Artículos de revistas sobre el tema "GP1BB"
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de Siqueira, Lucia Helena, Miriam P. Beltrame, Fernanda P. G. Cunha, Marina P. Colella, Joyce M. Annichino-Bizzacchi, Erich V. de Paula y Margareth C. Ozelo. "Six Novel Mutations Identified in the Glycoproteins Ib Alpha, Ib Beta and IX Genes Among Twenty-Two Unrelated Patients with Bernard-Soulier Syndrome in Brazil". Blood 118, n.º 21 (18 de noviembre de 2011): 1156. http://dx.doi.org/10.1182/blood.v118.21.1156.1156.
Texto completoBarozzi, Serena, Valeria Bozzi, Daniela De Rocco, Tania Giangregorio, Patrizia Noris, Anna Savoia y Alessandro Pecci. "A Novel Mutation in GP1BB Reveals the Role of the Cytoplasmic Domain of GPIbβ in the Pathophysiology of Bernard-Soulier Syndrome and GPIb-IX Complex Assembly". International Journal of Molecular Sciences 22, n.º 19 (22 de septiembre de 2021): 10190. http://dx.doi.org/10.3390/ijms221910190.
Texto completoTang, Jingrong, Sara Stern-Nezer, Po-Ching Liu, Ludmila Matyakhina, Michael Riordan, Naomi Luban, Peter Steinbach y Stephen Kaler. "Mutation in the leucine-rich repeat C-flanking region of platelet glycoprotein Ibβ impairs assembly of von Willebrand factor receptor". Thrombosis and Haemostasis 92, n.º 07 (2004): 75–88. http://dx.doi.org/10.1160/th04-02-0071.
Texto completoMekchay, Ponthip, Praewphan Ingrungruanglert, Kanya Suphapeetiporn, Darintr Sosothikul, Wilawan Ji-au, Supang Maneesri Le Grand, Nipan Israsena y Ponlapat Rojnuckarin. "Study of Bernard–Soulier Syndrome Megakaryocytes and Platelets Using Patient-Derived Induced Pluripotent Stem Cells". Thrombosis and Haemostasis 119, n.º 09 (28 de julio de 2019): 1461–70. http://dx.doi.org/10.1055/s-0039-1693409.
Texto completoSavoia, Anna, Shinji Kunishima, Patrizia Noris, Nuria Pujol-Moix, Dermot Kenny, Nurit Rosenberg, Margaret L. Rand et al. "International Consortium for the Study of Clinical and Molecular Aspects of Bernard-Soulier Syndrome". Blood 118, n.º 21 (18 de noviembre de 2011): 707. http://dx.doi.org/10.1182/blood.v118.21.707.707.
Texto completoBlanco-Luquin, Idoia, Blanca Acha, Amaya Urdánoz-Casado, Eva Gómez-Orte, Miren Roldan, Diego R. Pérez-Rodríguez, Juan Cabello y Maite Mendioroz. "NXN Gene Epigenetic Changes in an Adult Neurogenesis Model of Alzheimer’s Disease". Cells 11, n.º 7 (22 de marzo de 2022): 1069. http://dx.doi.org/10.3390/cells11071069.
Texto completoSivapalaratnam, Suthesh, Sarah K. Westbury, Jonathan C. Stephens, Daniel Greene, Kate Downes, Anne M. Kelly, Claire Lentaigne et al. "Rare variants in GP1BB are responsible for autosomal dominant macrothrombocytopenia". Blood 129, n.º 4 (26 de enero de 2017): 520–24. http://dx.doi.org/10.1182/blood-2016-08-732248.
Texto completoSivapalaratnam, Suthesh, Willem Ouwehand, Bridge Consortium y ThromboGenomics Consortium. "Rare Variants in GP1BB underlie Autosomal Dominant Macrothrombocytopenia; Findings of Large Unique Bleeding and Platelet Disorders Cohort". Blood 128, n.º 22 (2 de diciembre de 2016): 1359. http://dx.doi.org/10.1182/blood.v128.22.1359.1359.
Texto completoBartsch, Ingrid, Kirstin Sandrock, Francois Lanza, Paquita Nurden, Ina Hainmann, Anna Pavlova, Andreas Greinacher et al. "Deletion of human GP1BB and SEPT5 is associated with Bernard-Soulier syndrome, platelet secretion defect, polymicrogyria, and developmental delay". Thrombosis and Haemostasis 106, n.º 09 (2011): 475–83. http://dx.doi.org/10.1160/th11-05-0305.
Texto completoLouzil, 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, n.º 22 (19 de noviembre de 2022): 14386. http://dx.doi.org/10.3390/ijms232214386.
Texto completoWunderlich, Frank, Denis Delic, Daniela Gerovska y Marcos J. Araúzo-Bravo. "Vaccination Accelerates Liver-Intrinsic Expression of Megakaryocyte-Related Genes in Response to Blood-Stage Malaria". Vaccines 10, n.º 2 (14 de febrero de 2022): 287. http://dx.doi.org/10.3390/vaccines10020287.
Texto completoCutler, Jacky, Mike Mitchell, Hady Goubran y Geoffrey F. Savidge. "Familial Bernard-Soulier Syndrome Due to a Novel Ins/Del Mutation in Glycoprotein IX." Blood 106, n.º 11 (16 de noviembre de 2005): 2178. http://dx.doi.org/10.1182/blood.v106.11.2178.2178.
Texto completoFerrari, Silvia, Anna M. Lombardi, Irene Cortella, Maria A. Businaro, Antonella Bertomoro, Irene Di Pasquale y Fabrizio Fabris. "New heterozygous variant in GP1BB gene is responsible for an inherited form of macrothrombocytopenia". British Journal of Haematology 184, n.º 5 (12 de marzo de 2018): 855–58. http://dx.doi.org/10.1111/bjh.15176.
Texto completoOved, Joseph H., Michele P. Lambert, M. Anna Kowalska, Mortimer Poncz y Konrad Karczewski. "Analysis of the Frequency of Spontaneous, Functionally-Significant Mutations in Genes Associated with Platelet Disorders in >120,000 Healthy Individuals". Blood 132, Supplement 1 (29 de noviembre de 2018): 2438. http://dx.doi.org/10.1182/blood-2018-99-115567.
Texto completoLondon, Fredda S. "The PAR-1-Stimulated Platelet Subpopulation That Binds Factor Xa Also Expresses Matrixmetalloproteinase and Calpain Activities Resulting in Population-Specific GP1bα Shedding and Platelet Vesiculation." Blood 106, n.º 11 (16 de noviembre de 2005): 3563. http://dx.doi.org/10.1182/blood.v106.11.3563.3563.
Texto completoAl-Numair, Nouf, Khushnooda Ramzan, Laila Alquait, Meshal Alshehri, Faiqa Imtiaz y Tarek Owaidah. "A homozygous loss-of-function mutation in GP1BB causing variable clinical phenotypes in a family with Bernard–Soulier syndrome". Blood Coagulation & Fibrinolysis 32, n.º 5 (1 de marzo de 2021): 352–55. http://dx.doi.org/10.1097/mbc.0000000000001027.
Texto completoVaisvilas, M., V. Dirse, B. Aleksiuniene, I. Tamuliene, L. Cimbalistiene, A. Utkus y J. Rascon. "Acute pre-B lymphoblastic leukemia and congenital anomalies in a child with a de novo 22q11.1q11.22 duplication". Balkan Journal of Medical Genetics 21, n.º 1 (29 de octubre de 2018): 87–91. http://dx.doi.org/10.2478/bjmg-2018-0002.
Texto completoSzelenberger, Rafał, Michał Seweryn Karbownik, Michał Kacprzak, Ewelina Synowiec, Sylwia Michlewska, Michał Bijak, Marzenna Zielińska, Alina Olender y Joanna Saluk-Bijak. "Dysregulation in the Expression of Platelet Surface Receptors in Acute Coronary Syndrome Patients—Emphasis on P2Y12". Biology 11, n.º 5 (22 de abril de 2022): 644. http://dx.doi.org/10.3390/biology11050644.
Texto completoPeck, Rachel C., Sarah Westbury, Lucy Fitzgibbon, Neil V. Morgan, Jose Rivera, Walter H. Kahr, Nihr BioResource et al. "Comprehensive Description of Monoallelic GP1BA Variants Associated with Thrombocytopenia". Blood 136, Supplement 1 (5 de noviembre de 2020): 34–35. http://dx.doi.org/10.1182/blood-2020-133987.
Texto completoGissi, Davide, Viscardo Fabbri, Andrea Gabusi, Jacopo Lenzi, Luca Morandi, Sofia Melotti, Sofia Asioli et al. "Pre-Operative Evaluation of DNA Methylation Profile in Oral Squamous Cell Carcinoma Can Predict Tumor Aggressive Potential". International Journal of Molecular Sciences 21, n.º 18 (14 de septiembre de 2020): 6691. http://dx.doi.org/10.3390/ijms21186691.
Texto completoMao, Xiaohong, Xin Zhang, Xiaowei Zheng, Yongwu Chen, Zixue Xuan y Ping Huang. "Curcumin suppresses LGR5(+) colorectal cancer stem cells by inducing autophagy and via repressing TFAP2A-mediated ECM pathway". Journal of Natural Medicines 75, n.º 3 (13 de marzo de 2021): 590–601. http://dx.doi.org/10.1007/s11418-021-01505-1.
Texto completoMarkham, Stephen J., Lisa Bevilaqua, Haley Zarrin, Donna McDonald-McGinn, Elaine Zackai y Michele P. Lambert. "Detecting 22q11.2 Deletion Syndrome Using Flow Cytometry". Blood 124, n.º 21 (6 de diciembre de 2014): 4207. http://dx.doi.org/10.1182/blood.v124.21.4207.4207.
Texto completoRivera, Candido E., Prakash Vishnu, Gretchen Schaef Johns, Rajiv K. Pruthi y 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 de noviembre de 2018): 1158. http://dx.doi.org/10.1182/blood-2018-99-117995.
Texto completoArter, Zhaohui Liao, Caitlin Yatogo, Michael C. Chicka y Jeffrey L. Berenberg. "The Mystery of "Magic Blood" - Familial Macrothrombocytopenia Associated with a Novel Variant in GP1BA Gene". Blood 134, Supplement_1 (13 de noviembre de 2019): 2380. http://dx.doi.org/10.1182/blood-2019-122384.
Texto completoLian, Zheng, Milind Mahajan, Vincent Schulz, Erol Gulcicek, Diane Krause y Sherman M. Weissman. "Intermediate Steps In Erythroid, Megakaryocytic and Myeloid Lineage Specification". Blood 116, n.º 21 (19 de noviembre de 2010): 4778. http://dx.doi.org/10.1182/blood.v116.21.4778.4778.
Texto completoOnundarson, Pall Torfi, Elisabet R. Birgisdottir, Gudrun Bragadottir, Bylgja Hilmarsdottir, Brynja Gudmundsdottir, Brynjar Vidarsson y Magnus K. Magnusson. "Bernard-Soulier in Iceland. Bleeding Symptoms and Platelet Parameters in Patients, Carriers and Controls." Blood 108, n.º 11 (16 de noviembre de 2006): 1095. http://dx.doi.org/10.1182/blood.v108.11.1095.1095.
Texto completoBastida, 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, n.º 21 (6 de diciembre de 2014): 4210. http://dx.doi.org/10.1182/blood.v124.21.4210.4210.
Texto completoKitamura, Katsumasa, Yusuke Okuno, Kenichi Yoshida, Masashi Sanada, Yuichi Shiraishi, Hideki Muramatsu, Ryoji Kobayashi et al. "Functional Characterization of a Novel GFI1B Mutation Causing Congenital Macrothrombocytopenia". Blood 126, n.º 23 (3 de diciembre de 2015): 75. http://dx.doi.org/10.1182/blood.v126.23.75.75.
Texto completoNagy, Zoltan, Timo Vögtle, Mitchell J. Geer, Jun Mori, Silke Heising, Giada Di Nunzio, Ralph Gareus et al. "The Gp1ba-Cre transgenic mouse: a new model to delineate platelet and leukocyte functions". Blood 133, n.º 4 (24 de enero de 2019): 331–43. http://dx.doi.org/10.1182/blood-2018-09-877787.
Texto completoRabitzsch, G., J. Mair, P. Lechleitner, F. Noll, U. Hofmann, E. G. Krause, F. Dienstl y B. Puschendorf. "Immunoenzymometric assay of human glycogen phosphorylase isoenzyme BB in diagnosis of ischemic myocardial injury". Clinical Chemistry 41, n.º 7 (1 de julio de 1995): 966–78. http://dx.doi.org/10.1093/clinchem/41.7.966.
Texto completoPark, Kwang-Yeol, Ilknur Ay, Ross Avery, Juan Alfredo Caceres, Matthew S. Siket, Octavio M. Pontes-Neto, Hui Zheng et al. "New biomarker for acute ischaemic stroke: plasma glycogen phosphorylase isoenzyme BB". Journal of Neurology, Neurosurgery & Psychiatry 89, n.º 4 (13 de octubre de 2017): 404–9. http://dx.doi.org/10.1136/jnnp-2017-316084.
Texto completoBray, Paul F., Timothy D. Howard, Eric Vittinghoff, David C. Sane y David M. Herrington. "Effect of genetic variations in platelet glycoproteins Ibα and VI on the risk for coronary heart disease events in postmenopausal women taking hormone therapy". Blood 109, n.º 5 (14 de noviembre de 2006): 1862–69. http://dx.doi.org/10.1182/blood-2006-03-013151.
Texto completoUddin, Md Main, Mostafa M. H. Ibrahim y Karen P. Briski. "Glycogen Phosphorylase Isoform Regulation of Ventromedial Hypothalamic Nucleus Gluco-Regulatory Neuron 5′-AMP-Activated Protein Kinase and Transmitter Marker Protein Expression". ASN Neuro 13 (enero de 2021): 175909142110350. http://dx.doi.org/10.1177/17590914211035020.
Texto completoDi, Jia-Yin, Zong-Xin Zhang y Shao-Jun Xin. "Glycogen Phosphorylase Isoenzyme Bb, Myoglobin and BNP in ANT-Induced Cardiotoxicity". Open Life Sciences 13, n.º 1 (31 de diciembre de 2018): 561–68. http://dx.doi.org/10.1515/biol-2018-0067.
Texto completoSkalníková, Magdalena, Kateřina Staňo Kozubík, Jakub Trizuljak, Zuzana Vrzalová, Lenka Radová, Kamila Réblová, Radka Holbová et al. "A GP1BA Variant in a Czech Family with Monoallelic Bernard-Soulier Syndrome". International Journal of Molecular Sciences 23, n.º 2 (14 de enero de 2022): 885. http://dx.doi.org/10.3390/ijms23020885.
Texto completoGollomp, Kandace y Mortimer Poncz. "Gp1ba-Cre or Pf4-Cre: pick your poison". Blood 133, n.º 4 (24 de enero de 2019): 287–88. http://dx.doi.org/10.1182/blood-2018-11-887513.
Texto completoKruse, Alexandra, Alexa M. Sughroue, Patrick Morrissey, Claudia Tchatchouang, Guangheng Zhu, Marina Izak, Heyu Ni y James B. Bussel. "Response to TPO-Receptor Agonists: Role of Immature Platelet Fraction and Anti-GP1b". Blood 124, n.º 21 (6 de diciembre de 2014): 4190. http://dx.doi.org/10.1182/blood.v124.21.4190.4190.
Texto completoHamilton, Alexander, Margareth Ozelo, Jayne Leggo, Colleen Notley, Hannah Brown, Juan Pablo Frontroth, Anne Angelillo-Scherrer et al. "Frequency of Platelet type versus Type 2B von Willebrand Disease". Thrombosis and Haemostasis 105, n.º 03 (2011): 501–8. http://dx.doi.org/10.1160/th10-08-0523.
Texto completoAnnarapu, Gowtham K., Rashi Singhal, Avinash Gupta, Sheetal Chawla, Harish Batra, Tulika Seth y Prasenjit Guchhait. "HbS Binding to GP1bα Activates Platelets in Sickle Cell Disease". PLOS ONE 11, n.º 12 (9 de diciembre de 2016): e0167899. http://dx.doi.org/10.1371/journal.pone.0167899.
Texto completoGhalloussi, Dorsaf, Noémie Saut, Denis Bernot, Xavier Pillois, Philippe Rameau, Gérard Sébahoun, Marie-Christine Alessi, Hana Raslova y Véronique Baccini. "A new heterozygous mutation in GP1BA gene responsible for macrothrombocytopenia". British Journal of Haematology 183, n.º 3 (30 de octubre de 2017): 503–6. http://dx.doi.org/10.1111/bjh.14986.
Texto completoOthman, Maha y Jonas Emsley. "Gene of the issue: GP1BA gene mutations associated with bleeding". Platelets 28, n.º 8 (29 de septiembre de 2017): 832–36. http://dx.doi.org/10.1080/09537104.2017.1361526.
Texto completoBury, Loredana, Emanuela Falcinelli, Haripriya Kuchi Bhotla, Anna Maria Mezzasoma, Giuseppe Guglielmini, Alexander Tischer, Laurie Moon-Tasson, Matthew Auton y Paolo Gresele. "A p.Arg127Gln variant in GPIbα LRR5 allosterically enhances affinity for VWF: a novel form of platelet-type VWD". Blood Advances 6, n.º 7 (1 de abril de 2022): 2236–46. http://dx.doi.org/10.1182/bloodadvances.2021005463.
Texto completoWoods, Adriana, Analia Sanchez-Luceros, Emilse Bermejo, Juvenal Paiva, Maria Alberto, Silvia Grosso, Ana Kempfer y Maria Lazzari. "Identification of p.W246L As a Novel Mutation in the GP1BA Gene Responsible for Platelet-Type von Willebrand Disease". Seminars in Thrombosis and Hemostasis 40, n.º 02 (28 de enero de 2014): 151–60. http://dx.doi.org/10.1055/s-0033-1364183.
Texto completoSullivan, Spencer K., Jason A. Mills, Sevasti B. Koukouritaki, Karen K. Vo, Randolph B. Lyde, Prasuna Paluru, Guoha Zhao et al. "High-level transgene expression in induced pluripotent stem cell–derived megakaryocytes: correction of Glanzmann thrombasthenia". Blood 123, n.º 5 (30 de enero de 2014): 753–57. http://dx.doi.org/10.1182/blood-2013-10-530725.
Texto completoBurdorf, L., T. Zhang, E. Rybak, I. I. Salles, K. Broos, E. Welty, C. Avon et al. "295 Blocking GP1b-vWF Interaction by Anti-GP1b Fab Reduces Activation and Sequestration of Platelets in a Xenogeneic Pig Lung Perfusion Model". Journal of Heart and Lung Transplantation 30, n.º 4 (abril de 2011): S103. http://dx.doi.org/10.1016/j.healun.2011.01.302.
Texto completoMazzeffi, Michael, Shaheer Hasan, Ezeldeen Abuelkasem, Michael Meyer, Kristopher Deatrick, Bradley Taylor, Zachary Kon, Daniel Herr y Kenichi Tanaka. "Von Willebrand Factor-GP1bα Interactions in Venoarterial Extracorporeal Membrane Oxygenation Patients". Journal of Cardiothoracic and Vascular Anesthesia 33, n.º 8 (agosto de 2019): 2125–32. http://dx.doi.org/10.1053/j.jvca.2018.11.031.
Texto completoÖzdemir, Zeynep C., Yeter Düzenli Kar, Serdar Ceylaner y Özcan Bör. "A novel mutation in the GP1BA gene in Bernard–Soulier syndrome". Blood Coagulation & Fibrinolysis 31, n.º 1 (enero de 2020): 83–86. http://dx.doi.org/10.1097/mbc.0000000000000868.
Texto completoStavnichuk, Mariya, Zoltan Nagy, Yotis A. Senis y Svetlana V. Komarova. "Megakaryocyte-Driven Myelofibrosis Leads to Progressive Osteosclerosis in G6b-B Knockout Mice". Blood 134, Supplement_1 (13 de noviembre de 2019): 4199. http://dx.doi.org/10.1182/blood-2019-124186.
Texto completoNapit, Prabhat R., Abdulrahman Alhamyani, Khaggeswar Bheemanapally, Paul W. Sylvester y Karen P. Briski. "Sex-Dimorphic Glucocorticoid Receptor Regulation of Hypothalamic Primary Astrocyte Glycogen Metabolism: Interaction with Norepinephrine". Neuroglia 3, n.º 4 (17 de noviembre de 2022): 144–57. http://dx.doi.org/10.3390/neuroglia3040010.
Texto completoBadolia, Rachit, John Kostyak, Carol Dangelmaier y Satya Kunapuli. "Syk Activity Is Dispensable for Platelet GP1b-IX-V Signaling". International Journal of Molecular Sciences 18, n.º 6 (9 de junio de 2017): 1238. http://dx.doi.org/10.3390/ijms18061238.
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