Letteratura scientifica selezionata sul tema "Gray platelet syndrome"
Cita una fonte nei formati APA, MLA, Chicago, Harvard e in molti altri stili
Consulta la lista di attuali articoli, libri, tesi, atti di convegni e altre fonti scientifiche attinenti al tema "Gray platelet syndrome".
Accanto a ogni fonte nell'elenco di riferimenti c'è un pulsante "Aggiungi alla bibliografia". Premilo e genereremo automaticamente la citazione bibliografica dell'opera scelta nello stile citazionale di cui hai bisogno: APA, MLA, Harvard, Chicago, Vancouver ecc.
Puoi anche scaricare il testo completo della pubblicazione scientifica nel formato .pdf e leggere online l'abstract (il sommario) dell'opera se è presente nei metadati.
Articoli di riviste sul tema "Gray platelet syndrome":
Wills, E. J. "Gray Platelet Syndrome". Ultrastructural Pathology 13, n. 4 (gennaio 1989): 451–55. http://dx.doi.org/10.3109/01913128909048495.
Michelson, Alan D. "Gray platelet syndrome". Blood 121, n. 2 (10 gennaio 2013): 250. http://dx.doi.org/10.1182/blood-2012-09-455550.
Bain, Barbara J., e Manju Bhavnani. "Gray platelet syndrome". American Journal of Hematology 86, n. 12 (28 luglio 2011): 1027. http://dx.doi.org/10.1002/ajh.22055.
Rosa, Jean-Philippe. "The gray platelet syndrome". Sang thrombose vaisseaux 26, n. 5 (settembre 2014): 240–54. http://dx.doi.org/10.1684/stv.2014.0854.
Rosa, Jean-Philippe. "The gray platelet syndrome". Hématologie 19, n. 2 (marzo 2013): 123–35. http://dx.doi.org/10.1684/hma.2013.0793.
Baruch, Dominique, Theo Lindhout, Evelyne Dupuy e Jacques P. Caen. "Thrombin-Induced Platelet Factor Va Formation in Patients with a Gray Platelet Syndrome". Thrombosis and Haemostasis 58, n. 02 (1987): 768–71. http://dx.doi.org/10.1055/s-0038-1645967.
Tubman, Venée N., Jason E. Levine, Dean R. Campagna, Rita Monahan-Earley, Ann M. Dvorak, Ellis J. Neufeld e Mark D. Fleming. "X-linked gray platelet syndrome due to a GATA1 Arg216Gln mutation". Blood 109, n. 8 (5 gennaio 2007): 3297–99. http://dx.doi.org/10.1182/blood-2006-02-004101.
Köhler, Michael. "Treatment of Gray Platelet Syndrome". Thrombosis and Haemostasis 60, n. 01 (1988): 123. http://dx.doi.org/10.1055/s-0038-1647649.
Nurden, Paquita, Martine Jandrot-Perrus, Robert Combrié, Joelle Winckler, Veronique Arocas, Christelle Lecut, Jean-Max Pasquet, Thomas J. Kunicki e Alan T. Nurden. "Severe deficiency of glycoprotein VI in a patient with gray platelet syndrome". Blood 104, n. 1 (1 luglio 2004): 107–14. http://dx.doi.org/10.1182/blood-2003-11-3842.
Rao, A. Koneti, e Deepak A. Rao. "Gray platelet syndrome: immunity goes awry". Blood 136, n. 17 (22 ottobre 2020): 1898–900. http://dx.doi.org/10.1182/blood.2020008196.
Tesi sul tema "Gray platelet syndrome":
Delage, 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.
Recessive 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
Capitoli di libri sul tema "Gray platelet syndrome":
Timson, David J., Richard J. Reece, James B. Thoden, Hazel M. Holden, Andrea L. Utz, Beverly M. K. Biller, Eugen-Matthias Strehle et al. "Gray Platelet Syndrome". In Encyclopedia of Molecular Mechanisms of Disease, 758–59. Berlin, Heidelberg: Springer Berlin Heidelberg, 2009. http://dx.doi.org/10.1007/978-3-540-29676-8_735.
Shahraki, Hojat, Akbar Dorgalaleh e Barbara J. Bain. "Gray Platelet Syndrome (GPS)". In Congenital Bleeding Disorders, 379–96. Cham: Springer International Publishing, 2018. http://dx.doi.org/10.1007/978-3-319-76723-9_16.
Kianinodeh, Fatemeh, Maryam Sadat Hosseini e Barbara J. Bain. "Gray Platelet Syndrome: Diagnosis and Management". In Congenital Bleeding Disorders, 445–63. Cham: Springer International Publishing, 2023. http://dx.doi.org/10.1007/978-3-031-43156-2_17.
Vagts, Dierk A., Heike Kaltofen, Uta Emmig e Peter Biro. "Grey-Platelet-Syndrom (UK)/Gray-Platelet-Syndrom (USA)". In Anästhesie bei seltenen Erkrankungen, 1–2. Berlin, Heidelberg: Springer Berlin Heidelberg, 2018. http://dx.doi.org/10.1007/978-3-662-44368-2_108-1.
Köhler, M. "Grey-platelet-Syndrom: Pathophysiologie, Klinik, Diagnostik und Therapie". In Hämostaseologie, 67–71. Berlin, Heidelberg: Springer Berlin Heidelberg, 1999. http://dx.doi.org/10.1007/978-3-662-07673-6_9.
"Gray Platelet Syndrome". In Diagnostic Pathology: Blood and Bone Marrow, 322–25. Elsevier, 2018. http://dx.doi.org/10.1016/b978-0-323-39254-9.50068-4.
Pozdnyakova, Olga. "Gray Platelet Syndrome". In Hematopathology, 37–38. Elsevier, 2013. http://dx.doi.org/10.1016/b978-1-4377-1758-7.00016-6.
Atti di convegni sul tema "Gray platelet syndrome":
Levy-Toledano, S., J. Enouf, M. Lebret, R. Bredoux e J. P. Caen. "ABNORMAL CALCIUM TRANSPORT INTO MICROSOMES OF GRAY PLATELET SYNDROME". In XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1644747.
Mori, K., S. Suzuki, K. Sugai, Y. Akutsu, M. Ishikawa, H. Sakai e K. Hiwatashi. "INTRACELLULAR CA++ MOBILIZATION IN GRAY PLATELET SYNDROME. ELECTRONMICROSCOPIC STUDIES ON AEQUORIN LOADED PLATELETS". In XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1644558.
FACON, T., J. GOUPEMAND, C. CARON, M. ZANDECKI, M. H. ESTIENNE e A. COSSON. "GRAY PLATELET SYNDROME AND IDIOPATHIC PULMONARY FIBROSIS OCCURRING IN THE SAME PATIENT : A FORTUITOUS ASSOCIATION?" In XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1644559.
Legrand, C., V. Dubernard, N. Kieffer e A. T. Nurden. "USE OF A MONOCLONAL ANTIBODY TO MEASURE THE SURFACE EXPRESSION OF THROMBOSPONDIN FOLLOWING PLATELET ACTIVATION". In XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1643821.
Patscheke, H., e G. Mathieu. "MONITORING OF THE PLATELET ALPHA-GRANULE SECRETION IN THE AGGREGOMETER." In XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1643492.
Forestier, F., F. Daffos, C. Kaplan e P. Champeix. "PRENATAL DIAGNOSIS OF HEMORRHAGIC DISORDERS". In XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1644270.
Wautier, J. L., Y. Gruel, B. Boizard, J. P. Caen, F. Daffos e F. Forestier. "ANTENATAL DIAGNOSIS OF THROMBOPATHY". In XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1644271.
Cockbill, S. R., S. Heptinstall e H. B. Burmester. "A PLASMA FACTOR FROM A PATIENT WITH A BLEEDING TENDENCY CAUSES PLATELET SECRETION IN THE ABSENCE OF EXTRACELLULAR CALCIUM". In XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1643489.
Rendu, F., T. Hovig, P. Marche, M. Lebret, D. Tenza, J. Maclouf, J. P. Caen e S. Levy-Toledano. "MEMBRANE SIGNAL TRANSDUCTION IN PLATELETS WITH ALTERED RELEASE REACTION". In XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1644746.