BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

237 related articles for article (PubMed ID: 16790356)

  • 1. The effects of a dominant connexin32 mutant in myelinating Schwann cells.
    Jeng LJ; Balice-Gordon RJ; Messing A; Fischbeck KH; Scherer SS
    Mol Cell Neurosci; 2006 Jul; 32(3):283-98. PubMed ID: 16790356
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Transgenic expression of human connexin32 in myelinating Schwann cells prevents demyelination in connexin32-null mice.
    Scherer SS; Xu YT; Messing A; Willecke K; Fischbeck KH; Jeng LJ
    J Neurosci; 2005 Feb; 25(6):1550-9. PubMed ID: 15703409
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Connexin32 and X-linked Charcot-Marie-Tooth disease.
    Bone LJ; Deschênes SM; Balice-Gordon RJ; Fischbeck KH; Scherer SS
    Neurobiol Dis; 1997; 4(3-4):221-30. PubMed ID: 9361298
    [TBL] [Abstract][Full Text] [Related]  

  • 4. X-linked Charcot-Marie-Tooth disease and connexin32.
    Fischbeck KH; Abel A; Lin GS; Scherer SS
    Ann N Y Acad Sci; 1999 Sep; 883():36-41. PubMed ID: 10586227
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Prenylation-defective human connexin32 mutants are normally localized and function equivalently to wild-type connexin32 in myelinating Schwann cells.
    Huang Y; Sirkowski EE; Stickney JT; Scherer SS
    J Neurosci; 2005 Aug; 25(31):7111-20. PubMed ID: 16079393
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Functional analysis of connexin-32 mutants associated with X-linked dominant Charcot-Marie-Tooth disease.
    Wang HL; Chang WT; Yeh TH; Wu T; Chen MS; Wu CY
    Neurobiol Dis; 2004 Mar; 15(2):361-70. PubMed ID: 15006706
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Analysis of connexin expression during mouse Schwann cell development identifies connexin29 as a novel marker for the transition of neural crest to precursor cells.
    Li J; Habbes HW; Eiberger J; Willecke K; Dermietzel R; Meier C
    Glia; 2007 Jan; 55(1):93-103. PubMed ID: 17024657
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Expression pattern and functional characterization of connexin29 in transgenic mice.
    Eiberger J; Kibschull M; Strenzke N; Schober A; Büssow H; Wessig C; Djahed S; Reucher H; Koch DA; Lautermann J; Moser T; Winterhager E; Willecke K
    Glia; 2006 Apr; 53(6):601-11. PubMed ID: 16435366
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Altered gene expression in Schwann cells of connexin32 knockout animals.
    Nicholson SM; Gomès D; de Néchaud B; Bruzzone R
    J Neurosci Res; 2001 Oct; 66(1):23-36. PubMed ID: 11598999
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Connexin32 mutations cause loss of function in Schwann cells and oligodendrocytes leading to PNS and CNS myelination defects.
    Sargiannidou I; Vavlitou N; Aristodemou S; Hadjisavvas A; Kyriacou K; Scherer SS; Kleopa KA
    J Neurosci; 2009 Apr; 29(15):4736-49. PubMed ID: 19369543
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Intraneural GJB1 gene delivery improves nerve pathology in a model of X-linked Charcot-Marie-Tooth disease.
    Sargiannidou I; Kagiava A; Bashiardes S; Richter J; Christodoulou C; Scherer SS; Kleopa KA
    Ann Neurol; 2015 Aug; 78(2):303-16. PubMed ID: 26010264
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Connexin29 is uniquely distributed within myelinating glial cells of the central and peripheral nervous systems.
    Altevogt BM; Kleopa KA; Postma FR; Scherer SS; Paul DL
    J Neurosci; 2002 Aug; 22(15):6458-70. PubMed ID: 12151525
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Intrathecal gene therapy in mouse models expressing CMT1X mutations.
    Kagiava A; Karaiskos C; Richter J; Tryfonos C; Lapathitis G; Sargiannidou I; Christodoulou C; Kleopa KA
    Hum Mol Genet; 2018 Apr; 27(8):1460-1473. PubMed ID: 29462293
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Golgi-retained Cx32 mutants interfere with gene addition therapy for CMT1X.
    Kyriakoudi S; Sargiannidou I; Kagiava A; Olympiou M; Kleopa KA
    Hum Mol Genet; 2017 May; 26(9):1622-1633. PubMed ID: 28334782
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Gene expression profiling studies in regenerating nerves in a mouse model for CMT1X: uninjured Cx32-knockout peripheral nerves display expression profile of injured wild type nerves.
    Freidin M; Asche-Godin S; Abrams CK
    Exp Neurol; 2015 Jan; 263():339-49. PubMed ID: 25447941
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A second alternative transcript of the gap junction gene connexin32 is expressed in murine Schwann cells and modulated in injured sciatic nerve.
    Söhl G; Gillen C; Bosse F; Gleichmann M; Müller HW; Willecke K
    Eur J Cell Biol; 1996 Mar; 69(3):267-75. PubMed ID: 8900491
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Unique distributions of the gap junction proteins connexin29, connexin32, and connexin47 in oligodendrocytes.
    Kleopa KA; Orthmann JL; Enriquez A; Paul DL; Scherer SS
    Glia; 2004 Sep; 47(4):346-57. PubMed ID: 15293232
    [TBL] [Abstract][Full Text] [Related]  

  • 18. How do mutations in GJB1 cause X-linked Charcot-Marie-Tooth disease?
    Kleopa KA; Abrams CK; Scherer SS
    Brain Res; 2012 Dec; 1487():198-205. PubMed ID: 22771394
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Cellular mechanisms of connexin32 mutations associated with CNS manifestations.
    Kleopa KA; Yum SW; Scherer SS
    J Neurosci Res; 2002 Jun; 68(5):522-34. PubMed ID: 12111842
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Altered connexin expression after peripheral nerve injury.
    Chandross KJ; Kessler JA; Cohen RI; Simburger E; Spray DC; Bieri P; Dermietzel R
    Mol Cell Neurosci; 1996 Jun; 7(6):501-18. PubMed ID: 8875432
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 12.