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.
Pubmed for Handhelds
PUBMED FOR HANDHELDS
Journal Abstract Search
339 related items for PubMed ID: 10559784
1. 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 [Abstract] [Full Text] [Related]
2. 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 [Abstract] [Full Text] [Related]
3. 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 14; 883():310-20. PubMed ID: 10586256 [Abstract] [Full Text] [Related]
4. 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 14; 18(6):606-18. PubMed ID: 11749037 [Abstract] [Full Text] [Related]
5. Molecular bases of myelin formation as revealed by investigations on mice deficient in glial cell surface molecules. Martini R, Schachner M. Glia; 1997 Apr 14; 19(4):298-310. PubMed ID: 9097074 [Abstract] [Full Text] [Related]
6. 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 14; 883():91-108. PubMed ID: 10586235 [Abstract] [Full Text] [Related]
7. Developmental abnormalities in the nerves of peripheral myelin protein 22-deficient mice. Amici SA, Dunn WA, Notterpek L. J Neurosci Res; 2007 Feb 01; 85(2):238-49. PubMed ID: 17131416 [Abstract] [Full Text] [Related]
8. Identification of the regulatory region of the peripheral myelin protein 22 (PMP22) gene that directs temporal and spatial expression in development and regeneration of peripheral nerves. Maier M, Berger P, Nave KA, Suter U. Mol Cell Neurosci; 2002 May 01; 20(1):93-109. PubMed ID: 12056842 [Abstract] [Full Text] [Related]
9. 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 01; 25(1):83-94. PubMed ID: 14962742 [Abstract] [Full Text] [Related]
10. Peripheral myelin protein 22 kDa and protein zero: domain specific trans-interactions. Hasse B, Bosse F, Hanenberg H, Müller HW. Mol Cell Neurosci; 2004 Dec 01; 27(4):370-8. PubMed ID: 15555916 [Abstract] [Full Text] [Related]
11. Coexpression of PMP22 gene with MBP and P0 during de novo myelination and nerve repair. Kuhn G, Lie A, Wilms S, Müller HW. Glia; 1993 Aug 01; 8(4):256-64. PubMed ID: 7691737 [Abstract] [Full Text] [Related]
12. Formation and maintenance of the myelin sheath in the peripheral nerve: roles of cell adhesion molecules and the gap junction protein connexin 32. Martini R, Carenini S. Microsc Res Tech; 1998 Jun 01; 41(5):403-15. PubMed ID: 9672423 [Abstract] [Full Text] [Related]
13. Phenotypic differences between peripheral myelin protein-22 (PMP22) and myelin protein zero (P0) mutations associated with Charcot-Marie-Tooth-related diseases. Shames I, Fraser A, Colby J, Orfali W, Snipes GJ. J Neuropathol Exp Neurol; 2003 Jul 01; 62(7):751-64. PubMed ID: 12901701 [Abstract] [Full Text] [Related]
14. Temporal expression pattern of peripheral myelin protein 22 during in vivo and in vitro myelination. Notterpek L, Snipes GJ, Shooter EM. Glia; 1999 Feb 15; 25(4):358-69. PubMed ID: 10028918 [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 15; 60(6):714-24. PubMed ID: 10861783 [Abstract] [Full Text] [Related]
16. Myelin P0-protein, more than just a structural protein? Filbin MT, Tennekoon GI. Bioessays; 1992 Aug 15; 14(8):541-7. PubMed ID: 1285424 [Abstract] [Full Text] [Related]
17. 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 15; 25(2):165-78. PubMed ID: 9890631 [Abstract] [Full Text] [Related]
18. The myelin protein MAL affects peripheral nerve myelination: a new player influencing p75 neurotrophin receptor expression. Buser AM, Schmid D, Kern F, Erne B, Lazzati T, Schaeren-Wiemers N. Eur J Neurosci; 2009 Jun 15; 29(12):2276-90. PubMed ID: 19508690 [Abstract] [Full Text] [Related]
19. 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 15; 31(4):685-91. PubMed ID: 16458537 [Abstract] [Full Text] [Related]
20. Recombinant peripheral myelin protein P0 confers both adhesion and neurite outgrowth-promoting properties. Schneider-Schaulies J, von Brunn A, Schachner M. J Neurosci Res; 1990 Nov 15; 27(3):286-97. PubMed ID: 1711125 [Abstract] [Full Text] [Related] Page: [Next] [New Search]