Cyst expansion and regression in a mouse model of polycystic kidney disease (Q86296609)

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25 February 2020

title

Cyst expansion and regression in a mouse model of polycystic kidney disease (English)

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polycystic kidney disease

25 February 2020

main subject

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4

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25 February 2020

author name string

Hester Happé

1

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25 February 2020

Annemieke M van der Wal

2

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25 February 2020

Daniela C F Salvatori

3

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25 February 2020

Martijn H Breuning

5

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25 February 2020

Emile de Heer

6

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25 February 2020

Dorien J M Peters

7

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25 February 2020

language of work or name

English

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publication date

6 March 2013

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25 February 2020

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23466997 AND SRC:MED&resulttype=core&format=json

25 February 2020

volume

83

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25 February 2020

issue

6

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25 February 2020

page(s)

1099-1108

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Autosomal dominant polycystic kidney disease--more than a renal disease

25 February 2020

cites work

1 reference

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Pathogenic sequence for dissecting aneurysm formation in a hypomorphic polycystic kidney disease 1 mouse model

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The polycystic kidney disease 1 gene encodes a 14 kb transcript and lies within a duplicated region on chromosome 16. The European Polycystic Kidney Disease Consortium

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Selective cyclooxygenase-2 inhibition with celecoxib decreases angiotensin II-induced abdominal aortic aneurysm formation in mice

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Inhibition of autoregulated TGFbeta signaling simultaneously enhances proliferation and differentiation of kidney epithelium and promotes repair following renal ischemia

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Kidney-specific inactivation of the KIF3A subunit of kinesin-II inhibits renal ciliogenesis and produces polycystic kidney disease

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7 January 2021

Toxic tubular injury in kidneys from Pkd1-deletion mice accelerates cystogenesis accompanied by dysregulated planar cell polarity and canonical Wnt signaling pathways

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Macrophages promote cyst growth in polycystic kidney disease

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Exploring the full spectrum of macrophage activation

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Correlation of kidney function, volume and imaging findings, and PKHD1 mutations in 73 patients with autosomal recessive polycystic kidney disease

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Clinical consequences of PKHD1 mutations in 164 patients with autosomal-recessive polycystic kidney disease (ARPKD)

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Apoptosis and loss of renal tissue in polycystic kidney diseases

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Cyst formation and activation of the extracellular regulated kinase pathway after kidney specific inactivation of Pkd1.

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Curcumin inhibits cystogenesis by simultaneous interference of multiple signaling pathways: in vivo evidence from a Pkd1-deletion model.

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Intermediate Volume on Computed Tomography Imaging Defines a Fibrotic Compartment that Predicts Glomerular Filtration Rate Decline in Autosomal Dominant Polycystic Kidney Disease Patients

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Polycystic kidney disease: neoplasia in disguise

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mTOR inhibitors in polycystic kidney disease.

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Sirolimus and kidney growth in autosomal dominant polycystic kidney disease

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Dose-dependent effects of sirolimus on mTOR signaling and polycystic kidney disease

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7 January 2021