Showing results (321-330 of 628) with videos related to
Sort By:
Pageof 63
BMC Cancer|July 12, 2014
Stability of the CpG island methylator phenotype during glioma progression and identification of methylated loci in secondary glioblastomasVictoria K Hill, Thoraia Shinawi, Christopher J Ricketts, et al.Epigenetics|January 8, 2013
DNA methylation profiles of long- and short-term glioblastoma survivorsThoraia Shinawi, Victoria K Hill, Dietmar Krex, et al.Blood|May 3, 2002
Paraneoplastic erythrocytosis associated with an inactivating point mutation of the von Hippel-Lindau gene in a renal cell carcinomaMichael S Wiesener, Melchior Seyfarth, Christina Warnecke, et al.Lancet (London, England)|April 27, 2001
Germline SDHD mutation in familial phaeochromocytomaD Astuti, F Douglas, T W Lennard, et al.American Journal of Human Genetics|June 19, 2001
Gene mutations in the succinate dehydrogenase subunit SDHB cause susceptibility to familial pheochromocytoma and to familial paragangliomaD Astuti, F Latif, A Dallol, et al.European Journal of Cancer (Oxford, England : 1990)|July 27, 2002
Frequent 3p allele loss and epigenetic inactivation of the RASSF1A tumour suppressor gene from region 3p21.3 in head and neck squamous cell carcinomaR P Hogg, S Honorio, A Martinez, et al.Molecular Vision|April 21, 2010
Nonsense mutation in TMEM126A causing autosomal recessive optic atrophy and auditory neuropathyEsther Meyer, Michel Michaelides, Louise J Tee, et al.Cancer Chemotherapy and Pharmacology|January 17, 2025
A phase I study of MLN4924 and belinostat in relapsed/refractory acute myeloid leukemia or myelodysplastic syndromeKeri R Maher, Danielle Shafer, Dale Schaar, et al.JACC. Clinical Electrophysiology|May 31, 2024
Targeting Wavefront Discontinuity Lines for Scar-Related Ventricular Tachycardia Ablation: A Novel Functional Substrate Ablation ApproachTimothy R Maher, Benjamin L Freedman, Shu Yang, et al.Journal of Medical Genetics|July 1, 1991
Von Hippel-Lindau disease: a genetic studyE R Maher, L Iselius, J R Yates, et al.Pageof 63