283 related articles for article (PubMed ID: 29962935)
21. CHD2 pathogenic nonsense variant in a three-generation family with variable phenotype and a paracentric inversion 16: Case report.
Angelopoulou E; Theodosiou A; Papaevripidou I; Alexandrou A; Liehr T; Gyftodimou Y; Stefanou EG; Sismani C
Heliyon; 2023 Dec; 9(12):e22987. PubMed ID: 38125503
[TBL] [Abstract][Full Text] [Related]
22. Regulation of neuronal connectivity in the mammalian brain by chromatin remodeling.
Goodman JV; Bonni A
Curr Opin Neurobiol; 2019 Dec; 59():59-68. PubMed ID: 31146125
[TBL] [Abstract][Full Text] [Related]
23. Oligodendrocyte precursor survival and differentiation requires chromatin remodeling by Chd7 and Chd8.
Marie C; Clavairoly A; Frah M; Hmidan H; Yan J; Zhao C; Van Steenwinckel J; Daveau R; Zalc B; Hassan B; Thomas JL; Gressens P; Ravassard P; Moszer I; Martin DM; Lu QR; Parras C
Proc Natl Acad Sci U S A; 2018 Aug; 115(35):E8246-E8255. PubMed ID: 30108144
[TBL] [Abstract][Full Text] [Related]
24. Disruption of chromodomain helicase DNA binding protein 2 (CHD2) causes scoliosis.
Kulkarni S; Nagarajan P; Wall J; Donovan DJ; Donell RL; Ligon AH; Venkatachalam S; Quade BJ
Am J Med Genet A; 2008 May; 146A(9):1117-27. PubMed ID: 18386809
[TBL] [Abstract][Full Text] [Related]
25. Exome sequencing analysis in a pair of monozygotic twins re-evaluates the genetics behind their intellectual disability and reveals a CHD2 mutation.
Pinto AM; Bianciardi L; Mencarelli MA; Imperatore V; Di Marco C; Furini S; Suppiej A; Salviati L; Tenconi R; Ariani F; Mari F; Renieri A
Brain Dev; 2016 Jun; 38(6):590-6. PubMed ID: 26754451
[TBL] [Abstract][Full Text] [Related]
26. Functional DNA methylation signatures for autism spectrum disorder genomic risk loci: 16p11.2 deletions and CHD8 variants.
Siu MT; Butcher DT; Turinsky AL; Cytrynbaum C; Stavropoulos DJ; Walker S; Caluseriu O; Carter M; Lou Y; Nicolson R; Georgiades S; Szatmari P; Anagnostou E; Scherer SW; Choufani S; Brudno M; Weksberg R
Clin Epigenetics; 2019 Jul; 11(1):103. PubMed ID: 31311581
[TBL] [Abstract][Full Text] [Related]
27. Low-grade parental gonosomal mosaicism in CHD2 siblings with Smith-Magenis-like syndrome.
Cogliati F; Straniero L; Rimoldi V; Masciadri M; Perego S; Rinaldi B; Milani D; Gentilini D; Larizza L; Asselta R; Russo S; Bedeschi MF
Am J Med Genet B Neuropsychiatr Genet; 2024 Feb; ():e32976. PubMed ID: 38385826
[TBL] [Abstract][Full Text] [Related]
28. Generation of a rat monoclonal antibody specific for CHD2.
Harada A; Yoshimura S; Odawara J; Azuma M; Okada S; Nakamura M; Tachibana T; Ohkawa Y
Hybridoma (Larchmt); 2010 Apr; 29(2):173-7. PubMed ID: 20443711
[TBL] [Abstract][Full Text] [Related]
29. CHD2 variants are a risk factor for photosensitivity in epilepsy.
Galizia EC; Myers CT; Leu C; de Kovel CG; Afrikanova T; Cordero-Maldonado ML; Martins TG; Jacmin M; Drury S; Krishna Chinthapalli V; Muhle H; Pendziwiat M; Sander T; Ruppert AK; Møller RS; Thiele H; Krause R; Schubert J; Lehesjoki AE; Nürnberg P; Lerche H; ; Palotie A; Coppola A; Striano S; Gaudio LD; Boustred C; Schneider AL; Lench N; Jocic-Jakubi B; Covanis A; Capovilla G; Veggiotti P; Piccioli M; Parisi P; Cantonetti L; Sadleir LG; Mullen SA; Berkovic SF; Stephani U; Helbig I; Crawford AD; Esguerra CV; Kasteleijn-Nolst Trenité DG; Koeleman BP; Mefford HC; Scheffer IE; Sisodiya SM
Brain; 2015 May; 138(Pt 5):1198-207. PubMed ID: 25783594
[TBL] [Abstract][Full Text] [Related]
30. CHD2 mutations are a rare cause of generalized epilepsy with myoclonic-atonic seizures.
Trivisano M; Striano P; Sartorelli J; Giordano L; Traverso M; Accorsi P; Cappelletti S; Claps DJ; Vigevano F; Zara F; Specchio N
Epilepsy Behav; 2015 Oct; 51():53-6. PubMed ID: 26262932
[TBL] [Abstract][Full Text] [Related]
31. Dissecting genetics of spectrum of epilepsies with eyelid myoclonia by exome sequencing.
Coppola A; Krithika S; Iacomino M; Bobbili D; Balestrini S; Bagnasco I; Bilo L; Buti D; Casellato S; Cuccurullo C; Ferlazzo E; Leu C; Giordano L; Gobbi G; Hernandez-Hernandez L; Lench N; Martins H; Meletti S; Messana T; Nigro V; Pinelli M; Pippucci T; Bellampalli R; Salis B; Sofia V; Striano P; Striano S; Tassi L; Vignoli A; Vaudano AE; Viri M; Scheffer IE; May P; Zara F; Sisodiya SM
Epilepsia; 2024 Mar; 65(3):779-791. PubMed ID: 38088023
[TBL] [Abstract][Full Text] [Related]
32. Mutation of the SNF2 family member Chd2 affects mouse development and survival.
Marfella CG; Ohkawa Y; Coles AH; Garlick DS; Jones SN; Imbalzano AN
J Cell Physiol; 2006 Oct; 209(1):162-71. PubMed ID: 16810678
[TBL] [Abstract][Full Text] [Related]
33. From X-inactivation to neurodevelopment: CHD8-transcription factors (TFs) competitive binding at regulatory regions of CHD8 target genes can contribute to correct neuronal differentiation.
Cerase A; Avner P
Curr Res Neurobiol; 2023; 5():100114. PubMed ID: 38020809
[TBL] [Abstract][Full Text] [Related]
34. Chromodomain helicase DNA-binding protein 2 affects the repair of X-ray and UV-induced DNA damage.
Rajagopalan S; Nepa J; Venkatachalam S
Environ Mol Mutagen; 2012 Jan; 53(1):44-50. PubMed ID: 22223433
[TBL] [Abstract][Full Text] [Related]
35. Chd2 regulates chromatin for proper gene expression toward differentiation in mouse embryonic stem cells.
Semba Y; Harada A; Maehara K; Oki S; Meno C; Ueda J; Yamagata K; Suzuki A; Onimaru M; Nogami J; Okada S; Akashi K; Ohkawa Y
Nucleic Acids Res; 2017 Sep; 45(15):8758-8772. PubMed ID: 28549158
[TBL] [Abstract][Full Text] [Related]
36. Chromodomain helicase DNA-binding domain 2 maintains spermatogonial self-renewal by promoting chromatin accessibility and mRNA stability.
Min Z; Xin H; Liu X; Wan J; Fan Z; Rao X; Fan J; Yang L; Li D
iScience; 2022 Dec; 25(12):105552. PubMed ID: 36444304
[TBL] [Abstract][Full Text] [Related]
37. Genetic and expressional alterations of CHD genes in gastric and colorectal cancers.
Kim MS; Chung NG; Kang MR; Yoo NJ; Lee SH
Histopathology; 2011 Apr; 58(5):660-8. PubMed ID: 21447119
[TBL] [Abstract][Full Text] [Related]
38. Chromatin Remodeler CHD8 in Autism and Brain Development.
Hoffmann A; Spengler D
J Clin Med; 2021 Jan; 10(2):. PubMed ID: 33477995
[TBL] [Abstract][Full Text] [Related]
39. CHD1 and CHD2 are positive regulators of HIV-1 gene expression.
Rodgers MJ; Banks DJ; Bradley KA; Young JA
Virol J; 2014 Oct; 11():180. PubMed ID: 25297984
[TBL] [Abstract][Full Text] [Related]
40. A mutation in the mouse Chd2 chromatin remodeling enzyme results in a complex renal phenotype.
Marfella CG; Henninger N; LeBlanc SE; Krishnan N; Garlick DS; Holzman LB; Imbalzano AN
Kidney Blood Press Res; 2008; 31(6):421-32. PubMed ID: 19142019
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
