Detalles de la búsqueda
1.
Null and missense mutations of ERI1 cause a recessive phenotypic dichotomy in humans.
Am J Hum Genet
; 110(7): 1068-1085, 2023 07 06.
Artículo
en Inglés
| MEDLINE | ID: mdl-37352860
2.
Parkin deficiency promotes liver cancer metastasis by TMEFF1 transcription activation via TGF-ß/Smad2/3 pathway.
Acta Pharmacol Sin
; 2024 Mar 22.
Artículo
en Inglés
| MEDLINE | ID: mdl-38519646
3.
Ras inhibitor farnesylthiosalicylic acid conjugated with IR783 dye exhibits improved tumor-targeting and altered anti-breast cancer mechanisms in mice.
Acta Pharmacol Sin
; 43(7): 1843-1856, 2022 Jul.
Artículo
en Inglés
| MEDLINE | ID: mdl-34845369
4.
Spatial learning and memory deficits induced by prenatal glucocorticoid exposure depend on hippocampal CRHR1 and CXCL5 signaling in rats.
J Neuroinflammation
; 18(1): 85, 2021 Apr 02.
Artículo
en Inglés
| MEDLINE | ID: mdl-33810797
5.
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
6.
Isoptericola halalbus sp. nov., a halotolerant actinobacterium isolated from saline lake sediment.
Int J Syst Evol Microbiol
; 70(8): 4661-4667, 2020 Aug.
Artículo
en Inglés
| MEDLINE | ID: mdl-32687463
7.
Paracoccus luteus sp. nov., isolated from the intestine of grass carp.
Int J Syst Evol Microbiol
; 70(1): 543-549, 2020 Jan.
Artículo
en Inglés
| MEDLINE | ID: mdl-31647401
8.
Azospirillum thermophilum sp. nov., isolated from a hot spring.
Int J Syst Evol Microbiol
; 70(1): 550-554, 2020 Jan.
Artículo
en Inglés
| MEDLINE | ID: mdl-31651377
9.
CRH/CRHR1 mediates prenatal synthetic glucocorticoid programming of depression-like behavior across 2 generations.
FASEB J
; 32(8): 4258-4269, 2018 08.
Artículo
en Inglés
| MEDLINE | ID: mdl-29543532
10.
Design, synthesis and structure-activity relationship of diaryl-ureas with novel isoxazol[3,4-b]pyridine-3-amino-structure as multi-target inhibitors against receptor tyrosine kinase.
Bioorg Med Chem
; 26(16): 4735-4744, 2018 09 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-30121211
11.
Investigation of myocardial dysfunction using three-dimensional speckle tracking echocardiography in a genetic positive hypertrophic cardiomyopathy Chinese family.
Cardiol Young
; 28(9): 1106-1114, 2018 Sep.
Artículo
en Inglés
| MEDLINE | ID: mdl-29978770
12.
The Cumulative Effects of the MYH7-V878A and CACNA1C-A1594V Mutations in a Chinese Family with Hypertrophic Cardiomyopathy.
Cardiology
; 138(4): 228-237, 2017.
Artículo
en Inglés
| MEDLINE | ID: mdl-28866666
13.
Improvement of soybean transformation via Agrobacterium tumefaciens methods involving α-aminooxyacetic acid and sonication treatments enlightened by gene expression profile analysis.
Plant Cell Rep
; 35(6): 1259-71, 2016 Jun.
Artículo
en Inglés
| MEDLINE | ID: mdl-26960402
14.
The wheat NHX antiporter gene TaNHX2 confers salt tolerance in transgenic alfalfa by increasing the retention capacity of intracellular potassium.
Plant Mol Biol
; 87(3): 317-27, 2015 Feb.
Artículo
en Inglés
| MEDLINE | ID: mdl-25549607
15.
Studies on [5,6]-Fused Bicyclic Scaffolds Derivatives as Potent Dual B-RafV600E/KDR Inhibitors Using Docking and 3D-QSAR Approaches.
Int J Mol Sci
; 16(10): 24451-74, 2015 Oct 15.
Artículo
en Inglés
| MEDLINE | ID: mdl-26501259
16.
Protective effect of melatonin on bone marrow mesenchymal stem cells against hydrogen peroxide-induced apoptosis in vitro.
J Cell Biochem
; 114(10): 2346-55, 2013 Oct.
Artículo
en Inglés
| MEDLINE | ID: mdl-23824714
17.
Activation of cannabinoid type 2 receptor by JWH133 protects heart against ischemia/reperfusion-induced apoptosis.
Cell Physiol Biochem
; 31(4-5): 693-702, 2013.
Artículo
en Inglés
| MEDLINE | ID: mdl-23711495
18.
[Significance of high sensitivity C-reactive protein level for predicting risk of nonalcoholic fatty liver in type 2 diabetes mellitus patients].
Zhonghua Gan Zang Bing Za Zhi
; 21(1): 57-61, 2013 Jan.
Artículo
en Zh
| MEDLINE | ID: mdl-23663765
19.
[Study on antitumor effect of wutousan].
Zhong Yao Cai
; 36(8): 1301-4, 2013 Aug.
Artículo
en Zh
| MEDLINE | ID: mdl-24558831
20.
[Site-directed mutagenesis and protein expression of SCN5A gene associated with congenital long QT syndrome].
Zhongguo Dang Dai Er Ke Za Zhi
; 15(3): 223-6, 2013 Mar.
Artículo
en Zh
| MEDLINE | ID: mdl-23498767