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Franziska Seifert

Showing results (11-20 of 27) with videos related to

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Chemico-Biological Interactions|February 19, 2018
Synthesis and biological investigation of new carbonic anhydrase IX (CAIX) inhibitorsKranthi Vanchanagiri, Daniel Emmerich, Monique Bruschke, et al.
Molecules (Basel, Switzerland)|October 26, 2024
High Fluorescence of Phytochromes Does Not Require Chromophore ProtonationSagie Katz, Hoang Trong Phan, Fabian Rieder, et al.
Human Genetics|May 26, 2017
A recessive mutation in beta-IV-spectrin (SPTBN4) associates with congenital myopathy, neuropathy, and central deafnessEllen Knierim, Esther Gill, Franziska Seifert, et al.
Immunobiology|October 8, 2021
CD28 Superagonist D665-mediated activation of mouse regulatory T cells maintains their phenotype without loss of suppressive qualityJohanna C Wagner, Svenja Leicht, Manuela Hofmann, et al.
Biochemistry|May 4, 2007
Phosphorylation of serine 264 impedes active site accessibility in the E1 component of the human pyruvate dehydrogenase multienzyme complexFranziska Seifert, Ewa Ciszak, Lioubov Korotchkina, et al.
Neurology. Genetics|April 12, 2016
Recessive REEP1 mutation is associated with congenital axonal neuropathy and diaphragmatic palsyGudrun Schottmann, Dominik Seelow, Franziska Seifert, et al.
Biochemistry|October 18, 2006
Direct kinetic evidence for half-of-the-sites reactivity in the E1 component of the human pyruvate dehydrogenase multienzyme complex through alternating sites cofactor activationFranziska Seifert, Ralph Golbik, Johanna Brauer, et al.
Skeletal Muscle|July 7, 2016
Characterization of a Dmd (EGFP) reporter mouse as a tool to investigate dystrophin expressionMina V Petkova, Susanne Morales-Gonzales, Karima Relizani, et al.
Developmental Dynamics : an Official Publication of the American Association of Anatomists|April 22, 2006
A mutation in the zebrafish Na,K-ATPase subunit atp1a1a.1 provides genetic evidence that the sodium potassium pump contributes to left-right asymmetry downstream or in parallel to nodal flowElin Ellertsdottir, Julia Ganz, Katrin Dürr, et al.
Acta Neuropathologica|August 4, 2016
Kyphoscoliosis peptidase (KY) mutation causes a novel congenital myopathy with core targetoid defectsRachel Straussberg, Gudrun Schottmann, Menachem Sadeh, et al.
Pageof 3

Showing results (11-20 of 27) with videos related to

Sort By:
Pageof 3
Chemico-Biological Interactions|February 19, 2018
Synthesis and biological investigation of new carbonic anhydrase IX (CAIX) inhibitorsKranthi Vanchanagiri, Daniel Emmerich, Monique Bruschke, et al.
Molecules (Basel, Switzerland)|October 26, 2024
High Fluorescence of Phytochromes Does Not Require Chromophore ProtonationSagie Katz, Hoang Trong Phan, Fabian Rieder, et al.
Human Genetics|May 26, 2017
A recessive mutation in beta-IV-spectrin (SPTBN4) associates with congenital myopathy, neuropathy, and central deafnessEllen Knierim, Esther Gill, Franziska Seifert, et al.
Immunobiology|October 8, 2021
CD28 Superagonist D665-mediated activation of mouse regulatory T cells maintains their phenotype without loss of suppressive qualityJohanna C Wagner, Svenja Leicht, Manuela Hofmann, et al.
Biochemistry|May 4, 2007
Phosphorylation of serine 264 impedes active site accessibility in the E1 component of the human pyruvate dehydrogenase multienzyme complexFranziska Seifert, Ewa Ciszak, Lioubov Korotchkina, et al.
Neurology. Genetics|April 12, 2016
Recessive REEP1 mutation is associated with congenital axonal neuropathy and diaphragmatic palsyGudrun Schottmann, Dominik Seelow, Franziska Seifert, et al.
Biochemistry|October 18, 2006
Direct kinetic evidence for half-of-the-sites reactivity in the E1 component of the human pyruvate dehydrogenase multienzyme complex through alternating sites cofactor activationFranziska Seifert, Ralph Golbik, Johanna Brauer, et al.
Skeletal Muscle|July 7, 2016
Characterization of a Dmd (EGFP) reporter mouse as a tool to investigate dystrophin expressionMina V Petkova, Susanne Morales-Gonzales, Karima Relizani, et al.
Developmental Dynamics : an Official Publication of the American Association of Anatomists|April 22, 2006
A mutation in the zebrafish Na,K-ATPase subunit atp1a1a.1 provides genetic evidence that the sodium potassium pump contributes to left-right asymmetry downstream or in parallel to nodal flowElin Ellertsdottir, Julia Ganz, Katrin Dürr, et al.
Acta Neuropathologica|August 4, 2016
Kyphoscoliosis peptidase (KY) mutation causes a novel congenital myopathy with core targetoid defectsRachel Straussberg, Gudrun Schottmann, Menachem Sadeh, et al.
Pageof 3