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Martin Moorhead

Showing results (11-20 of 26) with videos related to

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Arthritis & Rheumatology (Hoboken, N.J.)|December 22, 2016
Discovery of T Cell Receptor β Motifs Specific to HLA-B27-Positive Ankylosing Spondylitis by Deep Repertoire Sequence AnalysisMalek Faham, Victoria Carlton, Martin Moorhead, et al.
Genome Biology|November 22, 2007
Analysis of molecular inversion probe performance for allele copy number determinationYuker Wang, Martin Moorhead, George Karlin-Neumann, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 4, 2009
High-throughput, high-accuracy array-based resequencingJianbiao Zheng, Martin Moorhead, Li Weng, et al.
Human Mutation|January 12, 2008
Rapid identification of somatic mutations in colorectal and breast cancer tissues using mismatch repair detection (MRD)Steven Bentivegna, Jianbiao Zheng, Eugeni Namsaraev, et al.
Human Gene Therapy|April 18, 2022
Cell-Selective Adeno-Associated Virus-Mediated <i>SCN1A</i> Gene Regulation Therapy Rescues Mortality and Seizure Phenotypes in a Dravet Syndrome Mouse Model and Is Well Tolerated in Nonhuman PrimatesAnnie Tanenhaus, Timothy Stowe, Andrew Young, et al.
The Lancet. Oncology|April 6, 2015
Circulating tumour DNA and CT monitoring in patients with untreated diffuse large B-cell lymphoma: a correlative biomarker studyMark Roschewski, Kieron Dunleavy, Stefania Pittaluga, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 6, 2005
Multiplexed variation scanning for 1,000 amplicons in hundreds of patients using mismatch repair detection (MRD) on tag arraysMalek Faham, Jianbiao Zheng, Martin Moorhead, et al.
BMC Medical Genomics|February 21, 2009
High quality copy number and genotype data from FFPE samples using Molecular Inversion Probe (MIP) microarraysYuker Wang, Victoria E H Carlton, George Karlin-Neumann, et al.
British Journal of Haematology|December 23, 2017
A comparison of minimal residual disease detection in autografts among ASO-qPCR, droplet digital PCR, and next-generation sequencing in patients with multiple myeloma who underwent autologous stem cell transplantationHiroyuki Takamatsu, Rachel K Wee, Yoshitaka Zaimoku, et al.
Nature Genetics|October 18, 2005
Population structure, differential bias and genomic control in a large-scale, case-control association studyDavid G Clayton, Neil M Walker, Deborah J Smyth, et al.
Pageof 3

Showing results (11-20 of 26) with videos related to

Sort By:
Pageof 3
Arthritis & Rheumatology (Hoboken, N.J.)|December 22, 2016
Discovery of T Cell Receptor β Motifs Specific to HLA-B27-Positive Ankylosing Spondylitis by Deep Repertoire Sequence AnalysisMalek Faham, Victoria Carlton, Martin Moorhead, et al.
Genome Biology|November 22, 2007
Analysis of molecular inversion probe performance for allele copy number determinationYuker Wang, Martin Moorhead, George Karlin-Neumann, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 4, 2009
High-throughput, high-accuracy array-based resequencingJianbiao Zheng, Martin Moorhead, Li Weng, et al.
Human Mutation|January 12, 2008
Rapid identification of somatic mutations in colorectal and breast cancer tissues using mismatch repair detection (MRD)Steven Bentivegna, Jianbiao Zheng, Eugeni Namsaraev, et al.
Human Gene Therapy|April 18, 2022
Cell-Selective Adeno-Associated Virus-Mediated <i>SCN1A</i> Gene Regulation Therapy Rescues Mortality and Seizure Phenotypes in a Dravet Syndrome Mouse Model and Is Well Tolerated in Nonhuman PrimatesAnnie Tanenhaus, Timothy Stowe, Andrew Young, et al.
The Lancet. Oncology|April 6, 2015
Circulating tumour DNA and CT monitoring in patients with untreated diffuse large B-cell lymphoma: a correlative biomarker studyMark Roschewski, Kieron Dunleavy, Stefania Pittaluga, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 6, 2005
Multiplexed variation scanning for 1,000 amplicons in hundreds of patients using mismatch repair detection (MRD) on tag arraysMalek Faham, Jianbiao Zheng, Martin Moorhead, et al.
BMC Medical Genomics|February 21, 2009
High quality copy number and genotype data from FFPE samples using Molecular Inversion Probe (MIP) microarraysYuker Wang, Victoria E H Carlton, George Karlin-Neumann, et al.
British Journal of Haematology|December 23, 2017
A comparison of minimal residual disease detection in autografts among ASO-qPCR, droplet digital PCR, and next-generation sequencing in patients with multiple myeloma who underwent autologous stem cell transplantationHiroyuki Takamatsu, Rachel K Wee, Yoshitaka Zaimoku, et al.
Nature Genetics|October 18, 2005
Population structure, differential bias and genomic control in a large-scale, case-control association studyDavid G Clayton, Neil M Walker, Deborah J Smyth, et al.
Pageof 3