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 *

187 related articles for article (PubMed ID: 8250577)

  • 1. The molecular genetics of basement membrane diseases.
    Marinkovich MP
    Arch Dermatol; 1993 Dec; 129(12):1557-65. PubMed ID: 8250577
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Ultrastructural findings in epidermolysis bullosa.
    Smith LT
    Arch Dermatol; 1993 Dec; 129(12):1578-84. PubMed ID: 7504435
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Human skin basement membrane in health and in autoimmune diseases.
    Chan LS
    Front Biosci; 1997 Jul; 2():d343-52. PubMed ID: 9232815
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [Epidermolysis bullosa].
    García Pérez A
    An R Acad Nac Med (Madr); 1999; 116(2):387-413; discussion 413-5. PubMed ID: 10682398
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Immunohistochemical, ultrastructural, and molecular features of Kindler syndrome distinguish it from dystrophic epidermolysis bullosa.
    Shimizu H; Sato M; Ban M; Kitajima Y; Ishizaki S; Harada T; Bruckner-Tuderman L; Fine JD; Burgeson R; Kon A; McGrath JA; Christiano AM; Uitto J; Nishikawa T
    Arch Dermatol; 1997 Sep; 133(9):1111-7. PubMed ID: 9301588
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Hemidesmosomes show abnormal association with the keratin filament network in junctional forms of epidermolysis bullosa.
    McMillan JR; McGrath JA; Tidman MJ; Eady RA
    J Invest Dermatol; 1998 Feb; 110(2):132-7. PubMed ID: 9457907
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [Hereditary epidermolysis bullosa: towards classification and genetic counseling based upon identification of molecular defects].
    Hovnanian A; de Prost Y
    Arch Pediatr; 1994 Nov; 1(11):1028-33. PubMed ID: 7530560
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Cell adhesion molecules and extracellular matrix components as target structures of autoimmunity].
    Moll R; Bahn H; Bayerl C; Moll I
    Verh Dtsch Ges Pathol; 1996; 80():67-79. PubMed ID: 9065056
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Hemidesmosomes and their unique transmembrane protein BP180.
    Hirako Y; Owaribe K
    Microsc Res Tech; 1998 Nov; 43(3):207-17. PubMed ID: 9840798
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Epidermolysis bullosa: hereditary skin fragility diseases as paradigms in cell biology.
    Eady RA; Dunnill MG
    Arch Dermatol Res; 1994; 287(1):2-9. PubMed ID: 7537032
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Acquired skin disease of hemidesmosomes.
    Zillikens D
    J Dermatol Sci; 1999 Jun; 20(2):134-54. PubMed ID: 10379705
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Compound heterozygosity for a nonsense mutation and a splice site mutation in the type VII collagen gene (COL7A1) in recessive dystrophic epidermolysis bullosa.
    Tamai K; Ishida-Yamamoto A; Matsuo S; Iizuka H; Hashimoto I; Christiano AM; Uitto J; McGrath JA
    Lab Invest; 1997 Feb; 76(2):209-17. PubMed ID: 9042157
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Granulocyte-derived elastase and gelatinase B are required for dermal-epidermal separation induced by autoantibodies from patients with epidermolysis bullosa acquisita and bullous pemphigoid.
    Shimanovich I; Mihai S; Oostingh GJ; Ilenchuk TT; Bröcker EB; Opdenakker G; Zillikens D; Sitaru C
    J Pathol; 2004 Dec; 204(5):519-27. PubMed ID: 15538734
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Genetic skin diseases.
    Francis JS
    Curr Opin Pediatr; 1994 Aug; 6(4):447-53. PubMed ID: 7951667
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Histology of supepidermal bullous dermatoses].
    Megahed M
    Verh Dtsch Ges Pathol; 1996; 80():223-8. PubMed ID: 9065014
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Ultrastructure and molecular pathogenesis of epidermolysis bullosa.
    Shinkuma S; McMillan JR; Shimizu H
    Clin Dermatol; 2011; 29(4):412-9. PubMed ID: 21679868
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Autoimmune and inherited subepidermal blistering diseases: advances in the clinic and the laboratory.
    Schmidt E; Zillikens D
    Adv Dermatol; 2000; 16():113-57; discussion 158. PubMed ID: 11094626
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [The dermo-epidermal junction and its acquired and hereditary pathology. A few recent advances].
    Ortonne JP
    Pathol Biol (Paris); 1992 Feb; 40(2):121-32. PubMed ID: 1608653
    [TBL] [Abstract][Full Text] [Related]  

  • 19. The carboxyl-terminal domain of type VII collagen is present at the basement membrane in recessive dystrophic epidermolysis bullosa.
    Rusenko KW; Gammon WR; Fine JD; Briggaman RA
    J Invest Dermatol; 1989 Apr; 92(4):623-7. PubMed ID: 2649597
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Do mutations in the basement membrane zone affect the human periodontium? Review with special reference to epidermolysis bullosa.
    Wiebe CB; Larjava HS
    J West Soc Periodontol Periodontal Abstr; 1998; 46(1):5-18. PubMed ID: 9709672
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.