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Thomas Ried

Showing results (21-30 of 257) with videos related to

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The Thoracic and Cardiovascular Surgeon|January 25, 2013
Successful treatment of pure aortic insufficiency with transapical implantation of the JenaValveSabine Bleiziffer, Domenico Mazzitelli, Christian Nöbauer, et al.
Nucleus (Austin, Tex.)|January 28, 2017
Chromosome conformation and gene expression patterns differ profoundly in human fibroblasts grown in spheroids versus monolayersHaiming Chen, Laura Seaman, Sijia Liu, et al.
Cellular Oncology : the Official Journal of the International Society for Cellular Oncology|July 11, 2006
Molecular cytogenetics: genomic imbalances in colorectal cancer and their clinical impactMarian Grade, Heinz Becker, Torsten Liersch, et al.
Biotechniques|May 11, 2007
Isolation and solubilization of proteins after TRIzol extraction of RNA and DNA from patient material following prolonged storageAmanda B Hummon, Sharlene R Lim, Michael J Difilippantonio, et al.
Nucleic Acids Research|March 9, 2013
Concurrent V(D)J recombination and DNA end instability increase interchromosomal trans-rearrangements in ATM-deficient thymocytesSteven Bowen, Darawalee Wangsa, Thomas Ried, et al.
Iscience|February 2, 2024
The fragile X locus is prone to spontaneous DNA damage that is preferentially repaired by nonhomologous end-joining to preserve genome integrityDaman Kumari, Rachel Adihe Lokanga, Cai McCann, et al.
Nature Protocols|April 5, 2007
Spectral karyotyping analysis of human and mouse chromosomesHesed M Padilla-Nash, Linda Barenboim-Stapleton, Michael J Difilippantonio, et al.
Advances in Experimental Medicine and Biology|December 14, 2006
From genome to proteome in tumor profiling: molecular events in colorectal cancer genesisJens K Habermann, Uwe J Roblick, Madhvi Upender, et al.
Oncogene|February 13, 2002
Centrosome abnormalities, recurring deletions of chromosome 4, and genomic amplification of HER2/neu define mouse mammary gland adenocarcinomas induced by mutant HER2/neuCristina Montagna, Eran R Andrechek, Hesed Padilla-Nash, et al.
Experimental Dermatology|January 16, 2007
Spectral karyotyping demonstrates genetically unstable skin-homing T lymphocytes in cutaneous T-cell lymphomaHesed M Padilla-Nash, Kaida Wu, Helle Just, et al.
Pageof 26

Showing results (21-30 of 257) with videos related to

Sort By:
Pageof 26
The Thoracic and Cardiovascular Surgeon|January 25, 2013
Successful treatment of pure aortic insufficiency with transapical implantation of the JenaValveSabine Bleiziffer, Domenico Mazzitelli, Christian Nöbauer, et al.
Nucleus (Austin, Tex.)|January 28, 2017
Chromosome conformation and gene expression patterns differ profoundly in human fibroblasts grown in spheroids versus monolayersHaiming Chen, Laura Seaman, Sijia Liu, et al.
Cellular Oncology : the Official Journal of the International Society for Cellular Oncology|July 11, 2006
Molecular cytogenetics: genomic imbalances in colorectal cancer and their clinical impactMarian Grade, Heinz Becker, Torsten Liersch, et al.
Biotechniques|May 11, 2007
Isolation and solubilization of proteins after TRIzol extraction of RNA and DNA from patient material following prolonged storageAmanda B Hummon, Sharlene R Lim, Michael J Difilippantonio, et al.
Nucleic Acids Research|March 9, 2013
Concurrent V(D)J recombination and DNA end instability increase interchromosomal trans-rearrangements in ATM-deficient thymocytesSteven Bowen, Darawalee Wangsa, Thomas Ried, et al.
Iscience|February 2, 2024
The fragile X locus is prone to spontaneous DNA damage that is preferentially repaired by nonhomologous end-joining to preserve genome integrityDaman Kumari, Rachel Adihe Lokanga, Cai McCann, et al.
Nature Protocols|April 5, 2007
Spectral karyotyping analysis of human and mouse chromosomesHesed M Padilla-Nash, Linda Barenboim-Stapleton, Michael J Difilippantonio, et al.
Advances in Experimental Medicine and Biology|December 14, 2006
From genome to proteome in tumor profiling: molecular events in colorectal cancer genesisJens K Habermann, Uwe J Roblick, Madhvi Upender, et al.
Oncogene|February 13, 2002
Centrosome abnormalities, recurring deletions of chromosome 4, and genomic amplification of HER2/neu define mouse mammary gland adenocarcinomas induced by mutant HER2/neuCristina Montagna, Eran R Andrechek, Hesed Padilla-Nash, et al.
Experimental Dermatology|January 16, 2007
Spectral karyotyping demonstrates genetically unstable skin-homing T lymphocytes in cutaneous T-cell lymphomaHesed M Padilla-Nash, Kaida Wu, Helle Just, et al.
Pageof 26