A compendium of validated pain genes.
A compendium of validated pain genes.
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DOI:
10.1002/wsbm.1570
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发表时间:
2022-11
影响因子:
3.1
通讯作者:
中科院分区:
文献类型:
--
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The development of novel pain therapeutics hinges on the identification and rigorous validation of potential targets. Model organisms provide a means to test the involvement of specific genes and regulatory elements in pain. Here we provide a list of genes linked to pain‐associated behaviors. We capitalize on results spanning over three decades to identify a set of 242 genes. They support a remarkable diversity of functions spanning action potential propagation, immune response, GPCR signaling, enzymatic catalysis, nucleic acid regulation, and intercellular signaling. Making use of existing tissue and single‐cell high‐throughput RNA sequencing datasets, we examine their patterns of expression. For each gene class, we discuss archetypal members, with an emphasis on opportunities for additional experimentation. Finally, we discuss how powerful and increasingly ubiquitous forward genetic screening approaches could be used to improve our ability to identify pain genes. Neurological Diseases > Genetics/Genomics/Epigenetics Neurological Diseases > Molecular and Cellular Physiology This article is categorized under: An overview of pain signaling pathways, with tissue expression patterns of 242 validated pain genes.
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影响因子:
15.9
作者:
Banerjee A;Larsen RS;Philpot BD;Paulsen O
通讯作者:
Paulsen O
影响因子:
25
作者:
Blanchard, Joel W.;Eade, Kevin T.;Szucs, Attila;Lo Sardo, Valentina;Tsunemoto, Rachel K.;Williams, Daniel;Sanna, Pietro Paolo;Baldwin, Kristin K.
通讯作者:
Baldwin, Kristin K.
影响因子:
64.8
作者:
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通讯作者:
Basbaum, AI
DOI:
10.1523/jneurosci.6103-09.2010
发表时间:
2010-08-25
期刊:
The Journal of neuroscience : the official journal of the Society for Neuroscience
影响因子:
--
作者:
Alter BJ;Zhao C;Karim F;Landreth GE;Gereau RW 4th
通讯作者:
Gereau RW 4th
影响因子:
27.4
作者:
Alawi KM;Russell FA;Aubdool AA;Srivastava S;Riffo-Vasquez Y;Baldissera L Jr;Thakore P;Saleque N;Fernandes ES;Walsh DA;Brain SD
通讯作者:
Brain SD