Page DC - Search Results

1

The human inactive X chromosome modulates expression of the active X chromosome.

San Roman AK, Godfrey AK, Skaletsky H, Bellott DW, Groff AF, Harris HL, Blanton LV, Hughes JF, Brown L, Phou S, Buscetta A, Kruszka P, Banks N, Dutra A, Pak E, Lasutschinkow PC, Keen C, Davis SM, Tartaglia NR, Samango-Sprouse C, Muenke M, Page DC. San Roman AK, et al. Among authors: page dc. Cell Genom. 2023 Feb 8;3(2):100259. doi: 10.1016/j.xgen.2023.100259. eCollection 2023 Feb 8. Cell Genom. 2023. PMID: 36819663 Free PMC article.

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: page dc. Science. 1992 Oct 2;258(5079):52-9. doi: 10.1126/science.1439769. Science. 1992. PMID: 1439769

3

Inactivation of the Rps4 gene on the mouse X chromosome.

Zinn AR, Bressler SL, Beer-Romero P, Adler DA, Chapman VM, Page DC, Disteche CM. Zinn AR, et al. Among authors: page dc. Genomics. 1991 Dec;11(4):1097-101. doi: 10.1016/0888-7543(91)90037-f. Genomics. 1991. PMID: 1783379

4

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. Genomics. 1990 May;7(1):37-46. doi: 10.1016/0888-7543(90)90516-w. Genomics. 1990. PMID: 1970799

5

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. Nature. 1990 Jul 19;346(6281):279-81. doi: 10.1038/346279a0. Nature. 1990. PMID: 1973823

6

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: page dc. 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.

7

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: page dc. Cell. 1990 Dec 21;63(6):1205-18. doi: 10.1016/0092-8674(90)90416-c. Cell. 1990. PMID: 2124517

8

Human sex-chromosome-specific repeats within a region of pseudoautosomal/Yq homology.

Fisher EM, Alitalo T, Luoh SW, de la Chapelle A, Page DC. Fisher EM, et al. Among authors: page dc. Genomics. 1990 Aug;7(4):625-8. doi: 10.1016/0888-7543(90)90209-d. Genomics. 1990. PMID: 2387589

9

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: page dc. Cell. 1989 Jun 30;57(7):1247-58. doi: 10.1016/0092-8674(89)90061-5. Cell. 1989. PMID: 2500252

10

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: page dc. Nature. 1989 Dec 7;342(6250):708-11. doi: 10.1038/342708a0. Nature. 1989. PMID: 2512506

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