Resultados globales: 24 registros encontrados en 0.02 segundos.
Artículos, Encontrados 19 registros
Documentos de investigación, Encontrados 5 registros
Artículos Encontrados 19 registros  1 - 10siguiente  ir al registro:
1.
10 p, 922.8 KB The Role of the Complement System in Chronic Inflammatory Demyelinating Polyneuropathy : Implications for Complement-Targeted Therapies / Querol, Luis (Institut d'Investigació Biomèdica Sant Pau) ; Hartung, Hans-Peter (Palacky University Olomouc) ; Lewis, Richard A. (Cedars Sinai Medical Center) ; van Doorn, Pieter A. (University Medical Center) ; Hammond, Timothy R. (Sanofi) ; Atassi, Nazem (Sanofi) ; Alonso-Alonso, Miguel (Sanofi) ; Dalakas, Marinos C. (Neuroimmunology National and Kapodistrian University of Athens Medical School) ; Universitat Autònoma de Barcelona
Chronic inflammatory demyelinating polyneuropathy (CIDP) is the most common, heterogeneous, immune-mediated neuropathy, characterized by predominant demyelination of motor and sensory nerves. CIDP follows a relapsing-remitting or a progressive course and causes substantial disability. [...]
2022 - 10.1007/s13311-022-01221-y
Neurotherapeutics, Vol. 19 Núm. 3 (april 2022) , p. 864-873  
2.
17 p, 887.0 KB IL-1 Family Cytokines in Inflammatory Dermatoses : Pathogenetic Role and Potential Therapeutic Implications / Iznardo, Helena (Institut d'Investigació Biomèdica Sant Pau) ; Puig Sanz, Lluís (Institut d'Investigació Biomèdica Sant Pau) ; Universitat Autònoma de Barcelona
The interleukin-1 (IL-1) family is involved in the correct functioning and regulation of the innate immune system, linking innate and adaptative immune responses. This complex family is composed by several cytokines, receptors, and co-receptors, all working in a balanced way to maintain homeostasis. [...]
2022 - 10.3390/ijms23169479
International journal of molecular sciences, Vol. 23 Núm. 16 (august 2022) , p. 9479  
3.
15 p, 2.7 MB Lysosomal lipid alterations caused by glucocerebrosidase deficiency promote lysosomal dysfunction, chaperone-mediated-autophagy deficiency, and alpha-synuclein pathology / Navarro, Alba (Hospital Universitari Vall d'Hebron. Institut de Recerca) ; Fernández González, Irene (Hospital Universitari Vall d'Hebron. Institut de Recerca) ; Riera del Brio, Jordi (Hospital Universitari Vall d'Hebron. Institut de Recerca) ; Montpeyó Garcia-Moreno, Marta (Hospital Universitari Vall d'Hebron. Institut de Recerca) ; Albert-Bayo, Mercé (Hospital Universitari Vall d'Hebron. Institut de Recerca) ; Lopez-Royo, Tresa (Hospital Universitari Vall d'Hebron. Institut de Recerca) ; Castillo-Sanchez, Pablo (Hospital Universitari Vall d'Hebron. Institut de Recerca) ; Carnicer-Cáceres, Clara (Institució Catalana de Recerca i Estudis Avançats) ; Arranz-Amo, Jose Antonio (Hospital Universitari Vall d'Hebron. Institut de Recerca) ; Castillo-Ribelles, Laura (Hospital Universitari Vall d'Hebron. Institut de Recerca) ; Pradas-Gracia, Eddie (Hospital Universitari Vall d'Hebron. Institut de Recerca) ; Casas, Josefina (Institut de Química Avançada de Catalunya) ; Vila Bover, Miquel (Hospital Universitari Vall d'Hebron. Institut de Recerca) ; Martinez-Vicente, Marta (Hospital Universitari Vall d'Hebron. Institut de Recerca) ; Universitat Autònoma de Barcelona
Mutations in the GBA gene that encodes the lysosomal enzyme β-glucocerebrosidase (GCase) are a major genetic risk factor for Parkinson's disease (PD). In this study, we generated a set of differentiated and stable human dopaminergic cell lines that express the two most prevalent GBA mutations as well as GBA knockout cell lines as a in vitro disease modeling system to study the relationship between mutant GBA and the abnormal accumulation of α-synuclein. [...]
2022 - 10.1038/s41531-022-00397-6
NPJ Parkinson's disease, Vol. 8 (october 2022)  
4.
9 p, 1.1 MB Outcomes of cystoid macular edema following Descemet's membrane endothelial keratoplasty in a referral center for keratoplasty in Spain : retrospective study / Moura-Coelho, Nuno (Hospital CUF Cascais) ; Papa-Vettorazzi, Renato (Instituto Microcirurgia Ocular) ; Santiesteban-García, Imalvet (Instituto Microcirurgia Ocular) ; Dias-Santos, Arnaldo (Centro Hospitalar Universitário Lisboa Central) ; Manero, Felicidad (Universitat Autònoma de Barcelona) ; Cunha, João Paulo (Escola Superior de Tecnologias da Saúde de Lisboa) ; Güell, Jose (Universitat Autònoma de Barcelona. Departament de Cirurgia)
The aim of this study was to analyze the outcomes of eyes with visually significant cystoid macular œdema (vs-CMO) after Descemet membrane endothelial keratoplasty (DMEK) in a referral center for keratoplasty in Spain. [...]
2023 - 10.1038/s41598-023-29127-5
Scientific reports, Vol. 13 (february 2023)  
5.
15 p, 2.0 MB Strain-specific interspecies interactions between co-isolated pairs of Staphylococcus aureus and Pseudomonas aeruginosa from patients with tracheobronchitis or bronchial colonization / Gomes Fernandes, Meissiner (Institut Germans Trias i Pujol. Hospital Universitari Germans Trias i Pujol) ; Gómez Camacho, Andromeda Celeste (Universitat Autònoma de Barcelona. Institut de Biotecnologia i de Biomedicina "Vicent Villar Palasí") ; Bravo, Marc (Universitat Autònoma de Barcelona. Departament de Genètica i de Microbiologia) ; Huedo Moreno, Pol (Universitat Autònoma de Barcelona. Institut de Biotecnologia i de Biomedicina "Vicent Villar Palasí") ; Coves, Xavier (Universitat Autònoma de Barcelona. Departament de Genètica i de Microbiologia) ; Prat i Aymerich, Cristina (Institut Germans Trias i Pujol. Hospital Universitari Germans Trias i Pujol) ; Gibert, Isidre (Universitat Autònoma de Barcelona. Departament de Genètica i de Microbiologia) ; Lacoma, Alicia (Institut Germans Trias i Pujol. Hospital Universitari Germans Trias i Pujol) ; Yero, Daniel (Universitat Autònoma de Barcelona. Institut de Biotecnologia i de Biomedicina "Vicent Villar Palasí")
Dual species interactions in co-isolated pairs of Staphylococcus aureus and Pseudomonas aeruginosa from patients with tracheobronchitis or bronchial colonization were examined. The genetic and phenotypic diversity between the isolates was high making the interactions detected strain-specific. [...]
2022 - 10.1038/s41598-022-07018-5
Scientific reports, Vol. 12 (March 2022) , art. 3374  
6.
26 p, 855.4 KB Pathogenesis, Diagnosis and Management of Obstetric Antiphospholipid Syndrome : A Comprehensive Review / Alijotas-Reig, Jaume (Universitat Autònoma de Barcelona. Departament de Medicina) ; Esteve-Valverde, Enrique (Althaia Xarxa Assistencial (Manresa)) ; Anunciación-Llunell, Ariadna (Hospital Universitari Vall d'Hebron. Institut de Recerca) ; Marques-Soares, Joana (Hospital Universitari Vall d'Hebron) ; Pardos-Gea, Josep (Hospital Universitari Vall d'Hebron) ; Miró-Mur, Francesc (Hospital Universitari Vall d'Hebron. Institut de Recerca)
Antiphospholipid syndrome is an autoimmune disorder characterized by vascular thrombosis and/or pregnancy morbidity associated with persistent antiphospholipid antibody positivity. Cases fulfilling the Sydney criteria for obstetric morbidity with no previous thrombosis are known as obstetric antiphospholipid syndrome (OAPS). [...]
2022 - 10.3390/jcm11030675
Journal of clinical medicine, Vol. 11 Núm. 3 (january 2022)  
7.
8 p, 1.7 MB Blastocystis sp. Carriage and Irritable Bowel Syndrome : Is the Association Already Established? / Salvador, Fernando (Hospital Universitari Vall d'Hebron. Institut de Recerca) ; Lobo Álvarez, Beatriz (Hospital Universitari Vall d'Hebron. Institut de Recerca) ; Goterris, Lidia (Hospital Universitari Vall d'Hebron. Institut de Recerca) ; Alonso Cotoner, Carmen (Hospital Universitari Vall d'Hebron. Institut de Recerca) ; Santos, Javier (Universitat Autònoma de Barcelona. Departament de Medicina) ; Sulleiro Igual, Elena (Hospital Universitari Vall d'Hebron. Institut de Recerca) ; Bailo, Begoña (National Centre of Microbiology, Instituto de Salud Carlos III, 28220 Madrid, Spain; (B.B.); (D.C.); (I.F.)) ; Carmena, David (National Centre of Microbiology, Instituto de Salud Carlos III, 28220 Madrid, Spain; (B.B.); (D.C.); (I.F.)) ; Sánchez-Montalvá, Adrián (Hospital Universitari Vall d'Hebron. Institut de Recerca) ; Bosch-Nicolau, Pau (Hospital Universitari Vall d'Hebron. Institut de Recerca) ; Espinosa-Pereiro, Juan (Hospital Universitari Vall d'Hebron. Institut de Recerca) ; Fuentes, Isabel (National Centre of Microbiology, Instituto de Salud Carlos III, 28220 Madrid, Spain; (B.B.); (D.C.); (I.F.)) ; Molina Romero, Israel (Hospital Universitari Vall d'Hebron. Institut de Recerca)
The intestinal protist Blastocystis sp. is one of the most common intestinal parasites observed in humans, and has a worldwide distribution, being more prevalent in developing countries. Although this parasite has been described decades ago, the pathogenic potential it is still not understood completely. [...]
2021 - 10.3390/biology10040340
Biology, Vol. 10 (april 2021)  
8.
10 p, 1012.8 KB Exploring the Role of IL-36 Cytokines as a New Target in Psoriatic Disease / Iznardo, Helena (Institut d'Investigació Biomèdica Sant Pau) ; Puig Sanz, Lluís (Universitat Autònoma de Barcelona. Departament de Medicina)
Unmet needs in the treatment of psoriasis call for novel therapeutic strategies. Pustular psoriasis and psoriatic arthritis often represent a therapeutic challenge. Focus on IL-36 cytokines offers an interesting approach, as the IL-36 axis has been appointed a critical driver of the autoinflammatory responses involved in pustular psoriasis. [...]
2021 - 10.3390/ijms22094344
International journal of molecular sciences, Vol. 22 (april 2021)  
9.
13 p, 2.4 MB The P1 Protein of Watermelon mosaic virus Compromises the Activity as RNA Silencing Suppressor of the P25 Protein of Cucurbit yellow stunting disorder virus / Domingo Calap, María Luisa (Centre de Recerca en Agrigenòmica) ; Chase, Ornela (Centre de Recerca en Agrigenòmica) ; Estapé, Mariona (Centre de Recerca en Agrigenòmica) ; Moreno, Ana Beatriz (Centre de Recerca en Agrigenòmica) ; Lopez-Moya, Juan Jose (Centre de Recerca en Agrigenòmica)
Mixed viral infections in plants involving a potyvirus and other unrelated virus often result in synergistic effects, with significant increases in accumulation of the non-potyvirus partner, as in the case of melon plants infected by the potyvirus Watermelon mosaic virus (WMV) and the crinivirus Cucurbit yellow stunting disorder virus (CYSDV). [...]
2021 - 10.3389/fmicb.2021.645530
Frontiers in microbiology, Vol. 12 (March 2021) , art. 645530  
10.
13 p, 4.6 MB Dynamics of CD4 and CD8 T-Cell Subsets and Inflammatory Biomarkers during Early and Chronic HIV Infection in Mozambican Adults / Pastor Palomo, Lucía (Institut Germans Trias i Pujol. Institut de Recerca de la Sida IrsiCaixa) ; Urrea, Victor (Institut Germans Trias i Pujol. Institut de Recerca de la Sida IrsiCaixa) ; Carrillo, Jorge (Institut Germans Trias i Pujol. Institut de Recerca de la Sida IrsiCaixa) ; Parker, Erica (School of Paediatrics and Child Health, University of Western Australia) ; Fuente-Soro, Laura (Institut de Salut Global de Barcelona) ; Jairoce, Chenjerai (Centro de Investigação em Saúde da Manhiça (CISM)) ; Mandomando, Inacio (Centro de Investigação em Saúde da Manhiça (CISM)) ; Naniche, Denise (Centro de Investigação em Saúde da Manhiça (CISM)) ; Blanco, Julià (Universitat de Vic - Universitat Central de Catalunya)
During primary HIV infection (PHI), there is a striking cascade response of inflammatory cytokines and many cells of the immune system show altered frequencies and signs of extensive activation. These changes have been shown to have a relevant role in predicting disease progression; however, the challenges of identifying PHI have resulted in a lack of critical information about the dynamics of early pathogenic events. [...]
2018 - 10.3389/fimmu.2017.01925
Frontiers in immunology, Vol. 8 (january 2018) , art. 1925  

Artículos : Encontrados 19 registros   1 - 10siguiente  ir al registro:
Documentos de investigación Encontrados 5 registros  
1.
3.9 MB The role of the polymerization of the mutated alpha-1 antitrypsin in the pathogenesis of lung and liver disease in patients with alpha-1 antitrypsin deficiency / Núñez Dubon, Alexa Gabriela ; Esquinas López, Cristina, dir. ; Miravitlles Fernández, Marc, dir. ; Ferrer Sancho, Jaume, 1958-, dir.
El dèficit d'alfa-1 antitripsina és una malaltia genètica rara que es caracteritza per presentar concentracions sèriques baixes d'alfa-1 antitripsina i pel plec i la polimerització de la proteïna en els hepatòcits. [...]
El deficit de alfa-1 antitripsina es una enfermedad genética rara que se caracteriza por presentar concentraciones séricas bajas de alfa-1 antitripsina y por el pliegue y polimerización de la proteína en los hepatocitos. [...]
Alpha-1 antitrypsin deficiency is a genetic condition that is characterized by low circulating levels of the alpha-1 antitrypsin (AAT) protein and by the misfolding and polymerisation of the protein within hepatocytes. [...]

2022  
2.
1 p, 2.5 MB Proteòmica i patogènia del virus de l'ébola / López Vivas, Alberto ; Ferrer-Miralles, Neus, dir. (Universitat Autònoma de Barcelona. Departament de Genètica i de Microbiologia) ; Universitat Autònoma de Barcelona. Facultat de Biociències
2015
Grau en Bioquímica [814]  
3.
1 p, 424.2 KB Methamphetamine effects on dopamine as model of schizophrenia pathogenesis / Sanchis Pérez, Neus M. ; Vivas Sabido, Nuria María, dir. (Universitat Autònoma de Barcelona. Departament de Farmacologia, de Terapèutica i de Toxicologia) ; Universitat Autònoma de Barcelona. Facultat de Biociències
2015
Grau en Ciències Biomèdiques [832]  
4.
172 p, 6.7 MB Haemophilus parasuis host-pathogen interactions in the respiratory tract / Bello-Orti, Bernardo ; Aragon, Virginia, dir. ; Accensi Alemany, Francesc, tut. ; Universitat Autònoma de Barcelona. Departament de Genètica i de Microbiologia
En el sector veterinario, la enfermedad de Glässer es un proceso patogénico frecuente que conduce a pérdidas económicas considerables. Esta enfermedad es causada por Haemophilus parasuis. Aunque se ha llevado a cabo un esfuerzo importante hacia la comprensión de los factores que intervienen en la evolución de la enfermedad, la falta de completa protección de las vacunas comerciales sugieren que debe dirigirse más trabajo hacia el estudio de este proceso patogénico. [...]
In the veterinary field, Glässer's disease is a common pathogenic process that leads to considerable economic losses. This disease is caused by Haemophilus parasuis. Although considerable effort has been focused towards understanding the factors involved in disease outcome, evidences of lack of complete protection of commercial vaccine formulations suggest that more work should be addressed towards understanding this pathogenic process. [...]

[Barcelona] : Universitat Autònoma de Barcelona, 2015  
5.
1 p, 1.6 MB The role of prion-like proteins in human diseases : TAF15 and HNRPDL / Ventura Molina, Júlia ; Ventura, Salvador, dir. (Universitat Autònoma de Barcelona. Departament de Bioquímica i de Biologia Molecular) ; Universitat Autònoma de Barcelona. Facultat de Biociències
2014
Grau en Biotecnologia [815]  

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