BIOLOGY AND GENETICS OF HEREDITARY MOTOR AND SENSORY NEUROPATHIES

被引：146

作者：

SUTER, U

SNIPES, GJ

机构：

[1] STANFORD UNIV, SCH MED, DEPT NEUROBIOL, STANFORD, CA 94305 USA

[2] STANFORD UNIV, SCH MED, DEPT PATHOL NEUROPATHOL, STANFORD, CA 94305 USA

来源：

ANNUAL REVIEW OF NEUROSCIENCE | 1995年 / 18卷

关键词：

MYELIN; TREMBLER; CHARCOT-MARIE-TOOTH DISEASE; HEREDITARY NEUROPATHY WITH LIABILITY TO PRESSURE PALSIES; PMP22; PO; CONNEXIN; 32;

D O I：

10.1146/annurev.neuro.18.1.45

中图分类号：

Q189 [神经科学];

学科分类号：

071006 ;

摘要：

引用

页码：45 / 75

页数：31

共 115 条

[71] THE GENE FOR THE PERIPHERAL MYELIN PROTEIN-PMP-22 IS A CANDIDATE FOR CHARCOT-MARIE-TOOTH DISEASE TYPE-1A [J].

PATEL, PI ;

ROA, BB ;

WELCHER, AA ;

SCHOENERSCOTT, R ;

TRASK, BJ ;

PENTAO, L ;

SNIPES, GJ ;

GARCIA, CA ;

FRANCKE, U ;

SHOOTER, EM ;

LUPSKI, JR ;

SUTER, U .

NATURE GENETICS, 1992, 1 (03) :159-165

[72] SCHWANN-CELL MITOSIS IN RESPONSE TO REGENERATING PERIPHERAL AXONS INVIVO [J].

PELLEGRINO, RG ;

SPENCER, PS .

BRAIN RESEARCH, 1985, 341 (01) :16-25

[73]

Peters A., 1991, FINE STRUCTURE NERVO

[74]

RAEYMAEKERS P, 1989, AM J HUM GENET, V45, P953

[75]

Raeymaekers P, 1991, Neuromuscul Disord, V1, P93, DOI 10.1016/0960-8966(91)90055-W

[76]

RAHMAN S, 1993, J BIOL CHEM, V268, P1260

[77]

Raine C., 1984, MYELIN, P1, DOI 10.1007/978-1-4757-1830-0_1

[78]

RASKIND WH, 1991, AM J HUM GENET, V49, P1355

[79] PREMATURE ARREST OF MYELIN FORMATION IN TRANSGENIC MICE WITH INCREASED PROTEOLIPID PROTEIN GENE DOSAGE [J].

READHEAD, C ;

SCHNEIDER, A ;

GRIFFITHS, I ;

NAVE, KA .

NEURON, 1994, 12 (03) :583-595

[80] EVIDENCE FOR A RECESSIVE PMP22 POINT MUTATION IN CHARCOT-MARIE-TOOTH DISEASE TYPE-1A [J].

ROA, BB ;

GARCIA, CA ;

LIU, PT ;

KILLIAN, JM ;

TRASK, BJ ;

SUTER, U ;

SNIPES, GJ ;

ORTIZLOPEZ, R ;

SHOOTER, EM ;

PATEL, PI ;

LUPSKI, JR .

NATURE GENETICS, 1993, 5 (02) :189-194

← 3 4 5 6 7 8 9 10 11 12 →