Literatura científica selecionada sobre o tema "BEACH-domain containing protein"
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Artigos de revistas sobre o assunto "BEACH-domain containing protein"
Liu, Xuezhao, Yang Li, Xin Wang, Ruxiao Xing, Kai Liu, Qiwen Gan, Changyong Tang et al. "The BEACH-containing protein WDR81 coordinates p62 and LC3C to promote aggrephagy". Journal of Cell Biology 216, n.º 5 (12 de abril de 2017): 1301–20. http://dx.doi.org/10.1083/jcb.201608039.
Texto completo da fonteTheisen, Derek J., Jesse T. Davidson, Carlos G. Briseño, Marco Gargaro, Elvin J. Lauron, Qiuling Wang, Pritesh Desai et al. "WDFY4 is required for cross-presentation in response to viral and tumor antigens". Science 362, n.º 6415 (8 de novembro de 2018): 694–99. http://dx.doi.org/10.1126/science.aat5030.
Texto completo da fonteAarts, Cathelijn E. M., Kate Downes, Arie J. Hoogendijk, Evelien G. G. Sprenkeler, Roel P. Gazendam, Rémi Favier, Marie Favier et al. "Neutrophil specific granule and NETosis defects in gray platelet syndrome". Blood Advances 5, n.º 2 (25 de janeiro de 2021): 549–64. http://dx.doi.org/10.1182/bloodadvances.2020002442.
Texto completo da fonteKahr, Walter H. "Molecular Triggers of Granule Formation in Megakaryocytes and Platelets". Blood 120, n.º 21 (16 de novembro de 2012): SCI—34—SCI—34. http://dx.doi.org/10.1182/blood.v120.21.sci-34.sci-34.
Texto completo da fonteSpitzer, S. G., B. J. Warn-Cramer, C. K. Kasper e S. P. Bajaj. "Replacement of isoleucine-397 by threonine in the clotting proteinase factor IXa (Los Angeles and Long Beach variants) affects macromolecular catalysis but not l-tosylarginine methyl ester hydrolysis. Lack of correlation between the ox brain prothrombin time and the mutation site in the variant proteins". Biochemical Journal 265, n.º 1 (1 de janeiro de 1990): 219–25. http://dx.doi.org/10.1042/bj2650219.
Texto completo da fonteCullinane, Andrew R., Alejandro A. Schäffer e Marjan Huizing. "The BEACH Is Hot: A LYST of Emerging Roles for BEACH-Domain Containing Proteins in Human Disease". Traffic 14, n.º 7 (24 de abril de 2013): 749–66. http://dx.doi.org/10.1111/tra.12069.
Texto completo da fonteLyu, Xia, Janine A. Lamb e Hector Chinoy. "The clinical relevance of WDFY4 in autoimmune diseases in diverse ancestral populations". Rheumatology, 20 de março de 2024. http://dx.doi.org/10.1093/rheumatology/keae183.
Texto completo da fonteWegner, Philine, Julia Drube, Lisa Ziegler, Birgit Strotmann, Raphaela Marquardt, Claudia Küchler, Marco Groth, Bernhard Nieswandt, Nico Andreas e Sebastian Drube. "The Neurobeachin‐like 2 protein (NBEAL2) controls the homeostatic level of the ribosomal protein RPS6 in mast cells". Immunology, 25 de janeiro de 2024. http://dx.doi.org/10.1111/imm.13756.
Texto completo da fonteCole, Eric S., Wolfgang Maier, Ewa Joachimiak, Yu-yang Jiang, Chinkyu Lee, Erik Collet, Carl Chmelik et al. "The Tetrahymena bcd1 mutant implicates endosome trafficking in ciliate, cortical pattern formation". Molecular Biology of the Cell, 10 de maio de 2023. http://dx.doi.org/10.1091/mbc.e22-11-0501.
Texto completo da fonteMuellerleile, Julia, Aline Blistein, Astrid Rohlmann, Frederieke Scheiwe, Markus Missler, Stephan W. Schwarzacher e Peter Jedlicka. "Enhanced LTP of population spikes in the dentate gyrus of mice haploinsufficient for neurobeachin". Scientific Reports 10, n.º 1 (29 de setembro de 2020). http://dx.doi.org/10.1038/s41598-020-72925-4.
Texto completo da fonteTeses / dissertações sobre o assunto "BEACH-domain containing protein"
Koebke, Eva [Verfasser], Martin [Gutachter] Hülskamp e Ute [Gutachter] Höcker. "The BEACH domain containing protein SPIRRIG in an interplay with TZF proteins and the characterization of SPIRRIG in M. polymorpha / Eva Koebke ; Gutachter: Martin Hülskamp, Ute Höcker". Köln : Universitäts- und Stadtbibliothek Köln, 2020. http://d-nb.info/122807187X/34.
Texto completo da fonteDelage, Laure. "Des déficiences génétiques comme modèles naturels pour l'étude de la régulation des checkpoints immunitaires et la caractérisation des réponses auto-immunes". Electronic Thesis or Diss., Université Paris Cité, 2021. http://www.theses.fr/2021UNIP5190.
Texto completo da fonteRecessive NBEAL2 mutations have been reported in patients with Gray Platelet Syndrome (GPS). This syndrome is characterized by a macro-thrombocytopenia, with platelets lacking alpha-granules, leading to bleeding disorders, often associated with splenomegaly. Thus, NBEAL2 plays a crucial role in the trafficking of alpha-granules in platelets. Moreover, our lab has also described NBEAL2 deficiencies in patients presenting clinical features of the autoimmune lymphoproliferative syndrome, suggesting a role of NBEAL2 in immune homeostasis and tolerance. A broader international cohort of GPS patients has been described, revealing immune system abnormalities (autoimmune diseases, autoantibodies, lymphopenia). If the role of NBEAL2 in the traffic of granules is often investigated, the exact mechanism leading to the development of autoimmune manifestations in GPS patients remains unknown. NBEAL2 belongs to a protein family involved in vesicular trafficking, all of which possess a conserved BEACH domain. Within this BEACH-domain containing proteins family, one of the closest members to NBEAL2 is LRBA. LRBA is involved in the recycling of CTLA-4, an inhibitory immune checkpoint. CTLA-4 plays a crucial role in the regulation of immune responses and tolerance. Recessive mutations of LRBA lead to similar clinical features as partial CTLA-4 deficiency: autoimmunity, lymphocytic infiltrations, and progressive B lymphopenia. Physiologically, LRBA prevents the lysosomal degradation of CTLA-4 and allows its recycling to the membrane. By analogy with LRBA, we investigated the importance of NBEAL2 in immune checkpoints intracellular trafficking and we brought new insights on its role in lymphocytes. Thus, NBEAL2 is a scaffold protein, binding LRBA, and involved in CTLA-4 trafficking as well as in vesicular trafficking in general. This work brings new knowledge to the regulation of CTLA-4 in activated T lymphocytes, a list of new partners for NBEAL2 protein and a new model of vesicular trafficking in which NBEAL2 is involved. Finally, a better understanding of the mechanisms leading to autoimmunity in patients with gray platelets syndrome could lead to better diagnosis and treatment management