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Heike Biebermann

Showing results (51-60 of 127) with videos related to

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Endocrine|February 14, 2009
A novel melanocortin-4 receptor gene mutation in a female patient with severe childhood obesityChristian L Roth, Michael Ludwig, Joachim Woelfle, et al.
Frontiers in Endocrinology|October 10, 2018
3-Iodothyronamine Activates a Set of Membrane Proteins in Murine Hypothalamic Cell LinesJulia Bräunig, Stefan Mergler, Sabine Jyrch, et al.
European Thyroid Journal|November 25, 2015
Trace Amine-Associated Receptor 1 Localization at the Apical Plasma Membrane Domain of Fisher Rat Thyroid Epithelial Cells Is Confined to CiliaJoanna Szumska, Maria Qatato, Maren Rehders, et al.
Endocrinology|July 14, 2007
Evolutionary aspects in evaluating mutations in the melanocortin 4 receptorClaudia Stäubert, Patrick Tarnow, Harald Brumm, et al.
Neuroendocrinology|February 14, 2012
MC4R dimerization in the paraventricular nucleus and GHSR/MC3R heterodimerization in the arcuate nucleus: is there relevance for body weight regulation?Anne Rediger, Carolin Leonie Piechowski, Kirk Habegger, et al.
Sexual Development : Genetics, Molecular Biology, Evolution, Endocrinology, Embryology, and Pathology of Sex Determination and Differentiation|February 10, 2015
A novel hemizygous mutation of MAMLD1 in a patient with 46,XY complete gonadal dysgenesisInge-Lore Ruiz-Arana, Angela Hübner, Cigdem Cetingdag, et al.
Molecular and Cellular Endocrinology|May 26, 2016
The long N-terminus of the human monocarboxylate transporter 8 is a target of ubiquitin-dependent proteasomal degradation which regulates protein expression and oligomerization capacityDenise Zwanziger, Mathias Schmidt, Jana Fischer, et al.
Plos One|November 11, 2011
Differential modulation of Beta-adrenergic receptor signaling by trace amine-associated receptor 1 agonistsGunnar Kleinau, Juliane Pratzka, Daniela Nürnberg, et al.
European Journal of Endocrinology|May 1, 2007
Screening for mutations in transcription factors in a Czech cohort of 170 patients with congenital and early-onset hypothyroidism: identification of a novel PAX8 mutation in dominantly inherited early-onset non-autoimmune hypothyroidismEva Al Taji, Heike Biebermann, Zdenka Límanová, et al.
The Journal of Clinical Endocrinology and Metabolism|November 20, 2013
Identification of PENDRIN (SLC26A4) mutations in patients with congenital hypothyroidism and "apparent" thyroid dysgenesisPeter Kühnen, Serap Turan, Sebastian Fröhler, et al.
Pageof 13

Showing results (51-60 of 127) with videos related to

Sort By:
Pageof 13
Endocrine|February 14, 2009
A novel melanocortin-4 receptor gene mutation in a female patient with severe childhood obesityChristian L Roth, Michael Ludwig, Joachim Woelfle, et al.
Frontiers in Endocrinology|October 10, 2018
3-Iodothyronamine Activates a Set of Membrane Proteins in Murine Hypothalamic Cell LinesJulia Bräunig, Stefan Mergler, Sabine Jyrch, et al.
European Thyroid Journal|November 25, 2015
Trace Amine-Associated Receptor 1 Localization at the Apical Plasma Membrane Domain of Fisher Rat Thyroid Epithelial Cells Is Confined to CiliaJoanna Szumska, Maria Qatato, Maren Rehders, et al.
Endocrinology|July 14, 2007
Evolutionary aspects in evaluating mutations in the melanocortin 4 receptorClaudia Stäubert, Patrick Tarnow, Harald Brumm, et al.
Neuroendocrinology|February 14, 2012
MC4R dimerization in the paraventricular nucleus and GHSR/MC3R heterodimerization in the arcuate nucleus: is there relevance for body weight regulation?Anne Rediger, Carolin Leonie Piechowski, Kirk Habegger, et al.
Sexual Development : Genetics, Molecular Biology, Evolution, Endocrinology, Embryology, and Pathology of Sex Determination and Differentiation|February 10, 2015
A novel hemizygous mutation of MAMLD1 in a patient with 46,XY complete gonadal dysgenesisInge-Lore Ruiz-Arana, Angela Hübner, Cigdem Cetingdag, et al.
Molecular and Cellular Endocrinology|May 26, 2016
The long N-terminus of the human monocarboxylate transporter 8 is a target of ubiquitin-dependent proteasomal degradation which regulates protein expression and oligomerization capacityDenise Zwanziger, Mathias Schmidt, Jana Fischer, et al.
Plos One|November 11, 2011
Differential modulation of Beta-adrenergic receptor signaling by trace amine-associated receptor 1 agonistsGunnar Kleinau, Juliane Pratzka, Daniela Nürnberg, et al.
European Journal of Endocrinology|May 1, 2007
Screening for mutations in transcription factors in a Czech cohort of 170 patients with congenital and early-onset hypothyroidism: identification of a novel PAX8 mutation in dominantly inherited early-onset non-autoimmune hypothyroidismEva Al Taji, Heike Biebermann, Zdenka Límanová, et al.
The Journal of Clinical Endocrinology and Metabolism|November 20, 2013
Identification of PENDRIN (SLC26A4) mutations in patients with congenital hypothyroidism and "apparent" thyroid dysgenesisPeter Kühnen, Serap Turan, Sebastian Fröhler, et al.
Pageof 13