Detalhe da pesquisa
1.
Physical activity practiced at a young age is associated with a less severe subsequent clinical presentation in facioscapulohumeral muscular dystrophy.
BMC Musculoskelet Disord
; 25(1): 35, 2024 Jan 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-38183077
2.
The FSHD jigsaw: are we placing the tiles in the right position?
Curr Opin Neurol
; 36(5): 455-463, 2023 10 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-37338810
3.
De novo variants and recombination at 4q35: Hints for preimplantation genetic testing in facioscapulohumeral muscular dystrophy.
Clin Genet
; 103(2): 242-246, 2023 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-36250762
4.
Interpretation of the Epigenetic Signature of Facioscapulohumeral Muscular Dystrophy in Light of Genotype-Phenotype Studies.
Int J Mol Sci
; 21(7)2020 Apr 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-32290091
5.
MicroRNA-196b is transcribed from an autonomous promoter and is directly regulated by Cdx2 and by posterior Hox proteins during embryogenesis.
Biochim Biophys Acta
; 1849(8): 1066-80, 2015 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-26141604
6.
HOX cluster-embedded micro-RNAs and cancer.
Biochim Biophys Acta Rev Cancer
; 1869(2): 230-247, 2018 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-29540308
7.
MafB is a downstream target of the IL-10/STAT3 signaling pathway, involved in the regulation of macrophage de-activation.
Biochim Biophys Acta
; 1843(5): 955-64, 2014 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-24472656
8.
The Orosomucoid 1 protein is involved in the vitamin D - mediated macrophage de-activation process.
Exp Cell Res
; 319(20): 3201-13, 2013 Dec 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-23973664
9.
Counseling and prenatal diagnosis in facioscapulohumeral muscular dystrophy: A retrospective study on a 13-year multidisciplinary approach.
Health Sci Rep
; 5(3): e614, 2022 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-35509380
10.
The Italian National Registry for FSHD: an enhanced data integration and an analytics framework towards Smart Health Care and Precision Medicine for a rare disease.
Orphanet J Rare Dis
; 16(1): 470, 2021 11 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-34736505
11.
Does DNA Methylation Matter in FSHD?
Genes (Basel)
; 11(3)2020 02 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-32121044
12.
Hoxd13 binds in vivo and regulates the expression of genes acting in key pathways for early limb and skeletal patterning.
Dev Biol
; 317(2): 497-507, 2008 May 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-18407260
13.
An autoregulatory loop controls the expression of the transcription factor NF-Y.
Biochim Biophys Acta Gene Regul Mech
; 1861(5): 509-518, 2018 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-29505822
14.
The miR-196b miRNA inhibits the GATA6 intestinal transcription factor and is upregulated in colon cancer patients.
Oncotarget
; 8(3): 4747-4759, 2017 Jan 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-27902469
15.
NUP98 fusion oncoproteins interact with the APC/C(Cdc20) as a pseudosubstrate and prevent mitotic checkpoint complex binding.
Cell Cycle
; 15(17): 2275-87, 2016 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-27097363
16.
NUP98 fusion oncoproteins promote aneuploidy by attenuating the mitotic spindle checkpoint.
Cancer Res
; 74(4): 1079-90, 2014 Feb 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-24371226
17.
HOXD13 binds DNA replication origins to promote origin licensing and is inhibited by geminin.
Mol Cell Biol
; 29(21): 5775-88, 2009 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-19703996
18.
Hoxd13 and Hoxa13 directly control the expression of the EphA7 Ephrin tyrosine kinase receptor in developing limbs.
J Biol Chem
; 281(4): 1992-9, 2006 Jan 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-16314414
19.
Pbx1/Pbx2 requirement for distal limb patterning is mediated by the hierarchical control of Hox gene spatial distribution and Shh expression.
Development
; 133(11): 2263-73, 2006 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-16672333
20.
A Pbx1-dependent genetic and transcriptional network regulates spleen ontogeny.
Development
; 132(13): 3113-26, 2005 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-15944191