Detalhe da pesquisa
1.
Impact of spliceosome mutations on RNA splicing in myelodysplasia: dysregulated genes/pathways and clinical associations.
Blood;
132(12): 1225-1240, 2018 09 20.
Artigo
em Inglês
| MEDLINE
| ID: mdl-29930011
2.
A versatile transgenic allele for mouse overexpression studies.
Mamm Genome;
26(11-12): 598-608, 2015 Dec.
Artigo
em Inglês
| MEDLINE
| ID: mdl-26369329
3.
Application of CRISPR/Cas9 genome editing to the study and treatment of disease.
Arch Toxicol;
89(7): 1023-34, 2015 Jul.
Artigo
em Inglês
| MEDLINE
| ID: mdl-25827103
4.
Effects of prolactin on movement disorders and APOE, GFAP, and PRL receptor gene expression following intracerebral hemorrhage in rats.
Iran J Basic Med Sci;
24(12): 1709-1716, 2021 Dec.
Artigo
em Inglês
| MEDLINE
| ID: mdl-35432801
5.
ASXL1 mutations are associated with distinct epigenomic alterations that lead to sensitivity to venetoclax and azacytidine.
Blood Cancer J;
11(9): 157, 2021 09 21.
Artigo
em Inglês
| MEDLINE
| ID: mdl-34548471
6.
Chronic stimulation of the hypothalamic vasoactive intestinal peptide receptor lengthens circadian period in mice and hamsters.
Am J Physiol Regul Integr Comp Physiol;
299(1): R379-85, 2010 Jul.
Artigo
em Inglês
| MEDLINE
| ID: mdl-20463182
7.
The protective effects of prolactin on brain injury.
Life Sci;
263: 118547, 2020 Dec 15.
Artigo
em Inglês
| MEDLINE
| ID: mdl-33038380
8.
Circadian clock genes in reproductive tissues and the developing conceptus.
Reprod Fertil Dev;
21(1): 1-9, 2009.
Artigo
em Inglês
| MEDLINE
| ID: mdl-19152739
9.
Application of induced pluripotent stem cell technology for the investigation of hematological disorders.
Adv Biol Regul;
71: 19-33, 2019 01.
Artigo
em Inglês
| MEDLINE
| ID: mdl-30341008
10.
Clustered Regularly Interspaced Short Palindromic Repeats/Cas9 Gene Editing Technique in Xenotransplantation.
Front Immunol;
9: 1711, 2018.
Artigo
em Inglês
| MEDLINE
| ID: mdl-30233563
11.
Generation of Knock-out Primary and Expanded Human NK Cells Using Cas9 Ribonucleoproteins.
J Vis Exp;
(136)2018 06 14.
Artigo
em Inglês
| MEDLINE
| ID: mdl-29985369
12.
The U2AF1S34F mutation induces lineage-specific splicing alterations in myelodysplastic syndromes.
J Clin Invest;
127(6): 2206-2221, 2017 Jun 01.
Artigo
em Inglês
| MEDLINE
| ID: mdl-28436936
13.
Impact of Splicing Factor Mutations on Pre-mRNA Splicing in the Myelodysplastic Syndromes.
Curr Pharm Des;
22(16): 2333-44, 2016.
Artigo
em Inglês
| MEDLINE
| ID: mdl-26916023
14.
Application of genome editing technologies to the study and treatment of hematological disease.
Adv Biol Regul;
60: 122-134, 2016 Jan.
Artigo
em Inglês
| MEDLINE
| ID: mdl-26433620
15.
ASXL1 mutation correction by CRISPR/Cas9 restores gene function in leukemia cells and increases survival in mouse xenografts.
Oncotarget;
6(42): 44061-71, 2015 Dec 29.
Artigo
em Inglês
| MEDLINE
| ID: mdl-26623729
16.
Combining gene mutation with gene expression data improves outcome prediction in myelodysplastic syndromes.
Nat Commun;
6: 5901, 2015 Jan 09.
Artigo
em Inglês
| MEDLINE
| ID: mdl-25574665
17.
SF3B1 mutations induce R-loop accumulation and DNA damage in MDS and leukemia cells with therapeutic implications.
Leukemia;
34(9): 2525-2530, 2020 09.
Artigo
em Inglês
| MEDLINE
| ID: mdl-32076118
18.
Embryonic development of circadian oscillations in the mouse hypothalamus.
J Biol Rhythms;
29(4): 299-310, 2014 Aug.
Artigo
em Inglês
| MEDLINE
| ID: mdl-25238858
19.
The role of splicing factor mutations in the pathogenesis of the myelodysplastic syndromes.
Adv Biol Regul;
54: 153-61, 2014 Jan.
Artigo
em Inglês
| MEDLINE
| ID: mdl-24080589
20.
The U2AF1S34F mutation induces lineage-specific splicing alterations in myelodysplastic syndromes.
J Clin Invest;
127(9): 3557, 2017 09 01.
Artigo
em Inglês
| MEDLINE
| ID: mdl-28862641