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David A Wheeler

Showing results (31-40 of 175) with videos related to

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Neuropathology and Applied Neurobiology|March 23, 2022
A CTNNB1-altered medulloblastoma shows the immunophenotypic, DNA methylation and transcriptomic profiles of SHH-activated, and not WNT-activated, medulloblastomaJason Chiang, Daniel C Moreira, Nicholas J Pytel, et al.
Genome Research|April 3, 2004
Genomic analysis of the nuclear receptor family: new insights into structure, regulation, and evolution from the rat genomeZhengdong Zhang, Paula E Burch, Austin J Cooney, et al.
Journal of Neuropathology and Experimental Neurology|January 11, 2017
Genomic Alterations of Adamantinomatous and Papillary CraniopharyngiomaTobias Goschzik, Marco Gessi, Verena Dreschmann, et al.
Leukemia & Lymphoma|September 17, 2013
Case series of patients with acute myeloid leukemia receiving hypomethylation therapy and retrospectively found to have IDH1 or IDH2 mutationsChristopher B Benton, Farhad Ravandi, Michael Andreeff, et al.
Genome Research|December 19, 2009
A SNP discovery method to assess variant allele probability from next-generation resequencing dataYufeng Shen, Zhengzheng Wan, Cristian Coarfa, et al.
Pediatric Blood & Cancer|December 21, 2012
Identification of TP53 as an acute lymphocytic leukemia susceptibility gene through exome sequencingBradford C Powell, Lichun Jiang, Donna M Muzny, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 22, 2024
Evaluation of Bayesian point-based system on the variant classification of hereditary cancer predisposition genesMohammad K Eldomery, Jamie L Maciaszek, Taylor Cain, et al.
Physiological Genomics|July 21, 2011
Resequencing of IRS2 reveals rare variants for obesity but not fasting glucose homeostasis in Hispanic childrenNancy F Butte, V Saroja Voruganti, Shelley A Cole, et al.
Biopreservation and Biobanking|June 20, 2018
National Cancer Institute Biospecimen Evidence-Based Practices: Harmonizing Procedures for Nucleic Acid Extraction from Formalin-Fixed, Paraffin-Embedded TissueSarah R Greytak, Kelly B Engel, Erik Zmuda, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|September 10, 2011
Disruptive TP53 mutation is associated with aggressive disease characteristics in an orthotopic murine model of oral tongue cancerDaisuke Sano, Tong-Xin Xie, Thomas J Ow, et al.
Pageof 18

Showing results (31-40 of 175) with videos related to

Sort By:
Pageof 18
Neuropathology and Applied Neurobiology|March 23, 2022
A CTNNB1-altered medulloblastoma shows the immunophenotypic, DNA methylation and transcriptomic profiles of SHH-activated, and not WNT-activated, medulloblastomaJason Chiang, Daniel C Moreira, Nicholas J Pytel, et al.
Genome Research|April 3, 2004
Genomic analysis of the nuclear receptor family: new insights into structure, regulation, and evolution from the rat genomeZhengdong Zhang, Paula E Burch, Austin J Cooney, et al.
Journal of Neuropathology and Experimental Neurology|January 11, 2017
Genomic Alterations of Adamantinomatous and Papillary CraniopharyngiomaTobias Goschzik, Marco Gessi, Verena Dreschmann, et al.
Leukemia & Lymphoma|September 17, 2013
Case series of patients with acute myeloid leukemia receiving hypomethylation therapy and retrospectively found to have IDH1 or IDH2 mutationsChristopher B Benton, Farhad Ravandi, Michael Andreeff, et al.
Genome Research|December 19, 2009
A SNP discovery method to assess variant allele probability from next-generation resequencing dataYufeng Shen, Zhengzheng Wan, Cristian Coarfa, et al.
Pediatric Blood & Cancer|December 21, 2012
Identification of TP53 as an acute lymphocytic leukemia susceptibility gene through exome sequencingBradford C Powell, Lichun Jiang, Donna M Muzny, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 22, 2024
Evaluation of Bayesian point-based system on the variant classification of hereditary cancer predisposition genesMohammad K Eldomery, Jamie L Maciaszek, Taylor Cain, et al.
Physiological Genomics|July 21, 2011
Resequencing of IRS2 reveals rare variants for obesity but not fasting glucose homeostasis in Hispanic childrenNancy F Butte, V Saroja Voruganti, Shelley A Cole, et al.
Biopreservation and Biobanking|June 20, 2018
National Cancer Institute Biospecimen Evidence-Based Practices: Harmonizing Procedures for Nucleic Acid Extraction from Formalin-Fixed, Paraffin-Embedded TissueSarah R Greytak, Kelly B Engel, Erik Zmuda, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|September 10, 2011
Disruptive TP53 mutation is associated with aggressive disease characteristics in an orthotopic murine model of oral tongue cancerDaisuke Sano, Tong-Xin Xie, Thomas J Ow, et al.
Pageof 18