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Peter Lohse

Showing results (21-30 of 121) with videos related to

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Fertility and Sterility|February 6, 2008
Common 677C-->T mutation of the 5,10-methylenetetrahydrofolate reductase gene affects follicular estradiol synthesisStephanie Hecht, Roman Pavlik, Peter Lohse, et al.
Der Nervenarzt|September 18, 2024
[Fatigue and sensorimotor instability : Neurologically controlled conversion of post-COVID-19 patients]Thomas Urban, Fritjof Reinhardt, Peter Lohse, et al.
Fertility and Sterility|April 13, 2011
Divergent effects of the 677C>T mutation of the 5,10-methylenetetrahydrofolate reductase (MTHFR) gene on ovarian responsiveness and anti-Müllerian hormone concentrationsRoman Pavlik, Stephanie Hecht, Robert Ochsenkühn, et al.
American Journal of Reproductive Immunology (New York, N.Y. : 1989)|August 30, 2008
Paternal thrombophilic gene mutations are not associated with recurrent miscarriageBettina Toth, Franziska Vocke, Nina Rogenhofer, et al.
Journal of Cardiothoracic Surgery|August 21, 2009
Gene polymorphisms in APOE, NOS3, and LIPC genes may be risk factors for cardiac adverse events after primary CABGSandra Eifert, Astrid Rasch, Andres Beiras-Fernandez, et al.
World Journal of Gastroenterology|April 9, 2005
Severe chronic diarrhea and weight loss in cholesteryl ester storage disease: a case reportUta Drebber, Matthias Andersen, Hans U Kasper, et al.
Cancer|July 13, 2002
Impact of thrombophilic gene mutations on thrombosis risk in patients with gastrointestinal carcinomaRudolf Pihusch, Gudrun Danzl, Michael Scholz, et al.
Experimental Hematology|October 5, 2010
A copy number repeat polymorphism in the transactivation domain of the CEPBA gene is possibly associated with a protective effect against acquired CEBPA mutations: an analysis in 1135 patients with AML and 187 healthy controlsSusanne Schnittger, Ulrike Bacher, Christiane Eder, et al.
Clinical and Experimental Rheumatology|October 22, 2015
Increased serum concentrations of neutrophil-derived protein S100A12 in heterozygous carriers of MEFV mutationsMareike Lieber, Tilmann Kallinich, Peter Lohse, et al.
Virchows Archiv : an International Journal of Pathology|May 27, 2008
Three German fibrinogen Aalpha-chain amyloidosis patients with the p.Glu526Val mutationMagdalena Eriksson, Stefan Schönland, Raoul Bergner, et al.
Pageof 13

Showing results (21-30 of 121) with videos related to

Sort By:
Pageof 13
Fertility and Sterility|February 6, 2008
Common 677C-->T mutation of the 5,10-methylenetetrahydrofolate reductase gene affects follicular estradiol synthesisStephanie Hecht, Roman Pavlik, Peter Lohse, et al.
Der Nervenarzt|September 18, 2024
[Fatigue and sensorimotor instability : Neurologically controlled conversion of post-COVID-19 patients]Thomas Urban, Fritjof Reinhardt, Peter Lohse, et al.
Fertility and Sterility|April 13, 2011
Divergent effects of the 677C>T mutation of the 5,10-methylenetetrahydrofolate reductase (MTHFR) gene on ovarian responsiveness and anti-Müllerian hormone concentrationsRoman Pavlik, Stephanie Hecht, Robert Ochsenkühn, et al.
American Journal of Reproductive Immunology (New York, N.Y. : 1989)|August 30, 2008
Paternal thrombophilic gene mutations are not associated with recurrent miscarriageBettina Toth, Franziska Vocke, Nina Rogenhofer, et al.
Journal of Cardiothoracic Surgery|August 21, 2009
Gene polymorphisms in APOE, NOS3, and LIPC genes may be risk factors for cardiac adverse events after primary CABGSandra Eifert, Astrid Rasch, Andres Beiras-Fernandez, et al.
World Journal of Gastroenterology|April 9, 2005
Severe chronic diarrhea and weight loss in cholesteryl ester storage disease: a case reportUta Drebber, Matthias Andersen, Hans U Kasper, et al.
Cancer|July 13, 2002
Impact of thrombophilic gene mutations on thrombosis risk in patients with gastrointestinal carcinomaRudolf Pihusch, Gudrun Danzl, Michael Scholz, et al.
Experimental Hematology|October 5, 2010
A copy number repeat polymorphism in the transactivation domain of the CEPBA gene is possibly associated with a protective effect against acquired CEBPA mutations: an analysis in 1135 patients with AML and 187 healthy controlsSusanne Schnittger, Ulrike Bacher, Christiane Eder, et al.
Clinical and Experimental Rheumatology|October 22, 2015
Increased serum concentrations of neutrophil-derived protein S100A12 in heterozygous carriers of MEFV mutationsMareike Lieber, Tilmann Kallinich, Peter Lohse, et al.
Virchows Archiv : an International Journal of Pathology|May 27, 2008
Three German fibrinogen Aalpha-chain amyloidosis patients with the p.Glu526Val mutationMagdalena Eriksson, Stefan Schönland, Raoul Bergner, et al.
Pageof 13