175 related articles for article (PubMed ID: 19116729)
1. Non-random X chromosome inactivation in Aicardi syndrome.
Eble TN; Sutton VR; Sangi-Haghpeykar H; Wang X; Jin W; Lewis RA; Fang P; Van den Veyver IB
Hum Genet; 2009 Mar; 125(2):211-6. PubMed ID: 19116729
[TBL] [Abstract][Full Text] [Related]
2. [X chromosome inactivation patterns in patients with Rett syndrome and their mothers and the parental origin of the priority inactive X chromosome].
Jiang SL; Bao XH; Song FY; Pan H; Li MR; Wu XR
Zhonghua Er Ke Za Zhi; 2006 Sep; 44(9):648-52. PubMed ID: 17217653
[TBL] [Abstract][Full Text] [Related]
3. X chromosome inactivation patterns in normal and X-linked hereditary nephropathy carrier dogs.
Bell RJ; Lees GE; Murphy KE
Cytogenet Genome Res; 2008; 122(1):37-40. PubMed ID: 18931484
[TBL] [Abstract][Full Text] [Related]
4. Molecular Mechanisms of Skewed X-Chromosome Inactivation in Female Hemophilia Patients-Lessons from Wide Genome Analyses.
Dardik R; Avishai E; Lalezari S; Barg AA; Levy-Mendelovich S; Budnik I; Barel O; Khavkin Y; Kenet G; Livnat T
Int J Mol Sci; 2021 Aug; 22(16):. PubMed ID: 34445777
[TBL] [Abstract][Full Text] [Related]
5. Skewed X chromosome inactivation in girls and female adolescents with autoimmune thyroid disease.
Santiwatana S; Mahachoklertwattana P; Limwongse C; Khlairit P; Pongratanakul S; Roothumnong E; Prangphan K; Choubtum L; Songdej D; Poomthavorn P
Clin Endocrinol (Oxf); 2018 Dec; 89(6):863-869. PubMed ID: 30229980
[TBL] [Abstract][Full Text] [Related]
6. Phenotype-genotype correlations in hemophilia A carriers are consistent with the binary role of the phase between F8 and X-chromosome inactivation.
Radic CP; Rossetti LC; Abelleyro MM; Tetzlaff T; Candela M; Neme D; Sciuccati G; Bonduel M; Medina-Acosta E; Larripa IB; de Tezanos Pinto M; De Brasi CD
J Thromb Haemost; 2015 Apr; 13(4):530-9. PubMed ID: 25611311
[TBL] [Abstract][Full Text] [Related]
7. X chromosome inactivation in Rett Syndrome and its correlations with MECP2 mutations and phenotype.
Xinhua Bao ; Shengling Jiang ; Fuying Song ; Hong Pan ; Meirong Li ; Wu XR
J Child Neurol; 2008 Jan; 23(1):22-5. PubMed ID: 18184939
[TBL] [Abstract][Full Text] [Related]
8. Characterization of X chromosome inactivation using integrated analysis of whole-exome and mRNA sequencing.
Szelinger S; Malenica I; Corneveaux JJ; Siniard AL; Kurdoglu AA; Ramsey KM; Schrauwen I; Trent JM; Narayanan V; Huentelman MJ; Craig DW
PLoS One; 2014; 9(12):e113036. PubMed ID: 25503791
[TBL] [Abstract][Full Text] [Related]
9. Understanding the Landscape of X-linked Variants Causing Intellectual Disability in Females Through Extreme X Chromosome Inactivation Skewing.
Vianna EQ; Piergiorge RM; Gonçalves AP; Dos Santos JM; Calassara V; Rosenberg C; Krepischi ACV; Boy da Silva RT; Dos Santos SR; Ribeiro MG; Machado FB; Medina-Acosta E; Pimentel MMG; Santos-Rebouças CB
Mol Neurobiol; 2020 Sep; 57(9):3671-3684. PubMed ID: 32564284
[TBL] [Abstract][Full Text] [Related]
10. A new sex-specific underlying mechanism for female schizophrenia: accelerated skewed X chromosome inactivation.
Zhang X; Li Y; Ma L; Zhang G; Liu M; Wang C; Zheng Y; Li R
Biol Sex Differ; 2020 Jul; 11(1):39. PubMed ID: 32680558
[TBL] [Abstract][Full Text] [Related]
11. X chromosome inactivation in women with alcoholism.
Manzardo AM; Henkhaus R; Hidaka B; Penick EC; Poje AB; Butler MG
Alcohol Clin Exp Res; 2012 Aug; 36(8):1325-9. PubMed ID: 22375556
[TBL] [Abstract][Full Text] [Related]
12. X inactivation and reactivation in X-linked diseases.
Vacca M; Della Ragione F; Scalabrì F; D'Esposito M
Semin Cell Dev Biol; 2016 Aug; 56():78-87. PubMed ID: 26994527
[TBL] [Abstract][Full Text] [Related]
13. Comparison of X-chromosome inactivation patterns in multiple tissues from human females.
Bittel DC; Theodoro MF; Kibiryeva N; Fischer W; Talebizadeh Z; Butler MG
J Med Genet; 2008 May; 45(5):309-13. PubMed ID: 18156436
[TBL] [Abstract][Full Text] [Related]
14. Skewed X-chromosome inactivation and XIST locus methylation levels do not contribute to the lower prevalence of Parkinson's disease in females.
Sharma A; Kaut O; Pavlova A; Fröhlich H; Ahmad A; Schmitt I; El-Maarri O; Oldenburg J; Wüllner U
Neurobiol Aging; 2017 Sep; 57():248.e1-248.e5. PubMed ID: 28663000
[TBL] [Abstract][Full Text] [Related]
15. Female Hunter syndrome caused by a single mutation and familial XCI skewing: implications for other X-linked disorders.
Kloska A; Jakóbkiewicz-Banecka J; Tylki-Szymańska A; Czartoryska B; Węgrzyn G
Clin Genet; 2011 Nov; 80(5):459-65. PubMed ID: 21062272
[TBL] [Abstract][Full Text] [Related]
16. Skewed X-chromosome inactivation in scleroderma.
Uz E; Loubiere LS; Gadi VK; Ozbalkan Z; Stewart J; Nelson JL; Ozcelik T
Clin Rev Allergy Immunol; 2008 Jun; 34(3):352-5. PubMed ID: 18157513
[TBL] [Abstract][Full Text] [Related]
17. Aneuploid rescue precedes X-chromosome inactivation and increases the incidence of its skewness by reducing the size of the embryonic progenitor cell pool.
Yoshida T; Miyado M; Mikami M; Suzuki E; Kinjo K; Matsubara K; Ogata T; Akutsu H; Kagami M; Fukami M
Hum Reprod; 2019 Sep; 34(9):1762-1769. PubMed ID: 31398259
[TBL] [Abstract][Full Text] [Related]
18. Female human pluripotent stem cells rapidly lose X chromosome inactivation marks and progress to a skewed methylation pattern during culture.
Geens M; Seriola A; Barbé L; Santalo J; Veiga A; Dée K; Van Haute L; Sermon K; Spits C
Mol Hum Reprod; 2016 Apr; 22(4):285-98. PubMed ID: 26786180
[TBL] [Abstract][Full Text] [Related]
19. Segregation of a totally skewed pattern of X chromosome inactivation in four familial cases of Rett syndrome without MECP2 mutation: implications for the disease.
Villard L; Lévy N; Xiang F; Kpebe A; Labelle V; Chevillard C; Zhang Z; Schwartz CE; Tardieu M; Chelly J; Anvret M; Fontès M
J Med Genet; 2001 Jul; 38(7):435-42. PubMed ID: 11432961
[TBL] [Abstract][Full Text] [Related]
20. X-chromosome inactivation patterns depend on age and tissue but not conception method in humans.
Juchniewicz P; Kloska A; Portalska K; Jakóbkiewicz-Banecka J; Węgrzyn G; Liss J; Głodek P; Tukaj S; Piotrowska E
Chromosome Res; 2023 Jan; 31(1):4. PubMed ID: 36695960
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]