The plasma membrane calcium pump in health and disease

FEBS Journal

Volumn 280, Issue 21, 2013, Pages 5385-5397

  Brini, Marisa ^a   Calì, Tito ^a   Ottolini, Denis ^a   Carafoli, Ernesto ^b  

^a UNIVERSITY OF PADOVA   (Italy)

^b VENETIAN INSTITUTE OF MOLECULAR MEDICINE   (Italy)

Author keywords

cerebellar ataxia; genetic deafness; plasma membrane Ca2+ pumps; PMCA mutations; pump isoforms

Indexed keywords

ADENOSINE TRIPHOSPHATASE (CALCIUM); CALCIUM CHANNEL P TYPE; CALCIUM ION; CALMODULIN; ENZYME VARIANT; ISOENZYME; SARCOPLASMIC RETICULUM CALCIUM TRANSPORTING ADENOSINE TRIPHOSPHATASE;

ALTERNATIVE RNA SPLICING; AMINO TERMINAL SEQUENCE; ATAXIA; BINDING AFFINITY; BINDING SITE; CALCIUM BINDING; CALCIUM CELL LEVEL; CALCIUM HOMEOSTASIS; CALCIUM SIGNALING; CALCIUM TRANSPORT; CARBOXY TERMINAL SEQUENCE; CELL MEMBRANE; CONFERENCE PAPER; CYTOSOL; ENZYME LOCALIZATION; ENZYME REGULATION; ENZYME STRUCTURE; EUKARYOTIC CELL; GENE FUNCTION; GENE LOCATION; GENE MUTATION; GENE PRODUCT; GENETIC DISORDER; HEARING IMPAIRMENT; HOUSEKEEPING GENE; HUMAN; MALIGNANT NEOPLASTIC DISEASE; MAMMAL; MOLECULAR MODEL; NONHUMAN; PHENOTYPE; PMCA1 GENE; PMCA2 GENE; PMCA3 GENE; PMCA4 GENE; PRIORITY JOURNAL; PROTEIN AGGREGATION; PROTEIN DEPHOSPHORYLATION; PROTEIN DOMAIN; PROTEIN PROTEIN INTERACTION; TISSUE SPECIFICITY;

CEREBELLAR ATAXIA; GENETIC DEAFNESS; PLASMA MEMBRANE CA2+ PUMPS; PMCA MUTATIONS; PUMP ISOFORMS;

ANIMALS; CELL MEMBRANE; GENETIC DISEASES, X-LINKED; HUMANS; MICE; PLASMA MEMBRANE CALCIUM-TRANSPORTING ATPASES;

EUKARYOTA; MAMMALIA; MUS;

EID: 84886087580     PISSN: 1742464X     EISSN: 17424658     Source Type: Journal    
DOI: 10.1111/febs.12193     Document Type: Conference Paper

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