Browsing by Title Facultad de Medicina

Now showing items 5528-5547 of 12961

    • Gene-gene interaction for nonsyndromic cleft lip with or without cleft palate in chilean case-parent trios 
      Suazo, José; Santos, José Luis; Colombo, Alicia; Pardo Vargas, Rosa (Elsevier, 2018-07)
      Objective: Nonsyndromic cleft lip with or without cleft palate (NSCL/P) is a birth defect for which several genes susceptibility genes been proposed. Consequently, it has been suggested that many of these genes belong to ...
    • General considerations, indications and contraindications for liver transplantation in Chile. A multicenter ... 
      Hepp K., Juan; Zapata, Rodrigo; Buckel, Erwin; Martínez, Jorge; Uribe, Mario; Díaz, Juan Carlos; Ferrario, Mario; Sanhueza, Edgar; Pérez, Rosa María; Hunter, Bessie; Ríos, Gloria; Humeres, Roberto; Poniachik Teller, Jaime; Oksenberg Reisberg, Dan; Arrese, Marco (2008)
      Liver transplantation is an excellent therapeutic option for terminal liver disease. During the last decades the results of liver transplantation have improved significantly with a patient survival rate of nearly 90% at ...
    • General Medicine in the present medical organization in Chile La Medicina General en la organización médica actual 
      Montero, Joaquín; Muñoz, Fernando; Rosselot Jaramillo, Eduardo; Valdivieso, Vicente; Barna, Roberto (1996)
      This is a round table organized by the Medical Society of Santiago, with the participation of physicians working at high positions at the Faculties of Medicine, Health Ministry and General and Familial Medical Society. ...
    • General practice: a theme in search of clarity Medicina general; un tema en busca de claridad. 
      Goic, (1993)
      Specialization is a consequence of the progress in knowledge and technology, and is essential to increase medical knowledge. Culturally, the population increasingly aspires to be attended by a specialist. On the other hand, ...
    • Generalized bullous fixed drug eruption successfully treated with cyclosporine 
      Vargas Mora, Pablo; García, Santiago; Valenzuela Ahumada, Fernando; Lopetegui Morales, Claudia (Wiley, 2020)
    • Generation and validation of a scale to measure physicians' wellbeing Validación de una escala para medir ... 
      Horwitz Campos, Nina; Bascuñán, Luz; Schattino, Irene; Acuña, Julia; Jiménez, Juan Pablo (2010)
      Background: The recent and ongoing changes in the structure and social organization of medicine have deeply transformed medical practice. Aim: To study the perception of these changes by physicians, the impact of these ...
    • Generation of monoclonal antibodies against 17α-hydroxyprogesterone for newborn screening of congenital ... 
      Morejón García, Greilys; García de la Rosa, Iria; González Reyes, Ernesto C.; Rubio Torres, Anett; Quintana Guerra, Joel M.; Hernández Marín, Milenén; Pérez Mora, Pedro L.; Feal Carballo, Sadys; Lafita Delfino, Yesdiley; Pupo Infante, Maylín; Castells Martínez, Eli (Elsevier B.V., 2018)
      © 2018 Elsevier B.V. Congenital adrenal hyperplasia (CAH) is an autosomal recessive disorder caused by the deficiency of one of the five enzymes involved in the biosynthesis of corticosteroids. The most common form of the ...
    • Generation of nonviral integration-free human iPS cell line KISCOi001-A from normal human fibroblasts, under ... 
      Inzunza, José; Arias Fuenzalida, Jonathan Lee; Segura Aguilar, Juan Ernesto; Nalvarte, Iván; Varshney, Mukesh (Elsevier, 2021)
      KISCOi001-A is a healthy feeder-free and fully characterized human induced pluripotent stem (iPS) cell line cultured under xeno-free and defined conditions. The cell line is generated from normal human foreskin fibroblasts ...
    • Genes as primary determinants of population level lateralisation 
      Concha, Miguel L. (2005)
      Vallortigara & Rogers (V & R) propose a fundamental role of the environment in determining population-level lateralisation and suggest that genes play no primary function in this phenomenon. Here I argue that genes involved ...
    • Genes related to long polar fimbriae of pathogenic Escherichia coli strains as reliable markers to identify ... 
      Torres, Alfredo G.; Blanco, Miguel; Valenzuela, Patricio; Slater, Terry M.; Patel, Shilpa D.; Dahbi, Ghizlane; López, Cecilia; Barriga, Ximena Fernández; Blanco, Jesús E.; Gomes, Tânia A.T.; Vidal Álvarez, Roberto; Blanco, Jorge (2009)
      Lpf (stands for long polar fimbriae) is one of the few adhesive factors of enterohemorrhagic Escherichia coli O157:H7 associated with colonization of the intestine. E. coli O157:H7 strains possess two lpf loci encoding ...
    • Genetic and biochemical characterization of d-arabinose dehydrogenase from Neurospora crassa 
      Carrasco,; Pincheira, Roxana; Ureta, G. (1981)
    • Genetic and environmental influences on ethanol consumption: Perspectives from preclinical research 
      Pautassi, Ricardo M.; Camarini, Rosana; Quadros, Isabel Marian; Miczek, Klaus A.; Israel Jacard, Yedy (Blackwell Publishing Ltd, 2010)
      Background: Alcohol use disorders (abuse and dependence, AUD) are multifactorial phenomena, depending on the interplay of environmental and genetic variables. Method: This review describes current developments in animal ...
    • Genetic and reproductive evidence of natural hybridization between the sister species rhinella atacamensis ... 
      Correa, Claudio L.; Méndez, Marco A.; Veloso, Alberto; Sallaberry Ayerza, Michel (2012)
      Rhinella atacamensis and Rhinella arunco are sister species which, together, are distributed from 25°S to 38°S in Chile. Until recently they were considered to be allopatric, with the dividing line around 32°S, but in 2007 ...
    • Genetic association of gastric cancer with miRNA clusters including the cancer-related genes MIR29, MIR25, ... 
      Espinosa-Parrilla, Yolanda; Muñoz, Xavier; Bonet, Catalina; Garcia, Nadia; Venceslá, Adoraciõn; Yiannakouris, Nikos; Naccarati, Alessio; Sieri, Sabina; Panico, Salvatore; Huerta, José M.; Barricarte, Aurelio; Menéndez, Virginia; Sánchez-Cantalejo, Emilio; Dorronsoro, (Wiley-Liss Inc., 2014)
      MicroRNAs (miRNAs) are post-transcriptional gene regulators involved in a wide range of biological processes including tumorigenesis. Deregulation of miRNA pathways has been associated with cancer but the contribution of ...
    • Genetic characterization and phylogeny of human T-cell lymphotropic virus type I from Chile 
      Ramirez, E.; Cartier Rovirosa, Luis; Villota, C.; Fernandez, J. (2002)
      Infection with Human T-Cell Lymphotropic Virus type I (HTLV-I) have been associated with the development of the HTLV-I associated myelopathy/tropical spastic paraparesis (HAM/TSP). Phylogenetic analyses of HTLV-I isolates ...
    • Genetic composition of Chilean aboriginal populations: HLA and other genetic marker variation 
      Llop Romero, Elena (1996)
      Phenotypes and gene frequencies for eight genetic systems are presented for five Chilean Indian tribes. Results agree with the pattern expected for Andean Indians. Genetic distances and dendrograms were obtained separately ...
    • Genetic composition of the Chilean population: the population from San Pedro de Atacama Composicion genética ... 
      Acuña Acuña, Jeannette; Llop Romero, Elena; Rothhammer Engel, Francisco (1994)
      This work describes the genetic composition of atacameños from San Pedro de Atacama. The results show that a) the contribution of non-indigenous genes is relatively low, in relation to the spanish immigration period. b) ...
    • Genetic composition of the Chilean population: the Yamanas from Ukika Composición genética de la población ... 
      Llop Romero, Elena; Harb,; Moreno Moreno, Claudia; Aspillaga, Angela; van de Maele,; Rothhammer Engel, Francisco (1994)
      The genetic composition of a group of 24 Yamana indians that survive in Puerto Williams, Navarino Island, Chile (parallel 55 south of Tierra del Fuego), was studied. Results showed that these indians have a different genetic ...
    • Genetic contributors to risk of schizophrenia in the presence of a 22q11.2 deletion 
      Cleynen, Isabelle; Engchuan, Worrawat; Hestand, Matthew S.; Heung, Tracy; Holleman, Aarón M.; Johnston, H. Richard; Monfeuga, Thomas; McDonald McGinn, Donna M.; Gur, Raquel E.; Morrow, Bernice E.; Swillen, Ann; Vorstman, Jacob A. S.; Bearden, Carrie E.; Chow, Eva W. C.; van den Bree, Marianne; Emanuel, Beverly S.; Vermeesch, Joris R.; Warren, Stephen T.; Owen, Michael J.; Chopra, Pankaj; Cutler, David J.; Duncan, Richard; Kotlar, Alex V.; Mulle, Jennifer G.; Voss, Anna J.; Zwick, Michael E.; Diacou, Alexander; Golden, Aaron; Guo, Tingwei; Lin, Jhih Rong; Wang, Tao; Zhang, Zhengdong; Zhao, Yingjie; Marshall, Christian; Merico, Daniele; Jin, Andrea; Lilley, Brenna; Salmons, Harold I.; Oanh, Tran; Pardinas, Antonio; Walters, James T. R.; Demaerel, Wolfram; Boot, Erik; Butcher, Nancy J.; Costain, Gregory A.; Lowther, Chelsea; Evers, Rens; van Amelsvoort, Therese A. M. J.; van Duin, Esther; Vingerhoets, Claudia; Breckpot, Jeroen; Devriendt, Koen; Vergaelen, Elfi; Vogels, Annick; Crowley, T. Blaine; McGinn, Daniel E.; Moss, Edward M.; Sharkus, Robert J.; Unolt, Marta; Zackai, Elaine H.; Calkins, Mónica E.; Gallagher, Robert S.; Gur, Rubén C.; Tang, Sunny X.; Fritsch Montero, Rosemarie; Ornstein Letelier, Claudia; Repetto, Gabriela M.; Breetvelt, Elemi; Duijff, Sasja N.; Fiksinski, Ania; Moss, Hayley; Niarchou, Maria; Murphy, Kieran C.; Prasad, Sarah E.; Daly, Eileen M.; Gudbrandsen, María; Murphy, Clodagh M.; Murphy, Declan G.; Buzzanca, Antonio; Di Fabio, Fabio; Digilio, María C.; Pontillo, María; Marino, Bruno; Vicari, Stefano; Coleman, Karlene; Cubells, Joseph F.; Ousley, Opal Y.; Carmel, Miri; Gothelf, Doron; Mekori Domachevsky, Ehud; Michaelovsky, Elena; Weinberger, Ronnie; Eliez, Stephan; Sandini, Corrado; Schneider, Maude; Bena, Frederique Sloan; Antshel, Kevin M.; Fremont, Wanda; Kates, Wendy R.; Belzeaux, Raoul; Busa, Tiffany; Schoch, Kelly; Shashi, Vandana; Simon, Tony J.; Tassone, Flora; Arango, Celso; Suner, Damia H.; Raventos Simic, Jasna; Epstein, Michael P.; Williams, Nigel M.; Bassett, Anne S. (Nature, 2020)
      Schizophrenia occurs in about one in four individuals with 22q11.2 deletion syndrome (22q11.2DS). The aim of this International Brain and Behavior 22q11.2DS Consortium (IBBC) study was to identify genetic factors that ...
    • Genetic contributors to serum uric acid levels in Mexicans and their effect on premature coronary artery disease 
      Macias-Kauffer, Luis R.; Villamil-Ramírez, Hugo; León-Mimila, Paola; Jacobo-Albavera, Leonor; Posadas-Romero, Carlos; Posadas-Sánchez, Rosalinda; López-Contreras, Blanca E.; Morán-Ramos, Sofía; Romero-Hidalgo, Sandra; Acuña Alonzo, Víctor; del-Río-Navarro, Blanca E (Elsevier Ireland Ltd, 2018)
      © 2018 Elsevier B.V.Background: Serum uric acid (SUA) is a heritable trait associated with cardiovascular risk factors and coronary artery disease (CAD). Genome wide association studies (GWAS) have identified several genes ...