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Katrin Hoffmann

Showing results (201-210 of 241) with videos related to

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Oncogene|August 5, 2018
Tumor penetrating peptides inhibiting MYC as a potent targeted therapeutic strategy for triple-negative breast cancersEdina Wang, Anabel Sorolla, Paula T Cunningham, et al.
Molecular Systems Biology|July 23, 2020
Disentangling molecular mechanisms regulating sensitization of interferon alpha signal transductionFrédérique Kok, Marcus Rosenblatt, Melissa Teusel, et al.
BMC Geriatrics|February 11, 2018
The delirium and population health informatics cohort study protocol: ascertaining the determinants and outcomes from delirium in a whole populationDaniel Davis, Sarah Richardson, Joanne Hornby, et al.
Plos One|December 21, 2023
A mixed methods PAR study investigating social capital as a resource for Black and other racially minoritised communities in the UK: A study protocolGeorgina Gnan, Zara Asif, Sanchika Campbell, et al.
American Journal of Human Genetics|July 11, 2006
Escobar syndrome is a prenatal myasthenia caused by disruption of the acetylcholine receptor fetal gamma subunitKatrin Hoffmann, Juliane S Muller, Sigmar Stricker, et al.
Annals of Surgery|July 5, 2022
Completion Pancreatectomy After Pancreatoduodenectomy: Who Needs It?Martin Loos, Anna-Katharina König, Nikolai von Winkler, et al.
Circulation|March 19, 2003
Mutations in the human muscle LIM protein gene in families with hypertrophic cardiomyopathyChristian Geier, Andreas Perrot, Cemil Ozcelik, et al.
Nature Genetics|July 16, 2002
Mutations in the gene encoding the lamin B receptor produce an altered nuclear morphology in granulocytes (Pelger-Huët anomaly)Katrin Hoffmann, Christine K Dreger, Ada L Olins, et al.
European Journal of Human Genetics : EJHG|July 9, 2009
Association of FTO variants with BMI and fat mass in the self-contained population of Sorbs in GermanyAnke Tönjes, Eleftheria Zeggini, Peter Kovacs, et al.
Human Molecular Genetics|February 26, 2015
Molecular mechanism of CHRDL1-mediated X-linked megalocornea in humans and in Xenopus modelThorsten Pfirrmann, Denise Emmerich, Peter Ruokonen, et al.
Pageof 25

Showing results (201-210 of 241) with videos related to

Sort By:
Pageof 25
Oncogene|August 5, 2018
Tumor penetrating peptides inhibiting MYC as a potent targeted therapeutic strategy for triple-negative breast cancersEdina Wang, Anabel Sorolla, Paula T Cunningham, et al.
Molecular Systems Biology|July 23, 2020
Disentangling molecular mechanisms regulating sensitization of interferon alpha signal transductionFrédérique Kok, Marcus Rosenblatt, Melissa Teusel, et al.
BMC Geriatrics|February 11, 2018
The delirium and population health informatics cohort study protocol: ascertaining the determinants and outcomes from delirium in a whole populationDaniel Davis, Sarah Richardson, Joanne Hornby, et al.
Plos One|December 21, 2023
A mixed methods PAR study investigating social capital as a resource for Black and other racially minoritised communities in the UK: A study protocolGeorgina Gnan, Zara Asif, Sanchika Campbell, et al.
American Journal of Human Genetics|July 11, 2006
Escobar syndrome is a prenatal myasthenia caused by disruption of the acetylcholine receptor fetal gamma subunitKatrin Hoffmann, Juliane S Muller, Sigmar Stricker, et al.
Annals of Surgery|July 5, 2022
Completion Pancreatectomy After Pancreatoduodenectomy: Who Needs It?Martin Loos, Anna-Katharina König, Nikolai von Winkler, et al.
Circulation|March 19, 2003
Mutations in the human muscle LIM protein gene in families with hypertrophic cardiomyopathyChristian Geier, Andreas Perrot, Cemil Ozcelik, et al.
Nature Genetics|July 16, 2002
Mutations in the gene encoding the lamin B receptor produce an altered nuclear morphology in granulocytes (Pelger-Huët anomaly)Katrin Hoffmann, Christine K Dreger, Ada L Olins, et al.
European Journal of Human Genetics : EJHG|July 9, 2009
Association of FTO variants with BMI and fat mass in the self-contained population of Sorbs in GermanyAnke Tönjes, Eleftheria Zeggini, Peter Kovacs, et al.
Human Molecular Genetics|February 26, 2015
Molecular mechanism of CHRDL1-mediated X-linked megalocornea in humans and in Xenopus modelThorsten Pfirrmann, Denise Emmerich, Peter Ruokonen, et al.
Pageof 25