Detalhe da pesquisa
1.
Biophysical mechanisms underlying tefluthrin-induced modulation of gating changes and resurgent current generation in the human Nav1.4 channel.
Pestic Biochem Physiol
; 200: 105833, 2024 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-38582596
2.
Patisiran, an RNAi therapeutic for hereditary transthyretin-mediated amyloidosis: Sub-analysis in Taiwanese patients from the APOLLO study.
J Formos Med Assoc
; 2024 Mar 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-38548524
3.
Growth of B16F10 cells is enhanced in DJ-1-deficiency pancreas.
Biochem Biophys Res Commun
; 682: 359-364, 2023 11 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-37839104
4.
A randomized, placebo-controlled study of givosiran in patients with acute hepatic porphyrias (ENVISION): Final (36-month) analysis of the Taiwan Cohort.
J Formos Med Assoc
; 2023 Dec 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-38044204
5.
FT895 Impairs Mitochondrial Function in Malignant Peripheral Nerve Sheath Tumor Cells.
Int J Mol Sci
; 25(1)2023 Dec 24.
Artigo
em Inglês
| MEDLINE | ID: mdl-38203448
6.
Efficacy of Tafamidis in Patients with Ala97Ser Hereditary Transthyretin Cardiac Amyloidosis: A Six-Month Follow-Up Study.
Acta Cardiol Sin
; 39(4): 619-627, 2023 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-37456942
7.
EXPLORE B: A prospective, long-term natural history study of patients with acute hepatic porphyria with chronic symptoms.
J Inherit Metab Dis
; 45(6): 1163-1174, 2022 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-36069414
8.
Comparison of clinical and neuroimaging features between NOTCH3 mutations and nongenetic spontaneous intracerebral haemorrhage.
Eur J Neurol
; 29(11): 3243-3254, 2022 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-35781912
9.
Cardiac manifestations and prognostic implications of hereditary transthyretin amyloidosis associated with transthyretin Ala97Ser.
J Formos Med Assoc
; 119(3): 693-700, 2020 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-31521469
10.
Changes of Resurgent Na+ Currents in the Nav1.4 Channel Resulting from an SCN4A Mutation Contributing to Sodium Channel Myotonia.
Int J Mol Sci
; 21(7)2020 Apr 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-32276507
11.
The Biophysical Basis Underlying Gating Changes in the p.V1316A Mutant Nav1.7 Channel and the Molecular Pathogenesis of Inherited Erythromelalgia.
PLoS Biol
; 14(9): e1002561, 2016 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-27653502
12.
Sudomotor innervation in transthyretin amyloid neuropathy: Pathology and functional correlates.
Ann Neurol
; 78(2): 272-83, 2015 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-25973863
13.
Growth hormone is increased in the lungs and enhances experimental lung metastasis of melanoma in DJ-1 KO mice.
BMC Cancer
; 16(1): 871, 2016 11 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-27825319
14.
Myopathy associated with COVID-19.
J Formos Med Assoc
; 120(3): 1022-1024, 2021 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-32800405
15.
Increased Histone Deacetylase Activity Involved in the Suppressed Invasion of Cancer Cells Survived from ALA-Mediated Photodynamic Treatment.
Int J Mol Sci
; 16(10): 23994-4010, 2015 Oct 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-26473836
16.
Detrimental effects of intracerebral haemorrhage on patients with CADASIL harbouring NOTCH3 R544C mutation.
J Neurol Neurosurg Psychiatry
; 90(7): 841-843, 2019 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-30309883
17.
Tafamidis improves myocardial longitudinal strain in A97S transthyretin cardiac amyloidosis.
Ther Adv Chronic Dis
; 15: 20406223231222828, 2024.
Artigo
em Inglês
| MEDLINE | ID: mdl-38223905
18.
Use of Technetium-99m-Pyrophosphate Single-Photon Emission Computed Tomography/Computed Tomography in Monitoring Therapeutic Changes of Eplontersen in Patients With Hereditary Transthyretin Amyloid Cardiomyopathy.
J Am Heart Assoc
; 13(2): e030512, 2024 Jan 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-38214277
19.
The influences of reserpine and imipramine on the 5-HT2 receptor binding site and its coupled second messenger in rat cerebral cortex.
Chin J Physiol
; 56(4): 199-208, 2013 Aug 31.
Artigo
em Inglês
| MEDLINE | ID: mdl-23806035
20.
Tafamidis decreased cardiac amyloidosis deposition in patients with Ala97Ser hereditary transthyretin cardiomyopathy: a 12-month follow-up cohort study.
Orphanet J Rare Dis
; 18(1): 289, 2023 09 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-37705003