Genetic reduction of the α1 Subunit of Na/K-ATPase corrects multiple hippocampal phenotypes in angelman syndrome

Cell Reports

Volumn 4, Issue 3, 2013, Pages 405-412

  Kaphzan, Hanoch ^a,b   Buffington, ShellyA ^c   Ramaraj, AkilaB ^a   Lingrel, JerryB ^d   Rasband, MatthewN ^c   Santini, Emanuela ^a   Klann, Eric ^a  

^a NEW YORK UNIVERSITY   (United States)

^b UNIVERSITY OF HAIFA   (Israel)

^c BAYLOR COLLEGE OF MEDICINE   (United States)

^d UNIVERSITY OF CINCINNATI COLLEGE OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ADENOSINE TRIPHOSPHATASE (POTASSIUM SODIUM); ADENOSINE TRIPHOSPHATASE (POTASSIUM SODIUM) ALPHA1 SUBUNIT; ANKYRIN; ANKYRIN G; SODIUM CHANNEL NAV1.6; UNCLASSIFIED DRUG;

ANIMAL CELL; ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; AXON INITIAL SEGMENT LENGTH; CONTROLLED STUDY; FEMALE; GENE DELETION; GENETIC MANIPULATION; GENETIC REDUCTION; GENOTYPE; HAPPY PUPPET SYNDROME; HETEROZYGOTE; HIPPOCAMPAL CA1 REGION; HIPPOCAMPAL CA3 REGION; KNOCKOUT MOUSE; LATENT PERIOD; LONG TERM MEMORY; LONG TERM POTENTIATION; MALE; MEMORY DISORDER; MOLECULAR DYNAMICS; MORPHOLOGY; MOUSE; NERVE CELL CHARACTERISTICS AND FUNCTIONS; NERVE CELL PLASTICITY; NERVE EXCITABILITY; NERVE FIBER MEMBRANE POTENTIAL; NEUROPATHOLOGY; NONHUMAN; PHENOTYPE; PRIORITY JOURNAL; PROTEIN EXPRESSION; PYRAMIDAL NERVE CELL; WILD TYPE;

MUS;

ANGELMAN SYNDROME; ANIMALS; ANKYRINS; DISEASE MODELS, ANIMAL; FEMALE; HIPPOCAMPUS; MALE; MICE; MICE, INBRED C57BL; NAV1.6 VOLTAGE-GATED SODIUM CHANNEL; NEURONS; PROTEIN SUBUNITS; SODIUM-POTASSIUM-EXCHANGING ATPASE;

EID: 84881615694     PISSN: None     EISSN: 22111247     Source Type: Journal    
DOI: 10.1016/j.celrep.2013.07.005     Document Type: Article

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