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Maura Agostini

Showing results (11-20 of 21) with videos related to

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Molecular and Cellular Biology|December 6, 2021
Structure-Guided Approach to Relieving Transcriptional Repression in Resistance to Thyroid Hormone αBeatriz Romartinez-Alonso, Maura Agostini, Heulyn Jones, et al.
The Journal of Clinical Endocrinology and Metabolism|March 21, 2014
A novel albumin gene mutation (R222I) in familial dysalbuminemic hyperthyroxinemiaNadia Schoenmakers, Carla Moran, Irene Campi, et al.
The Journal of Clinical Endocrinology and Metabolism|September 16, 2017
Anemia in Patients With Resistance to Thyroid Hormone α: A Role for Thyroid Hormone Receptor α in Human ErythropoiesisAnja L M van Gucht, Marcel E Meima, Carla Moran, et al.
Diabetes|April 7, 2018
A Pharmacogenetic Approach to the Treatment of Patients With <i>PPARG</i> MutationsMaura Agostini, Erik Schoenmakers, Junaid Beig, et al.
Cell Metabolism|October 3, 2006
Non-DNA binding, dominant-negative, human PPARgamma mutations cause lipodystrophic insulin resistanceMaura Agostini, Erik Schoenmakers, Catherine Mitchell, et al.
Diabetes|March 29, 2003
Human metabolic syndrome resulting from dominant-negative mutations in the nuclear receptor peroxisome proliferator-activated receptor-gammaDavid B Savage, Garry D Tan, Carlo L Acerini, et al.
Nature Genetics|November 8, 2016
Prospective functional classification of all possible missense variants in PPARGAmit R Majithia, Ben Tsuda, Maura Agostini, et al.
Nature Genetics|July 16, 2002
Digenic inheritance of severe insulin resistance in a human pedigreeDavid B Savage, Maura Agostini, Inês Barroso, 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.
Nature Communications|December 2, 2023
Selenoprotein deficiency disorder predisposes to aortic aneurysm formationErik Schoenmakers, Federica Marelli, Helle F Jørgensen, et al.
Pageof 3

Showing results (11-20 of 21) with videos related to

Sort By:
Pageof 3
Molecular and Cellular Biology|December 6, 2021
Structure-Guided Approach to Relieving Transcriptional Repression in Resistance to Thyroid Hormone αBeatriz Romartinez-Alonso, Maura Agostini, Heulyn Jones, et al.
The Journal of Clinical Endocrinology and Metabolism|March 21, 2014
A novel albumin gene mutation (R222I) in familial dysalbuminemic hyperthyroxinemiaNadia Schoenmakers, Carla Moran, Irene Campi, et al.
The Journal of Clinical Endocrinology and Metabolism|September 16, 2017
Anemia in Patients With Resistance to Thyroid Hormone α: A Role for Thyroid Hormone Receptor α in Human ErythropoiesisAnja L M van Gucht, Marcel E Meima, Carla Moran, et al.
Diabetes|April 7, 2018
A Pharmacogenetic Approach to the Treatment of Patients With <i>PPARG</i> MutationsMaura Agostini, Erik Schoenmakers, Junaid Beig, et al.
Cell Metabolism|October 3, 2006
Non-DNA binding, dominant-negative, human PPARgamma mutations cause lipodystrophic insulin resistanceMaura Agostini, Erik Schoenmakers, Catherine Mitchell, et al.
Diabetes|March 29, 2003
Human metabolic syndrome resulting from dominant-negative mutations in the nuclear receptor peroxisome proliferator-activated receptor-gammaDavid B Savage, Garry D Tan, Carlo L Acerini, et al.
Nature Genetics|November 8, 2016
Prospective functional classification of all possible missense variants in PPARGAmit R Majithia, Ben Tsuda, Maura Agostini, et al.
Nature Genetics|July 16, 2002
Digenic inheritance of severe insulin resistance in a human pedigreeDavid B Savage, Maura Agostini, Inês Barroso, 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.
Nature Communications|December 2, 2023
Selenoprotein deficiency disorder predisposes to aortic aneurysm formationErik Schoenmakers, Federica Marelli, Helle F Jørgensen, et al.
Pageof 3