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Items: 32


The formation of the thumb requires direct modulation of Gli3 transcription by Hoxa13.

Bastida MF, Pérez-Gómez R, Trofka A, Zhu J, Rada-Iglesias A, Sheth R, Stadler HS, Mackem S, Ros MA.

Proc Natl Acad Sci U S A. 2020 Jan 14;117(2):1090-1096. doi: 10.1073/pnas.1919470117. Epub 2020 Jan 2.


Development and functional characterization of a lncRNA-HIT conditional loss of function allele.

Carlson HL, Stadler HS.

Genesis. 2019 Dec 14:e23351. doi: 10.1002/dvg.23351. [Epub ahead of print]


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. 2016 Dec 13;17(11):2913-2926. doi: 10.1016/j.celrep.2016.11.039.


Evolution of Hoxa11 regulation in vertebrates is linked to the pentadactyl state.

Kherdjemil Y, Lalonde RL, Sheth R, Dumouchel A, de Martino G, Pineault KM, Wellik DM, Stadler HS, Akimenko MA, Kmita M.

Nature. 2016 Nov 3;539(7627):89-92. doi: 10.1038/nature19813. Epub 2016 Oct 5.


LncRNA-HIT Functions as an Epigenetic Regulator of Chondrogenesis through Its Recruitment of p100/CBP Complexes.

Carlson HL, Quinn JJ, Yang YW, Thornburg CK, Chang HY, Stadler HS.

PLoS Genet. 2015 Dec 3;11(12):e1005680. doi: 10.1371/journal.pgen.1005680. eCollection 2015 Dec.


Musculoskeletal integration at the wrist underlies the modular development of limb tendons.

Huang AH, Riordan TJ, Pryce B, Weibel JL, Watson SS, Long F, Lefebvre V, Harfe BD, Stadler HS, Akiyama H, Tufa SF, Keene DR, Schweitzer R.

Development. 2015 Jul 15;142(14):2431-41. doi: 10.1242/dev.122374. Epub 2015 Jun 10.


Chemical shift assignments of mouse HOXD13 DNA binding domain bound to duplex DNA.

Turner M, Zhang Y, Carlson HL, Stadler HS, Ames JB.

Biomol NMR Assign. 2015 Oct;9(2):267-70. doi: 10.1007/s12104-014-9589-4. Epub 2014 Dec 10.


HOXA13 regulates Aldh1a2 expression in the autopod to facilitate interdigital programmed cell death.

Shou S, Carlson HL, Perez WD, Stadler HS.

Dev Dyn. 2013 Jun;242(6):687-98. doi: 10.1002/dvdy.23966. Epub 2013 Apr 28.


Analysis of de novo HOXA13 polyalanine expansions supports replication slippage without repair in their generation.

Owens KM, Quinonez SC, Thomas PE, Keegan CE, Lefebvre N, Roulston D, Larsen CA, Stadler HS, Innis JW.

Am J Med Genet A. 2013 May;161A(5):1019-27. doi: 10.1002/ajmg.a.35843. Epub 2013 Mar 26.


Structural basis for sequence specific DNA binding and protein dimerization of HOXA13.

Zhang Y, Larsen CA, Stadler HS, Ames JB.

PLoS One. 2011;6(8):e23069. doi: 10.1371/journal.pone.0023069. Epub 2011 Aug 1.


Backbone chemical shift assignments of mouse HOXA13 DNA binding domain bound to duplex DNA.

Zhang Y, Thornburg CK, Stadler HS, Ames JB.

Biomol NMR Assign. 2010 Apr;4(1):97-9. doi: 10.1007/s12104-010-9216-y. Epub 2010 Mar 16.


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. 2010 Feb;239(2):446-57. doi: 10.1002/dvdy.22183.


(1)H, (15)N, and (13)C chemical shift assignments of mouse HOXA13 DNA binding domain.

Zhang Y, Thornburg CK, Stadler HS, Ames JB.

Biomol NMR Assign. 2009 Dec;3(2):199-201. doi: 10.1007/s12104-009-9174-4. Epub 2009 Jun 24.


Expression of prolyl 3-hydroxylase genes in embryonic and adult mouse tissues.

Vranka J, Stadler HS, Bächinger HP.

Cell Struct Funct. 2009;34(2):97-104. Epub 2009 Aug 1.


HOXA13 Is essential for placental vascular patterning and labyrinth endothelial specification.

Shaut CA, Keene DR, Sorensen LK, Li DY, Stadler HS.

PLoS Genet. 2008 May 16;4(5):e1000073. doi: 10.1371/journal.pgen.1000073.


A dermal HOX transcriptional program regulates site-specific epidermal fate.

Rinn JL, Wang JK, Allen N, Brugmann SA, Mikels AJ, Liu H, Ridky TW, Stadler HS, Nusse R, Helms JA, Chang HY.

Genes Dev. 2008 Feb 1;22(3):303-7. doi: 10.1101/gad.1610508.


Synthesis of diverse lactam carboxamides leading to the discovery of a new transcription-factor inhibitor.

Ng PY, Tang Y, Knosp WM, Stadler HS, Shaw JT.

Angew Chem Int Ed Engl. 2007;46(28):5352-5. No abstract available.


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. 2007 Apr;236(4):951-60.


Misexpression of Sox9 in mouse limb bud mesenchyme induces polydactyly and rescues hypodactyly mice.

Akiyama H, Stadler HS, Martin JF, Ishii TM, Beachy PA, Nakamura T, de Crombrugghe B.

Matrix Biol. 2007 May;26(4):224-33. Epub 2006 Dec 8.


Elucidation, quantitative refinement, and in vivo utilization of the HOXA13 DNA binding site.

Knosp WM, Saneyoshi C, Shou S, Bächinger HP, Stadler HS.

J Biol Chem. 2007 Mar 2;282(9):6843-53. Epub 2007 Jan 1.


Transcriptome analysis of the murine forelimb and hindlimb autopod.

Shou S, Scott V, Reed C, Hitzemann R, Stadler HS.

Dev Dyn. 2005 Sep;234(1):74-89.


Genitourinary functions of Hoxa13 and Hoxd13.

Scott V, Morgan EA, Stadler HS.

J Biochem. 2005 Jun;137(6):671-6. Review.


HOXA13 regulates the expression of bone morphogenetic proteins 2 and 7 to control distal limb morphogenesis.

Knosp WM, Scott V, Bächinger HP, Stadler HS.

Development. 2004 Sep;131(18):4581-92.


Loss of Bmp7 and Fgf8 signaling in Hoxa13-mutant mice causes hypospadia.

Morgan EA, Nguyen SB, Scott V, Stadler HS.

Development. 2003 Jul;130(14):3095-109.


Modelling genitourinary defects in mice: an emerging genetic and developmental system.

Stadler HS.

Nat Rev Genet. 2003 Jun;4(6):478-82. Review.


Roles of Hoxa1 and Hoxa2 in patterning the early hindbrain of the mouse.

Barrow JR, Stadler HS, Capecchi MR.

Development. 2000 Mar;127(5):933-44.


Detection of targeted GFP-Hox gene fusions during mouse embryogenesis.

Godwin AR, Stadler HS, Nakamura K, Capecchi MR.

Proc Natl Acad Sci U S A. 1998 Oct 27;95(22):13042-7.


Phylogenetic conservation and physical mapping of members of the H6 homeobox gene family.

Stadler HS, Murray JC, Leysens NJ, Goodfellow PJ, Solursh M.

Mamm Genome. 1995 Jun;6(6):383-8.


Identification and genetic mapping of a homeobox gene to the 4p16.1 region of human chromosome 4.

Stadler HS, Padanilam BJ, Buetow K, Murray JC, Solursh M.

Proc Natl Acad Sci U S A. 1992 Dec 1;89(23):11579-83.


Characterization of the human HOX 7 cDNA and identification of polymorphic markers.

Padanilam BJ, Stadler HS, Mills KA, McLeod LB, Solursh M, Lee B, Ramirez F, Buetow KH, Murray JC.

Hum Mol Genet. 1992 Sep;1(6):407-10.


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