Format
Sort by
Items per page

Send to

Choose Destination

Links from PubMed

Items: 1 to 20 of 173

1.

An SRY mutation causing human sex reversal resolves a general mechanism of structure-specific DNA recognition: application to the four-way DNA junction.

Peters R, King CY, Ukiyama E, Falsafi S, Donahoe PK, Weiss MA.

Biochemistry. 1995 Apr 11;34(14):4569-76.

PMID:
7718558
2.

Protein-directed DNA structure. I. Raman spectroscopy of a high-mobility-group box with application to human sex reversal.

Benevides JM, Chan G, Lu XJ, Olson WK, Weiss MA, Thomas GJ Jr.

Biochemistry. 2000 Jan 25;39(3):537-47.

PMID:
10642178
3.

Evolutionary conservation in the DNA-binding and -bending properties of HMG-boxes from SRY proteins of primates.

Pontiggia A, Whitfield S, Goodfellow PN, Lovell-Badge R, Bianchi ME.

Gene. 1995 Mar 10;154(2):277-80.

PMID:
7890177
4.

Structural basis for SRY-dependent 46-X,Y sex reversal: modulation of DNA bending by a naturally occurring point mutation.

Murphy EC, Zhurkin VB, Louis JM, Cornilescu G, Clore GM.

J Mol Biol. 2001 Sep 21;312(3):481-99.

PMID:
11563911
5.

Defective importin beta recognition and nuclear import of the sex-determining factor SRY are associated with XY sex-reversing mutations.

Harley VR, Layfield S, Mitchell CL, Forwood JK, John AP, Briggs LJ, McDowall SG, Jans DA.

Proc Natl Acad Sci U S A. 2003 Jun 10;100(12):7045-50. Epub 2003 May 22.

6.

Sry-directed sex reversal in transgenic mice is robust with respect to enhanced DNA bending: comparison of human and murine HMG boxes.

Phillips NB, Nikolskaya T, Jancso-Radek A, Ittah V, Jiang F, Singh R, Haas E, Weiss MA.

Biochemistry. 2004 Jun 8;43(22):7066-81.

PMID:
15170344
7.

Biochemical defects in eight SRY missense mutations causing XY gonadal dysgenesis.

Mitchell CL, Harley VR.

Mol Genet Metab. 2002 Nov;77(3):217-25.

PMID:
12409269
8.

SRY-directed DNA bending and human sex reversal: reassessment of a clinical mutation uncovers a global coupling between the HMG box and its tail.

Li B, Phillips NB, Jancso-Radek A, Ittah V, Singh R, Jones DN, Haas E, Weiss MA.

J Mol Biol. 2006 Jul 7;360(2):310-28. Epub 2006 May 9.

PMID:
16762365
9.

Two new novel point mutations localized upstream and downstream of the HMG box region of the SRY gene in three Indian 46,XY females with sex reversal and gonadal tumour formation.

Shahid M, Dhillion VS, Jain N, Hedau S, Diwakar S, Sachdeva P, Batra S, Das BC, Husain SA.

Mol Hum Reprod. 2004 Jul;10(7):521-6. Epub 2004 May 21.

PMID:
15155818
10.

Mutational analysis of SRY: nonsense and missense mutations in XY sex reversal.

Hawkins JR, Taylor A, Berta P, Levilliers J, Van der Auwera B, Goodfellow PN.

Hum Genet. 1992 Feb;88(4):471-4.

PMID:
1339396
11.
12.

Sry and Sox9: mammalian testis-determining genes.

Koopman P.

Cell Mol Life Sci. 1999 Jun;55(6-7):839-56. Review.

PMID:
10412367
13.

Human sex reversal due to impaired nuclear localization of SRY. A clinical correlation.

Li B, Zhang W, Chan G, Jancso-Radek A, Liu S, Weiss MA.

J Biol Chem. 2001 Dec 7;276(49):46480-4.

15.

Two novel mutations in SRY gene form Chinese sex reversal XY females.

Zhou C, Fu JJ, Li LY, Lu GX.

Yi Chuan Xue Bao. 2005 May;32(5):443-9.

PMID:
16018252
16.

A familial mutation in the testis-determining gene SRY shared by both sexes.

Jäger RJ, Harley VR, Pfeiffer RA, Goodfellow PN, Scherer G.

Hum Genet. 1992 Dec;90(4):350-5.

PMID:
1483689
17.
18.

Molecular basis of mammalian sexual determination: activation of Müllerian inhibiting substance gene expression by SRY.

Haqq CM, King CY, Ukiyama E, Falsafi S, Haqq TN, Donahoe PK, Weiss MA.

Science. 1994 Dec 2;266(5190):1494-500. Review. Erratum in: Science 1995 Jan 20;267(5196):317.

PMID:
7985018
19.

Loss of sequences 3' to the testis-determining gene, SRY, including the Y pseudoautosomal boundary associated with partial testicular determination.

McElreavey K, Vilain E, Barbaux S, Fuqua JS, Fechner PY, Souleyreau N, Doco-Fenzy M, Gabriel R, Quereux C, Fellous M, Berkovitz GD.

Proc Natl Acad Sci U S A. 1996 Aug 6;93(16):8590-4.

20.

A novel double nucleotide substitution in the HMG box of the SRY gene associated with Swyer syndrome.

Battiloro E, Angeletti B, Tozzi MC, Bruni L, Tondini S, Vignetti P, Verna R, D'Ambrosio E.

Hum Genet. 1997 Oct;100(5-6):585-7.

PMID:
9341876

Supplemental Content

Support Center