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

Volumn 98, Issue 20, 2001, Pages 11353-11358

Human disease-causing NOG missense mutations: Effects on noggin secretion, dimer formation, and bone morphogenetic protein binding

(9) Marcelino, Jose a Sciortino, Christopher M b Romero, Michael F b Ulatowski, Lynn M b Ballock, R Tracy b Economides, Aris N c Eimon, Peter M d Harland, Richard M d Warman, Matthew L a

a UNIVERSITY HOSPITALS OF CLEVELAND (United States)

b CASE WESTERN RESERVE UNIVERSITY SCHOOL OF MEDICINE (United States)

c REGENERON PHARMACEUTICALS INC (United States)

d UNIVERSITY OF CALIFORNIA (United States)

Author keywords

[No Author keywords available]

Indexed keywords

BONE MORPHOGENETIC PROTEIN; NOGGIN; POLYPEPTIDE;

ALLELE; ANIMAL CELL; ARTHRODESIS; ARTICLE; AUTOSOMAL DOMINANT DISORDER; CELL STRAIN COS1; CONGENITAL MALFORMATION; DIMERIZATION; DOSE RESPONSE; EMBRYO; HETEROZYGOSITY LOSS; MISSENSE MUTATION; NONHUMAN; OOCYTE; PHENOTYPE; PRIORITY JOURNAL; PROTEIN BINDING; PROTEIN EXPRESSION; PROTEIN SECRETION; REGULATORY MECHANISM; SPECIES DIFFERENCE; STRUCTURE ACTIVITY RELATION; SYNOSTOSIS; XENOPUS LAEVIS;

ANIMALS; BONE MORPHOGENETIC PROTEINS; CARRIER PROTEINS; CERCOPITHECUS AETHIOPS; COS CELLS; DIMERIZATION; DISULFIDES; FEMALE; HUMANS; MUTATION, MISSENSE; OOCYTES; PROTEIN BIOSYNTHESIS; PROTEINS; RECOMBINANT PROTEINS; SYNOSTOSIS; TRANSFECTION; XENOPUS LAEVIS;

ANIMALIA; XENOPUS LAEVIS;

EID: 0035949677 PISSN: 00278424 EISSN: None Source Type: Journal
DOI: 10.1073/pnas.201367598 Document Type: Article

Times cited : (78)

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