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Heike Biebermann

Showing results (71-80 of 127) with videos related to

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The Journal of Clinical Endocrinology and Metabolism|May 27, 2010
A new phenotype of nongoitrous and nonautoimmune hyperthyroidism caused by a heterozygous thyrotropin receptor mutation in transmembrane helix 6Franziska Winkler, Gunnar Kleinau, Patrick Tarnow, et al.
Plos One|November 19, 2010
Investigation of a genome wide association signal for obesity: synthetic association and haplotype analyses at the melanocortin 4 receptor gene locusAndré Scherag, Ivonne Jarick, Jessica Grothe, et al.
Human Mutation|August 19, 2007
Five novel mutations in steroidogenic factor 1 (SF1, NR5A1) in 46,XY patients with severe underandrogenization but without adrenal insufficiencyBirgit Köhler, Lin Lin, Bruno Ferraz-de-Souza, et al.
Journal of Molecular Endocrinology|May 16, 2013
Inhibition of melanocortin-4 receptor dimerization by substitutions in intracellular loop 2Carolin L Piechowski, Anne Rediger, Christina Lagemann, et al.
European Journal of Endocrinology|June 3, 2010
Association of variants in gastric inhibitory polypeptide receptor gene with impaired glucose homeostasis in obese children and adolescents from BerlinJeannine Sauber, Jessica Grothe, Maria Behm, et al.
Frontiers in Endocrinology|August 17, 2019
Signal Transduction and Pathogenic Modifications at the Melanocortin-4 Receptor: A Structural PerspectiveNicolas Heyder, Gunnar Kleinau, Michal Szczepek, et al.
Physiological Genomics|May 25, 2006
N-ethyl-N-nitrosourea-based generation of mouse models for mutant G protein-coupled receptorsJohannes Grosse, Patrick Tarnow, Holger Römpler, et al.
The Journal of Clinical Endocrinology and Metabolism|November 25, 2011
New pathogenic thyrotropin receptor mutations decipher differentiated activity switching at a conserved helix 6 motif of family A GPCRHeike Biebermann, Franziska Winkler, Daniela Handke, et al.
American Journal of Physiology. Renal Physiology|August 22, 2008
V2 vasopressin receptor deficiency causes changes in expression and function of renal and hypothalamic components involved in electrolyte and water homeostasisNicole Schliebe, Rainer Strotmann, Kathy Busse, et al.
Laboratory Investigation; a Journal of Technical Methods and Pathology|September 19, 2020
Ascorbate-induced oxidative stress mediates TRP channel activation and cytotoxicity in human etoposide-sensitive and -resistant retinoblastoma cellsJakub Oronowicz, Jacqueline Reinhard, Peter Sol Reinach, et al.
Pageof 13

Showing results (71-80 of 127) with videos related to

Sort By:
Pageof 13
The Journal of Clinical Endocrinology and Metabolism|May 27, 2010
A new phenotype of nongoitrous and nonautoimmune hyperthyroidism caused by a heterozygous thyrotropin receptor mutation in transmembrane helix 6Franziska Winkler, Gunnar Kleinau, Patrick Tarnow, et al.
Plos One|November 19, 2010
Investigation of a genome wide association signal for obesity: synthetic association and haplotype analyses at the melanocortin 4 receptor gene locusAndré Scherag, Ivonne Jarick, Jessica Grothe, et al.
Human Mutation|August 19, 2007
Five novel mutations in steroidogenic factor 1 (SF1, NR5A1) in 46,XY patients with severe underandrogenization but without adrenal insufficiencyBirgit Köhler, Lin Lin, Bruno Ferraz-de-Souza, et al.
Journal of Molecular Endocrinology|May 16, 2013
Inhibition of melanocortin-4 receptor dimerization by substitutions in intracellular loop 2Carolin L Piechowski, Anne Rediger, Christina Lagemann, et al.
European Journal of Endocrinology|June 3, 2010
Association of variants in gastric inhibitory polypeptide receptor gene with impaired glucose homeostasis in obese children and adolescents from BerlinJeannine Sauber, Jessica Grothe, Maria Behm, et al.
Frontiers in Endocrinology|August 17, 2019
Signal Transduction and Pathogenic Modifications at the Melanocortin-4 Receptor: A Structural PerspectiveNicolas Heyder, Gunnar Kleinau, Michal Szczepek, et al.
Physiological Genomics|May 25, 2006
N-ethyl-N-nitrosourea-based generation of mouse models for mutant G protein-coupled receptorsJohannes Grosse, Patrick Tarnow, Holger Römpler, et al.
The Journal of Clinical Endocrinology and Metabolism|November 25, 2011
New pathogenic thyrotropin receptor mutations decipher differentiated activity switching at a conserved helix 6 motif of family A GPCRHeike Biebermann, Franziska Winkler, Daniela Handke, et al.
American Journal of Physiology. Renal Physiology|August 22, 2008
V2 vasopressin receptor deficiency causes changes in expression and function of renal and hypothalamic components involved in electrolyte and water homeostasisNicole Schliebe, Rainer Strotmann, Kathy Busse, et al.
Laboratory Investigation; a Journal of Technical Methods and Pathology|September 19, 2020
Ascorbate-induced oxidative stress mediates TRP channel activation and cytotoxicity in human etoposide-sensitive and -resistant retinoblastoma cellsJakub Oronowicz, Jacqueline Reinhard, Peter Sol Reinach, et al.
Pageof 13