These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

178 related articles for article (PubMed ID: 34184264)

  • 1. WNT10A, dermatology and dentistry.
    Doolan BJ; Onoufriadis A; Kantaputra P; McGrath JA
    Br J Dermatol; 2021 Dec; 185(6):1105-1111. PubMed ID: 34184264
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Abnormal primary and permanent dentitions with ectodermal symptoms predict WNT10A deficiency.
    Bergendal B; Norderyd J; Zhou X; Klar J; Dahl N
    BMC Med Genet; 2016 Nov; 17(1):88. PubMed ID: 27881089
    [TBL] [Abstract][Full Text] [Related]  

  • 3. EDA, EDAR, EDARADD and WNT10A allelic variants in patients with ectodermal derivative impairment in the Spanish population.
    Martínez-Romero MC; Ballesta-Martínez MJ; López-González V; Sánchez-Soler MJ; Serrano-Antón AT; Barreda-Sánchez M; Rodriguez-Peña L; Martínez-Menchon MT; Frías-Iniesta J; Sánchez-Pedreño P; Carbonell-Meseguer P; Glover-López G; Guillén-Navarro E;
    Orphanet J Rare Dis; 2019 Dec; 14(1):281. PubMed ID: 31796081
    [TBL] [Abstract][Full Text] [Related]  

  • 4. The WNT10A gene in ectodermal dysplasias and selective tooth agenesis.
    Mues G; Bonds J; Xiang L; Vieira AR; Seymen F; Klein O; D'Souza RN
    Am J Med Genet A; 2014 Oct; 164A(10):2455-60. PubMed ID: 24700731
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Mutations in WNT10A are frequently involved in oligodontia associated with minor signs of ectodermal dysplasia.
    Plaisancié J; Bailleul-Forestier I; Gaston V; Vaysse F; Lacombe D; Holder-Espinasse M; Abramowicz M; Coubes C; Plessis G; Faivre L; Demeer B; Vincent-Delorme C; Dollfus H; Sigaudy S; Guillén-Navarro E; Verloes A; Jonveaux P; Martin-Coignard D; Colin E; Bieth E; Calvas P; Chassaing N
    Am J Med Genet A; 2013 Apr; 161A(4):671-8. PubMed ID: 23401279
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Distinct impacts of bi-allelic WNT10A mutations on the permanent and primary dentitions in odonto-onycho-dermal dysplasia.
    Yu M; Liu Y; Liu H; Wong SW; He H; Zhang X; Wang Y; Han D; Feng H
    Am J Med Genet A; 2019 Jan; 179(1):57-64. PubMed ID: 30569517
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Compound heterozygous WNT10A missense variations exacerbated the tooth agenesis caused by hypohidrotic ectodermal dysplasia.
    Liu Y; Sun J; Zhang C; Wu Y; Ma S; Li X; Wu X; Gao Q
    BMC Oral Health; 2024 Jan; 24(1):136. PubMed ID: 38280992
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Mutations in WNT10A are present in more than half of isolated hypodontia cases.
    van den Boogaard MJ; Créton M; Bronkhorst Y; van der Hout A; Hennekam E; Lindhout D; Cune M; Ploos van Amstel HK
    J Med Genet; 2012 May; 49(5):327-31. PubMed ID: 22581971
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Tricho-odonto-onycho-dermal dysplasia and WNT10A mutations.
    Kantaputra P; Kaewgahya M; Jotikasthira D; Kantaputra W
    Am J Med Genet A; 2014 Apr; 164A(4):1041-8. PubMed ID: 24458874
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Phenotypic characteristics of taurodontism and a novel WNT10A variant in non-syndromic oligodontia family.
    Zhao Y; Hou Y; Ren J; Gao X; Meng L; Liu Y; Xing C; Shen W
    Arch Oral Biol; 2023 Oct; 154():105759. PubMed ID: 37422997
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Involvement of and interaction between WNT10A and EDA mutations in tooth agenesis cases in the Chinese population.
    He H; Han D; Feng H; Qu H; Song S; Bai B; Zhang Z
    PLoS One; 2013; 8(11):e80393. PubMed ID: 24312213
    [TBL] [Abstract][Full Text] [Related]  

  • 12. WNT10A variants in relation to nonsyndromic hypodontia in eastern Slovak population.
    Grejtakova D; Gabrikova-Dojcakova D; Boronova I; Kyjovska L; Hubcejova J; Fecenkova M; Zigova M; Priganc M; Bernasovska J
    J Genet; 2018 Dec; 97(5):1169-1177. PubMed ID: 30555066
    [TBL] [Abstract][Full Text] [Related]  

  • 13. WNT10B mutations associated with isolated dental anomalies.
    Kantaputra PN; Hutsadaloi A; Kaewgahya M; Intachai W; German R; Koparal M; Leethanakul C; Tolun A; Ketudat Cairns JR
    Clin Genet; 2018 May; 93(5):992-999. PubMed ID: 29364501
    [TBL] [Abstract][Full Text] [Related]  

  • 14. WNT10A variants are associated with non-syndromic tooth agenesis in the general population.
    Song S; Zhao R; He H; Zhang J; Feng H; Lin L
    Hum Genet; 2014 Jan; 133(1):117-24. PubMed ID: 24043634
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Novel mutations identified in patients with tooth agenesis by whole-exome sequencing.
    Zhao K; Lian M; Zou D; Huang W; Zhou W; Shen Y; Wang F; Wu Y
    Oral Dis; 2019 Mar; 25(2):523-534. PubMed ID: 30417976
    [TBL] [Abstract][Full Text] [Related]  

  • 16. WNT10A coding variants and maxillary lateral incisor agenesis with associated dental anomalies.
    Mostowska A; Biedziak B; Zadurska M; Matuszewska-Trojan S; Jagodziński PP
    Eur J Oral Sci; 2015 Feb; 123(1):1-8. PubMed ID: 25545742
    [TBL] [Abstract][Full Text] [Related]  

  • 17. WNT10A mutations are a frequent cause of a broad spectrum of ectodermal dysplasias with sex-biased manifestation pattern in heterozygotes.
    Bohring A; Stamm T; Spaich C; Haase C; Spree K; Hehr U; Hoffmann M; Ledig S; Sel S; Wieacker P; Röpke A
    Am J Hum Genet; 2009 Jul; 85(1):97-105. PubMed ID: 19559398
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Odonto-onycho-dermal dysplasia in a patient homozygous for a WNT10A nonsense mutation and mild manifestations of ectodermal dysplasia in carriers of the mutation.
    Krøigård AB; Clemmensen O; Gjørup H; Hertz JM; Bygum A
    BMC Dermatol; 2016 Mar; 16():3. PubMed ID: 26964878
    [TBL] [Abstract][Full Text] [Related]  

  • 19. WNT10A gene is the second molecular candidate in a cohort of young Italian subjects with ectodermal derivative impairment (EDI).
    Guazzarotti L; Tadini G; Mancini GE; Sani I; Pisanelli S; Galderisi F; D'Auria E; Secondi R; Bottero A; Zuccotti GV
    Clin Genet; 2018 Mar; 93(3):693-698. PubMed ID: 28976000
    [TBL] [Abstract][Full Text] [Related]  

  • 20. WNT10A and isolated hypodontia.
    Kantaputra P; Sripathomsawat W
    Am J Med Genet A; 2011 May; 155A(5):1119-22. PubMed ID: 21484994
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.