BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

150 related articles for article (PubMed ID: 37001412)

  • 41. Hypohidrotic Ectodermal Dysplasia with c.28delG Mutation in Ectodysplasin A Gene and Severe Atopic Dermatitis Treated Successfully with Tofacitinib.
    Li X; Wu X; Elston DM; Zhang J; Zhou C
    Acta Derm Venereol; 2021 Jan; 101(1):adv00352. PubMed ID: 33196100
    [No Abstract]   [Full Text] [Related]  

  • 42. [Phenotypic and genetic analysis of a case with hypohidrotic ectodermal dysplasia due to Xq13.1 microdeletion].
    Mei D; Mei S; Chen G; Wang Y; Wang X; Zhang J; Chen X; Li D; Zhang Y
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2021 Mar; 38(3):219-223. PubMed ID: 33751528
    [TBL] [Abstract][Full Text] [Related]  

  • 43. A novel EDA gene mutation in a Spanish family with X-linked hypohidrotic ectodermal dysplasia.
    Cañueto J; Zafra-Cobo MI; Ciria S; Unamuno P; González-Sarmiento R
    Actas Dermosifiliogr; 2011 Nov; 102(9):722-5. PubMed ID: 21696697
    [TBL] [Abstract][Full Text] [Related]  

  • 44. Characterization of a novel gross deletion and insertion mutation in EDA gene causing hypohidrotic ectodermal dysplasia.
    Sun J; Chen L; Han S; He Y; Dumitru AG; Zhou W; Cai J; Qi M
    J Dermatol; 2021 Jan; 48(1):e29-e30. PubMed ID: 33180991
    [No Abstract]   [Full Text] [Related]  

  • 45. A novel EDA1 missense mutation in X-linked hypohidrotic ectodermal dysplasia.
    Wang X; Zhang Z; Yuan S; Ren J; Qu H; Zhang G; Chen W; Zheng S; Meng L; Bai J; Du Q; Yang D; Shen W
    Medicine (Baltimore); 2020 Mar; 99(11):e19244. PubMed ID: 32176048
    [TBL] [Abstract][Full Text] [Related]  

  • 46. Mutation Screening of the EDA Gene in Seven Chinese Families with X-Linked Hypohidrotic Ectodermal Dysplasia.
    Liu Y; Huang Y; Hua R; Zhao X; Yang W; Liu Y; Zhang X
    Genet Test Mol Biomarkers; 2018 Aug; 22(8):487-491. PubMed ID: 30117778
    [TBL] [Abstract][Full Text] [Related]  

  • 47. Hypohidrotic ectodermal dysplasia: clinical and molecular review.
    Reyes-Reali J; Mendoza-Ramos MI; Garrido-Guerrero E; Méndez-Catalá CF; Méndez-Cruz AR; Pozo-Molina G
    Int J Dermatol; 2018 Aug; 57(8):965-972. PubMed ID: 29855039
    [TBL] [Abstract][Full Text] [Related]  

  • 48. [Clinical and molecular study in a family with autosomal dominant hypohidrotic ectodermal dysplasia].
    Callea M; Cammarata-Scalisi F; Willoughby CE; Giglio SR; Sani I; Bargiacchi S; Traficante G; Bellacchio E; Tadini G; Yavuz I; Galeotti A; Clarich G
    Arch Argent Pediatr; 2017 Feb; 115(1):e34-e38. PubMed ID: 28097853
    [TBL] [Abstract][Full Text] [Related]  

  • 49. A novel 1-bp deletion mutation of the EDA gene in a Chinese Han family with X-linked hypohidrotic ectodermal dysplasia.
    Kong XD; Liu N; Shi HR; Yang YX
    J Dermatol; 2014 Jul; 41(7):659-61. PubMed ID: 24985548
    [No Abstract]   [Full Text] [Related]  

  • 50. First report of X-linked hypohidrotic ectodermal dysplasia with a hemizygous c.1142G > C in the EDA gene: variant of uncertain significance or new pathogenic variant?
    Tumminello M; Gangemi A; Matina F; Guardino M; Giuffrè BL; Corsello G
    Ital J Pediatr; 2021 Jun; 47(1):128. PubMed ID: 34078430
    [TBL] [Abstract][Full Text] [Related]  

  • 51. Mutation analysis of X-linked hypohidrotic ectodermal dysplasia in a Taiwanese family.
    Chao SC; Chung CH; Yang CC; Yang MH; Lee JY
    J Formos Med Assoc; 2003 Jun; 102(6):412-7. PubMed ID: 12923595
    [TBL] [Abstract][Full Text] [Related]  

  • 52. A novel large deletion that encompasses EDA and the downstream gene AWAT2 causes X-linked hypohidrotic/anhidrotic ectodermal dysplasia.
    Chaudhary AK; Sankar VH; Bashyam MD
    J Dermatol Sci; 2016 Oct; 84(1):105-107. PubMed ID: 27443954
    [No Abstract]   [Full Text] [Related]  

  • 53. [Mutations in the ED1 gene in families with X-linked hypohidrotic ectodermal dysplasia].
    Fan HL; Ye XQ; Shi B; Zhang YL; Bian Z
    Zhonghua Kou Qiang Yi Xue Za Zhi; 2007 May; 42(5):272-5. PubMed ID: 17686277
    [TBL] [Abstract][Full Text] [Related]  

  • 54. Structural insights into pathogenic mechanism of hypohidrotic ectodermal dysplasia caused by ectodysplasin A variants.
    Yu K; Huang C; Wan F; Jiang C; Chen J; Li X; Wang F; Wu J; Lei M; Wu Y
    Nat Commun; 2023 Feb; 14(1):767. PubMed ID: 36765055
    [TBL] [Abstract][Full Text] [Related]  

  • 55. Clinical and Molecular Genetic Analysis of Cases with Ectodermal Dysplasia.
    Yapijakis C; Douka A; Gintoni I; Agiannitopoulos K; Vlachakis D; Chrousos GP
    Adv Exp Med Biol; 2023; 1423():181-186. PubMed ID: 37525042
    [TBL] [Abstract][Full Text] [Related]  

  • 56. [Detection of
    Wu JY; Yu M; Sun SC; Fan ZZ; Zheng JL; Zhang LT; Feng HL; Liu Y; Han D
    Beijing Da Xue Xue Bao Yi Xue Ban; 2020 Dec; 53(1):24-33. PubMed ID: 33550332
    [TBL] [Abstract][Full Text] [Related]  

  • 57. A recurrent missense mutation in the EDAR gene causes severe autosomal recessive hypohidrotic ectodermal dysplasia in two consanguineous Kashmiri families.
    Sadia ; Foo JN; Khor CC; Jelani M; Ali G
    J Gene Med; 2019 Sep; 21(9):e3113. PubMed ID: 31310406
    [TBL] [Abstract][Full Text] [Related]  

  • 58. A new variant of the ectodysplasin A receptor death domain gene associated with anhidrotic ectodermal dysplasia in a Turkish family and its simple diagnosis by restriction fragment length polymorphism.
    Rencuzogullari E; Ezer BG
    Genes Genet Syst; 2023 Oct; 98(4):171-178. PubMed ID: 37673591
    [TBL] [Abstract][Full Text] [Related]  

  • 59. Novel mutation of EDA causes new asymmetrical X-linked hypohidrotic ectodermal dysplasia phenotypes in a female.
    Shen L; Liu C; Gao M; Li H; Zhang Y; Tian Q; Ni H; Peng P; Zhao R; Hu Z; Gao Y; Xia K; Bo Q; Guo H
    J Dermatol; 2019 Aug; 46(8):731-733. PubMed ID: 31241787
    [TBL] [Abstract][Full Text] [Related]  

  • 60. No evidence for preferential X-chromosome inactivation as the main cause of divergent phenotypes in sisters with X-linked hypohidrotic ectodermal dysplasia.
    Körber L; Schneider H; Fleischer N; Maier-Wohlfart S
    Orphanet J Rare Dis; 2021 Feb; 16(1):98. PubMed ID: 33622384
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 8.