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MLO: Medical Laboratory Observer
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July 27, 2018
Precision medicine and companion diagnostics join the battle against ovarian cancer
Debora Mancini-DiNardo, Krystal Brown
Current Protocols in Human Genetics
|
April 23, 2008
Selection of a platform for mutation detection
Victoria A Joshi, Debora Mancini-DiNardo, Birgit H Funke
Human Molecular Genetics
|
January 30, 2003
A differentially methylated region within the gene Kcnq1 functions as an imprinted promoter and silencer
Debora Mancini-DiNardo, Scott J S Steele, Robert S Ingram, et al.
Genes & Development
|
May 17, 2006
Elongation of the Kcnq1ot1 transcript is required for genomic imprinting of neighboring genes
Debora Mancini-Dinardo, Scott J S Steele, John M Levorse, et al.
Personalized Medicine
|
May 23, 2018
Platform evaluation for rapid genotyping of CYP2C9 and VKORC1 alleles
Victoria A Joshi, Elizabeth Duffy, Birgit H Funke, et al.
Cancer Genetics
|
March 11, 2017
Detection of somatic variants in peripheral blood lymphocytes using a next generation sequencing multigene pan cancer panel
Bradford Coffee, Hannah C Cox, John Kidd, et al.
Human Mutation
|
September 7, 2019
A substantial proportion of apparently heterozygous TP53 pathogenic variants detected with a next-generation sequencing hereditary pan-cancer panel are acquired somatically
Bradford Coffee, Hannah C Cox, Ryan Bernhisel, et al.
Molecular Cell
|
October 28, 2008
Kcnq1ot1 antisense noncoding RNA mediates lineage-specific transcriptional silencing through chromatin-level regulation
Radha Raman Pandey, Tanmoy Mondal, Faizaan Mohammad, et al.
Cancer Genetics
|
May 7, 2019
Prevalence and characteristics of likely-somatic variants in cancer susceptibility genes among individuals who had hereditary pan-cancer panel testing
Thomas P Slavin, Bradford Coffee, Ryan Bernhisel, et al.
Frontiers in Oncology
|
February 16, 2023
Discordance between germline genetic findings and abnormal tumor immunohistochemistry staining of mismatch repair proteins in individuals with suspected Lynch syndrome
Shujuan Pan, Hannah Cox, Jamie Willmott, et al.
Page
of 2
Search research articles
Search
Showing results (1-10 of 18) with videos related to
Sort By:
Page
of 2
MLO: Medical Laboratory Observer
|
July 27, 2018
Precision medicine and companion diagnostics join the battle against ovarian cancer
Debora Mancini-DiNardo, Krystal Brown
Current Protocols in Human Genetics
|
April 23, 2008
Selection of a platform for mutation detection
Victoria A Joshi, Debora Mancini-DiNardo, Birgit H Funke
Human Molecular Genetics
|
January 30, 2003
A differentially methylated region within the gene Kcnq1 functions as an imprinted promoter and silencer
Debora Mancini-DiNardo, Scott J S Steele, Robert S Ingram, et al.
Genes & Development
|
May 17, 2006
Elongation of the Kcnq1ot1 transcript is required for genomic imprinting of neighboring genes
Debora Mancini-Dinardo, Scott J S Steele, John M Levorse, et al.
Personalized Medicine
|
May 23, 2018
Platform evaluation for rapid genotyping of CYP2C9 and VKORC1 alleles
Victoria A Joshi, Elizabeth Duffy, Birgit H Funke, et al.
Cancer Genetics
|
March 11, 2017
Detection of somatic variants in peripheral blood lymphocytes using a next generation sequencing multigene pan cancer panel
Bradford Coffee, Hannah C Cox, John Kidd, et al.
Human Mutation
|
September 7, 2019
A substantial proportion of apparently heterozygous TP53 pathogenic variants detected with a next-generation sequencing hereditary pan-cancer panel are acquired somatically
Bradford Coffee, Hannah C Cox, Ryan Bernhisel, et al.
Molecular Cell
|
October 28, 2008
Kcnq1ot1 antisense noncoding RNA mediates lineage-specific transcriptional silencing through chromatin-level regulation
Radha Raman Pandey, Tanmoy Mondal, Faizaan Mohammad, et al.
Cancer Genetics
|
May 7, 2019
Prevalence and characteristics of likely-somatic variants in cancer susceptibility genes among individuals who had hereditary pan-cancer panel testing
Thomas P Slavin, Bradford Coffee, Ryan Bernhisel, et al.
Frontiers in Oncology
|
February 16, 2023
Discordance between germline genetic findings and abnormal tumor immunohistochemistry staining of mismatch repair proteins in individuals with suspected Lynch syndrome
Shujuan Pan, Hannah Cox, Jamie Willmott, et al.
Page
of 2