Clinical significance of Matrilin-3 gene polymorphism in Egyptian patients with primary knee osteoarthritis.

about

3'-UTR Polymorphisms of MTHFR and TS Associated with Osteoporotic Vertebral Compression Fracture Susceptibility in Postmenopausal Women.

P2860

Q51763541-C76AEEEF-1F8F-444E-89E0-B00FB8BA9A01

P2860

Clinical significance of Matrilin-3 gene polymorphism in Egyptian patients with primary knee osteoarthritis.

Item

http://www.wikidata.org/entity/Q41846024

description

2017 nî lūn-bûn

@nan

2017年の論文

@ja

2017年論文

@yue

2017年論文

@zh-hant

2017年論文

@zh-hk

2017年論文

@zh-mo

2017年論文

@zh-tw

2017年论文

@wuu

2017年论文

@zh

2017年论文

@zh-cn

name

Clinical significance of Matri ...... h primary knee osteoarthritis.

@en

type

Item

label

Clinical significance of Matri ...... h primary knee osteoarthritis.

@en

prefLabel

Clinical significance of Matri ...... h primary knee osteoarthritis.

@en

P1476

Clinical significance of Matri ...... h primary knee osteoarthritis.

@en

P2093

Amira I Mansour

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

Basma S Azab

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

Howyda M Kamal

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

Rasha M Fawzy

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

Safia M Diab

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

P2860

Genomewide scan for hand osteoarthritis: a novel mutation in matrilin-3.

Spondylo-epi-metaphyseal dysplasia (SEMD) matrilin 3 type: homozygote matrilin 3 mutation in a novel form of SEMD

A meta-analysis of genome-wide association studies identifies novel variants associated with osteoarthritis of the hip

Functional knockout of the matrilin-3 gene causes premature chondrocyte maturation to hypertrophy and increases bone mineral density and osteoarthritis

Radiological assessment of osteo-arthrosis

Characterization of human matrilin-3 (MATN3).

The matrilins: a novel family of oligomeric extracellular matrix proteins.

Prostaglandins and bone: physiology and pathophysiology.

Genetic, clinical and radiographic signs in knee osteoarthritis susceptibility.

Mutations in the region encoding the von Willebrand factor A domain of matrilin-3 are associated with multiple epiphyseal dysplasia.

P304

200-204

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

P31

scholarly article

P356

10.5152/EURJRHEUM.2016.16107

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

P433

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

P478

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

P577

2017-07-04T00:00:00Z

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

P698

28983412

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

P921

osteoarthritis

P932

5621842

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

Clinical significance of Matrilin-3 gene polymorphism in Egyptian patients with primary knee osteoarthritis.

about

P2860

P2860

Clinical significance of Matrilin-3 gene polymorphism in Egyptian patients with primary knee osteoarthritis.

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P577

P698

P921

P932

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P577

P698

P921

P932