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Items: 1 to 20 of 75

1.

SOX9 duplication linked to intersex in deer.

Kropatsch R, Dekomien G, Akkad DA, Gerding WM, Petrasch-Parwez E, Young ND, Altmüller J, Nürnberg P, Gasser RB, Epplen JT.

PLoS One. 2013 Sep 6;8(9):e73734. doi: 10.1371/journal.pone.0073734. eCollection 2013.

2.

Investigation of mutations in the SRY, SOX9, and DAX1 genes in sex reversal patients from the Sichuan region of China.

Chen L, Ding XP, Wei X, Li LX.

Genet Mol Res. 2014 Mar 12;13(1):1518-26. doi: 10.4238/2014.March.12.4.

3.

Deep sequencing of a candidate region harboring the SOX9 gene for the canine XX disorder of sex development.

Nowacka-Woszuk J, Szczerbal I, Pausch H, Hundi S, Hytönen MK, Grzemski A, Flisikowski K, Lohi H, Switonski M, Szydlowski M.

Anim Genet. 2017 Jun;48(3):330-337. doi: 10.1111/age.12538. Epub 2017 Jan 17.

PMID:
28094446
4.

Disruption of a long distance regulatory region upstream of SOX9 in isolated disorders of sex development.

Benko S, Gordon CT, Mallet D, Sreenivasan R, Thauvin-Robinet C, Brendehaug A, Thomas S, Bruland O, David M, Nicolino M, Labalme A, Sanlaville D, Callier P, Malan V, Huet F, Molven A, Dijoud F, Munnich A, Faivre L, Amiel J, Harley V, Houge G, Morel Y, Lyonnet S.

J Med Genet. 2011 Dec;48(12):825-30. doi: 10.1136/jmedgenet-2011-100255. Epub 2011 Nov 2.

PMID:
22051515
5.

Transcription of a protein-coding gene on B chromosomes of the Siberian roe deer (Capreolus pygargus).

Trifonov VA, Dementyeva PV, Larkin DM, O'Brien PC, Perelman PL, Yang F, Ferguson-Smith MA, Graphodatsky AS.

BMC Biol. 2013 Aug 6;11:90. doi: 10.1186/1741-7007-11-90.

6.

Copy number variation in the region harboring SOX9 gene in dogs with testicular/ovotesticular disorder of sex development (78,XX; SRY-negative).

Marcinkowska-Swojak M, Szczerbal I, Pausch H, Nowacka-Woszuk J, Flisikowski K, Dzimira S, Nizanski W, Payan-Carreira R, Fries R, Kozlowski P, Switonski M.

Sci Rep. 2015 Oct 1;5:14696. doi: 10.1038/srep14696.

7.
8.

Autosomal XX sex reversal caused by duplication of SOX9.

Huang B, Wang S, Ning Y, Lamb AN, Bartley J.

Am J Med Genet. 1999 Dec 3;87(4):349-53.

PMID:
10588843
9.

XX males SRY negative: a confirmed cause of infertility.

Vetro A, Ciccone R, Giorda R, Patricelli MG, Della Mina E, Forlino A, Zuffardi O.

J Med Genet. 2011 Oct;48(10):710-2. doi: 10.1136/jmedgenet-2011-100036. Epub 2011 Jun 7.

10.

Conserved regulatory modules in the Sox9 testis-specific enhancer predict roles for SOX, TCF/LEF, Forkhead, DMRT, and GATA proteins in vertebrate sex determination.

Bagheri-Fam S, Sinclair AH, Koopman P, Harley VR.

Int J Biochem Cell Biol. 2010 Mar;42(3):472-7. doi: 10.1016/j.biocel.2009.07.001. Epub 2009 Jul 16.

PMID:
19616114
11.

Loss of Fgfr2 leads to partial XY sex reversal.

Bagheri-Fam S, Sim H, Bernard P, Jayakody I, Taketo MM, Scherer G, Harley VR.

Dev Biol. 2008 Feb 1;314(1):71-83. Epub 2007 Nov 19.

15.

A molecular genetic approach for species identification of mammals and sex determination of birds in a forensic case of poaching from South Korea.

An J, Lee MY, Min MS, Lee MH, Lee H.

Forensic Sci Int. 2007 Mar 22;167(1):59-61. Epub 2006 Feb 7.

PMID:
16460896
16.

Analysis of medaka sox9 orthologue reveals a conserved role in germ cell maintenance.

Nakamura S, Watakabe I, Nishimura T, Toyoda A, Taniguchi Y, Tanaka M.

PLoS One. 2012;7(1):e29982. doi: 10.1371/journal.pone.0029982. Epub 2012 Jan 12.

17.

Identification of single-nucleotide polymorphisms of the prion protein gene in sika deer (Cervus nippon laiouanus).

Jeong HJ, Lee JB, Park SY, Song CS, Kim BS, Rho JR, Yoo MH, Jeong BH, Kim YS, Choi IS.

J Vet Sci. 2007 Sep;8(3):299-301.

18.

Genome-wide identification of Sox8-, and Sox9-dependent genes during early post-natal testis development in the mouse.

Chalmel F, Lardenois A, Georg I, Barrionuevo F, Demougin P, Jégou B, Scherer G, Primig M.

Andrology. 2013 Mar;1(2):281-92. doi: 10.1111/j.2047-2927.2012.00049.x. Epub 2013 Jan 13.

19.

Genetic variability and differentiation in Spanish roe deer (Capreolus capreolus): A phylogeographic reassessment within the European framework.

Royo LJ, Pajares G, Alvarez I, Fernández I, Goyache F.

Mol Phylogenet Evol. 2007 Jan;42(1):47-61. Epub 2006 May 26.

PMID:
16876438
20.

Heterozygous SOX9 mutations allowing for residual DNA-binding and transcriptional activation lead to the acampomelic variant of campomelic dysplasia.

Staffler A, Hammel M, Wahlbuhl M, Bidlingmaier C, Flemmer AW, Pagel P, Nicolai T, Wegner M, Holzinger A.

Hum Mutat. 2010 Jun;31(6):E1436-44. doi: 10.1002/humu.21238.

PMID:
20513132

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