Zobrazeno 1 - 10
of 25
pro vyhledávání: '"María Luisa Guevara"'
Autor:
María Luisa Guevara‐Fujita, Francia Huaman‐Dianderas, Daisy Obispo, Rodrigo Sánchez, Victor Barrenechea, Diana Rojas‐Málaga, Alejandro Estrada‐Cuzcano, Milana Trubnykova, Mario Cornejo‐Olivas, Victoria Marca, Bertha Gallardo, Milagros Dueñas‐Roque, Ana Protzel, Carlos Castañeda, Hugo Abarca, Luis Celis, Jorge La Serna‐Infantes, Ricardo Fujita
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 9, Iss 9, Pp n/a-n/a (2021)
Abstract Background We report the molecular analysis of the DMD gene in a group of Peruvian patients with Duchenne/Becker dystrophinopathy. This is the first study to thoroughly characterize mutations in this population. Methods We used the combinati
Externí odkaz:
https://doaj.org/article/eb9689d258c04b929b47d0d45d2093fd
Autor:
Francia DP Huaman-Dianderas, María Luisa Guevara-Fujita, DIana Rojas Málaga, Alejandro Estrada-Cuzcano, Ricardo Fujita
Publikováno v:
Revista Peruana de Medicina Experimental y Salud Pública, Vol 36, Iss 3, Pp 475-80 (2019)
Las distrofias musculares de Duchenne/Becker son enfermedades raras que reciben poca atención en nuestro medio. El objetivo del presente estudio fue implementar la técnica de amplificación múltiple dependiente de ligación por sondas (MLPA) y dem
Externí odkaz:
https://doaj.org/article/df5da08bf5384b3c8a639e04693ed36f
Autor:
Luis Olivares, María Villanueva, Elvira Aparicio, Aracelli Yauri, Rosa Medina, Noelia De la Sota, Doris Huerta, Luisa Negrón, María Luisa Guevara, José Sandoval, Ricardo Fujita, Oscar Acosta
Publikováno v:
Anales de la Facultad de Medicina, Vol 78, Iss 2, Pp 126-131 (2017)
Introducción: La farmacogenética tiene utilidad clínica para evaluar los efectos de los fármacos según perfil genético y aporta a la medicina poblacional y personalizada. La diabetes mellitus tipo 2 (DMT2) es una enfermedad prevalente en el Per
Externí odkaz:
https://doaj.org/article/8acfea976bc44bf1bd18971e8744481e
Autor:
Sergio Talavera Vargas-Machuca, Ismenia Gamboa Oré, Francia Huamán Dianderas, Ricardo Fujita Alarcón, María Luisa Fajardo Loo, María Luisa Guevara Gil
Publikováno v:
Horizonte Médico, Vol 17, Iss 3, Pp 73-78 (2017)
Medical genetics is rapidly advancing thanks to technologies that accurately define which genes are involved in the development of diseases. Some syndromes occur in the general population, and their diagnosis and treatment are important to provide
Externí odkaz:
https://doaj.org/article/9d410ab02f6b4c38a5403587a70cf6f2
Publikováno v:
Revista Peruana de Biología, Vol 18, Iss 2, Pp 261-263 (2011)
El test de micronúcleos en cultivo de linfocitos es una prueba validada para estudiar mutagenicidad. Consiste en detectar material nuclear interfásico dañado, producto de fragmentación cromosómica o errores de división nuclear en 2000 células
Externí odkaz:
https://doaj.org/article/b9b2c96d63a74473a81b7c1127d35b35
Autor:
Roman Romero-Ortuno, Frank Lizaraso-Soto, Ricardo Fujita, Teodoro J. Oscanoa, Y. B. Andia, O. Grimaldo, Edwin C. Cieza, María Luisa Guevara
Publikováno v:
Advances in Gerontology. 11:208-213
We explored the relationships between the use of Angiotensin II receptor blockers (ARBs), Angiotensin I-converting enzyme (ACE) genetic polymorphisms and memory performance in older adults, whilst controlling for confounders. Retrospective observatio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::015f720368d6d30c83e37b2d859f56d4
https://doi.org/10.1134/s2079057021020107
https://doi.org/10.1134/s2079057021020107
Autor:
Roman Romero-Ortuno, María Luisa Guevara, Teodoro J. Oscanoa, Edwin C. Cieza, Ricardo Fujita, Frank Lizaraso-Soto
Publikováno v:
Arterial Hypertension. 24:115-119
Background: Epidemiological studies have shown an association between the ACE gene I/D polymorphism with arterial hypertension, specifically the DD genotype, in different populations. The objective of this study is to evaluate the association between
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::436c64253403c873bf7d912eb6e967d1
https://doi.org/10.5603/ah.a2020.0011
https://doi.org/10.5603/ah.a2020.0011
Autor:
María Luisa Guevara, Roman Romero-Ortuno, Teodoro J. Oscanoa, Ricardo Fujita, Frank Lizaraso-Soto, Edwin C. Cieza
Publikováno v:
Annals of Human Biology. 47:309-312
Background: Some studies have suggested that the insertion(I)/deletion(D) polymorphism of the Angiotensin-Converting Enzyme (ACE) gene may be associated with human longevity, especially in centenar...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6967d2d11e67125f1f8c1a9b75931ac6
https://doi.org/10.1080/03014460.2020.1748227
https://doi.org/10.1080/03014460.2020.1748227
Autor:
Rauw, Wendy M., Gomez-Raya, Luis, Star, Laura, Øverland, Margareth, Delezie, Evelyne, Grivins, Mikelis, Karen T., Hamann, Marco, Pietropaoli, Klaassen, Michiel T., Klemetsdal, Gunnar, Gil, María Luisa Guevara, Torres, Olga, Dvergedal, Hanne, Formato, Giovanni
Externí odkaz:
https://hdl.handle.net/11250/3059781
Autor:
Ana Protzel, Ada Chávez-Gil, María Luisa Guevara-Fujita, Luis Venegas-Tresierra, Milagros M. Dueñas-Roque, Alexis Murillo, Verónica Ángeles-Villalba, Alejandro Zevallos-Morales, Ricardo Fujita, Miguel Guevara-Cruz
Publikováno v:
Repositorio Académico USMP
Universidad San Martín de Porres-USMP
USMP-Institucional
Universidad de San Martín de Porres
instacron:USMP
Genetics and Molecular Biology
Genetics and Molecular Biology, Volume: 43, Issue: 1, Article number: e20190126, Published: 27 FEB 2020
Genetics and Molecular Biology, Vol 43, Iss 1 (2020)
Universidad San Martín de Porres-USMP
USMP-Institucional
Universidad de San Martín de Porres
instacron:USMP
Genetics and Molecular Biology
Genetics and Molecular Biology, Volume: 43, Issue: 1, Article number: e20190126, Published: 27 FEB 2020
Genetics and Molecular Biology, Vol 43, Iss 1 (2020)
Hereditary Hemorrhagic Telangiectasia (HHT) is a rare disorder of vascular development. Common manifestations include epistaxis, telangiectasias and arteriovenous malformations (AVMs) in multiple organs. Most patients have deletions or missense mutat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::244c4c541935423971b4c0a6a88ff719