Detalhe da pesquisa
1.
Recognition and inhibition of SARS-CoV-2 by humoral innate immunity pattern recognition molecules.
Nat Immunol
; 23(2): 275-286, 2022 02.
Artigo
Inglês
| MEDLINE | ID: mdl-35102342
2.
Reply to: Hultström et al., Genetic determinants of mannose-binding lectin activity predispose to thromboembolic complications in critical COVID-19. Mannose-binding lectin genetics in COVID-19.
Nat Immunol
; 23(6): 865-867, 2022 06.
Artigo
Inglês
| MEDLINE | ID: mdl-35624207
3.
Needles in Haystacks: Understanding the Success of Selective Pairing of Nucleic Acids.
Int J Mol Sci
; 23(6)2022 Mar 12.
Artigo
Inglês
| MEDLINE | ID: mdl-35328493
4.
The Role of Epigenetics in Primary Biliary Cholangitis.
Int J Mol Sci
; 23(9)2022 Apr 28.
Artigo
Inglês
| MEDLINE | ID: mdl-35563266
5.
OxDNA to Study Species Interactions.
Entropy (Basel)
; 24(4)2022 Mar 26.
Artigo
Inglês
| MEDLINE | ID: mdl-35455121
6.
Hereditary Hypofibrinogenemia with Hepatic Storage.
Int J Mol Sci
; 21(21)2020 Oct 22.
Artigo
Inglês
| MEDLINE | ID: mdl-33105716
7.
Exploring the global landscape of genetic variation in coagulation factor XI deficiency.
Blood
; 130(4): e1-e6, 2017 07 27.
Artigo
Inglês
| MEDLINE | ID: mdl-28615222
8.
Understanding the Impact of Aberrant Splicing in Coagulation Factor V Deficiency.
Int J Mol Sci
; 20(4)2019 Feb 20.
Artigo
Inglês
| MEDLINE | ID: mdl-30791524
9.
Newtonian to non-newtonian fluid transition of a model transient network.
Soft Matter
; 14(17): 3288-3295, 2018 May 02.
Artigo
Inglês
| MEDLINE | ID: mdl-29691545
10.
miR-634 is a Pol III-dependent intronic microRNA regulating alternative-polyadenylated isoforms of its host gene PRKCA.
Biochim Biophys Acta Gen Subj
; 1861(5 Pt A): 1046-1056, 2017 May.
Artigo
Inglês
| MEDLINE | ID: mdl-28212793
11.
Fibrinogen as a Pleiotropic Protein Causing Human Diseases: The Mutational Burden of Aα, Bß, and γ Chains.
Int J Mol Sci
; 18(12)2017 Dec 14.
Artigo
Inglês
| MEDLINE | ID: mdl-29240685
12.
The Characterization of GSDMB Splicing and Backsplicing Profiles Identifies Novel Isoforms and a Circular RNA That Are Dysregulated in Multiple Sclerosis.
Int J Mol Sci
; 18(3)2017 Mar 07.
Artigo
Inglês
| MEDLINE | ID: mdl-28272342
13.
Saposin D variants are not a common cause of familial Parkinson's disease among Italians.
Brain
; 143(9): e71, 2020 09 01.
Artigo
Inglês
| MEDLINE | ID: mdl-32793950
14.
Phase behavior and critical activated dynamics of limited-valence DNA nanostars.
Proc Natl Acad Sci U S A
; 110(39): 15633-7, 2013 Sep 24.
Artigo
Inglês
| MEDLINE | ID: mdl-24019470
15.
Profiling the mutational landscape of coagulation factor V deficiency.
Haematologica
; 105(4): e180-e185, 2020 04.
Artigo
Inglês
| MEDLINE | ID: mdl-31399523
16.
Rare variants lowering the levels of coagulation factor X are protective against ischemic heart disease.
Haematologica
; 105(7): e365-e369, 2020 07.
Artigo
Inglês
| MEDLINE | ID: mdl-31699787
17.
Meta-Analysis of Multiple Sclerosis Microarray Data Reveals Dysregulation in RNA Splicing Regulatory Genes.
Int J Mol Sci
; 16(10): 23463-81, 2015 Sep 30.
Artigo
Inglês
| MEDLINE | ID: mdl-26437396
18.
Synthetic eco-evolutionary dynamics in simple molecular environment.
Elife
; 122024 Mar 26.
Artigo
Inglês
| MEDLINE | ID: mdl-38530348
19.
Notch1 regulates chemotaxis and proliferation by controlling the CC-chemokine receptors 5 and 9 in T cell acute lymphoblastic leukaemia.
J Pathol
; 226(5): 713-22, 2012 Apr.
Artigo
Inglês
| MEDLINE | ID: mdl-21984373
20.
Genetic susceptibility to severe COVID-19.
Infect Genet Evol
; 110: 105426, 2023 06.
Artigo
Inglês
| MEDLINE | ID: mdl-36934789