Accelerated podocyte detachment and progressive podocyte loss from glomeruli with age in Alport Syndrome.

about

Alport syndrome and Pierson syndrome: Diseases of the glomerular basement membrane.Nephrin is necessary for podocyte recovery following injury in an adult mature glomerulus.

P2860

Q52718217-BD99F7DA-6FD1-4885-B27B-7A3C7552DE43 Q55456867-C26076B8-96A3-4F18-A56F-B10CCB5D222D

P2860

Accelerated podocyte detachment and progressive podocyte loss from glomeruli with age in Alport Syndrome.

Item

http://www.wikidata.org/entity/Q38372746

description

2017 nî lūn-bûn

@nan

2017年の論文

@ja

2017年学术文章

@wuu

2017年学术文章

@zh-cn

2017年学术文章

@zh-hans

2017年学术文章

@zh-my

2017年学术文章

@zh-sg

2017年學術文章

@yue

2017年學術文章

@zh

2017年學術文章

@zh-hant

name

Accelerated podocyte detachmen ...... i with age in Alport Syndrome.

@en

type

Item

label

Accelerated podocyte detachmen ...... i with age in Alport Syndrome.

@en

prefLabel

Accelerated podocyte detachmen ...... i with age in Alport Syndrome.

@en

P1476

Accelerated podocyte detachmen ...... i with age in Alport Syndrome.

@en

P2093

Fang Wang

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

Fangrui Ding

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

Farsad Afshinnia

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

Jeffrey Hodgin

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

Jie Ding

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

Larysa Wickman

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

Su Q Wang

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

Yanqin Zhang

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

P2860

COL4A3/COL4A4 mutations producing focal segmental glomerulosclerosis and renal failure in thin basement membrane nephropathy

Identification of mutations in the alpha 3(IV) and alpha 4(IV) collagen genes in autosomal recessive Alport syndrome

Podometrics as a Potential Clinical Tool for Glomerular Disease Management

Role of the podocyte (and glomerular endothelium) in building the GBM

Identification of mutations in the COL4A5 collagen gene in Alport syndrome

Early angiotensin-converting enzyme inhibition in Alport syndrome delays renal failure and improves life expectancy.

A single-gene cause in 29.5% of cases of steroid-resistant nephrotic syndrome.

Rare hereditary COL4A3/COL4A4 variants may be mistaken for familial focal segmental glomerulosclerosis

The two kidney to one kidney transition and transplant glomerulopathy: a podocyte perspective

Urine podocyte mRNAs mark disease activity in IgA nephropathy.

P31

scholarly article

P356

10.1016/J.KINT.2017.05.017

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

P407

English

P50

Roger C Wiggins

P577

2017-07-26T00:00:00Z

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

P698

28754557

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

P932

5696060

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

Accelerated podocyte detachment and progressive podocyte loss from glomeruli with age in Alport Syndrome.

about

P2860

P2860

Accelerated podocyte detachment and progressive podocyte loss from glomeruli with age in Alport Syndrome.

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P31

P356

P407

P50

P577

P698

P932

P356

P1433

P1476

P2093

P2860

P31

P356

P407

P50

P577

P698

P932