Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Rosenda Peñaloza"'
Autor:
Margarita Camorlinga-Ponce, Guillermo Perez-Perez, Gerardo Gonzalez-Valencia, Irma Mendoza, Rosenda Peñaloza-Espinosa, Irma Ramos, Dangeruta Kersulyte, Adriana Reyes-Leon, Carolina Romo, Julio Granados, Leopoldo Muñoz, Douglas E Berg, Javier Torres
Publikováno v:
PLoS ONE, Vol 6, Iss 11, p e27212 (2011)
It is valuable to extend genotyping studies of Helicobacter pylori to strains from indigenous communities across the world to better define adaption, evolution, and associated diseases. We aimed to genetically characterize both human individuals and
Externí odkaz:
https://doaj.org/article/a32fb830cadf41ff8fd873657296adc6
Autor:
Thelma Canto-Cetina, Patricia Canto, Fabio Salamanca-Gómez, Samuel Canizales-Quinteros, Fernando Minauro-Sanmiguel, Ramón Mauricio Coral-Vázquez, Maricela Rodríguez-Cruz, Rosa María Ordoñez-Razo, Rosenda Peñaloza
Publikováno v:
Genetic Testing and Molecular Biomarkers. 14:237-240
Mutations on the delta-sarcoglycan gene have been associated with the development of both hypertrophic cardiomyopathy (HCM) and dilated cardiomyopathy. Recently, the polymorphism c.-94CG was associated with HCM in Japanese patients. The aim of our st
Autor:
Carmen Navarrete, Rosenda Peñaloza, J. Jorge Palacios, Beatriz Nieva, Brenda Melo-Nava, Fabio Salamanca, A. Rebeca Jaloma-Cruz, Diego Arenas, Herminia Benítez
Publikováno v:
Blood Cells, Molecules, and Diseases. 39:361-365
To investigate the origin of von Willebrand disease in Mexican Mestizo population, we analyzed exons 18, 19, 20, 28, 45, and 52 of the VWF gene from 34 Mexican Mestizo index cases, 28 of them affected but not related, using DNA amplification by polym
Autor:
Fabio Salamanca Gómez, Rosenda Peñaloza Espinoza, Carmen Navarrete, Rafael Martínez Gallegos, Diego Arenas Aranda, Herminia Benítez Aranda
Publikováno v:
American Journal of Hematology. 77:1-6
Variable nucleotide tandem repeats (VNTR) Int13, Int22, and St14 were analyzed to determine polymorphic distribution in normal individuals from Mexico's central region and their efficacy in detecting hemophilia A carriers. Polymerase chain reaction (
Autor:
Rosenda Peñaloza, Fabio Salamanca, Hector Mayani, Juan José Montesinos, E. Hernandez-Caballero, Diego Arenas
Publikováno v:
Leukemia Research. 31:395-397
Cell differentiation and four WT1 isoforms were assessed in CD34 + cells from patients with acute myelogenous leukemia in presence or absence of recombinant human GM-CSF and G-CSF, on days 0, 10 and 20 of culture. We found that WT1 isoforms expressio
Autor:
Brenda, Melo-Nava, Rosenda, Peñaloza
Publikováno v:
Revista de investigacion clinica; organo del Hospital de Enfermedades de la Nutricion. 59(5)
Von Willebrand Factor (VWF) is a large multimeric glycoprotein expressed in the megakaryocytes and endothelial cells of all vertebrates. It participates fundamentally in the primary and secondary hemostasis because it induces the adhesion of platelet
Autor:
Fabio Salamanca, Everardo Curiel-Quesada, Normand Garcia, Rosenda Peñaloza, Isabel Alvarado, Horacio Astudillo-de la Vega, Diego Arenas
Publikováno v:
BMC Cancer
BMC Cancer, Vol 5, Iss 1, p 93 (2005)
BMC Cancer, Vol 5, Iss 1, p 93 (2005)
Background Breast cancer is one of the most frequent causes of death in Mexican women over 35 years of age. At molecular level, changes in many genetic networks have been reported as associated with this neoplasia. To analyze these changes, we determ
Publikováno v:
Scopus-Elsevier
Several blood groups, ABO, Rh, Ss, Fy, Jk, and red cell acid phosphatase (ACP) types were studied in a native Mixteca population that has resided in Mexico City since 1950. Gene frequencies were obtained and used to establish admixture estimates with
Autor:
Carlos Zavala, Rosenda Peñaloza, Alejandro García-Carrancá, Carlos Alvarez, Teresa Ceras, Fabio Salamanca, Jaime Berumen
Publikováno v:
American journal of human biology : the official journal of the Human Biology Council. 7(1)
Five polymorphic restriction enzyme sites in the beta globin gene cluster (HindIII Gγ-Hind III Aγ-, Ava IIINV-2 β-and Hpa I and Bam HI 3'β-globin gene) were studied in individuals from 13 families: 13 homozygote patients for sickle cell anemia, t
Publikováno v:
Clinical genetics. 40(1)
Germinal mosaicism is reported in three siblings with Crouzon syndrome born to normal, unrelated parents. Other probable explanations for the features in this family are discussed.