BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

170 related articles for article (PubMed ID: 26176760)

  • 1. Mutations Affecting Keratin 10 Surface-Exposed Residues Highlight the Structural Basis of Phenotypic Variation in Epidermolytic Ichthyosis.
    Mirza H; Kumar A; Craiglow BG; Zhou J; Saraceni C; Torbeck R; Ragsdale B; Rehder P; Ranki A; Choate KA
    J Invest Dermatol; 2015 Dec; 135(12):3041-3050. PubMed ID: 26176760
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. 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]  

  • 4. Retinoids reduce formation of keratin aggregates in heat-stressed immortalized keratinocytes from an epidermolytic ichthyosis patient with a KRT10 mutation*.
    Li H; Törmä H
    Acta Derm Venereol; 2013 Jan; 93(1):44-9. PubMed ID: 22504942
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Splice site and deletion mutations in keratin (KRT1 and KRT10) genes: unusual phenotypic alterations in Scandinavian patients with epidermolytic hyperkeratosis.
    Virtanen M; Smith SK; Gedde-Dahl T; Vahlquist A; Bowden PE
    J Invest Dermatol; 2003 Nov; 121(5):1013-20. PubMed ID: 14708600
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. Epidermolytic Ichthyosis Sine Epidermolysis.
    Eskin-Schwartz M; Drozhdina M; Sarig O; Gat A; Jackman T; Isakov O; Shomron N; Samuelov L; Malchin N; Peled A; Vodo D; Hovnanian A; Ruzicka T; Koshkin S; Harmon RM; Koetsier JL; Green KJ; Paller AS; Sprecher E
    Am J Dermatopathol; 2017 Jun; 39(6):440-444. PubMed ID: 28121638
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Recessive epidermolytic ichthyosis results from loss of keratin 10 expression, regardless of the mutation location.
    Vodo D; Sarig O; Peled A; Samuelov L; Malchin N; Grafi-Cohen M; Sprecher E
    Clin Exp Dermatol; 2018 Mar; 43(2):187-190. PubMed ID: 29277919
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Ichthyosis with confetti caused by new and recurrent mutations in KRT10 associated with varying degrees of keratin 10 mis-localization.
    Pan Y; Feng C; Wang H; Lee M; Tang Z; Lin Z
    J Dermatol Sci; 2020 Apr; 98(1):35-40. PubMed ID: 32113649
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. A Novel non-sense Mutation in Keratin 10 Causes a Familial Case of Recessive Epidermolytic Ichthyosis.
    Gutierrez JA; Hannoush ZC; Vargas LG; Momany A; Garcia CC; Murray JC; Dunnwald M
    Mol Genet Genomic Med; 2013 Jul; 1(2):108-112. PubMed ID: 23957016
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A human keratin 10 knockout causes recessive epidermolytic hyperkeratosis.
    Müller FB; Huber M; Kinaciyan T; Hausser I; Schaffrath C; Krieg T; Hohl D; Korge BP; Arin MJ
    Hum Mol Genet; 2006 Apr; 15(7):1133-41. PubMed ID: 16505000
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Expanding the keratin mutation database: novel and recurrent mutations and genotype-phenotype correlations in 28 patients with epidermolytic ichthyosis.
    Arin MJ; Oji V; Emmert S; Hausser I; Traupe H; Krieg T; Grimberg G
    Br J Dermatol; 2011 Feb; 164(2):442-7. PubMed ID: 21271994
    [TBL] [Abstract][Full Text] [Related]  

  • 14. A novel substitution in keratin 10 in epidermolytic hyperkeratosis.
    Arin MJ; Longley MA; Anton-Lamprecht I; Kurze G; Huber M; Hohl D; Rothnagel JA; Roop DR
    J Invest Dermatol; 1999 Apr; 112(4):506-8. PubMed ID: 10201536
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Expanding the Clinical and Genetic Spectrum of KRT1, KRT2 and KRT10 Mutations in Keratinopathic Ichthyosis.
    Hotz A; Oji V; Bourrat E; Jonca N; Mazereeuw-Hautier J; Betz RC; Blume-Peytavi U; Stieler K; Morice-Picard F; Schönbuchner I; Markus S; Schlipf N; Fischer J
    Acta Derm Venereol; 2016 May; 96(4):473-8. PubMed ID: 26581228
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. Cyclic ichthyosis with epidermolytic hyperkeratosis: A phenotype conferred by mutations in the 2B domain of keratin K1.
    Sybert VP; Francis JS; Corden LD; Smith LT; Weaver M; Stephens K; McLean WH
    Am J Hum Genet; 1999 Mar; 64(3):732-8. PubMed ID: 10053007
    [TBL] [Abstract][Full Text] [Related]  

  • 18. The X-Ray Crystal Structure of the Keratin 1-Keratin 10 Helix 2B Heterodimer Reveals Molecular Surface Properties and Biochemical Insights into Human Skin Disease.
    Bunick CG; Milstone LM
    J Invest Dermatol; 2017 Jan; 137(1):142-150. PubMed ID: 27595935
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Generalized and naevoid epidermolytic ichthyosis in Denmark: clinical and mutational findings.
    Bygum A; Virtanen M; Brandrup F; Gånemo A; Sommerlund M; Strauss G; Vahlquist A
    Acta Derm Venereol; 2013 May; 93(3):309-13. PubMed ID: 22930352
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Mutations in the rod domain of keratin 2e in patients with ichthyosis bullosa of Siemens.
    Rothnagel JA; Traupe H; Wojcik S; Huber M; Hohl D; Pittelkow MR; Saeki H; Ishibashi Y; Roop DR
    Nat Genet; 1994 Aug; 7(4):485-90. PubMed ID: 7524919
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.