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 *

174 related articles for article (PubMed ID: 10586253)

  • 1. The absence of myelin P0 protein produces a novel molecular phenotype in Schwann cells.
    Menichella DM; Xu W; Jiang H; Sohi J; Vallat JM; Baron P; Kamholz J; Shy M
    Ann N Y Acad Sci; 1999 Sep; 883():281-93. PubMed ID: 10586253
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Protein zero is necessary for E-cadherin-mediated adherens junction formation in Schwann cells.
    Menichella DM; Arroyo EJ; Awatramani R; Xu T; Baron P; Vallat JM; Balsamo J; Lilien J; Scarlato G; Kamholz J; Scherer SS; Shy ME
    Mol Cell Neurosci; 2001 Dec; 18(6):606-18. PubMed ID: 11749037
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Regulation of myelin-specific gene expression. Relevance to CMT1.
    Kamholz J; Awatramani R; Menichella D; Jiang H; Xu W; Shy M
    Ann N Y Acad Sci; 1999 Sep; 883():91-108. PubMed ID: 10586235
    [TBL] [Abstract][Full Text] [Related]  

  • 4. The alpha-chemokine CXCL14 is up-regulated in the sciatic nerve of a mouse model of Charcot-Marie-Tooth disease type 1A and alters myelin gene expression in cultured Schwann cells.
    Barbaria EM; Kohl B; Buhren BA; Hasenpusch-Theil K; Kruse F; Küry P; Martini R; Müller HW
    Neurobiol Dis; 2009 Mar; 33(3):448-58. PubMed ID: 19111616
    [TBL] [Abstract][Full Text] [Related]  

  • 5. The Absence of Myelin P
    Menichella DM; Xu W; Jiang H; Sohi J; Vallat JM; Baron P; Kamholz J; Shy M
    Ann N Y Acad Sci; 1999 Oct; 883(1):281-293. PubMed ID: 29086945
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Effective gene transfer of lacZ and P0 into Schwann cells of P0-deficient mice.
    Guénard V; Schweitzer B; Flechsig E; Hemmi S; Martini R; Suter U; Schachner M
    Glia; 1999 Jan; 25(2):165-78. PubMed ID: 9890631
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Subtle roles of neural cell adhesion molecule and myelin-associated glycoprotein during Schwann cell spiralling in P0-deficient mice.
    Carenini S; Montag D; Schachner M; Martini R
    Glia; 1999 Sep; 27(3):203-12. PubMed ID: 10457367
    [TBL] [Abstract][Full Text] [Related]  

  • 8. New vistas on the pathomechanism of Charcot-Marie-Tooth and related peripheral neuropathies.
    Müller HW
    Ann N Y Acad Sci; 1999 Sep; 883():152-9. PubMed ID: 10586241
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Nerve conduction abnormalities and neuromyotonia in genetically engineered mouse models of human hereditary neuropathies.
    Zielasek J; Toyka KV
    Ann N Y Acad Sci; 1999 Sep; 883():310-20. PubMed ID: 10586256
    [TBL] [Abstract][Full Text] [Related]  

  • 10. P0-deficient knockout mice as tools to understand pathomechanisms in Charcot-Marie-Tooth 1B and P0-related Déjérine-Sottas syndrome.
    Martini R
    Ann N Y Acad Sci; 1999 Sep; 883():273-80. PubMed ID: 10586252
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Increase of MCP-1 (CCL2) in myelin mutant Schwann cells is mediated by MEK-ERK signaling pathway.
    Fischer S; Weishaupt A; Troppmair J; Martini R
    Glia; 2008 Jun; 56(8):836-43. PubMed ID: 18383340
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Major myelin protein gene (P0) mutation causes a novel form of axonal degeneration.
    Li J; Bai Y; Ianakova E; Grandis M; Uchwat F; Trostinskaia A; Krajewski KM; Garbern J; Kupsky WJ; Shy ME
    J Comp Neurol; 2006 Sep; 498(2):252-65. PubMed ID: 16856127
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Attenuated demyelination in the absence of the macrophage-restricted adhesion molecule sialoadhesin (Siglec-1) in mice heterozygously deficient in P0.
    Kobsar I; Oetke C; Kroner A; Wessig C; Crocker P; Martini R
    Mol Cell Neurosci; 2006 Apr; 31(4):685-91. PubMed ID: 16458537
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Neurofibromin, the neurofibromatosis type 1 Ras-GAP, is required for appropriate P0 expression and myelination.
    Rosenbaum T; Kim HA; Boissy YL; Ling B; Ratner N
    Ann N Y Acad Sci; 1999 Sep; 883():203-14. PubMed ID: 10586246
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Absence of P0 leads to the dysregulation of myelin gene expression and myelin morphogenesis.
    Xu W; Manichella D; Jiang H; Vallat JM; Lilien J; Baron P; Scarlato G; Kamholz J; Shy ME
    J Neurosci Res; 2000 Jun; 60(6):714-24. PubMed ID: 10861783
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Localization and functional roles of PMP22 in peripheral nerves of P0-deficient mice.
    Carenini S; Neuberg D; Schachner M; Suter U; Martini R
    Glia; 1999 Dec; 28(3):256-64. PubMed ID: 10559784
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Schwann cells and the pathogenesis of inherited motor and sensory neuropathies (Charcot-Marie-Tooth disease).
    Berger P; Niemann A; Suter U
    Glia; 2006 Sep; 54(4):243-57. PubMed ID: 16856148
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Proteolipid protein modulates preservation of peripheral axons and premature death when myelin protein zero is lacking.
    Patzig J; Kusch K; Fledrich R; Eichel MA; Lüders KA; Möbius W; Sereda MW; Nave KA; Martini R; Werner HB
    Glia; 2016 Jan; 64(1):155-74. PubMed ID: 26393339
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Altered expression of ion channel isoforms at the node of Ranvier in P0-deficient myelin mutants.
    Ulzheimer JC; Peles E; Levinson SR; Martini R
    Mol Cell Neurosci; 2004 Jan; 25(1):83-94. PubMed ID: 14962742
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Glomerular permeability is altered by loss of P0, a myelin protein expressed in glomerular epithelial cells.
    Plaisier E; Mougenot B; Verpont MC; Jouanneau C; Archelos JJ; Martini R; Kerjaschki D; Ronco P
    J Am Soc Nephrol; 2005 Nov; 16(11):3350-6. PubMed ID: 16162811
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.