BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

155 related articles for article (PubMed ID: 25495838)

  • 1. Extensive lentigo simplex, linear epidermolytic naevus and epidermolytic naevus comedonicus caused by a somatic mutation in KRT10.
    Samuelov L; Sarig O; Gat A; Halachmi S; Shalev S; Sprecher E
    Br J Dermatol; 2015 Jul; 173(1):293-6. PubMed ID: 25495838
    [No Abstract]   [Full Text] [Related]  

  • 2. Epidermolytic Acanthoma of the Genitalia Does Not Show Mutations in KRT1 or KRT10.
    Egozi-Reinman E; Avitan-Hersh E; Barzilai A; Indelman M; Bergman R
    Am J Dermatopathol; 2016 Feb; 38(2):164-5. PubMed ID: 26825163
    [No Abstract]   [Full Text] [Related]  

  • 3. A Child with Epidermolytic Ichthyosis from a Parent with Epidermolytic Nevus: Risk Evaluation of Transmission from Mosaic to Germline.
    Kono M; Suga Y; Akashi T; Ito Y; Takeichi T; Muro Y; Akiyama M
    J Invest Dermatol; 2017 Sep; 137(9):2024-2026. PubMed ID: 28532675
    [No Abstract]   [Full Text] [Related]  

  • 4. Lethal autosomal recessive epidermolytic ichthyosis due to a novel donor splice-site mutation in KRT10.
    Covaciu C; Castori M; De Luca N; Ghirri P; Nannipieri A; Ragone G; Zambruno G; Castiglia D
    Br J Dermatol; 2010 Jun; 162(6):1384-7. PubMed ID: 20302579
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Localized linear epidermolytic epidermal nevus of male genitalia with a recurrent keratin 10 mutation, p.Arg156His.
    Uchiyama K; Nakanishi G; Fujimoto N; Takikita M; Tanaka T
    Eur J Dermatol; 2013; 23(4):557-8. PubMed ID: 24001792
    [No Abstract]   [Full Text] [Related]  

  • 6. Bullous icthyosiform erythroderma with rickets in child of a parent with naevus unius lateralis.
    Bhat YJ; Baba AN; Manzoor S; Qayoom S; Ahmed SM
    Indian J Dermatol Venereol Leprol; 2010; 76(2):192-4. PubMed ID: 20228558
    [No Abstract]   [Full Text] [Related]  

  • 7. R156C mutation of keratin 10 causes mild form of epidermolytic hyperkeratosis.
    Haruna K; Suga Y; Mizuno Y; Hasegawa T; Kourou K; Matsuba S; Muramatsu S; Ikeda S
    J Dermatol; 2007 Aug; 34(8):545-8. PubMed ID: 17683385
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Epidermolytic ichthyosis due to a de novo missense mutation c.1307T> C; p.Leu436Pro in KRT10.
    Kuske M; Berndt K; Meinel G; Abraham S; Oji V; Reicherter K; Hörtnagel K; Beissert S; Bauer A
    J Dtsch Dermatol Ges; 2019 Jan; 17(1):82-84. PubMed ID: 30520551
    [No Abstract]   [Full Text] [Related]  

  • 9. A case of epidermolytic ichthyosis showing a very mild phenotype due to a novel tail extension mutation in KRT10.
    Kono M; Fukai K; Omura R; Sugawara K; Tsuruta D; Sugiura K; Akiyama M
    J Eur Acad Dermatol Venereol; 2017 Feb; 31(2):e68-e69. PubMed ID: 27225831
    [No Abstract]   [Full Text] [Related]  

  • 10. Epidermolytic hyperkeratosis with palmoplantar keratoderma in a patient with KRT10 mutation.
    Morais P; Mota A; Baudrier T; Lopes JM; Cerqueira R; Tavares P; Azevedo F
    Eur J Dermatol; 2009; 19(4):333-6. PubMed ID: 19443303
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Mutations in KRT10 in epidermolytic acanthoma.
    Cheraghlou S; Atzmony L; Roy SF; McNiff JM; Choate KA
    J Cutan Pathol; 2020 Jun; 47(6):524-529. PubMed ID: 32045015
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Case of epidermolytic ichthyosis (bullous congenial ichthyosiform erythroderma) with a novel L157P mutation in KRT10 complicated by hypercalcemia.
    Yamamoto M; Tsuda T; Otaki Y; Nakanishi T; Yamanishi K
    J Dermatol; 2012 Aug; 39(8):716-8. PubMed ID: 22035476
    [No Abstract]   [Full Text] [Related]  

  • 13. Extensive Post-zygotic Mosaicism of KRT1 or KRT10 Mutation Mimicking Classical Epider-molytic Ichthyosis.
    Severino-Freire M; Jonca N; Pichery M; Tournier E; Chassaing N; Mazereeuw-Hautier J
    Acta Derm Venereol; 2017 Mar; 97(3):387-388. PubMed ID: 27722766
    [No Abstract]   [Full Text] [Related]  

  • 14. New KRT10 gene mutation underlying the annular variant of bullous congenital ichthyosiform erythroderma with clinical worsening during pregnancy.
    Sheth N; Greenblatt D; McGrath JA
    Br J Dermatol; 2007 Sep; 157(3):602-4. PubMed ID: 17596149
    [No Abstract]   [Full Text] [Related]  

  • 15. The absence of BRAF, FGFR3, and PIK3CA mutations differentiates lentigo simplex from melanocytic nevus and solar lentigo.
    Hafner C; Stoehr R; van Oers JM; Zwarthoff EC; Hofstaedter F; Klein C; Landthaler M; Hartmann A; Vogt T
    J Invest Dermatol; 2009 Nov; 129(11):2730-5. PubMed ID: 19536147
    [No Abstract]   [Full Text] [Related]  

  • 16. S159P mutation of keratin 10 gene causes severe form of epidermolytic hyperkeratosis.
    Chen PJ; Li CX; Wen J; Peng YS; Zeng K; Zhang SQ; Tian X; Zhang XB
    J Eur Acad Dermatol Venereol; 2016 Oct; 30(10):e102-e104. PubMed ID: 26373619
    [No Abstract]   [Full Text] [Related]  

  • 17. Recessive epidermolytic hyperkeratosis caused by a previously unreported termination codon mutation in the keratin 10 gene.
    Terheyden P; Grimberg G; Hausser I; Rose C; Korge BP; Krieg T; Arin MJ
    J Invest Dermatol; 2009 Nov; 129(11):2721-3. PubMed ID: 19474805
    [No Abstract]   [Full Text] [Related]  

  • 18. Bullous congenital ichthyosiform erythroderma: a sporadic case produced by a new KRT10 gene mutation.
    Betlloch I; Lucas Costa A; Mataix J; Pérez-Crespo M; Ballester I
    Pediatr Dermatol; 2009; 26(4):489-91. PubMed ID: 19689541
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Mild recessive epidermolytic hyperkeratosis associated with a novel keratin 10 donor splice-site mutation in a family of Norfolk terrier dogs.
    Credille KM; Barnhart KF; Minor JS; Dunstan RW
    Br J Dermatol; 2005 Jul; 153(1):51-8. PubMed ID: 16029326
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Intrafamilial phenotypic heterogeneity of epidermolytic ichthyosis associated with a new missense mutation in keratin 10.
    Abdul-Wahab A; Takeichi T; Liu L; Stephens C; Akiyama M; McGrath JA
    Clin Exp Dermatol; 2016 Apr; 41(3):290-3. PubMed ID: 26338057
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.