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Paraskevi Salpea

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

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Molecular Immunology|August 22, 2008
Developmental and epigenetic regulation of the human TLR3 geneAnalia Porrás, Sarah Kozar, Valya Russanova, et al.
Endocrine-Related Cancer|October 7, 2015
Celecoxib reduces glucocorticoids in vitro and in a mouse model with adrenocortical hyperplasiaSisi Liu, Emmanouil Saloustros, Annabel Berthon, et al.
Human Molecular Genetics|August 7, 2015
Haploinsufficiency for either one of the type-II regulatory subunits of protein kinase A improves the bone phenotype of Prkar1a+/- miceSisi Liu, Emmanouil Saloustros, Edward L Mertz, et al.
Diabetes Research and Clinical Practice|September 14, 2019
Global and regional diabetes prevalence estimates for 2019 and projections for 2030 and 2045: Results from the International Diabetes Federation Diabetes Atlas, 9<sup>th</sup> editionPouya Saeedi, Inga Petersohn, Paraskevi Salpea, et al.
European Journal of Endocrinology|May 1, 2015
Germline PRKACA amplification causes variable phenotypes that may depend on the extent of the genomic defect: molecular mechanisms and clinical presentationsMaya B Lodish, Bo Yuan, Isaac Levy, et al.
The Lancet. Diabetes & Endocrinology|December 18, 2025
11th edition of the IDF Diabetes Atlas: global, regional, and national diabetes prevalence estimates for 2024 and projections for 2050Irini Genitsaridi, Paraskevi Salpea, Agus Salim, et al.
Diabetes Care|January 28, 2026
Global, Regional, and National Estimates of Undiagnosed Diabetes in Adults: Findings From the 2025 IDF Diabetes AtlasFelix Teufel, Katherine Orgutsova, Irini Genitsaridi, et al.
The Journal of Clinical Endocrinology and Metabolism|October 31, 2013
Deletions of the PRKAR1A locus at 17q24.2-q24.3 in Carney complex: genotype-phenotype correlations and implications for genetic testingParaskevi Salpea, Anelia Horvath, Edra London, et al.
European Journal of Endocrinology|January 24, 2021
DNAJC3 deficiency induces β-cell mitochondrial apoptosis and causes syndromic young-onset diabetesMaria Lytrivi, Valérie Senée, Paraskevi Salpea, et al.
Diabetologia|March 30, 2023
GLP-1R agonists demonstrate potential to treat Wolfram syndrome in human preclinical modelsVyron Gorgogietas, Bahareh Rajaei, Chae Heeyoung, et al.
Pageof 3

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

Sort By:
Pageof 3
Molecular Immunology|August 22, 2008
Developmental and epigenetic regulation of the human TLR3 geneAnalia Porrás, Sarah Kozar, Valya Russanova, et al.
Endocrine-Related Cancer|October 7, 2015
Celecoxib reduces glucocorticoids in vitro and in a mouse model with adrenocortical hyperplasiaSisi Liu, Emmanouil Saloustros, Annabel Berthon, et al.
Human Molecular Genetics|August 7, 2015
Haploinsufficiency for either one of the type-II regulatory subunits of protein kinase A improves the bone phenotype of Prkar1a+/- miceSisi Liu, Emmanouil Saloustros, Edward L Mertz, et al.
Diabetes Research and Clinical Practice|September 14, 2019
Global and regional diabetes prevalence estimates for 2019 and projections for 2030 and 2045: Results from the International Diabetes Federation Diabetes Atlas, 9<sup>th</sup> editionPouya Saeedi, Inga Petersohn, Paraskevi Salpea, et al.
European Journal of Endocrinology|May 1, 2015
Germline PRKACA amplification causes variable phenotypes that may depend on the extent of the genomic defect: molecular mechanisms and clinical presentationsMaya B Lodish, Bo Yuan, Isaac Levy, et al.
The Lancet. Diabetes & Endocrinology|December 18, 2025
11th edition of the IDF Diabetes Atlas: global, regional, and national diabetes prevalence estimates for 2024 and projections for 2050Irini Genitsaridi, Paraskevi Salpea, Agus Salim, et al.
Diabetes Care|January 28, 2026
Global, Regional, and National Estimates of Undiagnosed Diabetes in Adults: Findings From the 2025 IDF Diabetes AtlasFelix Teufel, Katherine Orgutsova, Irini Genitsaridi, et al.
The Journal of Clinical Endocrinology and Metabolism|October 31, 2013
Deletions of the PRKAR1A locus at 17q24.2-q24.3 in Carney complex: genotype-phenotype correlations and implications for genetic testingParaskevi Salpea, Anelia Horvath, Edra London, et al.
European Journal of Endocrinology|January 24, 2021
DNAJC3 deficiency induces β-cell mitochondrial apoptosis and causes syndromic young-onset diabetesMaria Lytrivi, Valérie Senée, Paraskevi Salpea, et al.
Diabetologia|March 30, 2023
GLP-1R agonists demonstrate potential to treat Wolfram syndrome in human preclinical modelsVyron Gorgogietas, Bahareh Rajaei, Chae Heeyoung, et al.
Pageof 3