Zobrazeno 1 - 10
of 12
pro vyhledávání: '"María Luisa Guevara-Fujita"'
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
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:
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
Autor:
Francia Dp, Huamán-Dianderas, María Luisa, Guevara-Fujita, Diana Rojas, Málaga, Alejandro, Estrada-Cuzcano, Ricardo, Fujita
Publikováno v:
Revista peruana de medicina experimental y salud publica. 36(3)
Duchenne and Becker muscular dystrophies are rare diseases that receive limited attention in our field. The objective of this study was to implement the Multiplex Ligation-dependent Probe Amplification technique (MLPA) and to demonstrate that it has
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::acac49604d2bf069aeae66862f37848f
https://pubmed.ncbi.nlm.nih.gov/31800942
https://pubmed.ncbi.nlm.nih.gov/31800942
Autor:
Pierina Danos, Stefano Giannoni‐Luza, Alexis Germán Murillo Carrasco, Oscar Acosta, Maria Luisa Guevara‐Fujita, José Manuel Cotrina Concha, Henry Guerra Miller, Joseph Pinto Oblitas, Alfredo Aguilar Cartagena, Jhajaira M. Araujo, Ricardo Fujita, José Luis Buleje Sono
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 11, Iss 12, Pp n/a-n/a (2023)
Abstract Background Promoter hypermethylation is one of the enabling mechanisms of hallmarks of cancer. Tumor suppressor genes like RARB and GSTP1 have been reported as hypermethylated in breast cancer tumors compared with normal tissues in several p
Externí odkaz:
https://doaj.org/article/c23afe1478b04c97a1a53d3df5a70f58
Publikováno v:
Horizonte Médico (Lima). 14:43-47
ldentification of a causative deletion of gastrointestinal stromal tumor (gist) by the analysis of the KlT and PDGFRA genes
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e8abd1e18ce706e3edd34298723f3485
https://doi.org/10.24265/horizmed.2014.v14n4.08
https://doi.org/10.24265/horizmed.2014.v14n4.08
Autor:
Susan L. Dagenais, Ann C. Burgess, George J. Brewer, Rob Loechel, Thomas W. Glover, María Luisa Guevara-Fujita, Vilma Yuzbasiyan-Gurkan, Diane E. Miller
Publikováno v:
Mammalian genome : official journal of the International Mammalian Genome Society. 10(7)
Canine copper toxicosis (CT) is an autosomal recessive disorder resulting in accumulation of copper at toxic levels in the liver owing to deficient excretion via the bile (Hardy et al. 1975). This disorder is prevalent in certain breeds, most notably
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c53cb1371c280b453b62856f4f739a19
https://pubmed.ncbi.nlm.nih.gov/10384054
https://pubmed.ncbi.nlm.nih.gov/10384054
Autor:
Jason Cook, Gerald A. Fishman, Anand Swaroop, Kinga Buraczynska, Helen A. Mintz-Hittner, Marcela Pena, Dennis R. Hoffman, Ricardo Fujita, Alan J. Mears, Stacey Fahrner, Dianna K H Wheaton, David G. Birch, Fanny Cortés, Cesar Vicencio, María Luisa Guevara-Fujita
Publikováno v:
Human Mutation. 17:151-151
X-linked forms of retinitis pigmentosa (XLRP) are among the most severe because of their early onset, often leading to significant visual impairment before the fourth decade. RP3, genetically localized at Xp21.1, accounts for 70% of XLRP in different
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::848f42b12d858c76139ee58d055ee0bf
https://doi.org/10.1002/1098-1004(200102)17:2<151::aid-humu7>3.0.co
https://doi.org/10.1002/1098-1004(200102)17:2<151::aid-humu7>3.0.co
Publikováno v:
Redalyc
Horizonte Médico (Lima); Vol. 14 Núm. 4 (2014): OCTUBRE-DICIEMBRE; 43-47
Horizonte Médico (Lima); Vol. 14 No. 4 (2014): OCTUBRE-DICIEMBRE; 43-47
Horizonte médico
Universidad de San Martín de Porres
instacron:USMP
Horizonte Médico (Lima); Vol. 14 Núm. 4 (2014): OCTUBRE-DICIEMBRE; 43-47
Horizonte Médico (Lima); Vol. 14 No. 4 (2014): OCTUBRE-DICIEMBRE; 43-47
Horizonte médico
Universidad de San Martín de Porres
instacron:USMP
ldentification of a causative deletion of gastrointestinal stromal tumor (gist) by the analysis of the KlT and PDGFRA genes
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::579e31adb3f17c9108d398651cb6f115
http://www.redalyc.org/articulo.oa?id=371637137008
http://www.redalyc.org/articulo.oa?id=371637137008