Detalhe da pesquisa
1.
Prospective Investigation of Optical Genome Mapping for Prenatal Genetic Diagnosis.
Clin Chem
; 70(6): 820-829, 2024 Jun 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-38517460
2.
Whole-genome resequencing uncovers diversity and selective sweep in Kazakh cattle.
Anim Genet
; 55(3): 377-386, 2024 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-38561945
3.
Infantile fibrosarcoma of the perineum with dorsal metastasis in a neonate: a case report original.
BMC Pediatr
; 23(1): 327, 2023 06 29.
Artigo
em Inglês
| MEDLINE | ID: mdl-37386422
4.
Genome-wide identification and analysis of TMT-based proteomes in longissimus dorsi tissue from Kazakh cattle and Xinjiang brown cattle.
Anim Biotechnol
; 34(4): 1261-1272, 2023 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-34965845
5.
Anxiety, depression, insomnia symptoms & associated factors among young to middle-aged adults during the resurgent epidemic of COVID-19: a cross-sectional study.
Psychol Health Med
; 28(5): 1336-1346, 2023 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-36334084
6.
New sonographic feature (C-sign) to improve the prenatal accuracy of jejunal atresia.
J Obstet Gynaecol Res
; 47(12): 4196-4202, 2021 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-34545663
7.
Estrogen regulation of cardiac cAMP-L-type Ca2+ channel pathway modulates sex differences in basal contraction and responses to ß2AR-mediated stress in left ventricular apical myocytes.
Cell Commun Signal
; 17(1): 34, 2019 04 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-30987657
8.
Rare Copy Number Variations Might Not be Involved in the Molecular Pathogenesis of PA-IVS in an Unselected Chinese Cohort.
Pediatr Cardiol
; 40(4): 762-767, 2019 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-30868185
9.
[Identification of ATP7B gene variant by combined use of Sanger sequencing, array CGH and quantitative PCR].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
; 36(12): 1183-1186, 2019 Dec 10.
Artigo
em Zh
| MEDLINE | ID: mdl-31813143
10.
TaGW2-6A allelic variation contributes to grain size possibly by regulating the expression of cytokinins and starch-related genes in wheat.
Planta
; 246(6): 1153-1163, 2017 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-28825220
11.
A modified multiplex ligation-dependent probe amplification method for the detection of 22q11.2 copy number variations in patients with congenital heart disease.
BMC Genomics
; 16: 364, 2015 May 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-25952753
12.
Chromosome microarray testing for patients with congenital heart defects reveals novel disease causing loci and high diagnostic yield.
BMC Genomics
; 15: 1127, 2014 Dec 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-25516202
13.
Research on the perception of the terrain image of the tourism destination based on multimodal user-generated content data.
PeerJ Comput Sci
; 10: e1801, 2024.
Artigo
em Inglês
| MEDLINE | ID: mdl-38435561
14.
A meta-analysis of immunogenicity and safety of two versus single-doses of influenza A (H1N1) vaccine in person living with HIV.
Int J STD AIDS
; 35(5): 326-336, 2024 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-38087772
15.
Molecular mechanism of Hfq-dependent sRNA1039 and sRNA1600 regulating antibiotic resistance and virulence in Shigella sonnei.
Int J Antimicrob Agents
; 63(2): 107070, 2024 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-38141834
16.
Characterization of six missense mutations in the tissue-nonspecific alkaline phosphatase (TNSALP) gene in Chinese children with hypophosphatasia.
Cell Physiol Biochem
; 32(3): 635-44, 2013.
Artigo
em Inglês
| MEDLINE | ID: mdl-24022022
17.
Involvement of RNA chaperone hfq in the regulation of antibiotic resistance and virulence in Shigella sonnei.
Res Microbiol
; 174(5): 104047, 2023 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-36868486
18.
Prenatal phenotype features and genetic etiology of the Williams-Beuren syndrome and literature review.
Front Pediatr
; 11: 1141665, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-37009295
19.
Intrauterine phenotype features of fetuses with 7q11.23 microduplication syndrome.
Orphanet J Rare Dis
; 18(1): 305, 2023 Sep 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-37759207
20.
Identification of LDLR mutations in two Chinese pedigrees with familial hypercholesterolemia.
J Pediatr Endocrinol Metab
; 25(7-8): 769-73, 2012.
Artigo
em Inglês
| MEDLINE | ID: mdl-23155708