Mario Torrado
Overview
Explore the profile of Mario Torrado including associated specialties, affiliations and a list of published articles.
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Articles
41
Citations
653
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Recent Articles
1.
Desmarini D, Truong D, Wilkinson-White L, Desphande C, Torrado M, Mackay J, et al.
Biomolecules
. 2022 Oct;
12(10).
PMID: 36291735
New antifungals with unique modes of action are urgently needed to treat the increasing global burden of invasive fungal infections. The fungal inositol polyphosphate kinase (IPK) pathway, comprised of IPKs...
2.
Torrado M, Maneiro E, Lamounier Junior A, Fernandez-Burriel M, Sanchez Giralt S, Martinez-Carapeto A, et al.
Sci Rep
. 2022 May;
12(1):7284.
PMID: 35508642
The finding of a genotype-negative hypertrophic cardiomyopathy (HCM) pedigree with several affected members indicating a familial origin of the disease has driven this study to discover causative gene variants. Genetic...
3.
Torrado M, Fernandez G, Ganoza C, Maneiro E, Garcia D, Sonicheva-Paterson N, et al.
NPJ Genom Med
. 2021 Mar;
6(1):21.
PMID: 33664273
Here we report an infant with clinical findings suggestive of Jervell and Lange-Nielsen syndrome (JLNS), including a prolonged QT interval (LQTS) and chronic bilateral sensorineural deafness. NGS analysis revealed one...
4.
Low J, Silva A, Sharifi Tabar M, Torrado M, Webb S, Parker B, et al.
Cell Rep
. 2020 Dec;
33(9):108450.
PMID: 33264611
The nucleosome remodeling and deacetylase (NuRD) complex is essential for metazoan development but has been refractory to biochemical analysis. We present an integrated analysis of the native mammalian NuRD complex,...
5.
Vitale G, Pasquale F, Leone O, Cenacchi G, Niro F, Torrado M, et al.
Can J Cardiol
. 2020 Jul;
36(9):1554.e1-1554.e3.
PMID: 32710830
The coexistence of GLA (Pro259Ser, c.775C>T) and MYBPC3 (c.1351+2T>C) mutations was found in a female patient with hypertrophic cardiomyopathy. Histology documented abundant vacuolisation with osmiophilic lamellar bodies and positive Gb3...
6.
Lopes L, Barbosa P, Torrado M, Quinn E, Merino A, Ochoa J, et al.
Circ Genom Precis Med
. 2020 May;
13(3):e002905.
PMID: 32396390
No abstract available.
7.
Zhong Y, Paudel B, Ryan D, Low J, Franck C, Patel K, et al.
Nat Commun
. 2020 Apr;
11(1):1519.
PMID: 32251276
Chromatin remodellers hydrolyse ATP to move nucleosomal DNA against histone octamers. The mechanism, however, is only partially resolved, and it is unclear if it is conserved among the four remodeller...
8.
Latham R, Torrado M, Atto B, Walshe J, Wilson R, Guss J, et al.
Mol Microbiol
. 2019 Nov;
113(2):381-398.
PMID: 31742788
Commensal bacteria serve as an important line of defense against colonisation by opportunisitic pathogens, but the underlying molecular mechanisms remain poorly explored. Here, we show that strains of a commensal...
9.
Link S, Spitzer R, Sana M, Torrado M, Volker-Albert M, Keilhauer E, et al.
Nat Commun
. 2018 Oct;
9(1):4300.
PMID: 30327463
Chromatin structure and function is regulated by reader proteins recognizing histone modifications and/or histone variants. We recently identified that PWWP2A tightly binds to H2A.Z-containing nucleosomes and is involved in mitotic...
10.
Torrado M, Maneiro E, Trujillo-Quintero J, Evangelista A, Mikhailov A, Monserrat L
Biomed Res Int
. 2018 Jul;
2018:3536495.
PMID: 30003093
Marfan syndrome (MFS) is an autosomal dominantly inherited connective tissue disorder, mostly caused by mutations in the fibrillin-1 () gene. We, by using targeted next-generation sequence analysis, identified a novel...