Detalhe da pesquisa
1.
Usage of compromised lung volume in monitoring steroid therapy on severe COVID-19.
Respir Res;
23(1): 105, 2022 Apr 29.
Artigo
em Inglês
| MEDLINE
| ID: mdl-35488261
2.
Association between LGR4 polymorphisms and peak bone mineral density and body composition.
J Bone Miner Metab;
38(5): 658-669, 2020 Sep.
Artigo
em Inglês
| MEDLINE
| ID: mdl-32399675
3.
Genetic variants in the PLS3 gene are associated with osteoporotic fractures in postmenopausal Chinese women.
Acta Pharmacol Sin;
40(9): 1212-1218, 2019 Sep.
Artigo
em Inglês
| MEDLINE
| ID: mdl-30837644
4.
Reports of 17 Chinese patients with tumor-induced osteomalacia.
J Bone Miner Metab;
35(3): 298-307, 2017 May.
Artigo
em Inglês
| MEDLINE
| ID: mdl-27085966
5.
Association between SNPs and haplotypes in the METTL21C gene and peak bone mineral density and body composition in Chinese male nuclear families.
J Bone Miner Metab;
35(4): 437-447, 2017 Jul.
Artigo
em Inglês
| MEDLINE
| ID: mdl-27628047
6.
Novel mutations of TCIRG1 cause a malignant and mild phenotype of autosomal recessive osteopetrosis (ARO) in four Chinese families.
Acta Pharmacol Sin;
38(11): 1456-1465, 2017 Nov.
Artigo
em Inglês
| MEDLINE
| ID: mdl-28816234
7.
OPG, RANKL, and RANK gene polymorphisms and the bone mineral density response to alendronate therapy in postmenopausal Chinese women with osteoporosis or osteopenia.
Pharmacogenet Genomics;
26(1): 12-9, 2016 Jan.
Artigo
em Inglês
| MEDLINE
| ID: mdl-26426211
8.
Two novel mutations of CLCN7 gene in Chinese families with autosomal dominant osteopetrosis (type II).
J Bone Miner Metab;
34(4): 440-6, 2016 Jul.
Artigo
em Inglês
| MEDLINE
| ID: mdl-26056022
9.
BMP7 gene polymorphisms are not associated with bone mineral density or osteoporotic fractures in postmenopausal Chinese women.
Acta Pharmacol Sin;
37(8): 1076-82, 2016 Aug.
Artigo
em Inglês
| MEDLINE
| ID: mdl-27264311
10.
Calcification of joints and arteries: second report with novel NT5E mutations and expansion of the phenotype.
J Hum Genet;
60(10): 561-4, 2015 Oct.
Artigo
em Inglês
| MEDLINE
| ID: mdl-26178434
11.
The efficacy and safety of weekly 35-mg risedronate dosing regimen for Chinese postmenopausal women with osteoporosis or osteopenia: 1-year data.
Acta Pharmacol Sin;
36(7): 841-6, 2015 Jul.
Artigo
em Inglês
| MEDLINE
| ID: mdl-26051110
12.
Post-genome wide association studies and functional analyses identify association of MPP7 gene variants with site-specific bone mineral density.
Hum Mol Genet;
21(7): 1648-57, 2012 Apr 01.
Artigo
em Inglês
| MEDLINE
| ID: mdl-22171069
13.
Serum osteocalcin levels are inversely associated with plasma glucose and body mass index in healthy Chinese women.
Acta Pharmacol Sin;
35(12): 1521-6, 2014 Dec.
Artigo
em Inglês
| MEDLINE
| ID: mdl-25327813
14.
Identification of a novel mutation in the CLCN5 gene in a Chinese family with Dent-1 disease.
Nephrology (Carlton);
19(2): 80-3, 2014 Feb.
Artigo
em Inglês
| MEDLINE
| ID: mdl-24428215
15.
Association of JAG1 with bone mineral density and osteoporotic fractures: a genome-wide association study and follow-up replication studies.
Am J Hum Genet;
86(2): 229-39, 2010 Feb 12.
Artigo
em Inglês
| MEDLINE
| ID: mdl-20096396
16.
Association of serum 25-hydroxyvitamin D with insulin resistance and ß-cell function in a healthy Chinese female population.
Acta Pharmacol Sin;
34(8): 1070-4, 2013 Aug.
Artigo
em Inglês
| MEDLINE
| ID: mdl-23770983
17.
Association of single nucleotide polymorphism Rs2236518 in PRDM16 gene with BMI in Chinese males.
Acta Pharmacol Sin;
34(5): 710-6, 2013 May.
Artigo
em Inglês
| MEDLINE
| ID: mdl-23524569
18.
Three novel PHEX gene mutations in four Chinese families with X-linked dominant hypophosphatemic rickets.
Biochem Biophys Res Commun;
423(4): 793-8, 2012 Jul 13.
Artigo
em Inglês
| MEDLINE
| ID: mdl-22713460
19.
The virulence gene and clinical phenotypes of osteopetrosis in the Chinese population: six novel mutations of the CLCN7 gene in twelve osteopetrosis families.
J Bone Miner Metab;
30(3): 338-48, 2012 May.
Artigo
em Inglês
| MEDLINE
| ID: mdl-21947783
20.
The identification of novel mutations in COL1A1, COL1A2, and LEPRE1 genes in Chinese patients with osteogenesis imperfecta.
J Bone Miner Metab;
30(1): 69-77, 2012 Jan.
Artigo
em Inglês
| MEDLINE
| ID: mdl-21667357