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Molecular Immunology
|
August 22, 2008
Developmental and epigenetic regulation of the human TLR3 gene
Analia 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 hyperplasia
Sisi 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+/- mice
Sisi 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> edition
Pouya 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 presentations
Maya 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 2050
Irini 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 Atlas
Felix 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 testing
Paraskevi 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 diabetes
Maria Lytrivi, Valérie Senée, Paraskevi Salpea, et al.
Diabetologia
|
March 30, 2023
GLP-1R agonists demonstrate potential to treat Wolfram syndrome in human preclinical models
Vyron Gorgogietas, Bahareh Rajaei, Chae Heeyoung, et al.
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Search research articles
Search
Showing results (11-20 of 21) with videos related to
Sort By:
Page
of 3
Molecular Immunology
|
August 22, 2008
Developmental and epigenetic regulation of the human TLR3 gene
Analia 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 hyperplasia
Sisi 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+/- mice
Sisi 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> edition
Pouya 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 presentations
Maya 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 2050
Irini 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 Atlas
Felix 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 testing
Paraskevi 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 diabetes
Maria Lytrivi, Valérie Senée, Paraskevi Salpea, et al.
Diabetologia
|
March 30, 2023
GLP-1R agonists demonstrate potential to treat Wolfram syndrome in human preclinical models
Vyron Gorgogietas, Bahareh Rajaei, Chae Heeyoung, et al.
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of 3