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Volumn 88, Issue 3, 1999, Pages 989-991

Identification of break points in mutated RMP22 gene in a new trembler (TR-Ncnp) mouse

Author keywords

[No Author keywords available]

Indexed keywords

MYELIN PROTEIN;

EID: 0032889851     PISSN: 03064522     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0306-4522(98)00402-3     Document Type: Note
Times cited : (3)

References (11)
  • 1
    • 0030883723 scopus 로고    scopus 로고
    • Analysis of compound heterozygous mice reveals that the trembler mutation can behave as a gain-of-function allele
    • Adlkofer K., Naef R. and Suter U. (1997) Analysis of compound heterozygous mice reveals that the trembler mutation can behave as a gain-of-function allele. J. Neurosci. Res. 49, 671-680.
    • (1997) J. Neurosci. Res. , vol.49 , pp. 671-680
    • Adlkofer, K.1    Naef, R.2    Suter, U.3
  • 2
    • 0027981751 scopus 로고
    • Molecular genetics of Charcot-Marie-Tooth disease and related neuropathies
    • Chance P. F. and Fischbeck K. H. (1994) Molecular genetics of Charcot-Marie-Tooth disease and related neuropathies. Hum. molec. Genet. 3, 1503-1507.
    • (1994) Hum. Molec. Genet. , vol.3 , pp. 1503-1507
    • Chance, P.F.1    Fischbeck, K.H.2
  • 3
    • 0028811634 scopus 로고
    • Axonal degeneration promotes abnormal accumulation of amyloid beta protein in ascending gracile tract of gracile axonal dystrophy (GAD) mouse
    • Ichihara N., Wu J., Chui D., Yamazaki K., Wakabayashi T. and Kikuchi T. (1995) Axonal degeneration promotes abnormal accumulation of amyloid beta protein in ascending gracile tract of gracile axonal dystrophy (GAD) mouse. Brain Res. 695, 173-178.
    • (1995) Brain Res. , vol.695 , pp. 173-178
    • Ichihara, N.1    Wu, J.2    Chui, D.3    Yamazaki, K.4    Wakabayashi, T.5    Kikuchi, T.6
  • 5
    • 0030900850 scopus 로고    scopus 로고
    • Aberrant protein trafficking in trembler suggests a disease mechanism for hereditary human peripheral neuropathies
    • Naef R., Adlkofer K., Lescher B. and Suter U. (1997) Aberrant protein trafficking in trembler suggests a disease mechanism for hereditary human peripheral neuropathies. Molec. cell. Neurosci. 9, 13-25.
    • (1997) Molec. Cell. Neurosci. , vol.9 , pp. 13-25
    • Naef, R.1    Adlkofer, K.2    Lescher, B.3    Suter, U.4
  • 6
    • 0030996714 scopus 로고    scopus 로고
    • Abnormal Schwann cell/axon interactions in the Trembler-J mouse
    • Robertson A. M., King R. H. M., Muddle J. R. and Thomas P. K. (1997) Abnormal Schwann cell/axon interactions in the Trembler-J mouse. J. Anat. 190, 423-432.
    • (1997) J. Anat. , vol.190 , pp. 423-432
    • Robertson, A.M.1    King, R.H.M.2    Muddle, J.R.3    Thomas, P.K.4
  • 7
    • 0029033094 scopus 로고
    • Mapping of the gracile axonal dystrophy (gad) gene to a region between D5Mit197 and D5Mit113 on proximal mouse chromosome 5
    • Suh J. G., Yamanishi T., Matsui K., Tanaka K. and Wada K. (1995) Mapping of the gracile axonal dystrophy (gad) gene to a region between D5Mit197 and D5Mit113 on proximal mouse chromosome 5. Genomics 27, 549-551.
    • (1995) Genomics , vol.27 , pp. 549-551
    • Suh, J.G.1    Yamanishi, T.2    Matsui, K.3    Tanaka, K.4    Wada, K.5
  • 8
    • 0030825570 scopus 로고    scopus 로고
    • An in-frame deletion in peripheral myelin protein-22 gene causes hypomyelination and cell death of the Schwann cells in the new trembler mutant mice
    • Suh J. G., Ichihara N., Saigou K., Nakabayashi O., Yamanishi T., Tanaka K., Wada K. and Kikuchi T. (1997) An in-frame deletion in peripheral myelin protein-22 gene causes hypomyelination and cell death of the Schwann cells in the new trembler mutant mice. Neuroscience 79, 735-744.
    • (1997) Neuroscience , vol.79 , pp. 735-744
    • Suh, J.G.1    Ichihara, N.2    Saigou, K.3    Nakabayashi, O.4    Yamanishi, T.5    Tanaka, K.6    Wada, K.7    Kikuchi, T.8


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.