Extracellular matrix remodeling and transforming growth factor-β signaling abnormalities induced by lamin A/C variants that cause lipodystrophy.

Item

http://www.wikidata.org/entity/Q38731010

description

2016 nî lūn-bûn

@nan

2016年の論文

@ja

2016年論文

@yue

2016年論文

@zh-hant

2016年論文

@zh-hk

2016年論文

@zh-mo

2016年論文

@zh-tw

2016年论文

@wuu

2016年论文

@zh

2016年论文

@zh-cn

name

Extracellular matrix remodelin ...... ants that cause lipodystrophy.

@en

type

Item

label

Extracellular matrix remodelin ...... ants that cause lipodystrophy.

@en

prefLabel

Extracellular matrix remodelin ...... ants that cause lipodystrophy.

@en

P1476

Extracellular matrix remodelin ...... iants that cause lipodystrophy

@en

P2093

Corinne Vigouroux

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

Howard J Worman

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

Jacqueline Capeau

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

Véronique Béréziat

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

Wei Wu

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

P2860

Real-time PCR based on SYBR-Green I fluorescence: an alternative to the TaqMan assay for a relative quantification of gene rearrangements, gene amplifications and micro gene deletions

Mutations in the gene encoding lamin A/C cause autosomal dominant Emery-Dreifuss muscular dystrophy

An in-frame deletion at the polymerase active site of POLD1 causes a multisystem disorder with lipodystrophy

Mandibuloacral dysplasia is caused by a mutation in LMNA-encoding lamin A/C

Homozygous defects in LMNA, encoding lamin A/C nuclear-envelope proteins, cause autosomal recessive axonal neuropathy in human (Charcot-Marie-Tooth disorder type 2) and mouse

Cleavage of structural proteins during the assembly of the head of bacteriophage T4

Structure of the globular tail of nuclear lamin

The Ig-like structure of the C-terminal domain of lamin A/C, mutated in muscular dystrophies, cardiomyopathy, and partial lipodystrophy

Missense mutations in the rod domain of the lamin A/C gene as causes of dilated cardiomyopathy and conduction-system disease

Nuclear lamin A/C R482Q mutation in canadian kindreds with Dunnigan-type familial partial lipodystrophy

P304

151-163

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

P31

scholarly article

P356

10.1194/JLR.M071381

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

P433

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

P478

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

P50

Caroline Le Dour

P577

2016-11-14T00:00:00Z

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

P698

27845687

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

P932

5234718

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