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 *

113 related articles for article (PubMed ID: 9754951)

  • 1. Plectin in the human central nervous system: predominant expression at pia/glia and endothelia/glia interfaces.
    Lie AA; Schröder R; Blümcke I; Magin TM; Wiestler OD; Elger CE
    Acta Neuropathol; 1998 Sep; 96(3):215-21. PubMed ID: 9754951
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Distribution of plectin, an intermediate filament-associated protein, in the adult rat central nervous system.
    Errante LD; Wiche G; Shaw G
    J Neurosci Res; 1994 Mar; 37(4):515-28. PubMed ID: 8021973
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Defective expression of plectin/HD1 in epidermolysis bullosa simplex with muscular dystrophy.
    Gache Y; Chavanas S; Lacour JP; Wiche G; Owaribe K; Meneguzzi G; Ortonne JP
    J Clin Invest; 1996 May; 97(10):2289-98. PubMed ID: 8636409
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Distribution of rSlo Ca2+-activated K+ channels in rat astrocyte perivascular endfeet.
    Price DL; Ludwig JW; Mi H; Schwarz TL; Ellisman MH
    Brain Res; 2002 Nov; 956(2):183-93. PubMed ID: 12445685
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Altered distribution of plectin/HD1 in dystrophinopathies.
    Schröder R; Mundegar RR; Treusch M; Schlegel U; Blümcke I; Owaribe K; Magin TM
    Eur J Cell Biol; 1997 Oct; 74(2):165-71. PubMed ID: 9352221
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Hippocampal loss of tenascin boundaries in Ammon's horn sclerosis.
    Scheffler B; Faissner A; Beck H; Behle K; Wolf HK; Wiestler OD; Blümcke I
    Glia; 1997 Jan; 19(1):35-46. PubMed ID: 8989566
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Epidermolysis bullosa simplex associated with muscular dystrophy: phenotype-genotype correlations and review of the literature.
    Shimizu H; Takizawa Y; Pulkkinen L; Murata S; Kawai M; Hachisuka H; Udono M; Uitto J; Nishikawa T
    J Am Acad Dermatol; 1999 Dec; 41(6):950-6. PubMed ID: 10570379
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Ultrastructural observations of astrocyte end-feet in the rat central nervous system.
    Nakazawa E; Ishikawa H
    J Neurocytol; 1998 Jun; 27(6):431-40. PubMed ID: 10192524
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Downstream effects of plectin mutations in epidermolysis bullosa simplex with muscular dystrophy.
    Winter L; Türk M; Harter PN; Mittelbronn M; Kornblum C; Norwood F; Jungbluth H; Thiel CT; Schlötzer-Schrehardt U; Schröder R
    Acta Neuropathol Commun; 2016 Apr; 4(1):44. PubMed ID: 27121971
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Expression of plectin and HD1 epitopes in patients with epidermolysis bullosa simplex associated with muscular dystrophy.
    Shimizu H; Masunaga T; Kurihara Y; Owaribe K; Wiche G; Pulkkinen L; Uitto J; Nishikawa T
    Arch Dermatol Res; 1999 Oct; 291(10):531-7. PubMed ID: 10552210
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Loss of plectin causes epidermolysis bullosa with muscular dystrophy: cDNA cloning and genomic organization.
    McLean WH; Pulkkinen L; Smith FJ; Rugg EL; Lane EB; Bullrich F; Burgeson RE; Amano S; Hudson DL; Owaribe K; McGrath JA; McMillan JR; Eady RA; Leigh IM; Christiano AM; Uitto J
    Genes Dev; 1996 Jul; 10(14):1724-35. PubMed ID: 8698233
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Disorganization of the desmin cytoskeleton and mitochondrial dysfunction in plectin-related epidermolysis bullosa simplex with muscular dystrophy.
    Schröder R; Kunz WS; Rouan F; Pfendner E; Tolksdorf K; Kappes-Horn K; Altenschmidt-Mehring M; Knoblich R; van der Ven PF; Reimann J; Fürst DO; Blümcke I; Vielhaber S; Zillikens D; Eming S; Klockgether T; Uitto J; Wiche G; Rolfs A
    J Neuropathol Exp Neurol; 2002 Jun; 61(6):520-30. PubMed ID: 12071635
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Plectin expression patterns determine two distinct subtypes of epidermolysis bullosa simplex.
    Natsuga K; Nishie W; Akiyama M; Nakamura H; Shinkuma S; McMillan JR; Nagasaki A; Has C; Ouchi T; Ishiko A; Hirako Y; Owaribe K; Sawamura D; Bruckner-Tuderman L; Shimizu H
    Hum Mutat; 2010 Mar; 31(3):308-16. PubMed ID: 20052759
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Plectin deficiency results in muscular dystrophy with epidermolysis bullosa.
    Smith FJ; Eady RA; Leigh IM; McMillan JR; Rugg EL; Kelsell DP; Bryant SP; Spurr NK; Geddes JF; Kirtschig G; Milana G; de Bono AG; Owaribe K; Wiche G; Pulkkinen L; Uitto J; McLean WH; Lane EB
    Nat Genet; 1996 Aug; 13(4):450-7. PubMed ID: 8696340
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Plectin immunopositivity appears in the astrocytes in the white matter but not in the gray matter after stab wounds.
    Kálmán M; Szabó A
    Brain Res; 2000 Feb; 857(1-2):291-4. PubMed ID: 10700580
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Life-long course and molecular characterization of the original Dutch family with epidermolysis bullosa simplex with muscular dystrophy due to a homozygous novel plectin point mutation.
    Koss-Harnes D; Høyheim B; Jonkman MF; de Groot WP; de Weerdt CJ; Nikolic B; Wiche G; Gedde-Dahl T
    Acta Derm Venereol; 2004; 84(2):124-31. PubMed ID: 15206692
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Homozygous deletion mutations in the plectin gene (PLEC1) in patients with epidermolysis bullosa simplex associated with late-onset muscular dystrophy.
    Pulkkinen L; Smith FJ; Shimizu H; Murata S; Yaoita H; Hachisuka H; Nishikawa T; McLean WH; Uitto J
    Hum Mol Genet; 1996 Oct; 5(10):1539-46. PubMed ID: 8894687
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Reactive changes of retinal astrocytes and Müller glial cells in kainate-induced neuroexcitotoxicity.
    Chang ML; Wu CH; Jiang-Shieh YF; Shieh JY; Wen CY
    J Anat; 2007 Jan; 210(1):54-65. PubMed ID: 17229283
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Plectin regulates the organization of glial fibrillary acidic protein in Alexander disease.
    Tian R; Gregor M; Wiche G; Goldman JE
    Am J Pathol; 2006 Mar; 168(3):888-97. PubMed ID: 16507904
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Plectin abnormality in epidermolysis bullosa simplex Ogna: non-responsiveness of basal keratinocytes to some anti-rat plectin antibodies.
    Koss-Harnes D; Jahnsen FL; Wiche G; Søyland E; Brandtzaeg P; Gedde-Dahl T
    Exp Dermatol; 1997 Feb; 6(1):41-8. PubMed ID: 9067706
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.