Zobrazeno 1 - 10
of 24
pro vyhledávání: '"Vicente Forero"'
Publikováno v:
Tecnociencia, Vol 24, Iss 2 (2022)
NASE (Network for Astronomy School Education) se constituyó en la Asamblea General de la IAU en Río de Janeiro en 2009 con el propósito de entrenar docentes en la enseñanza de la astronomía usando materiales baratos y fáciles de conseguir para
Externí odkaz:
https://doaj.org/article/c38d910551324b2b980caa9e43930f89
Autor:
Manoj Kumar Kashyap, Hiren Karathia, Deepak Kumar, Roberto Vera Alvarez, Jose Vicente Forero-Forero, Eider Moreno, Juliana Velez Lujan, Carlos Ivan Amaya-Chanaga, Newton Medeiros Vidal, Zhe Yu, Emanuela M. Ghia, Paula A. Lengerke-Diaz, Daniel Achinko, Michael Y. Choi, Laura Z. Rassenti, Leonardo Mariño-Ramírez, Stephen M. Mount, Sridhar Hannenhalli, Thomas J. Kipps, Januario E. Castro
Publikováno v:
Molecular Therapy: Nucleic Acids, Vol 35, Iss 2, Pp 102202- (2024)
Splicing factor 3b subunit 1 (SF3B1) is the largest subunit and core component of the spliceosome. Inhibition of SF3B1 was associated with an increase in broad intron retention (IR) on most transcripts, suggesting that IR can be used as a marker of s
Externí odkaz:
https://doaj.org/article/adf59c81f6f94126a63b606708311ab5
Autor:
Flora Tassone, Hiu Tung Tang, Laura Yuriko González-Teshima, Wilmar Saldarriaga, Jose Vicente Forero-Forero
Publikováno v:
Journal of Intellectual Disabilities. 26:800-807
Fragile X syndrome (FXS) has a classic phenotype, however its expression can be variable among full mutation males. This is secondary to variable methylation mosaicisms and the number of CGG triplet repeats in the non-coding region of the Fragile X M
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b0e88df85e2f223b5638e86814e37492
https://doi.org/10.1177/1744629521995346
https://doi.org/10.1177/1744629521995346
Autor:
Manoj Kumar Kashyap, Hiren Karathia, Deepak Kumar, Roberto Vera Alvarez, Paula A Lengerke-Diaz, Jose Vicente Forero-Forero, Eider Moreno, Juliana Velez Lujan, Carlos Ivan Amaya-Chanaga, Newton Medeiros Vidal, Zhe Yu, Daniel Achinko, Emanuela M. Ghia, Michael Y. Choi, Laura Z. Rassenti, Leonardo Mariño-Ramírez, Stephen M. Mount, Sridhar Hannenhalli, Thomas J. Kipps, Januario E. Castro
BackgroundAlternative splicing (AS) is a fundamental process in eukaryotes contributing to the diversity of mRNA isoforms with variable ratios of intron/exon. SF3B1 is a pivotal protein of the spliceosome machinery. Mutations in the SF3B1 gene have p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e9780fc833c4337eeaff49ae6153d3bf
https://doi.org/10.21203/rs.3.rs-1622375/v1
https://doi.org/10.21203/rs.3.rs-1622375/v1
Autor:
Laura María Rodríguez Santa, Laura Yuriko González Teshima, Jose Vicente Forero Forero, Andres Orlando Castillo Giraldo
Publikováno v:
Journal of Pregnancy, Vol 2015 (2015)
In recent years, microRNAs (miRNAs) have been the focus of research for their role in posttranscriptional regulation and as potential biomarkers of risk for disease development. Their identification in specific physiological processes, like angiogene
Externí odkaz:
https://doaj.org/article/7893a4762d3c45cfb2abe90d49f90d85
Autor:
Mohamed A. Kharfan-Dabaja, Allison C. Rosenthal, Paula A. Lengerke-Diaz, Zaid Abdel Rahman, Jose Vicente Forero-Forero, Januario E. Castro, Eider F. Moreno-Cortes, Megan Melody
Publikováno v:
Hematology/oncology and stem cell therapy.
Objective/background Despite the success of chimeric antigen receptor (CAR) T-cell therapy in patients with aggressive non-Hodgkin lymphoma (aNHL), some patients still fail treatment, and their prognosis is dismal. Methods We performed a retrospectiv
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::37ae87963ff8f562cc63a563401cafb9
https://pubmed.ncbi.nlm.nih.gov/34562407
https://pubmed.ncbi.nlm.nih.gov/34562407
Autor:
Carlos A. Fandiño Losada, Laura Y. González Teshima, José Vicente Forero F., Carolina Isaza de Lourido, José Rafael Tovar C., Julián Ramírez Cheyne, Marisol Silva, Sergio Aguilar Gaxiola, Flora Tassone, Wilmar Saldarriaga Gil, Randi J. Hagerman
Este libro cuenta cómo se logra demostrar que Ricaurte es un conglomerado genético de síndrome X frágil (SXF) con la prevalencia más alta en el mundo a través de un proyecto de investigación cofinanciado entre la Universidad del Valle y el ins
Autor:
Eider Felipe Moreno, Natalie Booth, Paula A Lengerke Diaz, Januario E. Castro, Daniela A. Castro-Martinez, Jose Vicente Forero-Forero, Juan Esteban Garcia-Robledo
Publikováno v:
Journal of Clinical Oncology. 39:e14516-e14516
e14516 Background: IEC are arguably the most promising therapy in oncology, and FDA approvals for CAR T cells are a testament to their real potential. This has led to a great growth of clinical trials (CT), making the evaluation of their associated d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::99151468d56058b8e60e0fae5ee4fb8a
https://doi.org/10.1200/jco.2021.39.15_suppl.e14516
https://doi.org/10.1200/jco.2021.39.15_suppl.e14516
Autor:
Paula A. Lengerke-Diaz, Januario E. Castro, Jose Vicente Forero-Forero, Eider F. Moreno-Cortes
Publikováno v:
Critical Reviews in Oncology/Hematology. 159:103239
There is a rapid growth of published data associated with chimeric antigen receptor (CAR) T-cells, and its evaluation is becoming challenging. We performed a review of the ClinicalTrials.gov database, searching for clinical trials using CAR T-cell th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::88e950f11d9eb9a511c7730fbbfa726c
https://doi.org/10.1016/j.critrevonc.2021.103239
https://doi.org/10.1016/j.critrevonc.2021.103239
Autor:
Laura Yuriko González-Teshima, Antonio Madrid, Jose Vicente Forero-Forero, Wilmar Saldarriaga, Julián Ramírez-Cheyne
Publikováno v:
Revista Colombiana de Cardiología, Vol 23, Iss 5, Pp 443-452 (2016)
ResumenEl síndrome de deleción 22q11 consiste en una agrupación variable de características fenotípicas secundarias a la pérdida del material genético localizado en la banda 22q11.2. El espectro de deleción del 22q11 abarca varios síndromes,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::80c3140145cf13c2778189a08d363cec