Genetic deletion of Cadm4 results in myelin abnormalities resembling Charcot-Marie-Tooth neuropathy

Journal of Neuroscience

Volumn 33, Issue 27, 2013, Pages 10950-10961

  Golan, Neev ^a   Kartvelishvily, Elena ^a   Spiegel, Ivo ^a   Salomon, Daniela ^a   Sabanay, Helena ^a   Rechav, Katya ^a   Vainshtein, Anya ^a   Frechter, Shahar ^a   Maik Rachline, Galia ^a   Eshed Eisenbach, Yael ^a   Momoi, Takashi ^b   Peles, Elior ^a  

^a WEIZMANN INSTITUTE OF SCIENCE   (Israel)

^b INTERNATIONAL UNIVERSITY OF HEALTH AND WELFARE   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

CADM1 PROTEIN; PROTEIN; UNCLASSIFIED DRUG;

ANIMAL TISSUE; ANTIBODY LABELING; ARTICLE; CONTROLLED STUDY; ELECTRON MICROSCOPY; ELECTROPHYSIOLOGY; GENE DELETION; IMMUNOREACTIVITY; MOTOR PERFORMANCE; MOUSE; MYELIN DEFICIENCY; NERVE CONDUCTION; NEUROPATHY; NONHUMAN; PERIPHERAL NERVOUS SYSTEM; PRIORITY JOURNAL; REVERSE TRANSCRIPTION POLYMERASE CHAIN REACTION; RNA ANALYSIS; WESTERN BLOTTING;

ANIMALS; CELL ADHESION MOLECULES; CHARCOT-MARIE-TOOTH DISEASE; GENE DELETION; IMMUNOGLOBULINS; MICE; MICE, 129 STRAIN; MICE, KNOCKOUT; MICE, TRANSGENIC; MYELIN SHEATH; NERVE FIBERS, MYELINATED;

EID: 84880495720     PISSN: 02706474     EISSN: 15292401     Source Type: Journal    
DOI: 10.1523/JNEUROSCI.0571-13.2013     Document Type: Article

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