Trp-p8, a novel prostate-specific gene, is up-regulated in prostate cancer and other malignancies and shares high homology with transient receptor potential calcium channel proteins.
By L. Tsavaler, M. Shapero, S. Morkowski, R. Laus. Cancer Research, 2001
634 citations recorded by the source corpus.
View Paper: https://www.semanticscholar.org/paper/adb865b9c3feef637df5d16cfb36776276b16fa3
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Citations in the corpus
- The trp ion channel family (2001, background): “The related TRPM8 or Trp-p8 is a protein with 41% sequence identity to TRPM2, without an apparent Nudix hydrolase moti”
- Calcium and cancer: targeting Ca2+ transport (2007, background): “68 )) concurrent with an increase in Ca 2+ influx channel expression (TRPM8 (Ref”
- Identification of a cold receptor reveals a general role for TRP channels in thermosensation (2002, background): “Further search of the literature showed that CMR1 is 92% identical to a human sequence originally identified as a prostate-specific transcrip”
- An introduction to TRP channels. (2006, background): “Although first identified in prostate, in which it is proposed to be an androgenresponsive channel (160), TRPM8 has been most convincingly described as a cold- and menthol-activated nonselective cation channel with prominent voltagedependent gating properties (71, 161–163).”
- TRP Channels (2012, unknown): “It is also known as Mucolipin2 MCOLN2).”