Zobrazeno 1 - 10
of 34
pro vyhledávání: '"Aspasia Destouni"'
Autor:
Iliana Kalaboki, Dionysios Koulougliotis, Dimitra Kleisiari, Eleni Melliou, Prokopios Magiatis, Adamantia Kampioti, Effimia Eriotou, Aspasia Destouni
Publikováno v:
Foods, Vol 10, Iss 12, p 3009 (2021)
Background: The phenolic fraction of extra virgin olive oil (EVOO) has disease preventive and health-promoting properties which are supported by numerous studies. As such, EVOO is defined as a functional food. The aim of the present study was to char
Externí odkaz:
https://doaj.org/article/485d839068494ac3b11510e9a5e3240b
Autor:
Arunika Das, Aspasia Destouni
Publikováno v:
Human Reproduction. 38:195-203
The post-reproductive phase or menopause in females is triggered by a physiological timer that depends on a threshold of follicle number in the ovary. Curiously, reproductive senescence appears to be decoupled from chronological age and is instead th
Autor:
D. Parker Kelley, Lucas Albrechet‐Souza, Shealan Cruise, Rajani Maiya, Aspasia Destouni, Siva S. V. P. Sakamuri, Alexander Duplooy, Meghan Hibicke, Charles Nichols, Prasad V. G. Katakam, Nicholas W. Gilpin, Joseph Francis
Publikováno v:
Genes, Brain and Behavior. 22
Autor:
D. Parker Kelley, Katy Venable, Aspasia Destouni, Gerald Billac, Philip Ebenezer, Krisztian Stadler, Charles Nichols, Steven Barker, Joseph Francis
Publikováno v:
ACS chemical neuroscience. 13(2)
Post-traumatic stress disorder (PTSD) is associated with cognitive deficits, oxidative stress, and inflammation. Animal models have recapitulated features of PTSD, but no comparative RNA sequencing analysis of differentially expressed genes (DEGs) in
Autor:
Aspasia Tsezou, Konstantinos C. Tsolis, Evanthia Mourmoura, Ioanna V. Papathanasiou, Charalampos Balis, Anastassios Economou, Aspasia Destouni
BACKGROUND: Knee osteoarthritis (OA) is one of the most common structural OA disorders globally. Incomplete understanding of the fundamental biological aspects of osteoarthritis underlies the current lack of effective treatment or disease modifying d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::478f2bdc2c979c221e4ae608971846f6
https://lirias.kuleuven.be/handle/123456789/684257
https://lirias.kuleuven.be/handle/123456789/684257
Autor:
Arunika Das, Aiko Iwata-Otsubo, Aspasia Destouni, Jennine M. Dawicki-McKenna, Katelyn G. Boese, Ben E. Black, Michael A. Lampson
Publikováno v:
Nature cell biology. 24(5)
Centromeres are defined epigenetically by the histone H3 variant CENP-A. The propagation cycle by which pre-existing CENP-A nucleosomes serve as templates for nascent assembly predicts the epigenetic memory of weakened centromeres. Using a mouse mode
Autor:
Masoud Zamani Esteki, Eric Legius, Cindy Melotte, Thomy de Ravel, Karen Peeraer, Joris Vermeesch, Christel Meuleman, Thiery Voet, Eftychia Dimitriadou, Ellen Denayer, Jia Ding, Sophie Debrock, Aspasia Destouni, Heleen Masset, Kris Van Den Bogaert
Publikováno v:
Human Reproduction, 33(12), 2302-2311. Oxford University Press
Human Reproduction (Oxford, England)
Human Reproduction
Human Reproduction (Oxford, England)
Human Reproduction
STUDY QUESTION: Can genome-wide haplotyping increase success following preimplantation genetic testing for a monogenic disorder (PGT-M) by including zygotes with absence of pronuclei (0PN) or the presence of only one pronucleus (1PN)? SUMMARY ANSWER:
Autor:
Joris Vermeesch, Olga Tšuiko, Kris Van Den Bogaert, Tatjana Jatsenko, Karen Peeraer, Masoud Zamani Esteki, Ellen Denayer, Eftychia Dimitriadou, Jia Ding, Cindy Melotte, Sophie Debrock, Aspasia Destouni, Thierry Voet
Publikováno v:
Human Reproduction, 35(3), 718-726. Oxford University Press
STUDY QUESTION Is it possible to haplotype parents using parental siblings to leverage preimplantation genetic testing (PGT) for monogenic diseases and aneuploidy (comprehensive PGT) by genome-wide haplotyping? SUMMARY ANSWER We imputed identity-by-s
Autor:
Jessie Theuns, Katrien Omer François, Han G. Brunner, Masoud Zamani Esteki, Edith Coonen, Thierry Voet, Joris Vermeesch, Dennis Lorson, Cindy Melotte, Rebecca Richards, Olga Tšuiko, Sophie Debrock, Marion Drüsedau, Aspasia Destouni, Karen Peeraer, Scott Happe, Jos Dreesen, Aimee D C Paulussen, Kasper W.J. Derks, Benoit Devogelaere, Jeroen Meekels, Eftychia Dimitriadou, Josien G. Derhaag, Chris M. J. van Uum, Joke Allemeersch, Heleen Masset, Christine E. M. de Die-Smulders
Publikováno v:
Human Reproduction, 34(8), 1608-1619. Oxford University Press
STUDY QUESTION Can reduced representation genome sequencing offer an alternative to single nucleotide polymorphism (SNP) arrays as a generic and genome-wide approach for comprehensive preimplantation genetic testing for monogenic disorders (PGT-M), a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8c1229938ce0d6716326966d017670c6
https://cris.maastrichtuniversity.nl/en/publications/f063b5a1-1e6d-47e4-ab82-b9762610e7b5
https://cris.maastrichtuniversity.nl/en/publications/f063b5a1-1e6d-47e4-ab82-b9762610e7b5
Autor:
Aspasia Destouni, Joanne Traeger-Synodinos, Georgia Kakourou, Sophia Kitsiou-Tzeli, Myrto Poulou, Christina Vrettou, Maria Tzetis
Publikováno v:
Journal of Cystic Fibrosis. 15:163-170
Background Institutions offering CF-PGD face the challenge of developing and optimizing single cell genotyping protocols that should cover for the extremely heterogeneous CF mutation spectrum. Here we report the development and successful clinical ap