Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Meritxell Espino Guarch"'
Autor:
Clara Mayayo-Vallverdú, Miguel López de Heredia, Esther Prat, Laura González, Meritxell Espino Guarch, Clara Vilches, Lourdes Muñoz, Miguel A. Asensi, Carmen Serra, Amadeu Llebaria, Mercedes Casado, Rafael Artuch, Gloria Garrabou, Pablo M. Garcia-Roves, Federico V. Pallardó, Virginia Nunes
Publikováno v:
Redox Biology, Vol 64, Iss , Pp 102801- (2023)
The high recurrence rate of cystine lithiasis observed in cystinuria patients highlights the need for new therapeutic options to address this chronic disease. There is growing evidence of an antioxidant defect in cystinuria, which has led to test ant
Externí odkaz:
https://doaj.org/article/af072a2d640d476fa7f993ce82b38f63
Autor:
Meritxell Espino Guarch, Mariona Font-Llitjós, Silvia Murillo-Cuesta, Ekaitz Errasti- Murugarren, Adelaida M Celaya, Giorgia Girotto, Dragana Vuckovic, Massimo Mezzavilla, Clara Vilches, Susanna Bodoy, Ignasi Sahún, Laura González, Esther Prat, Antonio Zorzano, Mara Dierssen, Isabel Varela-Nieto, Paolo Gasparini, Manuel Palacín, Virginia Nunes
Publikováno v:
eLife, Vol 7 (2018)
Age-related hearing loss (ARHL) is the most common sensory deficit in the elderly. The disease has a multifactorial etiology with both environmental and genetic factors involved being largely unknown. SLC7A8/SLC3A2 heterodimer is a neutral amino acid
Externí odkaz:
https://doaj.org/article/503c7861f97c46ce95ce9813d6079273
Autor:
Junfeng Ji, Vivek Sharma, Suxia Qi, Meritxell Espino Guarch, Ping Zhao, Zhiwei Luo, Wenxia Fan, Yu Wang, Faridah Mbabaali, Dante Neculai, Miguel Angel Esteban, John D. McPherson, Nizar N. Batada
Publikováno v:
Stem Cell Reports, Vol 2, Iss 1, Pp 44-51 (2014)
Somatic cells can be reprogrammed to induced pluripotent stem cells (iPSCs) using oncogenic transcription factors. However, this method leads to genetic aberrations in iPSCs via unknown mechanisms, which may limit their clinical use. Here, we demonst
Externí odkaz:
https://doaj.org/article/54bf8bd69ce348f08e3045105f8f2540
Autor:
Ekaitz Errasti-Murugarren, Joana Fort, Paola Bartoccioni, Lucía Díaz, Els Pardon, Xavier Carpena, Meritxell Espino-Guarch, Antonio Zorzano, Christine Ziegler, Jan Steyaert, Juan Fernández-Recio, Ignacio Fita, Manuel Palacín
Publikováno v:
Nature Communications, Vol 10, Iss 1, Pp 1-12 (2019)
L-Amino acid Transporters (LATs) are asymmetric amino acid exchangers. Here the authors determine the crystal structure of a prokaryotic LAT, the alanine-serine-cysteine exchanger (BasC) and identify key residues for asymmetric substrate interaction
Externí odkaz:
https://doaj.org/article/02f00387781745f491d1d369e1db2215
Autor:
Tracy Augustine, Fariada Badri, Selvasankar Murugesan, Meritxell Espino Guarch, Mohammad Ameen Al-Aghbar, Rana El Nahas, Anthony Akobeng, Mamoun Elawad, Souhaila Al Khodor, Mehdi Adeli, Nicholas van Panhuys
Publikováno v:
Qatar medical journal. 2022(2)
Allergic diseases constitute significant health and economic issues in both developed and developing nations, with epidemiological studies demonstrating a rapid increase in the global prevalence of food allergy among the pediatric population. Cow mil
Autor:
Mohammad, Ameen Al-Aghbar, Tracy, Augustine, Meritxell, Espino Guarch, Rana, El Nahas, Ghalia, Missous, Nicholas, van Panhuys
Publikováno v:
Qatar Medical Journal. 2022
The chain of events that leads to the sensitization of the immune system to environmental antigens, resulting in the onset of allergic disease, has been studied in great detail over the past 30 years. However, during this time, the rate of allergic d
Autor:
Tracy Augustine, Mohammad Ameen Al-Aghbar, Moza Al-Kowari, Meritxell Espino-Guarch, Nicholas van Panhuys
Publikováno v:
Frontiers in Immunology. 13
Asthma is ranked among the most common chronic conditions and has become a significant public health issue due to the recent and rapid increase in its prevalence. Investigations into the underlying genetic factors predict a heritable component for it
Autor:
Moza, Alkowari, Meritxell, Espino-Guarch, Sahar, Daas, Doua, Abdelrahman, Waseem, Hasan, Navaneethakrishnan, Krishnamoorthy, Abbirami, Sathappan, Patrick, Sheehan, Nicholas Van, Panhuys, The Qatar Genome Program Research Consortium, Xavier, Estivill
Publikováno v:
International journal of molecular sciences. 23(6)
Hereditary hearing loss (HHL) is a common genetic disorder accounting for at least 60% of pre-lingual deafness in children, of which 70% is inherited in an autosomal recessive pattern. The long tradition of consanguinity among the Qatari population h
Autor:
Meritxell Espino Guarch, Mariona Font-Llitjós, Silvia Murillo-Cuesta, Ekaitz Errasti- Murugarren, Adelaida M Celaya, Giorgia Girotto, Dragana Vuckovic, Massimo Mezzavilla, Clara Vilches, Susanna Bodoy, Ignasi Sahún, Laura González, Esther Prat, Antonio Zorzano, Mara Dierssen, Isabel Varela-Nieto, Paolo Gasparini, Manuel Palacín, Virginia Nunes
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c9f085c49dc75859850a63f067f5fc17
https://doi.org/10.7554/elife.31511.028
https://doi.org/10.7554/elife.31511.028