Detalhe da pesquisa
1.
ETV4 plays a role on the primary events during the adenoma-adenocarcinoma progression in colorectal cancer.
BMC Cancer
; 21(1): 207, 2021 Mar 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-33648461
2.
mRNA Expression and Methylation of the RAD51, ATM, ATR, BRCA1, and BRCA2 Genes in Gastric Adenocarcinoma.
Biomark Insights
; 19: 11772719231225206, 2024.
Artigo
em Inglês
| MEDLINE | ID: mdl-38293680
3.
1031-1034delTAAC (Leu125Stop): a novel familial UBE3A mutation causing Angelman syndrome in two siblings showing distinct phenotypes.
BMC Med Genet
; 13: 124, 2012 Dec 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-23256887
4.
Role of NFKB2 on the early myeloid differentiation of CD34+ hematopoietic stem/progenitor cells.
Differentiation
; 80(4-5): 195-203, 2010.
Artigo
em Inglês
| MEDLINE | ID: mdl-20708837
5.
Repetitive stress fracture: a warning sign of genetic susceptibility to fracture? A case report of a heterozygous variant in SERPINF1.
Arch Endocrinol Metab
; 65(4): 500-504, 2021 Nov 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-34283899
6.
Maple syrup urine disease in Brazilian patients: variants and clinical phenotype heterogeneity.
Orphanet J Rare Dis
; 15(1): 309, 2020 11 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-33131499
7.
miR-450a Acts as a Tumor Suppressor in Ovarian Cancer by Regulating Energy Metabolism.
Cancer Res
; 79(13): 3294-3305, 2019 07 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-31101765
8.
Contribution of SLC26A4 to the molecular diagnosis of nonsyndromic prelingual sensorineural hearing loss in a Brazilian cohort.
BMC Res Notes
; 11(1): 546, 2018 Aug 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-30068397
9.
Highly expressed placental miRNAs control key biological processes in human cancer cell lines.
Oncotarget
; 9(34): 23554-23563, 2018 May 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-29805755
10.
Placenta-Enriched LincRNAs MIR503HG and LINC00629 Decrease Migration and Invasion Potential of JEG-3 Cell Line.
PLoS One
; 11(3): e0151560, 2016.
Artigo
em Inglês
| MEDLINE | ID: mdl-27023770
11.
A further case of a Prader-Willi syndrome phenotype in a patient with Angelman syndrome molecular defect.
Arq Neuropsiquiatr
; 60(4): 1011-4, 2002 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-12563398
12.
A further case of a Prader-Willi syndrome phenotype in a patient with Angelman syndrome molecular defect
Arq. neuropsiquiatr
; 60(4): 1011-1014, Dec. 2002. ilus, tab
Artigo
em Inglês
| LILACS | ID: lil-326179