BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

408 related articles for article (PubMed ID: 9028791)

  • 1. 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]  

  • 2. 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]  

  • 3. 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]  

  • 4. 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]  

  • 5. 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]  

  • 6. 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]  

  • 7. 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]  

  • 8. Selective involvement of keratins K1 and K10 in the cytoskeletal abnormality of epidermolytic hyperkeratosis (bullous congenital ichthyosiform erythroderma).
    Ishida-Yamamoto A; McGrath JA; Judge MR; Leigh IM; Lane EB; Eady RA
    J Invest Dermatol; 1992 Jul; 99(1):19-26. PubMed ID: 1376754
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Mutations in the non-helical linker segment L1-2 of keratin 5 in patients with Weber-Cockayne epidermolysis bullosa simplex.
    Chan YM; Yu QC; LeBlanc-Straceski J; Christiano A; Pulkkinen L; Kucherlapati RS; Uitto J; Fuchs E
    J Cell Sci; 1994 Apr; 107 ( Pt 4)():765-74. PubMed ID: 7520042
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. Atypical epidermolytic palmoplantar keratoderma presentation associated with a mutation in the keratin 1 gene.
    Terron-Kwiatkowski A; Terrinoni A; Didona B; Melino G; Atherton DJ; Irvine AD; McLean WH
    Br J Dermatol; 2004 Jun; 150(6):1096-103. PubMed ID: 15214894
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. A mutation in human keratin K6b produces a phenocopy of the K17 disorder pachyonychia congenita type 2.
    Smith FJ; Jonkman MF; van Goor H; Coleman CM; Covello SP; Uitto J; McLean WH
    Hum Mol Genet; 1998 Jul; 7(7):1143-8. PubMed ID: 9618173
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [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]  

  • 15. 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]  

  • 16. An atypical form of bullous congenital ichthyosiform erythroderma is caused by a mutation in the L12 linker region of keratin 1.
    Kremer H; Lavrijsen AP; McLean WH; Lane EB; Melchers D; Ruiter DJ; Mariman EC; Steijlen PM
    J Invest Dermatol; 1998 Dec; 111(6):1224-6. PubMed ID: 9856846
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Disruption of the suprabasal keratin network by mutation M150T in the helix initiation motif of keratin 10 does not affect cornified cell envelope formation in human epidermis.
    Akiyama M; Takizawa Y; Sawamura D; Matsuo I; Shimizu H
    Exp Dermatol; 2003 Oct; 12(5):638-45. PubMed ID: 14705805
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Lessons from disorders of epidermal differentiation-associated keratins.
    Ishida-Yamamoto A; Takahashi H; Iizuka H
    Histol Histopathol; 2002 Jan; 17(1):331-8. PubMed ID: 11813882
    [TBL] [Abstract][Full Text] [Related]  

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

  • 20. The genetic basis of epidermolytic hyperkeratosis: a disorder of differentiation-specific epidermal keratin genes.
    Cheng J; Syder AJ; Yu QC; Letai A; Paller AS; Fuchs E
    Cell; 1992 Sep; 70(5):811-9. PubMed ID: 1381287
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 21.