Zobrazeno 1 - 10
of 100
pro vyhledávání: '"Koutsoulidou A"'
Autor:
Despina Charalambous, Michalis Christoforou, Krystallo Christou, Melina Christou, Antonis Ververis, Marios Andreou, Kyproula Christodoulou, Andrie Koutsoulidou, Christoforos Papachrysostomou, Maria Pantelidou
Publikováno v:
Plants, Vol 13, Iss 14, p 1982 (2024)
The purpose of this study was to identify the saponin and phenolic components in root extracts of Saponaria officinalis, a widespread species, found in Cyprus. A total of six major saponins, including gypsogenin and gypsogenic acid derivatives, as we
Externí odkaz:
https://doaj.org/article/2a140fd43d644af6b1e91dbf4f978895
Autor:
Andrea C. Kakouri, Demetris Koutalianos, Andrie Koutsoulidou, Anastasis Oulas, Marios Tomazou, Nikoletta Nikolenko, Chris Turner, Andreas Roos, Anna Lusakowska, Katarzyna Janiszewska, George K. Papadimas, Constantinos Papadopoulos, Evangelia Kararizou, Eleni Zamba Papanicolaou, Grainne Gorman, Hanns Lochmüller, George M. Spyrou, Leonidas A. Phylactou
Publikováno v:
RNA Biology, Vol 19, Iss 1, Pp 507-518 (2022)
Muscular dystrophies are a group of rare and severe inherited disorders mainly affecting the muscle tissue. Duchene Muscular Dystrophy, Myotonic Dystrophy types 1 and 2, Limb Girdle Muscular Dystrophy and Facioscapulohumeral Muscular Dystrophy are so
Externí odkaz:
https://doaj.org/article/fce9b866c9544801aef48904f2cb8776
Akademický článek
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Autor:
Koutsoulidou, Andrie, Koutalianos, Demetris, Georgiou, Kristia, Kakouri, Andrea C., Oulas, Anastasis, Tomazou, Marios, Kyriakides, Tassos C., Roos, Andreas, Papadimas, George K., Papadopoulos, Constantinos, Kararizou, Evangelia, Spyrou, George M., Zamba Papanicolaou, Eleni, Lochmüller, Hanns, Phylactou, Leonidas A.
Publikováno v:
In Neuromuscular Disorders April 2022 32(4):332-346
Autor:
Demetris Koutalianos, Andrie Koutsoulidou, Chrystalla Mytidou, Andrea C. Kakouri, Anastasis Oulas, Marios Tomazou, Tassos C. Kyriakides, Marianna Prokopi, Konstantinos Kapnisis, Nikoletta Nikolenko, Chris Turner, Anna Lusakowska, Katarzyna Janiszewska, George K. Papadimas, Constantinos Papadopoulos, Evangelia Kararizou, George M. Spyrou, Geneviève Gourdon, Eleni Zamba Papanicolaou, Grainne Gorman, Andreas Anayiotos, Hanns Lochmüller, Leonidas A. Phylactou
Publikováno v:
Molecular Therapy: Methods & Clinical Development, Vol 23, Iss , Pp 169-183 (2021)
Myotonic dystrophy type 1 (DM1) is the most common adult-onset muscular dystrophy, primarily characterized by muscle wasting and weakness. Many biomarkers already exist in the rapidly developing biomarker research field that aim to improve patients
Externí odkaz:
https://doaj.org/article/0df8908873d4446eb6c45e3b522382e8
Autor:
Charalambous, Despina, Christoforou, Michalis, Christou, Krystallo, Christou, Melina, Ververis, Antonis, Andreou, Marios, Christodoulou, Kyproula, Koutsoulidou, Andrie, Papachrysostomou, Christoforos, Pantelidou, Maria
Publikováno v:
Plants (2223-7747); Jul2024, Vol. 13 Issue 14, p1982, 17p
Publikováno v:
Molecular Therapy: Methods & Clinical Development, Vol 18, Iss , Pp 230-239 (2020)
Muscular dystrophies are a group of inherited disorders that primarily affect the muscle tissues. Across the muscular dystrophies, symptoms commonly compromise the quality of life in all areas of functioning. It is well noted that muscular dystrophie
Externí odkaz:
https://doaj.org/article/a005b3d6a80a443caf3a1a30df08bcbb
Autor:
Chrystalla Mytidou, Andrie Koutsoulidou, Margarita Zachariou, Marianna Prokopi, Konstantinos Kapnisis, George M. Spyrou, Andreas Anayiotos, Leonidas A. Phylactou
Publikováno v:
Frontiers in Physiology, Vol 12 (2021)
Skeletal muscle growth and maintenance depend on two tightly regulated processes, myogenesis and muscle regeneration. Both processes involve a series of crucial regulatory molecules including muscle-specific microRNAs, known as myomiRs. We recently s
Externí odkaz:
https://doaj.org/article/86f3128605ab452590a0feba08a9e1c5
Autor:
Michaella Georgiadou, Melina Christou, Kleitos Sokratous, Jesper Wengel, Kyriaki Michailidou, Kyriacos Kyriacou, Andrie Koutsoulidou, Nikolaos P. Mastroyiannopoulos, Leonidas A. Phylactou
Publikováno v:
Pharmaceuticals, Vol 14, Iss 11, p 1113 (2021)
Duchenne muscular dystrophy (DMD) is a fatal disorder characterised by progressive muscle wasting. It is caused by mutations in the dystrophin gene, which disrupt the open reading frame leading to the loss of functional dystrophin protein in muscle f
Externí odkaz:
https://doaj.org/article/859912fa29444673b665f4b3783ea3bc
Akademický článek
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K zobrazení výsledku je třeba se přihlásit.