Brown L - Search Results

1

Polymorphism for a 1.6-Mb deletion of the human Y chromosome persists through balance between recurrent mutation and haploid selection.

Repping S, Skaletsky H, Brown L, van Daalen SK, Korver CM, Pyntikova T, Kuroda-Kawaguchi T, de Vries JW, Oates RD, Silber S, van der Veen F, Page DC, Rozen S. Repping S, et al. Among authors: brown l. Nat Genet. 2003 Nov;35(3):247-51. doi: 10.1038/ng1250. Epub 2003 Oct 5. Nat Genet. 2003. PMID: 14528305

2

The human Y chromosome: a 43-interval map based on naturally occurring deletions.

Vollrath D, Foote S, Hilton A, Brown LG, Beer-Romero P, Bogan JS, Page DC. Vollrath D, et al. Among authors: brown lg. Science. 1992 Oct 2;258(5079):52-9. doi: 10.1126/science.1439769. Science. 1992. PMID: 1439769

3

Chromosomal localization of ZFX--a human gene that escapes X inactivation--and its murine homologs.

Page DC, Disteche CM, Simpson EM, de la Chapelle A, Andersson M, Alitalo T, Brown LG, Green P, Akots G. Page DC, et al. Among authors: brown lg. Genomics. 1990 May;7(1):37-46. doi: 10.1016/0888-7543(90)90516-w. Genomics. 1990. PMID: 1970799

4

Additional deletion in sex-determining region of human Y chromosome resolves paradox of X,t(Y;22) female.

Page DC, Fisher EM, McGillivray B, Brown LG. Page DC, et al. Among authors: brown lg. Nature. 1990 Jul 19;346(6281):279-81. doi: 10.1038/346279a0. Nature. 1990. PMID: 1973823

5

Mouse Zfx protein is similar to Zfy-2: each contains an acidic activating domain and 13 zinc fingers.

Mardon G, Luoh SW, Simpson EM, Gill G, Brown LG, Page DC. Mardon G, et al. Among authors: brown lg. Mol Cell Biol. 1990 Feb;10(2):681-8. doi: 10.1128/mcb.10.2.681-688.1990. Mol Cell Biol. 1990. PMID: 2105457 Free PMC article.

6

Homologous ribosomal protein genes on the human X and Y chromosomes: escape from X inactivation and possible implications for Turner syndrome.

Fisher EM, Beer-Romero P, Brown LG, Ridley A, McNeil JA, Lawrence JB, Willard HF, Bieber FR, Page DC. Fisher EM, et al. Among authors: brown lg. Cell. 1990 Dec 21;63(6):1205-18. doi: 10.1016/0092-8674(90)90416-c. Cell. 1990. PMID: 2124517

7

ZFX has a gene structure similar to ZFY, the putative human sex determinant, and escapes X inactivation.

Schneider-Gädicke A, Beer-Romero P, Brown LG, Nussbaum R, Page DC. Schneider-Gädicke A, et al. Among authors: brown lg. Cell. 1989 Jun 30;57(7):1247-58. doi: 10.1016/0092-8674(89)90061-5. Cell. 1989. PMID: 2500252

8

Putative transcription activator with alternative isoforms encoded by human ZFX gene.

Schneider-Gädicke A, Beer-Romero P, Brown LG, Mardon G, Luoh SW, Page DC. Schneider-Gädicke A, et al. Among authors: brown lg. Nature. 1989 Dec 7;342(6250):708-11. doi: 10.1038/342708a0. Nature. 1989. PMID: 2512506

9

Exchange of terminal portions of X- and Y-chromosomal short arms in human XX males.

Page DC, Brown LG, de la Chapelle A. Page DC, et al. Among authors: brown lg. Nature. 1987 Jul 30-Aug 5;328(6129):437-40. doi: 10.1038/328437a0. Nature. 1987. PMID: 2886915

10

An XXX male resulting from paternal X-Y interchange and maternal X-X nondisjunction.

Annerén G, Andersson M, Page DC, Brown LG, Berg M, Läckgren G, Gustavson KH, de la Chapelle A. Annerén G, et al. Among authors: brown lg. Am J Hum Genet. 1987 Oct;41(4):594-604. Am J Hum Genet. 1987. PMID: 2889356 Free PMC article.

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