Zobrazeno 1 - 10
of 21
pro vyhledávání: '"Dimitrios, Ioannou"'
Autor:
George Anifandis, Tyl H Taylor, Christina I Messini, Katerina Chatzimeletiou, Alexandros Daponte, Dimitrios Ioannou, Helen G Tempest
Publikováno v:
Medicina, Vol 57, Iss 9, p 946 (2021)
Cryopreservation of human gametes and embryos as well as human reproductive tissues has been characterized as an essential process and aspect of assisted reproductive technology (ART). Notably, sperm cryopreservation is a fundamental aspect of cryopr
Externí odkaz:
https://doaj.org/article/8b18eec9910447b79d9362307767a0fe
Autor:
Dimitrios Ioannou
Η διατριβή αποτελεί μια απόπειρα διερεύνησης των τρόπων με τους οποίους τα Εξάρχεια, μια ιστορική συνοικία του Αθηναϊκού κέντρου, απέκτ
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c905008d333cb4b7e1f0eec977ee7da9
https://doi.org/10.12681/eadd/37432
https://doi.org/10.12681/eadd/37432
Autor:
Dimitrios Ioannou, Lakshmi Kandukuri, Ameer Quadri, Victor Becerra, Joe Leigh Simpson, Helen G Tempest
Publikováno v:
PLoS ONE, Vol 10, Iss 3, p e0118886 (2015)
The higher-order organization of chromatin is well-established, with chromosomes occupying distinct positions within the interphase nucleus. Chromatin is susceptible to, and constantly assaulted by both endogenous and exogenous threats. However, the
Externí odkaz:
https://doaj.org/article/b27dfc4b34f743298af8fd9219aa89ec
Background: Narrow aortic bifurcation (NAB) is considered as a risk factor for endograft limb thrombosis. The purpose of the study was to investigate the effect of narrow aortic bifurcation on outcomes of elective endovascular aneurysm repair (EVAR).
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2127::26d663486e6b58d29243d2c3bfa793af
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3029179
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3029179
Autor:
Dimitrios Ioannou, Helen G. Tempest
Publikováno v:
Systems Biology in Reproductive Medicine. 64:518-534
The spermatozoon is considered by many to be a silent vessel whose only function is to safely deliver the paternal genome to the maternal oocyte. As a result, the paternal contribution to fertilization and embryogenesis is frequently overlooked. Howe
Publikováno v:
Scientific Reports
The organization of chromosomes in sperm nuclei has been proposed to possess a unique “hairpin-loop” arrangement, which is hypothesized to aid in the ordered exodus of the paternal genome following fertilization. This study simultaneously assesse
Publikováno v:
Panminerva medica. 58(2)
Fluorescence in-situ hybridization (FISH) revolutionized cytogenetics using fluorescently labelled probes with high affinity with target (nuclear) DNA. By the early 1990s FISH was adopted as a means of preimplantation genetic diagnosis (PGD) sexing f
Meiotic Nondisjunction: Insights into the Origin and Significance of Aneuploidy in Human Spermatozoa
Autor:
Dimitrios, Ioannou, Helen G, Tempest
Publikováno v:
Advances in experimental medicine and biology. 868
Chromosome aneuploidy refers to changes in the chromosome complement of a genome and can include gain or loss of genetic material. The human genome is delicately balanced, and for the most part perturbations in the chromosome complement are often inc
Autor:
Helen G. Tempest, Joe Leigh Simpson, Ameer Quadri, Dimitrios Ioannou, Lakshmi Kandukuri, Victor N. Becerra
Publikováno v:
PLoS ONE, Vol 10, Iss 3, p e0118886 (2015)
PLoS ONE
PLoS ONE
The higher-order organization of chromatin is well-established, with chromosomes occupying distinct positions within the interphase nucleus. Chromatin is susceptible to, and constantly assaulted by both endogenous and exogenous threats. However, the
Meiotic Nondisjunction: Insights into the Origin and Significance of Aneuploidy in Human Spermatozoa
Autor:
Helen G. Tempest, Dimitrios Ioannou
Publikováno v:
Advances in Experimental Medicine and Biology ISBN: 9783319188805
Chromosome aneuploidy refers to changes in the chromosome complement of a genome and can include gain or loss of genetic material. The human genome is delicately balanced, and for the most part perturbations in the chromosome complement are often inc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c5851a1fe670c280b5a1eacf1e08c7d3
https://doi.org/10.1007/978-3-319-18881-2_1
https://doi.org/10.1007/978-3-319-18881-2_1