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Peter Bugert

Showing results (131-140 of 174) with videos related to

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Journal of Autoimmunity|December 31, 2013
Late-onset myasthenia gravis - CTLA4(low) genotype association and low-for-age thymic output of naïve T cellsWen-Yu Chuang, Philipp Ströbel, Anna-Lena Bohlender-Willke, et al.
Hamostaseologie|January 27, 2025
The Diagnostic Assessment of Inherited Platelet Function Defects - Part 1: An Overview of the Diagnostic Approach and Laboratory MethodsGero Hoepner, Karina Althaus, Jens Müller, et al.
Breast Cancer Research and Treatment|April 15, 2014
Clinical and molecular characterization of the BRCA2 p.Asn3124Ile variant reveals substantial evidence for pathogenic significanceHarald Martin Surowy, Christian Sutter, Max Mittnacht, et al.
Carcinogenesis|April 21, 2017
The association between breast cancer and S100P methylation in peripheral blood by multicenter case-control studiesRongxi Yang, Sarah Stöcker, Sarah Schott, et al.
Hamostaseologie|January 27, 2025
The Diagnostic Assessment of Platelet Function Defects - Part 2: Update on Platelet DisordersKarina Althaus, Gero Hoepner, Barbara Zieger, et al.
Plos One|June 6, 2012
Genetic analyses of heme oxygenase 1 (HMOX1) in different forms of pancreatitisSebastian Weis, Moritz Jesinghaus, Peter Kovacs, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|March 25, 2005
Association of NCOA3 polymorphisms with breast cancer riskBarbara Burwinkel, Michael Wirtenberger, Rüdiger Klaes, et al.
International Journal of Cancer|September 13, 2014
DNA methylation array analyses identified breast cancer-associated HYAL2 methylation in peripheral bloodRongxi Yang, Katrin Pfütze, Manuela Zucknick, et al.
Journal of Medical Genetics|April 24, 2010
A BRCA1 promoter variant (rs11655505) and breast cancer riskPaolo Verderio, Sara Pizzamiglio, Melissa C Southey, et al.
Breast Cancer Research and Treatment|January 10, 2012
Molecular and clinical characterization of an in frame deletion of uncertain clinical significance in the BRCA2 geneMichelle G Rath, Farnoosh Fathali-Zadeh, Anne Langheinz, et al.
Pageof 18

Showing results (131-140 of 174) with videos related to

Sort By:
Pageof 18
Journal of Autoimmunity|December 31, 2013
Late-onset myasthenia gravis - CTLA4(low) genotype association and low-for-age thymic output of naïve T cellsWen-Yu Chuang, Philipp Ströbel, Anna-Lena Bohlender-Willke, et al.
Hamostaseologie|January 27, 2025
The Diagnostic Assessment of Inherited Platelet Function Defects - Part 1: An Overview of the Diagnostic Approach and Laboratory MethodsGero Hoepner, Karina Althaus, Jens Müller, et al.
Breast Cancer Research and Treatment|April 15, 2014
Clinical and molecular characterization of the BRCA2 p.Asn3124Ile variant reveals substantial evidence for pathogenic significanceHarald Martin Surowy, Christian Sutter, Max Mittnacht, et al.
Carcinogenesis|April 21, 2017
The association between breast cancer and S100P methylation in peripheral blood by multicenter case-control studiesRongxi Yang, Sarah Stöcker, Sarah Schott, et al.
Hamostaseologie|January 27, 2025
The Diagnostic Assessment of Platelet Function Defects - Part 2: Update on Platelet DisordersKarina Althaus, Gero Hoepner, Barbara Zieger, et al.
Plos One|June 6, 2012
Genetic analyses of heme oxygenase 1 (HMOX1) in different forms of pancreatitisSebastian Weis, Moritz Jesinghaus, Peter Kovacs, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|March 25, 2005
Association of NCOA3 polymorphisms with breast cancer riskBarbara Burwinkel, Michael Wirtenberger, Rüdiger Klaes, et al.
International Journal of Cancer|September 13, 2014
DNA methylation array analyses identified breast cancer-associated HYAL2 methylation in peripheral bloodRongxi Yang, Katrin Pfütze, Manuela Zucknick, et al.
Journal of Medical Genetics|April 24, 2010
A BRCA1 promoter variant (rs11655505) and breast cancer riskPaolo Verderio, Sara Pizzamiglio, Melissa C Southey, et al.
Breast Cancer Research and Treatment|January 10, 2012
Molecular and clinical characterization of an in frame deletion of uncertain clinical significance in the BRCA2 geneMichelle G Rath, Farnoosh Fathali-Zadeh, Anne Langheinz, et al.
Pageof 18