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TRPP Cation Channels
Known as:
TRPP Cation Channels [Chemical/Ingredient]
, Cation Channels, TRPP
, Polycystins
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A subgroup of TRP cation channels that are widely expressed in various cell types. Defects are associated with POLYCYSTIC KIDNEY DISEASES.
National Institutes of Health
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Related topics
Related topics
11 relations
In Blood
Process of secretion
agonists
antagonists & inhibitors
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Narrower (2)
polycystic kidney disease 1 protein
polycystic kidney disease 2 protein
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
Review
2014
Review
2014
Polycystin-1 cleavage and the regulation of transcriptional pathways
David M Merrick
,
C. Bertuccio
,
Hannah C. Chapin
,
M. Lal
,
V. Chauvet
,
M. Caplan
Pediatric nephrology (Berlin, West)
2014
Corpus ID: 23351481
Autosomal dominant polycystic kidney disease (ADPKD) is the most common genetic cause of end-stage renal disease, affecting…
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Review
2013
Review
2013
Multidrug Therapy for Polycystic Kidney Disease: A Review and Perspective
G. Aguiari
,
L. Catizone
,
L. del Senno
American Journal of Nephrology
2013
Corpus ID: 2469321
Autosomal dominant polycystic kidney disease (ADPKD) is a renal disorder characterized by the development of cysts in both…
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Highly Cited
2009
Highly Cited
2009
Characterization of primary cilia in human airway smooth muscle cells.
Jun Wu
,
H. Du
,
Xiangling Wang
,
C. Mei
,
G. Sieck
,
Q. Qian
Chest
2009
Corpus ID: 25758343
BACKGROUND Considerable evidence indicates a key role for primary cilia of mammalian cells in mechanochemical sensing…
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Review
2006
Review
2006
Molecular pathogenesis of autosomal dominant polycystic kidney disease
B. Yoder
,
S. Mulroy
,
Hannah E. Eustace
,
C. Boucher
,
R. Sandford
Expert Reviews in Molecular Medicine
2006
Corpus ID: 28159373
Autosomal dominant polycystic kidney disease (ADPKD) is one of the commonest inherited human disorders yet remains relatively…
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Review
2005
Review
2005
Subcellular localization and trafficking of polycystins
M. Köttgen
,
G. Walz
Pflügers Archiv
2005
Corpus ID: 6118825
Polycystin-2 is a member of the transient receptor potential (TRP) family of ion channels that is mutated in autosomal dominant…
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2005
2005
Primary cilia of inv/inv mouse renal epithelial cells sense physiological fluid flow: bending of primary cilia and Ca2+ influx.
D. Shiba
,
T. Takamatsu
,
T. Yokoyama
Cell Structure and Function
2005
Corpus ID: 10063685
Primary cilia are hypothesized to act as a mechanical sensor to detect renal tubular fluid flow. Anomalous structure of primary…
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Review
2004
Review
2004
Polycystins: what polycystic kidney disease tells us about sperm
A. Kierszenbaum
Molecular Reproduction and Development
2004
Corpus ID: 9420080
Experimental evidence indicates that the membrane‐associated proteins polycystin‐1 and polycystin‐2 operate as a receptor‐calcium…
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2002
2002
Modulation of the human polycystin‐L channel by voltage and divalent cations
Yan Liu
,
Qiang Li
,
+4 authors
Xing-Zhen Chen
FEBS Letters
2002
Corpus ID: 3150744
Review
2001
Review
2001
Autosomal dominant polycystic kidney disease: modification of disease progression
D. Peters
,
M. Breuning
The Lancet
2001
Corpus ID: 45804785
Highly Cited
1968
Highly Cited
1968
Radiolarian Skeletons: Solution at Depths
W. Berger
Science
1968
Corpus ID: 23628628
Radiolarian skeletons were placed at several depths on the taut mooring wire of a buoy in the central Pacific for 4 months…
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