Genetic linkage of Paget disease of the bone to chromosome 18q - Wikidata - awgldk - TriplyDB

Genetic linkage of Paget disease of the bone to chromosome 18q

Genetic linkage of Paget disease of the bone to chromosome 18q

http://www.wikidata.org/entity/Q24677166

about

Paget disease of bone: mapping of two loci at 5q35-qter and 5q31.The mechanism of hearing loss in Paget's disease of bone.Somatic mutations in SQSTM1 detected in affected tissues from patients with sporadic Paget's disease of bone.The role of osteogenic cells in the pathophysiology of Paget's disease.Common mechanisms of osteosarcoma and Paget's disease.Detecting low penetrance genes in cancer: the way ahead.Genomewide search in familial Paget disease of bone shows evidence of genetic heterogeneity with candidate loci on chromosomes 2q36, 10p13, and 5q35 Paget's disease of bone and genetic disorders of RANKL/OPG/RANK/NF-kappaB signaling.Emerging strategies and therapies for treatment of Paget's disease of bone.Paget disease of bone.Paget's Disease of Bone: A Review of Epidemiology, Pathophysiology and Management The role of immune cells and inflammatory cytokines in Paget's disease and multiple myeloma.Mechanisms of disease: genetics of Paget's disease of bone and related disorders.The spine in Paget's disease Recurrent mutation of the gene encoding sequestosome 1 (SQSTM1/p62) in Paget disease of bone Linkage of Paget disease of bone to a novel region on human chromosome 18q23.Clinical and Genetic Advances in Paget's Disease of Bone: a Review.c-FMS inhibitors: a patent review.Characteristics and familial aggregation of Paget's disease of bone in Italy.Inheritance of osteosarcoma and Paget's disease of bone: a familial loss of heterozygosity study Sequestosome 1: mutation frequencies, haplotypes, and phenotypes in familial Paget's disease of bone.Identification of the Arg1086His mutation in the alpha subunit of the voltage-dependent calcium channel (CACNA1S) in a North American family with malignant hyperthermia.Update on the epidemiology of Paget's disease of bone.Heterogeneity in familial dominant Paget disease of bone and muscular dystrophy.Cochlear implantation in a patient with Paget's disease.Genetic variation in the TNFRSF11A gene encoding RANK is associated with susceptibility to Paget's disease of bone.Paget's disease with craniofacial and skeletal bone involvement.A putative role for c-Fos in the pathophysiology of Paget's disease.Chronic recurrent multifocal osteomyelitis (CRMO): evidence for a susceptibility gene located on chromosome 18q21.3-18q22 Lack of mutations in the RANK gene in Spanish patients with Paget disease of bone

P2860

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P2860

Genetic linkage of Paget disease of the bone to chromosome 18q

http://www.wikidata.org/entity/Q24677166

description

1997 nî lūn-bûn

@nan

1997 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած

@hyw

1997 թվականի նոյեմբերին հրատարակված գիտական հոդված

@hy

1997年の論文

@ja

1997年論文

@yue

1997年論文

@zh-hant

1997年論文

@zh-hk

1997年論文

@zh-mo

1997年論文

@zh-tw

1997年论文

@wuu

name

Genetic linkage of Paget disease of the bone to chromosome 18q

@ast

Genetic linkage of Paget disease of the bone to chromosome 18q

@en

Genetic linkage of Paget disease of the bone to chromosome 18q

@nl

type

label

Genetic linkage of Paget disease of the bone to chromosome 18q

@ast

Genetic linkage of Paget disease of the bone to chromosome 18q

@en

Genetic linkage of Paget disease of the bone to chromosome 18q

@nl

prefLabel

Genetic linkage of Paget disease of the bone to chromosome 18q

@ast

Genetic linkage of Paget disease of the bone to chromosome 18q

@en

Genetic linkage of Paget disease of the bone to chromosome 18q

@nl

P1433

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P1476

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P433

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P478

Q24677166-219A5DC0-14CB-4C65-9770-A9AC1B1E5618

P577

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P5875

Q24677166-16B27418-E856-46AF-9158-E5854ED7B066

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P932

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P356

P1433

American Journal of Human Genetics

P1476

Genetic linkage of Paget disease of the bone to chromosome 18q

@en

P2093

B Otterund

http://www.w3.org/2001/XMLSchema#string

F R Singer

http://www.w3.org/2001/XMLSchema#string

G D Roodman

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J D Cody

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M Leppert

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R J Leach

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T B Lewis

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P2860

Strategies for multilocus linkage analysis in humans

A comprehensive genetic map of the human genome based on 5,264 microsatellites

Genetic linkage of familial expansile osteolysis to chromosome 18q

Linkage of early-onset familial breast cancer to chromosome 17q21

Polymorphic DNA region adjacent to the 5' end of the human insulin gene

A family study of Paget's disease of bone.

Distribution of Paget's disease in England, Wales and Scotland and a possible relationship with vitamin D deficiency in childhood

Ultrastructural features of the osteoclasts from Paget's disease of bone in relation to a viral aetiology.

Osteoclast ultrastructure in Paget's disease.

Clinical features and pharmacologic treatment of Paget's disease.

P304

1117-22

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P31

scholarly article

P356

10.1086/301601

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P407

P433

5

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P478

61

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P577

1997-11-01T00:00:00Z

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P5875

13883869

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P698

9345096

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P932

1716035

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