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Items: 1 to 20 of 172

1.

An infertile 45,X male with a SRY-bearing chromosome 13: a clinical case report and literature review.

Peng D, Zhang YS, Zhang XY, Hu C, Liu MH, Liu RZ.

J Assist Reprod Genet. 2015 Jan;32(1):107-9. doi: 10.1007/s10815-014-0376-z. Epub 2014 Nov 6.

2.

Sex-determination gene SRY potentially associates with poor prognosis but not sex bias in hepatocellular carcinoma.

Xue TC, Zhang L, Ren ZG, Chen RX, Cui JF, Ge NL, Ye SL.

Dig Dis Sci. 2015 Feb;60(2):427-35. doi: 10.1007/s10620-014-3377-y. Epub 2014 Oct 2.

PMID:
25274159
3.

Structure-function relationships in human testis-determining factor SRY: an aromatic buttress underlies the specific DNA-bending surface of a high mobility group (HMG) box.

Racca JD, Chen YS, Maloy JD, Wickramasinghe N, Phillips NB, Weiss MA.

J Biol Chem. 2014 Nov 21;289(47):32410-29. doi: 10.1074/jbc.M114.597526. Epub 2014 Sep 24.

4.

Transient neuroprotection by SRY upregulation in dopamine cells following injury in males.

Czech DP, Lee J, Correia J, Loke H, Möller EK, Harley VR.

Endocrinology. 2014 Jul;155(7):2602-12. doi: 10.1210/en.2013-2158. Epub 2014 Apr 7.

PMID:
24708242
5.

Inherited human sex reversal due to impaired nucleocytoplasmic trafficking of SRY defines a male transcriptional threshold.

Chen YS, Racca JD, Phillips NB, Weiss MA.

Proc Natl Acad Sci U S A. 2013 Sep 17;110(38):E3567-76. doi: 10.1073/pnas.1300828110. Epub 2013 Sep 3.

6.

Comparative SRY incorporation on the regulatory regions of pluripotency/differentiation genes in human embryonic carcinoma cells after retinoic acid induction.

Kakhki SA, Shahhoseini M, Salekdeh GH.

Mol Cell Biochem. 2013 Apr;376(1-2):145-50. doi: 10.1007/s11010-013-1562-5. Epub 2013 Jan 30.

PMID:
23361361
7.

The human testis-determining factor SRY localizes in midbrain dopamine neurons and regulates multiple components of catecholamine synthesis and metabolism.

Czech DP, Lee J, Sim H, Parish CL, Vilain E, Harley VR.

J Neurochem. 2012 Jul;122(2):260-71. doi: 10.1111/j.1471-4159.2012.07782.x. Epub 2012 Jun 8.

8.

A novel SRY mutation leads to asymmetric SOX9 activation and is responsible for mixed 46,XY gonadal dysgenesis.

Klee P, Béna F, Birraux J, Dahoun S, Dirlewanger M, Girardin C, Plotton I, Rougemont AL, Morel Y, Schwitzgebel VM.

Horm Res Paediatr. 2012;78(3):188-92. doi: 10.1159/000336925. Epub 2012 Mar 22.

PMID:
22441105
9.

46, XY gonadal dysgenesis: new SRY point mutation in two siblings with paternal germ line mosaicism.

Stoppa-Vaucher S, Ayabe T, Paquette J, Patey N, Francoeur D, Vuissoz JM, Deladoëy J, Samuels ME, Ogata T, Deal CL.

Clin Genet. 2012 Dec;82(6):505-13. doi: 10.1111/j.1399-0004.2011.01832.x. Epub 2012 Jan 30.

PMID:
22288726
10.

A novel missense mutation in the high mobility group domain of SRY drastically reduces its DNA-binding capacity and causes paternally transmitted 46,XY complete gonadal dysgenesis.

Filges I, Kunz C, Miny P, Boesch N, Szinnai G, Wenzel F, Tschudin S, Zumsteg U, Heinimann K.

Fertil Steril. 2011 Oct;96(4):851-5. doi: 10.1016/j.fertnstert.2011.07.1137. Epub 2011 Aug 24.

PMID:
21868002
11.

Mammalian testis-determining factor SRY and the enigma of inherited human sex reversal: frustrated induced fit in a bent protein-DNA complex.

Phillips NB, Racca J, Chen YS, Singh R, Jancso-Radek A, Radek JT, Wickramasinghe NP, Haas E, Weiss MA.

J Biol Chem. 2011 Oct 21;286(42):36787-807. doi: 10.1074/jbc.M111.260091. Epub 2011 Aug 17.

12.

SRY-specific cell free fetal DNA in maternal plasma in twin pregnancies throughout gestation.

Orendi K, Klein K, Krampl-Bettelheim E, Nuk M, Holzapfel-Bauer M, Magnet E, Griesbacher A, Lang U, Pertl B.

Placenta. 2011 Aug;32(8):611-5. doi: 10.1016/j.placenta.2011.03.009. Epub 2011 Jun 21.

PMID:
21696822
13.

Dual nuclear import mechanisms of sex determining factor SRY: intracellular Ca2+ as a switch.

Kaur G, Jans DA.

FASEB J. 2011 Feb;25(2):665-75. doi: 10.1096/fj.10-173351. Epub 2010 Nov 4.

PMID:
21051653
14.

The role of SRY mutations in the etiology of gonadal dysgenesis in patients with 45,X/46,XY disorder of sex development and variants.

Nishi MY, Costa EM, Oliveira SB, Mendonca BB, Domenice S.

Horm Res Paediatr. 2011;75(1):26-31. doi: 10.1159/000316536. Epub 2010 Aug 12.

PMID:
20699606
15.

An SRY-deleted XXY female resulting from a paternally inherited t(Y;22).

Kim J, Kim SH, Song J, Choi JR, Kim HS, Lee KA.

Ann Clin Lab Sci. 2010 Summer;40(3):295-9.

PMID:
20689145
16.

Calmodulin-dependent nuclear import of HMG-box family nuclear factors: importance of the role of SRY in sex reversal.

Kaur G, Delluc-Clavieres A, Poon IK, Forwood JK, Glover DJ, Jans DA.

Biochem J. 2010 Aug 15;430(1):39-48. doi: 10.1042/BJ20091758.

17.

Nonsyndromic 46,XX Testicular Disorders of Sex Development.

Délot EC, Vilain EJ.

In: Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean LJH, Stephens K, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993-2018.
2003 Oct 30 [updated 2015 May 7].

18.

Review of the Y chromosome, Sry and hypertension.

Ely D, Underwood A, Dunphy G, Boehme S, Turner M, Milsted A.

Steroids. 2010 Nov;75(11):747-53. doi: 10.1016/j.steroids.2009.10.015. Epub 2009 Nov 13. Review.

19.

Analysis of the SRY gene in a girl with 45,X/46,XY genotype.

Akbas E, Soylemez F, Hallioglu O, Polat S, Turkoz G.

Genet Couns. 2009;20(3):249-54.

PMID:
19852431
20.

Mixed gonadal dysgenesis with 45,X/46,X,idic(Y)/46,XY,idic(Y) karyotype.

Caglayan AO, Demiryilmaz F, Kendirci M, Ozyazgan I, Akalin H, Bittmann S.

Genet Couns. 2009;20(2):173-9.

PMID:
19650415

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