Gotowa bibliografia na temat „Diffuse midline glioma (DMG)”
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Artykuły w czasopismach na temat "Diffuse midline glioma (DMG)"
Barron, Tara, Belgin Yalçın, Aaron Mochizuki, Evan Cantor, Kiarash Shamardani, Dana Tlais, Andrea Franson i in. "CNSC-01. GABAERGIC NEURON-TO-GLIOMA SYNAPSES IN DIFFUSE MIDLINE GLIOMAS". Neuro-Oncology 25, Supplement_1 (1.06.2023): i11. http://dx.doi.org/10.1093/neuonc/noad073.044.
Pełny tekst źródłaAl Sharie, Sarah, Dima Abu Laban, Jamil Nazzal, Shahad Iqneibi, Sura Ghnaimat, Abdallah Al-Ani i Maysa Al-Hussaini. "Midline Gliomas: A Retrospective Study from a Cancer Center in the Middle East". Cancers 15, nr 18 (13.09.2023): 4545. http://dx.doi.org/10.3390/cancers15184545.
Pełny tekst źródłaIbdah, Haleem, Shervin Pejhan, Lee Ang, Cynthia Hawkins, Barbara Fisher, Joseph Megyesi i Maria MacDonald. "CEREBELLAR DIFFUSE MIDLINE GLIOMA, H3K27M ALTERED IN A FIFTY-FIVE-YEAR-OLD PATIENT". Neuro-Oncology Advances 5, Supplement_2 (1.07.2023): i6. http://dx.doi.org/10.1093/noajnl/vdad071.026.
Pełny tekst źródłaChoi, Seonah, In-Ho Jung, Jaejoon Lim, Ju Hyung Moon, Eui Hyun Kim, Se Hoon Kim, Seok-Gu Kang i Jong Hee Chang. "PATH-06. SURVIVAL ANALYSIS FOR ADULT MIDLINE GLIOMA: DO ADULT MIDLINE GLIOMAS WITH THE H3 K27M MUTATION REALLY HAVE POOR PROGNOSIS?" Neuro-Oncology 24, Supplement_7 (1.11.2022): vii150—vii151. http://dx.doi.org/10.1093/neuonc/noac209.579.
Pełny tekst źródłaNakatogawa, Hirokazu, Hiroshi Kawaji, Nobuhide Hayashi, Junya Fukai, Noriyuki Kijima, Tomoko Shofuda, Ema Yoshioka i in. "10184-BT-14 CLINICAL FEATURE OF HEMISPHERIC GLIOMA WITH H3F3A, PEDIATRIC-TYPE HIGH GRADE GLIOMA, H3 K27-ALTERED, NEC AND DIFFUSE HEMISPHERIC GLIOMA, H3 G34-MUTANT, CNS WHO GRADE 4". Neuro-Oncology Advances 5, Supplement_5 (1.12.2023): v18—v19. http://dx.doi.org/10.1093/noajnl/vdad141.074.
Pełny tekst źródłaMorscio, Julie, Sandra Jacobs i Frederik De Smet. "DIPG-55. DISSECTING THE ECOSYSTEM OF PEDIATRIC DIFFUSE MIDLINE GLIOMA". Neuro-Oncology 26, Supplement_4 (18.06.2024): 0. http://dx.doi.org/10.1093/neuonc/noae064.108.
Pełny tekst źródłaKnowles, Truman, Shejuan An, Tina Huang, Jin Qi i Amanda Saratsis. "DIPG-01. LIN28B EXPRESSION IN DIFFUSE MIDLINE GLIOMA". Neuro-Oncology 25, Supplement_1 (1.06.2023): i12. http://dx.doi.org/10.1093/neuonc/noad073.048.
Pełny tekst źródłaKnowles, Truman, Shejuan An, Tina Huang, Jin Qi i Amanda Saratsis. "CSIG-11. LIN28B EXPRESSION IN DIFFUSE MIDLINE GLIOMA". Neuro-Oncology 25, Supplement_5 (1.11.2023): v42. http://dx.doi.org/10.1093/neuonc/noad179.0167.
Pełny tekst źródłaKnowles, Truman, Shejuan An, Tina Huang, Jin Qi i Amanda Saratsis. "DIPG-02. LIN28B EXPRESSION IN DIFFUSE MIDLINE GLIOMA". Neuro-Oncology 26, Supplement_4 (18.06.2024): 0. http://dx.doi.org/10.1093/neuonc/noae064.056.
Pełny tekst źródłaLarsen, Alexandra Giantini, Maricruz Rivera, David Pisapia, Sameer Farouk Sait, Matthias Karajannis, Jeffrey Greenfield i Mark Souweidane. "DIPG-44. DIFFUSE MIDLINE GLIOMA WITH EXTRACRANIAL METASTASIS". Neuro-Oncology 25, Supplement_1 (1.06.2023): i23. http://dx.doi.org/10.1093/neuonc/noad073.091.
Pełny tekst źródłaRozprawy doktorskie na temat "Diffuse midline glioma (DMG)"
Rakotomalala-Andrianasolo, Andria. "Développement et caractérisation de modèles cellulaires pour l'étude du rôle de l'oncohistone H3.3 K27M dans le phénotype agressif et la réponse aux thérapies des gliomes pédiatriques diffus de la ligne médiane". Electronic Thesis or Diss., Université de Lille (2022-....), 2024. http://www.theses.fr/2024ULILS015.
Pełny tekst źródłaH3K27-altered DMG treatment is one of the most significant challenges in pediatric neuro-oncology,with no improvement in patient survival over the past 50 years. In 2012, it was shown that DMGs harbor a specific histone 3 mutation (oncohistone) called H3.3 K27M with a very high prevalence (70-80% of cases). Although theH3.3 K27M impact on the epigenetic landscape has been well described, studies are needed to understand betterits role in DMG cells’ aggressiveness and response to therapies.To study the H3.3 K27M mutation impact on DMG cell phenotypes precisely, we developed andcharacterized pediatric high-grade glioma isogenic cellular models induced and knock-out for the oncohistone.Using these models, we aimed to decipher the oncohistone impact on DMG cell biology and response to anticancertherapies, including radiation therapy, the only current standard of care for DMGs. Characterization of our H3.3 K27M-induced pediatric supratentorial glioma cell lines reveals that the oncohistone affects the response to ionizing radiations and specific targeted therapies in a cellular context-dependentway. Based on these results, we settled to characterize oncohistone biological impacts in a more relevant cellular context of DMG. In that sense, we established H3.3 K27M knock-out cellular models and characterized them regarding their parental DMG H3.3 K27M mutated cell lines. Through omic (transcriptomic and proteomic)and cell metabolism characterizations of these models, we notably showed the H3.3 K27M mutation impact on DMG cells’ lipid metabolism. In 3D spheroid models, this H3.3 K27M-induced lipid metabolism rewiring appeared conditioned by microenvironment factors still under investigation.On the other hand, a functional pharmacological screen identified H3.3 K27M-driven dependencies tospecific DNA repair pathways. In addition, ongoing radiobiological characterization of our models indicates anH3.3 K27M-associated radiosensitivity correlating with a decrease in DNA repair efficiency following ionizingradiations. Beyond this DNA repair impact, our pharmacological screen also revealed an H3.3 K27M-relatedsensitivity to cardiac glycoside drugs. This result makes sense with our transcriptomic data showing enrichmentin genes involved in cardiomyopathies and ion homeostasis among differentially expressed genes with theoncohistone. In this context, we began unraveling the molecular and biological processes underlying thisH3.3 K27M-driven effect.Finally, we used our isogenic cellular models to show that the H3.3 K27M oncohistone drives lipidmetabolism modifications. These metabolic changes could prime H3K27-altered DMG cells to specific regulatedcell death pathways (e.g., ferroptosis) and affect the response to certain therapies. Moreover, the H3.3 K27Mseems to drive specific sensitivities, notably to radiation therapy and cardiac glycoside drugs. Understanding the underlying molecular mechanisms governing these H3.3 K27M-associated Achille heels could highlight newinsights into the oncohistone role in DMG cells and provide rationales for developing new therapeutic strategies
Trisolini, Elena. "Targeted molecular characterization of adult midline and circumscribed gliomas for the identification of new potential targets for personalized therapy". Doctoral thesis, Università del Piemonte Orientale, 2020. http://hdl.handle.net/11579/114872.
Pełny tekst źródłaKsiążki na temat "Diffuse midline glioma (DMG)"
Kleihues, Paul, Elisabeth Rushing i Hiroko Ohgaki. The 2016 revision of the WHO classification of tumours of the central nervous system. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780199651870.003.0001.
Pełny tekst źródłaCzęści książek na temat "Diffuse midline glioma (DMG)"
Noureldine, Mohammad Hassan A., Nir Shimony i George I. Jallo. "Diffuse Midline Glioma – Diffuse Intrinsic Pontine Glioma". W Brainstem Tumors, 159–93. Cham: Springer International Publishing, 2020. http://dx.doi.org/10.1007/978-3-030-38774-7_8.
Pełny tekst źródłaLiu, Dongyou. "Chordoid Glioma, Angiocentric Glioma, and Diffuse Midline Glioma". W Tumors and Cancers, 31–36. Boca Raton : Taylor & Francis, 2018. | Series: Pocket guides to biomedical sciences | “A CRC title, part of the Taylor & Francis imprint, a member of the Taylor & Francis Group, the academic division of T&F Informa plc.”: CRC Press, 2017. http://dx.doi.org/10.1201/9781315120522-6.
Pełny tekst źródłaSait, Sameer Farouk, Morgan Freret i Matthias Karajannis. "Pediatric High-Grade Glioma". W Neuro-Oncology Compendium for the Boards and Clinical Practice, redaktorzy Maciej M. Mrugala, Na Tosha N. Gatson, Sylvia C. Kurz, Kathryn S. Nevel i Jennifer L. Clarke, 267—C18.P333. Oxford University PressNew York, 2023. http://dx.doi.org/10.1093/med/9780197573778.003.0018.
Pełny tekst źródłaCarabenciov, Ivan D., i Michael W. Ruff. "Progressive Bilateral Arm Pain, Gait Disturbance, Constipation, and Urinary Retention". W Mayo Clinic Cases in Neuroimmunology, redaktorzy Andrew McKeon, B. Mark Keegan i W. Oliver Tobin, 231–32. Oxford University Press, 2021. http://dx.doi.org/10.1093/med/9780197583425.003.0075.
Pełny tekst źródłaStreszczenia konferencji na temat "Diffuse midline glioma (DMG)"
Borsuk, Robyn, Lanlan Zhou, Rishi Lulla i Wafik El-Deiry. "Abstract 5407: Novel imipridone combination therapies targeting oncohistone H3K27M mutant diffuse midline glioma (DMG)". W Proceedings: AACR Annual Meeting 2020; April 27-28, 2020 and June 22-24, 2020; Philadelphia, PA. American Association for Cancer Research, 2020. http://dx.doi.org/10.1158/1538-7445.am2020-5407.
Pełny tekst źródłaMinns, Hanna, Oscar Padilla, Hong-Jian Wei, Robyn D. Gartrell, Andrea Webster-Carrion, Masih Tazhibi, Nicholas McQuillan i in. "53 Inducing immune response with FLASH and conventional radiation in diffuse midline glioma (DMG)". W SITC 38th Annual Meeting (SITC 2023) Abstracts. BMJ Publishing Group Ltd, 2023. http://dx.doi.org/10.1136/jitc-2023-sitc2023.0053.
Pełny tekst źródłaBorsuk, Robyn, Lanlan Zhou, Yiqun Zhang, Varun V. Prabhu, Joshua E. Allen, Nikos Tapinos, Rishi Lulla i Wafik S. El-Deiry. "Abstract 635: Response to novel imipridone combination therapies targeting H3K27M mutant diffuse midline glioma (DMG)". W Proceedings: AACR Annual Meeting 2021; April 10-15, 2021 and May 17-21, 2021; Philadelphia, PA. American Association for Cancer Research, 2021. http://dx.doi.org/10.1158/1538-7445.am2021-635.
Pełny tekst źródłaCheney, Allison R., Lauren M. Sanders, Lucas Seninge, Holly C. Beale, Ellen Towle Kephart, Jacob Pfeil, Katrina Learned i in. "Abstract B06: Candidate differentiation stall in epithelial mesenchymal transition in H3K27M diffuse midline glioma". W Abstracts: AACR Special Conference on the Advances in Pediatric Cancer Research; September 17-20, 2019; Montreal, QC, Canada. American Association for Cancer Research, 2020. http://dx.doi.org/10.1158/1538-7445.pedca19-b06.
Pełny tekst źródłaWeidert, Frances, Christina Von Roemeling, James McGuiness, Jonathan Chardon-Robles, Nagheme Thomas, Anna Devries, Sadeem Qdaisat i in. "1398 Immune responses and long-term survival with mRNA vaccine targeting diffuse midline glioma". W SITC 38th Annual Meeting (SITC 2023) Abstracts. BMJ Publishing Group Ltd, 2023. http://dx.doi.org/10.1136/jitc-2023-sitc2023.1398.
Pełny tekst źródłaMathes, Stephanie, Nicolas Gerber, Marion Rizo, Michael Grotzer, Ana Guerreiro-Stücklin, Javad Nazarian i Sabine Müller. "Clinical Research for Pediatric Patients Suffering from a Diffuse Midline Glioma: Limits, Challenges and Perspectives". W RExPO23. REPO4EU, 2023. http://dx.doi.org/10.58647/rexpo.23012.
Pełny tekst źródłaWernicke, Caroline M., Birgit Geoerger, Olaf Witt, Christof Kramm, Stefan Burdach i Irene Teichert von Luettichau. "Unusual Course of a Diffuse Midline Glioma Exhibits Upcoming Therapeutic Options through Novel Molecular Genetic Analyses". W Abstracts of the 45th Annual Meeting of the Society for Neuropediatrics. Georg Thieme Verlag KG, 2019. http://dx.doi.org/10.1055/s-0039-1698205.
Pełny tekst źródłaMartinez, Payton, Jane J. Song, Kang-Ho Song, Mark Borden, Genna Nault, Jenna Steiner, Natalie Serkova i in. "Enhancing Delivery and Efficacy of Panobinostat for Diffuse Midline Glioma through Focused Ultrasound-Mediated Blood-Brain Barrier Opening". W 2023 IEEE International Ultrasonics Symposium (IUS). IEEE, 2023. http://dx.doi.org/10.1109/ius51837.2023.10306559.
Pełny tekst źródłaMount, Christopher W., Robbie Majzner, Shree Sundaresh, Evan P. Arnold, Meena Kadapakkam, Samuel Haile, Louai Labanieh i in. "Abstract 958: Anti-GD2 chimeric antigen receptor T cells as a potent immunotherapy regimen in xenograft models of histone 3 K27M mutant diffuse midline glioma". W Proceedings: AACR Annual Meeting 2018; April 14-18, 2018; Chicago, IL. American Association for Cancer Research, 2018. http://dx.doi.org/10.1158/1538-7445.am2018-958.
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