BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

267 related articles for article (PubMed ID: 34753942)

  • 41. Mutations in SWI/SNF chromatin remodeling complex gene ARID1B cause Coffin-Siris syndrome.
    Santen GW; Aten E; Sun Y; Almomani R; Gilissen C; Nielsen M; Kant SG; Snoeck IN; Peeters EA; Hilhorst-Hofstee Y; Wessels MW; den Hollander NS; Ruivenkamp CA; van Ommen GJ; Breuning MH; den Dunnen JT; van Haeringen A; Kriek M
    Nat Genet; 2012 Mar; 44(4):379-80. PubMed ID: 22426309
    [TBL] [Abstract][Full Text] [Related]  

  • 42. 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]  

  • 43. Protein destabilization underlies pathogenic missense mutations in ARID1B.
    Mermet-Meillon F; Mercan S; Bauer-Probst B; Allard C; Bleu M; Calkins K; Knehr J; Altorfer M; Naumann U; Sprouffske K; Barys L; Sesterhenn F; Galli GG
    Nat Struct Mol Biol; 2024 Feb; ():. PubMed ID: 38347147
    [TBL] [Abstract][Full Text] [Related]  

  • 44. Establishment of an induced pluripotent stem cell (iPSC) line SDQLCHi045-A from peripheral blood mononuclear cells of a patient with Coffin-Siris syndrome 1 carrying a mutation in ARID1B gene.
    Yang X; Liu C; Zhang H; Lv Y; Li Y; Li Z; Liu Y; Gai Z
    Stem Cell Res; 2023 Feb; 66():102982. PubMed ID: 36473251
    [TBL] [Abstract][Full Text] [Related]  

  • 45. ARID1A facilitates KRAS signaling-regulated enhancer activity in an AP1-dependent manner in colorectal cancer cells.
    Sen M; Wang X; Hamdan FH; Rapp J; Eggert J; Kosinsky RL; Wegwitz F; Kutschat AP; Younesi FS; Gaedcke J; Grade M; Hessmann E; Papantonis A; Strӧbel P; Johnsen SA
    Clin Epigenetics; 2019 Jun; 11(1):92. PubMed ID: 31217031
    [TBL] [Abstract][Full Text] [Related]  

  • 46. Expanding the Circuitry of Pluripotency by Selective Isolation of Chromatin-Associated Proteins.
    Rafiee MR; Girardot C; Sigismondo G; Krijgsveld J
    Mol Cell; 2016 Nov; 64(3):624-635. PubMed ID: 27773674
    [TBL] [Abstract][Full Text] [Related]  

  • 47. The BAF and PRC2 Complex Subunits Dpf2 and Eed Antagonistically Converge on Tbx3 to Control ESC Differentiation.
    Zhang W; Chronis C; Chen X; Zhang H; Spalinskas R; Pardo M; Chen L; Wu G; Zhu Z; Yu Y; Yu L; Choudhary J; Nichols J; Parast MM; Greber B; Sahlén P; Plath K
    Cell Stem Cell; 2019 Jan; 24(1):138-152.e8. PubMed ID: 30609396
    [TBL] [Abstract][Full Text] [Related]  

  • 48. The Tumor Suppressor ARID1A Controls Global Transcription via Pausing of RNA Polymerase II.
    Trizzino M; Barbieri E; Petracovici A; Wu S; Welsh SA; Owens TA; Licciulli S; Zhang R; Gardini A
    Cell Rep; 2018 Jun; 23(13):3933-3945. PubMed ID: 29949775
    [TBL] [Abstract][Full Text] [Related]  

  • 49. Epilepsy features in ARID1B-related Coffin-Siris syndrome.
    Proietti J; Amadori E; Striano P; Ricci E; Cordelli DM; Bana C; Dilena R; Gardella E; Klint Nielsen JE; Pisani F; Lo Barco T; Fiorini E; Fontana E; Darra F; Dalla Bernardina B; Cantalupo G
    Epileptic Disord; 2021 Dec; 23(6):865-874. PubMed ID: 34730517
    [TBL] [Abstract][Full Text] [Related]  

  • 50. Coffin-Siris Syndrome-1: Report of five cases from Asian populations with truncating mutations in the ARID1B gene.
    Lian S; Ting TW; Lai AHM; Tan ES; Wei H; Cham B; Tan EC
    J Neurol Sci; 2020 Jul; 414():116819. PubMed ID: 32339967
    [TBL] [Abstract][Full Text] [Related]  

  • 51. Coffin-Siris Syndrome with obesity, macrocephaly, hepatomegaly and hyperinsulinism caused by a mutation in the ARID1B gene.
    Vals MA; Õiglane-Shlik E; Nõukas M; Shor R; Peet A; Kals M; Kivistik PA; Metspalu A; Õunap K
    Eur J Hum Genet; 2014 Nov; 22(11):1327-9. PubMed ID: 24569609
    [TBL] [Abstract][Full Text] [Related]  

  • 52. Mutational Landscapes and Phenotypic Spectrum of SWI/SNF-Related Intellectual Disability Disorders.
    Bögershausen N; Wollnik B
    Front Mol Neurosci; 2018; 11():252. PubMed ID: 30123105
    [TBL] [Abstract][Full Text] [Related]  

  • 53. Mutations affecting components of the SWI/SNF complex cause Coffin-Siris syndrome.
    Tsurusaki Y; Okamoto N; Ohashi H; Kosho T; Imai Y; Hibi-Ko Y; Kaname T; Naritomi K; Kawame H; Wakui K; Fukushima Y; Homma T; Kato M; Hiraki Y; Yamagata T; Yano S; Mizuno S; Sakazume S; Ishii T; Nagai T; Shiina M; Ogata K; Ohta T; Niikawa N; Miyatake S; Okada I; Mizuguchi T; Doi H; Saitsu H; Miyake N; Matsumoto N
    Nat Genet; 2012 Mar; 44(4):376-8. PubMed ID: 22426308
    [TBL] [Abstract][Full Text] [Related]  

  • 54. SWI/SNF factors required for cellular resistance to DNA damage include ARID1A and ARID1B and show interdependent protein stability.
    Watanabe R; Ui A; Kanno S; Ogiwara H; Nagase T; Kohno T; Yasui A
    Cancer Res; 2014 May; 74(9):2465-75. PubMed ID: 24788099
    [TBL] [Abstract][Full Text] [Related]  

  • 55. 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]  

  • 56. MUC1-C Activates the BAF (mSWI/SNF) Complex in Prostate Cancer Stem Cells.
    Hagiwara M; Yasumizu Y; Yamashita N; Rajabi H; Fushimi A; Long MD; Li W; Bhattacharya A; Ahmad R; Oya M; Liu S; Kufe D
    Cancer Res; 2021 Feb; 81(4):1111-1122. PubMed ID: 33323379
    [TBL] [Abstract][Full Text] [Related]  

  • 57. Neural crest survival and differentiation in zebrafish depends on mont blanc/tfap2a gene function.
    Barrallo-Gimeno A; Holzschuh J; Driever W; Knapik EW
    Development; 2004 Apr; 131(7):1463-77. PubMed ID: 14985255
    [TBL] [Abstract][Full Text] [Related]  

  • 58. Folate Receptor Alpha Upregulates Oct4, Sox2 and Klf4 and Downregulates miR-138 and miR-let-7 in Cranial Neural Crest Cells.
    Mohanty V; Shah A; Allender E; Siddiqui MR; Monick S; Ichi S; Mania-Farnell B; G McLone D; Tomita T; Mayanil CS
    Stem Cells; 2016 Nov; 34(11):2721-2732. PubMed ID: 27300003
    [TBL] [Abstract][Full Text] [Related]  

  • 59. Subunits of ARID1 serve as novel biomarkers for the sensitivity to immune checkpoint inhibitors and prognosis of advanced non-small cell lung cancer.
    Sun D; Tian L; Zhu Y; Wo Y; Liu Q; Liu S; Li H; Hou H
    Mol Med; 2020 Aug; 26(1):78. PubMed ID: 32791957
    [TBL] [Abstract][Full Text] [Related]  

  • 60. Multiple roles of Sox2, an HMG-box transcription factor in avian neural crest development.
    Wakamatsu Y; Endo Y; Osumi N; Weston JA
    Dev Dyn; 2004 Jan; 229(1):74-86. PubMed ID: 14699579
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 14.