Sclerosteosis: neurogenetic and pathophysiologic analysis of an American kinship.
about
Osteocyte control of bone formation via sclerostin, a novel BMP antagonistPolymorphisms in the sclerosteosis/van Buchem disease gene (SOST) region are associated with bone-mineral density in elderly whites.Bone dysplasia sclerosteosis results from loss of the SOST gene product, a novel cystine knot-containing proteinSclerostin is an osteocyte-expressed negative regulator of bone formation, but not a classical BMP antagonistIdentification of a 52 kb deletion downstream of the SOST gene in patients with van Buchem diseaseFrom disease to treatment: from rare skeletal disorders to treatments for osteoporosisA 52-kb deletion in the SOST-MEOX1 intergenic region on 17q12-q21 is associated with van Buchem disease in the Dutch populationCbfa1/RUNX2 directs specific expression of the sclerosteosis gene (SOST)Single-dose, placebo-controlled, randomized study of AMG 785, a sclerostin monoclonal antibodyManagement of trigeminal neuralgia in sclerosteosisWise regulates bone deposition through genetic interactions with Lrp5Serum sclerostin levels negatively correlate with parathyroid hormone levels and free estrogen index in postmenopausal women.Sclerostin: current knowledge and future perspectives.Localization of the gene for sclerosteosis to the van Buchem disease-gene region on chromosome 17q12-q21Romosozumab for the treatment of osteoporosis.Expression of sclerostin in the developing zebrafish (Danio rerio) brain and skeleton.Sclerosing bone dysplasias--a target-site approach.The sclerostin-neutralizing antibody AbD09097 recognizes an epitope adjacent to sclerostin's binding site for the Wnt co-receptor LRP6Sclerostin: a gem from the genome leads to bone-building antibodies.Sclerostin monoclonal antibody therapy with AMG 785: a potential treatment for osteoporosis.Sclerostin: therapeutic horizons based upon its actions.Sclerostin: a possible target for the management of cancer-induced bone disease.The Lrp4R1170Q Homozygous Knock-In Mouse Recapitulates the Bone Phenotype of Sclerosteosis in Humans.TGF-β Family Signaling in Connective Tissue and Skeletal Diseases.Sclerosteosis in a Spanish male: first report in a person of Mediterranean origin.Retinochoroidal (optociliary) shunt veins, blindness and optic atrophy: a non-specific sign of chronic optic nerve compression.The natural history of sclerosteosis.Dental and oral manifestations of sclerosteosis.An auditory profile of sclerosteosis.Antibodies in Phase III Studies for Immunological Disorders
P2860
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P2860
Sclerosteosis: neurogenetic and pathophysiologic analysis of an American kinship.
description
1983 nî lūn-bûn
@nan
1983年の論文
@ja
1983年学术文章
@wuu
1983年学术文章
@zh-cn
1983年学术文章
@zh-hans
1983年学术文章
@zh-my
1983年学术文章
@zh-sg
1983年學術文章
@yue
1983年學術文章
@zh
1983年學術文章
@zh-hant
name
Sclerosteosis: neurogenetic and pathophysiologic analysis of an American kinship.
@en
Sclerosteosis: neurogenetic and pathophysiologic analysis of an American kinship.
@nl
type
label
Sclerosteosis: neurogenetic and pathophysiologic analysis of an American kinship.
@en
Sclerosteosis: neurogenetic and pathophysiologic analysis of an American kinship.
@nl
prefLabel
Sclerosteosis: neurogenetic and pathophysiologic analysis of an American kinship.
@en
Sclerosteosis: neurogenetic and pathophysiologic analysis of an American kinship.
@nl
P2093
P356
P1433
P1476
Sclerosteosis: neurogenetic and pathophysiologic analysis of an American kinship.
@en
P2093
McKeever P
Schlesinger S
Teitelbaum SL
P304
P356
10.1212/WNL.33.3.267
P407
P577
1983-03-01T00:00:00Z