Neuroligin trafficking deficiencies arising from mutations in the α/β-hydrolase fold protein family

Journal of Biological Chemistry

Volumn 285, Issue 37, 2010, Pages 28674-28682

  De Jaco, Antonella ^a,c,d   Lin, Michael Z ^a,e   Dubi, Noga ^a   Comoletti, Davide ^a   Miller, Meghan T ^a   Camp, Shelley ^a   Ellisman, Mark ^b   Butko, Margaret T ^a   Tsien, Roger Y ^a   Taylor, Palmer ^a  

^a UNIVERSITY OF CALIFORNIA   (United States)

^b UNIVERSITY OF CALIFORNIA   (United States)

^c SAPIENZA UNIVERSITY OF ROME   (Italy)

^d Pasteur Institute   (Italy)

^e Stanford University   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ADHESION PROTEINS; CONGENITAL DISORDERS; DENDRITIC SPINE; DOMAIN INFLUENCE; ENDOPLASMIC RETICULUM; FUNCTIONAL DIVERSITY; HIPPOCAMPAL NEURONS; HYDROLASES; IN-VITRO; MISFOLDING; MUTANT PROTEINS; NERVOUS SYSTEM; PROCESSING RATES; PROTEASOMES; PROTEIN FAMILY; SECRETORY PATHWAYS; STRUCTURAL MOTIFS; THYROGLOBULIN;

PROTEINS;

ALPHA HYDROLASE; BETA HYDROLASE; HYDROLASE; NEUROLIGIN; PROTEASOME; UNCLASSIFIED DRUG; MEMBRANE PROTEIN; NERVE CELL ADHESION MOLECULE; NERVE PROTEIN; NEUROLIGIN 3;

ARTICLE; CONTROLLED STUDY; DENDRITIC SPINE; ENDOCRINE DISEASE; ENDOPLASMIC RETICULUM; GENE MUTATION; GLYCOSYLATION; HIPPOCAMPUS; HUMAN; HUMAN CELL; IMMUNOPRECIPITATION; NEUROLOGIC DISEASE; NONHUMAN; PRIORITY JOURNAL; PROTEIN DEGRADATION; PROTEIN DOMAIN; PROTEIN FOLDING; PROTEIN INTERACTION; PROTEIN LOCALIZATION; PROTEIN TRANSPORT; RAT; AMINO ACID SUBSTITUTION; ANIMAL; AUTISM; CELL LINE; CONGENITAL HYPOTHYROIDISM; DENDRITE; GENETICS; METABOLISM; MISSENSE MUTATION; PROTEIN MOTIF; PROTEIN PROCESSING; PROTEIN TERTIARY STRUCTURE;

AMINO ACID MOTIFS; AMINO ACID SUBSTITUTION; ANIMALS; AUTISTIC DISORDER; CELL ADHESION MOLECULES, NEURONAL; CELL LINE; CONGENITAL HYPOTHYROIDISM; DENDRITES; HIPPOCAMPUS; HUMANS; HYDROLASES; MEMBRANE PROTEINS; MUTATION, MISSENSE; NERVE TISSUE PROTEINS; PROTEIN FOLDING; PROTEIN PROCESSING, POST-TRANSLATIONAL; PROTEIN STRUCTURE, TERTIARY; PROTEIN TRANSPORT; RATS;

EID: 77956507581     PISSN: 00219258     EISSN: 1083351X     Source Type: Journal    
DOI: 10.1074/jbc.M110.139519     Document Type: Article

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