BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

278 related articles for article (PubMed ID: 28301459)

  • 1. Blepharocheilodontic syndrome is a CDH1 pathway-related disorder due to mutations in CDH1 and CTNND1.
    Ghoumid J; Stichelbout M; Jourdain AS; Frenois F; Lejeune-Dumoulin S; Alex-Cordier MP; Lebrun M; Guerreschi P; Duquennoy-Martinot V; Vinchon M; Ferri J; Jung M; Vicaire S; Vanlerberghe C; Escande F; Petit F; Manouvrier-Hanu S
    Genet Med; 2017 Sep; 19(9):1013-1021. PubMed ID: 28301459
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Variants in members of the cadherin-catenin complex, CDH1 and CTNND1, cause blepharocheilodontic syndrome.
    Kievit A; Tessadori F; Douben H; Jordens I; Maurice M; Hoogeboom J; Hennekam R; Nampoothiri S; Kayserili H; Castori M; Whiteford M; Motter C; Melver C; Cunningham M; Hing A; Kokitsu-Nakata NM; Vendramini-Pittoli S; Richieri-Costa A; Baas AF; Breugem CC; Duran K; Massink M; Derksen PWB; van IJcken WFJ; van Unen L; Santos-Simarro F; Lapunzina P; Gil-da Silva Lopes VL; Lustosa-Mendes E; Krall M; Slavotinek A; Martinez-Glez V; Bakkers J; van Gassen KLI; de Klein A; van den Boogaard MH; van Haaften G
    Eur J Hum Genet; 2018 Feb; 26(2):210-219. PubMed ID: 29348693
    [TBL] [Abstract][Full Text] [Related]  

  • 3. CDH1-related blepharocheilodontic syndrome is associated with diffuse gastric cancer risk.
    LeBlanc S; Naveen D; Haan E; Barnett C; Rawlings L; Roscioli T; Poplawski N
    Am J Med Genet A; 2020 Jul; 182(7):1780-1784. PubMed ID: 32302040
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Novel truncating mutations in CTNND1 cause a dominant craniofacial and cardiac syndrome.
    Alharatani R; Ververi A; Beleza-Meireles A; Ji W; Mis E; Patterson QT; Griffin JN; Bhujel N; Chang CA; Dixit A; Konstantino M; Healy C; Hannan S; Neo N; Cash A; Li D; Bhoj E; Zackai EH; Cleaver R; Baralle D; McEntagart M; Newbury-Ecob R; Scott R; Hurst JA; Au PYB; Hosey MT; Khokha M; Marciano DK; Lakhani SA; Liu KJ
    Hum Mol Genet; 2020 Jul; 29(11):1900-1921. PubMed ID: 32196547
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Mutations in the Epithelial Cadherin-p120-Catenin Complex Cause Mendelian Non-Syndromic Cleft Lip with or without Cleft Palate.
    Cox LL; Cox TC; Moreno Uribe LM; Zhu Y; Richter CT; Nidey N; Standley JM; Deng M; Blue E; Chong JX; Yang Y; Carstens RP; Anand D; Lachke SA; Smith JD; Dorschner MO; Bedell B; Kirk E; Hing AV; Venselaar H; Valencia-Ramirez LC; Bamshad MJ; Glass IA; Cooper JA; Haan E; Nickerson DA; van Bokhoven H; Zhou H; Krahn KN; Buckley MF; Murray JC; Lidral AC; Roscioli T
    Am J Hum Genet; 2018 Jun; 102(6):1143-1157. PubMed ID: 29805042
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Clinical spectrum and pleiotropic nature of
    Figueiredo J; Melo S; Carneiro P; Moreira AM; Fernandes MS; Ribeiro AS; Guilford P; Paredes J; Seruca R
    J Med Genet; 2019 Apr; 56(4):199-208. PubMed ID: 30661051
    [No Abstract]   [Full Text] [Related]  

  • 7. A Novel
    Du S; Yang Y; Yi P; Luo J; Liu T; Chen R; Liu CJ; Ma T; Li Y; Wang C; Weng J; Liu M; Zhang L; Yang B; Zeng X; Liu JY
    Genet Test Mol Biomarkers; 2019 Nov; 23(11):759-765. PubMed ID: 31638429
    [No Abstract]   [Full Text] [Related]  

  • 8. Cleft lip/palate and hereditary diffuse gastric cancer: report of a family harboring a CDH1 c.687 + 1G > A germline mutation and review of the literature.
    Obermair F; Rammer M; Burghofer J; Malli T; Schossig A; Wimmer K; Kranewitter W; Mayrbaeurl B; Duba HC; Webersinke G
    Fam Cancer; 2019 Apr; 18(2):253-260. PubMed ID: 30306390
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Imperforate anus is a rare associated finding in blepharocheilodontic syndrome.
    Weaver KN; Rutledge KD; Grant JH; Robin NH
    Am J Med Genet A; 2010 Feb; 152A(2):438-40. PubMed ID: 20101698
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Cleft lip/palate and CDH1/E-cadherin mutations in families with hereditary diffuse gastric cancer.
    Frebourg T; Oliveira C; Hochain P; Karam R; Manouvrier S; Graziadio C; Vekemans M; Hartmann A; Baert-Desurmont S; Alexandre C; Lejeune Dumoulin S; Marroni C; Martin C; Castedo S; Lovett M; Winston J; Machado JC; Attié T; Jabs EW; Cai J; Pellerin P; Triboulet JP; Scotte M; Le Pessot F; Hedouin A; Carneiro F; Blayau M; Seruca R
    J Med Genet; 2006 Feb; 43(2):138-42. PubMed ID: 15831593
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Rare Variants in the Epithelial Cadherin Gene Underlying the Genetic Etiology of Nonsyndromic Cleft Lip with or without Cleft Palate.
    Brito LA; Yamamoto GL; Melo S; Malcher C; Ferreira SG; Figueiredo J; Alvizi L; Kobayashi GS; Naslavsky MS; Alonso N; Felix TM; Zatz M; Seruca R; Passos-Bueno MR
    Hum Mutat; 2015 Nov; 36(11):1029-33. PubMed ID: 26123647
    [TBL] [Abstract][Full Text] [Related]  

  • 12.
    Selvanathan A; Nixon CY; Zhu Y; Scietti L; Forneris F; Uribe LMM; Lidral AC; Jezewski PA; Mulliken JB; Murray JC; Buckley MF; Cox TC; Roscioli T
    Genes (Basel); 2020 Apr; 11(4):. PubMed ID: 32260281
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Resolving clinical diagnoses for syndromic cleft lip and/or palate phenotypes using whole-exome sequencing.
    Pengelly RJ; Upstill-Goddard R; Arias L; Martinez J; Gibson J; Knut M; Collins AL; Ennis S; Collins A; Briceno I
    Clin Genet; 2015 Nov; 88(5):441-9. PubMed ID: 25441681
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Variants of the CDH1 (E-Cadherin) Gene Associated with Oral Clefts in the Thai Population.
    Ittiwut R; Ittiwut C; Siriwan P; Chichareon V; Suphapeetiporn K; Shotelersuk V
    Genet Test Mol Biomarkers; 2016 Jul; 20(7):406-9. PubMed ID: 27227907
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Identification of germline mutations in the cancer predisposing gene CDH1 in patients with orofacial clefts.
    Vogelaar IP; Figueiredo J; van Rooij IA; Simões-Correia J; van der Post RS; Melo S; Seruca R; Carels CE; Ligtenberg MJ; Hoogerbrugge N
    Hum Mol Genet; 2013 Mar; 22(5):919-26. PubMed ID: 23197654
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Exome sequencing-based identification of mutations in non-syndromic genes among individuals with apparently syndromic features.
    Nishi E; Masuda K; Arakawa M; Kawame H; Kosho T; Kitahara M; Kubota N; Hidaka E; Katoh Y; Shirahige K; Izumi K
    Am J Med Genet A; 2016 Nov; 170(11):2889-2894. PubMed ID: 27566442
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Expanding the genetic and phenotypic spectrum of popliteal pterygium disorders.
    Leslie EJ; O'Sullivan J; Cunningham ML; Singh A; Goudy SL; Ababneh F; Alsubaie L; Ch'ng GS; van der Laar IM; Hoogeboom AJ; Dunnwald M; Kapoor S; Jiramongkolchai P; Standley J; Manak JR; Murray JC; Dixon MJ
    Am J Med Genet A; 2015 Mar; 167A(3):545-52. PubMed ID: 25691407
    [TBL] [Abstract][Full Text] [Related]  

  • 18. AXIN2 and CDH1 polymorphisms, tooth agenesis, and oral clefts.
    Letra A; Menezes R; Granjeiro JM; Vieira AR
    Birth Defects Res A Clin Mol Teratol; 2009 Feb; 85(2):169-73. PubMed ID: 18683894
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Three GLI2 mutations combined potentially underlie non-syndromic cleft lip with or without cleft palate in a Chinese pedigree.
    Meng P; Zhao H; Huang W; Zhang Y; Zhong W; Zhang M; Jia P; Zhou Z; Maimaitili G; Chen F; Zhang J; Lin J
    Mol Genet Genomic Med; 2019 Sep; 7(9):e714. PubMed ID: 31386309
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Associations of CDH1 germline variant location and cancer phenotype in families with hereditary diffuse gastric cancer (HDGC).
    Lo W; Zhu B; Sabesan A; Wu HH; Powers A; Sorber RA; Ravichandran S; Chen I; McDuffie LA; Quadri HS; Beane JD; Calzone K; Miettinen MM; Hewitt SM; Koh C; Heller T; Wacholder S; Rudloff U
    J Med Genet; 2019 Jun; 56(6):370-379. PubMed ID: 30745422
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 14.