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Association of bone morphogenetic proteins with otosclerosis.

Association of bone morphogenetic proteins with otosclerosis.

http://www.wikidata.org/entity/Q37158695

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A genome-wide analysis identifies genetic variants in the RELN gene associated with otosclerosis Mutations and altered expression of SERPINF1 in patients with familial otosclerosis Genetic analyses of bone morphogenetic protein 2, 4 and 7 in congenital combined pituitary hormone deficiency.Cochlear otosclerosis.Phenotype characterization and sequence analysis of BMP2 and BMP4 variants in two Mexican families with oligodontia.Differences in gene expression between the otic capsule and other bones.Establishment of Immortalized BMP2/4 Double Knock-Out Osteoblastic Cells Is Essential for Study of Osteoblast Growth, Differentiation, and Osteogenesis Gene expression analysis of human otosclerotic stapedial footplates.Constructing genomic maps of positive selection in humans: where do we go from here?Detection of otosclerosis-specific measles virus receptor (cd46) protein isoforms.Otosclerosis Associated with a De Novo Mutation -832G > A in the TGFB1 Gene Promoter Causing a Decreased Expression Level.The rs39335 polymorphism of the RELN gene is not associated with otosclerosis in a southern Italian population Rare variants in BMP2 and BMP4 found in otosclerosis patients reduce Smad signaling.Perspectives of pharmacological treatment in otosclerosis.HLA class I polymorphisms in Tunisian patients with otosclerosis.Associations of polymorphisms in the bone morphogenetic protein-2 gene with risk and prognosis of osteosarcoma in a Chinese population.Association of COL1A1 and TGFB1 polymorphisms with otosclerosis in a Tunisian population.Identification of target proteins involved in cochlear otosclerosis.Exclusion of TNFRSF11B as Candidate Gene for Otosclerosis in Campania Population.Involvement of T-cell receptor-beta alterations in the development of otosclerosis linked to OTSC2.Genetic association and altered gene expression of osteoprotegerin in otosclerosis patients.Genetic association and gene expression profiles of TGFB1 and the contribution of TGFB1 to otosclerosis susceptibility.Expression of bone morphogenetic protein 2, 4, 5, and 7 correlates with histological activity of otosclerotic foci

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Association of bone morphogenetic proteins with otosclerosis.

http://www.wikidata.org/entity/Q37158695

description

article científic

@ca

article scientifique

@fr

articolo scientifico

@it

artigo científico

@pt

bilimsel makale

@tr

scientific article published on April 2008

@en

vedecký článok

@sk

vetenskaplig artikel

@sv

videnskabelig artikel

@da

vědecký článek

@cs

name

Association of bone morphogenetic proteins with otosclerosis.

@en

Association of bone morphogenetic proteins with otosclerosis.

@nl

type

label

Association of bone morphogenetic proteins with otosclerosis.

@en

Association of bone morphogenetic proteins with otosclerosis.

@nl

prefLabel

Association of bone morphogenetic proteins with otosclerosis.

@en

Association of bone morphogenetic proteins with otosclerosis.

@nl

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Journal of Bone and Mineral Research

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Association of bone morphogenetic proteins with otosclerosis.

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Cor R W J Cremers

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Erik Fransen

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Erwin Offeciers

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Frank Declau

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Ingeborg Dhooge

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Jeroen R Huyghe

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Kathleen Vanderstraeten

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Megan Ealy

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Melissa Thys

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Nele Dieltjens

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P2860

Heterozygous mutations in the gene encoding noggin affect human joint morphogenesis

Large-scale evidence for the effect of the COLIA1 Sp1 polymorphism on osteoporosis outcomes: the GENOMOS study.

Novel regulators of bone formation: molecular clones and activities

Single-nucleotide polymorphisms in the COL1A1 regulatory regions are associated with otosclerosis

The Spemann organizer signal noggin binds and inactivates bone morphogenetic protein 4

The human CD46 molecule is a receptor for measles virus (Edmonston strain)

The diastrophic dysplasia gene encodes a novel sulfate transporter: positional cloning by fine-structure linkage disequilibrium mapping

Autosomal dominant stapes ankylosis with broad thumbs and toes, hyperopia, and skeletal anomalies is caused by heterozygous nonsense and frameshift mutations in NOG, the gene encoding noggin.

A haplotype map of the human genome

Statistical significance for genomewide studies

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507-516

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scholarly article

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10.1359/JBMR.071112

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4

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23

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Paul Van de Heyning

Isabelle Schrauwen

Mireille Claustres

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2008-04-01T00:00:00Z

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5826079

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18021008

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