Artículos de revistas sobre el tema "GP1BA"
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Peck, 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 completode 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 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 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 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 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 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 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 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 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 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 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 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 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 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 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 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 completoShen, Jun, Xiao-Chang Chen, Wang-Jun Li, Qiu Han, Chun Chen, Jing-Min Lu, Jin-Yu Zheng y Shou-Ru Xue. "Identification of Parkinson’s disease-related pathways and potential risk factors". Journal of International Medical Research 48, n.º 10 (octubre de 2020): 030006052095719. http://dx.doi.org/10.1177/0300060520957197.
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 completoOthman, M. "Differential identification of PT-VWD from type 2B VWD and GP1BA nomenclature issues". British Journal of Haematology 142, n.º 2 (julio de 2008): 312–14. http://dx.doi.org/10.1111/j.1365-2141.2008.07171.x.
Texto completoMohamed, Sara, Martina Di Palma, Michela Faleschini, Daniela De Benedittis, Maria Luisa Moleti, Luisa Cardarelli, Anna Maria Testi, Giovanna Palumbo, Anna Savoia y Fiorina Giona. "Chronic Thrombocytopenia in Children: What Could It Hide?" Blood 136, Supplement 1 (5 de noviembre de 2020): 33–34. http://dx.doi.org/10.1182/blood-2020-138651.
Texto completoLavenu-Bombled, Cécile, Corinne Guitton, Arnaud Dupuis, Marie-Jeanne Baas, Céline Desconclois, Marie Dreyfus, Renhao Li et al. "A novel platelet-type von Willebrand disease mutation (GP1BA p.Met255Ile) associated with type 2B “Malmö/New York” von Willebrand disease". Thrombosis and Haemostasis 116, n.º 12 (noviembre de 2016): 1070–78. http://dx.doi.org/10.1160/th16-06-0438.
Texto completoTrizuljak, Jakub, Kateřina Staňo Kozubík, Lenka Radová, Michaela Pešová, Karol Pál, Kamila Réblová, Olga Stehlíková et al. "A novel germline mutation in GP1BA gene N-terminal domain in monoallelic Bernard-Soulier syndrome". Platelets 29, n.º 8 (17 de octubre de 2018): 827–33. http://dx.doi.org/10.1080/09537104.2018.1529300.
Texto completoAli, Shahnaz, Shrimati Shetty y Kanjaksha Ghosh. "A novel mutation in GP1BA gene leads to mono-allelic Bernard Soulier syndrome form of macrothrombocytopenia". Blood Coagulation & Fibrinolysis 28, n.º 1 (enero de 2017): 94–95. http://dx.doi.org/10.1097/mbc.0000000000000530.
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 completoMonteiro, Manuel, Luis Almeida, Mariana Morais y Luis Dias. "Bernard Soulier syndrome: a rare, frequently misdiagnosed and poorly managed bleeding disorder". BMJ Case Reports 14, n.º 8 (agosto de 2021): e243518. http://dx.doi.org/10.1136/bcr-2021-243518.
Texto completoKanaji, Taisuke, Susan Russell, Janet Cunningham, Kenji Izuhara, Joan E. B. Fox y Jerry Ware. "Megakaryocyte proliferation and ploidy regulated by the cytoplasmic tail of glycoprotein Ibα". Blood 104, n.º 10 (15 de noviembre de 2004): 3161–68. http://dx.doi.org/10.1182/blood-2004-03-0893.
Texto completoStavnichuk, Mariya y Svetlana V. Komarova. "Megakaryocyte-bone cell interactions: lessons from mouse models of experimental myelofibrosis and related disorders". American Journal of Physiology-Cell Physiology 322, n.º 2 (1 de febrero de 2022): C177—C184. http://dx.doi.org/10.1152/ajpcell.00328.2021.
Texto completoShlebak, Abdul, Anthony Poles, Richard Manning, Shaikha Almuhareb, Josu De La Funte, Mike Mitchell y Geoff Lucas. "A Novel Homozygous c.800C>G Substitution in GP1BA Exon 2 in a Kuwaiti Family with Bernard-Soulier Syndrome". Acta Haematologica 134, n.º 3 (2015): 193–98. http://dx.doi.org/10.1159/000381328.
Texto completoV. Anisimova, A., A. S. Gunchenko, A. Yu. Ikonnikova, S. S. Galkin, M. A. Avdonina, T. V. Nasedkina y Z. Abdukhalikova. "Study of the Role of Polymorphism of ACE, GP1BA, PDE4D Genes and Clinical Features in the Development of Cerebrovascular Diseases". International Journal of Sciences 8, n.º 03 (2019): 97–101. http://dx.doi.org/10.18483/ijsci.1975.
Texto completoLi, Xingchuan, Song Wang, Jiusi Wu, Haidong Wang, Jing Wang, Xiangyu Dong y Ni Zhang. "A Case of Bernard-Soulier Syndrome due to a Novel Homozygous Missense Mutation in an Exon of the GP1BA Gene". Acta Haematologica 143, n.º 1 (12 de julio de 2019): 60–64. http://dx.doi.org/10.1159/000500797.
Texto completoSkvortsova, V. I., E. A. Koltsova, Ekaterina Igorevna Kimelfeld, S. A. Limborskaya, P. A. Slominsky y T. V. Tupitsyna. "Analysis of the contribution of -5t/c polymorphism in the GP1BA gene to the development of ischemic stroke in young patients". Neurology, neuropsychiatry, Psychosomatics, n.º 4 (15 de diciembre de 2012): 39. http://dx.doi.org/10.14412/2074-2711-2012-419.
Texto completoShorikov, E. "C0376: Platelets Aggregation in Relation to Polymorphism of GP1BA-Trombocyte Receptor Gene at Patients with Arterial Hypertension and Diabetes Mellitus Type 2". Thrombosis Research 133 (mayo de 2014): S82. http://dx.doi.org/10.1016/s0049-3848(14)50266-6.
Texto completoGindele, Réka, Adrienne Kerényi, Judit Kállai, György Pfliegler, Ágota Schlammadinger, István Szegedi, Tamás Major et al. "Resolving Differential Diagnostic Problems in von Willebrand Disease, in Fibrinogen Disorders, in Prekallikrein Deficiency and in Hereditary Hemorrhagic Telangiectasia by Next-Generation Sequencing". Life 11, n.º 3 (5 de marzo de 2021): 202. http://dx.doi.org/10.3390/life11030202.
Texto completoKunicki, Thomas J., Augusto B. Federici, Daniel R. Salomon, James A. Koziol, Steven R. Head, Tony S. Mondala, Jeffrey D. Chismar, Luciano Baronciani, Maria Teresa Canciani y Ian R. Peake. "An association of candidate gene haplotypes and bleeding severity in von Willebrand disease (VWD) type 1 pedigrees". Blood 104, n.º 8 (15 de octubre de 2004): 2359–67. http://dx.doi.org/10.1182/blood-2004-01-0349.
Texto completoEnayat, Said, Shirin Ravanbod, Maryam Rassoulzadegan, Mohammad Jazebi, Shirin Tarighat, Fereydoun Ala, Jonas Emsley y Maha Othman. "A novel D235Y mutation in the GP1BA gene enhances platelet interaction with von Willebrand factor in an Iranian family with platelet-type von Willebrand disease". Thrombosis and Haemostasis 108, n.º 11 (2012): 946–54. http://dx.doi.org/10.1160/th12-04-0189.
Texto completoWandall, Hans H., Anne Louise Sørensen, Sunita Patel, Jennifer Richardson, Joseph E. Italiano, Victoria Rumjantseva, Eric P. Bennett, Henrik Clausen, Thomas P. Stossel y John H. Hartwig. "Megakaryocytes Package and Deliver Golgi-Associated Glycosyltransferases into Platelets and to Platelet Surfaces Using Dense Granules." Blood 106, n.º 11 (16 de noviembre de 2005): 1643. http://dx.doi.org/10.1182/blood.v106.11.1643.1643.
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 completoTupitsyna, T. V., E. A. Bondarenko, S. A. Kravchenko, P. F. Tatarskyy, I. M. Shetova, N. A. Shamalov, S. M. Kuznetsova et al. "Comparative analysis of associations between polymorphic variants of the F2, F5, GP1BA, and ACE genes and the risk of developing stroke in Russian and Ukrainian populations". Molecular Genetics, Microbiology and Virology 28, n.º 1 (enero de 2013): 8–14. http://dx.doi.org/10.3103/s0891416813010072.
Texto completoFrontroth, Juan Pablo, Mirta Hepner, Gabriela Sciuccati, Aurora Feliú Torres, Graciela Pieroni y Mariana Bonduel. "Prospective study of low-dose ristocetin-induced platelet aggregation to identify type 2B von Willebrand disease (VWD) and platelet-type VWD in children". Thrombosis and Haemostasis 104, n.º 12 (2010): 1158–65. http://dx.doi.org/10.1160/th10-04-0213.
Texto completoLi, Yang, Guoqing Li, Fu Wang, Xiaoshan Wu, Zhifang Wu, Jinsong Wang, Chunmei Zhang, Junqi He, Hao Wang y Songlin Wang. "Integrated Analysis of LncRNA-mRNA Coexpression in the Extracellular Matrix of Developing Deciduous Teeth in Miniature Pigs". BioMed Research International 2019 (23 de enero de 2019): 1–9. http://dx.doi.org/10.1155/2019/6159490.
Texto completoВеремеева, В. В., Н. А. Бухвальд, Э. В. Дашкевич y Н. Г. Седляр. "Development of the Integrated Algorithm for Examining Women with a Risk of Hereditary Thrombophilia in Planning Pregnancy". Гематология. Трансфузиология. Восточная Европа, n.º 2 (6 de julio de 2020): 208–16. http://dx.doi.org/10.34883/pi.2020.6.2.006.
Texto completoVan der Reijden, Bert A., Davide Monteferrario, Nikhita Bolar, Anna Marneth, Konnie Hebeda, Saskia Bergevoet, Hans Veenstra et al. "A Dominant-Negative GFI1B Mutation in Gray Platelet Syndrome". Blood 122, n.º 21 (15 de noviembre de 2013): LBA—3—LBA—3. http://dx.doi.org/10.1182/blood.v122.21.lba-3.lba-3.
Texto completoSemashchenko, K. S., T. S. Mongush, A. A. Kosinova, T. N. Subbotina y Y. I. Grinshtein. "Study the Association of Nucleotide Polymorphisms in Platelet Receptor and Cytochrome P450 Genes with the Development of Resistance to Antiplatelet Drugs in Patients with Coronary Artery Disease". Rational Pharmacotherapy in Cardiology 18, n.º 3 (6 de julio de 2022): 289–96. http://dx.doi.org/10.20996/1819-6446-2022-06-15.
Texto completoKunicki, Thomas J., Daniel Diaz, Shirley A. Williams, Richard W. Farndale y Diane J. Nugent. "The Integrin α2 Dimorphism E534K Modulates Platelet Binding to Decorin but Not Collagen I",. Blood 118, n.º 21 (18 de noviembre de 2011): 3256. http://dx.doi.org/10.1182/blood.v118.21.3256.3256.
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.
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