Polycystic kidney disease - where gene dosage counts

about

Kidney: polycystic kidney disease.Therapeutic targets for polycystic kidney disease.Is the light at the end of the tunnel nigh? A review of ADPKD focusing on the burden of disease and tolvaptan as a new treatment.

P2860

Q34436755-96636BA3-F630-4FD2-872F-2B4F52ED82DD Q38578289-B5372224-78A5-4B6A-B8B0-F11B78703146 Q50024807-A16B5AC6-5D03-406C-9D0E-B0DFED1C09BD

P2860

Polycystic kidney disease - where gene dosage counts

Item

http://www.wikidata.org/entity/Q27012746

description

2014 nî lūn-bûn

@nan

2014 թուականին հրատարակուած գիտական յօդուած

@hyw

2014 թվականին հրատարակված գիտական հոդված

@hy

2014年の論文

@ja

2014年論文

@yue

2014年論文

@zh-hant

2014年論文

@zh-hk

2014年論文

@zh-mo

2014年論文

@zh-tw

2014年论文

@wuu

name

Polycystic kidney disease - where gene dosage counts

@ast

Polycystic kidney disease - where gene dosage counts

@en

Polycystic kidney disease - where gene dosage counts

@nl

type

Item

label

Polycystic kidney disease - where gene dosage counts

@ast

Polycystic kidney disease - where gene dosage counts

@en

Polycystic kidney disease - where gene dosage counts

@nl

prefLabel

Polycystic kidney disease - where gene dosage counts

@ast

Polycystic kidney disease - where gene dosage counts

@en

Polycystic kidney disease - where gene dosage counts

@nl

P1476

Polycystic kidney disease - where gene dosage counts

@en

P2093

Cherie Stayner

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

Michael Eccles

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

P2860

Perinatal lethality with kidney and pancreas defects in mice with a targetted Pkd1 mutation

A genetic interaction network of five genes for human polycystic kidney and liver diseases defines polycystin-1 as the central determinant of cyst formation

Pkd1 transgenic mice: adult model of polycystic kidney disease with extrarenal and renal phenotypes.

Genetics and pathogenesis of polycystic kidney disease.

Reduced ciliary polycystin-2 in induced pluripotent stem cells from polycystic kidney disease patients with PKD1 mutations

Renal cystic diseases: a review.

Prenatal diagnosis of autosomal recessive polycystic kidney disease (ARPKD): molecular genetics, clinical experience, and fetal morphology.

Defining a link with autosomal-dominant polycystic kidney disease in mice with congenitally low expression of Pkd1

Incompletely penetrant PKD1 alleles mimic the renal manifestations of ARPKD.

c-Met and NF-κB-dependent overexpression of Wnt7a and -7b and Pax2 promotes cystogenesis in polycystic kidney disease.

P304

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

P31

scholarly article

P356

10.12703/P6-24

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

P407

English

P478

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

P577

2014-01-01T00:00:00Z

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

P5875

261883911

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

P698

24765529

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

P932

3974567

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

Polycystic kidney disease - where gene dosage counts

about

P2860

P2860

Polycystic kidney disease - where gene dosage counts

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P304

P31

P356

P407

P478

P577

P5875

P698

P932

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P407

P478

P577

P5875

P698

P932