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Pavlos Fanis

Showing results (21-30 of 36) with videos related to

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Hormones (Athens, Greece)|July 11, 2016
A novel MC4R deletion coexisting with FTO and MC1R gene variants, causes severe early onset obesityVassos Neocleous, Christos Shammas, Marie M Phelan, et al.
Molecular & Cellular Proteomics : MCP|August 9, 2012
Five friends of methylated chromatin target of protein-arginine-methyltransferase[prmt]-1 (chtop), a complex linking arginine methylation to desumoylationPavlos Fanis, Nynke Gillemans, Ali Aghajanirefah, et al.
Frontiers in Integrative Neuroscience|September 25, 2020
Neurophysiological and Genetic Findings in Patients With Juvenile Myoclonic EpilepsyStefani Stefani, Ioanna Kousiappa, Nicoletta Nicolaou, et al.
Orphanet Journal of Rare Diseases|April 29, 2025
Co-segregation of the c.489+3A>G variant with p.Cys1400Ter pathogenic CFTR mutation in Cyprus: prevalence and clinical implicationsPanayiotis K Yiallouros, Pinelopi Anagnostopoulou, Panayiotis Kouis, et al.
Molecular and Cellular Biology|October 28, 2009
Friend of Prmt1, a novel chromatin target of protein arginine methyltransferasesThamar Bryn van Dijk, Nynke Gillemans, Claudia Stein, et al.
Endocrine Connections|May 31, 2023
Reduced serum concentrations of biomarkers reflecting Leydig and Sertoli cell function in male patients with congenital adrenal hyperplasiaTrine Holm Johannsen, Jakob Albrethsen, Vassos Neocleous, et al.
International Journal of Endocrinology|May 11, 2017
Variations in the 3'UTR of the <i>CYP21A2</i> Gene in Heterozygous Females with HyperandrogenaemiaVassos Neocleous, Pavlos Fanis, Meropi Toumba, et al.
Hormone and Metabolic Research = Hormon- Und Stoffwechselforschung = Hormones Et Metabolisme|September 11, 2019
The Spectrum of Genetic Defects in Congenital Adrenal Hyperplasia in the Population of Cyprus: A Retrospective AnalysisVassos Neocleous, Pavlos Fanis, Meropi Toumba, et al.
Plos One|July 21, 2021
Molecular epidemiology of SARS-CoV-2 in CyprusJan Richter, Pavlos Fanis, Christina Tryfonos, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|November 12, 2020
Late diagnosis of 3β-Hydroxysteroid dehydrogenase deficiency: the pivotal role of gas chromatography-mass spectrometry urinary steroid metabolome analysis and a novel homozygous nonsense mutation in the <i>HSD3B2</i> genePavlos Fanis, Vassos Neocleous, Konstantina Kosta, et al.
Pageof 4

Showing results (21-30 of 36) with videos related to

Sort By:
Pageof 4
Hormones (Athens, Greece)|July 11, 2016
A novel MC4R deletion coexisting with FTO and MC1R gene variants, causes severe early onset obesityVassos Neocleous, Christos Shammas, Marie M Phelan, et al.
Molecular & Cellular Proteomics : MCP|August 9, 2012
Five friends of methylated chromatin target of protein-arginine-methyltransferase[prmt]-1 (chtop), a complex linking arginine methylation to desumoylationPavlos Fanis, Nynke Gillemans, Ali Aghajanirefah, et al.
Frontiers in Integrative Neuroscience|September 25, 2020
Neurophysiological and Genetic Findings in Patients With Juvenile Myoclonic EpilepsyStefani Stefani, Ioanna Kousiappa, Nicoletta Nicolaou, et al.
Orphanet Journal of Rare Diseases|April 29, 2025
Co-segregation of the c.489+3A>G variant with p.Cys1400Ter pathogenic CFTR mutation in Cyprus: prevalence and clinical implicationsPanayiotis K Yiallouros, Pinelopi Anagnostopoulou, Panayiotis Kouis, et al.
Molecular and Cellular Biology|October 28, 2009
Friend of Prmt1, a novel chromatin target of protein arginine methyltransferasesThamar Bryn van Dijk, Nynke Gillemans, Claudia Stein, et al.
Endocrine Connections|May 31, 2023
Reduced serum concentrations of biomarkers reflecting Leydig and Sertoli cell function in male patients with congenital adrenal hyperplasiaTrine Holm Johannsen, Jakob Albrethsen, Vassos Neocleous, et al.
International Journal of Endocrinology|May 11, 2017
Variations in the 3'UTR of the <i>CYP21A2</i> Gene in Heterozygous Females with HyperandrogenaemiaVassos Neocleous, Pavlos Fanis, Meropi Toumba, et al.
Hormone and Metabolic Research = Hormon- Und Stoffwechselforschung = Hormones Et Metabolisme|September 11, 2019
The Spectrum of Genetic Defects in Congenital Adrenal Hyperplasia in the Population of Cyprus: A Retrospective AnalysisVassos Neocleous, Pavlos Fanis, Meropi Toumba, et al.
Plos One|July 21, 2021
Molecular epidemiology of SARS-CoV-2 in CyprusJan Richter, Pavlos Fanis, Christina Tryfonos, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|November 12, 2020
Late diagnosis of 3β-Hydroxysteroid dehydrogenase deficiency: the pivotal role of gas chromatography-mass spectrometry urinary steroid metabolome analysis and a novel homozygous nonsense mutation in the <i>HSD3B2</i> genePavlos Fanis, Vassos Neocleous, Konstantina Kosta, et al.
Pageof 4