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 *

347 related articles for article (PubMed ID: 19587453)

  • 1. Epidermolysis bullosa simplex: a paradigm for disorders of tissue fragility.
    Coulombe PA; Kerns ML; Fuchs E
    J Clin Invest; 2009 Jul; 119(7):1784-93. PubMed ID: 19587453
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Defining keratin protein function in skin epithelia: epidermolysis bullosa simplex and its aftermath.
    Coulombe PA; Lee CH
    J Invest Dermatol; 2012 Mar; 132(3 Pt 2):763-75. PubMed ID: 22277943
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Threonine 150 Phosphorylation of Keratin 5 Is Linked to Epidermolysis Bullosa Simplex and Regulates Filament Assembly and Cell Viability.
    Sawant M; Schwarz N; Windoffer R; Magin TM; Krieger J; Mücke N; Obara B; Jankowski V; Jankowski J; Wally V; Lettner T; Leube RE
    J Invest Dermatol; 2018 Mar; 138(3):627-636. PubMed ID: 29080682
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Mutations in KRT5 and KRT14 cause epidermolysis bullosa simplex in 75% of the patients.
    Bolling MC; Lemmink HH; Jansen GH; Jonkman MF
    Br J Dermatol; 2011 Mar; 164(3):637-44. PubMed ID: 21375516
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Complete cytolysis and neonatal lethality in keratin 5 knockout mice reveal its fundamental role in skin integrity and in epidermolysis bullosa simplex.
    Peters B; Kirfel J; Büssow H; Vidal M; Magin TM
    Mol Biol Cell; 2001 Jun; 12(6):1775-89. PubMed ID: 11408584
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Distinct Impact of Two Keratin Mutations Causing Epidermolysis Bullosa Simplex on Keratinocyte Adhesion and Stiffness.
    Homberg M; Ramms L; Schwarz N; Dreissen G; Leube RE; Merkel R; Hoffmann B; Magin TM
    J Invest Dermatol; 2015 Oct; 135(10):2437-2445. PubMed ID: 25961909
    [TBL] [Abstract][Full Text] [Related]  

  • 7. In silico analysis of all point mutations on the 2B domain of K5/K14 causing epidermolysis bullosa simplex: a genotype-phenotype correlation.
    Banerjee S; Wu Q; Yu P; Qi M; Li C
    Mol Biosyst; 2014 Oct; 10(10):2567-77. PubMed ID: 25017986
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Keratins as an Inflammation Trigger Point in Epidermolysis Bullosa Simplex.
    Evtushenko NA; Beilin AK; Kosykh AV; Vorotelyak EA; Gurskaya NG
    Int J Mol Sci; 2021 Nov; 22(22):. PubMed ID: 34830328
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Identification of novel and known KRT5 and KRT14 mutations in 53 patients with epidermolysis bullosa simplex: correlation between genotype and phenotype.
    Arin MJ; Grimberg G; Schumann H; De Almeida H; Chang YR; Tadini G; Kohlhase J; Krieg T; Bruckner-Tuderman L; Has C
    Br J Dermatol; 2010 Jun; 162(6):1365-9. PubMed ID: 20199538
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Cytokines as genetic modifiers in K5-/- mice and in human epidermolysis bullosa simplex.
    Roth W; Reuter U; Wohlenberg C; Bruckner-Tuderman L; Magin TM
    Hum Mutat; 2009 May; 30(5):832-41. PubMed ID: 19267394
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Novel and recurrent mutations in Keratin 5 and 14 in Korean patients with Epidermolysis bullosa simplex.
    Kang TW; Lee JS; Kim SE; Oh SW; Kim SC
    J Dermatol Sci; 2010 Feb; 57(2):90-4. PubMed ID: 20060687
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A Drosophila Model of Epidermolysis Bullosa Simplex.
    Bohnekamp J; Cryderman DE; Paululat A; Baccam GC; Wallrath LL; Magin TM
    J Invest Dermatol; 2015 Aug; 135(8):2031-2039. PubMed ID: 25830653
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Epidermolysis bullosa simplex in Scotland caused by a spectrum of keratin mutations.
    Rugg EL; Horn HM; Smith FJ; Wilson NJ; Hill AJ; Magee GJ; Shemanko CS; Baty DU; Tidman MJ; Lane EB
    J Invest Dermatol; 2007 Mar; 127(3):574-80. PubMed ID: 17039244
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Keratin 14-null cells as a model to test the efficacy of gene therapy approaches in epithelial cells.
    D'Alessandro M; Coats SE; Jonkmann MF; Leigh IM; Lane EB
    J Invest Dermatol; 2011 Jul; 131(7):1412-9. PubMed ID: 21326298
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Keratins and epidermolysis bullosa simplex.
    Khani P; Ghazi F; Zekri A; Nasri F; Behrangi E; Aghdam AM; Mirzaei H
    J Cell Physiol; 2018 Jan; 234(1):289-297. PubMed ID: 30078200
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Mutation analysis of keratin 5 and keratin 14 genes in a family with epidermolysis bullosa simplex with mottled pigmentation].
    Liu X; Xia L; Wang JX; Hao YJ; Yang J; Liu FQ; Guo R
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2011 Dec; 28(6):612-5. PubMed ID: 22161089
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Human-Induced Pluripotent Stem Cell‒Derived Keratinocytes, a Useful Model to Identify and Explore the Pathological Phenotype of Epidermolysis Bullosa Simplex.
    Coutier J; Bonnette M; Martineau S; Mercadier A; Domingues S; Saidani M; Jarrige M; Polveche H; Darle A; Holic N; Hadj-Rabia S; Bodemer C; Lemaitre G; Martinat C; Baldeschi C
    J Invest Dermatol; 2022 Oct; 142(10):2695-2705.e11. PubMed ID: 35490743
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Atypical epidermolysis bullosa simplex with a missense keratin 14 mutation p.Arg125Cys.
    Tsuruta D; Sowa J; Tateishi C; Obase Y; Tsubura A; Fukumoto T; Ishii M; Kobayashi H; Sakaguchi S; Hashimoto T; Hamada T
    J Dermatol; 2011 Dec; 38(12):1177-9. PubMed ID: 21967011
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Development of allele-specific therapeutic siRNA for keratin 5 mutations in epidermolysis bullosa simplex.
    Atkinson SD; McGilligan VE; Liao H; Szeverenyi I; Smith FJ; Moore CB; McLean WH
    J Invest Dermatol; 2011 Oct; 131(10):2079-86. PubMed ID: 21716320
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A Review of 52 Pedigrees with Epidermolysis Bullosa Simplex Identifying Ten Novel Mutations in KRT5 and KRT14 in Australia.
    Kim EN; Harris AG; Bingham LJ; Yan W; Su JC; Murrell DF
    Acta Derm Venereol; 2017 Oct; 97(9):1114-1119. PubMed ID: 28561874
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 18.