Detalhe da pesquisa
1.
Haplotype-specific MAPK3 expression in 16p11.2 deletion contributes to variable neurodevelopment.
Brain
; 146(8): 3347-3363, 2023 08 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-36869767
2.
Application of MFI-5 in severe complications and unfavorable outcomes after radical resection of colorectal cancer.
World J Surg Oncol
; 21(1): 307, 2023 Sep 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-37752577
3.
CRISPR/Cas9-mediated ß-globin gene knockout in rabbits recapitulates human ß-thalassemia.
J Biol Chem
; 296: 100464, 2021.
Artigo
em Inglês
| MEDLINE | ID: mdl-33639162
4.
Identification of a novel TBX5 c.755 + 1 G > A variant and related pathogenesis in a family with Holt-Oram syndrome.
Am J Med Genet A
; 188(1): 58-70, 2022 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-34490705
5.
Mesenchymal stem cells from different sources show distinct therapeutic effects in hyperoxia-induced bronchopulmonary dysplasia in rats.
J Cell Mol Med
; 25(17): 8558-8566, 2021 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-34322990
6.
Different culture method changing CD105 expression in amniotic fluid MSCs without affecting differentiation ability or immune function.
J Cell Mol Med
; 24(7): 4212-4222, 2020 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-32119193
7.
Efficient gene correction of an aberrant splice site in ß-thalassaemia iPSCs by CRISPR/Cas9 and single-strand oligodeoxynucleotides.
J Cell Mol Med
; 23(12): 8046-8057, 2019 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-31631510
8.
The phenomena of balanced effect between α-globin gene and of ß-globin gene.
BMC Med Genet
; 19(1): 145, 2018 08 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-30119651
9.
B-cell lymphoma 2 inhibitor ABT-737 induces Beclin1- and reactive oxygen species-dependent autophagy in Adriamycin-resistant human hepatocellular carcinoma cells.
Tumour Biol
; 39(3): 1010428317695965, 2017 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-28351336
10.
Chromosomal aneuploidies and copy number variations in posterior fossa abnormalities diagnosed by prenatal ultrasonography.
Prenat Diagn
; 37(11): 1160-1168, 2017 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-28940600
11.
Psychomotor retardation with a 1q42.11-q42.12 deletion.
Hereditas
; 154: 6, 2017.
Artigo
em Inglês
| MEDLINE | ID: mdl-28286461
12.
Chromosomal microarray analysis in prenatal diagnosis.
Clin Exp Obstet Gynecol
; 44(2): 177-179, 2017.
Artigo
em Inglês
| MEDLINE | ID: mdl-29746015
13.
Prenatal Diagnosis of a Case of Norrie Disease with Late Development of Bilateral Ocular Malformation.
Fetal Pediatr Pathol
; 36(3): 240-245, 2017 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-28394646
14.
A Rare de novo Interstitial Duplication at 4p15.2 in a Boy with Severe Congenital Heart Defects, Limb Anomalies, Hypogonadism, and Global Developmental Delay.
Cytogenet Genome Res
; 150(2): 112-117, 2016.
Artigo
em Inglês
| MEDLINE | ID: mdl-28030855
15.
Paternal Uniparental Disomy of Chromosome 14 with Hypospadias.
Cytogenet Genome Res
; 148(4): 256-61, 2016.
Artigo
em Inglês
| MEDLINE | ID: mdl-27300571
16.
Prenatal diagnosis of submicroscopic chromosomal aberrations in fetuses with ventricular septal defects by chromosomal microarray-based analysis.
Prenat Diagn
; 36(13): 1178-1184, 2016 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-27794163
17.
MCDA twins with discordant malformations: submicroscopic chromosomal anomalies detected by chromosomal microarray analysis and clinical outcomes.
Prenat Diagn
; 36(8): 766-74, 2016 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-27315788
18.
Unexpected Detection of HbH-CS in a Pregnant Woman by Assessing HbA1c Using Capillary Electrophoresis.
Clin Lab
; 62(7): 1357-1361, 2016 Jul 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-28164640
19.
[Prenatal diagnosis of 1p36.3 microdeletion in a fetus with complex heart defect].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
; 33(3): 353-6, 2016 Jun.
Artigo
em Zh
| MEDLINE | ID: mdl-27264820
20.
[Application of single nucleotide polymorphism-based array analysis for prenatal diagnosis of a fetus with de novo derivative chromosome].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
; 33(5): 678-81, 2016 Oct.
Artigo
em Zh
| MEDLINE | ID: mdl-27577222