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Ulrich Schweizer

Showing results (111-120 of 129) with videos related to

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The Biochemical Journal|November 1, 2008
The selenocysteine tRNA STAF-binding region is essential for adequate selenocysteine tRNA status, selenoprotein expression and early age survival of miceBradley A Carlson, Ulrich Schweizer, Christine Perella, et al.
Journal of Molecular Endocrinology|September 21, 2022
Lack of L-type amino acid transporter 2 in murine thyroid tissue induces autophagyVaishnavi Venugopalan, Maren Rehders, Jonas Weber, et al.
International Journal of Molecular Sciences|January 20, 2021
The Thyroid Hormone Transporter Mct8 Restricts Cathepsin-Mediated Thyroglobulin Processing in Male Mice through Thyroid Auto-Regulatory Mechanisms That Encompass AutophagyVaishnavi Venugopalan, Alaa Al-Hashimi, Maren Rehders, et al.
Plos One|March 6, 2013
Selenium and selenoprotein deficiencies induce widespread pyogranuloma formation in mice, while high levels of dietary selenium decrease liver tumor size driven by TGFαMohamed E Moustafa, Bradley A Carlson, Miriam R Anver, et al.
Cellular Oncology (Dordrecht, Netherlands)|June 2, 2026
DIO3 associates with sorting nexins and endosomal trafficking networks in ovarian cancerDaniel Maman-Shinar, Shachar Vanmak, David Bern, et al.
European Journal of Endocrinology|August 5, 2011
Monocarboxylate transporter 8 deficiency: altered thyroid morphology and persistent high triiodothyronine/thyroxine ratio after thyroidectomyEva K Wirth, Sien-Yi Sheu, Jazmin Chiu-Ugalde, et al.
Physiology & Behavior|November 9, 2011
The HPA axis modulates the CNS melanocortin control of liver triacylglyceride metabolismPetra Wiedmer, Nilika Chaudhary, Michaela Rath, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|July 31, 2009
Neuronal 3',3,5-triiodothyronine (T3) uptake and behavioral phenotype of mice deficient in Mct8, the neuronal T3 transporter mutated in Allan-Herndon-Dudley syndromeEva K Wirth, Stephan Roth, Cristiane Blechschmidt, et al.
Free Radical Biology & Medicine|February 25, 2017
Homozygous mutation in TXNRD1 is associated with genetic generalized epilepsyAlexei P Kudin, Gregor Baron, Gábor Zsurka, et al.
The Biochemical Journal|May 22, 2016
Selenophosphate synthetase 1 is an essential protein with roles in regulation of redox homoeostasis in mammalsRyuta Tobe, Bradley A Carlson, Jang Hoe Huh, et al.
Pageof 13

Showing results (111-120 of 129) with videos related to

Sort By:
Pageof 13
The Biochemical Journal|November 1, 2008
The selenocysteine tRNA STAF-binding region is essential for adequate selenocysteine tRNA status, selenoprotein expression and early age survival of miceBradley A Carlson, Ulrich Schweizer, Christine Perella, et al.
Journal of Molecular Endocrinology|September 21, 2022
Lack of L-type amino acid transporter 2 in murine thyroid tissue induces autophagyVaishnavi Venugopalan, Maren Rehders, Jonas Weber, et al.
International Journal of Molecular Sciences|January 20, 2021
The Thyroid Hormone Transporter Mct8 Restricts Cathepsin-Mediated Thyroglobulin Processing in Male Mice through Thyroid Auto-Regulatory Mechanisms That Encompass AutophagyVaishnavi Venugopalan, Alaa Al-Hashimi, Maren Rehders, et al.
Plos One|March 6, 2013
Selenium and selenoprotein deficiencies induce widespread pyogranuloma formation in mice, while high levels of dietary selenium decrease liver tumor size driven by TGFαMohamed E Moustafa, Bradley A Carlson, Miriam R Anver, et al.
Cellular Oncology (Dordrecht, Netherlands)|June 2, 2026
DIO3 associates with sorting nexins and endosomal trafficking networks in ovarian cancerDaniel Maman-Shinar, Shachar Vanmak, David Bern, et al.
European Journal of Endocrinology|August 5, 2011
Monocarboxylate transporter 8 deficiency: altered thyroid morphology and persistent high triiodothyronine/thyroxine ratio after thyroidectomyEva K Wirth, Sien-Yi Sheu, Jazmin Chiu-Ugalde, et al.
Physiology & Behavior|November 9, 2011
The HPA axis modulates the CNS melanocortin control of liver triacylglyceride metabolismPetra Wiedmer, Nilika Chaudhary, Michaela Rath, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|July 31, 2009
Neuronal 3',3,5-triiodothyronine (T3) uptake and behavioral phenotype of mice deficient in Mct8, the neuronal T3 transporter mutated in Allan-Herndon-Dudley syndromeEva K Wirth, Stephan Roth, Cristiane Blechschmidt, et al.
Free Radical Biology & Medicine|February 25, 2017
Homozygous mutation in TXNRD1 is associated with genetic generalized epilepsyAlexei P Kudin, Gregor Baron, Gábor Zsurka, et al.
The Biochemical Journal|May 22, 2016
Selenophosphate synthetase 1 is an essential protein with roles in regulation of redox homoeostasis in mammalsRyuta Tobe, Bradley A Carlson, Jang Hoe Huh, et al.
Pageof 13