BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

173 related articles for article (PubMed ID: 32335881)

  • 1. [Analysis of a case with Mowat-Wilson syndrome caused by ZEB2 gene variant].
    Ma J; Liu Y; Zhang K; Lyu Y; Gao M; Wang D; Gai Z; Liu Y
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2020 May; 37(5):539-542. PubMed ID: 32335881
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [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
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2022 Aug; 39(8):889-892. PubMed ID: 35929943
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [Analysis of ZEB2 gene variation in two patients with Mowat-Wilson syndrome].
    Cao X; Deng X; Zou Z; Liu C; Zhao Y; Ren J; Liu Y
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2022 Feb; 39(2):152-156. PubMed ID: 35076910
    [TBL] [Abstract][Full Text] [Related]  

  • 4. A novel nonsense mutation of ZEB2 gene in a Chinese patient with Mowat-Wilson syndrome.
    Hu Y; Peng Q; Ma K; Li S; Rao C; Zhong B; Lu X
    J Clin Lab Anal; 2020 Sep; 34(9):e23413. PubMed ID: 32519765
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Novel Zeb2 gene variation in the Mowat Wilson syndrome (MWS).
    Moore SW; Fieggen K; Honey E; Zaahl M
    J Pediatr Surg; 2016 Feb; 51(2):268-71. PubMed ID: 26852091
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Clinical characteristics of Polish patients with molecularly confirmed Mowat-Wilson syndrome.
    Jakubiak A; Szczałuba K; Badura-Stronka M; Kutkowska-Kaźmierczak A; Jakubiuk-Tomaszuk A; Chilarska T; Pilch J; Braun-Walicka N; Castaneda J; Wołyńska K; Wiśniewska M; Kugaudo M; Bielecka M; Pesz K; Wierzba J; Latos-Bieleńska A; Obersztyn E; Krajewska-Walasek M; Śmigiel R
    J Appl Genet; 2021 Sep; 62(3):477-485. PubMed ID: 33982229
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Early Infantile Epileptic Encephalopathy with a de novo variant in ZEB2 identified by exome sequencing.
    Babkina N; Deignan JL; Lee H; Vilain E; Sankar R; Giurgea I; Mowat D; Graham JM
    Eur J Med Genet; 2016 Feb; 59(2):70-4. PubMed ID: 26721324
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Fetal diagnosis of Mowat-Wilson syndrome by whole exome sequencing.
    Evans CA; Pinner J; Chan CY; Bowyer L; Mowat D; Buckley MF; Roscioli T
    Am J Med Genet A; 2019 Oct; 179(10):2152-2157. PubMed ID: 31321886
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Age-dependent epileptic encephalopathy associated with an unusual co-occurrence of ZEB2 and SCN1A variants.
    Nardello R; Fontana A; Mangano GD; Efthymiou S; Salpietro V; Houlden H; Mangano S
    Epileptic Disord; 2020 Feb; 22(1):111-115. PubMed ID: 32031527
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Mowat-Wilson syndrome presenting with fever-associated seizures.
    Seo SE; Kim SH; Lee ST; Choi JR; Lee JS; Kim HD; Kang HC
    Epileptic Disord; 2017 Dec; 19(4):481-485. PubMed ID: 29258970
    [TBL] [Abstract][Full Text] [Related]  

  • 11. The spectrum of ZEB2 mutations causing the Mowat-Wilson syndrome in Japanese populations.
    Yamada Y; Nomura N; Yamada K; Matsuo M; Suzuki Y; Sameshima K; Kimura R; Yamamoto Y; Fukushi D; Fukuhara Y; Ishihara N; Nishi E; Imataka G; Suzumura H; Hamano S; Shimizu K; Iwakoshi M; Ohama K; Ohta A; Wakamoto H; Kajita M; Miura K; Yokochi K; Kosaki K; Kuroda T; Kosaki R; Hiraki Y; Saito K; Mizuno S; Kurosawa K; Okamoto N; Wakamatsu N
    Am J Med Genet A; 2014 Aug; 164A(8):1899-908. PubMed ID: 24715670
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Neurological Phenotype of Mowat-Wilson Syndrome.
    Cordelli DM; Di Pisa V; Fetta A; Garavelli L; Maltoni L; Soliani L; Ricci E
    Genes (Basel); 2021 Jun; 12(7):. PubMed ID: 34199024
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Congenital tracheal stenosis in Mowat-Wilson syndrome with nonsense mutation of ZEB2 gene.
    Lin LC; Wen WH; Chen PT
    Pediatr Neonatol; 2024 Mar; 65(2):202-203. PubMed ID: 37980276
    [No Abstract]   [Full Text] [Related]  

  • 14. [Prenatal diagnosis of a fetus with Mowat-Wilson syndrome].
    Hu R; Luo X; Li Y; Lu J; Huang W
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2019 Dec; 36(12):1203-1205. PubMed ID: 31813148
    [TBL] [Abstract][Full Text] [Related]  

  • 15. A Diagnosis to Consider in Intellectual Disability: Mowat-Wilson Syndrome.
    Kilic E; Cetinkaya A; Utine GE; Boduroğlu K
    J Child Neurol; 2016 Jun; 31(7):913-7. PubMed ID: 26809768
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Mowat-Wilson Syndrome: Case Report and Review of
    St Peter C; Hossain WA; Lovell S; Rafi SK; Butler MG
    Int J Mol Sci; 2024 Feb; 25(5):. PubMed ID: 38474085
    [TBL] [Abstract][Full Text] [Related]  

  • 17. ZEB2 zinc-finger missense mutations lead to hypomorphic alleles and a mild Mowat-Wilson syndrome.
    Ghoumid J; Drevillon L; Alavi-Naini SM; Bondurand N; Rio M; Briand-Suleau A; Nasser M; Goodwin L; Raymond P; Yanicostas C; Goossens M; Lyonnet S; Mowat D; Amiel J; Soussi-Yanicostas N; Giurgea I
    Hum Mol Genet; 2013 Jul; 22(13):2652-61. PubMed ID: 23466526
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Critical involvement of ZEB2 in collagen fibrillogenesis: the molecular similarity between Mowat-Wilson syndrome and Ehlers-Danlos syndrome.
    Teraishi M; Takaishi M; Nakajima K; Ikeda M; Higashi Y; Shimoda S; Asada Y; Hijikata A; Ohara O; Hiraki Y; Mizuno S; Fukada T; Furukawa T; Wakamatsu N; Sano S
    Sci Rep; 2017 Apr; 7():46565. PubMed ID: 28422173
    [TBL] [Abstract][Full Text] [Related]  

  • 19. ZEB2, the Mowat-Wilson Syndrome Transcription Factor: Confirmations, Novel Functions, and Continuing Surprises.
    Birkhoff JC; Huylebroeck D; Conidi A
    Genes (Basel); 2021 Jul; 12(7):. PubMed ID: 34356053
    [TBL] [Abstract][Full Text] [Related]  

  • 20. The Role of ZEB2 in Human CD8 T Lymphocytes: Clinical and Cellular Immune Profiling in Mowat-Wilson Syndrome.
    Frith K; Munier CML; Hastings L; Mowat D; Wilson M; Seddiki N; Macintosh R; Kelleher AD; Gray P; Zaunders JJ
    Int J Mol Sci; 2021 May; 22(10):. PubMed ID: 34070208
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.