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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.
5 cascade and the transient receptor potential melastatin 1 (TRPM1) cation channel.
6 metabotropic glutamate receptor 6 to the TRP melastatin 1 (TRPM1) channel to transmit signals from ph
7 aining G(alphao), and the cation channel TRP melastatin 1 (TRPM1).
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
10                 Transient receptor potential melastatin-1 (TRPM1) is essential for the light-induced
11 try (SOCE), the transient receptor potential melastatin 2 (TRPM2) channel contributes to Ca(2+) relea
12 try through the transient receptor potential melastatin 2 (TRPM2) channel in macrophages.
13                 Transient receptor potential melastatin 2 (TRPM2) channel is known to be a cellular r
14             The transient receptor potential melastatin 2 (TRPM2) channel plays a key role in redox s
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
19                 Transient receptor potential melastatin 2 (TRPM2) ion channel has an essential functi
20                 Transient Receptor Potential Melastatin 2 (TRPM2) is a Ca(2+)-permeable cation channe
21                 Transient receptor potential melastatin 2 (TRPM2) is a Ca(2+)-permeable cation channe
22                 Transient Receptor Potential Melastatin 2 (TRPM2) is a Ca(2+)-permeable channel gated
23                 Transient receptor potential melastatin 2 (TRPM2) is a calcium-permeable channel acti
24                 Transient Receptor Potential Melastatin 2 (TRPM2) is a cation channel important for t
25         Transient receptor potential channel melastatin 2 (TRPM2) is highly expressed in cancer and h
26  cation channel transient receptor potential melastatin 2 (TRPM2) plays a key role in pathogen-evoked
27 rmeable channel Transient Receptor Potential Melastatin 2 (TRPM2).
28 tella vectensis Transient Receptor Potential Melastatin 2), the species variant of the human apoptosi
29             The transient potential receptor melastatin-2 (TRPM2) channel has emerged as an important
30 DP ribose opens transient receptor potential melastatin-2 (TRPM2) channels in endothelial cells leadi
31                 Transient Receptor Potential Melastatin-2 (TRPM2) ion channel is emerging as a great
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
37                 Transient receptor potential melastatin 3 (TRPM3) channels are activated by heat, and
38                 Transient Receptor Potential Melastatin 3 (TRPM3) is a Ca(2+) permeable non-selective
39                 Transient receptor potential melastatin 3 (TRPM3) is a calcium-permeable nonselective
40                 Transient receptor potential melastatin 3 (TRPM3) is a heat-activated ion channel exp
41                 Transient receptor potential melastatin 3 (TRPM3) is a nonselective cation channel th
42                 Transient receptor potential melastatin 3 ion channel (TRPM3) belongs to the TRP fami
43  stimulation of transient receptor potential melastatin-3 (TRPM3) channels.
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
47             The transient receptor potential melastatin 4 (TRPM4) channel contributes to disease seve
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
50 ltage-dependent transient receptor potential melastatin 4 (TRPM4) channels.
51                 Transient receptor potential melastatin 4 (TRPM4) is a Ca(2+) -activated nonselective
52           Transient receptor potential (TRP) melastatin 4 (TRPM4) is a widely expressed cation channe
53 dently enhances transient receptor potential melastatin 4 (TRPM4), a Ca2+-activated nonselective (CAN
54 bly of Sur1 and transient receptor potential melastatin 4 (Trpm4).
55 )1.6, and transient receptor potential [TRP] melastatin 4 [TRPM4]) both regulate excitability and gen
56           Transient receptor potential (TRP) melastatin 4 and 5 (TRPM4 and TRPM5), two calcium-activa
57 ucted by TRPM4 (transient receptor potential melastatin 4) channels in native cerebral artery smooth
58 a-gustducin and transient receptor potential melastatin 5.
59 n and restoring transient receptor potential melastatin 6 expression in the DCT.
60 n, and restored transient receptor potential melastatin 6 expression.
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
64 n activates the transient receptor potential melastatin 7 (TRPM7) channel.
65                 Transient receptor potential melastatin 7 (TRPM7) channels are novel Ca(2+)-permeable
66 n DIO acting on transient receptor potential melastatin 7 (Trpm7) channels in CB.
67                 Transient receptor potential melastatin 7 (TRPM7) channels represent the major magnes
68                 Transient receptor potential melastatin 7 (TRPM7) is a bifunctional protein containin
69                 Transient receptor potential melastatin 7 (TRPM7) is a broadly expressed, non-selecti
70                 Transient receptor potential melastatin 7 (TRPM7) is a divalent ion channel with a C-
71                 Transient receptor potential melastatin 7 (TRPM7) is a newly found gene essential to
72   ABSTRACT: The transient receptor potential melastatin 7 (TRPM7) is a protein that combines an ion c
73                 Transient receptor potential melastatin 7 (TRPM7) is a ubiquitously expressed Mg(2+)-
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 (
78 of MSCs through Transient receptor potential melastatin 7 (TRPM7)-Osterix axis.
79 ermeable TRPM7 (transient receptor potential melastatin 7) channels.
80          TRPM7 (transient-receptor-potential melastatin 7) is an ion channel with alpha-kinase functi
81 enthol receptor transient receptor potential melastatin 8 (TRPM8) and compared its behavior with that
82                 Transient receptor potential melastatin 8 (TRPM8) and transient receptor potential va
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
85             The transient receptor potential melastatin 8 (TRPM8) channel is the primary molecular tr
86 nthol-activated transient receptor potential melastatin 8 (TRPM8) channels are thought to be regulate
87                 Transient receptor potential melastatin 8 (TRPM8) channels are well known as sensors
88 nthol-activated transient receptor potential melastatin 8 (TRPM8) channels diminishes over time in th
89 nthol-activated transient receptor potential melastatin 8 (TRPM8) channels.
90             The transient receptor potential melastatin 8 (TRPM8) ion channel is a major sensor of en
91             The transient receptor potential melastatin 8 (TRPM8) ion channel is a major sensor of en
92             The transient receptor potential melastatin 8 (TRPM8) ion channel is the primary detector
93                 Transient receptor potential melastatin 8 (TRPM8) ion channel represents a valuable p
94  interacts with transient receptor potential melastatin 8 (TRPM8) ion channels in cold-sensitive sens
95 nthol-sensitive transient receptor potential melastatin 8 (TRPM8) ion channels.
96                 Transient receptor potential melastatin 8 (TRPM8) is a nonselective cation channel ex
97                 Transient receptor potential melastatin 8 (TRPM8) is a temperature- and menthol-sensi
98                 Transient receptor potential melastatin 8 (TRPM8) is crucially involved in pain modul
99                        One such channel--TRP melastatin 8 (TRPM8) or cold and menthol receptor 1 (CMR
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
104 enthol receptor transient receptor potential melastatin 8 (TRPM8).
105 d-gated channel transient receptor potential melastatin 8 (TRPM8).
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
109 receptor TRPM8 (transient receptor potential melastatin 8) on trigeminal afferents.
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
116 tagonist of the transient receptor potential melastatin-8 (TRPM8) channel.
117                 Transient Receptor Potential Melastatin-8 (TRPM8), a recently identified member of th
118  diesel exhaust PM > crystalline silica; TRP melastatin-8 is also robustly activated by CFA1, whereas
119 man melanomas characterized by low levels of melastatin and miR-211.
120 further divided into TRPC (canonical), TRPM (melastatin), and TRPV (vanilloid) subfamilies.
121 umor suppressive activity is not mediated by melastatin but instead by a microRNA (miR-211) hosted wi
122                 Transient receptor potential melastatin channel subfamily member 2 (TRPM2) has an ess
123                                      The TRP melastatin channels TRPM2 and TRPM3 have a role in pain
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
126 n, whereas primary melanomas showed variable melastatin expression.
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
129                                          The melastatin-family transient receptor potential 2 (TRPM2)
130                                    The mouse melastatin gene contains 27 exons and spans at least 58
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
133 a member of the Transient-Receptor-Potential Melastatin ion channel family.
134                                              Melastatin is greatly downregulated in metastatic melano
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
137        The gene transient receptor potential-melastatin-like 7 (Trpm7) encodes a protein that functio
138 l disruption of transient receptor potential-melastatin-like 7 (Trpm7) in mice results in embryonic l
139                 Transient receptor potential melastatin-like 7 (TRPM7) is a channel protein that also
140                 Transient receptor potential melastatin-like 7 channel (TRPM7) is a ubiquitous, const
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.
145                 Transient receptor potential melastatin member 4 (TRPM4) channels are nonselective mo
146 reen identified transient receptor potential melastatin member 4 (TRPM4), a calcium-activated, ATP-in
147             The transient receptor potential melastatin member 7 (TRPM7) and member 6 (TRPM6) are div
148                 Transient receptor potential melastatin member 8 (TRPM8) is a calcium ion (Ca(2+))-pe
149           Transient receptor potential (TRP) melastatin member 8 (TRPM8), which is a calcium-permeabl
150 ceptor potential cation channel subfamily M (melastatin) member 8 play a crucial role.
151 amily includes the putative tumor suppressor melastatin (MLSN) and is a poorly characterized group of
152                                              Melastatin (MLSN-1), a novel melanocyte-specific gene re
153                                      Uniform melastatin mRNA expression in the primary tumor was corr
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
156                            Downregulation of melastatin mRNA in the primary cutaneous tumor is a prog
157  I patients whose tumors diffusely expressed melastatin mRNA was 100%, whereas in stage I patients wi
158                                              Melastatin mRNA was evaluated by in situ hybridization i
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
161  terminus domain (CTD) of the cold-activated melastatin receptor channel, TRPM8.
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
165             The transient receptor potential melastatin-related channel 2 (TRPM2) is a nonselective c
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
168           TRPM6 and TRPM7 are members of the melastatin-related transient receptor potential (TRPM) s
169                                              Melastatin-related transient receptor potential channel
170                                          The melastatin-related transient receptor potential channel
171 variants in the transient receptor potential melastatin-related type 3 gene (TRPM3) have been associa
172                         Used in combination, melastatin status and tumor thickness allow for the iden
173          Multivariate analysis revealed that melastatin status, mitotic rate, and tumor thickness inf
174 nsient receptor potential ion channel in the melastatin subfamily (TRPM(PZQ))-however, little is know
175                                          The melastatin subfamily (TRPM) channels have N-terminal dom
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
180                                          The melastatin subfamily of the transient receptor potential
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
183             The transient receptor potential melastatin-subfamily member 7 (TRPM7) is a ubiquitously
184 his analysis identified a novel gene, termed melastatin, that is expressed at high levels in poorly m
185                                              Melastatin transcripts were not detected in melanoma met
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
188                 Transient receptor potential melastatin (TRPM) cation channels are polymodal sensors
189    Finally, two transient receptor potential melastatin (TRPM) channels, GON-2 and GTL-2, mediate thi
190                                      The TRP-melastatin (TRPM) subfamily includes the putative tumor
191             The transient receptor potential melastatin (TRPM) tetrameric cation channels are involve
192 amilies: classical (TRPC), vanilloid (TRPV), melastatin (TRPM), muclopins (TRPML), polycystin (TRPP),
193             The transient receptor potential melastatin (TRPM)-3 channel is critical for various phys
194 h in turn opens transient receptor potential melastatin (TRPM)2 channels.
195 studies have demonstrated that expression of melastatin/TRPM1 strongly predicts nonmetastatic propens
196             The transient receptor potential melastatin type 6 (TRPM6) epithelial Mg(2+) channels par
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
199             The transient receptor potential melastatin type 8 (TRPM8) is a nonselective cation chann
200 dulation of the transient receptor potential melastatin type 8 (TRPM8) is currently under investigati
201                                              Melastatin was also found to be differentially expressed
202           Benign nevi express high levels of melastatin, whereas primary melanomas showed variable me
203          We recently described a novel gene, melastatin, whose expression is inversely correlated wit

 
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