Showing 1 - 7 results of 7 for search 'S Glentis', query time: 0.05s
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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 by M Chappell, L Breda, A Guerra, V Ghiaccio, M Fedorky, D Jarocha, K Gollomp, N Teawtrakul, S Glentis, A Kattamis, S Rivella
Published 2022-01-01
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The Diverse Genomic Landscape of Diamond–Blackfan Anemia: Two Novel Variants and a Mini-Review by Iordanis Pelagiadis, Ioannis Kyriakidis, Nikolaos Katzilakis, Chrysoula Kosmeri, Danai Veltra, Christalena Sofocleous, Stavros Glentis, Antonis Kattamis, Alexandros Makis, Eftichia Stiakaki
Published 2023-11-01
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3
A Novel Variant in the <i>TP53</i> Gene Causing Li–Fraumeni Syndrome by Dimitrios T. Papadimitriou, Constantine A. Stratakis, Antonis Kattamis, Stavros Glentis, Constantine Dimitrakakis, George P. Spyridis, Panagiotis Christopoulos, George Mastorakos, Nikolaos F. Vlahos, Nicoletta Iacovidou
Published 2023-06-01
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4
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 by S. Rivella, M. Chappell, D. Jarocha, L. Breda, V. Ghiaccio, M. Fedorky, M. Triebwasser, A. Guerra, K. Gollomp, N. Teawtrakul, S. Glentis, A. Kattamis, O. Abdulmalik
Published 2022-06-01
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P798: DIAMOND BLACKFAN ANEMIA MAY ESCAPE DIAGNOSIS UP TO ADULTHOOD; A REPORT FROM THE UPDATED GREEK REGISTRY by Polyxeni Delaporta, Christalena Sofocleous, Stavros Glentis, Danai Veltra, Sophia Polychronopoulou, Lydia Kossiva, Alexandros Makis, Marina Economou, Nikolaos Katzilakis, Eftychia Steiakaki, Theodoros Marinakis, Stavroula Kostaridou, Antonis Kattamis
Published 2023-08-01
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Identifying novel regulatory effects for clinically relevant genes through the study of the Greek population by Konstantinos Rouskas, Efthymia A. Katsareli, Charalampia Amerikanou, Alexandros C. Dimopoulos, Stavros Glentis, Alexandra Kalantzi, Anargyros Skoulakis, Nikolaos Panousis, Halit Ongen, Deborah Bielser, Alexandra Planchon, Luciana Romano, Vaggelis Harokopos, Martin Reczko, Panagiotis Moulos, Ioannis Griniatsos, Theodoros Diamantis, Emmanouil T. Dermitzakis, Jiannis Ragoussis, George Dedoussis, Antigone S. Dimas
Published 2023-08-01
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Rare variant enrichment analysis supports GREB1L as a contributory driver gene in the etiology of Mayer-Rokitansky-Küster-Hauser syndrome by Angad Jolly, Haowei Du, Christelle Borel, Na Chen, Sen Zhao, Christopher M. Grochowski, Ruizhi Duan, Jawid M. Fatih, Moez Dawood, Sejal Salvi, Shalini N. Jhangiani, Donna M. Muzny, André Koch, Konstantinos Rouskas, Stavros Glentis, Efthymios Deligeoroglou, Flora Bacopoulou, Carol A. Wise, Jennifer E. Dietrich, Ignatia B. Van den Veyver, Antigone S. Dimas, Sara Brucker, V. Reid Sutton, Richard A. Gibbs, Stylianos E. Antonarakis, Nan Wu, Zeynep H. Coban-Akdemir, Lan Zhu, Jennifer E. Posey, James R. Lupski
Published 2023-07-01
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