Zeitschriftenartikel zum Thema „NBEAL2“
Geben Sie eine Quelle nach APA, MLA, Chicago, Harvard und anderen Zitierweisen an
Machen Sie sich mit Top-50 Zeitschriftenartikel für die Forschung zum Thema "NBEAL2" bekannt.
Neben jedem Werk im Literaturverzeichnis ist die Option "Zur Bibliographie hinzufügen" verfügbar. Nutzen Sie sie, wird Ihre bibliographische Angabe des gewählten Werkes nach der nötigen Zitierweise (APA, MLA, Harvard, Chicago, Vancouver usw.) automatisch gestaltet.
Sie können auch den vollen Text der wissenschaftlichen Publikation im PDF-Format herunterladen und eine Online-Annotation der Arbeit lesen, wenn die relevanten Parameter in den Metadaten verfügbar sind.
Sehen Sie die Zeitschriftenartikel für verschiedene Spezialgebieten durch und erstellen Sie Ihre Bibliographie auf korrekte Weise.
Noetzli, Leila, Natalie Smith, Gary Brodsky und Jorge Di Paola. „Expression Patterns Of NBEAL2 In Human Tissues and a Megakaryocytic Cell Line“. Blood 122, Nr. 21 (15.11.2013): 1075. http://dx.doi.org/10.1182/blood.v122.21.1075.1075.
Der volle Inhalt der QuelleLo, Richard W., Ling Li, Fred G. Pluthero, Richard Leung, Koji Eto und Walter H. A. Kahr. „The endoplasmic reticulum protein SEC22B interacts with NBEAL2 and is required for megakaryocyte α-granule biogenesis“. Blood 136, Nr. 6 (06.08.2020): 715–25. http://dx.doi.org/10.1182/blood.2019004276.
Der volle Inhalt der QuelleKahr, Walter H. A., Richard W. Lo, Ling Li, Fred G. Pluthero, Hilary Christensen, Ran Ni, Nima Vaezzadeh et al. „Abnormal megakaryocyte development and platelet function in Nbeal2−/− mice“. Blood 122, Nr. 19 (07.11.2013): 3349–58. http://dx.doi.org/10.1182/blood-2013-04-499491.
Der volle Inhalt der QuelleDarling, Thayer K., Michael P. Schenk, Chengjing C. Zhou, Franklin M. Maloba, Patrice N. Mimche, Jonathan M. Gibbins, Shawn M. Jobe und Tracey J. Lamb. „Platelet α-granules contribute to organ-specific pathologies in a mouse model of severe malaria“. Blood Advances 4, Nr. 1 (31.12.2019): 1–8. http://dx.doi.org/10.1182/bloodadvances.2019000773.
Der volle Inhalt der QuelleMayer, Louisa, Maria Jasztal, Mercedes Pardo, Salvadora Aguera de Haro, Janine Collins, Tadbir K. Bariana, Peter A. Smethurst et al. „Nbeal2 interacts with Dock7, Sec16a, and Vac14“. Blood 131, Nr. 9 (01.03.2018): 1000–1011. http://dx.doi.org/10.1182/blood-2017-08-800359.
Der volle Inhalt der QuelleAarts, 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, Nr. 2 (25.01.2021): 549–64. http://dx.doi.org/10.1182/bloodadvances.2020002442.
Der volle Inhalt der QuelleTang, Yuling, Hongping Wu, Caiyun Huo, Shumei Zou, Yanxin Hu und Hanchun Yang. „Transcriptomic Profiling of Mouse Mast Cells upon Pathogenic Avian H5N1 and Pandemic H1N1 Influenza a Virus Infection“. Viruses 14, Nr. 2 (29.01.2022): 292. http://dx.doi.org/10.3390/v14020292.
Der volle Inhalt der QuelleDi Paola, Jorge. „Novel Congenital Platelet Disorders“. Blood 128, Nr. 22 (02.12.2016): SCI—39—SCI—39. http://dx.doi.org/10.1182/blood.v128.22.sci-39.sci-39.
Der volle Inhalt der QuelleKim, Dongjune A., Katrina J. Ashworth, Jorge Di Paola und David N. Ku. „Platelet α-granules are required for occlusive high-shear-rate thrombosis“. Blood Advances 4, Nr. 14 (22.07.2020): 3258–67. http://dx.doi.org/10.1182/bloodadvances.2020002117.
Der volle Inhalt der QuelleGuerrero, Jose A., Cavan Bennett, Louise van der Weyden, Harriet McKinney, Melody Chin, Paquita Nurden, Zoe McIntyre et al. „Gray platelet syndrome: proinflammatory megakaryocytes and α-granule loss cause myelofibrosis and confer metastasis resistance in mice“. Blood 124, Nr. 24 (04.12.2014): 3624–35. http://dx.doi.org/10.1182/blood-2014-04-566760.
Der volle Inhalt der QuelleSims, Matthew C., Louisa Mayer, Janine H. Collins, Tadbir K. Bariana, Karyn Megy, Cecile Lavenu-Bombled, Denis Seyres et al. „Novel manifestations of immune dysregulation and granule defects in gray platelet syndrome“. Blood 136, Nr. 17 (22.10.2020): 1956–67. http://dx.doi.org/10.1182/blood.2019004776.
Der volle Inhalt der QuelleShinde, Vishal, Nara Sobreira, Elizabeth S. Wohler, George Maiti, Nan Hu, Giuliana Silvestri, Sonia George et al. „Pathogenic alleles in microtubule, secretory granule and extracellular matrix-related genes in familial keratoconus“. Human Molecular Genetics 30, Nr. 8 (17.03.2021): 658–71. http://dx.doi.org/10.1093/hmg/ddab075.
Der volle Inhalt der QuelleReed, Jenna, Margot Deckers, Philippe Van den Steen, Aaron Petrey, Brian D. Evavold und Tracey Lamb. „Deciphering the role of platelet alpha granules in alveolar-capillary breakdown in severe malaria“. Journal of Immunology 210, Nr. 1_Supplement (01.05.2023): 241.13. http://dx.doi.org/10.4049/jimmunol.210.supp.241.13.
Der volle Inhalt der QuelleBottega, Roberta, Elena Nicchia, Caterina Alfano, Ana C. Glembotsky, Annalisa Pastore, Debora Bertaggia-Calderara, Bettina Bisig et al. „Gray platelet syndrome: Novel mutations of the NBEAL2 gene“. American Journal of Hematology 92, Nr. 2 (17.01.2017): E20—E22. http://dx.doi.org/10.1002/ajh.24610.
Der volle Inhalt der QuellePluthero, Fred G., Jorge Di Paola, Manuel D. Carcao und Walter H. A. Kahr. „NBEAL2 mutations and bleeding in patients with gray platelet syndrome“. Platelets 29, Nr. 6 (05.06.2018): 632–35. http://dx.doi.org/10.1080/09537104.2018.1478405.
Der volle Inhalt der QuelleNand, Sucha, Manuel O. Diaz, David E. Marinier, Mark A. Walshauser, Amy B. Rosenfeld, Laura C. Michaelis, Patrick J. Stiff und Xiaowu Gai. „Germ-Line and Somatic Mutations in Familial Myeloproliferative Neoplasms (MPNs). a Pilot Study“. Blood 124, Nr. 21 (06.12.2014): 3214. http://dx.doi.org/10.1182/blood.v124.21.3214.3214.
Der volle Inhalt der QuelleDeppermann, Carsten, Deya Cherpokova, Paquita Nurden, Jan-Niklas Schulz, Ina Thielmann, Peter Kraft, Timo Vögtle et al. „Gray platelet syndrome and defective thrombo-inflammation in Nbeal2-deficient mice“. Journal of Clinical Investigation 123, Nr. 8 (01.07.2013): 3331–42. http://dx.doi.org/10.1172/jci69210.
Der volle Inhalt der QuelleKahr, Walter HA, Jesse Hinckley, Ling Li, Hansjörg Schwertz, Hilary Christensen, Jesse W. Rowley, Fred G. Pluthero et al. „Mutations in NBEAL2, encoding a BEACH protein, cause gray platelet syndrome“. Nature Genetics 43, Nr. 8 (17.07.2011): 738–40. http://dx.doi.org/10.1038/ng.884.
Der volle Inhalt der QuelleWijgaerts, Anouck, Christine Wittevrongel, Chantal Thys, Timothy Devos, Kathelijne Peerlinck, Marloes R. Tijssen, Chris Van Geet und Kathleen Freson. „The transcription factor GATA1 regulates NBEAL2 expression through a long-distance enhancer“. Haematologica 102, Nr. 4 (12.01.2017): 695–706. http://dx.doi.org/10.3324/haematol.2016.152777.
Der volle Inhalt der QuelleSowerby, John M., David C. Thomas, Simon Clare, Marion Espéli, Jose A. Guerrero, Kim Hoenderdos, Katherine Harcourt et al. „NBEAL2 is required for neutrophil and NK cell function and pathogen defense“. Journal of Clinical Investigation 127, Nr. 9 (07.08.2017): 3521–26. http://dx.doi.org/10.1172/jci91684.
Der volle Inhalt der QuelleTomberg, Kärt, Rami Khoriaty, Randal J. Westrick, Heather E. Fairfield, Laura G. Reinholdt, Gary L. Brodsky, Pavel Davizon-Castillo, David Ginsburg und Jorge Di Paola. „Spontaneous 8bp Deletion in Nbeal2 Recapitulates the Gray Platelet Syndrome in Mice“. PLOS ONE 11, Nr. 3 (07.03.2016): e0150852. http://dx.doi.org/10.1371/journal.pone.0150852.
Der volle Inhalt der QuelleAlbers, Cornelis A., Ana Cvejic, Rémi Favier, Evelien E. Bouwmans, Marie-Christine Alessi, Paul Bertone, Gregory Jordan et al. „Exome sequencing identifies NBEAL2 as the causative gene for gray platelet syndrome“. Nature Genetics 43, Nr. 8 (17.07.2011): 735–37. http://dx.doi.org/10.1038/ng.885.
Der volle Inhalt der QuelleBottega, R., A. Pecci, E. De Candia, N. Pujol-Moix, P. G. Heller, P. Noris, D. De Rocco et al. „Correlation between platelet phenotype and NBEAL2 genotype in patients with congenital thrombocytopenia and -granule deficiency“. Haematologica 98, Nr. 6 (25.10.2012): 868–74. http://dx.doi.org/10.3324/haematol.2012.075861.
Der volle Inhalt der QuelleBarg, A., E. Avishai, R. Dardik, S. Levy-Mendelovich, O. Cohen, B. Roth Jelinek, O. Barel, T. Livnat und G. Kenet. „PB1390 Gray Platelet Syndrome- Novel NBEAL2 Pathogenic Variants and Hemostasis Evaluation by Global Coagulation Assays“. Research and Practice in Thrombosis and Haemostasis 7 (Oktober 2023): 101518. http://dx.doi.org/10.1016/j.rpth.2023.101518.
Der volle Inhalt der QuelleCao, Lijuan, Jian Su, Jiaming Li, Ziqiang Yu, Xia Bai, Zhaoyue Wang, Lijun Xia und Changgeng Ruan. „A novel nonsense NBEAL2 gene mutation causing severe bleeding in a patient with gray platelet syndrome“. Platelets 29, Nr. 3 (15.05.2017): 288–91. http://dx.doi.org/10.1080/09537104.2017.1306041.
Der volle Inhalt der QuelleGunay-Aygun, Meral, Tzipora C. Falik-Zaccai, Thierry Vilboux, Yifat Zivony-Elboum, Fatma Gumruk, Mualla Cetin, Morad Khayat et al. „NBEAL2 is mutated in gray platelet syndrome and is required for biogenesis of platelet α-granules“. Nature Genetics 43, Nr. 8 (17.07.2011): 732–34. http://dx.doi.org/10.1038/ng.883.
Der volle Inhalt der QuelleRiley, Roger, Asad Khan, Shella Pai, Laura Warmke, Marcus Winkler und William Gunning. „A Case of Chronic Thrombocytopenia in a 17-Year-Old Female“. Laboratory Medicine 50, Nr. 4 (22.06.2019): 406–20. http://dx.doi.org/10.1093/labmed/lmz013.
Der volle Inhalt der QuelleCoenen, D., und S. Whiteheart. „PB1402 NBEAL2 and the Intragranular Proteoglycan, Serglycin, Both Contribute to the Initiation and Progression of Aortic Aneurysms“. Research and Practice in Thrombosis and Haemostasis 7 (Oktober 2023): 101685. http://dx.doi.org/10.1016/j.rpth.2023.101685.
Der volle Inhalt der QuelleLo, Richard W., Ling Li, Richard Leung, Fred G. Pluthero und Walter H. A. Kahr. „NBEAL2 (Neurobeachin-Like 2) Is Required for Retention of Cargo Proteins by α-Granules During Their Production by Megakaryocytes“. Arteriosclerosis, Thrombosis, and Vascular Biology 38, Nr. 10 (Oktober 2018): 2435–47. http://dx.doi.org/10.1161/atvbaha.118.311270.
Der volle Inhalt der QuelleLouzil, Jan, Jana Stikarova, Dana Provaznikova, Ingrid Hrachovinova, Tereza Fenclova, Jan Musil, Martin Radek et al. „Diagnosing Czech Patients with Inherited Platelet Disorders“. International Journal of Molecular Sciences 23, Nr. 22 (19.11.2022): 14386. http://dx.doi.org/10.3390/ijms232214386.
Der volle Inhalt der QuelleUrban, Denisa, Ling Li, Hilary Christensen, Fred G. Pluthero, Shao Zun Chen, Michael Puhacz, Parvesh M. Garg et al. „The VPS33B-binding protein VPS16B is required in megakaryocyte and platelet α-granule biogenesis“. Blood 120, Nr. 25 (13.12.2012): 5032–40. http://dx.doi.org/10.1182/blood-2012-05-431205.
Der volle Inhalt der QuelleMohamed, Sara, Martina Di Palma, Michela Faleschini, Daniela De Benedittis, Maria Luisa Moleti, Luisa Cardarelli, Anna Maria Testi, Giovanna Palumbo, Anna Savoia und Fiorina Giona. „Chronic Thrombocytopenia in Children: What Could It Hide?“ Blood 136, Supplement 1 (05.11.2020): 33–34. http://dx.doi.org/10.1182/blood-2020-138651.
Der volle Inhalt der QuelleJia, Siyuan, Yunyan He, Meirong Lu, Ning Liao, Yonghong Lei, Nikuze Lauriane, Kairong Liang und Hongying Wei. „Identification of novel pathogenic F13A1 mutation and novel NBEAL2 gene missense mutation in a pedigree with hereditary congenital factor XIII deficiency“. Gene 702 (Juni 2019): 143–47. http://dx.doi.org/10.1016/j.gene.2019.03.067.
Der volle Inhalt der QuelleCollins, J., H. Foster, L. Mayer, A. Crosby, A. Evans, W. Lau, S. Mason et al. „PB0355 Knock-in of Homozygous NBEAL2 Variants to Model Gray Platelet Syndrome in Megakaryocytes Derived from CRISPR-Cas9-edited Pluripotent Stem Cells“. Research and Practice in Thrombosis and Haemostasis 7 (Oktober 2023): 101493. http://dx.doi.org/10.1016/j.rpth.2023.101493.
Der volle Inhalt der QuelleKahr, Walter H. „Molecular Triggers of Granule Formation in Megakaryocytes and Platelets“. Blood 120, Nr. 21 (16.11.2012): SCI—34—SCI—34. http://dx.doi.org/10.1182/blood.v120.21.sci-34.sci-34.
Der volle Inhalt der QuelleShibata, Yusuke, Kazuhito Kawakita und Daigo Takemoto. „Age-Related Resistance of Nicotiana benthamiana Against Hemibiotrophic Pathogen Phytophthora infestans Requires Both Ethylene- and Salicylic Acid–Mediated Signaling Pathways“. Molecular Plant-Microbe Interactions® 23, Nr. 9 (September 2010): 1130–42. http://dx.doi.org/10.1094/mpmi-23-9-1130.
Der volle Inhalt der QuelleLuo, Fangxiu, Jialu Zhao, Yubao Chen, Zhenping Peng, Ran An, Yeling Lu und Jiaming Li. „Clinical and Molecular Characteristics of Megakaryocytes in Myelodysplastic Syndrome“. Global Medical Genetics 11, Nr. 02 (Juni 2024): 187–95. http://dx.doi.org/10.1055/s-0044-1787752.
Der volle Inhalt der QuelleNaik, Gurudatta, Dongquan Chen, Michael Crowley, David Crossman, Katherine C. Sexton, William E. Grizzle, Amitkumar N. Mehta und Guru Sonpavde. „Whole-exome sequencing (WES) of penile squamous cell carcinoma (PSCC) to identify multiple recurrent mutations.“ Journal of Clinical Oncology 34, Nr. 2_suppl (10.01.2016): 484. http://dx.doi.org/10.1200/jco.2016.34.2_suppl.484.
Der volle Inhalt der QuelleAbraham, Shirley M., Dong Chen, Karen Simon, Thomas Markello und William A. Gahl. „GFI1B Mutation Associated Alpha-Delta Platelet Storage-Pool Deficiency: A Case Report and Its Potential Important Implication“. Blood 128, Nr. 22 (02.12.2016): 3727. http://dx.doi.org/10.1182/blood.v128.22.3727.3727.
Der volle Inhalt der QuelleVincent, Benjamin G., Darshan Singh, Michael Wu, Sally A. Hunsucker, Gheath Alatrash, Kathryn Ruisaard, Pariya Sukhumalchandra et al. „RNA-Seq Expression Profiling of AML Stem Cells Reveals Differential Expression of Lineage Differentiation Markers and Novel Splice Variants.“ Blood 120, Nr. 21 (16.11.2012): 2502. http://dx.doi.org/10.1182/blood.v120.21.2502.2502.
Der volle Inhalt der QuelleRivera, Candido E., Prakash Vishnu, Gretchen Schaef Johns, Rajiv K. Pruthi und Dong Chen. „Identification of a Novel Heterozygous Mutation (c.2213T>G;p.Leu738Arg) in Platelet Glycoprotein ITGB3 gene in a Patient with Glanzmann's Thrombasthenia“. Blood 132, Supplement 1 (29.11.2018): 1158. http://dx.doi.org/10.1182/blood-2018-99-117995.
Der volle Inhalt der QuelleKapoor, Urvi, Shipra Kaicker, Jenny Shek, Robyn Gartrell und Monica Bhatia. „Two Hit Theory for the Pathogenesis of Type 3 Congenital Amegakaryocytic Thrombocytopenia“. Blood 142, Supplement 1 (28.11.2023): 5454. http://dx.doi.org/10.1182/blood-2023-190490.
Der volle Inhalt der QuelleBastida, Jose Maria, Mónica del Rey, Rocío Benito, Isabel Sanchez-Guiu, Susana Riesco, Maria Jesús Peñarrubia, Rosa Fisac et al. „Design and Validate of Next-Generation Sequencing Panel for Inherited Platelet Disorders“. Blood 124, Nr. 21 (06.12.2014): 4210. http://dx.doi.org/10.1182/blood.v124.21.4210.4210.
Der volle Inhalt der QuelleOchi, Yotaro, Kenichi Yoshida, Ying-Jung Huang, Ming-Chung Kuo, Yusuke Shiozawa, Yasuhito Nannya, Yuichi Shiraishi et al. „Molecular Profiling of Blastic Transformation in Chronic Myeloid Leukemia“. Blood 132, Supplement 1 (29.11.2018): 1725. http://dx.doi.org/10.1182/blood-2018-99-114512.
Der volle Inhalt der QuelleLim, Ken-Hong, Yu-Cheng Chang, Yi-Hao Chiang, Huan-Chau Lin, Chiao-Yi Chang, Ching-Sung Lin, Ling Huang et al. „Overexpression of Calr Mutants Perturbs Developmental Hematopoiesis in Zebrafish Embryos“. Blood 128, Nr. 22 (02.12.2016): 4282. http://dx.doi.org/10.1182/blood.v128.22.4282.4282.
Der volle Inhalt der QuelleJingyao, Ma, Zhenping Chen, Huiqing LIU, Jialu Zhang, Hao GU und Runhui Wu. „Application of High-Throughput Sequencing in the Diagnosis of Inherited Immune-Thrombocytopenia from Children Chronic/Refractory ITP“. Blood 134, Supplement_1 (13.11.2019): 86. http://dx.doi.org/10.1182/blood-2019-126771.
Der volle Inhalt der QuelleBloom, A. Anthony, Kevin W. Bowman, Junjie Liu, Alexandra G. Konings, John R. Worden, Nicholas C. Parazoo, Victoria Meyer et al. „Lagged effects regulate the inter-annual variability of the tropical carbon balance“. Biogeosciences 17, Nr. 24 (17.12.2020): 6393–422. http://dx.doi.org/10.5194/bg-17-6393-2020.
Der volle Inhalt der QuelleSingh, Ram Sewak, Demissie Jobir Gelmecha, Satyasis Mishra, Gemechu Dengia und Devendra Kumar Sinha. „A Novel Machine Learning Approach for Detection of Coronary Artery Disease Using Reduced Non-linear and Chaos Features“. International Journal Bioautomation 26, Nr. 3 (September 2022): 273–96. http://dx.doi.org/10.7546/ijba.2022.26.3.000786.
Der volle Inhalt der QuelleChen-Liang, Tzu Hua, Ana M. Hurtado López, Laura Palomo, Teresa Bernal Del Castillo, Mar Tormo, Maria Lourdes Hermosin, María-José Jimenez et al. „Germline and Acquired Genetic Variants in Myelodysplastic Syndromes in Young Adults without a Preexisting Disorder or Organ Dysfunction“. Blood 132, Supplement 1 (29.11.2018): 4339. http://dx.doi.org/10.1182/blood-2018-99-116045.
Der volle Inhalt der QuelleZhang, Biao, Chao Song, Xuchu Jiang und Ying Li. „Electricity price forecast based on the STL-TCN-NBEATS model“. Heliyon 9, Nr. 1 (Januar 2023): e13029. http://dx.doi.org/10.1016/j.heliyon.2023.e13029.
Der volle Inhalt der Quelle