Zobrazeno 1 - 10
of 212
pro vyhledávání: '"Zachaki A"'
Autor:
Manola, Kalliopi N.1 (AUTHOR) pmanola@ipta.demokritos.gr, Zachaki, Sophia1 (AUTHOR) katerinakak@hotmail.com, Kakosaiou, Katerina1 (AUTHOR) mrshcn@gmail.com, Ioannidou, Agapi1 (AUTHOR) mar_ka@ipta.demokritos.gr, Kalomoiraki, Marina1 (AUTHOR), Rampias, Theodoros2 (AUTHOR) pmanola@ipta.demokritos.gr
Publikováno v:
Life (2075-1729). Oct2024, Vol. 14 Issue 10, p1311. 13p.
Autor:
Kalliopi N. Manola, Sophia Zachaki, Katerina Kakosaiou, Agapi Ioannidou, Marina Kalomoiraki, Theodoros Rampias
Publikováno v:
Life, Vol 14, Iss 10, p 1311 (2024)
Background: Aberrant gene promoter methylation is one of the hallmarks of Acute Myeloid Leukemia (AML). RAD21 is an important gene, implicated in sister chromatids cohesion, DNA repair, the regulation of gene transcription, apoptosis and hematopoiesi
Externí odkaz:
https://doaj.org/article/3a469e817f0649c08518c81fdced3f33
Akademický článek
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Autor:
Elisavet Kouvidi, Hara Tsimela, Leandros Lazaros, Kalliopi N Manola, Sophia Zachaki, Ruxandra Dobrescu, Konstantinos Sfakianoudis, Theodora Tsoni, Christina Katsidi, Haralambia Tsarouha, Emmanuel Kanavakis, Ariadni Mavrou
Publikováno v:
Journal of Human Reproductive Sciences, Vol 15, Iss 3, Pp 307-317 (2022)
46,XX male sex reversal syndrome is a rare genetic cause of male infertility. We report on two new cases of this syndrome in men presenting with hypogonadism and infertility. Cytogenetic and molecular analysis was performed in both patients. An exten
Externí odkaz:
https://doaj.org/article/a6a515c629cd4f0597776ef60a30578d
Autor:
Zachaki, Sophia, Kalomoiraki, Marina, Kouvidi, Elisavet, Promponas, Emmanuel, Syrkos, Stefanos, Panopoulou, Birgit, Pantou, Amelia, Mavrou, Ariadni, Kanavakis, Emmanuel, Manola, Kalliopi N.
Publikováno v:
In European Journal of Obstetrics & Gynecology and Reproductive Biology September 2021 264:212-218
Autor:
Kouvidi, Elisavet, Tsarouha, Haralambia, Zachaki, Sophia, Katsidi, Christina, Tsimela, Hara, Pantou, Amelia, Kanavakis, Emmanuel, Mavrou, Ariadni
Publikováno v:
Cytogenetic & Genome Research; 2024, Vol. 163 Issue 5/6, p274-278, 5p
Autor:
Elisavet Kouvidi, Haralambia Tsarouha, Christina Katsidi, Sophia Zachaki, Nikolaos Nitsos, Sofia Samourgianidi, Amelia Pantou, Lazaros Leandros, Emmanouel Kanavakis, Ariadni Mavrou
Publikováno v:
OBM Genetics. :1-17
Chromosomal abnormalities represent a significant genetic cause of male infertility because they impair spermatogenesis. The objective of the current study was to determine the prevalence and distribution of chromosomal abnormalities in Greek men wit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::68a1581020ab4017bb8127f675001f55
https://doi.org/10.21926/obm.genet.2301178
https://doi.org/10.21926/obm.genet.2301178
Publikováno v:
Balkan Journal of Medical Genetics, Vol 21, Iss 2, Pp 63-67 (2018)
A novel de novo paracentric inversion of the long arm of chromosome 20 [inv(20)(q13.1q13.3)], detected by conventional karyotyping in a 14-year-old boy with mental retardation is described. Further investigation by array comparative genomic hybridiza
Externí odkaz:
https://doaj.org/article/7e2dd82776644a21930ccca5fa05b9f7
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
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Autor:
Daraki, Aggeliki, Kakosaiou, Katerina, Zachaki, Sophia, Sambani, Constantina, Aleporou-Marinou, Vassiliki, Kollia, Panagoula, Manola, Kalliopi N. *
Publikováno v:
In Cancer Genetics November 2016 209(11):525-533