Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Antonia, Angelopoulou"'
Autor:
Vasileios L. Zogopoulos, Georgia Saxami, Apostolos Malatras, Antonia Angelopoulou, Chih-Hung Jen, William J. Duddy, Gerasimos Daras, Polydefkis Hatzopoulos, David R. Westhead, Ioannis Michalopoulos
Publikováno v:
iScience, Vol 24, Iss 8, Pp 102848- (2021)
Summary: Gene coexpression analysis refers to the discovery of sets of genes which exhibit similar expression patterns across multiple transcriptomic data sets, such as microarray experiment data of public repositories. Arabidopsis Coexpression Tool
Externí odkaz:
https://doaj.org/article/91928281b65f438d9705d5ef422a8fa2
Autor:
Christos, Yapijakis, Stefania, Kalogera, Antonia, Angelopoulou, Georgios, Paraskevas, Elisabeth, Kapaki
Publikováno v:
Advances in experimental medicine and biology. 1339
Oculodentodigital syndrome (ODDS) is a rare genetic disorder caused by mutations in the gap junction GJA1 gene encoding connexin-43 (chromosome 6q22). A typical ODDS case is presented.A 40-year-old male patient was examined neurologically and genetic
Autor:
Antonia, Angelopoulou, Dimitrios, Vlachakis, George P, Chrousos, Nikolaos, Cosmidis, Christos, Yapijakis
Publikováno v:
Advances in experimental medicine and biology. 1339
One of the most common genetic causes associated with thrombophilia is mutation G20210A of the coagulation factor II (F2) gene.Data collected from 355 unrelated Greeks examined for the mutation G20210A over a period of two decades were anonymously an
Autor:
Christos, Yapijakis, Antonis, Vylliotis, Antonia, Angelopoulou, Mary, Adamopoulou, George P, Chrousos, Costas, Voumvourakis
Publikováno v:
Advances in experimental medicine and biology. 1339
Frontometaphyseal dysplasia 1 (FMD1) is a rare X-linked craniofacial syndrome belonging in the otopalatodigital spectrum of disorders. Here we present a case with severe FMD1 that was caused by a mutation in the FLNA gene located on Xq28.A diagnosis
Autor:
Christos Yapijakis, Stefania Kalogera, Antonia Angelopoulou, Georgios Paraskevas, Elisabeth Kapaki
Publikováno v:
GeNeDis 2020 ISBN: 9783030787868
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::69748db4a8043cd5a51639ee16c185a0
https://doi.org/10.1007/978-3-030-78787-5_39
https://doi.org/10.1007/978-3-030-78787-5_39
Autor:
Antonia Angelopoulou, Dimitrios Vlachakis, George P. Chrousos, Nikolaos Cosmidis, Christos Yapijakis
Publikováno v:
GeNeDis 2020 ISBN: 9783030787868
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f7471ebcee780bb7032b29deb9f76f5c
https://doi.org/10.1007/978-3-030-78787-5_40
https://doi.org/10.1007/978-3-030-78787-5_40
Autor:
Christos Yapijakis, Antonis Vylliotis, Antonia Angelopoulou, Mary Adamopoulou, George P. Chrousos, Costas Voumvourakis
Publikováno v:
GeNeDis 2020 ISBN: 9783030787868
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::26c904ce942177725ed91b3b29fbc393
https://doi.org/10.1007/978-3-030-78787-5_38
https://doi.org/10.1007/978-3-030-78787-5_38
Publikováno v:
Advances in experimental medicine and biology. 1195
X-linked spinal and bulbar muscular atrophy (SBMA), also known as Kennedy syndrome, is an adult-onset neurodegenerative disorder characterized by slowly progressive muscle atrophy and other severe symptoms gradually leading to reduced mobility and ul
Publikováno v:
Advances in experimental medicine and biology. 1195
Chromosome 18q deletion syndrome (18q-) is a rare chromosomal disorder with phenotypic variability, including mental deficiency, short stature, hypotonia, cleft palate, and hearing impairment. We present a case with features of 18q- syndrome who had
Publikováno v:
Advances in Experimental Medicine and Biology ISBN: 9783030326326
Introduction: Chromosome 18q deletion syndrome (18q-) is a rare chromosomal disorder with phenotypic variability, including mental deficiency, short stature, hypotonia, cleft palate, and hearing impairment. We present a case with features of 18q- syn
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c7eaa2b7d8644ad28ddebf09ed4610a2
https://doi.org/10.1007/978-3-030-32633-3_22
https://doi.org/10.1007/978-3-030-32633-3_22