 Polycystic Kidney Diseases
"Polycystic Kidney Diseases" 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.
Hereditary diseases that are characterized by the progressive expansion of a large number of tightly packed CYSTS within the KIDNEYS. They include diseases with autosomal dominant and autosomal recessive inheritance.
| Descriptor ID |
D007690
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| MeSH Number(s) |
C12.777.419.403.875 C13.351.968.419.403.875
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| Concept/Terms |
Polycystic Kidney Diseases- Polycystic Kidney Diseases
- Disease, Polycystic Kidney
- Diseases, Polycystic Kidney
- Kidney Disease, Polycystic
- Kidney Diseases, Polycystic
- Polycystic Kidney Disease
- Polycystic Renal Disease
- Disease, Polycystic Renal
- Diseases, Polycystic Renal
- Polycystic Renal Diseases
- Renal Disease, Polycystic
- Renal Diseases, Polycystic
Kidney, Polycystic- Kidney, Polycystic
- Kidneys, Polycystic
- Polycystic Kidneys
- Polycystic Kidney
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Below are MeSH descriptors whose meaning is more general than "Polycystic Kidney Diseases".
Below are MeSH descriptors whose meaning is more specific than "Polycystic Kidney Diseases".
This graph shows the total number of publications written about "Polycystic Kidney Diseases" by people in this website by year, and whether "Polycystic Kidney Diseases" was a major or minor topic of these publications.
To see the data from this visualization as text, click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 1983 | 1 | 0 | 1 | | 1985 | 1 | 1 | 2 | | 1990 | 0 | 1 | 1 | | 1994 | 2 | 0 | 2 | | 1997 | 1 | 0 | 1 | | 1999 | 1 | 0 | 1 | | 2000 | 0 | 1 | 1 | | 2001 | 1 | 0 | 1 | | 2004 | 1 | 0 | 1 | | 2010 | 1 | 0 | 1 | | 2011 | 1 | 0 | 1 | | 2012 | 0 | 1 | 1 | | 2013 | 1 | 0 | 1 | | 2018 | 1 | 0 | 1 |
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Below are the most recent publications written about "Polycystic Kidney Diseases" by people in Profiles.
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Rahbari-Oskoui FF, Chapman AB. Hypoxia-Inducible Factor 1a (HIF-1a), Angiopoietin-2 (ANG-2) and Endocan: Novel Biomarkers of Disease Progression Involving Polycystic Kidney Disease. Am J Nephrol. 2018; 47(4):228-230.
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Bae KT, Tao C, Wang J, Kaya D, Wu Z, Bae JT, Chapman AB, Torres VE, Grantham JJ, Mrug M, Bennett WM, Flessner MF, Landsittel DP. Novel approach to estimate kidney and cyst volumes using mid-slice magnetic resonance images in polycystic kidney disease. Am J Nephrol. 2013; 38(4):333-41.
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Araç D, Boucard AA, Bolliger MF, Nguyen J, Soltis SM, Südhof TC, Brunger AT. A novel evolutionarily conserved domain of cell-adhesion GPCRs mediates autoproteolysis. EMBO J. 2012 Mar 21; 31(6):1364-78.
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Chapman AB, Wei W. Imaging approaches to patients with polycystic kidney disease. Semin Nephrol. 2011 May; 31(3):237-44.
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Akkina S, Becker BN. MicroRNAs in kidney function and disease. Transl Res. 2011 Apr; 157(4):236-40.
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Torres VE, Boletta A, Chapman A, Gattone V, Pei Y, Qian Q, Wallace DP, Weimbs T, Wüthrich RP. Prospects for mTOR inhibitor use in patients with polycystic kidney disease and hamartomatous diseases. Clin J Am Soc Nephrol. 2010 Jul; 5(7):1312-29.
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Basu J, Compitello G, Stromberg G, Willard HF, Van Bokkelen G. Efficient assembly of de novo human artificial chromosomes from large genomic loci. BMC Biotechnol. 2005 Jul 05; 5:21.
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Powell CR, Tata S, Govani MV, Chien GW, Orvieto MA, Shalhav AL. Transplantation of a cadaveric polycystic kidney in a patient with autosomal dominant polycystic kidney disease: long-term outcome. Transplant Proc. 2004 Jun; 36(5):1288-92.
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Dunn MD, Portis AJ, Naughton C, Shalhav A, McDougall EM, Clayman RV. Laparoscopic cyst marsupialization in patients with autosomal dominant polycystic kidney disease. J Urol. 2001 Jun; 165(6 Pt 1):1888-92.
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Bingham C, Ellard S, Allen L, Bulman M, Shepherd M, Frayling T, Berry PJ, Clark PM, Lindner T, Bell GI, Ryffel GU, Nicholls AJ, Hattersley AT. Abnormal nephron development associated with a frameshift mutation in the transcription factor hepatocyte nuclear factor-1 beta. Kidney Int. 2000 Mar; 57(3):898-907.
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