206 related articles for article (PubMed ID: 26994527)
1. 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]
2. 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]
3. [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]
4. Skewed X chromosome inactivation failed to explain the normal phenotype of a carrier female with MECP2 mutation resulting in Rett syndrome.
Takahashi S; Ohinata J; Makita Y; Suzuki N; Araki A; Sasaki A; Murono K; Tanaka H; Fujieda K
Clin Genet; 2008 Mar; 73(3):257-61. PubMed ID: 18190595
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. Genetic and pharmacological reactivation of the mammalian inactive X chromosome.
Bhatnagar S; Zhu X; Ou J; Lin L; Chamberlain L; Zhu LJ; Wajapeyee N; Green MR
Proc Natl Acad Sci U S A; 2014 Sep; 111(35):12591-8. PubMed ID: 25136103
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. 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]
9. MECP2 mutant allele in a boy with Rett syndrome and his unaffected heterozygous mother.
Dayer AG; Bottani A; Bouchardy I; Fluss J; Antonarakis SE; Haenggeli CA; Morris MA
Brain Dev; 2007 Jan; 29(1):47-50. PubMed ID: 16844334
[TBL] [Abstract][Full Text] [Related]
10. Increased skewing of X chromosome inactivation in Rett syndrome patients and their mothers.
Knudsen GP; Neilson TC; Pedersen J; Kerr A; Schwartz M; Hulten M; Bailey ME; Orstavik KH
Eur J Hum Genet; 2006 Nov; 14(11):1189-94. PubMed ID: 16823396
[TBL] [Abstract][Full Text] [Related]
11. The Role of X-Chromosome Inactivation in Retinal Development and Disease.
Fahim AT; Daiger SP
Adv Exp Med Biol; 2016; 854():325-31. PubMed ID: 26427428
[TBL] [Abstract][Full Text] [Related]
12. [Analysis of the parental origin of de novo MECP2 mutations and X chromosome inactivation in fifteen sporadic cases with Rett syndrome].
Zhu XW; Pan H; Li MR; Bao XH; Zhang JJ; Wu XR
Zhonghua Er Ke Za Zhi; 2009 Aug; 47(8):565-9. PubMed ID: 19951486
[TBL] [Abstract][Full Text] [Related]
13. X-chromosome inactivation: implications in human disease.
Pereira G; Dória S
J Genet; 2021; 100():. PubMed ID: 34553695
[TBL] [Abstract][Full Text] [Related]
14. A Rett syndrome patient with a ring X chromosome: further evidence for skewing of X inactivation and heterogeneity in the aetiology of the disease.
Rosenberg C; Wouters CH; Szuhai K; Dorland R; Pearson P; Poll-The BT; Colombijn RM; Breuning M; Lindhout D
Eur J Hum Genet; 2001 Mar; 9(3):171-7. PubMed ID: 11313755
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. Dosage Compensation in Females with X-Linked Metabolic Disorders.
Juchniewicz P; Piotrowska E; Kloska A; Podlacha M; Mantej J; Węgrzyn G; Tukaj S; Jakóbkiewicz-Banecka J
Int J Mol Sci; 2021 Apr; 22(9):. PubMed ID: 33925963
[TBL] [Abstract][Full Text] [Related]
17. Developmental regulation of X-chromosome inactivation.
Payer B
Semin Cell Dev Biol; 2016 Aug; 56():88-99. PubMed ID: 27112543
[TBL] [Abstract][Full Text] [Related]
18. Analysis of X-inactivation status in a Rett syndrome natural history study cohort.
Fang X; Butler KM; Abidi F; Gass J; Beisang A; Feyma T; Ryther RC; Standridge S; Heydemann P; Jones M; Haas R; Lieberman DN; Marsh ED; Benke TA; Skinner S; Neul JL; Percy AK; Friez MJ; Caylor RC
Mol Genet Genomic Med; 2022 May; 10(5):e1917. PubMed ID: 35318820
[TBL] [Abstract][Full Text] [Related]
19. X-inactivation and human disease: X-linked dominant male-lethal disorders.
Franco B; Ballabio A
Curr Opin Genet Dev; 2006 Jun; 16(3):254-9. PubMed ID: 16650755
[TBL] [Abstract][Full Text] [Related]
20. Balanced X chromosome inactivation patterns in the Rett syndrome brain.
Shahbazian MD; Sun Y; Zoghbi HY
Am J Med Genet; 2002 Aug; 111(2):164-8. PubMed ID: 12210344
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]