"Kidney Diseases, Cystic" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
A heterogeneous group of hereditary and acquired disorders in which the KIDNEY contains one or more CYSTS unilaterally or bilaterally (KIDNEY, CYSTIC).
| Descriptor ID |
D052177
|
| MeSH Number(s) |
C12.777.419.403 C13.351.968.419.403
|
| Concept/Terms |
Kidney Diseases, Cystic- Kidney Diseases, Cystic
- Cystic Kidney Disease
- Disease, Cystic Kidney
- Diseases, Cystic Kidney
- Kidney Disease, Cystic
- Cystic Kidney Diseases
- Cystic Renal Diseases
- Cystic Renal Disease
- Disease, Cystic Renal
- Diseases, Cystic Renal
- Renal Disease, Cystic
- Renal Diseases, Cystic
Kidney, Cystic- Kidney, Cystic
- Cystic Kidney
- Cystic Kidneys
- Kidneys, Cystic
|
Below are MeSH descriptors whose meaning is more general than "Kidney Diseases, Cystic".
Below are MeSH descriptors whose meaning is more specific than "Kidney Diseases, Cystic".
This graph shows the total number of publications written about "Kidney Diseases, Cystic" by people in this website by year, and whether "Kidney Diseases, Cystic" was a major or minor topic of these publications.
To see the data from this visualization as text,
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| Year | Major Topic | Minor Topic | Total |
|---|
| 2002 | 1 | 0 | 1 |
| 2012 | 1 | 0 | 1 |
| 2013 | 1 | 0 | 1 |
| 2017 | 2 | 0 | 2 |
| 2018 | 1 | 0 | 1 |
| 2019 | 1 | 0 | 1 |
| 2020 | 1 | 0 | 1 |
| 2022 | 0 | 1 | 1 |
| 2023 | 1 | 0 | 1 |
| 2024 | 0 | 1 | 1 |
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Below are the most recent publications written about "Kidney Diseases, Cystic" by people in Profiles.
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Osteopontin deletion attenuates cyst growth but exacerbates fibrosis in mice with cystic kidney disease. Physiol Rep. 2024 Sep; 12(17):e70038.
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Single-molecule imaging in the primary cilium. Methods Cell Biol. 2023; 176:59-83.
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The Joubert-Meckel-Nephronophthisis Spectrum of Ciliopathies. Annu Rev Genomics Hum Genet. 2022 08 31; 23:301-329.
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Dysfunction of the ciliary ARMC9/TOGARAM1 protein module causes Joubert syndrome. J Clin Invest. 2020 08 03; 130(8):4423-4439.
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Tissue-Resident Macrophages Promote Renal Cystic Disease. J Am Soc Nephrol. 2019 10; 30(10):1841-1856.
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Primary cilia disruption differentially affects the infiltrating and resident macrophage compartment in the liver. Am J Physiol Gastrointest Liver Physiol. 2018 06 01; 314(6):G677-G689.
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Super-resolution microscopy reveals that disruption of ciliary transition-zone architecture causes Joubert syndrome. Nat Cell Biol. 2017 Oct; 19(10):1178-1188.
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Mutations in ARMC9, which Encodes a Basal Body Protein, Cause Joubert Syndrome in Humans and Ciliopathy Phenotypes in Zebrafish. Am J Hum Genet. 2017 Jul 06; 101(1):23-36.
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Case report: Multimodality imaging of a cystic nephroma. Radiol Technol. 2013 Jul-Aug; 84(6):559-66.
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Unilateral renal cystic disease. Kidney Int. 2012 Jan; 81(2):220.