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Etienne Sochett

Showing results (41-50 of 56) with videos related to

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BMC Medical Genetics|April 11, 2012
Mutations in LRP5 cause primary osteoporosis without features of OI by reducing Wnt signaling activityJohanna Korvala, Harald Jüppner, Outi Mäkitie, et al.
Molecular & Cellular Proteomics : MCP|December 28, 2019
Peptidomic Analysis of Urine from Youths with Early Type 1 Diabetes Reveals Novel Bioactivity of Uromodulin Peptides <i>In Vitro</i>Julie A D Van, Sergi Clotet-Freixas, Joyce Zhou, et al.
European Heart Journal|March 14, 2019
Elevated high-density lipoprotein in adolescents with Type 1 diabetes is associated with endothelial dysfunction in the presence of systemic inflammationScott T Chiesa, Marietta Charakida, Eve McLoughlin, et al.
The Journal of Clinical Endocrinology and Metabolism|June 14, 2021
Mild Idiopathic Infantile Hypercalcemia-Part 1: Biochemical and Genetic FindingsNina Lenherr-Taube, Edwin J Young, Michelle Furman, et al.
Cardiovascular Diabetology|February 17, 2016
Early changes in cardiovascular structure and function in adolescents with type 1 diabetesTimothy J Bradley, Cameron Slorach, Farid H Mahmud, et al.
American Journal of Human Genetics|June 2, 2015
Recessive osteogenesis imperfecta caused by missense mutations in SPARCRoberto Mendoza-Londono, Somayyeh Fahiminiya, Jacek Majewski, et al.
Diabetes Care|February 21, 2016
Association Between Plasma Uric Acid Levels and Cardiorenal Function in Adolescents With Type 1 DiabetesYuliya Lytvyn, Farid H Mahmud, Denis Daneman, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|February 26, 2019
Renal Hemodynamic Function and RAAS Activation Over the Natural History of Type 1 DiabetesYuliya Lytvyn, Petter Bjornstad, Julie A Lovshin, et al.
Diabetes, Obesity & Metabolism|February 15, 2019
Association between uric acid, renal haemodynamics and arterial stiffness over the natural history of type 1 diabetesYuliya Lytvyn, Petter Bjornstad, Julie A Lovshin, et al.
Plos One|December 17, 2013
Identification and functional characterization of three NoLS (nucleolar localisation signals) mutations of the CDC73 geneValerio Pazienza, Annamaria la Torre, Filomena Baorda, et al.
Pageof 6

Showing results (41-50 of 56) with videos related to

Sort By:
Pageof 6
BMC Medical Genetics|April 11, 2012
Mutations in LRP5 cause primary osteoporosis without features of OI by reducing Wnt signaling activityJohanna Korvala, Harald Jüppner, Outi Mäkitie, et al.
Molecular & Cellular Proteomics : MCP|December 28, 2019
Peptidomic Analysis of Urine from Youths with Early Type 1 Diabetes Reveals Novel Bioactivity of Uromodulin Peptides <i>In Vitro</i>Julie A D Van, Sergi Clotet-Freixas, Joyce Zhou, et al.
European Heart Journal|March 14, 2019
Elevated high-density lipoprotein in adolescents with Type 1 diabetes is associated with endothelial dysfunction in the presence of systemic inflammationScott T Chiesa, Marietta Charakida, Eve McLoughlin, et al.
The Journal of Clinical Endocrinology and Metabolism|June 14, 2021
Mild Idiopathic Infantile Hypercalcemia-Part 1: Biochemical and Genetic FindingsNina Lenherr-Taube, Edwin J Young, Michelle Furman, et al.
Cardiovascular Diabetology|February 17, 2016
Early changes in cardiovascular structure and function in adolescents with type 1 diabetesTimothy J Bradley, Cameron Slorach, Farid H Mahmud, et al.
American Journal of Human Genetics|June 2, 2015
Recessive osteogenesis imperfecta caused by missense mutations in SPARCRoberto Mendoza-Londono, Somayyeh Fahiminiya, Jacek Majewski, et al.
Diabetes Care|February 21, 2016
Association Between Plasma Uric Acid Levels and Cardiorenal Function in Adolescents With Type 1 DiabetesYuliya Lytvyn, Farid H Mahmud, Denis Daneman, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|February 26, 2019
Renal Hemodynamic Function and RAAS Activation Over the Natural History of Type 1 DiabetesYuliya Lytvyn, Petter Bjornstad, Julie A Lovshin, et al.
Diabetes, Obesity & Metabolism|February 15, 2019
Association between uric acid, renal haemodynamics and arterial stiffness over the natural history of type 1 diabetesYuliya Lytvyn, Petter Bjornstad, Julie A Lovshin, et al.
Plos One|December 17, 2013
Identification and functional characterization of three NoLS (nucleolar localisation signals) mutations of the CDC73 geneValerio Pazienza, Annamaria la Torre, Filomena Baorda, et al.
Pageof 6