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Heike Biebermann

Showing results (21-30 of 127) with videos related to

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Endocrine Development|September 6, 2017
Treatment of Diabetes and Obesity by Rationally Designed Peptide Agonists Functioning at Multiple Metabolic ReceptorsNoushafarin Khajavi, Heike Biebermann, Matthias Tschöp, et al.
Handbook of Experimental Pharmacology|January 18, 2012
The neuroendocrine circuitry controlled by POMC, MSH, and AGRPHeike Biebermann, Peter Kühnen, Gunnar Kleinau, et al.
Endocrine Reviews|May 7, 2013
Novel insights on thyroid-stimulating hormone receptor signal transductionGunnar Kleinau, Susanne Neumann, Annette Grüters, et al.
The Journal of Biological Chemistry|September 25, 2003
Mutationally induced disulfide bond formation within the third extracellular loop causes melanocortin 4 receptor inactivation in patients with obesityPatrick Tarnow, Torsten Schoneberg, Heiko Krude, et al.
Obesity Facts|March 22, 2012
Identification of the translation start site of the human melanocortin 3 receptorPatrick Tarnow, Anne Rediger, Angela Schulz, et al.
Plos One|December 10, 2016
Insights into Basal Signaling Regulation, Oligomerization, and Structural Organization of the Human G-Protein Coupled Receptor 83Anne Müller, Julia Catherine Berkmann, Patrick Scheerer, et al.
Pediatric Diabetes|April 27, 2011
Proinsulin and the proinsulin/insulin ratio in overweight and obese children and adolescents: relation to clinical parameters, insulin resistance, and impaired glucose regulationCarlotta von Berghes, Georg Brabant, Heike Biebermann, et al.
Experimental and Clinical Endocrinology & Diabetes : Official Journal, German Society of Endocrinology [And] German Diabetes Association|April 4, 2020
Allan-Herndon-Dudley-Syndrome: Considerations about the Brain Phenotype with Implications for Treatment StrategiesHeiko Krude, Heike Biebermann, Markus Schuelke, et al.
Diabetes|November 25, 2003
Autosomal-dominant mode of inheritance of a melanocortin-4 receptor mutation in a patient with severe early-onset obesity is due to a dominant-negative effect caused by receptor dimerizationHeike Biebermann, Heiko Krude, Andrea Elsner, et al.
The Journal of Clinical Endocrinology and Metabolism|October 5, 2002
Congenital central hypothyroidism due to homozygous thyrotropin beta 313 Delta T mutation is caused by a Founder effectHarald Brumm, Arne Pfeufer, Heike Biebermann, et al.
Pageof 13

Showing results (21-30 of 127) with videos related to

Sort By:
Pageof 13
Endocrine Development|September 6, 2017
Treatment of Diabetes and Obesity by Rationally Designed Peptide Agonists Functioning at Multiple Metabolic ReceptorsNoushafarin Khajavi, Heike Biebermann, Matthias Tschöp, et al.
Handbook of Experimental Pharmacology|January 18, 2012
The neuroendocrine circuitry controlled by POMC, MSH, and AGRPHeike Biebermann, Peter Kühnen, Gunnar Kleinau, et al.
Endocrine Reviews|May 7, 2013
Novel insights on thyroid-stimulating hormone receptor signal transductionGunnar Kleinau, Susanne Neumann, Annette Grüters, et al.
The Journal of Biological Chemistry|September 25, 2003
Mutationally induced disulfide bond formation within the third extracellular loop causes melanocortin 4 receptor inactivation in patients with obesityPatrick Tarnow, Torsten Schoneberg, Heiko Krude, et al.
Obesity Facts|March 22, 2012
Identification of the translation start site of the human melanocortin 3 receptorPatrick Tarnow, Anne Rediger, Angela Schulz, et al.
Plos One|December 10, 2016
Insights into Basal Signaling Regulation, Oligomerization, and Structural Organization of the Human G-Protein Coupled Receptor 83Anne Müller, Julia Catherine Berkmann, Patrick Scheerer, et al.
Pediatric Diabetes|April 27, 2011
Proinsulin and the proinsulin/insulin ratio in overweight and obese children and adolescents: relation to clinical parameters, insulin resistance, and impaired glucose regulationCarlotta von Berghes, Georg Brabant, Heike Biebermann, et al.
Experimental and Clinical Endocrinology & Diabetes : Official Journal, German Society of Endocrinology [And] German Diabetes Association|April 4, 2020
Allan-Herndon-Dudley-Syndrome: Considerations about the Brain Phenotype with Implications for Treatment StrategiesHeiko Krude, Heike Biebermann, Markus Schuelke, et al.
Diabetes|November 25, 2003
Autosomal-dominant mode of inheritance of a melanocortin-4 receptor mutation in a patient with severe early-onset obesity is due to a dominant-negative effect caused by receptor dimerizationHeike Biebermann, Heiko Krude, Andrea Elsner, et al.
The Journal of Clinical Endocrinology and Metabolism|October 5, 2002
Congenital central hypothyroidism due to homozygous thyrotropin beta 313 Delta T mutation is caused by a Founder effectHarald Brumm, Arne Pfeufer, Heike Biebermann, et al.
Pageof 13