Detalhe da pesquisa
1.
Overexpression of AQP5 Was Detected in Axillary Sweat Glands of Primary Focal Hyperhidrosis Patients.
Dermatology
; 232(2): 150-5, 2016.
Artigo
em Inglês
| MEDLINE | ID: mdl-26930592
2.
Abnormal function of EPHA2/p.R957P mutant in congenital cataract.
Int J Ophthalmol
; 17(6): 1007-1017, 2024.
Artigo
em Inglês
| MEDLINE | ID: mdl-38895685
3.
A novel mutation impairing the tertiary structure and stability of γC-crystallin (CRYGC) leads to cataract formation in humans and zebrafish lens.
Hum Mutat
; 33(2): 391-401, 2012 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-22052681
4.
A recognition survey of granular corneal dystrophy type 2 genetic detection in China.
Int J Ophthalmol
; 13(12): 1976-1982, 2020.
Artigo
em Inglês
| MEDLINE | ID: mdl-33344199
5.
[A novel PAX6 mutation (c.1286delC) in the patients with hereditary congenital aniridia.].
Yi Chuan
; 30(10): 1301-6, 2008 Oct.
Artigo
em Zh
| MEDLINE | ID: mdl-18930890
6.
A recurrent G367R mutation in MYOC associated with juvenile open angle glaucoma in a large Chinese family.
Int J Ophthalmol
; 11(3): 369-374, 2018.
Artigo
em Inglês
| MEDLINE | ID: mdl-29600168
7.
[Rapid genetic screening of Leber's hereditary optic neuropathy with mtDNA G11778A mutation by AS-PCR with whole blood].
Zhonghua Yan Ke Za Zhi
; 41(3): 243-5, 2005 Mar.
Artigo
em Zh
| MEDLINE | ID: mdl-15840367
8.
Efficient removal of uranium from aqueous solution by zero-valent iron nanoparticle and its graphene composite.
J Hazard Mater
; 290: 26-33, 2015 Jun 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-25734531
9.
Formation of N-heterocyclic diphosphine ligands from Ag(I)-assisted condensation reactions between bdppeda and formaldehyde and their binuclear silver(I) complexes.
Dalton Trans
; 41(27): 8447-54, 2012 Jul 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-22647979
10.
[Expression of recombinant human BMP-6 in Escherichia coli and its purification and bioassay in vitro].
Sheng Wu Gong Cheng Xue Bao
; 19(5): 556-60, 2003 Sep.
Artigo
em Zh
| MEDLINE | ID: mdl-15969083