Molecular characterization of V59E NIS, a Na+/I- symporter mutant that causes congenital I- transport defect

Endocrinology

Volumn 149, Issue 6, 2008, Pages 3077-3084

  Reed Tsur, Mia D ^a   De La Vieja, Antonio ^a,b   Ginter, Christopher S ^a,c   Carrasco, Nancy ^a  

^a ALBERT EINSTEIN COLLEGE OF MEDICINE   (United States)

^b INSTITUTO DE INVESTIGACIONES BIOMÉDICAS ALBERTO SOLS   (Spain)

^c WEILL CORNELL MEDICAL COLLEGE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

COTRANSPORTER; IODINE; SODIUM;

ANIMAL CELL; ARTICLE; CELL CULTURE; CONTROLLED STUDY; GENETIC TRANSFECTION; GOITER; HYPOTHYROIDISM; IMMUNOBLOTTING; NONHUMAN; PHENOTYPE; PRIORITY JOURNAL; PROTEIN ANALYSIS; PROTEIN EXPRESSION;

AMINO ACID SUBSTITUTION; ANIMALS; BIOLOGICAL TRANSPORT; CERCOPITHECUS AETHIOPS; COS CELLS; DNA, COMPLEMENTARY; GENETIC DISEASES, INBORN; HAPLORHINI; HUMANS; IODIDES; KINETICS; MODELS, MOLECULAR; MUTAGENESIS, SITE-DIRECTED; POLYMORPHISM, SINGLE NUCLEOTIDE; PROTEIN CONFORMATION; SYMPORTERS;

EID: 44249090228     PISSN: 00137227     EISSN: 00137227     Source Type: Journal    
DOI: 10.1210/en.2008-0027     Document Type: Article

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