Search Results - D. Williams Parsons

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  1. 1
    An 11 base pair duplication in exon 6 of the SMN gene produces a type I spinal muscular atrophy (SMA) phenotype: further evidence for SMN as the primary SMA-determining gene

    An 11 base pair duplication in exon 6 of the SMN gene produces a type I spinal muscular atrophy (SMA) phenotype: further evidence for SMN as the primary SMA-determining gene by D. Williams Parsons

    Published 1996
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  2. 2
    Biological and clinical significance of somatic mutations in Langerhans cell histiocytosis and related histiocytic neoplastic disorders

    Biological and clinical significance of somatic mutations in Langerhans cell histiocytosis and related histiocytic neoplastic disorders by Carl E. Allen, D. Williams Parsons

    Published 2015
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  3. 3
    IDH1 and IDH2: Not Your Typical Oncogenes

    IDH1 and IDH2: Not Your Typical Oncogenes by Zachary J. Reitman, D. Williams Parsons, Hai Yan

    Published 2010
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  4. 4
    Precision Medicine in Pediatric Oncology

    Precision Medicine in Pediatric Oncology by Kieuhoa T. Vo, D. Williams Parsons, Nita L. Seibel

    Published 2019
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  5. 5
    STUDIES ON THE MODE OF ACTION OF THE ADRENOCORTICOTROPIC HORMONE

    STUDIES ON THE MODE OF ACTION OF THE ADRENOCORTICOTROPIC HORMONE by Seymour B. Koritz, Fernand G. Péron, D. Williams Parsons

    Published 1958
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  6. 6
    On the Exogenous Requirements for the Action of ACTH in Vitro on Rat Adrenal Glands

    On the Exogenous Requirements for the Action of ACTH in Vitro on Rat Adrenal Glands by Fernand G. Péron, Seymour B. Koritz, D. Williams Parsons

    Published 1958
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  7. 7
    Mutant Metabolic Enzymes Are at the Origin of Gliomas

    Mutant Metabolic Enzymes Are at the Origin of Gliomas by Hai Yan, Darell D. Bigner, Victor E. Velculescu, D. Williams Parsons

    Published 2009
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  8. 8
    Sodium ion channel mutations in glioblastoma patients correlate with shorter survival

    Sodium ion channel mutations in glioblastoma patients correlate with shorter survival by Avadhut D. Joshi, D. Williams Parsons, Victor E. Velculescu, Gregory J. Riggins

    Published 2011
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  9. 9
    Precision medicine in pediatric oncology: Lessons learned and next steps

    Precision medicine in pediatric oncology: Lessons learned and next steps by Rajen Mody, John R. Prensner, Jessica N. Everett, D. Williams Parsons, Arul M. Chinnaiyan

    Published 2016
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  10. 10
    Intragenic telSMN Mutations: Frequency, Distribution, Evidence of a Founder Effect, and Modification of the Spinal Muscular Atrophy Phenotype by cenSMN Copy Number

    Intragenic telSMN Mutations: Frequency, Distribution, Evidence of a Founder Effect, and Modification of the Spinal Muscular Atrophy Phenotype by cenSMN Copy Number by D. Williams Parsons, Patricia McAndrew, ST Iannaccone, Jerry R. Mendell, Arthur H.M. Burghes, T. Prior

    Published 1998
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  11. 11
    Epitope Landscape in Breast and Colorectal Cancer

    Epitope Landscape in Breast and Colorectal Cancer by Neil H. Segal, D. Williams Parsons, Karl S. Peggs, Victor E. Velculescu, Ken W Kinzler, Bert Vogelstein, James P. Allison

    Published 2008
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  12. 12
    Germline Findings in Tumor-Only Sequencing: Points to Consider for Clinicians and Laboratories: Table 1.

    Germline Findings in Tumor-Only Sequencing: Points to Consider for Clinicians and Laboratories: Table 1. by Victoria M. Raymond, Stacy W. Gray, Sameek Roychowdhury, Steven Joffe, Arul M. Chinnaiyan, D. Williams Parsons, Sharon E. Plon

    Published 2015
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  13. 13
    Identification of Proximal Spinal Muscular Atrophy Carriers and Patients by Analysis of SMNT and SMNC Gene Copy Number

    Identification of Proximal Spinal Muscular Atrophy Carriers and Patients by Analysis of SMNT and SMNC Gene Copy Number by Patricia McAndrew, D. Williams Parsons, Louise R. Simard, Camille Rochette, Peter N. Ray, Jerry R. Mendell, Thomas W. Prior, Arthur H.M. Burghes

    Published 1997
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  14. 14
    The Challenge of Informed Consent and Return of Results in Translational Genomics: Empirical Analysis and Recommendations

    The Challenge of Informed Consent and Return of Results in Translational Genomics: Empirical Analysis and Recommendations by Gail E. Henderson, Susan M. Wolf, Kristine J. Kuczynski, Steven Joffe, Richard R. Sharp, D. Williams Parsons, Bartha Maria Knoppers, Joon‐Ho Yu, Paul S. Appelbaum

    Published 2014
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  15. 15
    Parental Perspectives on Whole-Exome Sequencing in Pediatric Cancer: A Typology of Perceived Utility

    Parental Perspectives on Whole-Exome Sequencing in Pediatric Cancer: A Typology of Perceived Utility by Janet Malek, Melody J. Slashinski, Jill O. Robinson, Amanda M. Gutierrez, D. Williams Parsons, Sharon E. Plon, Laurence B. McCullough, Amy L. McGuire

    Published 2017
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  16. 16
    Is Whole-Exome Sequencing an Ethically Disruptive Technology? Perspectives of Pediatric Oncologists and Parents of Pediatric Patients With Solid Tumors

    Is Whole-Exome Sequencing an Ethically Disruptive Technology? Perspectives of Pediatric Oncologists and Parents of Pediatric Patients With Solid Tumors by Laurence B. McCullough, Melody J. Slashinski, Amy L. McGuire, Richard L. Street, Christine M. Eng, Richard A. Gibbs, D. Williams Parsons, Sharon E. Plon

    Published 2015
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  17. 17
    Target and Agent Prioritization for the Children’s Oncology Group—National Cancer Institute Pediatric MATCH Trial

    Target and Agent Prioritization for the Children’s Oncology Group—National Cancer Institute Pediatric MATCH Trial by Carl E. Allen, Theodore W. Laetsch, Rajen Mody, Meredith S. Irwin, Megan S. Lim, Peter C. Adamson, Nita L. Seibel, D. Williams Parsons, Y. Jae Cho, Katherine A. Janeway

    Published 2016
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  18. 18
    A multidimensional analysis of genes mutated in breast and colorectal cancers

    A multidimensional analysis of genes mutated in breast and colorectal cancers by Jimmy Lin, Christine Gan, Xiaosong Zhang, Siân Jones, Tobias Sjöblom, Laura D. Wood, D. Williams Parsons, Nickolas Papadopoulos, Kenneth W. Kinzler, Bert Vogelstein, Giovanni Parmigiani, Victor E. Velculescu

    Published 2007
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  19. 19
    Reliable tumor detection by whole-genome methylation sequencing of cell-free DNA in cerebrospinal fluid of pediatric medulloblastoma

    Reliable tumor detection by whole-genome methylation sequencing of cell-free DNA in cerebrospinal fluid of pediatric medulloblastoma by Jia Li, Sibo Zhao, Minjung Lee, Yue Yin, Jin Li, Yubin Zhou, Leomar Y. Ballester, Yoshua Esquenazi, Roderick H. Dashwood, Peter J. Davies, D. Williams Parsons, Xiao‐Nan Li, Yun Huang, Deqiang Sun

    Published 2020
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  20. 20
    Obtaining informed consent for clinical tumor and germline exome sequencing of newly diagnosed childhood cancer patients

    Obtaining informed consent for clinical tumor and germline exome sequencing of newly diagnosed childhood cancer patients by Sarah Scollon, Katie Bergstrom, Robin A. Kerstein, Tao Wang, Susan G. Hilsenbeck, Uma Ramamurthy, Richard A. Gibbs, Christine M. Eng, Murali Chintagumpala, Stacey L. Berg, Laurence B. McCullough, Amy L. McGuire, Sharon E. Plon, D. Williams Parsons

    Published 2014
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