Detalhe da pesquisa
1.
A Mettl16/m6A/mybl2b/Igf2bp1 axis ensures cell cycle progression of embryonic hematopoietic stem and progenitor cells.
EMBO J
; 43(10): 1990-2014, 2024 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-38605226
2.
Association between quality of discharge teaching and self-management in patients after percutaneous coronary intervention: A chain mediation model.
J Clin Nurs
; 2024 May 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-38764246
3.
A novel homozygous mutation in ACTL7A leads to male infertility.
Mol Genet Genomics
; 298(2): 353-360, 2023 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-36574082
4.
Coexistence of tet(A) and blaKPC-2 in the ST11 hypervirulent tigecycline- and carbapenem-resistant Klebsiella pneumoniae isolated from a blood sample.
Eur J Clin Microbiol Infect Dis
; 42(1): 23-31, 2023 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-36322255
5.
Mutation in nuclear pore component NUP155 leads to atrial fibrillation and early sudden cardiac death.
Cell
; 135(6): 1017-27, 2008 Dec 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-19070573
6.
Actl7a deficiency in mice leads to male infertility and fertilization failure.
Biochem Biophys Res Commun
; 623: 154-161, 2022 10 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-35921706
7.
Two novel STAT1 mutations cause Mendelian susceptibility to mycobacterial disease.
Biochem Biophys Res Commun
; 591: 124-129, 2022 02 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-34815077
8.
A novel microdeletion upstream of HOXD13 in a Chinese family with synpolydactyly.
Am J Med Genet A
; 188(1): 31-36, 2022 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-34467619
9.
Potential Genes Associated with COVID-19 and Comorbidity.
Int J Med Sci
; 19(2): 402-415, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-35165525
10.
Comparison of the effectiveness and safety of insulin and oral hypoglycemic drugs in the treatment of gestational diabetes mellitus: a meta-analysis of 26 randomized controlled trials.
Gynecol Endocrinol
; 38(4): 303-309, 2022 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-34907818
11.
Novel mutations in ZP2 and ZP3 cause female infertility in three patients.
J Assist Reprod Genet
; 39(5): 1205-1215, 2022 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-35366744
12.
Inhibition of gastric cancer cell apoptosis by long noncoding RNA TRPM2-AS via mitogen-activated protein kinase and activators of transduction-3.
J Gastroenterol Hepatol
; 36(1): 186-195, 2021 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-32424838
13.
Human intracellular ISG15 prevents interferon-α/ß over-amplification and auto-inflammation.
Nature
; 517(7532): 89-93, 2015 Jan 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-25307056
14.
A novel mutation in ZP3 causes empty follicle syndrome and abnormal zona pellucida formation.
J Assist Reprod Genet
; 38(1): 251-259, 2021 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-33140178
15.
Juvenile-Onset Kufs Disease in a Chinese Consanguineous Family due to CLN6 Mutation.
Neurodegener Dis
; 21(5-6): 126-131, 2021.
Artigo
em Inglês
| MEDLINE | ID: mdl-35609511
16.
Deficiency of SCAMP5 leads to pediatric epilepsy and dysregulation of neurotransmitter release in the brain.
Hum Genet
; 139(4): 545-555, 2020 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-32020363
17.
A novel UBE2A mutation in a Chinese family with X-linked intellectual disability.
J Gene Med
; 22(8): e3191, 2020 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-32222108
18.
Novel mutations in ZP1 and ZP2 cause primary infertility due to empty follicle syndrome and abnormal zona pellucida.
J Assist Reprod Genet
; 37(11): 2853-2860, 2020 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-32829425
19.
Novel homozygous mutations in PATL2 lead to female infertility with oocyte maturation arrest.
J Assist Reprod Genet
; 37(4): 841-847, 2020 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-32048119
20.
Identification of functional lncRNAs in gastric cancer by integrative analysis of GEO and TCGA data.
J Cell Biochem
; 120(10): 17898-17911, 2019 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-31135068