Showing results (41-50 of 50) with videos related to

Sort By:
Pageof 5
You have reached the last page of results.This site can display upto 50 results.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|February 10, 2019
Comprehensive Genetic Characterization of Human Thyroid Cancer Cell Lines: A Validated Panel for Preclinical StudiesIñigo Landa, Nikita Pozdeyev, Christopher Korch, et al.
Endocrine-Related Cancer|September 25, 2009
Overexpression and activation of EGFR and VEGFR2 in medullary thyroid carcinomas is related to metastasisCristina Rodríguez-Antona, Judith Pallares, Cristina Montero-Conde, et al.
Cancer Research|July 19, 2012
Hematologic β-tubulin VI isoform exhibits genetic variability that influences paclitaxel toxicityLuis J Leandro-García, Susanna Leskelä, Lucía Inglada-Pérez, et al.
International Journal of Cancer|April 10, 2015
Thyroid cancer GWAS identifies 10q26.12 and 6q14.1 as novel susceptibility loci and reveals genetic heterogeneity among populationsVeronika Mancikova, Raquel Cruz, Lucía Inglada-Pérez, et al.
Cancer Research|October 3, 2007
Association study of 69 genes in the ret pathway identifies low-penetrance loci in sporadic medullary thyroid carcinomaSergio Ruiz-Llorente, Cristina Montero-Conde, Roger L Milne, et al.
The American Journal of Pathology|December 4, 2012
Differential gene expression of medullary thyroid carcinoma reveals specific markers associated with genetic conditionsAgnieszka Maliszewska, Luis J Leandro-Garcia, Esmeralda Castelblanco, et al.
Molecular Endocrinology (Baltimore, Md.)|October 29, 2010
Research resource: Transcriptional profiling reveals different pseudohypoxic signatures in SDHB and VHL-related pheochromocytomasElena López-Jiménez, Gonzalo Gómez-López, L Javier Leandro-García, et al.
Nature Genetics|June 21, 2011
Exome sequencing identifies MAX mutations as a cause of hereditary pheochromocytomaIñaki Comino-Méndez, Francisco J Gracia-Aznárez, Francesca Schiavi, et al.
Nature|October 8, 2015
Alternative transcription initiation leads to expression of a novel ALK isoform in cancerThomas Wiesner, William Lee, Anna C Obenauf, et al.
Plos Genetics|September 5, 2009
The variant rs1867277 in FOXE1 gene confers thyroid cancer susceptibility through the recruitment of USF1/USF2 transcription factorsIñigo Landa, Sergio Ruiz-Llorente, Cristina Montero-Conde, et al.
Pageof 5