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1 this leads to closure of the TRPM1 channel (melastatin).
2 icroRNA (miR-211) hosted within an intron of melastatin.
3 hannel, subfamily M, member 1, also known as melastatin.
4 arity to several vertebrate genes, including melastatin.
6 metabotropic glutamate receptor 6 to the TRP melastatin 1 (TRPM1) channel to transmit signals from ph
8 Go , closure of transient receptor potential melastatin 1 channels and hyperpolarization of these cel
9 ressed from the transient receptor potential melastatin 1 intronic region, regulates oxidative phosph
11 try (SOCE), the transient receptor potential melastatin 2 (TRPM2) channel contributes to Ca(2+) relea
15 neurons express transient receptor potential melastatin 2 (TRPM2) channels that underlie NMDA-induced
16 cation channel transient receptor potential melastatin 2 (TRPM2) exhibit essential roles in FPP-indu
17 variant of the transient receptor potential melastatin 2 (TRPM2) gene may confer susceptibility to t
18 cation channel transient receptor potential melastatin 2 (TRPM2) in a murine model of kidney ischemi
26 cation channel transient receptor potential melastatin 2 (TRPM2) plays a key role in pathogen-evoked
28 tella vectensis Transient Receptor Potential Melastatin 2), the species variant of the human apoptosi
30 DP ribose opens transient receptor potential melastatin-2 (TRPM2) channels in endothelial cells leadi
32 ble ion channel transient receptor potential melastatin-2 (TRPM2), previously implicated in persisten
33 TIONALE: TRPM2 (transient receptor potential melastatin-2) expressed in endothelial cells (ECs) is a
34 ent receptor potential ankyrin 1 (TRPA1) and melastatin 3 (TRPM3) are transduction channels of sensor
35 ent receptor potential ankyrin 1 (TRPA1) and melastatin 3 (TRPM3) are transduction channels of sensor
36 (MFA), that the Transient Receptor Potential Melastatin 3 (TRPM3) channel promotes the growth of clea
44 urea receptor 1-transient receptor potential melastatin 4 (SUR1-TRPM4) cation channel is a key underl
45 e non-selective Transient Receptor Potential Melastatin 4 (TRPM4) cation channel is abundantly expres
46 d K(+) (BK) and transient receptor potential melastatin 4 (TRPM4) cation channels linked to disruptio
48 ive deletion of transient receptor potential melastatin 4 (TRPM4) channels in mouse cardiomyocytes re
49 x through transient receptor potential (TRP) melastatin 4 (TRPM4) channels to cause membrane depolari
53 dently enhances transient receptor potential melastatin 4 (TRPM4), a Ca2+-activated nonselective (CAN
55 )1.6, and transient receptor potential [TRP] melastatin 4 [TRPM4]) both regulate excitability and gen
57 ucted by TRPM4 (transient receptor potential melastatin 4) channels in native cerebral artery smooth
61 gnesium channel transient receptor potential melastatin 6, and NCC phosphorylation, all of which were
62 tivation of the transient receptor potential melastatin 7 (TRPM7) channel promotes extracellular calc
63 (2+) conducting transient receptor potential melastatin 7 (TRPM7) channel-enzyme (chanzyme) has been
72 ABSTRACT: The transient receptor potential melastatin 7 (TRPM7) is a protein that combines an ion c
74 r inhibition of transient receptor potential melastatin 7 (TRPM7) reduces store-operated calcium entr
75 re we show that Transient Receptor Potential Melastatin 7 (TRPM7), a divalent-permeant channel-kinase
76 ous variants in transient receptor potential melastatin 7 (TRPM7), a ubiquitously expressed ion chann
77 e find that the transient receptor potential melastatin 7 (TRPM7)-associated Mg2+ -inhibited cation (
81 enthol receptor transient receptor potential melastatin 8 (TRPM8) and compared its behavior with that
83 l ganglion, the transient receptor potential melastatin 8 (TRPM8) channel is a Ca(2+)-permeable catio
84 nthol-sensitive transient receptor potential melastatin 8 (TRPM8) channel is important for both physi
86 nthol-activated transient receptor potential melastatin 8 (TRPM8) channels are thought to be regulate
88 nthol-activated transient receptor potential melastatin 8 (TRPM8) channels diminishes over time in th
94 interacts with transient receptor potential melastatin 8 (TRPM8) ion channels in cold-sensitive sens
100 is detected by transient receptor potential melastatin 8 (TRPM8), a nonselective cation channel expr
101 nthol activates transient receptor potential melastatin 8 (TRPM8), an ion channel also activated by c
102 aling receptor, Transient Receptor Potential Melastatin 8 (TRPM8), regulates dimorphic sexual and soc
103 hibited robust, transient receptor potential melastatin 8 (TRPM8)-dependent discharges at room temper
106 vanilloid 1 and transient receptor potential melastatin 8 in sensory neurons and causes mechanical hy
107 receptor TRPM8 (transient receptor potential melastatin 8) has been suggested to play a role in cold
108 vanilloid 1 and transient receptor potential melastatin 8) in primary sensory neurons using both phar
110 pport a role of transient receptor potential melastatin 8-mediated facilitation of synaptic strength
111 sitive channel transient receptor potential (melastatin)-8 (TRPM8), heterologously expressed in Chine
112 port that human transient receptor potential melastatin-8 (TRPM8) and an N-terminally truncated TRPM8
113 ll-length human transient receptor potential melastatin-8 (TRPM8) but did not inhibit activation by m
114 In the same experimental setup, blocking the melastatin-8 (TRPM8) channel with AMG2850 (30 mg/kg) att
115 imation via the transient receptor potential melastatin-8 (TRPM8) channel without evoking nociceptive
118 diesel exhaust PM > crystalline silica; TRP melastatin-8 is also robustly activated by CFA1, whereas
121 umor suppressive activity is not mediated by melastatin but instead by a microRNA (miR-211) hosted wi
124 human primary cutaneous melanomas examined, melastatin expression appeared to correlate inversely wi
125 ssion pattern observed suggests that loss of melastatin expression is an indicator of melanoma aggres
127 dermal transient receptor potential channel, melastatin family (TRPM) channel GTL-2 and IP(3)R-stimul
128 belongs to the Transient Receptor Potential Melastatin family of ion channels and is a divalent cati
131 r via the TRPM (transient receptor potential melastatin) gene, GON-2, which may sense the intestinal
132 PZQ activates a transient receptor potential melastatin ion channel (TRPM(PZQ)) in schistosomes by en
135 lcium-permeable channel, transient potential melastatin-like 2 (TRPM2), via stimulation of poly-ADP-r
136 We found that transient receptor potential-melastatin-like 7 (TRPM7) channel expression regulated E
138 l disruption of transient receptor potential-melastatin-like 7 (Trpm7) in mice results in embryonic l
141 lected against via suppression of the entire melastatin locus during human melanoma progression.
142 ate was 90% +/- 7%, whereas in patients with melastatin loss, the disease-free survival rate was 51%
143 A was 100%, whereas in stage I patients with melastatin loss, the disease-free survival rate was 77%
144 sion criterion, TRP polycystic (P)3, and TPR melastatin (M)8 were found to be uniquely adipospecific.
146 reen identified transient receptor potential melastatin member 4 (TRPM4), a calcium-activated, ATP-in
151 amily includes the putative tumor suppressor melastatin (MLSN) and is a poorly characterized group of
154 erformed to assess the prognostic utility of melastatin mRNA expression while adjusting for other pro
155 udied the relationship between expression of melastatin mRNA in the primary cutaneous tumor and progn
157 I patients whose tumors diffusely expressed melastatin mRNA was 100%, whereas in stage I patients wi
159 II disease whose tumors diffusely expressed melastatin mRNA, the 8-year disease-free survival rate w
160 the mouse are consistent with involvement of melastatin mutations in the mouse ruby-eye-2 defect, con
162 Increasing expression of miR-211 but not melastatin reduced migration and invasion of malignant a
163 that the transient receptor potential (TRP) melastatin related 7 (TRPM7) is the molecular basis of t
164 a member of the transient receptor potential melastatin-related (TRPM) family of cation channels, whi
166 cation channel that belongs to the family of melastatin-related transient receptor potential (TRPM) c
167 ium (Ca(2+))-permeable cation channel of the melastatin-related transient receptor potential (TRPM) i
171 variants in the transient receptor potential melastatin-related type 3 gene (TRPM3) have been associa
174 nsient receptor potential ion channel in the melastatin subfamily (TRPM(PZQ))-however, little is know
176 , inhibitors of transient receptor potential melastatin subfamily 4 (TRPM4), intracellular introducti
177 rent carried by transient receptor potential melastatin subfamily 4 channels via type 2 inositol 1,4,
178 mate receptor 6/transient receptor potential melastatin subfamily M member 1-signaling (mGluR6/TRPM1-
179 et identified within the S1-S4 domain of the Melastatin subfamily member TRPM8, the mammalian sensor
181 nsient receptor potential ion channel of the melastatin subfamily, named TRPM(MCLZ), as a parasite ta
182 nsient receptor potential ion channel of the melastatin subfamily, TRPM8, is a major cold receptor in
184 his analysis identified a novel gene, termed melastatin, that is expressed at high levels in poorly m
186 cation channel transient receptor potential melastatin (TRPM) 4 is involved in the control of Ca(2+)
187 lycosylation of transient receptor potential melastatin (Trpm) 4b, a membrane glycoprotein that regul
189 Finally, two transient receptor potential melastatin (TRPM) channels, GON-2 and GTL-2, mediate thi
192 amilies: classical (TRPC), vanilloid (TRPV), melastatin (TRPM), muclopins (TRPML), polycystin (TRPP),
195 studies have demonstrated that expression of melastatin/TRPM1 strongly predicts nonmetastatic propens
197 Mg(2+) channel transient receptor potential melastatin type 6 that determines the final urinary Mg(2
198 sensors such as transient receptor potential melastatin type 8 (TRPM8) have been identified, the neur
200 dulation of the transient receptor potential melastatin type 8 (TRPM8) is currently under investigati