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 *

166 related articles for article (PubMed ID: 20410354)

  • 1. TP63 gene mutations in Chinese P63 syndrome patients.
    Yin W; Ye X; Shi L; Wang QK; Jin H; Wang P; Bian Z
    J Dent Res; 2010 Aug; 89(8):813-7. PubMed ID: 20410354
    [TBL] [Abstract][Full Text] [Related]  

  • 2. EEC- and ADULT-associated TP63 mutations exhibit functional heterogeneity toward P63 responsive sequences.
    Monti P; Russo D; Bocciardi R; Foggetti G; Menichini P; Divizia MT; Lerone M; Graziano C; Wischmeijer A; Viadiu H; Ravazzolo R; Inga A; Fronza G
    Hum Mutat; 2013 Jun; 34(6):894-904. PubMed ID: 23463580
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Cleft palate and ADULT phenotype in a patient with a novel TP63 mutation suggests lumping of EEC/LM/ADULT syndromes into a unique entity: ELA syndrome.
    Prontera P; Garelli E; Isidori I; Mencarelli A; Carando A; Silengo MC; Donti E
    Am J Med Genet A; 2011 Nov; 155A(11):2746-9. PubMed ID: 21990121
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Analysis of the p63 gene in classical EEC syndrome, related syndromes, and non-syndromic orofacial clefts.
    Barrow LL; van Bokhoven H; Daack-Hirsch S; Andersen T; van Beersum SE; Gorlin R; Murray JC
    J Med Genet; 2002 Aug; 39(8):559-66. PubMed ID: 12161593
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Analysis of large phenotypic variability of EEC and SHFM4 syndromes caused by K193E mutation of the TP63 gene.
    Wei J; Xue Y; Wu L; Ma J; Yi X; Zhang J; Lu B; Li C; Shi D; Shi S; Feng X; Cai T
    PLoS One; 2012; 7(5):e35337. PubMed ID: 22574117
    [TBL] [Abstract][Full Text] [Related]  

  • 6. A spectrum of TP63-related disorders with eight affected individuals in five unrelated families.
    Soğukpınar M; Utine GE; Boduroğlu K; Şimşek-Kiper PÖ
    Eur J Med Genet; 2024 Apr; 68():104911. PubMed ID: 38281558
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [Heterozygous TP63 mutation in a Chinese patient with ectrodactyly-ectodermal dysplasia clefting syndrome without clefting].
    Han D; Wu H; Zhang XX; Feng HL
    Zhonghua Kou Qiang Yi Xue Za Zhi; 2010 Dec; 45(12):767-9. PubMed ID: 21211247
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Functional characterization of a novel TP63 mutation in a family with overlapping features of Rapp-Hodgkin/AEC/ADULT syndromes.
    Serra V; Castori M; Paradisi M; Bui L; Melino G; Terrinoni A
    Am J Med Genet A; 2011 Dec; 155A(12):3104-9. PubMed ID: 22069181
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A novel H208D TP63 mutation in a familial case of ectrodactyly-ectodermal dysplasia-cleft lip/palate syndrome without clefting.
    Sorasio L; Biamino E; Garelli E; Ferrero GB; Silengo MC
    Clin Exp Dermatol; 2009 Dec; 34(8):e726-8. PubMed ID: 19663851
    [TBL] [Abstract][Full Text] [Related]  

  • 10. ADULT syndrome due to an R243W mutation in TP63.
    Berk DR; Armstrong NL; Shinawi M; Whelan AJ
    Int J Dermatol; 2012 Jun; 51(6):693-6. PubMed ID: 22607287
    [TBL] [Abstract][Full Text] [Related]  

  • 11. EEC-LM-ADULT syndrome caused by R319H mutation in TP63 with ectrodactyly, syndactyly, and teeth anomaly: A case report.
    Otsuki Y; Ueda K; Nuri T; Satoh C; Maekawa R; Yoshiura KI
    Medicine (Baltimore); 2020 Oct; 99(44):e22816. PubMed ID: 33126320
    [TBL] [Abstract][Full Text] [Related]  

  • 12. p63-associated disorders.
    Rinne T; Brunner HG; van Bokhoven H
    Cell Cycle; 2007 Feb; 6(3):262-8. PubMed ID: 17224651
    [TBL] [Abstract][Full Text] [Related]  

  • 13. EEC syndrome, Arg227Gln TP63 mutation and micturition difficulties: Is there a genotype-phenotype correlation?
    Maclean K; Holme SA; Gilmour E; Taylor M; Scheffer H; Graf N; Smith GH; Onikul E; van Bokhoven H; Moss C; Adès LC
    Am J Med Genet A; 2007 May; 143A(10):1114-9. PubMed ID: 17431922
    [TBL] [Abstract][Full Text] [Related]  

  • 14. A novel mutation (c.1010G>T; p.R337L) in TP63 as a cause of split-hand/foot malformation with hypodontia.
    Jin JY; Zeng L; Li K; He JQ; Pang X; Huang H; Xiang R; Tang JY
    J Gene Med; 2019 Oct; 21(10):e3122. PubMed ID: 31420900
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Molecular basis of EEC (ectrodactyly, ectodermal dysplasia, clefting) syndrome: five new mutations in the DNA-binding domain of the TP63 gene and genotype-phenotype correlation.
    Clements SE; Techanukul T; Coman D; Mellerio JE; McGrath JA
    Br J Dermatol; 2010 Jan; 162(1):201-7. PubMed ID: 19903181
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Tooth defects of EEC and AEC syndrome caused by heterozygous TP63 mutations in three Chinese families and genotype-phenotype correlation analyses of TP63-related disorders.
    Zheng J; Liu H; Zhan Y; Liu Y; Wong SW; Cai T; Feng H; Han D
    Mol Genet Genomic Med; 2019 Jun; 7(6):e704. PubMed ID: 31050217
    [TBL] [Abstract][Full Text] [Related]  

  • 17. p63 Gene mutations in eec syndrome, limb-mammary syndrome, and isolated split hand-split foot malformation suggest a genotype-phenotype correlation.
    van Bokhoven H; Hamel BC; Bamshad M; Sangiorgi E; Gurrieri F; Duijf PH; Vanmolkot KR; van Beusekom E; van Beersum SE; Celli J; Merkx GF; Tenconi R; Fryns JP; Verloes A; Newbury-Ecob RA; Raas-Rotschild A; Majewski F; Beemer FA; Janecke A; Chitayat D; Crisponi G; Kayserili H; Yates JR; Neri G; Brunner HG
    Am J Hum Genet; 2001 Sep; 69(3):481-92. PubMed ID: 11462173
    [TBL] [Abstract][Full Text] [Related]  

  • 18. ADULT syndrome caused by a mutation previously associated with EEC syndrome.
    Avitan-Hersh E; Indelman M; Bergman R; Sprecher E
    Pediatr Dermatol; 2010; 27(6):643-5. PubMed ID: 21078104
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A case of ankyloblepharon, ectodermal dysplasia, and cleft lip/palate syndrome with ectrodactyly: are the p63 syndromes distinct after all?
    Chiu YE; Drolet BA; Duffy KJ; Holland KE
    Pediatr Dermatol; 2011; 28(1):15-9. PubMed ID: 19793345
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Differentially Expressed Genes in EEC and LMS Syndromes.
    Yin W; Song Y; Du Y; Bian Z
    PLoS One; 2015; 10(6):e0129432. PubMed ID: 26075610
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.