A mutation in Tpst2 encoding tyrosylprotein sulfotransferase causes dwarfism associated with hypothyroidism

Molecular Endocrinology

Volumn 21, Issue 7, 2007, Pages 1713-1721

  Sasaki, Nobuya ^a   Hosoda, Yayoi ^a   Nagata, Aogu ^a   Ding, Ming ^b,c   Cheng, Ji Ming ^b,c   Miyamoto, Tomomi ^b   Okano, Shinya ^a,d   Asano, Atsushi ^a,e   Miyoshi, Ichiro ^b   Agui, Takashi ^a  

^a HOKKAIDO UNIVERSITY   (Japan)

^b NAGOYA CITY UNIV MEDICAL SCHOOL   (Japan)

^c SOUTHERN ILLINOIS UNIVERSITY SCHOOL OF MEDICINE   (United States)

^d TOHOKU UNIVERSITY GRADUATE SCHOOL OF MEDICINE   (Japan)

^e TOTTORI UNIVERSITY   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

CYCLIC AMP; PROTEIN TYROSINE KINASE; SULFOTRANSFERASE; THYROTROPIN RECEPTOR; TYROSINE SULFATE; TYROSYLPROTEIN SULFOTRANSFERASE 2; UNCLASSIFIED DRUG;

ANIMAL CELL; ARTICLE; CONTROLLED STUDY; DWARFISM; FEMALE; FIBROBLAST; GENE MUTATION; GROWTH RETARDATION; HYPOTHYROIDISM; MALE; MISSENSE MUTATION; NONHUMAN; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL; PROTEIN EXPRESSION; SULFATION; THYROID FUNCTION; THYROID GLAND;

AMINO ACID SEQUENCE; ANIMALS; BASE SEQUENCE; CONGENITAL HYPOTHYROIDISM; DNA PRIMERS; DWARFISM; FEMALE; GENETIC COMPLEMENTATION TEST; MALE; MICE; MICE, INBRED C57BL; MICE, MUTANT STRAINS; MICE, TRANSGENIC; MOLECULAR SEQUENCE DATA; MUTATION, MISSENSE; PHENOTYPE; PROTEIN PROCESSING, POST-TRANSLATIONAL; RECEPTORS, THYROTROPIN; SEQUENCE HOMOLOGY, AMINO ACID; SIGNAL TRANSDUCTION; SUBSTRATE SPECIFICITY; SULFOTRANSFERASES; THYROTROPIN;

MUS;

EID: 34347234581     PISSN: 08888809     EISSN: None     Source Type: Journal    
DOI: 10.1210/me.2007-0040     Document Type: Article

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