These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
135 related articles for article (PubMed ID: 2347586)
21. Preferential X-chromosome inactivation, DNA methylation and imprinting. Monk M; Grant M Dev Suppl; 1990; ():55-62. PubMed ID: 2090431 [TBL] [Abstract][Full Text] [Related]
22. Variable X-chromosome DNA methylation patterns detected with probe M27 beta in a series of lymphoid and myeloid malignancies. Hodges E; Howell WM; Boyd Y; Smith JL Br J Haematol; 1991 Mar; 77(3):315-22. PubMed ID: 2012755 [TBL] [Abstract][Full Text] [Related]
24. X inactivation analysis and DNA methylation studies of the ubiquitin activating enzyme E1 and PCTAIRE-1 genes in human and mouse. Carrel L; Clemson CM; Dunn JM; Miller AP; Hunt PA; Lawrence JB; Willard HF Hum Mol Genet; 1996 Mar; 5(3):391-401. PubMed ID: 8852665 [TBL] [Abstract][Full Text] [Related]
27. An X chromosome inactivation assay based on differential methylation of a CpG island coupled to a VNTR polymorphism at the 5' end of the monoamine oxidase A gene. Hendriks RW; Chen ZY; Hinds H; Schuurman RK; Craig IW Hum Mol Genet; 1992 Jun; 1(3):187-94. PubMed ID: 1303176 [TBL] [Abstract][Full Text] [Related]
28. Diagnosis of Wiskott-Aldrich syndrome by analysis of the X chromosome inactivation patterns in maternal leucocyte populations using the hypervariable DXS255 locus. Hendriks RW; De Weers M; Mensink RG; Kraakman ME; Mollee-Versteegde IF; Veerman AJ; Sandkuyl LA; Schuurman RK Clin Exp Immunol; 1991 May; 84(2):219-22. PubMed ID: 1709069 [TBL] [Abstract][Full Text] [Related]
29. Clonal analysis of human tumors with M27 beta, a highly informative polymorphic X chromosomal probe. Fey MF; Peter HJ; Hinds HL; Zimmermann A; Liechti-Gallati S; Gerber H; Studer H; Tobler A J Clin Invest; 1992 May; 89(5):1438-44. PubMed ID: 1349026 [TBL] [Abstract][Full Text] [Related]
30. Biochemical and molecular analysis of an X-linked case of Leigh syndrome associated with thiamin-responsive pyruvate dehydrogenase deficiency. Naito E; Ito M; Yokota I; Saijo T; Matsuda J; Osaka H; Kimura S; Kuroda Y J Inherit Metab Dis; 1997 Aug; 20(4):539-48. PubMed ID: 9266390 [TBL] [Abstract][Full Text] [Related]
31. A study of X chromosome activity in two incontinentia pigmenti families with probable linkage to Xq28. Curtis AR; Lindsay S; Boye E; Clarke AJ; Landy SJ; Bhattacharya SS Eur J Hum Genet; 1994; 2(1):51-8. PubMed ID: 7913867 [TBL] [Abstract][Full Text] [Related]
32. X-chromosome localization of the functional gene for the E1 alpha subunit of the human pyruvate dehydrogenase complex. Brown RM; Dahl HH; Brown GK Genomics; 1989 Feb; 4(2):174-81. PubMed ID: 2737678 [TBL] [Abstract][Full Text] [Related]
33. A new assay for the analysis of X-chromosome inactivation based on methylation-specific PCR. Kubota T; Nonoyama S; Tonoki H; Masuno M; Imaizumi K; Kojima M; Wakui K; Shimadzu M; Fukushima Y Hum Genet; 1999 Jan; 104(1):49-55. PubMed ID: 10071192 [TBL] [Abstract][Full Text] [Related]
34. An assay for X inactivation based on differential methylation at the fragile X locus, FMR1. Carrel L; Willard HF Am J Med Genet; 1996 Jul; 64(1):27-30. PubMed ID: 8826444 [TBL] [Abstract][Full Text] [Related]
35. Mutations in the X-linked pyruvate dehydrogenase (E1) alpha subunit gene (PDHA1) in patients with a pyruvate dehydrogenase complex deficiency. Lissens W; De Meirleir L; Seneca S; Liebaers I; Brown GK; Brown RM; Ito M; Naito E; Kuroda Y; Kerr DS; Wexler ID; Patel MS; Robinson BH; Seyda A Hum Mutat; 2000; 15(3):209-19. PubMed ID: 10679936 [TBL] [Abstract][Full Text] [Related]
36. Mutations in the X-linked E1 alpha subunit of pyruvate dehydrogenase leading to deficiency of the pyruvate dehydrogenase complex. Chun K; MacKay N; Petrova-Benedict R; Robinson BH Hum Mol Genet; 1993 Apr; 2(4):449-54. PubMed ID: 8504306 [TBL] [Abstract][Full Text] [Related]
37. Association of cerebral dysgenesis and lactic acidemia with X-linked PDH E1 alpha subunit mutations in females. Otero LJ; Brown GK; Silver K; Arnold DL; Matthews PM Pediatr Neurol; 1995 Nov; 13(4):327-32. PubMed ID: 8771169 [TBL] [Abstract][Full Text] [Related]
38. Association between nonrandom X-chromosome inactivation and BRCA1 mutation in germline DNA of patients with ovarian cancer. Buller RE; Sood AK; Lallas T; Buekers T; Skilling JS J Natl Cancer Inst; 1999 Feb; 91(4):339-46. PubMed ID: 10050867 [TBL] [Abstract][Full Text] [Related]
39. Molecular detection of altered X-inactivation patterns in the diagnosis of genetic disease. Malcolm S J Inherit Metab Dis; 1992; 15(4):514-7. PubMed ID: 1528011 [TBL] [Abstract][Full Text] [Related]
40. Variability of X chromosome inactivation: effect on levels of TIMP1 RNA and role of DNA methylation. Anderson CL; Brown CJ Hum Genet; 2002 Mar; 110(3):271-8. PubMed ID: 11935340 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]