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1 this leads to closure of the TRPM1 channel (melastatin).
2 arity to several vertebrate genes, including melastatin.
3 icroRNA (miR-211) hosted within an intron of melastatin.
4 hannel, subfamily M, member 1, also known as 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
14 neurons express transient receptor potential melastatin 2 (TRPM2) channels that underlie NMDA-induced
15 variant of the transient receptor potential melastatin 2 (TRPM2) gene may confer susceptibility to t
16 cation channel transient receptor potential melastatin 2 (TRPM2) in a murine model of kidney ischemi
21 cation channel transient receptor potential melastatin 2 (TRPM2) plays a key role in pathogen-evoked
23 DP ribose opens transient receptor potential melastatin-2 (TRPM2) channels in endothelial cells leadi
24 TIONALE: TRPM2 (transient receptor potential melastatin-2) expressed in endothelial cells (ECs) is a
25 (MFA), that the Transient Receptor Potential Melastatin 3 (TRPM3) channel promotes the growth of clea
30 e non-selective Transient Receptor Potential Melastatin 4 (TRPM4) cation channel is abundantly expres
31 x through transient receptor potential (TRP) melastatin 4 (TRPM4) channels to cause membrane depolari
33 dently enhances transient receptor potential melastatin 4 (TRPM4), a Ca2+-activated nonselective (CAN
36 (2+) conducting transient receptor potential melastatin 7 (TRPM7) channel-enzyme (chanzyme) has been
43 ABSTRACT: The transient receptor potential melastatin 7 (TRPM7) is a protein that combines an ion c
45 r inhibition of transient receptor potential melastatin 7 (TRPM7) reduces store-operated calcium entr
46 re we show that Transient Receptor Potential Melastatin 7 (TRPM7), a divalent-permeant channel-kinase
47 e find that the transient receptor potential melastatin 7 (TRPM7)-associated Mg2+ -inhibited cation (
51 enthol receptor transient receptor potential melastatin 8 (TRPM8) and compared its behavior with that
53 l ganglion, the transient receptor potential melastatin 8 (TRPM8) channel is a Ca(2+)-permeable catio
54 nthol-activated transient receptor potential melastatin 8 (TRPM8) channels are thought to be regulate
55 nthol-activated transient receptor potential melastatin 8 (TRPM8) channels diminishes over time in th
59 interacts with transient receptor potential melastatin 8 (TRPM8) ion channels in cold-sensitive sens
62 is detected by transient receptor potential melastatin 8 (TRPM8), a nonselective cation channel expr
63 nthol activates transient receptor potential melastatin 8 (TRPM8), an ion channel also activated by c
65 receptor TRPM8 (transient receptor potential melastatin 8) has been suggested to play a role in cold
66 pport a role of transient receptor potential melastatin 8-mediated facilitation of synaptic strength
67 sitive channel transient receptor potential (melastatin)-8 (TRPM8), heterologously expressed in Chine
68 port that human transient receptor potential melastatin-8 (TRPM8) and an N-terminally truncated TRPM8
69 In the same experimental setup, blocking the melastatin-8 (TRPM8) channel with AMG2850 (30 mg/kg) att
70 imation via the transient receptor potential melastatin-8 (TRPM8) channel without evoking nociceptive
73 diesel exhaust PM > crystalline silica; TRP melastatin-8 is also robustly activated by CFA1, whereas
76 umor suppressive activity is not mediated by melastatin but instead by a microRNA (miR-211) hosted wi
77 human primary cutaneous melanomas examined, melastatin expression appeared to correlate inversely wi
78 ssion pattern observed suggests that loss of melastatin expression is an indicator of melanoma aggres
80 dermal transient receptor potential channel, melastatin family (TRPM) channel GTL-2 and IP(3)R-stimul
85 lcium-permeable channel, transient potential melastatin-like 2 (TRPM2), via stimulation of poly-ADP-r
86 We found that transient receptor potential-melastatin-like 7 (TRPM7) channel expression regulated E
88 l disruption of transient receptor potential-melastatin-like 7 (Trpm7) in mice results in embryonic l
92 ate was 90% +/- 7%, whereas in patients with melastatin loss, the disease-free survival rate was 51%
93 A was 100%, whereas in stage I patients with melastatin loss, the disease-free survival rate was 77%
94 sion criterion, TRP polycystic (P)3, and TPR melastatin (M)8 were found to be uniquely adipospecific.
96 amily includes the putative tumor suppressor melastatin (MLSN) and is a poorly characterized group of
99 erformed to assess the prognostic utility of melastatin mRNA expression while adjusting for other pro
100 udied the relationship between expression of melastatin mRNA in the primary cutaneous tumor and progn
102 I patients whose tumors diffusely expressed melastatin mRNA was 100%, whereas in stage I patients wi
104 II disease whose tumors diffusely expressed melastatin mRNA, the 8-year disease-free survival rate w
105 the mouse are consistent with involvement of melastatin mutations in the mouse ruby-eye-2 defect, con
106 Increasing expression of miR-211 but not melastatin reduced migration and invasion of malignant a
107 that the transient receptor potential (TRP) melastatin related 7 (TRPM7) is the molecular basis of t
108 a member of the transient receptor potential melastatin-related (TRPM) family of cation channels, whi
110 cation channel that belongs to the family of melastatin-related transient receptor potential (TRPM) c
111 ium (Ca(2+))-permeable cation channel of the melastatin-related transient receptor potential (TRPM) i
118 , inhibitors of transient receptor potential melastatin subfamily 4 (TRPM4), intracellular introducti
119 rent carried by transient receptor potential melastatin subfamily 4 channels via type 2 inositol 1,4,
120 mate receptor 6/transient receptor potential melastatin subfamily M member 1-signaling (mGluR6/TRPM1-
121 nsient receptor potential ion channel of the melastatin subfamily, TRPM8, is a major cold receptor in
122 his analysis identified a novel gene, termed melastatin, that is expressed at high levels in poorly m
124 cation channel transient receptor potential melastatin (TRPM) 4 is involved in the control of Ca(2+)
125 lycosylation of transient receptor potential melastatin (Trpm) 4b, a membrane glycoprotein that regul
128 amilies: classical (TRPC), vanilloid (TRPV), melastatin (TRPM), muclopins (TRPML), polycystin (TRPP),
131 studies have demonstrated that expression of melastatin/TRPM1 strongly predicts nonmetastatic propens
133 Mg(2+) channel transient receptor potential melastatin type 6 that determines the final urinary Mg(2
135 dulation of the transient receptor potential melastatin type 8 (TRPM8) is currently under investigati
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