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Elena Bochukova

Showing results (1-10 of 5) with videos related to

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Molecular Genetics and Metabolism|June 27, 2013
Severe obesity and diabetes insipidus in a patient with PCSK1 deficiencyGraeme R Frank, Joyce Fox, Ninfa Candela, et al.
Cell Death & Disease|July 15, 2025
Simvastatin suppresses spinal cord metastasis of medulloblastoma at clinically significant dosesCharley Comer, Kian Cotton, Christopher Edwards, et al.
Epigenetics|November 25, 2021
An integrative epi-transcriptomic approach identifies the human cartilage chitinase 3-like protein 2 (<i>CHI3L2)</i> as a potential mediator of B12 deficiency in adipocytesB William Ogunkolade, Antonysunil Adaikalakoteswari, Shirleny Romualdo Cardoso, et al.
The Journal of Clinical Investigation|February 9, 2016
Mutation in human selenocysteine transfer RNA selectively disrupts selenoprotein synthesisErik Schoenmakers, Bradley Carlson, Maura Agostini, et al.
The New England Journal of Medicine|December 16, 2011
A mutation in the thyroid hormone receptor alpha geneElena Bochukova, Nadia Schoenmakers, Maura Agostini, et al.
Pageof 1

Showing results (1-10 of 5) with videos related to

Sort By:
Pageof 1
Molecular Genetics and Metabolism|June 27, 2013
Severe obesity and diabetes insipidus in a patient with PCSK1 deficiencyGraeme R Frank, Joyce Fox, Ninfa Candela, et al.
Cell Death & Disease|July 15, 2025
Simvastatin suppresses spinal cord metastasis of medulloblastoma at clinically significant dosesCharley Comer, Kian Cotton, Christopher Edwards, et al.
Epigenetics|November 25, 2021
An integrative epi-transcriptomic approach identifies the human cartilage chitinase 3-like protein 2 (<i>CHI3L2)</i> as a potential mediator of B12 deficiency in adipocytesB William Ogunkolade, Antonysunil Adaikalakoteswari, Shirleny Romualdo Cardoso, et al.
The Journal of Clinical Investigation|February 9, 2016
Mutation in human selenocysteine transfer RNA selectively disrupts selenoprotein synthesisErik Schoenmakers, Bradley Carlson, Maura Agostini, et al.
The New England Journal of Medicine|December 16, 2011
A mutation in the thyroid hormone receptor alpha geneElena Bochukova, Nadia Schoenmakers, Maura Agostini, et al.
Pageof 1