142 related articles for article (PubMed ID: 31981384)
1. De Novo ARID1B mutations cause growth delay associated with aberrant Wnt/β-catenin signaling.
Liu X; Hu G; Ye J; Ye B; Shen N; Tao Y; Zhang X; Fan Y; Liu H; Zhang Z; Fang D; Gu X; Mo X; Yu Y
Hum Mutat; 2020 May; 41(5):1012-1024. PubMed ID: 31981384
[TBL] [Abstract][Full Text] [Related]
2. Chromatin-Remodeling-Factor ARID1B Represses Wnt/β-Catenin Signaling.
Vasileiou G; Ekici AB; Uebe S; Zweier C; Hoyer J; Engels H; Behrens J; Reis A; Hadjihannas MV
Am J Hum Genet; 2015 Sep; 97(3):445-56. PubMed ID: 26340334
[TBL] [Abstract][Full Text] [Related]
3. A novel familial autosomal dominant mutation in ARID1B causing neurodevelopmental delays, short stature, and dysmorphic features.
Smith JA; Holden KR; Friez MJ; Jones JR; Lyons MJ
Am J Med Genet A; 2016 Dec; 170(12):3313-3318. PubMed ID: 27570168
[TBL] [Abstract][Full Text] [Related]
4. De novo mutations in ARID1B associated with both syndromic and non-syndromic short stature.
Yu Y; Yao R; Wang L; Fan Y; Huang X; Hirschhorn J; Dauber A; Shen Y
BMC Genomics; 2015 Sep; 16(1):701. PubMed ID: 26376624
[TBL] [Abstract][Full Text] [Related]
5. Corpus callosum abnormalities, intellectual disability, speech impairment, and autism in patients with haploinsufficiency of ARID1B.
Halgren C; Kjaergaard S; Bak M; Hansen C; El-Schich Z; Anderson CM; Henriksen KF; Hjalgrim H; Kirchhoff M; Bijlsma EK; Nielsen M; den Hollander NS; Ruivenkamp CA; Isidor B; Le Caignec C; Zannolli R; Mucciolo M; Renieri A; Mari F; Anderlid BM; Andrieux J; Dieux A; Tommerup N; Bache I
Clin Genet; 2012 Sep; 82(3):248-55. PubMed ID: 21801163
[TBL] [Abstract][Full Text] [Related]
6. Corpus callosum metrics predict severity of visuospatial and neuromotor dysfunctions in ARID1B mutations with Coffin-Siris syndrome.
Demily C; Duwime C; Lopez C; Hemimou C; Poisson A; Plasse J; Robert MP; Dénier C; Rossi M; Franck N; Besmond C; Barcia G; Boddaert N; Munnich A; Vaivre-Douret L
Psychiatr Genet; 2019 Dec; 29(6):237-242. PubMed ID: 30933046
[TBL] [Abstract][Full Text] [Related]
7. Striking phenotypic overlap between Nicolaides-Baraitser and Coffin-Siris syndromes in monozygotic twins with ARID1B intragenic deletion.
Pascolini G; Valiante M; Bottillo I; Laino L; Fleischer N; Ferraris A; Grammatico P
Eur J Med Genet; 2020 Mar; 63(3):103739. PubMed ID: 31421289
[TBL] [Abstract][Full Text] [Related]
8. YAP1 negatively regulates chondrocyte differentiation partly by activating the β-catenin signaling pathway.
Yang B; Sun H; Song F; Yu M; Wu Y; Wang J
Int J Biochem Cell Biol; 2017 Jun; 87():104-113. PubMed ID: 28438716
[TBL] [Abstract][Full Text] [Related]
9. Knockdown of Kmt2d leads to growth impairment by activating the Akt/β-catenin signaling pathway.
Shangguan H; Huang X; Lin J; Chen R
G3 (Bethesda); 2024 Mar; 14(3):. PubMed ID: 38263533
[TBL] [Abstract][Full Text] [Related]
10. A novel microduplication of ARID1B: Clinical, genetic, and proteomic findings.
Seabra CM; Szoko N; Erdin S; Ragavendran A; Stortchevoi A; Maciel P; Lundberg K; Schlatzer D; Smith J; Talkowski ME; Gusella JF; Natowicz MR
Am J Med Genet A; 2017 Sep; 173(9):2478-2484. PubMed ID: 28691782
[TBL] [Abstract][Full Text] [Related]
11. Neurobiology of ARID1B haploinsufficiency related to neurodevelopmental and psychiatric disorders.
Moffat JJ; Smith AL; Jung EM; Ka M; Kim WY
Mol Psychiatry; 2022 Jan; 27(1):476-489. PubMed ID: 33686214
[TBL] [Abstract][Full Text] [Related]
12. Two novel EIF2S3 mutations associated with syndromic intellectual disability with severe microcephaly, growth retardation, and epilepsy.
Moortgat S; Désir J; Benoit V; Boulanger S; Pendeville H; Nassogne MC; Lederer D; Maystadt I
Am J Med Genet A; 2016 Nov; 170(11):2927-2933. PubMed ID: 27333055
[TBL] [Abstract][Full Text] [Related]
13. Disruption of the ARID1B and ADAMTS6 loci due to a t(5;6)(q12.3;q25.3) in a patient with developmental delay.
Malli T; Duba HC; Erdel M; Marschon R; Kranewitter W; Deutschbauer S; Kralik J; Diel E; Güenther B; Mueller D; Webersinke G
Am J Med Genet A; 2014 Dec; 164A(12):3126-31. PubMed ID: 25250687
[TBL] [Abstract][Full Text] [Related]
14. Essential Roles for ARID1B in Dendritic Arborization and Spine Morphology of Developing Pyramidal Neurons.
Ka M; Chopra DA; Dravid SM; Kim WY
J Neurosci; 2016 Mar; 36(9):2723-42. PubMed ID: 26937011
[TBL] [Abstract][Full Text] [Related]
15. Clinical correlations of mutations affecting six components of the SWI/SNF complex: detailed description of 21 patients and a review of the literature.
Kosho T; Okamoto N; Ohashi H; Tsurusaki Y; Imai Y; Hibi-Ko Y; Kawame H; Homma T; Tanabe S; Kato M; Hiraki Y; Yamagata T; Yano S; Sakazume S; Ishii T; Nagai T; Ohta T; Niikawa N; Mizuno S; Kaname T; Naritomi K; Narumi Y; Wakui K; Fukushima Y; Miyatake S; Mizuguchi T; Saitsu H; Miyake N; Matsumoto N
Am J Med Genet A; 2013 Jun; 161A(6):1221-37. PubMed ID: 23637025
[TBL] [Abstract][Full Text] [Related]
16. Insertional Mutagenesis Identifies a STAT3/Arid1b/β-catenin Pathway Driving Neurofibroma Initiation.
Wu J; Keng VW; Patmore DM; Kendall JJ; Patel AV; Jousma E; Jessen WJ; Choi K; Tschida BR; Silverstein KA; Fan D; Schwartz EB; Fuchs JR; Zou Y; Kim MO; Dombi E; Levy DE; Huang G; Cancelas JA; Stemmer-Rachamimov AO; Spinner RJ; Largaespada DA; Ratner N
Cell Rep; 2016 Mar; 14(8):1979-90. PubMed ID: 26904939
[TBL] [Abstract][Full Text] [Related]
17. [Zinc finger protein 521 suppresses osteogenic differentiation of rat mesenchymal stem cells by inhibiting the Wnt/beta-catenin signaling pathway].
Xie XT; Zhan XL; Hu ZH
Mol Biol (Mosk); 2017; 51(3):464-472. PubMed ID: 28707663
[TBL] [Abstract][Full Text] [Related]
18. Coffin-Siris syndrome and the BAF complex: genotype-phenotype study in 63 patients.
Santen GW; Aten E; Vulto-van Silfhout AT; Pottinger C; van Bon BW; van Minderhout IJ; Snowdowne R; van der Lans CA; Boogaard M; Linssen MM; Vijfhuizen L; van der Wielen MJ; Vollebregt MJ; ; Breuning MH; Kriek M; van Haeringen A; den Dunnen JT; Hoischen A; Clayton-Smith J; de Vries BB; Hennekam RC; van Belzen MJ
Hum Mutat; 2013 Nov; 34(11):1519-28. PubMed ID: 23929686
[TBL] [Abstract][Full Text] [Related]
19. Fibulin-4 reduces extracellular matrix production and suppresses chondrocyte differentiation via DKK1- mediated canonical Wnt/β-catenin signaling.
Shangguan L; Ning G; Luo Z; Zhou Y
Int J Biol Macromol; 2017 Jun; 99():293-299. PubMed ID: 28238906
[TBL] [Abstract][Full Text] [Related]
20. Alterations in GRHL2-OVOL2-ZEB1 axis and aberrant activation of Wnt signaling lead to altered gene transcription in posterior polymorphous corneal dystrophy.
Chung DD; Zhang W; Jatavallabhula K; Barrington A; Jung J; Aldave AJ
Exp Eye Res; 2019 Nov; 188():107696. PubMed ID: 31233731
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]