Zobrazeno 1 - 10
of 46
pro vyhledávání: '"Diego Arenas Aranda"'
Autor:
Manuel Nolasco‑Quiroga, Marisol Rosas‑Díaz, José Moreno, Leticia Rocha‑Zavaleta, Gerardo Vázquez‑Gómez, Isabel Alvarado Cabrero, Ricardo Godínez‑Aguilar, María José López‑Ibarra, Patricia Piña‑Sánchez, Diego Arenas Aranda, Fabio Salamanca Gómez
Publikováno v:
Oncology Letters
Focal adhesion kinase (FAK) is a non-receptor tyrosine kinase that is expressed in most human cell types (example: Epithelial cells, fibroblasts and endothelial), it serves a key role in the control of cell survival, proliferation and motility. The a
Autor:
Diego Arenas-Aranda, Emilio Castellanos-Juárez, Luis Benítez-Bribiesca, Hugo A Ceja-Rangel, Patricia Sánchez-Suárez, Rubicelia Peñaroja-Flores, Patricio Gariglio
Publikováno v:
Tumor Biology. 37:11917-11926
Maintenance of telomere length is one function of human telomerase that is crucial for the survival of cancer cells and cancer progression. Both telomeres and telomerase have been proposed as possible biomarkers of cancer risk and cancer invasiveness
Autor:
D Juárez-Melchor, Eunice López-Muñoz, J Villa-Morales, G Gutiérrez-Iglesias, F Minauro-Sanmiguel, Diego Arenas-Aranda, J Aguirre-Hernández, Normand García-Hernández
Publikováno v:
Genetics and Molecular Research. 14:8326-8337
Neurofibromatosis type I is an autosomal dominant disease with complete penetrance and variable age-dependent expressivity. It is caused by heterozygous mutations in neurofibromin 1 (NF1). These occur throughout the length of the gene, with no appare
Publikováno v:
Boletín Médico del Hospital Infantil de México, Vol 71, Iss 6, Pp 387-395 (2014)
ResumenEn México, la microtia presenta una prevalencia de 7.37/10,000 recién nacidos, la cual es más alta que la reportada en otras poblaciones; por ejemplo, en Estados Unidos es de 2-3/10,000 recién nacidos. Se define como la malformación cong
Autor:
Diego Arenas-Aranda, Cristian P Miguez-Muñoz, Ana Claudia Velázquez-Wong, María Antonieta de Jesús Araujo-Solís, Miguel Ángel Velázquez-Flores, Ruth Ruiz Esparza-Garrido, Fabio Salamanca-Gómez, Alan Cárdenas-Conejo, Juan Carlos Huicochea-Montiel
Publikováno v:
Cytogenetic and Genome Research. 144:183-189
We report on a 16-year-old girl with a complex phenotype, including intellectual disability, facial dysmorphisms, and obesity. During her infancy, she presented with weak sucking, global developmental delay, and later with excessive eating with centr
Autor:
Diego Arenas-Aranda, Sergio Encarnación-Guevara, Fabio Salamanca-Gómez, A. G. Martínez-Batallar, Miguel Ángel Velázquez-Flores, Ruth Ruiz Esparza-Garrido, Georgina Siordia-Reyes, Enrique López-Aguilar, Magdalena Hernández-Ortiz, Jaime Diegopérez-Ramírez
Publikováno v:
Journal of Proteomics. 94:162-175
Pediatric astrocytomas, a leading cause of death associated with cancer, are the most common primary central nervous system tumors found in children. Most studies of these tumors focus on adults, not on children. We examined the global protein and mi
Autor:
Luis Arturo Baiza-Gutman, Leticia Moreno-Fierros, Rubí Viedma-Rodríguez, Diego Arenas-Aranda, Alejandro García-Carrancá, Fabio Salamanca-Gómez
Publikováno v:
International Journal of Oncology
Apoptosis is controlled by the BCL-2 family of proteins, which can be divided into three different subclasses based on the conservation of BCL-2 homology domains. BIK is a founding member of the BH3-only pro-apoptotic protein family. BIK is predomina
Autor:
Diego Arenas-Aranda, Raquel Chávez-Torres, Calzada-Mendoza Claudia Camelia, Marta Elena Hernández-Caballero, José Alfredo Sierra-Ramírez
Publikováno v:
British Journal of Medicine and Medical Research. 3:351-360
Aim: To explore, in one patient, the possibility that D-bifunctional protein (D-BP) deficiency affects telomere length, and to determine the profile of genetic expression. Presentation of Case: Due to the symptoms of a newborn and his family backgrou
Autor:
Guadalupe Quiñonez-Silva, Félix Recillas-Targa, Luis Benítez-Bribiesca, Diego Arenas Aranda, Mercedes Dávalos-Salas, Patricia Ostrosky-Wegman
Publikováno v:
Clinical Epigenetics
Background Retinoblastoma is a malignant tumor of the retina in children G; −188T > G] sequence variant that is found in peripheral blood lymphocytes and tumor DNA. Unexpectedly, it was the mother who transmitted this variant to two more generation
Autor:
Fabio Salamanca-Gómez, Eunice López-Muñoz, Adelina Hernández-Zarco, Normand García-Hernández, Gelasio Zarco-Espinosa, Isabel Alvarado-Cabrero, Diego Arenas-Aranda
Publikováno v:
Clinical and Translational Oncology. 14:586-591
The purpose of this study is to determine the association between the BIK/NBK gene expression and estrogen receptor alpha expression. We determined the association of BIK/NBK gene expression by real time quantitative reverse transcription polymerase