Torthaí cuardaigh - Colin C. Pritchard
- 1 - 20 toradh as 89 á dtaispeáint
- Téigh chuig an gcéad leathanach eile
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Molecular Alterations and Biomarkers in Colorectal Cancer de réir William M. Grady, Colin C. Pritchard
Foilsithe / Cruthaithe 2013Revisão -
2
DNA-Repair Gene Mutations in Metastatic Prostate Cancer de réir Colin C. Pritchard, Kenneth Offit, Peter S. Nelson
Foilsithe / Cruthaithe 2016Carta -
3
MicroRNA profiling: approaches and considerations de réir Colin C. Pritchard, Heather H. Cheng, Muneesh Tewari
Foilsithe / Cruthaithe 2012Revisão -
4
Lynch Syndrome: From Screening to Diagnosis to Treatment in the Era of Modern Molecular Oncology de réir Stacey A. Cohen, Colin C. Pritchard, Gail P. Jarvik
Foilsithe / Cruthaithe 2019Revisão -
5
Project normal: Defining normal variance in mouse gene expression de réir Colin C. Pritchard, Li Hsu, Jeffrey J. Delrow, Peter S. Nelson
Foilsithe / Cruthaithe 2001Artigo -
6
Design and Analysis for Studying microRNAs in Human Disease: A Primer on -Omic Technologies de réir Viswam S. Nair, Colin C. Pritchard, Muneesh Tewari, John P. A. Ioannidis
Foilsithe / Cruthaithe 2014Revisão -
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Biallelic Inactivation of BRCA2 in Platinum-sensitive Metastatic Castration-resistant Prostate Cancer de réir Heather H. Cheng, Colin C. Pritchard, Thomas E. Boyd, Peter S. Nelson, Bruce Montgomery
Foilsithe / Cruthaithe 2015Artigo -
9
The effects of genomic germline variant reclassification on clinical cancer care de réir Thomas P. Slavin, Sophia Manjarrez, Colin C. Pritchard, Stacy W. Gray, Jeffrey N. Weitzel
Foilsithe / Cruthaithe 2019Artigo -
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11
Microsatellite Instability Detection by Next Generation Sequencing de réir Stephen J. Salipante, Sheena M. Scroggins, Heather L. Hampel, Emily H. Turner, Colin C. Pritchard
Foilsithe / Cruthaithe 2014Artigo -
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13
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14
Colon and Endometrial Cancers With Mismatch Repair Deficiency Can Arise From Somatic, Rather Than Germline, Mutations de réir Sigurdís Haraldsdóttir, Heather Hampel, Jerneja Tomšič, Wendy L. Frankel, Rachel Pearlman, Albert de la Chapelle, Colin C. Pritchard
Foilsithe / Cruthaithe 2014Artigo -
15
CADD score has limited clinical validity for the identification of pathogenic variants in noncoding regions in a hereditary cancer panel de réir Cheryl Mather, Sean D. Mooney, Stephen J. Salipante, Sheena Scroggins, David Wu, Colin C. Pritchard, Brian H. Shirts
Foilsithe / Cruthaithe 2016Artigo -
16
Conserved Gene Expression Programs Integrate Mammalian Prostate Development and Tumorigenesis de réir Colin C. Pritchard, Brig Mecham, Ruth F. Dumpit, Ilsa M. Coleman, M. Bhattacharjee, Qian Chen, Robert A. Sikes, Peter S. Nelson
Foilsithe / Cruthaithe 2009Artigo -
17
Systematic misclassification of missense variants in BRCA1 and BRCA2 “coldspots” de réir Jennifer N. Dines, Brian H. Shirts, Thomas P. Slavin, Tom Walsh, Mary‐Claire King, Douglas M. Fowler, Colin C. Pritchard
Foilsithe / Cruthaithe 2020Artigo -
18
Increased Expression of Osteopontin Contributes to the Progression of Prostate Cancer de réir Ani C. Khodavirdi, Zhigang Song, Shangxin Yang, Zhong Chen, Shunyou Wang, Hong Wu, Colin C. Pritchard, Peter S. Nelson, Pradip Roy‐Burman
Foilsithe / Cruthaithe 2006Artigo -
19
Accurate Pan-Cancer Molecular Diagnosis of Microsatellite Instability by Single-Molecule Molecular Inversion Probe Capture and High-Throughput Sequencing de réir Adam Waalkes, Nahum Smith, Kelsi Penewit, Jennifer A. Hempelmann, Eric Q. Konnick, Ronald J. Hause, Colin C. Pritchard, Stephen J. Salipante
Foilsithe / Cruthaithe 2018Artigo -
20
Two-stain immunohistochemical screening for Lynch syndrome in colorectal cancer may fail to detect mismatch repair deficiency de réir Rachel Pearlman, Michael J. Markow, Deborah A. Knight, Wei Chen, Christina A. Arnold, Colin C. Pritchard, Heather Hampel, Wendy L. Frankel
Foilsithe / Cruthaithe 2018Artigo
Uirlisí cuardaigh:
Ábhair a bhaineann le hábhar
Biology
Medicine
Genetics
Cancer
Gene
Internal medicine
Oncology
Prostate cancer
Cancer research
Mutation
Prostate
Germline mutation
Computational biology
Colorectal cancer
Pathology
DNA mismatch repair
Bioinformatics
Allele
Germline
DNA sequencing
Lynch syndrome
Microsatellite
Microsatellite instability
Gynecology
MLH1
DNA
MSH2
MSH6
Phenotype
Computer science