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.
Clinical efficiency of simultaneous CNV-seq and whole-exome sequencing for testing fetal structural anomalies.
J Transl Med
; 20(1): 10, 2022 01 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-34980134
3.
Decidual vascular endothelial cells promote maternal-fetal immune tolerance by inducing regulatory T cells through canonical Notch1 signaling.
Immunol Cell Biol
; 94(5): 458-69, 2016 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-26714886
4.
Evaluating ClinGen variant curation expert panels' application of PVS1 code.
Eur J Med Genet
; 67: 104909, 2024 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-38199457
5.
Anlotinib for Metastatic Progressed Pheochromocytoma and Paraganglioma: A Retrospective Study of Real-World Data.
J Endocr Soc
; 8(6): bvae061, 2024 Apr 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-38650712
6.
Paternal cadmium exposure induces glucolipid metabolic reprogramming in offspring mice via PPAR signaling pathway.
Chemosphere
; 339: 139592, 2023 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-37482320
7.
Prenatal diagnosis and outcomes in 320 fetuses with nasal bone anomalies.
Front Genet
; 14: 1170720, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-37693318
8.
Prenatal whole-exome sequencing for fetal structural anomalies: a retrospective analysis of 145 Chinese cases.
BMC Med Genomics
; 16(1): 262, 2023 10 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-37880672
9.
Identification of a novel 10.3 kb deletion causing α0-thalassemia by third-generation sequencing: Pedigree analysis and genetic diagnosis.
Clin Biochem
; 113: 64-69, 2023 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-36610469
10.
Decidual vascular endothelial cells promote maternal-fetal immune tolerance by inducing regulatory T cells through canonical Notch1 signaling.
Immunol Cell Biol
; 95(4): 416, 2017 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-28439122
11.
Prenatal diagnosis and genetic counseling of a 10p11.23q11.21 duplication associated with normal phenotype.
Mol Cytogenet
; 15(1): 21, 2022 Jun 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-35659699
12.
Clinical and genetic study of three families with 15q11q13 duplications.
Taiwan J Obstet Gynecol
; 61(4): 717-721, 2022 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-35779929
13.
Two novel truncating variants of the ASPM gene identified in a nonconsanguineous Chinese family associated with primary microcephaly.
Clin Dysmorphol
; 31(1): 1-5, 2022 Jan 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-34693918
14.
Perinatal outcomes of prenatal cases testing positive for trisomy 9 by noninvasive prenatal testing.
Taiwan J Obstet Gynecol
; 61(6): 965-970, 2022 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-36427999
15.
[Genetic Mutation Characteristics of Glucose-6-Phosphate Dehydrogenase Deficiency Patients in Wuhan].
Zhongguo Shi Yan Xue Ye Xue Za Zhi
; 30(1): 244-249, 2022 Feb.
Artigo
em Zh
| MEDLINE | ID: mdl-35123635
16.
The prevalence and outcomes of α- and ß-thalassemia among pregnant women in Hubei Province, Central China: An observational study.
Medicine (Baltimore)
; 101(9): e28790, 2022 Mar 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-35244037
17.
A feasibility study of noninvasive prenatal diagnosis in facioscapulohumeral muscular dystrophy type 1 in a Chinese family.
Front Genet
; 13: 1046096, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-36386852
18.
Genomic architecture of fetal central nervous system anomalies using whole-genome sequencing.
NPJ Genom Med
; 7(1): 31, 2022 May 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-35562572
19.
Genetic deconvolution of fetal and maternal cell-free DNA in maternal plasma enables next-generation non-invasive prenatal screening.
Cell Discov
; 8(1): 109, 2022 Oct 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-36229437
20.
[Hb Bart's Quantitative Analysis in the Screening of α-Thalassemia].
Zhongguo Shi Yan Xue Ye Xue Za Zhi
; 29(6): 1903-1906, 2021 Dec.
Artigo
em Zh
| MEDLINE | ID: mdl-34893131