Detalhe da pesquisa
1.
Osthole inhibits the migration and invasion of highly metastatic breast cancer cells by suppressing ITGα3/ITGß5 signaling.
Acta Pharmacol Sin
; 43(6): 1544-1555, 2022 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-34426644
2.
LncRNA MAFG-AS1 facilitates the migration and invasion of NSCLC cell via sponging miR-339-5p from MMP15.
Cell Biol Int
; 43(4): 384-393, 2019 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-30599080
3.
The Significance of Crochetage on the R wave of an Electrocardiogram for the Early Diagnosis of Pediatric Secundum Atrial Septal Defect.
Pediatr Cardiol
; 39(5): 1031-1035, 2018 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-29564520
4.
Novel mutations in FKBP10 in Chinese patients with osteogenesis imperfecta and their treatment with zoledronic acid.
J Hum Genet
; 62(2): 205-211, 2017 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-27762305
5.
Novel Mutations in SERPINF1 Result in Rare Osteogenesis Imperfecta Type VI.
Calcif Tissue Int
; 100(1): 55-66, 2017 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-27796462
6.
Wenshen Zhuanggu formula effectively suppresses breast cancer bone metastases in a mouse Xenograft model.
Acta Pharmacol Sin
; 38(10): 1369-1380, 2017 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-28414206
7.
Two novel mutations in TMEM38B result in rare autosomal recessive osteogenesis imperfecta.
J Hum Genet
; 61(6): 539-45, 2016 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-26911354
8.
THE CLINICAL CHARACTERISTICS AND EFFICACY OF BISPHOSPHONATES IN AUDLT PATIENTS WITH OSTEOGENESIS IMPERGECTA.
Endocr Pract
; 22(11): 1267-1276, 2016 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-27482615
9.
Alteration of gene expression profiling including GPR174 and GNG2 is associated with vasovagal syncope.
Pediatr Cardiol
; 36(3): 475-80, 2015 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-25367286
10.
[Attenuation and mechanism of endoplasmic reticulum stress-mediated hepatocyte apoptosis in rats with alcohol-induced liver injury by qinggan huoxue recipe and its disassembled formulas].
Zhongguo Zhong Xi Yi Jie He Za Zhi
; 31(5): 653-8, 2011 May.
Artigo
em Chinês
| MEDLINE | ID: mdl-21812268
11.
[Role of PERK/eIF2a signaling pathway in hepatocyte apoptosis of alcoholic liver injury rats].
Zhonghua Gan Zang Bing Za Zhi
; 18(10): 768-72, 2010 Oct.
Artigo
em Chinês
| MEDLINE | ID: mdl-21059295
12.
Characterization of the complete chloroplast genome of Calophaca sinica Rehd.
Mitochondrial DNA B Resour
; 5(1): 614-615, 2020 Jan 14.
Artigo
em Inglês
| MEDLINE | ID: mdl-33366671
13.
[Clinical investigation of the clinical management and therapeutic strategies to the first human case infected by influenza A/H5N1 in Guizhou Province].
Zhonghua Jie He He Hu Xi Za Zhi
; 32(5): 342-6, 2009 May.
Artigo
em Chinês
| MEDLINE | ID: mdl-19799067
14.
[A discussion about the tactics of mechanical ventilation for acute respiratory distress occurring in the first case of influenza A (H5N1) in Guizhou Province].
Zhongguo Wei Zhong Bing Ji Jiu Yi Xue
; 21(4): 237-9, 2009 Apr.
Artigo
em Chinês
| MEDLINE | ID: mdl-19374794
15.
Confinement of polysulfides within bi-functional metal-organic frameworks for high performance lithium-sulfur batteries.
Nanoscale
; 10(6): 2774-2780, 2018 Feb 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-29323375
16.
Extremely low level of serum pigment epithelium-derived factor is a special biomarker of Chinese osteogenesis imperfecta patients with SERPINF1 mutations.
Clin Chim Acta
; 478: 216-221, 2018 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-29104038
17.
A novel mutation in CLDN16 results in rare familial hypomagnesaemia with hypercalciuria and nephrocalcinosis in a Chinese family.
Clin Chim Acta
; 457: 69-74, 2016 Jun 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-27067446
18.
The analysis of DKK1 polymorphisms in relation to skeletal phenotypes and bone response to alendronate treatment in Chinese postmenopausal women.
Pharmacogenomics
; 17(3): 209-17, 2016 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-26780085
19.
A cryptic balanced translocation involving COL1A2 gene disruption cause a rare type of osteogenesis imperfecta.
Clin Chim Acta
; 460: 33-9, 2016 Sep 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-27312322
20.
[Association between the polymorphism of GNB3C825T gene and vasovagal syncope in children].
Zhonghua Er Ke Za Zhi
; 48(12): 896-9, 2010 Dec.
Artigo
em Chinês
| MEDLINE | ID: mdl-21215181