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Fujita, Ricardo (33)
Guevara Fujita, María Luisa (8)Sandoval Sandoval, José Raul (8)Acosta, Óscar (5)Jota, Marilza S. (5)Lacerda, Daniela R. (5)Santos, Fabrício R. (5)Acosta, Oscar (4)Revollo, Susana (4)Sandoval, José R. (4)... View MoreSubjectMutación (6)Polimorfismo genético (6)576.5 - Genética (5)572.8 - Genética bioquímica (4)617.7 - Oftalmología (4)Genética de población (4)576 - Genética y evolución (3)Cromosomas humanos Y (3)Filogeografía (3)Genética humana (3)... View MoreDate Issued2010 - 2020 (22)2000 - 2009 (10)1998 - 1999 (1)

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Genetics and genomics in Peru: Clinical and research perspective 

Guio, Heinner; Poterico, Julio A.; Levano, Kelly S.; Cornejo‐Olivas, Mario; Mazzetti, Pilar; Manassero‐Morales, Gioconda; Ugarte‐Gil, Manuel F.; Acevedo‐Vásquez, Eduardo; Dueñas‐Roque, Milagros; Piscoya, Alejandro; Fujita, Ricardo; Sanchez, Cesar; Casavilca‐Zambrano, Sandro; Jaramillo‐Valverde, Luis; Sullcahuaman‐Allende, Yasser; Iglesias‐Pedraz, Juan M.; Abarca‐Barriga, Hugo (Wiley Open Access, 2018-12-25)
Acceso abierto
Peruvians currently preserve in their DNA the history of 2.5 million years of human evolution and 150,000 years of migration from Africa to Peru or the Americas. The development of Genetics and Genomics in the clinical and ...
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Peruvian horse sickness virus and Yunnan orbivirus, isolated from vertebrates and mosquitoes in Peru and Australia 

Attoui, Houssam; Mendez-Lopez, Maria Rosario; Rao, Shujing; Hurtado-Alendes, Ana; Lizaraso-Caparo, Frank; Mohd Jaafar, Fauziah; Samuel, Alan R.; Belhouchet, Mourad; Pritchard, Lindsay I.; Melville, Lorna; Weir, Richard P.; Hyatt, Alex D.; Davis, Steven S.; Lunt, Ross; Calisher, Charles H.; Tesh, Robert B.; Fujita, Ricardo; Mertens, Peter P. C. (Elsevier B.V., 2009-11-25)
Acceso abierto
During 1997, two new viruses were isolated from outbreaks of disease that occurred in horses, donkeys, cattle and sheep in Peru. Genome characterization showed that the virus isolated from horses (with neurological disorders, ...
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A Novel Locus (RP24) for X-linked Retinitis Pigmentosa Maps to Xq26-27 

Gieser, Linn; Fujita, Ricardo; Göring, Harald H.H.; Ott, Jurg; Hoffman, Dennis R.; Cideciyan, Artur V.; Birch, David G.; Jacobson, Samuel G.; Swaroop, Anand (Cell Press, 1998-11)
Acceso abierto
Two genetic loci, RP2 and RP3, for X-linked retinitis pigmentosa (XLRP) have been localized to Xp11.3-11.23 and Xp21.1, respectively. RP3 appears to account for 70% of XLRP families; however, mutations in the RPGR gene ...
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The current genomic landscape of western south america: andes, amazonia, and pacific coast. 

Sandoval, José R.; Acosta, Oscar; Zurita, Camilo; Aguilar-Campos, Abraham; Tito-Álvarez, Ana M.; Serrano-Osuna, Ricardo; Gray, Russell D.; Mafessoni, Fabrizio; Heggarty, Paul; Shimizu, Kentaro K.; Fujita, Ricardo; Stoneking, Mark; Pugach, Irina; Fehren-Schmitz, Lars (Society for Molecular Biology and Evolution, 2019-12)
Acceso abierto
Studies of Native South American genetic diversity have helped to shed light on the peopling and differentiation of the continent, but available data are sparse for the major ecogeographic domains. These include the Pacific ...
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From colorectal cancer pattern to the characterization of individuals at risk: picture for genetic research in Latin America 

Vaccaro, Carlos Alberto; López-Kostner, Francisco; Della Valle, Adriana; Palmero, Edenir Inez; Rossi, Benedito Mauro; Antelo, Marina; Solano, Angela; Carraro, Dirce Maria; Forones, Nora Manoukian; Bohorquez, Mabel; Lino-Silva, Leonardo S.; Buleje, Jose; Spirandelli, Florencia; Abe-Sandes, Kiyoko; Nascimento, Ivana; Sullcahuaman, Yasser; Sarroca, Carlos; Gonzalez, Maria Laura; Herrando, Alberto Ignacio; Alvarez, Karin; Neffa, Florencia; Galvao, Henrique Camposreis; Esperon, Patricia; Golubicki, Mariano; Cisterna, Daniel; Cardoso, Florencia C.; Torrezan, Giovana Tardin; Aguiar Junior, Samuel; Pimenta, Celia Aparecida Marques; da Cruz Formiga, Maria Nirvana; Santos, Erika; Sa, Caroline U.; Oliveira, Edite P.; Fujita, Ricardo; Spirandelli, Enrique; Jimenez, Geiner; Guindalini, Rodrigo Santa Cruz; de Azevedo, Renata Gondim Meira Velame; Bueno, Larissa Souza Mario; Nogueira, Sonia Tereza dos Santos; Torres Loarte, Mariela; Padron, Jorge; Castro-Mujica, Maria del Carmen; Sanchez del Monte, Julio; Caballero, Carmelo; Muñeton Peña, Carlos Mario; Pinto, Joseph; Barletta-Carrillo, Claudia; Gutiérrez Angulo, Melva; Piñero, Tamara; Montenegro Beltran, Paola; Ashton-Prolla, Patricia; Rodriguez, Yenni; Quispe, Richard; Rossi, Norma Teresa; Martin, Claudia; Chialina, Sergio; Kalfayan, Pablo German; Bazo-Alvarez, Juan Carlos; Recalde Cañete, Alcides; Dominguez-Barrera, Constantino; Nuñez, Lina; Da Silva, Sabrina Daniela; Balavarca, Yesilda; Wernhoff, Patrik; Plazzer, John-Paul; Moller, Pal; Hovig, Eivind; Dominguez-Valentin, Mev (John Wiley & Sons Ltd, 2019-05-17)
Acceso abierto
Colorectal cancer (CRC) is one of the most common cancers in Latin America and the Caribbean, with the highest rates reported for Uruguay, Brazil and Argentina. We provide a global snapshot of the CRC patterns, how screening ...
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Novel mutation in ENG gene causing Hereditary Hemorrhagic Telangiectasia in a Peruvian family 

Zevallos-Morales, Alejandro; Murillo, Alexis; Dueñas-Roque, Milagros M.; Prötzel, Ana; Venegas-Tresierra, Luis; Ángeles-Villalba, Verónica; Guevara-Cruz, Miguel; Chávez-Gil, Ada; Fujita, Ricardo; Guevara-Fujita, Maria L. (Sociedade Brasileira de Genética, 2020)
Acceso abierto
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 ...
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Extreme High Prevalence of a Defective Mannose-Binding Lectin (MBL2 ) Genotype in Native South American West Andean Populations 

Sandoval Sandoval, José Raul; Madsen, Hans O.; De Stefano, Gianfranco; Descailleaux-Dulanto, Jaime; Velazquez Reinoso, Margarita Rosa Eugenia; Ñique Carbajal, César; Fujita, Ricardo; Garred, Peter (PLOS ONE, 2014)
Acceso abierto
Mannose-binding lectin (MBL) is one of the five recognition molecules in the lectin complement pathway. Common variant alleles in the promoter and structural regions of the human MBL gene (MBL2) influence the stability ...
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Three Novel Polymorphic Microsatellite Markers for the Glaucoma Locus GLC1B by Datamining Tetranucleotide Repeats on Chromosome 2p12-q12 

Murga Zamalloa, Carlos; Guevara Fujita, María Luisa; Estrada-Cuzcano, Alejandro; Fujita, Ricardo (Genetics and Molecular Biology, 2009)
Acceso abierto
In order to identify new markers around the glaucoma locus GLC1B as a tool to refine its critical region at 2p11.2-2q11.2, we searched the critical region sequence obtained from the UCSC database for tetranucleotide (GATA)n ...
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Variabilidad genética de la respuesta inflamatoria. I. Polimorfismo -511 C/T en el gen IL1β en diferentes subpoblaciones peruanas 

Acosta, Óscar; Solano, Luis; Huerta, Doris; Oré, Daniel; Sandoval Sandoval, José Raul; Figueroa, José; Fujita, Ricardo (Anales de la Facultad de Medicina, 2012)
Acceso abierto
El polimorfismo -511 citosina/timina (-511 C/T) en la región promotora del gen interleuquina 1 beta (IL1β) está implicado en la producción diferencial de la citoquina y por tanto puede estar asociado a la respuesta ...
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Optimización del test de micronúcleos en linfocitos cultivados usando una metodología de gradiente y frotis 

Castillo, Erika; Guevara Fujita, María Luisa; Fujita, Ricardo (Revista Peruana de Biología, 2011-08-25)
Acceso abierto
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 ...
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