal R, Gorowara S, Singh K
Scand J Gastroenterol. 1993
PubMed ID: 8235442
-
Organization and expression of mouse Hox3 cluster genes.
Goto J, Miyabayashi T, Wakamatsu Y, Takahashi N, Muramatsu M
Mol Gen Genet. 1993
PubMed ID: 8099712
-
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
-
Vertebrate homeobox gene nomenclature.
Scott MP
Cell. 1992
PubMed ID: 1358459
-
Lactoferrin expression in the mouse reproductive tract during the natural estrous cycle: correlation with circulating estradiol and progesterone.
Walmer DK, Wrona MA, Hughes CL, Nelson KG
Endocrinology. 1992
PubMed ID: 1505477
-
Respecification of vertebral identities by retinoic acid.
Kessel M
Development. 1992
PubMed ID: 1358593
-
Analysis of mouse Evx genes: Evx-1 displays graded expression in the primitive streak.
Dush MK, Martin GR
Dev Biol. 1992
PubMed ID: 1349539
-
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
-
Inactivation of muscle chloride channel by transposon insertion in myotonic mice.
Steinmeyer K, Klocke R, Ortland C, Gronemeier M, Jockusch H, Gründer S, Jentsch TJ
Nature. 1991
PubMed ID: 1659665
-
Homeotic transformations of murine vertebrae and concomitant alteration of Hox codes induced by retinoic acid.
Kessel M, Gruss P
Cell. 1991
PubMed ID: 1680565
-
Nomenclature for human homeobox genes.
McAlpine PJ, Shows TB
Genomics. 1990
PubMed ID: 1973146
-
Position-specific activity of the Hox1.1 promoter in transgenic mice.
Püschel AW, Balling R, Gruss P
Development. 1990
PubMed ID: 1971214
-
The human HOX gene family.
Acampora D, D'Esposito M, Faiella A, Pannese M, Migliaccio E, Morelli F, Stornaiuolo A, Nigro V, Simeone A, Boncinelli E
Nucleic Acids Res. 1989
PubMed ID: 2574852
-
Anterior boundaries of Hox gene expression in mesoderm-derived structures correlate with the linear gene order along the chromosome.
Dressler GR, Gruss P
Differentiation. 1989
PubMed ID: 2575552
-
Craniofacial abnormalities induced by ectopic expression of the homeobox gene Hox-1.1 in transgenic mice.
Balling R, Mutter G, Gruss P, Kessel M
Cell. 1989
PubMed ID: 2568891
-
Production of chimaeric mice containing embryonic stem (ES) cells carrying a homoeobox Hox 1.1 allele mutated by homologous recombination.
Zimmer A, Gruss P
Nature. 1989
PubMed ID: 2563901
-
Organization of human class I homeobox genes.
Boncinelli E, Acampora D, Pannese M, D'Esposito M, Somma R, Gaudino G, Stornaiuolo A, Cafiero M, Faiella A, Simeone A
Genome. 1989
PubMed ID: 2576652
-
Primary structure and nuclear localization of a murine homeodomain protein.
Kessel M, Schulze F, Fibi M, Gruss P
Proc Natl Acad Sci U S A. 1987
PubMed ID: 2885847
-
Expression of a homeo domain protein in noncontact-inhibited cultured cells and postmitotic neurons.
Odenwald WF, Taylor CF, Palmer-Hill FJ, Friedrich V, Tani M, Lazzarini RA
Genes Dev. 1987
PubMed ID: 2890554
-
Genetic and cytogenetic localisation of the homeo box containing genes on mouse chromosome 6 and human chromosome 7.
Bućan M, Yang-Feng T, Colberg-Poley AM, Wolgemuth DJ, Guenet JL, Francke U, Lehrach H
EMBO J. 1986
PubMed ID: 2878803
-
Sequential expression of murine homeo box genes during F9 EC cell differentiation.
Breier G, Bućan M, Francke U, Colberg-Poley AM, Gruss P
EMBO J. 1986
PubMed ID: 2877873
-
Clustered homeo boxes are differentially expressed during murine development.
Colberg-Poley AM, Voss SD, Chowdhury K, Stewart CL, Wagner EF, Gruss P
Cell. 1985
PubMed ID: 2416462
-
Structural analysis of murine genes containing homoeo box sequences and their expression in embryonal carcinoma cells.
Colberg-Poley AM, Voss SD, Chowdhury K, Gruss P
Nature. 1985
PubMed ID: 2986010
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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