Resultats globals: 9 registres trobats en 0.03 segons.
Articles, 6 registres trobats
Documents de recerca, 3 registres trobats
Articles 6 registres trobats  
1.
15 p, 620.2 KB Endometrial gene expression profile of pregnant sows with extreme phenotypes for reproductive efficiency / Córdoba, Sarai (Centre de Recerca en Agrigenòmica) ; Balcells Ortega, Ingrid (Centre de Recerca en Agrigenòmica) ; Castelló, Anna (Centre de Recerca en Agrigenòmica) ; Ovilo, Cristina (Instituto Nacional de Investigación y Tecnología Agraria y Alimentaria) ; Noguera Jiménez, José Luis (Institut de Recerca i Tecnologia Agroalimentàries) ; Timoneda i Heredia, Oriol (Centre de Recerca en Agrigenòmica) ; Sánchez Bonastre, Armando (Centre de Recerca en Agrigenòmica) ; Universitat Autònoma de Barcelona. Departament de Genètica Animal
2015 0) and low (L, EBV 0) prolificacy phenotypes. For each sample, mRNA and small RNA libraries were RNA-sequenced, identifying 141 genes and 10 miRNAs differentially expressed between H and L groups. We selected four miRNAs based on their role in reproduction, and five genes displaying the highest differences and a positive mapping into known reproductive QTLs for RT-qPCR validation on the whole extreme population. Significant differences were validated for genes: PTGS2 (p = 0.03; H/L ratio = 3.50), PTHLH (p = 0.03; H/L ratio = 3.69), MMP8 (p = 0.01; H/L ratio = 4.41) and SCNN1G (p = 0.04; H/L ratio = 3.42). Although selected miRNAs showed similar expression levels between H and L groups, significant correlation was found between the expression level of ssc-miR-133a (p 0.01) and sscmiR-92a (p 0.01) and validated genes. These results provide a better understanding of the genetic architecture of prolificacy-related traits and embryo implantation failure in pigs. - 10.1038/srep14416
Scientific reports, Vol. 5 (October 2015) , art. 14416  
2.
14 p, 745.8 KB Functional comparison of XPF missense mutations associated to multiple DNA repair disorders / Marín, Maria (Universitat Autònoma de Barcelona. Departament de Genètica i de Microbiologia) ; Ramírez de Haro, Ma. José (María José) (Universitat Autònoma de Barcelona. Departament de Genètica i de Microbiologia) ; Aza-Carmona, Miriam (Universitat Autònoma de Barcelona. Departament de Genètica i de Microbiologia) ; Jia, Nan (Nagoya University. Research Institute of Environmental Medicine) ; Ogi, Tomoo (Nagoya University. Research Institute of Environmental Medicine) ; Bogliolo, Massimo (Universitat Autònoma de Barcelona. Departament de Genètica i de Microbiologia) ; Surrallés i Calonge, Jordi (Universitat Autònoma de Barcelona. Departament de Genètica i de Microbiologia)
XPF endonuclease is one of the most important DNA repair proteins. Encoded by XPF/ERCC4, XPF provides the enzymatic activity of XPF-ERCC1 heterodimer, an endonuclease that incises at the 5' side of various DNA lesions. [...]
2019 - 10.3390/genes10010060
Genes, Vol. 10, Núm. 1 (January 2019) , art. 60  
3.
7 p, 385.6 KB Secondary metabolite profiling, growth profiles and other tools for species recognition and important Aspergillus mycotoxins / Frisvad, J.C. (Center for Microbial Biotechnology, BioCentrum-DTU, Technical University of Denmark) ; Larsen, T.O. (Center for Microbial Biotechnology, BioCentrum-DTU, Technical University of Denmark) ; de Vries, R. (Microbiology, Utrecht University) ; Meijer, M. (Microbiology, Utrecht University) ; Houbraken, J. (CBS Fungal Biodiversity Centre) ; Cabañes Sáenz, Francisco Javier (Universitat Autònoma de Barcelona. Departament de Sanitat i d'Anatomia Animals) ; Ehrlich, K. (Southern Regional Research Center/ARS/USDA) ; Samson, R.A. (CBS Fungal Biodiversity Centre)
Species in the genus Aspergillus have been classified primarily based on morphological features. Sequencing of house-hold genes has also been used in Aspergillus taxonomy and phylogeny, while extrolites and physiological features have been used less frequently. [...]
2007
Studies in Mycology, Vol. 59 (2007) , p. 31-37  
4.
8 p, 727.2 KB Rare diseases, rare presentations : recognizing atypical inherited kidney disease phenotypes in the age of genomics / Ars Criach, Elisabet (Institut d'Investigació Biomèdica Sant Pau) ; Torra Balcells, Roser (Institut d'Investigació Biomèdica Sant Pau)
A significant percentage of adults (10%) and children (20%) on renal replacement therapy have an inherited kidney disease (IKD). The new genomic era, ushered in by the next generation sequencing techniques, has contributed to the identification of new genes and facilitated the genetic diagnosis of the highly heterogeneous IKDs. [...]
2017 - 10.1093/ckj/sfx051
Clinical Kidney Journal, Vol. 10 (july 2017) , p. 586-593  
5.
7 p, 215.9 KB Evaluation of Rapid Progressors in HIV Infection as an Extreme Phenotype / Olson, Ashley D. (University College London. Medical Research Council Clinical Trials Unit (United Kingdom)) ; Guiguet, Marguerite (Université Pierre et Marie Curie (France)) ; Zangerle, Robert (Innsbruck Medical University (Austria)) ; Gill, John (University of Calgary (Canada)) ; Perez-Hoyos, Santiago (Vall d'Hebrón Institut de Recerca (VHIR)) ; Lodi, Sara (Instituto de Salud Carlos III) ; Ghosn, Jade (CHU Bicêtre. Service de Médecine Interne et Maladies Infectieuses (France)) ; Dorrucci, Maria (Istituto Superiore di Sanità (Italy)) ; Johnson, Anne (University College London. Institute of Epidemiology and Health Care (United Kingdom)) ; Sannes, Mette (Ulleval University Hospital (Norway)) ; Moreno, Santiago (Hospital Universitario Ramón y Cajal) ; Porter, Kholoud (University College London. Medical Research Council Clinical Trials Unit (United Kingdom)) ; Universitat Autònoma de Barcelona
Supplemental Digital Content is Available in the Text. Rapid CD4 cell loss represents an HIV phenotype used to identify causal variants of accelerated disease progression. The optimal rate and threshold for identifying this extreme phenotype in recently infected individuals is unclear. [...]
2014 - 10.1097/QAI.0000000000000240
Journal of acquired immune deficiency syndromes (1999), Vol. 67, Issue 1 (September 2014) , p. 15-21  
6.
15 p, 2.1 MB CD300f immunoreceptor contributes to peripheral nerve regeneration by the modulation of macrophage inflammatory phenotype. / Peluffo, Hugo (Institut Pasteur de Montevideo. Laboratorio de Neuroinflamación y Terapia Génica) ; Solari-Saquieres, Patricia (Institut Pasteur de Montevideo. Laboratorio de Neuroinflamación y Terapia Génica) ; Negro-Demontel, María Luciana (Institut Pasteur de Montevideo. Laboratorio de Neuroinflamación y Terapia Génica) ; Francos Quijorna, Isaac (Universitat Autònoma de Barcelona. Institut de Neurociències) ; Navarro, Xavier (Universitat Autònoma de Barcelona. Departament de Biologia Cel·lular, de Fisiologia i d'Immunologia) ; López Vales, Rubén (Universitat Autònoma de Barcelona. Institut de Neurociències) ; Sayós, Joan (Vall d'Hebron Institut de Recerca) ; Lago, Natalia (Institut Pasteur de Montevideo. Laboratorio de Neuroinflamación y Terapia Génica)
Background: It has recently become evident that activating/inhibitory cell surface immune receptors play a critical role in regulating immune and inflammatory processes in the central nervous system (CNS). [...]
2015 - 10.1186/s12974-015-0364-y
Journal of neuroinflammation, Vol. 12, No. 145 (2015)  

Documents de recerca 3 registres trobats  
1.
1 p, 428.3 KB The plan B of tumor cells : an insight into the ALT mechanism / Rodríguez Paz, Adrià ; Tusell Padrós, Laura, dir. (Universitat Autònoma de Barcelona. Departament de Biologia Cel·lular, de Fisiologia i d'Immunologia) ; Universitat Autònoma de Barcelona. Facultat de Biociències
2015
Graduat o Graduada en Ciències Biomèdiques [832]  
2.
226 p, 4.2 MB Factores genéticos asociados a la degeneración lobar frontotemporal. Análisis de susceptibilidad genética y correlación fenotipo-genotipo / Hernández Ruiz, Mª Isabel ; Ruiz Laza, Agustín, dir. ; Boada Rovira, Mercé, dir. ; Blesa Gonzalez, Rafael, dir. ; Álvarez Sabin, José ; Universitat Autònoma de Barcelona. Departament de Medicina
La Degeneración Lobar Frontotemporal es un grupo heterogéneo de enfermedades, la segunda causa más frecuente de demencia en edad presenil y la que presenta el mayor número de casos hereditarios. Se caracteriza por una gran variabilidad clínica, genética e histopatológica. [...]
Frontotemporal Lobar Degeneration is a heterogeneous group of disorders, the second most frequent cause of early dementia and the one with the highest number of inherited cases. It is characterized by considerable variability in clinical, genetic and histopathologic features. [...]

[Barcelona] : Universitat Autònoma de Barcelona, 2015  
3.
1 p, 674.2 KB Mitochondrial dysfunction and longevity : how does malfunction increase lifespan? / Zurita Carpio, Alberto ; Pereira dos Santos, Cristina Maria, dir. (Universitat Autònoma de Barcelona. Departament de Biologia Animal, de Biologia Vegetal i d'Ecologia) ; Universitat Autònoma de Barcelona. Facultat de Biociències
2014
Graduat o Graduada en Ciències Biomèdiques [832]  

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