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

[Cystic kidney diseases].

Der Internist - 1 Apr 2012

Zerres K, Ortiz Brüchle N

Abstract excerpt

Cystic kidney diseases are clinically and genetically heterogeneous. The most important entities are autosomal-dominant and autosomal-recessive polycystic kidney diseases. The proteins encoded by the involved genes are referred to as cystoproteins, which are located predominantly in the primary cilia. Primary cilia play an important role in cyst formation. Inherited polycystic kidney diseases belong to the...

Topics

Join the communities discussing this publication.

Early Diagnosis
Genetic Predisposition to Disease
Genetic Testing
Kidney Diseases, Cystic
Polymorphism, Single Nucleotide

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Source

Identifiers

PMID: 22410941
DOI: 10.1007/s00108-011-2985-2

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 1 Sept 2026.

Community interpretation

Discuss the evidence

Ask a question, add context or challenge an interpretation. Community activity is separate from scientific evidence strength.

0

discussions

0

replies

Citations encouraged

Claims remain attributable.

No discussion yet

Be the first to add a careful, cited interpretation.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

[Cystic kidney diseases].PMID 22410941Read ↗

Cystic diseases of the kidney: molecular biology and genetics.Semantic proximity Read ↗

Renal cystic disease and associated ciliopathiesSemantic proximity Read ↗

Renal Pathology of CiliopathiesSemantic proximity Read ↗

Genetic and Clinical Evaluation of Pediatric Cystic Kidney Diseases: Autosomal Dominant and Autosomal Recessive Polycystic Kidney Disease.Semantic proximity Read ↗

Diagnosis, pathogenesis, and treatment prospects in cystic kidney disease.Semantic proximity Read ↗

Cilia and centrosomes: a unifying pathogenic concept for cystic kidney disease?Semantic proximity Read ↗

Nephronophthisis-Pathobiology and Molecular Pathogenesis of a Rare Kidney Genetic Disease.Semantic proximity Read ↗

Update on autosomal dominant polycystic kidney disease.Semantic proximity Read ↗

Molecular genetics of renal ciliopathies.Semantic proximity Read ↗

The Classification of Renal Cystic Diseases and Other Congenital Malformations of the Kidney and Urinary TractSemantic proximity Read ↗

Hereditary Renal Cystic Disorders: Imaging of the Kidneys and Beyond.Semantic proximity Read ↗

Polycystic Kidney DiseaseSemantic proximity Read ↗

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