Detalhe da pesquisa
1.
Gravitational Raman Scattering in Effective Field Theory: A Scalar Tidal Matching at O(G
Phys Rev Lett
; 132(13): 131401, 2024 Mar 29.
Artigo
em Inglês
| MEDLINE | ID: mdl-38613266
2.
Astroglial Kir4.1 in the lateral habenula drives neuronal bursts in depression.
Nature
; 554(7692): 323-327, 2018 02 14.
Artigo
em Inglês
| MEDLINE | ID: mdl-29446379
3.
Role of Ion Channels in the Chemotransduction and Mechanotransduction in Digestive Function and Feeding Behavior.
Int J Mol Sci
; 23(16)2022 Aug 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-36012643
4.
Biallelic loss-of-function mutations in JAM2 cause primary familial brain calcification.
Brain
; 143(2): 491-502, 2020 02 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-31851307
5.
Ultrasonic Control of Neural Activity through Activation of the Mechanosensitive Channel MscL.
Nano Lett
; 18(7): 4148-4155, 2018 07 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-29916253
6.
[Application of mechanosensitive channels in sonogenetics].
Zhejiang Da Xue Xue Bao Yi Xue Ban
; 48(1): 34-38, 2019 05 25.
Artigo
em Zh
| MEDLINE | ID: mdl-31102355
7.
[I1363T mutation induces the defects in fast inactivation of human skeletal muscle voltage-gated sodium channel].
Zhejiang Da Xue Xue Bao Yi Xue Ban
; 48(1): 12-18, 2019 05 25.
Artigo
em Zh
| MEDLINE | ID: mdl-31102352
8.
Identification and Characterization of the Neisseria gonorrhoeae MscS-Like Mechanosensitive Channel.
Infect Immun
; 86(6)2018 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-29581189
9.
Mechanical coupling of the multiple structural elements of the large-conductance mechanosensitive channel during expansion.
Proc Natl Acad Sci U S A
; 112(34): 10726-31, 2015 Aug 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-26261325
10.
N1366S mutation of human skeletal muscle sodium channel causes paramyotonia congenita.
J Physiol
; 595(22): 6837-6850, 2017 11 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-28940424
11.
Tunable circular polarization selective surfaces for low-THz applications using patterned graphene.
Opt Express
; 23(6): 7227-36, 2015 Mar 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-25837067
12.
Mechanosensitive channel MscL gating transitions coupling with constriction point shift.
Protein Sci
; 33(4): e4965, 2024 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-38501596
13.
Clinical analysis and functional characterization of KCNQ2-related developmental and epileptic encephalopathy.
Front Mol Neurosci
; 16: 1205265, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-37497102
14.
Mechanosensitive channel MscL induces non-apoptotic cell death and its suppression of tumor growth by ultrasound.
Front Chem
; 11: 1130563, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-36936526
15.
Clinical comparison and functional study of the L703P: a recurrent mutation in human SCN4A that causes sodium channel myotonia.
Neuromuscul Disord
; 32(10): 811-819, 2022 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-36050252
16.
Differential Functional Changes of Nav1.2 Channel Causing SCN2A-Related Epilepsy and Status Epilepticus During Slow Sleep.
Front Neurol
; 12: 653517, 2021.
Artigo
em Inglês
| MEDLINE | ID: mdl-34093402
17.
Hydrophobic Gate of Mechanosensitive Channel of Large Conductance in Lipid Bilayers Revealed by Solid-State NMR Spectroscopy.
J Phys Chem B
; 125(10): 2477-2490, 2021 03 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-33685127
18.
An open-pore structure of the mechanosensitive channel MscL derived by determining transmembrane domain interactions upon gating.
FASEB J
; 23(7): 2197-204, 2009 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-19261722
19.
Pivotal role of the glycine-rich TM3 helix in gating the MscS mechanosensitive channel.
Nat Struct Mol Biol
; 12(2): 113-9, 2005 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-15665866
20.
Electrophysiological features: The next precise step for SCN2A developmental epileptic encephalopathy.
Mol Genet Genomic Med
; 8(7): e1250, 2020 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-32400968