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Results: 1 to 20 of 100

1.

The homeobox transcription factor HOXA9 is a regulator of SHOX in U2OS cells and chicken micromass cultures.

Durand C, Decker E, Roeth R, Schneider KU, Rappold G.

PLoS One. 2012;7(9):e45369. doi: 10.1371/journal.pone.0045369. Epub 2012 Sep 20.

PMID:
23028966
[PubMed - indexed for MEDLINE]
Free PMC Article
2.

FGFR3 is a target of the homeobox transcription factor SHOX in limb development.

Decker E, Durand C, Bender S, Rödelsperger C, Glaser A, Hecht J, Schneider KU, Rappold G.

Hum Mol Genet. 2011 Apr 15;20(8):1524-35. doi: 10.1093/hmg/ddr030. Epub 2011 Jan 27.

PMID:
21273290
[PubMed - indexed for MEDLINE]
Free Article
3.

Expression of the short stature homeobox gene Shox is restricted by proximal and distal signals in chick limb buds and affects the length of skeletal elements.

Tiecke E, Bangs F, Blaschke R, Farrell ER, Rappold G, Tickle C.

Dev Biol. 2006 Oct 15;298(2):585-96. Epub 2006 Jul 12.

PMID:
16904661
[PubMed - indexed for MEDLINE]
Free Article
4.

Enhancer elements upstream of the SHOX gene are active in the developing limb.

Durand C, Bangs F, Signolet J, Decker E, Tickle C, Rappold G.

Eur J Hum Genet. 2010 May;18(5):527-32. doi: 10.1038/ejhg.2009.216. Epub 2009 Dec 9.

PMID:
19997128
[PubMed - indexed for MEDLINE]
Free PMC Article
5.

Identification of the first recurrent PAR1 deletion in Léri-Weill dyschondrosteosis and idiopathic short stature reveals the presence of a novel SHOX enhancer.

Benito-Sanz S, Royo JL, Barroso E, Paumard-Hernández B, Barreda-Bonis AC, Liu P, Gracía R, Lupski JR, Campos-Barros Á, Gómez-Skarmeta JL, Heath KE.

J Med Genet. 2012 Jul;49(7):442-50. doi: 10.1136/jmedgenet-2011-100678.

PMID:
22791839
[PubMed - indexed for MEDLINE]
6.

Long-range conserved non-coding SHOX sequences regulate expression in developing chicken limb and are associated with short stature phenotypes in human patients.

Sabherwal N, Bangs F, Röth R, Weiss B, Jantz K, Tiecke E, Hinkel GK, Spaich C, Hauffa BP, van der Kamp H, Kapeller J, Tickle C, Rappold G.

Hum Mol Genet. 2007 Jan 15;16(2):210-22. Epub 2007 Jan 2.

PMID:
17200153
[PubMed - indexed for MEDLINE]
Free Article
7.

The Leri-Weill and Turner syndrome homeobox gene SHOX encodes a cell-type specific transcriptional activator.

Rao E, Blaschke RJ, Marchini A, Niesler B, Burnett M, Rappold GA.

Hum Mol Genet. 2001 Dec 15;10(26):3083-91.

PMID:
11751690
[PubMed - indexed for MEDLINE]
Free Article
8.

HOXA9 activates transcription of the gene encoding gp91Phox during myeloid differentiation.

Bei L, Lu Y, Eklund EA.

J Biol Chem. 2005 Apr 1;280(13):12359-70. Epub 2005 Jan 28.

PMID:
15681849
[PubMed - indexed for MEDLINE]
Free Article
9.

BNP is a transcriptional target of the short stature homeobox gene SHOX.

Marchini A, Häcker B, Marttila T, Hesse V, Emons J, Weiss B, Karperien M, Rappold G.

Hum Mol Genet. 2007 Dec 15;16(24):3081-7. Epub 2007 Sep 19.

PMID:
17881654
[PubMed - indexed for MEDLINE]
Free Article
10.

SHOX interacts with the chondrogenic transcription factors SOX5 and SOX6 to activate the aggrecan enhancer.

Aza-Carmona M, Shears DJ, Yuste-Checa P, Barca-Tierno V, Hisado-Oliva A, Belinchón A, Benito-Sanz S, Rodríguez JI, Argente J, Campos-Barros A, Scambler PJ, Heath KE.

Hum Mol Genet. 2011 Apr 15;20(8):1547-59. doi: 10.1093/hmg/ddr032. Epub 2011 Jan 24.

PMID:
21262861
[PubMed - indexed for MEDLINE]
Free Article
11.

Enhancer deletions of the SHOX gene as a frequent cause of short stature: the essential role of a 250 kb downstream regulatory domain.

Chen J, Wildhardt G, Zhong Z, Röth R, Weiss B, Steinberger D, Decker J, Blum WF, Rappold G.

J Med Genet. 2009 Dec;46(12):834-9. doi: 10.1136/jmg.2009.067785. Epub 2009 Jul 2.

PMID:
19578035
[PubMed - indexed for MEDLINE]
Free PMC Article
12.

Identification of novel SHOX target genes in the developing limb using a transgenic mouse model.

Beiser KU, Glaser A, Kleinschmidt K, Scholl I, Röth R, Li L, Gretz N, Mechtersheimer G, Karperien M, Marchini A, Richter W, Rappold GA.

PLoS One. 2014 Jun 2;9(6):e98543. doi: 10.1371/journal.pone.0098543. eCollection 2014.

PMID:
24887312
[PubMed - in process]
Free PMC Article
13.

Impairment of SHOX nuclear localization as a cause for Léri-Weill syndrome.

Sabherwal N, Schneider KU, Blaschke RJ, Marchini A, Rappold G.

J Cell Sci. 2004 Jun 15;117(Pt 14):3041-8. Epub 2004 Jun 1.

PMID:
15173321
[PubMed - indexed for MEDLINE]
Free Article
14.

SHOX at a glance: from gene to protein.

Marchini A, Rappold G, Schneider KU.

Arch Physiol Biochem. 2007 Jun;113(3):116-23. Review.

PMID:
17922307
[PubMed - indexed for MEDLINE]
15.

KLF4 and PBX1 directly regulate NANOG expression in human embryonic stem cells.

Chan KK, Zhang J, Chia NY, Chan YS, Sim HS, Tan KS, Oh SK, Ng HH, Choo AB.

Stem Cells. 2009 Sep;27(9):2114-25. doi: 10.1002/stem.143.

PMID:
19522013
[PubMed - indexed for MEDLINE]
Free Article
16.

New roles of SHOX as regulator of target genes.

Rappold GA, Durand C, Decker E, Marchini A, Schneider KU.

Pediatr Endocrinol Rev. 2012 May;9 Suppl 2:733-8.

PMID:
22946287
[PubMed - indexed for MEDLINE]
17.

Identification and characterization of Hoxa9 binding sites in hematopoietic cells.

Huang Y, Sitwala K, Bronstein J, Sanders D, Dandekar M, Collins C, Robertson G, MacDonald J, Cezard T, Bilenky M, Thiessen N, Zhao Y, Zeng T, Hirst M, Hero A, Jones S, Hess JL.

Blood. 2012 Jan 12;119(2):388-98. doi: 10.1182/blood-2011-03-341081. Epub 2011 Nov 9.

PMID:
22072553
[PubMed - indexed for MEDLINE]
Free PMC Article
18.

PBX1 and MEIS1 up-regulate SOX3 gene expression by direct interaction with a consensus binding site within the basal promoter region.

Mojsin M, Stevanovic M.

Biochem J. 2009 Dec 14;425(1):107-16. doi: 10.1042/BJ20090694.

PMID:
19799567
[PubMed - indexed for MEDLINE]
Free Article
19.

The short stature homeobox gene SHOX is involved in skeletal abnormalities in Turner syndrome.

Clement-Jones M, Schiller S, Rao E, Blaschke RJ, Zuniga A, Zeller R, Robson SC, Binder G, Glass I, Strachan T, Lindsay S, Rappold GA.

Hum Mol Genet. 2000 Mar 22;9(5):695-702.

PMID:
10749976
[PubMed - indexed for MEDLINE]
Free Article
20.

[From gene to disease; from SHOX to Lèri-Weill dyschondrosteosis, Turner syndrome and idiopathic short stature].

Kant SG, Drop SL.

Ned Tijdschr Geneeskd. 2001 Jul 28;145(30):1456-9. Review. Dutch.

PMID:
11503314
[PubMed - indexed for MEDLINE]

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