Zobrazeno 1 - 10
of 128
pro vyhledávání: '"Chromosome 11q"'
Publikováno v:
BMC Cancer, Vol 24, Iss 1, Pp 1-12 (2024)
Abstract Background Neuroblastoma exhibits substantial heterogeneity, which is intricately linked to various genetic alterations. We aimed to explore immune status in the peripheral blood and prognosis of patients with neuroblastoma with different ge
Externí odkaz:
https://doaj.org/article/a04455106ee2470ab51cef5d7730c505
Autor:
George Mason, Rhian Aghajani, Brieanna Dance, Jad Othman, Linda Goodwin, William Stevenson, Naomi Mackinlay
Publikováno v:
eJHaem, Vol 5, Iss 2, Pp 397-402 (2024)
Abstract Casitas B‐cell lineage (CBL) syndrome is a rare RASopathy known to predispose to CBL‐mutated juvenile myelomonocytic leukemia (JMML) in childhood. Adulthood acute myeloid leukemia arising out of a genetic aberrancies consistent with prio
Externí odkaz:
https://doaj.org/article/be6894524438416b854e6584a15e142c
Akademický článek
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Autor:
Kaylee M. Keller, Thomas F. Eleveld, Linda Schild, Kim van den Handel, Marlinde van den Boogaard, Vicky Amo-Addae, Selma Eising, Kimberley Ober, Bianca Koopmans, Leendert Looijenga, Godelieve A.M. Tytgat, Bauke Ylstra, Jan J. Molenaar, M. Emmy M. Dolman, Sander R. van Hooff
Publikováno v:
Frontiers in Oncology, Vol 12 (2022)
Neuroblastoma is the most common extracranial solid tumor found in children and despite intense multi-modal therapeutic approaches, low overall survival rates of high-risk patients persist. Tumors with heterozygous loss of chromosome 11q and MYCN amp
Externí odkaz:
https://doaj.org/article/2046bd60d71d42bd8c11809b13f2595a
Autor:
Chih-Ping Chen, Liang-Kai Wang, Pei-Chen Wu, Tung-Yao Chang, Schu-Rern Chern, Peih-Shan Wu, Yen-Ni Chen, Shin-Wen Chen, Chen-Chi Lee, Chien-Wen Yang, Wayseen Wang
Publikováno v:
Taiwanese Journal of Obstetrics & Gynecology, Vol 56, Iss 1, Pp 102-105 (2017)
Objective: We present molecular cytogenetic characterization of Jacobsen syndrome (11q23.3-q25 deletion) in a fetus associated with double outlet right ventricle (DORV), hypoplastic left heart syndrome (HLHS), and ductus venosus (DV) agenesis on pren
Externí odkaz:
https://doaj.org/article/291a17a5ef6540e7a58513bb248bcf5d
Autor:
Keller, Kaylee M., Eleveld, Thomas F., Schild, Linda, van den Handel, Kim, van den Boogaard, Marlinde, Amo-Addae, Vicky, Eising, Selma, Ober, Kimberley, Koopmans, Bianca, Looijenga, Leendert, Tytgat, Godelieve A.M., Ylstra, Bauke, Molenaar, Jan J., Dolman, M. Emmy M., van Hooff, Sander R., Afd Pharmaceutics, Pharmaceutics
Publikováno v:
Frontiers in Oncology, 12, 1. Frontiers Media S.A.
Frontiers in Oncology, 12:929123. Frontiers Media S.A.
Frontiers in oncology, 12:929123. Frontiers Media S.A.
Keller, K M, Eleveld, T F, Schild, L, van den Handel, K, van den Boogaard, M, Amo-Addae, V, Eising, S, Ober, K, Koopmans, B, Looijenga, L, Tytgat, G A M, Ylstra, B, Molenaar, J J, Dolman, M E M & van Hooff, S R 2022, ' Chromosome 11q loss and MYCN amplification demonstrate synthetic lethality with checkpoint kinase 1 inhibition in neuroblastoma ', Frontiers in Oncology, vol. 12, 929123 . https://doi.org/10.3389/fonc.2022.929123
Frontiers in Oncology, 12:929123. Frontiers Media S.A.
Frontiers in oncology, 12:929123. Frontiers Media S.A.
Keller, K M, Eleveld, T F, Schild, L, van den Handel, K, van den Boogaard, M, Amo-Addae, V, Eising, S, Ober, K, Koopmans, B, Looijenga, L, Tytgat, G A M, Ylstra, B, Molenaar, J J, Dolman, M E M & van Hooff, S R 2022, ' Chromosome 11q loss and MYCN amplification demonstrate synthetic lethality with checkpoint kinase 1 inhibition in neuroblastoma ', Frontiers in Oncology, vol. 12, 929123 . https://doi.org/10.3389/fonc.2022.929123
Neuroblastoma is the most common extracranial solid tumor found in children and despite intense multi-modal therapeutic approaches, low overall survival rates of high-risk patients persist. Tumors with heterozygous loss of chromosome 11q and MYCN amp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::329aea7d7c7654768bccaddc20ad5c25
https://dspace.library.uu.nl/handle/1874/425877
https://dspace.library.uu.nl/handle/1874/425877
Autor:
Elise J. Huisman, A. Rick Brooimans, Samone Mayer, Marieke Joosten, Louis de Bont, Mariëlle Dekker, Elisabeth L. M. Rammeloo, Frans J. Smiers, P. Martin van Hagen, C. Michel Zwaan, Masja de Haas, Marjon H. Cnossen, Virgil A. S. H. Dalm
Publikováno v:
Journal of Clinical Immunology, 42(7), 1521-1534. Springer New York
Journal of Clinical Immunology, 42(7), 1521-1534. SPRINGER/PLENUM PUBLISHERS
Journal of Clinical Immunology, 42(7), 1521-1534. SPRINGER/PLENUM PUBLISHERS
Disorders of the long arm of chromosome 11 (11q) are rare and involve various chromosomal regions. Patients with 11q disorders, including Jacobsen syndrome, often present with a susceptibility for bacterial and prolonged viral and fungal infections p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2ca718bf5f5e533186a2221bd954adec
https://hdl.handle.net/1887/3565001
https://hdl.handle.net/1887/3565001
Akademický článek
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Autor:
Au‐Yeung, Rex K. H., Arias Padilla, Laura, Zimmermann, Martin, Oschlies, Ilske, Siebert, Reiner, Woessmann, Wilhelm, Burkhardt, Birgit, Klapper, Wolfram
Summary Large B‐cell lymphoma with IRF4 rearrangement, and Burkitt‐like lymphoma with 11q aberration are two provisional lymphoma entities in the 2017 revision of the WHO classification of lymphoid neoplasms. Despite being more frequent in young
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::69f97f64f9744e920eede0f8ff18aacf
Akademický článek
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