Detalhe da pesquisa
1.
Hemolysis-driven IFNα production impairs erythropoiesis by negatively regulating EPO signaling in sickle cell disease.
Blood
; 143(11): 1018-1031, 2024 Mar 14.
Artigo
em Inglês
| MEDLINE | ID: mdl-38127913
2.
Impairment of human terminal erythroid differentiation by histone deacetylase 5 deficiency.
Blood
; 138(17): 1615-1627, 2021 10 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-34036344
3.
Stage-specific dual function: EZH2 regulates human erythropoiesis by eliciting histone and non-histone methylation.
Haematologica
; 108(9): 2487-2502, 2023 09 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-37021526
4.
Analyses of erythropoiesis from embryonic stem cell-CD34+ and cord blood-CD34+ cells reveal mechanisms for defective expansion and enucleation of embryomic stem cell-erythroid cells.
J Cell Mol Med
; 26(8): 2404-2416, 2022 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-35249258
5.
Identification and transcriptome analysis of erythroblastic island macrophages.
Blood
; 134(5): 480-491, 2019 08 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-31101625
6.
TET2 deficiency leads to stem cell factor-dependent clonal expansion of dysfunctional erythroid progenitors.
Blood
; 132(22): 2406-2417, 2018 11 29.
Artigo
em Inglês
| MEDLINE | ID: mdl-30254129
7.
Knockdown of spliceosome U2AF1 significantly inhibits the development of human erythroid cells.
J Cell Mol Med
; 23(8): 5076-5086, 2019 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-31144421
8.
Predicting risk of pulmonary infection in patients with primary membranous nephropathy on immunosuppressive therapy: The AIM-7C score.
Nephrology (Carlton)
; 24(10): 1009-1016, 2019 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-30499223
9.
DNA methylation aberrations rather than polymorphisms of FZD3 gene increase the risk of spina bifida in a high-risk region for neural tube defects.
Birth Defects Res A Clin Mol Teratol
; 103(1): 37-44, 2015 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-25131656
10.
DNMT1 regulates human erythropoiesis by modulating cell cycle and endoplasmic reticulum stress in a stage-specific manner.
Cell Death Differ
; 2024 May 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-38719927
11.
Altered methylation of IGF2 DMR0 is associated with neural tube defects.
Mol Cell Biochem
; 380(1-2): 33-42, 2013 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-23690138
12.
Comprehensive Characterization and Global Transcriptome Analysis of Human Fetal Liver Terminal Erythropoiesis.
Genomics Proteomics Bioinformatics
; 2023 Aug 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-37657739
13.
Glutamate carboxypeptidase II gene polymorphisms and neural tube defects in a high-risk Chinese population.
Metab Brain Dis
; 27(1): 59-65, 2012 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-22124883
14.
Sanfilippo syndrome type B, a lysosomal storage disease, is also a tauopathy.
Proc Natl Acad Sci U S A
; 106(20): 8332-7, 2009 May 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-19416848
15.
DNA methylation status of DNAJA4 is essential for human erythropoiesis.
Epigenomics
; 14(20): 1249-1267, 2022 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-36420716
16.
Carbon Dots as a Potential Therapeutic Agent for the Treatment of Cancer-Related Anemia.
Adv Mater
; 34(19): e2200905, 2022 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-35294781
17.
Vesicular formation regulated by ERK/MAPK pathway mediates human erythroblast enucleation.
Blood Adv
; 5(22): 4648-4661, 2021 11 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-34551066
18.
Disparate effects of methicillin-resistant Staphylococcus aureus infection on renal function in IgA-dominant infection-associated glomerulonephritis and menstrual toxic shock syndrome: a case report and literature review.
J Int Med Res
; 48(8): 300060520933810, 2020 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-32776805
19.
Low folate concentration impacts mismatch repair deficiency in neural tube defects.
Epigenomics
; 12(1): 5-18, 2020 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-31769301
20.
Recombination rates of human microRNA.
Biochem Biophys Res Commun
; 379(3): 702-5, 2009 Feb 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-19133229