Detalhe da pesquisa
1.
Post-translational modifications in diabetic cardiomyopathy.
J Cell Mol Med
; 28(7): e18158, 2024 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-38494853
2.
Regulation of N6 -methyladenosine modification in erythropoiesis and thalassemia.
Clin Genet
; 2024 Mar 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-38488342
3.
Peripheral blood circular RNA circ-0008102 may serve as a novel clinical biomarker in beta-thalassemia patients.
Eur J Pediatr
; 183(3): 1367-1379, 2024 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-38165465
4.
Intrauterine ultrasound phenotyping, molecular characteristics, and postnatal follow-up of fetuses with the 15q11.2 BP1-BP2 microdeletion syndrome: a single-center, retrospective clinical study.
BMC Pregnancy Childbirth
; 24(1): 23, 2024 Jan 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-38172840
5.
Causal associations between leisure sedentary behaviors and sleep status with frailty: insight from Mendelian randomization study.
BMC Geriatr
; 24(1): 168, 2024 Feb 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-38368347
6.
Genetic analysis, ultrasound phenotype, and pregnancy outcomes of fetuses with Xp22.33 or Yp11.32 microdeletions.
J Perinat Med
; 52(1): 96-101, 2024 Jan 29.
Artigo
em Inglês
| MEDLINE | ID: mdl-37846158
7.
First Report of Filipino ß0-Thalassemia/ß-Thalassemia in a Chinese Family.
Hemoglobin
; 48(1): 34-38, 2024 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-38192212
8.
Recombinase Polymerase Amplification Combined with Lateral Flow Dipstick Assay for the Rapid and Sensitive Detection of Pseudo-nitzschia multiseries.
Int J Mol Sci
; 25(2)2024 Jan 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-38279350
9.
[Advance of research on the role of BCL11A in the occurrence and treatment of ß-Thalassemia].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
; 41(4): 417-425, 2024 Apr 10.
Artigo
em Zh
| MEDLINE | ID: mdl-38565506
10.
Pathogenic copy number variations are associated with foetal short femur length in a tertiary referral centre study.
J Cell Mol Med
; 27(16): 2354-2361, 2023 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-37401003
11.
A novel PLS1 c.981+1G>A variant causes autosomal-dominant hereditary hearing loss in a family.
Clin Genet
; 103(4): 413-423, 2023 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-36537221
12.
Activating transcription factor 4 in erythroid development and [Formula: see text]-thalassemia: a powerful regulator with therapeutic potential.
Ann Hematol
; 2023 Oct 31.
Artigo
em Inglês
| MEDLINE | ID: mdl-37906269
13.
Immune and cytokine alterations and RNA-sequencing analysis in gestational tissues from pregnant women after recovery from COVID-19.
BMC Infect Dis
; 23(1): 620, 2023 Sep 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-37735363
14.
Analysis of retest reliability for pregnant women undergoing cfDNA testing with a no-call result.
Mol Biol Rep
; 50(9): 7649-7657, 2023 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-37535243
15.
Probing the local structure of FLiBe melts and solidified salts by in situ high-temperature NMR.
Phys Chem Chem Phys
; 25(29): 19446-19452, 2023 Jul 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-37403714
16.
Fetal genetic findings by chromosomal microarray analysis and karyotyping for fetal growth restriction without structural malformations at a territory referral center: 10-year experience.
BMC Pregnancy Childbirth
; 23(1): 73, 2023 Jan 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-36703098
17.
Ultrasonographic characteristics, genetic features, and maternal and fetal outcomes in fetuses with omphalocele in China: a single tertiary center study.
BMC Pregnancy Childbirth
; 23(1): 679, 2023 Sep 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-37726736
18.
Prenatal diagnosis of non-mosaic sex chromosome abnormalities: a 10-year experience from a tertiary referral center.
J Perinat Med
; 51(7): 904-912, 2023 Sep 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-37138453
19.
MALS-Net: A Multi-Head Attention-Based LSTM Sequence-to-Sequence Network for Socio-Temporal Interaction Modelling and Trajectory Prediction.
Sensors (Basel)
; 23(1)2023 Jan 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-36617127
20.
[Analysis of clinical phenotype and pathogenic variant of a fetus with Cornelia de Lange syndrome type II].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
; 40(5): 568-571, 2023 May 10.
Artigo
em Zh
| MEDLINE | ID: mdl-37102291