Detalhe da pesquisa
1.
Novel, pathogenic insertion variant of GSDME associates with autosomal dominant hearing loss in a large Chinese pedigree.
J Cell Mol Med
; 28(1): e18004, 2024 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-37864300
2.
Transcript isoforms of Reep6 have distinct functions in the retina.
Hum Mol Genet
; 30(21): 1907-1918, 2021 10 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-34104971
3.
HSPA6 and its role in cancers and other diseases.
Mol Biol Rep
; 49(11): 10565-10577, 2022 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-35666422
4.
Impact of TMPRSS2 Expression, Mutation Prognostics, and Small Molecule (CD, AD, TQ, and TQFL12) Inhibition on Pan-Cancer Tumors and Susceptibility to SARS-CoV-2.
Molecules
; 27(21)2022 Nov 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-36364238
5.
Prostate adenocarcinoma and COVID-19: The possible impacts of TMPRSS2 expressions in susceptibility to SARS-CoV-2.
J Cell Mol Med
; 25(8): 4157-4165, 2021 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-33609069
6.
TQFL12, a novel synthetic derivative of TQ, inhibits triple-negative breast cancer metastasis and invasion through activating AMPK/ACC pathway.
J Cell Mol Med
; 25(21): 10101-10110, 2021 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-34609056
7.
Noncoding mutation in RPGRIP1 contributes to inherited retinal degenerations.
Mol Vis
; 27: 95-106, 2021.
Artigo
em Inglês
| MEDLINE | ID: mdl-33907365
8.
Technical note: multi-alleles at the DYS385ab locus with high frequency in a Han Chinese population from southwestern China.
Int J Legal Med
; 135(5): 1737-1741, 2021 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-33844081
9.
A novel, homozygous nonsense variant of the CDHR1 gene in a Chinese family causes autosomal recessive retinal dystrophy by NGS-based genetic diagnosis.
J Cell Mol Med
; 22(11): 5662-5669, 2018 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-30160356
10.
Identification of a novel RPGRIP1 mutation in an Iranian family with leber congenital amaurosis by exome sequencing.
J Cell Mol Med
; 22(3): 1733-1742, 2018 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-29193763
11.
A novel homozygous variant of GPR98 causes usher syndrome type IIC in a consanguineous Chinese family by next generation sequencing.
BMC Med Genet
; 19(1): 99, 2018 06 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-29890953
12.
A novel splicing mutation in the PRPH2 gene causes autosomal dominant retinitis pigmentosa in a Chinese pedigree.
J Cell Mol Med
; 23(5): 3776-3780, 2019 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-30892800
13.
Two years of a pilot virtual melanoma education program for adolescents in Texas: Assessing knowledge gaps and demographic disparities.
Proc (Bayl Univ Med Cent)
; 37(2): 361-365, 2024.
Artigo
em Inglês
| MEDLINE | ID: mdl-38343485
14.
Skin, hair, and nail supplements advertised on Instagram.
Proc (Bayl Univ Med Cent)
; 36(1): 38-40, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-36578583
15.
Telehealth reform post-public health emergency: crucial next steps.
Proc (Bayl Univ Med Cent)
; 36(2): 269-271, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-36876246
16.
Mental health trends among medical students.
Proc (Bayl Univ Med Cent)
; 36(3): 408-410, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-37091765
17.
Novel pathogenic CERKL variant in Iranian familial with inherited retinal dystrophies: genotype-phenotype correlation.
3 Biotech
; 13(6): 166, 2023 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-37162806
18.
Demographics of Skin Cancer Knowledge Among Middle and High Schoolers in Texas.
Dermatol Pract Concept
; 13(1)2023 01 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-36892336
19.
Isotretinoin, Vitamin A Supplements, and Unintended Pregnancies in Post Roe v. Wade America.
Cureus
; 14(11): e31442, 2022 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-36523684
20.
A novel stop codon mutation of TSPAN12 gene in Chinese patients with familial exudative vitreoretinopathy.
Ophthalmic Genet
; 43(2): 210-217, 2022 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-34738848