Detalhe da pesquisa
1.
Congenital anemia reveals distinct targeting mechanisms for master transcription factor GATA1.
Blood
; 139(16): 2534-2546, 2022 04 21.
Artigo
Inglês
| MEDLINE | ID: mdl-35030251
2.
Preoperative autologous blood donation for kidney transplant and end-stage renal disease patients: A single-center study.
Transfus Apher Sci
; 60(4): 103149, 2021 Aug.
Artigo
Inglês
| MEDLINE | ID: mdl-34148766
3.
Clinical usefulness of cell-free and concentrated ascites reinfusion therapy (CART) in combination with chemotherapy for malignant ascites: a post-marketing surveillance study.
Int J Clin Oncol
; 26(6): 1130-1138, 2021 Jun.
Artigo
Inglês
| MEDLINE | ID: mdl-33761026
4.
Enzymatic Changes in Red Blood Cells of Diamond-Blackfan Anemia.
Tohoku J Exp Med
; 255(1): 49-55, 2021 09.
Artigo
Inglês
| MEDLINE | ID: mdl-34526430
5.
[Hereditary hemolytic anemia in newborns: clinical significance of genetic diagnosis].
Rinsho Ketsueki
; 61(5): 484-490, 2020.
Artigo
Japonês
| MEDLINE | ID: mdl-32507813
6.
Erythrocyte glutathione is a novel biomarker of Diamond-Blackfan anemia.
Blood Cells Mol Dis
; 59: 31-6, 2016 07.
Artigo
Inglês
| MEDLINE | ID: mdl-27282564
7.
ATP11C is a major flippase in human erythrocytes and its defect causes congenital hemolytic anemia.
Haematologica
; 101(5): 559-65, 2016 05.
Artigo
Inglês
| MEDLINE | ID: mdl-26944472
8.
Clinical Trial on the Safety and Tolerability of Personalized Cancer Vaccines Using Human Platelet Lysate-Induced Antigen-Presenting Cells.
Cancers (Basel)
; 15(14)2023 Jul 14.
Artigo
Inglês
| MEDLINE | ID: mdl-37509288
9.
Variant spectrum of PIEZO1 and KCNN4 in Japanese patients with dehydrated hereditary stomatocytosis.
Hum Genome Var
; 10(1): 8, 2023 Mar 02.
Artigo
Inglês
| MEDLINE | ID: mdl-36864026
10.
Dyserythropoietic anaemia with an intronic GATA1 splicing mutation in patients suspected to have Diamond-Blackfan anaemia.
EJHaem
; 3(1): 163-167, 2022 Feb.
Artigo
Inglês
| MEDLINE | ID: mdl-35846220
11.
Novel COL4A1 mutations identified in infants with congenital hemolytic anemia in association with brain malformations.
Hum Genome Var
; 7(1): 42, 2020 Nov 27.
Artigo
Inglês
| MEDLINE | ID: mdl-33298904
12.
Ribosomal protein S19 deficiency leads to reduced proliferation and increased apoptosis but does not affect terminal erythroid differentiation in a cell line model of Diamond-Blackfan anemia.
Stem Cells
; 26(2): 323-9, 2008 Feb.
Artigo
Inglês
| MEDLINE | ID: mdl-17962699
13.
KLF1 mutation E325K induces cell cycle arrest in erythroid cells differentiated from congenital dyserythropoietic anemia patient-specific induced pluripotent stem cells.
Exp Hematol
; 73: 25-37.e8, 2019 05.
Artigo
Inglês
| MEDLINE | ID: mdl-30876823
14.
Transgenic rescue of hemolytic anemia due to red blood cell pyruvate kinase deficiency.
Haematologica
; 92(6): 731-7, 2007 Jun.
Artigo
Inglês
| MEDLINE | ID: mdl-17550844
15.
Safety and efficacy of cell-free and concentrated ascites reinfusion therapy (CART) in refractory ascites: Post-marketing surveillance results.
PLoS One
; 12(5): e0177303, 2017.
Artigo
Inglês
| MEDLINE | ID: mdl-28510606
16.
Candesartan prevents angiotensin II-induced facilitation of hypoxic neuronal damage through PKCdelta inhibition.
Brain Res Mol Brain Res
; 135(1-2): 134-40, 2005 Apr 27.
Artigo
Inglês
| MEDLINE | ID: mdl-15857676
17.
Quantitative assessment of contaminating tumor cells in autologous peripheral blood stem cells of B-cell non-Hodgkin lymphomas using immunoglobulin heavy chain gene allele-specific oligonucleotide real-time quantitative-polymerase chain reaction.
Leuk Res
; 27(10): 925-34, 2003 Oct.
Artigo
Inglês
| MEDLINE | ID: mdl-12860013
18.
A road map toward defining the role of Smad signaling in hematopoietic stem cells.
Stem Cells
; 24(4): 1128-36, 2006 Apr.
Artigo
Inglês
| MEDLINE | ID: mdl-16357343
19.
Smad7 promotes self-renewal of hematopoietic stem cells.
Blood
; 108(13): 4246-54, 2006 Dec 15.
Artigo
Inglês
| MEDLINE | ID: mdl-16917010
20.
Development of cellular models for ribosomal protein S19 (RPS19)-deficient diamond-blackfan anemia using inducible expression of siRNA against RPS19.
Mol Ther
; 11(4): 627-37, 2005 Apr.
Artigo
Inglês
| MEDLINE | ID: mdl-15771965