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Eduardo Fernandez-Rebollo

Showing results (1-10 of 17) with videos related to

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Stem Cell Research & Therapy|April 20, 2018
Effects of senolytic drugs on human mesenchymal stromal cellsClara Grezella, Eduardo Fernandez-Rebollo, Julia Franzen, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|September 20, 2017
Primary Osteoporosis Is Not Reflected by Disease-Specific DNA Methylation or Accelerated Epigenetic Age in BloodEduardo Fernandez-Rebollo, Monika Eipel, Lothar Seefried, et al.
Clinical Endocrinology|April 9, 2008
New mutation type in pseudohypoparathyroidism type IaEduardo Fernandez-Rebollo, Raquel Barrio, Gustavo Pérez-Nanclares, et al.
Stem Cell Reports|January 28, 2020
Senescence-Associated Metabolomic Phenotype in Primary and iPSC-Derived Mesenchymal Stromal CellsEduardo Fernandez-Rebollo, Julia Franzen, Roman Goetzke, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|February 26, 2011
Gsα activity is reduced in erythrocyte membranes of patients with psedohypoparathyroidism due to epigenetic alterations at the GNAS locusCelia Zazo, Susanne Thiele, Cesar Martín, et al.
The Journal of Clinical Endocrinology and Metabolism|April 12, 2012
Detection of hypomethylation syndrome among patients with epigenetic alterations at the GNAS locusGustavo Perez-Nanclares, Valeria Romanelli, Sonia Mayo, et al.
The Journal of Clinical Endocrinology and Metabolism|December 17, 2009
Intragenic GNAS deletion involving exon A/B in pseudohypoparathyroidism type 1A resulting in an apparent loss of exon A/B methylation: potential for misdiagnosis of pseudohypoparathyroidism type 1BEduardo Fernandez-Rebollo, Beatriz García-Cuartero, Intza Garin, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|August 20, 2013
Postnatal establishment of allelic Gαs silencing as a plausible explanation for delayed onset of parathyroid hormone resistance owing to heterozygous Gαs disruptionSerap Turan, Eduardo Fernandez-Rebollo, Cumhur Aydin, et al.
Plos One|October 3, 2013
Gastric inhibitory polypeptide receptor methylation in newly diagnosed, drug-naïve patients with type 2 diabetes: a case-control studySilvia Canivell, Elena G Ruano, Antoni Sisó-Almirall, et al.
Plos One|June 11, 2014
Differential methylation of TCF7L2 promoter in peripheral blood DNA in newly diagnosed, drug-naïve patients with type 2 diabetesSilvia Canivell, Elena G Ruano, Antoni Sisó-Almirall, et al.
Pageof 2

Showing results (1-10 of 17) with videos related to

Sort By:
Pageof 2
Stem Cell Research & Therapy|April 20, 2018
Effects of senolytic drugs on human mesenchymal stromal cellsClara Grezella, Eduardo Fernandez-Rebollo, Julia Franzen, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|September 20, 2017
Primary Osteoporosis Is Not Reflected by Disease-Specific DNA Methylation or Accelerated Epigenetic Age in BloodEduardo Fernandez-Rebollo, Monika Eipel, Lothar Seefried, et al.
Clinical Endocrinology|April 9, 2008
New mutation type in pseudohypoparathyroidism type IaEduardo Fernandez-Rebollo, Raquel Barrio, Gustavo Pérez-Nanclares, et al.
Stem Cell Reports|January 28, 2020
Senescence-Associated Metabolomic Phenotype in Primary and iPSC-Derived Mesenchymal Stromal CellsEduardo Fernandez-Rebollo, Julia Franzen, Roman Goetzke, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|February 26, 2011
Gsα activity is reduced in erythrocyte membranes of patients with psedohypoparathyroidism due to epigenetic alterations at the GNAS locusCelia Zazo, Susanne Thiele, Cesar Martín, et al.
The Journal of Clinical Endocrinology and Metabolism|April 12, 2012
Detection of hypomethylation syndrome among patients with epigenetic alterations at the GNAS locusGustavo Perez-Nanclares, Valeria Romanelli, Sonia Mayo, et al.
The Journal of Clinical Endocrinology and Metabolism|December 17, 2009
Intragenic GNAS deletion involving exon A/B in pseudohypoparathyroidism type 1A resulting in an apparent loss of exon A/B methylation: potential for misdiagnosis of pseudohypoparathyroidism type 1BEduardo Fernandez-Rebollo, Beatriz García-Cuartero, Intza Garin, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|August 20, 2013
Postnatal establishment of allelic Gαs silencing as a plausible explanation for delayed onset of parathyroid hormone resistance owing to heterozygous Gαs disruptionSerap Turan, Eduardo Fernandez-Rebollo, Cumhur Aydin, et al.
Plos One|October 3, 2013
Gastric inhibitory polypeptide receptor methylation in newly diagnosed, drug-naïve patients with type 2 diabetes: a case-control studySilvia Canivell, Elena G Ruano, Antoni Sisó-Almirall, et al.
Plos One|June 11, 2014
Differential methylation of TCF7L2 promoter in peripheral blood DNA in newly diagnosed, drug-naïve patients with type 2 diabetesSilvia Canivell, Elena G Ruano, Antoni Sisó-Almirall, et al.
Pageof 2