Detalhe da pesquisa
1.
Next-Generation Sequencing of Breast Cancer in the Neoadjuvant Setting.
Pathobiology
; 91(2): 114-120, 2024.
Artigo
Inglês
| MEDLINE | ID: mdl-37660687
2.
European Real-World Assessment of the Clinical Validity of a CE-IVD Panel for Ultra-Fast Next-Generation Sequencing in Solid Tumors.
Int J Mol Sci
; 24(18)2023 Sep 07.
Artigo
Inglês
| MEDLINE | ID: mdl-37762091
3.
S100P is a molecular determinant of E-cadherin function in gastric cancer.
Cell Commun Signal
; 17(1): 155, 2019 11 25.
Artigo
Inglês
| MEDLINE | ID: mdl-31767037
4.
Blue intensity matters for cell cycle profiling in fluorescence DAPI-stained images.
Lab Invest
; 97(5): 615-625, 2017 05.
Artigo
Inglês
| MEDLINE | ID: mdl-28263290
5.
ATX-3, CDC-48 and UBXN-5: a new trimolecular complex in Caenorhabditis elegans.
Biochem Biophys Res Commun
; 386(4): 575-81, 2009 Sep 04.
Artigo
Inglês
| MEDLINE | ID: mdl-19545544
6.
NEDD8: a new ataxin-3 interactor.
Biochim Biophys Acta
; 1773(11): 1619-27, 2007 Nov.
Artigo
Inglês
| MEDLINE | ID: mdl-17935801
7.
The C677T polymorphism in MTHFR is not associated with migraine in Portugal.
Dis Markers
; 25(2): 107-13, 2008.
Artigo
Inglês
| MEDLINE | ID: mdl-18957721
8.
Inherited and acquired risk factors and their combined effects in pediatric stroke.
Pediatr Neurol
; 28(2): 134-8, 2003 Feb.
Artigo
Inglês
| MEDLINE | ID: mdl-12699865
9.
Molecular sexing and analysis of CHD1-Z and CHD1-W sequence variations in wild common quail (Coturnix c. coturnix) and domesticated Japanese quail (Coturnix c. japonica).
J Genet
; 90(2): e39-43, 2011 Aug 18.
Artigo
Inglês
| MEDLINE | ID: mdl-21873772
10.
Nonsense mutation in TITF1 in a Portuguese family with benign hereditary chorea.
Neurogenetics
; 6(4): 209-15, 2005 Dec.
Artigo
Inglês
| MEDLINE | ID: mdl-16220345
11.
A novel H101Q mutation causes PKCgamma loss in spinocerebellar ataxia type 14.
J Hum Genet
; 50(10): 523-529, 2005.
Artigo
Inglês
| MEDLINE | ID: mdl-16189624