Hakutulokset - Colin C. Pritchard

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  1. 1
    Molecular Alterations and Biomarkers in Colorectal Cancer

    Molecular Alterations and Biomarkers in Colorectal Cancer Tekijä William M. Grady, Colin C. Pritchard

    Julkaistu 2013
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  2. 2
    DNA-Repair Gene Mutations in Metastatic Prostate Cancer

    DNA-Repair Gene Mutations in Metastatic Prostate Cancer Tekijä Colin C. Pritchard, Kenneth Offit, Peter S. Nelson

    Julkaistu 2016
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  3. 3
    MicroRNA profiling: approaches and considerations

    MicroRNA profiling: approaches and considerations Tekijä Colin C. Pritchard, Heather H. Cheng, Muneesh Tewari

    Julkaistu 2012
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  4. 4
    Lynch Syndrome: From Screening to Diagnosis to Treatment in the Era of Modern Molecular Oncology

    Lynch Syndrome: From Screening to Diagnosis to Treatment in the Era of Modern Molecular Oncology Tekijä Stacey A. Cohen, Colin C. Pritchard, Gail P. Jarvik

    Julkaistu 2019
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  5. 5
    Project normal: Defining normal variance in mouse gene expression

    Project normal: Defining normal variance in mouse gene expression Tekijä Colin C. Pritchard, Li Hsu, Jeffrey J. Delrow, Peter S. Nelson

    Julkaistu 2001
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  6. 6
    Design and Analysis for Studying microRNAs in Human Disease: A Primer on -Omic Technologies

    Design and Analysis for Studying microRNAs in Human Disease: A Primer on -Omic Technologies Tekijä Viswam S. Nair, Colin C. Pritchard, Muneesh Tewari, John P. A. Ioannidis

    Julkaistu 2014
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  7. 7
    MSIplus for Integrated Colorectal Cancer Molecular Testing by Next-Generation Sequencing

    MSIplus for Integrated Colorectal Cancer Molecular Testing by Next-Generation Sequencing Tekijä Jennifer A. Hempelmann, Sheena M. Scroggins, Colin C. Pritchard, Stephen J. Salipante

    Julkaistu 2015
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  8. 8
    Biallelic Inactivation of BRCA2 in Platinum-sensitive Metastatic Castration-resistant Prostate Cancer

    Biallelic Inactivation of BRCA2 in Platinum-sensitive Metastatic Castration-resistant Prostate Cancer Tekijä Heather H. Cheng, Colin C. Pritchard, Thomas E. Boyd, Peter S. Nelson, Bruce Montgomery

    Julkaistu 2015
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  9. 9
    The effects of genomic germline variant reclassification on clinical cancer care

    The effects of genomic germline variant reclassification on clinical cancer care Tekijä Thomas P. Slavin, Sophia Manjarrez, Colin C. Pritchard, Stacy W. Gray, Jeffrey N. Weitzel

    Julkaistu 2019
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  10. 10
    Single molecule molecular inversion probes for targeted, high-accuracy detection of low-frequency variation

    Single molecule molecular inversion probes for targeted, high-accuracy detection of low-frequency variation Tekijä Joseph B. Hiatt, Colin C. Pritchard, Stephen J. Salipante, Brian J. O’Roak, Jay Shendure

    Julkaistu 2013
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  11. 11
    Microsatellite Instability Detection by Next Generation Sequencing

    Microsatellite Instability Detection by Next Generation Sequencing Tekijä Stephen J. Salipante, Sheena M. Scroggins, Heather L. Hampel, Emily H. Turner, Colin C. Pritchard

    Julkaistu 2014
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  12. 12
    Significance and implications of FDA approval of pembrolizumab for biomarker-defined disease

    Significance and implications of FDA approval of pembrolizumab for biomarker-defined disease Tekijä Michael Boyiadzis, John M. Kirkwood, John L. Marshall, Colin C. Pritchard, Nilofer S. Azad, James L. Gulley

    Julkaistu 2018
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  13. 13
    Hematopoietic cells and osteoblasts are derived from a common marrow progenitor after bone marrow transplantation

    Hematopoietic cells and osteoblasts are derived from a common marrow progenitor after bone marrow transplantation Tekijä Massimo Dominici, Colin C. Pritchard, John E. Garlits, Ted J. Hofmann, Derek A. Persons, Edwin M. Horwitz

    Julkaistu 2004
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  14. 14
    Colon and Endometrial Cancers With Mismatch Repair Deficiency Can Arise From Somatic, Rather Than Germline, Mutations

    Colon and Endometrial Cancers With Mismatch Repair Deficiency Can Arise From Somatic, Rather Than Germline, Mutations Tekijä Sigurdís Haraldsdóttir, Heather Hampel, Jerneja Tomšič, Wendy L. Frankel, Rachel Pearlman, Albert de la Chapelle, Colin C. Pritchard

    Julkaistu 2014
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  15. 15
    CADD score has limited clinical validity for the identification of pathogenic variants in noncoding regions in a hereditary cancer panel

    CADD score has limited clinical validity for the identification of pathogenic variants in noncoding regions in a hereditary cancer panel Tekijä Cheryl Mather, Sean D. Mooney, Stephen J. Salipante, Sheena Scroggins, David Wu, Colin C. Pritchard, Brian H. Shirts

    Julkaistu 2016
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  16. 16
    Conserved Gene Expression Programs Integrate Mammalian Prostate Development and Tumorigenesis

    Conserved Gene Expression Programs Integrate Mammalian Prostate Development and Tumorigenesis Tekijä Colin C. Pritchard, Brig Mecham, Ruth F. Dumpit, Ilsa M. Coleman, M. Bhattacharjee, Qian Chen, Robert A. Sikes, Peter S. Nelson

    Julkaistu 2009
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  17. 17
    Systematic misclassification of missense variants in BRCA1 and BRCA2 “coldspots”

    Systematic misclassification of missense variants in BRCA1 and BRCA2 “coldspots” Tekijä Jennifer N. Dines, Brian H. Shirts, Thomas P. Slavin, Tom Walsh, Mary‐Claire King, Douglas M. Fowler, Colin C. Pritchard

    Julkaistu 2020
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  18. 18
    Increased Expression of Osteopontin Contributes to the Progression of Prostate Cancer

    Increased Expression of Osteopontin Contributes to the Progression of Prostate Cancer Tekijä Ani C. Khodavirdi, Zhigang Song, Shangxin Yang, Zhong Chen, Shunyou Wang, Hong Wu, Colin C. Pritchard, Peter S. Nelson, Pradip Roy‐Burman

    Julkaistu 2006
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  19. 19
    Accurate Pan-Cancer Molecular Diagnosis of Microsatellite Instability by Single-Molecule Molecular Inversion Probe Capture and High-Throughput Sequencing

    Accurate Pan-Cancer Molecular Diagnosis of Microsatellite Instability by Single-Molecule Molecular Inversion Probe Capture and High-Throughput Sequencing Tekijä Adam Waalkes, Nahum Smith, Kelsi Penewit, Jennifer A. Hempelmann, Eric Q. Konnick, Ronald J. Hause, Colin C. Pritchard, Stephen J. Salipante

    Julkaistu 2018
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  20. 20
    Two-stain immunohistochemical screening for Lynch syndrome in colorectal cancer may fail to detect mismatch repair deficiency

    Two-stain immunohistochemical screening for Lynch syndrome in colorectal cancer may fail to detect mismatch repair deficiency Tekijä Rachel Pearlman, Michael J. Markow, Deborah A. Knight, Wei Chen, Christina A. Arnold, Colin C. Pritchard, Heather Hampel, Wendy L. Frankel

    Julkaistu 2018
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