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Jonas Rutishauser

Showing results (11-20 of 63) with videos related to

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Swiss Medical Weekly|October 29, 2013
Medical care of type 2 diabetes mellitus in light of international and national recommendations: a retrospective analysisKonstantin Burgmann, Sandra Fatio, Beat Jordi, et al.
JCEM Case Reports|November 1, 2023
Diagnosis and Treatment of Hereditary Central Diabetes Insipidus in a Swiss Family With a Mutation in the <i>AVP</i> GeneLorena Wyniger, Nicole Beuret, Jonas Rutishauser, et al.
Vitamins and Hormones|March 7, 2020
Amyloid-like aggregation of provasopressinMartin Spiess, Nicole Beuret, Cristina Prescianotto Baschong, et al.
Swiss Medical Weekly|June 22, 2017
Predictors of re-exacerbation after an index exacerbation of chronic obstructive pulmonary disease in the REDUCE randomised clinical trialBrigitte Engel, Christian Schindler, Jörg D Leuppi, et al.
Experientia Supplementum (2012)|October 8, 2019
Hereditary Neurohypophyseal Diabetes InsipidusJonas Rutishauser, Nicole Beuret, Cristina Prescianotto-Baschong, et al.
Lancet (London, England)|April 15, 2004
Chest pain after travel to the tropicsLuigia Elzi, Michael Decker, Manuel Battegay, et al.
International Journal of Clinical Pharmacy|November 5, 2022
Renal insufficiency and magnesium deficiency correlate with a decreased formation of biologically active cholecalciferol: a retrospective observational studyJean-Pierre Rothen, Jonas Rutishauser, Isabelle Arnet, et al.
The Journal of Biological Chemistry|March 5, 2004
Expression of regulated secretory proteins is sufficient to generate granule-like structures in constitutively secreting cellsNicole Beuret, Hansruedi Stettler, Anja Renold, et al.
Molecular and Cellular Endocrinology|December 1, 2019
Role of protein aggregation and degradation in autosomal dominant neurohypophyseal diabetes insipidusMartin Spiess, Michael Friberg, Nicole Beuret, et al.
Journal of Cell Science|October 15, 2009
Dominant pro-vasopressin mutants that cause diabetes insipidus form disulfide-linked fibrillar aggregates in the endoplasmic reticulumJulia Birk, Michael A Friberg, Cristina Prescianotto-Baschong, et al.
Pageof 7

Showing results (11-20 of 63) with videos related to

Sort By:
Pageof 7
Swiss Medical Weekly|October 29, 2013
Medical care of type 2 diabetes mellitus in light of international and national recommendations: a retrospective analysisKonstantin Burgmann, Sandra Fatio, Beat Jordi, et al.
JCEM Case Reports|November 1, 2023
Diagnosis and Treatment of Hereditary Central Diabetes Insipidus in a Swiss Family With a Mutation in the <i>AVP</i> GeneLorena Wyniger, Nicole Beuret, Jonas Rutishauser, et al.
Vitamins and Hormones|March 7, 2020
Amyloid-like aggregation of provasopressinMartin Spiess, Nicole Beuret, Cristina Prescianotto Baschong, et al.
Swiss Medical Weekly|June 22, 2017
Predictors of re-exacerbation after an index exacerbation of chronic obstructive pulmonary disease in the REDUCE randomised clinical trialBrigitte Engel, Christian Schindler, Jörg D Leuppi, et al.
Experientia Supplementum (2012)|October 8, 2019
Hereditary Neurohypophyseal Diabetes InsipidusJonas Rutishauser, Nicole Beuret, Cristina Prescianotto-Baschong, et al.
Lancet (London, England)|April 15, 2004
Chest pain after travel to the tropicsLuigia Elzi, Michael Decker, Manuel Battegay, et al.
International Journal of Clinical Pharmacy|November 5, 2022
Renal insufficiency and magnesium deficiency correlate with a decreased formation of biologically active cholecalciferol: a retrospective observational studyJean-Pierre Rothen, Jonas Rutishauser, Isabelle Arnet, et al.
The Journal of Biological Chemistry|March 5, 2004
Expression of regulated secretory proteins is sufficient to generate granule-like structures in constitutively secreting cellsNicole Beuret, Hansruedi Stettler, Anja Renold, et al.
Molecular and Cellular Endocrinology|December 1, 2019
Role of protein aggregation and degradation in autosomal dominant neurohypophyseal diabetes insipidusMartin Spiess, Michael Friberg, Nicole Beuret, et al.
Journal of Cell Science|October 15, 2009
Dominant pro-vasopressin mutants that cause diabetes insipidus form disulfide-linked fibrillar aggregates in the endoplasmic reticulumJulia Birk, Michael A Friberg, Cristina Prescianotto-Baschong, et al.
Pageof 7