Detalles de la búsqueda
1.
[Analysis of phenotype and MYH7 gene variant in a family of patients with hypertrophic cardiomyopathy].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
; 39(8): 873-876, 2022 Aug 10.
Artículo
en Zh
| MEDLINE | ID: mdl-35929939
2.
Predictors of cardiac involvement and survival in patients with primary systemic light-chain amyloidosis: roles of the clinical, chemical, and 3-D speckle tracking echocardiography parameters.
BMC Cardiovasc Disord
; 21(1): 43, 2021 01 21.
Artículo
en Inglés
| MEDLINE | ID: mdl-33478398
3.
Gender- and age-related differences in distinct phenotypes of hypertrophic cardiomyopathy-associated mutation MYBPC3-E334K.
Heart Vessels
; 36(10): 1525-1535, 2021 Oct.
Artículo
en Inglés
| MEDLINE | ID: mdl-33830315
4.
Quantitative Analysis of Left Ventricular Flow Dynamics in Latent Obstructive Hypertrophic Cardiomyopathy Using Vector Flow Mapping.
Cardiology
; 145(4): 227-235, 2020.
Artículo
en Inglés
| MEDLINE | ID: mdl-32097929
5.
[Analysis of genotype-phenotype correlation for a novel MYH7-D554Y mutation identified in an ethnic Han Chinese pedigree affected with hypertrophic cardiomyopathy].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
; 35(5): 667-671, 2018 Oct 10.
Artículo
en Zh
| MEDLINE | ID: mdl-30298491
6.
East Asian-Specific Common Variant in TNNI3 Predisposes to Hypertrophic Cardiomyopathy.
Circulation
; 142(21): 2086-2089, 2020 11 24.
Artículo
en Inglés
| MEDLINE | ID: mdl-33078954
7.
Efficacy and safety of 1550-nm fractional laser in the treatment of acne scars in Chinese patients: A split-face comparative study.
J Cosmet Laser Ther
; 18(6): 312-6, 2016 Oct.
Artículo
en Inglés
| MEDLINE | ID: mdl-27183153
8.
Efficacy and safety of fractional Q-switched 1064-nm neodymium-doped yttrium aluminum garnet laser in the treatment of melasma in Chinese patients.
Lasers Med Sci
; 31(8): 1657-1663, 2016 Nov.
Artículo
en Inglés
| MEDLINE | ID: mdl-27450275
9.
Intermittent hypoxia preconditioning-induced epileptic tolerance by upregulation of monocarboxylate transporter 4 expression in rat hippocampal astrocytes.
Neurochem Res
; 39(11): 2160-9, 2014 Nov.
Artículo
en Inglés
| MEDLINE | ID: mdl-25146899
10.
SurfPro-NN: A 3D point cloud neural network for the scoring of protein-protein docking models based on surfaces features and protein language models.
Comput Biol Chem
; : 108067, 2024 Apr 04.
Artículo
en Inglés
| MEDLINE | ID: mdl-38714420
11.
The computational rules of cross-modality suppression in the visual posterior sylvian area.
iScience
; 26(6): 106973, 2023 Jun 16.
Artículo
en Inglés
| MEDLINE | ID: mdl-37378331
12.
Monkey plays Pac-Man with compositional strategies and hierarchical decision-making.
Elife
; 112022 03 14.
Artículo
en Inglés
| MEDLINE | ID: mdl-35286255
13.
Revealing nonlinear neural decoding by analyzing choices.
Nat Commun
; 12(1): 6557, 2021 11 16.
Artículo
en Inglés
| MEDLINE | ID: mdl-34785652
14.
Vitiligo Skin Biomarkers Associated With Favorable Therapeutic Response.
Front Immunol
; 12: 613031, 2021.
Artículo
en Inglés
| MEDLINE | ID: mdl-33815367
15.
FSTL1-USP10-Notch1 Signaling Axis Protects Against Cardiac Dysfunction Through Inhibition of Myocardial Fibrosis in Diabetic Mice.
Front Cell Dev Biol
; 9: 757068, 2021.
Artículo
en Inglés
| MEDLINE | ID: mdl-34957094
16.
Clinical and molecular characterization of seven patients with Danon disease.
Exp Ther Med
; 21(4): 395, 2021 Apr.
Artículo
en Inglés
| MEDLINE | ID: mdl-33680117
17.
Early Onset of Combined Oxidative Phosphorylation Deficiency in Two Chinese Brothers Caused by a Homozygous (Leu275Phe) Mutation in the C1QBP Gene.
Front Pediatr
; 8: 583047, 2020.
Artículo
en Inglés
| MEDLINE | ID: mdl-33344382
18.
A Peptide-Functionalized Magnetic Nanoplatform-Loaded Melatonin for Targeted Amelioration of Fibrosis in Pressure Overload-Induced Cardiac Hypertrophy.
Int J Nanomedicine
; 15: 1321-1333, 2020.
Artículo
en Inglés
| MEDLINE | ID: mdl-32161461
19.
Genetic analysis of monoallelic double MYH7 mutations responsible for familial hypertrophic cardiomyopathy.
Mol Med Rep
; 20(6): 5229-5238, 2019 Dec.
Artículo
en Inglés
| MEDLINE | ID: mdl-31638223
20.
Novel phenotype-genotype correlations of hypertrophic cardiomyopathy caused by mutation in α-actin and myosin-binding protein genes in three unrelated Chinese families.
J Cardiol
; 73(5): 438-444, 2019 05.
Artículo
en Inglés
| MEDLINE | ID: mdl-30600190