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Ester Ballana
Ester Ballana
PI, IrsiCaixa-IGTP
在 irsicaixa.es 的电子邮件经过验证
标题
引用次数
引用次数
年份
Deletion of the late cornified envelope LCE3B and LCE3C genes as a susceptibility factor for psoriasis
R De Cid, E Riveira-Munoz, PLJM Zeeuwen, J Robarge, W Liao, ...
Nature genetics 41 (2), 211-215, 2009
6212009
Transmission of COVID-19 in 282 clusters in Catalonia, Spain: a cohort study
M Marks, P Millat-Martinez, D Ouchi, C h Roberts, A Alemany, ...
The Lancet Infectious Diseases 21 (5), 629-636, 2021
3892021
Hydroxychloroquine for early treatment of adults with mild coronavirus disease 2019: a randomized, controlled trial
O Mitjà, M Corbacho-Monné, M Ubals, C Tebé, J Peñafiel, A Tobias, ...
Clinical Infectious Diseases 73 (11), e4073-e4081, 2021
3712021
Prevalence and evolutionary origins of the del (GJB6-D13S1830) mutation in the DFNB1 locus in hearing-impaired subjects: a multicenter study
I Del Castillo, MA Moreno-Pelayo, FJ Del Castillo, Z Brownstein, S Marlin, ...
The American Journal of Human Genetics 73 (6), 1452-1458, 2003
3592003
A cluster-randomized trial of hydroxychloroquine for prevention of Covid-19
O Mitjà, M Corbacho-Monné, M Ubals, A Alemany, C Suñer, C Tebe, ...
New England Journal of Medicine 384 (5), 417-427, 2021
2892021
Mutation in TRMU related to transfer RNA modification modulates the phenotypic expression of the deafness-associated mitochondrial 12S ribosomal RNA mutations
MX Guan, Q Yan, X Li, Y Bykhovskaya, J Gallo-Teran, P Hajek, N Umeda, ...
The American Journal of Human Genetics 79 (2), 291-302, 2006
2672006
Nonmuscle myosin heavy-chain gene MYH14 is expressed in cochlea and mutated in patients affected by autosomal dominant hearing impairment (DFNA4)
F Donaudy, R Snoeckx, M Pfister, HP Zenner, N Blin, M Di Stazio, ...
The American Journal of Human Genetics 74 (4), 770-776, 2004
1982004
Cell cycle control and HIV-1 susceptibility are linked by CDK6-dependent CDK2 phosphorylation of SAMHD1 in myeloid and lymphoid cells
E Pauls, A Ruiz, R Badia, M Permanyer, A Gubern, E Riveira-Muñoz, ...
The Journal of Immunology 193 (4), 1988-1997, 2014
1622014
Endocytosis of HIV: anything goes
M Permanyer, E Ballana, JA Esté
Trends in microbiology 18 (12), 543-551, 2010
1242010
SAMHD1: at the crossroads of cell proliferation, immune responses, and virus restriction
E Ballana, JA Esté
Trends in microbiology 23 (11), 680-692, 2015
1062015
Mitochondrial 12S rRNA gene mutations affect RNA secondary structure and lead to variable penetrance in hearing impairment
E Ballana, E Morales, R Rabionet, B Montserrat, M Ventayol, O Bravo, ...
Biochemical and biophysical research communications 341 (4), 950-957, 2006
932006
Connexins and deafness Homepage
E Ballana
http://davinci. crg. es/deafness/, 2005
922005
An integrated genetic and functional analysis of the role of type II transmembrane serine proteases (TMPRSSs) in hearing loss
M Guipponi, MY Toh, J Tan, D Park, K Hanson, E Ballana, D Kwong, ...
Human mutation 29 (1), 130-141, 2008
812008
Espin gene (ESPN) mutations associated with autosomal dominant hearing loss cause defects in microvillar elongation or organisation
F Donaudy, L Zheng, R Ficarella, E Ballana, M Carella, S Melchionda, ...
Journal of medical genetics 43 (2), 157-161, 2006
792006
Cochlear alterations in deaf and unaffected subjects carrying the deafness-associated A1555G mutation in the mitochondrial 12S rRNA gene
O Bravo, E Ballana, X Estivill
Biochemical and biophysical research communications 344 (2), 511-516, 2006
772006
CD32 expression is associated to T-cell activation and is not a marker of the HIV-1 reservoir
R Badia, E Ballana, M Castellví, E García-Vidal, M Pujantell, B Clotet, ...
Nature communications 9 (1), 2739, 2018
752018
Restriction of HIV-1 replication in primary macrophages by IL-12 and IL-18 through the upregulation of SAMHD1
E Pauls, E Jimenez, A Ruiz, M Permanyer, E Ballana, H Costa, ...
The Journal of Immunology 190 (9), 4736-4741, 2013
752013
p21 regulates the HIV-1 restriction factor SAMHD1
E Pauls, A Ruiz, E Riveira-Muñoz, M Permanyer, R Badia, B Clotet, ...
Proceedings of the National Academy of Sciences 111 (14), E1322-E1324, 2014
692014
Detection of unrecognized low‐level mtDNA heteroplasmy may explain the variable phenotypic expressivity of apparently homoplasmic mtDNA mutations
E Ballana, N Govea, R De Cid, C Garcia, C Arribas, J Rosell, X Estivill
Human mutation 29 (2), 248-257, 2008
682008
Palbociclib, a selective inhibitor of cyclin-dependent kinase4/6, blocks HIV-1 reverse transcription through the control of sterile α motif and HD domain-containing protein-1 …
E Pauls, R Badia, J Torres-Torronteras, A Ruiz, M Permanyer, ...
Aids 28 (15), 2213-2222, 2014
592014
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