Citations for
1HOXA13, HOXD13
Distal Limb Patterning Requires Modulation of cis-Regulatory Activities by HOX13.
Sheth R, Barozzi I, Langlais D, Osterwalder M, Nemec S, Carlson HL, Stadler HS, Visel A, Drouin J, Kmita M.
Cell Rep 17(11):2913-2926. doi: 10.1016/j.celrep.2016.11.039. 2016
2HOXA13, HOXD13
HOX13 proteins: the molecular switcher in Hoxd bimodal regulation.
Ros MA.
Genes Dev 30(10):1135-7. doi: 10.1101/gad.283598.116. 2016
3ALDH1A2, HOXA13
HOXA13 regulates Aldh1a2 expression in the autopod to facilitate interdigital programmed cell death.
Shou S, Carlson HL, Perez WD, Stadler HS.
Dev Dyn 242(6):687-98. doi: 10.1002/dvdy.23966. Epub 2013 Apr 28. 2013
4HOXA10, HOXA13
HOXA10 and HOXA13 sequence variations in human female genital malformations including congenital absence of the uterus and vagina.
Ekici AB, Strissel PL, Oppelt PG, Renner SP, Brucker S, Beckmann MW, Strick R.
Gene 518(2):267-72. doi: 10.1016/j.gene.2013.01.030. Epub 2013 Jan 30. 2013
5HOXA13
Recruitment of 5' Hoxa genes in the allantois is essential for proper extra-embryonic function in placental mammals.
Scotti M, Kmita M.
Development 139(4):731-9. doi: 10.1242/dev.075408. Epub 2012 Jan 4. 2012
6HOXA13
Structural basis for sequence specific DNA binding and protein dimerization of HOXA13.
Zhang Y, Larsen CA, Stadler HS, Ames JB.
PLoS One 6(8):e23069. doi: 10.1371/journal.pone.0023069. Epub 2011 Aug 1. 2011
7GDF5, HOXA13
Survival of Hoxa13 homozygous mutants reveals a novel role in digit patterning and appendicular skeletal development.
Perez WD, Weller CR, Shou S, Stadler HS.
Dev Dyn 239(2):446-57. doi: 10.1002/dvdy.22183. 2010
8HFG, HOXA13
A novel mutation of HOXA13 in a family with hand-foot-genital syndrome and the role of polyalanine expansions in the spectrum of Müllerian fusion anomalies.
Jorgensen EM, Ruman JI, Doherty L, Taylor HS.
Fertil Steril 94(4):1235-8. doi: 10.1016/j.fertnstert.2009.05.057. Epub 2009 Jul 9. 2010
9HFG, HOXA13
A novel mutation of HOXA13 in a family with hand-foot-genital syndrome and the role of polyalanine expansions in the spectrum of Müllerian fusion anomalies.
Jorgensen EM, Ruman JI, Doherty L, Taylor HS.
Fertil Steril 94(4):1235-8. doi: 10.1016/j.fertnstert.2009.05.057. Epub 2009 Jul 9. 2010
10HOXA13
HOXA13 promotes cancer cell growth and predicts poor survival of patients with esophageal squamous cell carcinoma.
Gu ZD, Shen LY, Wang H, Chen XM, Li Y, Ning T, Chen KN.
Cancer Res 69(12):4969-73. doi: 10.1158/0008-5472.CAN-08-4546. Epub 2009 Jun 2. 2009
11FOXF1, HOXA13, TEK
HOXA13 Is essential for placental vascular patterning and labyrinth endothelial specification.
Shaut CA, Keene DR, Sorensen LK, Li DY, Stadler HS.
PLoS Genet 4(5):e1000073. doi: 10.1371/journal.pgen.1000073. 2008
12HOXA13, HFG
Molecular characterization of HOXA13 polyalanine expansion proteins in hand-foot-genital syndrome.
Utsch B, McCabe CD, Galbraith K, Gonzalez R, Born M, Dštsch J, Ludwig M, Reutter H, Innis JW.
Am J Med Genet A 143(24):3161-8. 2007
13EPHA6, EPHA7, HOXA13
HOXA13 directly regulates EphA6 and EphA7 expression in the genital tubercle vascular endothelia.
Shaut CA, Saneyoshi C, Morgan EA, Knosp WM, Sexton DR, Stadler HS.
Dev Dyn 236(4):951-60. 2007
14HOXA13
A genomic approach to the identification and characterization of HOXA13 functional binding elements.
McCabe CD, Innis JW.
Nucleic Acids Res 33(21):6782-94. Print 2005. 2005
15HOXA13, HFG
Polyalanine expansion in HOXA13: three new affected families and the molecular consequences in a mouse model.
Innis JW, Mortlock D, Chen Z, Ludwig M, Williams ME, Williams TM, Doyle CD, Shao Z, Glynn M, Mikulic D, Lehmann K, Mundlos S, Utsch B.
Hum Mol Genet 13(22):2841-51. Epub 2004 Sep 22. 2004
16WTAP, HOXA13
Exclusion of WTAP and HOXA13 as candidate genes for isolated hypospadias.
Utsch B, Kaya A, Ozburun A, Lentze MJ, Albers N, Ludwig M.
Scand J Urol Nephrol 37(6):498-501. 2003
17HFG, HOXA13
A novel stable polyalanine [poly(A)] expansion in the HOXA13 gene associated with hand-foot-genital syndrome: proper function of poly(A)-harbouring transcription factors depends on a critical repeat length?
Utsch B, Becker K, Brock D, Lentze MJ, Bidlingmaier F, Ludwig M.
Hum Genet 110(5):488-94. Review. 2002
18HOXA13, NUP98
The chromosome translocation t(7;11)(p15;p15) in acute myeloid leukemia results in fusion of the NUP98 gene with a HOXA cluster gene, HOXA13, but not HOXA9.
Taketani T, Taki T, Ono R, Kobayashi Y, Ida K, Hayashi Y.
Genes Chromosomes Cancer 34(4):437-43. 2002
19GTMS, HOXA13
A HOXA13 allele with a missense mutation in the homeobox and a dinucleotide deletion in the promoter underlies Guttmacher syndrome.
Innis JW, Goodman FR, Bacchelli C, Williams TM, Mortlock DP, Sateesh P, Scambler PJ, McKinnon W, Guttmacher AE.
Hum Mutat 19(5):573-4. 2002
20HFG, HOXA13
Novel HOXA13 mutations and the phenotypic spectrum of hand-foot-genital syndrome.
Goodman FR, Bacchelli C, Brady AF, Brueton LA, Fryns JP, Mortlock DP, Innis JW, Holmes LB, Donnenfeld AE, Feingold M, Beemer FA, Hennekam RC, Scambler PJ.
Am J Hum Genet 67(1):197-202. 2000
21HOXA13
Hoxa-13 gene mutation results in abnormal seminal vesicle and prostate development.
Podlasek CA, et al.
J Urol 161(5):1655-61. 1999
22HFG, HOXA13
Mutation of HOXA13 in hand-foot-genital syndrome.
Mortlock DP, et al.
Nat Genet 15 : 179-180. 1997