BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

202 related articles for article (PubMed ID: 32906216)

  • 1. Comparative analysis of rare EDAR mutations and tooth agenesis pattern in EDAR- and EDA-associated nonsyndromic oligodontia.
    Zhang L; Yu M; Wong SW; Qu H; Cai T; Liu Y; Liu H; Fan Z; Zheng J; Zhou Y; Feng H; Han D
    Hum Mutat; 2020 Nov; 41(11):1957-1966. PubMed ID: 32906216
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Deleterious Variants in
    Parveen A; Khan SA; Mirza MU; Bashir H; Arshad F; Iqbal M; Ahmad W; Wahab A; Fiaz A; Naz S; Ashraf F; Mobeen T; Aziz S; Ahmed SS; Muhammad N; Hassib NF; Mostafa MI; Gaboon NE; Gul R; Khan S; Froeyen M; Shoaib M; Wasif N
    Int J Mol Sci; 2019 Oct; 20(21):. PubMed ID: 31652981
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. Gene Mutations of the Three Ectodysplasin Pathway Key Players (
    Ahmed HA; El-Kamah GY; Rabie E; Mostafa MI; Abouzaid MR; Hassib NF; Mehrez MI; Abdel-Kader MA; Mohsen YH; Zada SK; Amr KS; Sayed ISM
    Genes (Basel); 2021 Sep; 12(9):. PubMed ID: 34573371
    [TBL] [Abstract][Full Text] [Related]  

  • 5. A novel EDAR missense mutation identified by whole-exome sequencing with non-syndromic tooth agenesis in a Chinese family.
    Zhang H; Kong X; Ren J; Yuan S; Liu C; Hou Y; Liu Y; Meng L; Zhang G; Du Q; Shen W
    Mol Genet Genomic Med; 2021 Jun; 9(6):e1684. PubMed ID: 33943035
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. EDAR-induced hypohidrotic ectodermal dysplasia: a clinical study on signs and symptoms in individuals with a heterozygous c.1072C > T mutation.
    Kieri CF; Bergendal B; Lind LK; Schmitt-Egenolf M; Stecksén-Blicks C
    BMC Med Genet; 2014 May; 15():57. PubMed ID: 24884697
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Missense mutations in EDA and EDAR genes cause dominant syndromic tooth agenesis.
    Andreoni F; Sgattoni C; Bencardino D; Simonetti O; Forabosco A; Magnani M
    Mol Genet Genomic Med; 2021 Jan; 9(1):e1555. PubMed ID: 33205897
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Genetic analysis: Wnt and other pathways in nonsyndromic tooth agenesis.
    Yu M; Wong SW; Han D; Cai T
    Oral Dis; 2019 Apr; 25(3):646-651. PubMed ID: 29969831
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Novel EDAR mutation in tooth agenesis and variable associated features.
    Mumtaz S; Nalbant G; Yıldız Bölükbaşı E; Huma Z; Ahmad N; Tolun A; Malik S
    Eur J Med Genet; 2020 Sep; 63(9):103926. PubMed ID: 32325225
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Non-syndromic tooth agenesis associated with a nonsense mutation in ectodysplasin-A (EDA).
    Nikopensius T; Annilo T; Jagomägi T; Gilissen C; Kals M; Krjutškov K; Mägi R; Eelmets M; Gerst-Talas U; Remm M; Saag M; Hoischen A; Metspalu A
    J Dent Res; 2013 Jun; 92(6):507-11. PubMed ID: 23603338
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [Whole exome sequencing and analysis of hypohidrotic ectodermal dysplasia patients].
    Liu XY; Zhu JX; Zhao YM
    Zhonghua Kou Qiang Yi Xue Za Zhi; 2022 Feb; 57(2):155-161. PubMed ID: 35152651
    [No Abstract]   [Full Text] [Related]  

  • 13. X-linked and autosomal recessive Hypohidrotic Ectodermal Dysplasia: genotypic-dental phenotypic findings.
    Clauss F; Chassaing N; Smahi A; Vincent MC; Calvas P; Molla M; Lesot H; Alembik Y; Hadj-Rabia S; Bodemer C; Manière MC; Schmittbuhl M
    Clin Genet; 2010 Sep; 78(3):257-66. PubMed ID: 20236127
    [TBL] [Abstract][Full Text] [Related]  

  • 14. De novo EDA mutations: Variable expression in two Egyptian families.
    Gaczkowska A; Abdalla EM; Dowidar KM; Elhady GM; Jagodzinski PP; Mostowska A
    Arch Oral Biol; 2016 Aug; 68():21-8. PubMed ID: 27054699
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Candidate gene analysis of tooth agenesis identifies novel mutations in six genes and suggests significant role for WNT and EDA signaling and allele combinations.
    Arte S; Parmanen S; Pirinen S; Alaluusua S; Nieminen P
    PLoS One; 2013; 8(8):e73705. PubMed ID: 23991204
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Novel EDA or EDAR Mutations Identified in Patients with X-Linked Hypohidrotic Ectodermal Dysplasia or Non-Syndromic Tooth Agenesis.
    Zeng B; Zhao Q; Li S; Lu H; Lu J; Ma L; Zhao W; Yu D
    Genes (Basel); 2017 Oct; 8(10):. PubMed ID: 28981473
    [No Abstract]   [Full Text] [Related]  

  • 17. Mutations in MSX1, PAX9 and MMP20 genes in Saudi Arabian patients with tooth agenesis.
    Shahid M; Balto HA; Al-Hammad N; Joshi S; Khalil HS; Somily AM; Sinjilawi NA; Al-Ghamdi S; Faiyaz-Ul-Haque M; Dhillon VS
    Eur J Med Genet; 2016 Aug; 59(8):377-85. PubMed ID: 27365112
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Novel missense mutation in the EDA gene in a family affected by oligodontia.
    Ruiz-Heiland G; Jabir S; Wende W; Blecher S; Bock N; Ruf S
    J Orofac Orthop; 2016 Jan; 77(1):31-8. PubMed ID: 26753551
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. A founder ectodysplasin A receptor (EDAR) mutation results in a high frequency of the autosomal recessive form of hypohidrotic ectodermal dysplasia in India.
    Bashyam MD; Chaudhary AK; Reddy EC; Reddy V; Acharya V; Nagarajaram HA; Devi AR; Bashyam L; Dalal AB; Gupta N; Kabra M; Agarwal M; Phadke SR; Tainwala R; Kumar R; Hariharan SV
    Br J Dermatol; 2012 Apr; 166(4):819-29. PubMed ID: 22032522
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.