PubMed for id: 341067

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37890485,37641719,37323203,36980900,36676725,36406119,36353360,36345475,36082562,35929943,35709987,35658366,35646055,35140087,35076910,34810354,34619538,34466018,34199024,34070208,34012377,33997095,33982229,33974257,33510600,33344924,33199988,32980962,32539836,32519765,32469269,32335881,32252596,32196960,31813148,31376723,31321886,31285160,31104665,30573661,30083364,29954473,29922981,29721247,29300384,29258970,28690488,28501473,28422173,28096981,28094084,27831545,27687363,26852091,26809768,26686679,26156877,26012591,25899569,25795985,25608121,25123255,25028418,24715670,24282181,24092421,24029077,23610866,23523603,23427518,23322667,23243526,23001561,22486326,22246645,21957361,21893004,21497296,21336163,20428734,20301585,20158378,20145308,20093881,19842203,19764599,19302864,19215041,18445050,18259761,18230842,17958891,17932455,17478475,17203459,17103451,16688751,16532472,16150342,16088920,16053902,15908750,15006694,14681759,12746390,11891681,31553157,29172423,27754667,23540268,12522767,12451214,37828049,37735378,35274783,34356053,33118233,33046754,32950463,32628253,32031527,30590588,30266271,30056076,29326173,28455101,27799067,27591083,27385012,27294509,26721324,26654950,26193487,25741725,25566742,25497574,24779060,24401652,24243579,24161570,24058414,23312518,23152852,20206619,20125191,19236961,18812405,18792984,18351671,18182442,17644613,17223398,16443855,15065106,38013828,37228682,36092668,35876393,35844343,35066687,34766667,34736638,34524300,34215578,32988076,32799525,32367346,31119937,31052408,29093661,28947381,27617128,27174633,26705424,25633232,24093039,22106903,21283754,21143296,20967904,18075983,16521475,10782939,10750432,22365546,37982893,37958648,37948459,37891621,37679133,37676292,37610449,37585461,37490568,37460708,37453721,37432072,37418029,37372360,37278766,37267769,37061531,37047673,37017437,36995257,36922279,36902033,36857021,36790471,36772973,36749416,36738110,36606638,36586783,36581449,36564622,36555308,36536313,36534156,36521661,36454543,36454299,36443333,36404533,36382711,36319675,36300492,36248794,36214716,36198237,36166100,36142117,36097644,36062518,35980364,35836014,35816394,35790984,35777734,35725288,35695198,35650007,35595348,35567578,35488810,35443634,35322726,35166674,35115551,35091706,34993837,34981673,34956076,34933715,34880446,34830235,34818877,34792104,34761964,34752660,34667088,34655156,34597781,34575824,34561316,34545688,34472202,34471485,34455465,34414975,34272903,34171997,34171448,34156257,34147087,34121091,34100550,34092334,34042275,34006365,33983112,33961858,33958373,33938072,33917126,33913579,33853325,33834290,33812987,33804586,33784990,33756487,33754314,33750457,33741501,33736665,33720042,33674768,33630212,33567347,33561610,33557787,33557656,33515383,33514916,33474713,33465467,33444820,33442921,33433679,33421311,33392852,33375093,33342844,33294994,33276791,33260622,33234331,33202966,33178831,33113016,33103535,33098347,33076379,33047879,33043602,33020172,32993133,32959905,32958024,32948616,32948239,32942321,32939943,32934297,32914730,32849667,32839936,32838606,32809970,32777409,32748823,32665298,32600305,32514992,32507977,32418639,32414519,32380506,32364585,32335897,32335870,32297806,32277595,32275061,32236665,32150337,32139661,32066630,32053512,31983649,31939867,31903518,31896937,31827238,31789936,31767031,31738640,31715421,31707728,31692235,31666091,31647312,31644668,31642440,31609069,31590591,31576467,31551465,31542828,31519213,31444792,31442438,31421289,31417183,31413121,31394080,31364476,31358688,31355911,31263958,31256294,31250547,31247956,31240788,31183986,31181311,31170185,31162149,31129106,31107799,31079897,31037734,30999961,30970187,30925032,30911172,30892814,30885557,30822775,30799307,30786110,30686516,30663199,30644554,30636638,30631982,30616633,30607663,30602132,30594740,30549420,30518452,30502294,30487245,30445974,30443988,30430282,30410491,30394532,30386901,30386900,30386899,30315601,30284348,30244542,30244530,30238602,30227298,30218169,30217742,30180823,30178219,30102486,30079626,30073757,30062828,30056070,30031151,30005639,29965875,29956457,29895226,29764583,29696799,29695640,29688570,29681101,29678817,29656294,29654647,29634418,29626357,29622757,29605259,29601828,29600337,29573576,29549028,29484400,29483666,29477871,29439660,29429387,29393463,29383490,29379196,29377512,29336779,29300049,29286936,29274487,29261189,29253842,29249648,29224790,29160006,29106856,29098737,29093530,29090971,29078343,29034068,28965333,28930629,28924375,28919319,28855726,28799054,28784882[uid]

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Mowat-Wilson syndrome factor ZEB2 controls early formation of human neural crest through BMP signaling modulation.

Charney RM, Prasad MS, Juan-Sing C, Patel LJ, Hernandez JC, Wu J, García-Castro MI. Charney RM, et al. Stem Cell Reports. 2023 Nov 14;18(11):2254-2267. doi: 10.1016/j.stemcr.2023.10.002. Epub 2023 Oct 26. Stem Cell Reports. 2023. PMID: 37890485 Free PMC article.

Clinical Characteristics and Novel ZEB2 Gene Mutation Analysis of Three Chinese Patients with Mowat-Wilson Syndrome.

Han X, Zhang Q, Wang C, Han B. Han X, et al. Pharmgenomics Pers Med. 2023 Aug 23;16:777-783. doi: 10.2147/PGPM.S414161. eCollection 2023. Pharmgenomics Pers Med. 2023. PMID: 37641719 Free PMC article.

Mutated Transcripts of ZEB2 Do Not Undergo Nonsense-Mediated Decay in Mowat-Wilson Syndrome.

Güleray Lafcı N, Karaosmanoglu B, Taskiran EZ, Simsek-Kiper PO, Utine GE. Güleray Lafcı N, et al. Mol Syndromol. 2023 Jun;14(3):258-265. doi: 10.1159/000528769. Epub 2023 Feb 20. Mol Syndromol. 2023. PMID: 37323203 Free PMC article.

Zeb2 DNA-Binding Sites in Neuroprogenitor Cells Reveal Autoregulation and Affirm Neurodevelopmental Defects, Including in Mowat-Wilson Syndrome.

Birkhoff JC, Korporaal AL, Brouwer RWW, Nowosad K, Milazzo C, Mouratidou L, van den Hout MCGN, van IJcken WFJ, Huylebroeck D, Conidi A. Birkhoff JC, et al. Genes (Basel). 2023 Mar 2;14(3):629. doi: 10.3390/genes14030629. Genes (Basel). 2023. PMID: 36980900 Free PMC article.

First Case Report of Developmental Bilateral Cataract with a Novel Mutation in the ZEB2 Gene Observed in Mowat-Wilson Syndrome.

Tronina A, Świerczyńska M, Filipek E. Tronina A, et al. Medicina (Kaunas). 2023 Jan 2;59(1):101. doi: 10.3390/medicina59010101. Medicina (Kaunas). 2023. PMID: 36676725 Free PMC article.

Physical, language, neurodevelopment and phenotype-genotype correlation of Chinese patients with Mowat-Wilson syndrome.

Wu L, Wang J, Wang L, Xu Q, Zhou B, Zhang Z, Li Q, Wang H, Han L, Jiang Q, Wang L. Wu L, et al. Front Genet. 2022 Nov 3;13:1016677. doi: 10.3389/fgene.2022.1016677. eCollection 2022. Front Genet. 2022. PMID: 36406119 Free PMC article.

ZEB2 haploinsufficient Mowat-Wilson syndrome induced pluripotent stem cells show disrupted GABAergic transcriptional regulation and function.

Schuster J, Klar J, Khalfallah A, Laan L, Hoeber J, Fatima A, Sequeira VM, Jin Z, Korol SV, Huss M, Nordgren A, Anderlid BM, Gallant C, Birnir B, Dahl N. Schuster J, et al. Front Mol Neurosci. 2022 Oct 24;15:988993. doi: 10.3389/fnmol.2022.988993. eCollection 2022. Front Mol Neurosci. 2022. PMID: 36353360 Free PMC article.

Mowat-Wilson Syndrome as a Differential Diagnosis in Patients with Congenital Heart Defects and Dysmorphic Facies.

Pachajoa H, Gomez-Pineda E, Giraldo-Ocampo S, Lores J. Pachajoa H, et al. Pharmgenomics Pers Med. 2022 Nov 1;15:913-918. doi: 10.2147/PGPM.S380908. eCollection 2022. Pharmgenomics Pers Med. 2022. PMID: 36345475 Free PMC article.

[Clinical characteristics and genetic analysis of 3 children with Mowat-Wilson syndrome].

Zhou T, Wang Y, Liang D, Chen L, Ye F, Cao H, Tong G. Zhou T, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2022 Sep 10;39(9):944-948. doi: 10.3760/cma.j.cn511374-20210829-00703. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2022. PMID: 36082562 Chinese.

[Analysis of a case with Mowat-Wilson syndrome due to nonsense variant of ZEB2 gene].

She M, Zhao Z, Shi P, Gao S, Kong X. She M, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2022 Aug 10;39(8):889-892. doi: 10.3760/cma.j.cn511374-20210510-00393. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2022. PMID: 35929943 Chinese.

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