- Home
- Publications
- Publication Search
- Publication Details
Title
The history of TRP channels, a commentary and reflection
Authors
Keywords
-
Journal
PFLUGERS ARCHIV-EUROPEAN JOURNAL OF PHYSIOLOGY
Volume 461, Issue 5, Pages 499-506
Publisher
Springer Nature
Online
2011-02-01
DOI
10.1007/s00424-010-0920-3
References
Ask authors/readers for more resources
Related references
Note: Only part of the references are listed.- Drosophila TRPA1 Channel Is Required to Avoid the Naturally Occurring Insect Repellent Citronellal
- (2010) Young Kwon et al. CURRENT BIOLOGY
- The History of theDrosophilaTRP Channel: The Birth of a New Channel Superfamily
- (2010) Baruch Minke JOURNAL OF NEUROGENETICS
- Light-avoidance-mediating photoreceptors tile the Drosophila larval body wall
- (2010) Yang Xiang et al. NATURE
- C. elegans phototransduction requires a G protein–dependent cGMP pathway and a taste receptor homolog
- (2010) Jie Liu et al. NATURE NEUROSCIENCE
- C. elegans TRP Family Protein TRP-4 Is a Pore-Forming Subunit of a Native Mechanotransduction Channel
- (2010) Lijun Kang et al. NEURON
- A Gain-of-Function Mutation in TRPA1 Causes Familial Episodic Pain Syndrome
- (2010) Barbara Kremeyer et al. NEURON
- Transient receptor potential channelopathies
- (2010) Bernd Nilius et al. PFLUGERS ARCHIV-EUROPEAN JOURNAL OF PHYSIOLOGY
- Drosophila TRPA1 channel mediates chemical avoidance in gustatory receptor neurons
- (2010) S. H. Kim et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- Mutations in the Gene Encoding the Calcium-Permeable Ion Channel TRPV4 Produce Spondylometaphyseal Dysplasia, Kozlowski Type and Metatropic Dysplasia
- (2009) Deborah Krakow et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Mutations in TRPM1 Are a Common Cause of Complete Congenital Stationary Night Blindness
- (2009) Maria M. van Genderen et al. AMERICAN JOURNAL OF HUMAN GENETICS
- TRPM1 Is Mutated in Patients with Autosomal-Recessive Complete Congenital Stationary Night Blindness
- (2009) Isabelle Audo et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Recessive Mutations of the Gene TRPM1 Abrogate ON Bipolar Cell Function and Cause Complete Congenital Stationary Night Blindness in Humans
- (2009) Zheng Li et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Impaired endocytosis of the ion channel TRPM4 is associated with human progressive familial heart block type I
- (2009) Martin Kruse et al. JOURNAL OF CLINICAL INVESTIGATION
- Alterations in the ankyrin domain of TRPV4 cause congenital distal SMA, scapuloperoneal SMA and HMSN2C
- (2009) Michaela Auer-Grumbach et al. NATURE GENETICS
- Scapuloperoneal spinal muscular atrophy and CMT2C are allelic disorders caused by alterations in TRPV4
- (2009) Han-Xiang Deng et al. NATURE GENETICS
- Mutations in TRPV4 cause Charcot-Marie-Tooth disease type 2C
- (2009) Guida Landouré et al. NATURE GENETICS
- Motor Deficit in a Drosophila Model of Mucolipidosis Type IV due to Defective Clearance of Apoptotic Cells
- (2008) Kartik Venkatachalam et al. CELL
- Transient receptor potential channels meet phosphoinositides
- (2008) Bernd Nilius et al. EMBO JOURNAL
- Gain-of-function mutations in TRPV4 cause autosomal dominant brachyolmia
- (2008) Matthew J Rock et al. NATURE GENETICS
- Control of thermotactic behavior via coupling of a TRP channel to a phospholipase C signaling cascade
- (2008) Young Kwon et al. NATURE NEUROSCIENCE
- Altered functional properties of a TRPM2 variant in Guamanian ALS and PD
- (2008) M. C. Hermosura et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- Neuronal TRP channels: thermometers, pathfinders and life-savers
- (2008) Karel Talavera et al. TRENDS IN NEUROSCIENCES
Discover Peeref hubs
Discuss science. Find collaborators. Network.
Join a conversationFind the ideal target journal for your manuscript
Explore over 38,000 international journals covering a vast array of academic fields.
Search