Skin in the game: Video-game–related cutaneous pathologies in adolescents

por Kyriakou, Georgia, Glentis, Apostolos
Publicado 2021

The Diverse Genomic Landscape of Diamond–Blackfan Anemia: Two Novel Variants and a Mini-Review

por Pelagiadis, Iordanis, Kyriakidis, Ioannis, Katzilakis, Nikolaos, Kosmeri, Chrysoula, Veltra, Danai, Sofocleous, Christalena, Glentis, Stavros, Kattamis, Antonis, Makis, Alexandros, Stiakaki, Eftichia
Publicado 2023

S104: A SEVERE MOUSE MODEL OF ALPHA-THALASSEMIA SHOWS ABNORMAL IRON METABOLISM, ERYTHROPOIESIS AND COAGULATION, AND CAN BE RESCUED BY A NOVEL GENE THERAPY APPROACH

por Chappell, M, Breda, L, Guerra, A, Ghiaccio, V, Fedorky, M, Jarocha, D, Gollomp, K, Teawtrakul, N, Glentis, S, Kattamis, A, Rivella, S
Publicado 2022

A Novel Variant in the TP53 Gene Causing Li–Fraumeni Syndrome

por Papadimitriou, Dimitrios T., Stratakis, Constantine A., Kattamis, Antonis, Glentis, Stavros, Dimitrakakis, Constantine, Spyridis, George P., Christopoulos, Panagiotis, Mastorakos, George, Vlahos, Nikolaos F., Iacovidou, Nicoletta
Publicado 2023

P1521: A SEVERE MOUSE MODEL OF ALPHA-THALASSEMIA SHOWS ABNORMAL IRON METABOLISM, ERYTHROPOIESIS AND COAGULATION, AND CAN BE RESCUED BY A NOVEL GENE THERAPY APPROACH

por Rivella, S., Chappell, M., Jarocha, D., Breda, L., Ghiaccio, V., Fedorky, M., Triebwasser, M., Guerra, A., Gollomp, K., Teawtrakul, N., Glentis, S., Kattamis, A., Abdulmalik, O.
Publicado 2022

P798: DIAMOND BLACKFAN ANEMIA MAY ESCAPE DIAGNOSIS UP TO ADULTHOOD; A REPORT FROM THE UPDATED GREEK REGISTRY

por Delaporta, Polyxeni, Sofocleous, Christalena, Glentis, Stavros, Veltra, Danai, Polychronopoulou, Sophia, Kossiva, Lydia, Makis, Alexandros, Economou, Marina, Katzilakis, Nikolaos, Steiakaki, Eftychia, Marinakis, Theodoros, Kostaridou, Stavroula, Kattamis, Antonis
Publicado 2023

Exome Sequencing in BRCA1- and BRCA2-Negative Greek Families Identifies MDM1 and NBEAL1 as Candidate Risk Genes for Hereditary Breast Cancer

por Glentis, Stavros, Dimopoulos, Alexandros C., Rouskas, Konstantinos, Ntritsos, George, Evangelou, Evangelos, Narod, Steven A., Mes-Masson, Anne-Marie, Foulkes, William D., Rivera, Barbara, Tonin, Patricia N., Ragoussis, Jiannis, Dimas, Antigone S.
Publicado 2019

The emergence of spontaneous coordinated epithelial rotation on cylindrical curved surfaces

por Glentis, Alexandros, Blanch-Mercader, Carles, Balasubramaniam, Lakshmi, Saw, Thuan Beng, d’Alessandro, Joseph, Janel, Sebastien, Douanier, Audrey, Delaval, Benedicte, Lafont, Frank, Lim, Chwee Teck, Delacour, Delphine, Prost, Jacques, Xi, Wang, Ladoux, Benoit
Publicado 2022

Cancer-associated fibroblasts induce metalloprotease-independent cancer cell invasion of the basement membrane

por Glentis, Alexandros, Oertle, Philipp, Mariani, Pascale, Chikina, Aleksandra, El Marjou, Fatima, Attieh, Youmna, Zaccarini, Francois, Lae, Marick, Loew, Damarys, Dingli, Florent, Sirven, Philemon, Schoumacher, Marie, Gurchenkov, Basile G., Plodinec, Marija, Vignjevic, Danijela Matic
Publicado 2017

Author Correction: Cancer-associated fibroblasts induce metalloprotease-independent cancer cell invasion of the basement membrane

por Glentis, Alexandros, Oertle, Philipp, Mariani, Pascale, Chikina, Aleksandra, El Marjou, Fatima, Attieh, Youmna, Zaccarini, Francois, Lae, Marick, Loew, Damarys, Dingli, Florent, Sirven, Philemon, Schoumacher, Marie, Gurchenkov, Basile G., Plodinec, Marija, Vignjevic, Danijela Matic
Publicado 2018

SETDB1 fuels the lung cancer phenotype by modulating epigenome, 3D genome organization and chromatin mechanical properties

por Zakharova, Vlada V, Magnitov, Mikhail D, Del Maestro, Laurence, Ulianov, Sergey V, Glentis, Alexandros, Uyanik, Burhan, Williart, Alice, Karpukhina, Anna, Demidov, Oleg, Joliot, Veronique, Vassetzky, Yegor S, Mège, René-Marc, Piel, Matthieu, Razin, Sergey V, Ait-Si-Ali, Slimane
Publicado 2022

Current recommendations for clinical surveillance and genetic testing in rhabdoid tumor predisposition: a report from the SIOPE Host Genome Working Group

por Frühwald, M. C., Nemes, K., Boztug, H., Cornips, M. C. A., Evans, D. G., Farah, R., Glentis, S., Jorgensen, M., Katsibardi, K., Hirsch, S., Jahnukainen, K., Kventsel, I., Kerl, K., Kratz, C. P., Pajtler, K. W., Kordes, U., Ridola, V., Stutz, E., Bourdeaut, F.
Publicado 2021

Identifying novel regulatory effects for clinically relevant genes through the study of the Greek population

por Rouskas, Konstantinos, Katsareli, Efthymia A., Amerikanou, Charalampia, Dimopoulos, Alexandros C., Glentis, Stavros, Kalantzi, Alexandra, Skoulakis, Anargyros, Panousis, Nikolaos, Ongen, Halit, Bielser, Deborah, Planchon, Alexandra, Romano, Luciana, Harokopos, Vaggelis, Reczko, Martin, Moulos, Panagiotis, Griniatsos, Ioannis, Diamantis, Theodoros, Dermitzakis, Emmanouil T., Ragoussis, Jiannis, Dedoussis, George, Dimas, Antigone S.
Publicado 2023

Rare variant enrichment analysis supports GREB1L as a contributory driver gene in the etiology of Mayer-Rokitansky-Küster-Hauser syndrome

por Jolly, Angad, Du, Haowei, Borel, Christelle, Chen, Na, Zhao, Sen, Grochowski, Christopher M., Duan, Ruizhi, Fatih, Jawid M., Dawood, Moez, Salvi, Sejal, Jhangiani, Shalini N., Muzny, Donna M., Koch, André, Rouskas, Konstantinos, Glentis, Stavros, Deligeoroglou, Efthymios, Bacopoulou, Flora, Wise, Carol A., Dietrich, Jennifer E., Van den Veyver, Ignatia B., Dimas, Antigone S., Brucker, Sara, Sutton, V. Reid, Gibbs, Richard A., Antonarakis, Stylianos E., Wu, Nan, Coban-Akdemir, Zeynep H., Zhu, Lan, Posey, Jennifer E., Lupski, James R.
Publicado 2023