Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Structure and function of the pancreas in the polycystic kidney rat.

Pancreas - 1 Nov 2012

Yi Lanjuan, Naruse Satoru, Furuya Sonoko, Yamamoto Akiko, Nakakuki Miyuki, Nagao Shizuko, Yoshihara Daisuke, Ko Shigeru B H, Wei Muxin, Kondo Takaharu, Ishiguro Hiroshi

Abstract excerpt

OBJECTIVES: Mutation in the Pkhd1 gene that encodes a ciliary protein, fibrocystin, causes multiple cysts in the kidneys and liver in the polycystic kidney (PCK) rat, a model for human autosomal recessive PCK disease. To clarify the role of primary cilia in the pancreatic duct, we examined the st...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Amylases
Share to Aquaporin 1
Share to Bile

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Carbachol

Share to Pancreatic Ducts

Share to Polycystic Kidney Diseases

Share to Rats, Sprague-Dawley

Share to Receptors, Cell Surface

Source

Identifiers

PMID: 22647734
DOI: 10.1097/MPA.0b013e31824c12f9

Genes

AQP1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-22647734-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 4 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Structure and function of the pancreas in the polycystic kidney rat.PMID 22647734Read ↗

Physiologic mechanisms underlying polycystic kidney disease.Semantic proximity Read ↗

Biliary dysgenesis in the PCK rat, an orthologous model of autosomal recessive polycystic kidney disease.Semantic proximity Read ↗

A mouse model of autosomal recessive polycystic kidney disease with biliary duct and proximal tubule dilatation.Semantic proximity Read ↗

Mouse models of polycystic kidney disease induced by defects of ciliary proteins.Semantic proximity Read ↗

Molecular basis of autosomal recessive polycystic kidney disease (ARPKD).Semantic proximity Read ↗

Ciliogenic pancreatopathy reveals a link between ciliopathies and exocrine pancreatic diseaseSemantic proximity Read ↗

Biliary and pancreatic dysgenesis in mice harboring a mutation in Pkhd1.Semantic proximity Read ↗

Pancreatic cyst development: insights from von Hippel-Lindau diseaseSemantic proximity Read ↗

Cholangiocyte primary cilia in liver health and diseaseSemantic proximity Read ↗

Fibrocystin/polyductin modulates renal tubular formation by regulating polycystin-2 expression and function.Semantic proximity Read ↗

Polycystins 1 and 2 mediate mechanosensation in the primary cilium of kidney cells.Semantic proximity Read ↗

Therapeutic Targets in Polycystic Liver DiseaseSemantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.