Functional evaluation of autism-associated mutations in NHE9

Nature Communications

Volumn 4, Issue , 2013, Pages

  Kondapalli, Kalyan C ^a   Hack, Anniesha ^a   Schushan, Maya ^b   Landau, Meytal ^c   Ben Tal, Nir ^b   Rao, Rajini ^a  

^a JOHNS HOPKINS UNIVERSITY SCHOOL OF MEDICINE   (United States)

^b TEL AVIV UNIVERSITY   (Israel)

^c TECHNION ISRAEL INSTITUTE OF TECHNOLOGY   (Israel)

Author keywords

[No Author keywords available]

Indexed keywords

ANTIPORTER; GLUTAMIC ACID; NEUROTRANSMITTER; NHE9 PROTEIN; TRANSFERRIN; TRANSFERRIN RECEPTOR; UNCLASSIFIED DRUG;

CRYSTAL STRUCTURE; GENE EXPRESSION; GENETIC ANALYSIS; HUMAN GEOGRAPHY; MEMBRANE; MICROBIAL COMMUNITY; MUTATION; NEUROLOGY; PHENOTYPIC PLASTICITY; PROTEIN;

ALKALINIZATION; ANIMAL CELL; ARTICLE; ASTROCYTE; AUTISM; CONTROLLED STUDY; CRYSTAL STRUCTURE; DISEASE ASSOCIATION; ENDOSOME; EVALUATION; GENE; GENETIC COMPLEMENTATION; GENETIC CONSERVATION; HUMAN; LOSS OF FUNCTION MUTATION; MOUSE; MUTATION; NONHUMAN; PH; PHENOTYPE; PROTEIN EXPRESSION; SYNAPTIC MEMBRANE;

AMINO ACID SEQUENCE; ANIMALS; ASTROCYTES; AUTISTIC DISORDER; CEREBRAL CORTEX; CONSERVED SEQUENCE; ENDOSOMES; ESCHERICHIA COLI PROTEINS; EXCITATORY AMINO ACID TRANSPORTER 1; GENE EXPRESSION REGULATION; GENETIC COMPLEMENTATION TEST; GLUTAMIC ACID; HUMANS; MICE; MODELS, MOLECULAR; MOLECULAR SEQUENCE DATA; MUTATION; PRIMARY CELL CULTURE; RECEPTORS, TRANSFERRIN; SACCHAROMYCES CEREVISIAE; SODIUM-HYDROGEN ANTIPORTER; STRUCTURAL HOMOLOGY, PROTEIN;

EID: 84885145782     PISSN: None     EISSN: 20411723     Source Type: Journal    
DOI: 10.1038/ncomms3510     Document Type: Article

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