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1.
Hesperetin Induces Autophagy and Delayed Apoptosis by Modulating the AMPK/Akt/mTOR Pathway in Human Leukemia Cells In Vitro.
Curr Issues Mol Biol
; 45(2): 1587-1600, 2023 Feb 13.
Artículo
en Inglés
| MEDLINE | ID: mdl-36826047
2.
Origin and timing of de novo variants implicated in type 2 von Willebrand disease.
J Cell Mol Med
; 26(21): 5403-5413, 2022 11.
Artículo
en Inglés
| MEDLINE | ID: mdl-36226571
3.
Deep vein thrombosis after major orthopedic surgery in Taiwan: A prospective cross-sectional study and literature review.
J Formos Med Assoc
; 121(8): 1541-1549, 2022 Aug.
Artículo
en Inglés
| MEDLINE | ID: mdl-35033412
4.
Clinical features and genetic defect in six index patients with congenital fibrinogen disorders: Three novel mutations with one common mutation in Taiwan's population.
Haemophilia
; 27(6): 1022-1027, 2021 Nov.
Artículo
en Inglés
| MEDLINE | ID: mdl-34460979
5.
Pitavastatin and metformin synergistically activate apoptosis and autophagy in pancreatic cancer cells.
Environ Toxicol
; 36(8): 1491-1503, 2021 Aug.
Artículo
en Inglés
| MEDLINE | ID: mdl-33886150
6.
Butein induces cellular senescence through reactive oxygen species-mediated p53 activation in osteosarcoma U-2 OS cells.
Environ Toxicol
; 36(5): 773-781, 2021 May.
Artículo
en Inglés
| MEDLINE | ID: mdl-33325610
7.
Acquired FXIII inhibitor: Patient characteristics and treatment outcome, a case series in Taiwan.
J Formos Med Assoc
; 120(1 Pt 2): 411-414, 2021 Jan.
Artículo
en Inglés
| MEDLINE | ID: mdl-32513506
8.
Inherited coagulation factor VII deficiency in Taiwan: Two novel F7 variants with relevant regional features in 33 patients.
Haemophilia
; 2024 May 23.
Artículo
en Inglés
| MEDLINE | ID: mdl-38783550
9.
A common polymorphism decreases LRP1 mRNA stability and is associated with increased plasma factor VIII levels.
Biochim Biophys Acta Mol Basis Dis
; 1863(6): 1690-1698, 2017 06.
Artículo
en Inglés
| MEDLINE | ID: mdl-28431990
10.
A distinct common p.Gln317* mutation among causative LMAN1 genetic mutations of combined factor V and factor VIII deficiency in five Taiwanese families.
Haemophilia
; 28(1): e28-e31, 2022 Jan.
Artículo
en Inglés
| MEDLINE | ID: mdl-34766420
11.
Shortened Activated Partial Thromboplastin Time Is Associated With Acute Ischemic Stroke, Stroke Severity, and Neurological Worsening.
J Stroke Cerebrovasc Dis
; 24(10): 2270-6, 2015 Oct.
Artículo
en Inglés
| MEDLINE | ID: mdl-26169548
12.
Azacitidine-Hesperetin Combination Induces S-phase Cell Cycle Arrest and Apoptosis in Human Leukemia Cells.
Anticancer Res
; 44(3): 1033-1044, 2024 Mar.
Artículo
en Inglés
| MEDLINE | ID: mdl-38423637
13.
The impact factors on the cost and length of stay among acute ischemic stroke.
J Stroke Cerebrovasc Dis
; 22(7): e152-8, 2013 Oct.
Artículo
en Inglés
| MEDLINE | ID: mdl-23253537
14.
Congenital factor V deficiency in Taiwan: identification of a novel variant p.Tyr1813 ∗ and two variants specific to East Asians.
Blood Coagul Fibrinolysis
; 34(1): 8-13, 2023 Jan 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-35946468
15.
A large family of hereditary spherocytosis and a rare case of hereditary elliptocytosis with a novel SPTA1 mutation underdiagnosed in Taiwan: A case report and literature review.
Medicine (Baltimore)
; 102(4): e32708, 2023 Jan 27.
Artículo
en Inglés
| MEDLINE | ID: mdl-36705355
16.
Negative impact of the hypopnea index or duration increase after a non-frame work surgery in patients with very severe obstructive sleep apnea.
Sci Rep
; 12(1): 2251, 2022 02 10.
Artículo
en Inglés
| MEDLINE | ID: mdl-35145170
17.
Respiratory Arousals in Patients with Very Severe Obstructive Sleep Apnea and How They Change after a Non-Framework Surgery.
Healthcare (Basel)
; 10(5)2022 May 13.
Artículo
en Inglés
| MEDLINE | ID: mdl-35628039
18.
Electrophysiological features of Hirayama disease.
Muscle Nerve
; 44(2): 185-90, 2011 Aug.
Artículo
en Inglés
| MEDLINE | ID: mdl-21755506
19.
First reported case of congenital thrombotic thrombocytopenic purpura in Taiwan with novel mutation of ADAMTS13 gene.
Int J Hematol
; 113(5): 760-764, 2021 May.
Artículo
en Inglés
| MEDLINE | ID: mdl-33387295
20.
A family with an MYH9-related disorder with different phenotypes masquerading as immune thrombocytopaenia: an underreported disorder in Taiwan.
Int J Hematol
; 112(6): 878-882, 2020 Dec.
Artículo
en Inglés
| MEDLINE | ID: mdl-32712863