A single amino acid change in the acetylcholinesterase-like domain of thyroglobulin causes congenital goiter with hypothyroidism in the cog/cog mouse: A model of human endoplasmic reticulum storage diseases

Proceedings of the National Academy of Sciences of the United States of America

Volumn 95, Issue 17, 1998, Pages 9909-9913

  Kim, Paul S ^a,d   Hossain, Shaikh Abu ^a   Park, Young Nam ^b   Lee, Ike ^c   Yoo, Sung Eun ^a   Arvan, Peter ^b  

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

^b ALBERT EINSTEIN COLLEGE OF MEDICINE   (United States)

^c BETH ISRAEL DEACONESS MEDICAL CENTER   (United States)

^d Medical Science Building 5564 ^*  (United States)

Author keywords

[No Author keywords available]

Indexed keywords

THYROGLOBULIN;

AMINO ACID SUBSTITUTION; ANIMAL CELL; ANIMAL TISSUE; ARTICLE; ENDOPLASMIC RETICULUM; GOITER; HORMONE SYNTHESIS; HYPOTHYROIDISM; IODINATION; MOUSE; NONHUMAN; PRIORITY JOURNAL; THYROID HORMONE RELEASE;

ACETYLCHOLINESTERASE; AMINO ACID SEQUENCE; ANIMALS; BASE SEQUENCE; BIOLOGICAL TRANSPORT, ACTIVE; CLONING, MOLECULAR; CONGENITAL HYPOTHYROIDISM; COS CELLS; DISEASE MODELS, ANIMAL; DNA, COMPLEMENTARY; ENDOPLASMIC RETICULUM; GENE EXPRESSION; GOITER; HUMANS; HYPOTHYROIDISM; MICE; MICE, INBRED AKR; MICE, MUTANT STRAINS; MOLECULAR SEQUENCE DATA; MUTAGENESIS, SITE-DIRECTED; POINT MUTATION; THYROGLOBULIN;

ANIMALIA;

EID: 0032544022     PISSN: 00278424     EISSN: None     Source Type: Journal    
DOI: 10.1073/pnas.95.17.9909     Document Type: Article

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