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 *

241 related articles for article (PubMed ID: 10354017)

  • 1. Human keratin diseases: the increasing spectrum of disease and subtlety of the phenotype-genotype correlation.
    Irvine AD; McLean WH
    Br J Dermatol; 1999 May; 140(5):815-28. PubMed ID: 10354017
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Human keratin diseases: hereditary fragility of specific epithelial tissues.
    Corden LD; McLean WH
    Exp Dermatol; 1996 Dec; 5(6):297-307. PubMed ID: 9028791
    [TBL] [Abstract][Full Text] [Related]  

  • 3. The molecular genetics of keratin disorders.
    Smith F
    Am J Clin Dermatol; 2003; 4(5):347-64. PubMed ID: 12688839
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Keratin gene mutations in disorders of human skin and its appendages.
    Chamcheu JC; Siddiqui IA; Syed DN; Adhami VM; Liovic M; Mukhtar H
    Arch Biochem Biophys; 2011 Apr; 508(2):123-37. PubMed ID: 21176769
    [TBL] [Abstract][Full Text] [Related]  

  • 5. The keratins and their disorders.
    Rugg EL; Leigh IM
    Am J Med Genet C Semin Med Genet; 2004 Nov; 131C(1):4-11. PubMed ID: 15452838
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Keratin disorders: from gene to therapy.
    McLean WH; Moore CB
    Hum Mol Genet; 2011 Oct; 20(R2):R189-97. PubMed ID: 21890491
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Keratins and skin disorders.
    Lane EB; McLean WH
    J Pathol; 2004 Nov; 204(4):355-66. PubMed ID: 15495218
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Proteomic profiling reveals KRT6C as a probable hereterodimer partner for KRT9: New insights into re-classifying epidermolytic palmoplantar keratoderma (EPPK) and a milder form of pachyonychia congenita (PC-K6c) as a group of genetic cutaneous disorders.
    Li P; Qi J; Zhong Y; Ding A; Xiao H
    J Proteomics; 2023 Sep; 287():104971. PubMed ID: 37467889
    [TBL] [Abstract][Full Text] [Related]  

  • 9. The molecular basis for inherited bullous diseases.
    Korge BP; Krieg T
    J Mol Med (Berl); 1996 Feb; 74(2):59-70. PubMed ID: 8820401
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Keratins and skin disease.
    Knöbel M; O'Toole EA; Smith FJ
    Cell Tissue Res; 2015 Jun; 360(3):583-9. PubMed ID: 25620412
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Novel mutations in keratin 16 gene underly focal non-epidermolytic palmoplantar keratoderma (NEPPK) in two families.
    Shamsher MK; Navsaria HA; Stevens HP; Ratnavel RC; Purkis PE; Kelsell DP; McLean WH; Cook LJ; Griffiths WA; Gschmeissner S
    Hum Mol Genet; 1995 Oct; 4(10):1875-81. PubMed ID: 8595410
    [TBL] [Abstract][Full Text] [Related]  

  • 12. New mutations in keratin 1 that cause bullous congenital ichthyosiform erythroderma and keratin 2e that cause ichthyosis bullosa of Siemens.
    Whittock NV; Ashton GH; Griffiths WA; Eady RA; McGrath JA
    Br J Dermatol; 2001 Aug; 145(2):330-5. PubMed ID: 11531804
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Arginine in the beginning of the 1A rod domain of the keratin 10 gene is the hot spot for the mutation in epidermolytic hyperkeratosis.
    Yang JM; Nam K; Kim SW; Jung SY; Min HG; Yeo UC; Park KB; Lee JH; Suhr KB; Park JK; Lee ES
    J Dermatol Sci; 1999 Feb; 19(2):126-33. PubMed ID: 10098704
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Mutations in the genes for epidermal keratins in epidermolysis bullosa and epidermolytic hyperkeratosis.
    Leigh IM; Lane EB
    Arch Dermatol; 1993 Dec; 129(12):1571-7. PubMed ID: 7504434
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Genetic disorders of keratin: are scarring alopecias a sub-set?
    Rothnagel JA; Longley MA; Holder RA; Bundman DS; Seki T; Bickenbach JR; Roop DR
    J Dermatol Sci; 1994 Jul; 7 Suppl():S164-9. PubMed ID: 7528048
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Identification of clinically useful predictive genetic variants in pachyonychia congenita.
    Samuelov L; Sarig O; Adir N; Pavlovsky M; Smith FJ; Schwartz J; Hansen CD; Sprecher E
    Clin Exp Dermatol; 2021 Jul; 46(5):867-873. PubMed ID: 33486795
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Inherited abnormalities of the epidermis caused by mutation of keratins].
    Hohl D
    Ann Dermatol Venereol; 1995; 122(4):162-6. PubMed ID: 8526410
    [TBL] [Abstract][Full Text] [Related]  

  • 18. How do keratinizing disorders and blistering disorders overlap?
    Hamada T; Tsuruta D; Fukuda S; Ishii N; Teye K; Numata S; Dainichi T; Karashima T; Ohata C; Furumura M; Hashimoto T
    Exp Dermatol; 2013 Feb; 22(2):83-7. PubMed ID: 23039137
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Keratin diseases].
    Jensen PK; Sørensen CB; Andresen BS; Brandrup F; Veien NK; Buus SK; Gregersen N; Bolund L
    Ugeskr Laeger; 2000 Mar; 162(13):1867-72. PubMed ID: 10765692
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Keratin 9 point mutation in the pedigree of epidermolytic hereditary palmoplantar keratoderma perturbs keratin intermediate filament network formation.
    Kobayashi S; Tanaka T; Matsuyoshi N; Imamura S
    FEBS Lett; 1996 May; 386(2-3):149-55. PubMed ID: 8647270
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 13.