288 related articles for article (PubMed ID: 26181491)
21. Novel mutations in cyclin-dependent kinase-like 5 (CDKL5) gene in Indian cases of Rett syndrome.
Das DK; Mehta B; Menon SR; Raha S; Udani V
Neuromolecular Med; 2013 Mar; 15(1):218-25. PubMed ID: 23242510
[TBL] [Abstract][Full Text] [Related]
22. A novel variant of the putative demethylase gene, s-JMJD1C, is a coactivator of the AR.
Wolf SS; Patchev VK; Obendorf M
Arch Biochem Biophys; 2007 Apr; 460(1):56-66. PubMed ID: 17353003
[TBL] [Abstract][Full Text] [Related]
23. Learning disability and myoclonic epilepsy associated with apparently synonymous but splice-disrupting JMJD1C variant that led to 21 bp deletion of the transcript.
Yamada M; Sokoda T; Uehara T; Suzuki H; Takenouchi T; Yagihashi T; Maruo Y; Kosaki K
Am J Med Genet A; 2020 Dec; 182(12):3064-3067. PubMed ID: 32996679
[No Abstract] [Full Text] [Related]
24. The histone demethylase JMJD1C regulates CPS1 expression and promotes the proliferation of paroxysmal nocturnal haemoglobinuria clones through cell metabolic reprogramming.
Chen Y; Liu H; Wang C; Chen W; Li L; Wu J; Wang G; Ling GS; Fu R
Br J Haematol; 2024 Jun; 204(6):2468-2479. PubMed ID: 38650379
[TBL] [Abstract][Full Text] [Related]
25. Spectrum of MECP2 mutations in New Zealand Rett syndrome patients.
Raizis AM; Saleem M; MacKay R; George PM
N Z Med J; 2009 Jun; 122(1296):21-8. PubMed ID: 19652677
[TBL] [Abstract][Full Text] [Related]
26. Inhibition of histone demethylase JMJD1C attenuates cardiac hypertrophy and fibrosis induced by angiotensin II.
Zhang S; Lu Y; Jiang C
J Recept Signal Transduct Res; 2020 Aug; 40(4):339-347. PubMed ID: 32122211
[TBL] [Abstract][Full Text] [Related]
27. KDM5C mutational screening among males with intellectual disability suggestive of X-Linked inheritance and review of the literature.
Gonçalves TF; Gonçalves AP; Fintelman Rodrigues N; dos Santos JM; Pimentel MM; Santos-Rebouças CB
Eur J Med Genet; 2014 Mar; 57(4):138-44. PubMed ID: 24583395
[TBL] [Abstract][Full Text] [Related]
28. Disruption of PHF21A causes syndromic intellectual disability with craniofacial anomalies, epilepsy, hypotonia, and neurobehavioral problems including autism.
Kim HG; Rosenfeld JA; Scott DA; Bénédicte G; Labonne JD; Brown J; McGuire M; Mahida S; Naidu S; Gutierrez J; Lesca G; des Portes V; Bruel AL; Sorlin A; Xia F; Capri Y; Muller E; McKnight D; Torti E; Rüschendorf F; Hummel O; Islam Z; Kolatkar PR; Layman LC; Ryu D; Kong IK; Madan-Khetarpal S; Kim CH
Mol Autism; 2019; 10():35. PubMed ID: 31649809
[TBL] [Abstract][Full Text] [Related]
29. Comparative analysis of the autism‑related variants between different autistic children in a family pedigree.
Shen L; Li P; Zheng T; Luo M; Zhang S; Huang Y; Hu Y; Li H
Mol Med Rep; 2021 Oct; 24(4):. PubMed ID: 34368859
[TBL] [Abstract][Full Text] [Related]
30. Mutation analysis of the MECP2 gene in British and Italian Rett syndrome females.
Vacca M; Filippini F; Budillon A; Rossi V; Mercadante G; Manzati E; Gualandi F; Bigoni S; Trabanelli C; Pini G; Calzolari E; Ferlini A; Meloni I; Hayek G; Zappella M; Renieri A; D'Urso M; D'Esposito M; MacDonald F; Kerr A; Dhanjal S; Hultén M
J Mol Med (Berl); 2001; 78(11):648-55. PubMed ID: 11269512
[TBL] [Abstract][Full Text] [Related]
31. The phenotypic consequences of MECP2 mutations extend beyond Rett syndrome.
Hammer S; Dorrani N; Dragich J; Kudo S; Schanen C
Ment Retard Dev Disabil Res Rev; 2002; 8(2):94-8. PubMed ID: 12112734
[TBL] [Abstract][Full Text] [Related]
32. Current developments in the genetics of Rett and Rett-like syndrome.
Ehrhart F; Sangani NB; Curfs LMG
Curr Opin Psychiatry; 2018 Mar; 31(2):103-108. PubMed ID: 29206688
[TBL] [Abstract][Full Text] [Related]
33. A novel variant in NEUROD2 in a patient with Rett-like phenotype points to Glu130 codon as a mutational hotspot.
Politano D; Gana S; Pezzotti E; Berardinelli A; Pasca L; Carmen Barbero V; Pichiecchio A; Maria Valente E; Errichiello E
Brain Dev; 2023 Mar; 45(3):179-184. PubMed ID: 36446697
[TBL] [Abstract][Full Text] [Related]
34. First report of an unusual novel double mutation affecting the transcription repression domain of MeCP2 and causing a severe phenotype of Rett syndrome: Molecular analyses and computational investigation.
Ghorbel R; Ghorbel R; Rouissi A; Fendri-Kriaa N; Ben Salah G; Belguith N; Ammar-Keskes L; Gouider-Khouja N; Fakhfakh F
Biochem Biophys Res Commun; 2018 Feb; 497(1):93-101. PubMed ID: 29421650
[TBL] [Abstract][Full Text] [Related]
35. JMJD1C Regulates Megakaryopoiesis in In Vitro Models through the Actin Network.
Wang J; Liu X; Wang H; Qin L; Feng A; Qi D; Wang H; Zhao Y; Kong L; Wang H; Wang L; Hu Z; Xu X
Cells; 2022 Nov; 11(22):. PubMed ID: 36429088
[TBL] [Abstract][Full Text] [Related]
36. An atypical 12q24.31 microdeletion implicates six genes including a histone demethylase KDM2B and a histone methyltransferase SETD1B in syndromic intellectual disability.
Labonne JD; Lee KH; Iwase S; Kong IK; Diamond MP; Layman LC; Kim CH; Kim HG
Hum Genet; 2016 Jul; 135(7):757-71. PubMed ID: 27106595
[TBL] [Abstract][Full Text] [Related]
37. shRNA screening identifies JMJD1C as being required for leukemia maintenance.
Sroczynska P; Cruickshank VA; Bukowski JP; Miyagi S; Bagger FO; Walfridsson J; Schuster MB; Porse B; Helin K
Blood; 2014 Mar; 123(12):1870-82. PubMed ID: 24501218
[TBL] [Abstract][Full Text] [Related]
38. Histone Modifier Genes Alter Conotruncal Heart Phenotypes in 22q11.2 Deletion Syndrome.
Guo T; Chung JH; Wang T; McDonald-McGinn DM; Kates WR; Hawuła W; Coleman K; Zackai E; Emanuel BS; Morrow BE
Am J Hum Genet; 2015 Dec; 97(6):869-77. PubMed ID: 26608785
[TBL] [Abstract][Full Text] [Related]
39. Role of H3K4 demethylases in complex neurodevelopmental diseases.
Wynder C; Stalker L; Doughty ML
Epigenomics; 2010 Jun; 2(3):407-18. PubMed ID: 22121901
[TBL] [Abstract][Full Text] [Related]
40. Polymorphisms in JMJD1C are associated with pubertal onset in boys and reproductive function in men.
Mørup N; Busch AS; Bang AK; Nordkap L; Nielsen JE; Rajpert-De Meyts E; Juul A; Jørgensen N; Almstrup K
Sci Rep; 2017 Dec; 7(1):17242. PubMed ID: 29222425
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
