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Thomas J Corydon

Showing results (21-30 of 114) with videos related to

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Clinical Endocrinology|December 18, 2003
Impaired trafficking of mutated AVP prohormone in cells expressing rare disease genes causing autosomal dominant familial neurohypophyseal diabetes insipidusJane H Christensen, Charlotte Siggaard, Thomas J Corydon, et al.
Seminars in Cancer Biology|March 28, 2019
The role of SOX family members in solid tumours and metastasisDaniela Grimm, Johann Bauer, Petra Wise, et al.
Experimental Eye Research|July 20, 2023
Porcine models of choroidal neovascularization: A systematic reviewThomas Stax Jakobsen, Bjørn K Fabian-Jessing, Silja Hansen, et al.
The Journal of Clinical Endocrinology and Metabolism|September 10, 2004
Differential cellular handling of defective arginine vasopressin (AVP) prohormones in cells expressing mutations of the AVP gene associated with autosomal dominant and recessive familial neurohypophyseal diabetes insipidusJane H Christensen, Charlotte Siggaard, Thomas J Corydon, et al.
Journal of Inherited Metabolic Disease|October 7, 2008
Mitochondrial fatty acid oxidation defects--remaining challengesNiels Gregersen, Brage S Andresen, Christina B Pedersen, et al.
Cancer Cell International|February 28, 2014
An eEF1A1 truncation encoded by PTI-1 exerts its oncogenic effect inside the nucleusLouise D Dahl, Thomas J Corydon, Liina Ränkel, et al.
Molecular Genetics and Metabolism|April 23, 2003
Expression of short-chain acyl-CoA dehydrogenase (SCAD) proteins in the liver of SCAD deficient mice after hydrodynamic gene transferDavid A Holm, Frederik Dagnaes-Hansen, Henrik Simonsen, et al.
Journal of Biomedical Informatics|November 1, 2019
Augmenting cancer cell proteomics with cellular images - A semantic approach to understand focal adhesionThomas J Bauer, Erich Gombocz, Marcus Krüger, et al.
Human Molecular Genetics|May 22, 2012
Molecular mechanisms of riboflavin responsiveness in patients with ETF-QO variations and multiple acyl-CoA dehydrogenation deficiencyNanna Cornelius, Frank E Frerman, Thomas J Corydon, et al.
Neuroendocrinology|June 28, 2018
A Novel Synonymous Variant in the AVP Gene Associated with Autosomal Dominant Familial Neurohypophyseal Diabetes Insipidus Causes Partial RNA MissplicingHelene Kvistgaard, Jane H Christensen, Jan-Ove Johansson, et al.
Pageof 12

Showing results (21-30 of 114) with videos related to

Sort By:
Pageof 12
Clinical Endocrinology|December 18, 2003
Impaired trafficking of mutated AVP prohormone in cells expressing rare disease genes causing autosomal dominant familial neurohypophyseal diabetes insipidusJane H Christensen, Charlotte Siggaard, Thomas J Corydon, et al.
Seminars in Cancer Biology|March 28, 2019
The role of SOX family members in solid tumours and metastasisDaniela Grimm, Johann Bauer, Petra Wise, et al.
Experimental Eye Research|July 20, 2023
Porcine models of choroidal neovascularization: A systematic reviewThomas Stax Jakobsen, Bjørn K Fabian-Jessing, Silja Hansen, et al.
The Journal of Clinical Endocrinology and Metabolism|September 10, 2004
Differential cellular handling of defective arginine vasopressin (AVP) prohormones in cells expressing mutations of the AVP gene associated with autosomal dominant and recessive familial neurohypophyseal diabetes insipidusJane H Christensen, Charlotte Siggaard, Thomas J Corydon, et al.
Journal of Inherited Metabolic Disease|October 7, 2008
Mitochondrial fatty acid oxidation defects--remaining challengesNiels Gregersen, Brage S Andresen, Christina B Pedersen, et al.
Cancer Cell International|February 28, 2014
An eEF1A1 truncation encoded by PTI-1 exerts its oncogenic effect inside the nucleusLouise D Dahl, Thomas J Corydon, Liina Ränkel, et al.
Molecular Genetics and Metabolism|April 23, 2003
Expression of short-chain acyl-CoA dehydrogenase (SCAD) proteins in the liver of SCAD deficient mice after hydrodynamic gene transferDavid A Holm, Frederik Dagnaes-Hansen, Henrik Simonsen, et al.
Journal of Biomedical Informatics|November 1, 2019
Augmenting cancer cell proteomics with cellular images - A semantic approach to understand focal adhesionThomas J Bauer, Erich Gombocz, Marcus Krüger, et al.
Human Molecular Genetics|May 22, 2012
Molecular mechanisms of riboflavin responsiveness in patients with ETF-QO variations and multiple acyl-CoA dehydrogenation deficiencyNanna Cornelius, Frank E Frerman, Thomas J Corydon, et al.
Neuroendocrinology|June 28, 2018
A Novel Synonymous Variant in the AVP Gene Associated with Autosomal Dominant Familial Neurohypophyseal Diabetes Insipidus Causes Partial RNA MissplicingHelene Kvistgaard, Jane H Christensen, Jan-Ove Johansson, et al.
Pageof 12