Detalhe da pesquisa
1.
Further confirmation of the association of SLC12A2 with non-syndromic autosomal-dominant hearing impairment.
J Hum Genet
; 66(12): 1169-1175, 2021 Dec.
Artigo
Inglês
| MEDLINE | ID: mdl-34226616
2.
Chemoresistance to Cancer Treatment: Benzo-α-Pyrene as Friend or Foe?
Molecules
; 23(4)2018 04 17.
Artigo
Inglês
| MEDLINE | ID: mdl-29673198
3.
The African-387 C>T TGFB1 variant is functional and associates with the ophthalmoplegic complication in juvenile myasthenia gravis.
J Hum Genet
; 61(4): 307-16, 2016 Apr.
Artigo
Inglês
| MEDLINE | ID: mdl-26632886
4.
Definition of the variables affecting efficacy of immunodepletion ex vivo of peripheral blood progenitor cell grafts by alemtuzumab (Campath in the bag).
Biol Blood Marrow Transplant
; 19(12): 1753-9, 2013 Dec.
Artigo
Inglês
| MEDLINE | ID: mdl-24120379
5.
A novel function for a redox-related LEA protein (SAG21/AtLEA5) in root development and biotic stress responses.
Plant Cell Environ
; 35(2): 418-29, 2012 Feb.
Artigo
Inglês
| MEDLINE | ID: mdl-21736589
6.
PMA-induced up-regulation of TBX3 is mediated by AP-1 and contributes to breast cancer cell migration.
Biochem J
; 433(1): 145-53, 2011 Jan 01.
Artigo
Inglês
| MEDLINE | ID: mdl-20942798
7.
Cell-based analysis of CLIC5A and SLC12A2 variants associated with hearing impairment in two African families.
Front Genet
; 13: 924904, 2022.
Artigo
Inglês
| MEDLINE | ID: mdl-36035115
8.
Activation-Induced Cytidine Deaminase Promotes Proliferation and Enhances Chemoresistance and Migration in B-cell Lymphoma.
Anticancer Res
; 41(1): 237-247, 2021 Jan.
Artigo
Inglês
| MEDLINE | ID: mdl-33419818
9.
HIV-1 Transactivator of Transcription (Tat) Co-operates With AP-1 Factors to Enhance c-MYC Transcription.
Front Cell Dev Biol
; 9: 693706, 2021.
Artigo
Inglês
| MEDLINE | ID: mdl-34277639
10.
Modulation of Cellular MicroRNA by HIV-1 in Burkitt Lymphoma Cells-A Pathway to Promoting Oncogenesis.
Genes (Basel)
; 12(9)2021 08 24.
Artigo
Inglês
| MEDLINE | ID: mdl-34573283
11.
Whole exome sequencing reveals a biallelic frameshift mutation in GRXCR2 in hearing impairment in Cameroon.
Mol Genet Genomic Med
; 9(3): e1609, 2021 03.
Artigo
Inglês
| MEDLINE | ID: mdl-33528103
12.
A Monoallelic Variant in REST Is Associated with Non-Syndromic Autosomal Dominant Hearing Impairment in a South African Family.
Genes (Basel)
; 12(11)2021 11 06.
Artigo
Inglês
| MEDLINE | ID: mdl-34828371
13.
Phosphorylation of histone H3 by protein kinase C signaling plays a critical role in the regulation of the developmentally important TBX2 gene.
J Biol Chem
; 284(39): 26368-76, 2009 Sep 25.
Artigo
Inglês
| MEDLINE | ID: mdl-19633291
14.
Activation-induced cytidine deaminase: in sickness and in health.
J Cancer Res Clin Oncol
; 146(11): 2721-2730, 2020 Nov.
Artigo
Inglês
| MEDLINE | ID: mdl-32772231
15.
Bi-Allelic Novel Variants in CLIC5 Identified in a Cameroonian Multiplex Family with Non-Syndromic Hearing Impairment.
Genes (Basel)
; 11(11)2020 10 23.
Artigo
Inglês
| MEDLINE | ID: mdl-33114113
16.
Hydroxyurea down-regulates BCL11A, KLF-1 and MYB through miRNA-mediated actions to induce γ-globin expression: implications for new therapeutic approaches of sickle cell disease.
Clin Transl Med
; 5(1): 15, 2016 Mar.
Artigo
Inglês
| MEDLINE | ID: mdl-27056246
17.
The T-box transcription factor, TBX3, is a key substrate of AKT3 in melanomagenesis.
Oncotarget
; 6(3): 1821-33, 2015 Jan 30.
Artigo
Inglês
| MEDLINE | ID: mdl-25595898
18.
The T-Box factor TBX3 is important in S-phase and is regulated by c-Myc and cyclin A-CDK2.
Cell Cycle
; 14(19): 3173-83, 2015.
Artigo
Inglês
| MEDLINE | ID: mdl-26266831
19.
A systematic review of known mechanisms of hydroxyurea-induced fetal hemoglobin for treatment of sickle cell disease.
Expert Rev Hematol
; 8(5): 669-79, 2015 Oct.
Artigo
Inglês
| MEDLINE | ID: mdl-26327494
20.
Serine and proline-rich ligands enriched via phage-display technology show preferential binding to BCR/ABL expressing cells.
Hematol Oncol Stem Cell Ther
; 7(1): 32-40, 2014 Mar.
Artigo
Inglês
| MEDLINE | ID: mdl-24480037