28 results on '"Glentis, Stavros"'
Search Results
2. Use of HSC-targeted LNP to generate a mouse model of lethal α-thalassemia and treatment via lentiviral gene therapy
3. Identifying novel regulatory effects for clinically relevant genes through the study of the Greek population
4. Rare variant enrichment analysis supports GREB1L as a contributory driver gene in the etiology of Mayer-Rokitansky-Küster-Hauser syndrome
5. Soft Tissue Undifferentiated Sarcoma Carrying a Novel Onecut1::Nutm1 Fusion.
6. A method to comprehensively identify germline SNVs, INDELs and CNVs from whole exome sequencing data of BRCA1/2 negative breast cancer patients
7. The Diverse Genomic Landscape of Diamond–Blackfan Anemia: Two Novel Variants and a Mini-Review
8. A Novel Variant in the TP53 Gene Causing Li–Fraumeni Syndrome
9. Periodic veganism in healthy individuals improves blood lipids, reduces low-grade inflammation, but impairs bone health: the FastBio study
10. Identifying novel regulatory effects for clinically relevant genes through the study of the Greek population
11. Ischemic stroke in a pediatric patient with very rare coexistence of sickle‐cell/β‐thalassemia and neurofibromatosis type 1
12. High Incidence of Clonal Hematopoiesis in Transfusion-Dependent Thalassemia Patients
13. Lnp-Targeting Hematopoietic Stem Cells and Lentiviral Gene Transfer to Generate and Rescue a Novel Mouse Model of Lethal Alpha-Thalassemia
14. PATH-13. Methylation analysis in the diagnosis of pediatric CNS tumors; a single center experience
15. Perturbations of genes essential for Müllerian duct and Wölffian duct development in Mayer-Rokitansky-Küster-Hauser syndrome
16. A Severe Mouse Model of Alpha-Thalassemia to Study Abnormal Iron Metabolism and Erythropoiesis, Hematopoietic Stem Cell Behavior and Development of a Gene Therapy Approach for Its Treatment
17. Prevalence of BRCA1 mutations among 403 women with triple-negative breast cancer: implications for genetic screening selection criteria: a Hellenic Cooperative Oncology Group Study
18. A Novel Variant of the CYCS Gene Alters Apoptosis of Megakaryocytes in a Family with Thrombocytopenia
19. Perturbations of genes essential for Müllerian duct and Wölffian duct development in Mayer-Rokitansky-Küster-Hauser syndrome
20. Children Diagnosed with Acute Leukemia of Ambiguous Lineage (ALAL) Benefit from Acute Myeloid Leukemia (AML) Treatment Protocols: A Retrospective Analysis from a Single Center
21. Surveillance recommendations for DICER1 pathogenic variant carriers: a report from the SIOPE Host Genome Working Group and CanGene-CanVar Clinical Guideline Working Group.
22. Exome Sequencing in BRCA1- and BRCA2-Negative Greek Families Identifies MDM1 and NBEAL1 as Candidate Risk Genes for Hereditary Breast Cancer
23. Congenital extracranial extrarenal rhabdoid tumor: A rare clinicopathologic entity and diagnostic challenge
24. P798: DIAMOND BLACKFAN ANEMIA MAY ESCAPE DIAGNOSIS UP TO ADULTHOOD; A REPORT FROM THE UPDATED GREEK REGISTRY.
25. A Novel Variant of the CYCSGene Alters Apoptosis of Megakaryocytes in a Family with Thrombocytopenia
26. Molecular comparison of single cell MDA products derived from different cell types
27. Women’s Perception of Information and Experiences of Nuchal Translucency Screening in Greece
28. Chemotherapy-free approach with arsenic trioxide and <italic>all-trans</italic> retinoic acid in children with acute promyelocytic leukemia.
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