Zobrazeno 1 - 10
of 20
pro vyhledávání: '"Indira Tirado-Hurtado"'
Publikováno v:
The Saudi Journal of Gastroenterology, Vol 28, Iss 5, Pp 393-394 (2022)
Externí odkaz:
https://doaj.org/article/df2cc19d1c3a4d86a43149bffc26d5d5
Autor:
Pilar Mazzetti, Miguel Inca-Martínez, Indira Tirado-Hurtado, Karina Milla-Neyra, Gustavo Silva-Paredes, Anastasia Vishnevetsky, Mario Cornejo-Olivas
Publikováno v:
Revista Peruana de Medicina Experimental y Salud Pública, Vol 32, Iss 4, Pp 787-793 (2015)
Neurogenetics is an emerging discipline in Peru that links basic research with clinical practice. The Neurogenetics Research Center located in Lima, Peru is the only unit dedicated to the specialized care of neurogenetic diseases in the country. From
Externí odkaz:
https://doaj.org/article/2827b5325e014361966c390fdcddcdf2
Publikováno v:
Frontiers in Oncology, Vol 8 (2018)
DNA damage inducible transcript 4 (DDIT4) gene is expressed under stress situations turning off the metabolic activity triggered by the mammalian target of rapamycin (mTOR). Several in vitro and in vivo works have demonstrated the ability of DDIT4 to
Externí odkaz:
https://doaj.org/article/bcbb59c097a14f31b0de42c414dd4c36
Autor:
Pilar Mazzetti, Miguel Inca-Martínez, Indira Tirado-Hurtado, Karina Milla-Neyra, Gustavo Silva-Paredes, Anastasia Vishnevetsky, Mario Cornejo-Olivas
Publikováno v:
Revista Peruana de Medicina Experimental y Salud Pública, Vol 32, Iss 4, Pp 787-793
La neurogenética es una disciplina emergente en el Perú que vincula la investigación básica con la práctica clínica. El Centro de Investigación Básica en Neurogenética, es el único centro en el Perú dedicado a la atención especializada de
Externí odkaz:
https://doaj.org/article/db76016a9c8647899837cf9d2f70eb1d
Autor:
Pilar Mazzetti, Miguel Inca-Martínez, Indira Tirado-Hurtado, Karina Milla-Neyra, Gustavo Silva-Paredes, Anastasia Vishnevetsky, Mario Cornejo-Olivas
Publikováno v:
Revista Peruana de Medicina Experimental y Salud Pública, Vol 32, Iss 4, Pp 787-793
La neurogenética es una disciplina emergente en el Perú que vincula la investigación básica con la práctica clínica. El Centro de Investigación Básica en Neurogenética, es el único centro en el Perú dedicado a la atención especializada de
Externí odkaz:
https://doaj.org/article/268a53b550384cb89dd7baf5cad5c96e
Autor:
Daniel J Enriquez, Indira Tirado-Hurtado, Patricia Rioja, Jackeline Macetas, Jorge Luna-Abanto
Publikováno v:
World Journal of Clinical Oncology
Background Myeloid sarcoma (MS) is a rare hematologic malignancy defined as an extramedullary tumor of immature granulocytic cells. It can occur as primary or de novo and be associated with myelodysplasia or myeloproliferative neoplasms. The most fre
Autor:
Ina Pérez, Christian Cortez, Julio Coyotupac, Joseph A. Pinto, José Alva, Carlos Munive, Jesús Bernal, Indira Tirado-Hurtado, Alfredo Goytendia, Lilian Castilho, Erika Rojas
Publikováno v:
Transfusion and Apheresis Science. 58:453-456
Blood banks in developing countries have limited capability to typify common blood groups creating disparities in the access to blood units for patients with rare blood genotypes. We report the case of a Peruvian woman with metastatic breast cancer w
Autor:
Luis J. Schwarz, Richard Ponce, Cristian Carlos, Alejandro Alfaro, Joseph A. Pinto, Williams Fajardo, Luciana Lancho, Indira Tirado-Hurtado, Layonel Torres, Michael Ayudant
Publikováno v:
Critical Reviews in Oncology/Hematology. 134:22-30
Helicobacter pylori (H. pylori) is a cosmopolite bacteria and the main responsible for the high burden of gastric cancer in developing countries, such as Peru. In this review, we describe some historical facts in the H. Pylori discovery, the first re
Publikováno v:
Saudi Journal of Gastroenterology. 28:393
Autor:
Maria Ketelaar, Michael R. Hayden, Colin J. D. Ross, Miguel Inca-Martinez, Pilar Mazzetti, Jennifer A. Collins, Ramy A. Slama, Mario Cornejo-Olivas, Indira Tirado-Hurtado, Diego Véliz-Otani, Galen E.B. Wright, Chris Kay
Publikováno v:
European Journal of Human Genetics. 25:332-340
Huntington disease (HD) is a dominant neurodegenerative disorder caused by a CAG repeat expansion in the Huntingtin (HTT) gene. HD occurs worldwide, but the causative mutation is found on different HTT haplotypes in distinct ethnic groups. In Latin A