Detalhe da pesquisa
1.
Subclones with variants of uncertain clinical significance might contribute to ineffective hemopoiesis and leukemia predisposition.
Eur J Haematol
; 111(5): 729-741, 2023 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-37501402
2.
Intragenic Deletion in MACROD2: A Family with Complex Phenotypes Including Microcephaly, Intellectual Disability, Polydactyly, Renal and Pancreatic Malformations.
Cytogenet Genome Res
; 158(1): 25-31, 2019.
Artigo
em Inglês
| MEDLINE | ID: mdl-31055587
3.
Fast Detection of a BRCA2 Large Genomic Duplication by Next Generation Sequencing as a Single Procedure: A Case Report.
Int J Mol Sci
; 18(11)2017 Nov 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-29165356
4.
CGH array for the identification of a compound heterozygous mutation in the CYP1B1 gene in a patient with bilateral anterior segment dysgenesis.
Clin Chem Lab Med
; 57(4): e63-e66, 2019 03 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-30207287
5.
c-Kit M541L variant is related to ineffective hemopoiesis predisposing to clonal evolution in 3D in vitro biomimetic co-culture model of bone marrow niche.
Heliyon
; 8(12): e11998, 2022 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-36478848
6.
Clinical efficacy of azacytidine and venetoclax and prognostic impact of Tim-3 and galectin-9 in acute myeloid leukemia and high-risk myelodysplastic syndromes: A single-center real-life experience.
Front Pharmacol
; 13: 1052060, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-36618908
7.
Purinergic Modulation of Spinal Neuroglial Maladaptive Plasticity Following Peripheral Nerve Injury.
Mol Neurobiol
; 52(3): 1440-1457, 2015 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-25352445