Detalhe da pesquisa
1.
Disease-associated mutations impacting BC-loop flexibility trigger long-range transthyretin tetramer destabilization and aggregation.
J Biol Chem
; 297(3): 101039, 2021 09.
Artigo
Inglês
| MEDLINE | ID: mdl-34343569
2.
Community Mortality Due to Respiratory Syncytial Virus in Argentina: Population-based Surveillance Study.
Clin Infect Dis
; 73(Suppl_3): S210-S217, 2021 09 02.
Artigo
Inglês
| MEDLINE | ID: mdl-34472572
3.
Conformational Isomerization Involving Conserved Proline Residues Modulates Oligomerization of the NS1 Interferon Response Inhibitor from the Syncytial Respiratory Virus.
Biochemistry
; 58(26): 2883-2892, 2019 07 02.
Artigo
Inglês
| MEDLINE | ID: mdl-31243994
4.
Intrinsic Disorder to Order Transitions in the Scaffold Phosphoprotein P from the Respiratory Syncytial Virus RNA Polymerase Complex.
Biochemistry
; 55(10): 1441-54, 2016 Mar 15.
Artigo
Inglês
| MEDLINE | ID: mdl-26901160
5.
Fine modulation of the respiratory syncytial virus M2-1 protein quaternary structure by reversible zinc removal from its Cys(3)-His(1) motif.
Biochemistry
; 52(39): 6779-89, 2013 Oct 01.
Artigo
Inglês
| MEDLINE | ID: mdl-23984912
6.
Molten Globule Driven and Self-downmodulated Phase Separation of a Viral Factory Scaffold.
J Mol Biol
; 435(16): 168153, 2023 08 15.
Artigo
Inglês
| MEDLINE | ID: mdl-37210029
7.
Modular unfolding and dissociation of the human respiratory syncytial virus phosphoprotein p and its interaction with the m(2-1) antiterminator: a singular tetramer-tetramer interface arrangement.
Biochemistry
; 51(41): 8100-10, 2012 Oct 16.
Artigo
Inglês
| MEDLINE | ID: mdl-22978633
8.
The respiratory syncytial virus transcription antiterminator M(2-1) is a highly stable, zinc binding tetramer with strong pH-dependent dissociation and a monomeric unfolding intermediate.
Biochemistry
; 50(40): 8529-39, 2011 Oct 11.
Artigo
Inglês
| MEDLINE | ID: mdl-21877705
9.
Prion soft amyloid core driven self-assembly of globular proteins into bioactive nanofibrils.
Nanoscale
; 11(26): 12680-12694, 2019 Jul 14.
Artigo
Inglês
| MEDLINE | ID: mdl-31237592
10.
Identification and characterization of four PAX8 rare sequence variants (p.T225M, p.L233L, p.G336S and p.A439A) in patients with congenital hypothyroidism and dysgenetic thyroid glands.
Clin Endocrinol (Oxf)
; 68(5): 828-35, 2008 May.
Artigo
Inglês
| MEDLINE | ID: mdl-17980011
11.
Mechanism of Tetramer Dissociation, Unfolding, and Oligomer Assembly of Pneumovirus M2-1 Transcription Antiterminators.
ACS Omega
; 3(11): 14732-14745, 2018 Nov 30.
Artigo
Inglês
| MEDLINE | ID: mdl-30555987
12.
Cooperative RNA Recognition by a Viral Transcription Antiterminator.
J Mol Biol
; 430(6): 777-792, 2018 03 16.
Artigo
Inglês
| MEDLINE | ID: mdl-29414675
13.
Plasticity in the Oxidative Folding Pathway of the High Affinity Nerita Versicolor Carboxypeptidase Inhibitor (NvCI).
Sci Rep
; 7(1): 5457, 2017 07 14.
Artigo
Inglês
| MEDLINE | ID: mdl-28710462
14.
[The thyroid as a model for molecular mechanisms in genetic diseases]. / La tiroides como modelo de mecanismos moleculares en enfermedades geneticas.
Medicina (B Aires)
; 65(3): 257-67, 2005.
Artigo
Espanhol
| MEDLINE | ID: mdl-16042141
15.
Five novel inactivating mutations in the thyroid peroxidase gene responsible for congenital goiter and iodide organification defect.
Hum Mutat
; 22(3): 259, 2003 Sep.
Artigo
Inglês
| MEDLINE | ID: mdl-12938097
16.
Genetics and phenomics of hypothyroidism and goiter due to thyroglobulin mutations.
Mol Cell Endocrinol
; 322(1-2): 44-55, 2010 Jun 30.
Artigo
Inglês
| MEDLINE | ID: mdl-20093166
17.
Identification and characterization of new variants of three associated SNPs and a microsatellite in the TSH receptor gene which are useful for genetic studies.
Mol Cell Probes
; 22(5-6): 281-6, 2008.
Artigo
Inglês
| MEDLINE | ID: mdl-18652889
18.
Congenital hypothyroidism with goitre caused by new mutations in the thyroglobulin gene.
Clin Endocrinol (Oxf)
; 67(3): 351-7, 2007 Sep.
Artigo
Inglês
| MEDLINE | ID: mdl-17532758
19.
Three mutations (p.Q36H, p.G418fsX482, and g.IVS19-2A>C) in the dual oxidase 2 gene responsible for congenital goiter and iodide organification defect.
Clin Chem
; 52(2): 182-91, 2006 Feb.
Artigo
Inglês
| MEDLINE | ID: mdl-16322276
20.
La tiroides como modelo de mecanismos moleculares en enfermedades geneticas. / [The thyroid as a model for molecular mechanisms in genetic diseases]
Medicina [B Aires]
; 65(3): 257-67, 2005.
Artigo
Espanhol
| BINACIS | ID: bin-38298