170 related articles for article (PubMed ID: 30779428)
21. Turner syndrome: the case of the missing sex chromosome.
Zinn AR; Page DC; Fisher EM
Trends Genet; 1993 Mar; 9(3):90-3. PubMed ID: 8488568
[TBL] [Abstract][Full Text] [Related]
22. Expression of selected genes escaping from X inactivation in the 41, XX(Y)* mouse model for Klinefelter's syndrome.
Werler S; Poplinski A; Gromoll J; Wistuba J
Acta Paediatr; 2011 Jun; 100(6):885-91. PubMed ID: 21241365
[TBL] [Abstract][Full Text] [Related]
23. A proposed path by which genes common to mammalian X and Y chromosomes evolve to become X inactivated.
Jegalian K; Page DC
Nature; 1998 Aug; 394(6695):776-80. PubMed ID: 9723615
[TBL] [Abstract][Full Text] [Related]
24. Escape from X chromosome inactivation is an intrinsic property of the Jarid1c locus.
Li N; Carrel L
Proc Natl Acad Sci U S A; 2008 Nov; 105(44):17055-60. PubMed ID: 18971342
[TBL] [Abstract][Full Text] [Related]
25. Methylation status of genes escaping from X-chromosome inactivation in patients with X-chromosome rearrangements.
Kawashima S; Hattori A; Suzuki E; Matsubara K; Toki M; Kosaki R; Hasegawa Y; Nakabayashi K; Fukami M; Kagami M
Clin Epigenetics; 2021 Jun; 13(1):134. PubMed ID: 34193245
[TBL] [Abstract][Full Text] [Related]
26. Maintenance of X inactivation of the Rps4, Zfx, and Ube1 genes in a mouse in vitro system.
Bressler SL; Lee KH; Adler DA; Chapman VM; Disteche CM
Somat Cell Mol Genet; 1993 Jan; 19(1):29-37. PubMed ID: 7681608
[TBL] [Abstract][Full Text] [Related]
27. Silencing of X-Linked MicroRNAs by Meiotic Sex Chromosome Inactivation.
Royo H; Seitz H; ElInati E; Peters AH; Stadler MB; Turner JM
PLoS Genet; 2015 Oct; 11(10):e1005461. PubMed ID: 26509798
[TBL] [Abstract][Full Text] [Related]
28. Derivation of consensus inactivation status for X-linked genes from genome-wide studies.
Balaton BP; Cotton AM; Brown CJ
Biol Sex Differ; 2015; 6():35. PubMed ID: 26719789
[TBL] [Abstract][Full Text] [Related]
29. Phenotype in X chromosome rearrangements: pitfalls of X inactivation study.
Schluth C; Cossée M; Girard-Lemaire F; Carelle N; Dollfus H; Jeandidier E; Flori E
Pathol Biol (Paris); 2007 Feb; 55(1):29-36. PubMed ID: 16690229
[TBL] [Abstract][Full Text] [Related]
30. The eXceptional nature of the X chromosome.
Balaton BP; Dixon-McDougall T; Peeters SB; Brown CJ
Hum Mol Genet; 2018 Aug; 27(R2):R242-R249. PubMed ID: 29701779
[TBL] [Abstract][Full Text] [Related]
31. A cross-species comparison of X-chromosome inactivation in Eutheria.
Yen ZC; Meyer IM; Karalic S; Brown CJ
Genomics; 2007 Oct; 90(4):453-63. PubMed ID: 17728098
[TBL] [Abstract][Full Text] [Related]
32. Landscape of DNA methylation on the X chromosome reflects CpG density, functional chromatin state and X-chromosome inactivation.
Cotton AM; Price EM; Jones MJ; Balaton BP; Kobor MS; Brown CJ
Hum Mol Genet; 2015 Mar; 24(6):1528-39. PubMed ID: 25381334
[TBL] [Abstract][Full Text] [Related]
33. Genes that escape X-inactivation in humans have high intraspecific variability in expression, are associated with mental impairment but are not slow evolving.
Zhang Y; Castillo-Morales A; Jiang M; Zhu Y; Hu L; Urrutia AO; Kong X; Hurst LD
Mol Biol Evol; 2013 Dec; 30(12):2588-601. PubMed ID: 24023392
[TBL] [Abstract][Full Text] [Related]
34. PHOG, a candidate gene for involvement in the short stature of Turner syndrome.
Ellison JW; Wardak Z; Young MF; Gehron Robey P; Laig-Webster M; Chiong W
Hum Mol Genet; 1997 Aug; 6(8):1341-7. PubMed ID: 9259282
[TBL] [Abstract][Full Text] [Related]
35. Identification of a cluster of X-linked imprinted genes in mice.
Raefski AS; O'Neill MJ
Nat Genet; 2005 Jun; 37(6):620-4. PubMed ID: 15908953
[TBL] [Abstract][Full Text] [Related]
36. An evaluation of the inactive mouse X chromosome in somatic cell hybrids.
Salido EC; Passage MB; Yen PH; Shapiro LJ; Mohandas TK
Somat Cell Mol Genet; 1993 Jan; 19(1):65-71. PubMed ID: 8460399
[TBL] [Abstract][Full Text] [Related]
37. The mouse as a model of fundamental concepts related to Turner syndrome.
Arnold AP
Am J Med Genet C Semin Med Genet; 2019 Mar; 181(1):76-85. PubMed ID: 30779420
[TBL] [Abstract][Full Text] [Related]
38. Rps4 maps near the inactivation center on the mouse X chromosome.
Hamvas RM; Zinn A; Keer JT; Fisher EM; Beer-Romero P; Brown SD; Page DC
Genomics; 1992 Feb; 12(2):363-7. PubMed ID: 1740345
[TBL] [Abstract][Full Text] [Related]
39. Ullrich-Turner syndrome is not caused by haploinsufficiency of RPS4X.
Geerkens C; Just W; Held KR; Vogel W
Hum Genet; 1996 Jan; 97(1):39-44. PubMed ID: 8557258
[TBL] [Abstract][Full Text] [Related]
40. Identification of common differentially expressed genes in Turner (45,X) and Klinefelter (47,XXY) syndromes using bioinformatics analysis.
Manotas MC; Calderón JC; López-Kleine L; Suárez-Obando F; Moreno OM; Rojas A
Mol Genet Genomic Med; 2020 Nov; 8(11):e1503. PubMed ID: 32959501
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]