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Platelets Volume 30, 2019 - Issue 4
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Gene of the Issue

RASGRP2 gene variations associated with platelet dysfunction and bleeding

Verónica Palma-BarquerosServicio de Hematología y Oncología Médica, Hospital Universitario Morales Meseguer, Centro Regional de Hemodonación, Universidad de Murcia, Murcia, SpainORCID Iconhttp://orcid.org/0000-0002-5699-0053View further author information
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Juan Ruiz-PividalServicio de Hematología y Oncología Médica, Hospital Universitario Morales Meseguer, Centro Regional de Hemodonación, Universidad de Murcia, Murcia, SpainView further author information
,
Natalia BohdanServicio de Hematología y Oncología Médica, Hospital Universitario Morales Meseguer, Centro Regional de Hemodonación, Universidad de Murcia, Murcia, SpainView further author information
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Vicente VicenteServicio de Hematología y Oncología Médica, Hospital Universitario Morales Meseguer, Centro Regional de Hemodonación, Universidad de Murcia, Murcia, SpainView further author information
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Jose Maria BastidaDepartment of Hematology, IBSAL-Hospital Universitario de Salamanca, Salamanca, SpainORCID Iconhttp://orcid.org/0000-0002-8007-3909View further author information
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María LozanoServicio de Hematología y Oncología Médica, Hospital Universitario Morales Meseguer, Centro Regional de Hemodonación, Universidad de Murcia, Murcia, Spain;On behalf of the “Inherited Platelet Disorders Project”, Hemorrhagic Diathesis Working Group SETH.ORCID Iconhttp://orcid.org/0000-0003-3148-7037View further author information
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José RiveraServicio de Hematología y Oncología Médica, Hospital Universitario Morales Meseguer, Centro Regional de Hemodonación, Universidad de Murcia, Murcia, Spain;On behalf of the “Inherited Platelet Disorders Project”, Hemorrhagic Diathesis Working Group SETH.Correspondence[email protected]
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Pages 535-539 | Received 29 Dec 2018, Accepted 16 Feb 2019, Published online: 08 Mar 2019

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Essa Alharby, Mohammad A Bakhsh, Alia M Albalawi, Sultan O Almutairi, Jamil A Hashmi & Sulman Basit. (2020) A novel missense variant in the RASGRP2 gene in patients with moderate to severe bleeding disorder. Platelets 31:5, pages 646-651.
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Articles from other publishers (10)

Tanvi Rudran, Silvio Antoniak, Matthew J. Flick, Mark H. Ginsberg, Alisa S. Wolberg, Wolfgang Bergmeier & Robert H. Lee. (2023) Protease-activated receptors and glycoprotein VI cooperatively drive the platelet component in thromboelastography. Journal of Thrombosis and Haemostasis 21:8, pages 2236-2247.
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Kateryna Kalyta, Weronika Stelmaszczyk, Dominika Szczęśniak, Lidia Kotuła, Paula Dobosz & Magdalena Mroczek. (2023) The Spectrum of the Heterozygous Effect in Biallelic Mendelian Diseases—The Symptomatic Heterozygote Issue. Genes 14:8, pages 1562.
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Hao Wang, Zhenzhen Lin, Zhe Nian, Wei Zhang, Wenxu Liu, Fei Yan, Zengtuan Xiao, Xia Wang, Zhenfa Zhang, Zhenyi Ma & Zhe Liu. (2022) Hematopoietic transcription factor GFI1 promotes anchorage independence by sustaining ERK activity in cancer cells. Journal of Clinical Investigation 132:17.
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Sara Morais, Mónica Pereira, Catarina Lau, Ana Gonçalves, Catarina Monteiro, Marta Gonçalves, Jorge Oliveira, Lurdes Moreira, Eugénia Cruz, Rosário Santos & Margarida Lima. (2021) CalDAG-GEFI Deficiency in a Family with Symptomatic Heterozygous and Homozygous Carriers of a Likely Pathogenic Variant in RASGRP2. International Journal of Molecular Sciences 22:22, pages 12423.
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Verónica Palma-Barqueros, Nuria Revilla, Ana Sánchez, Ana Zamora Cánovas, Agustín Rodriguez-Alén, Ana Marín-Quílez, José Ramón González-Porras, Vicente Vicente, María Luisa Lozano, José María Bastida & José Rivera. (2021) Inherited Platelet Disorders: An Updated Overview. International Journal of Molecular Sciences 22:9, pages 4521.
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Robert H. Lee, Raj S. Kasthuri & Wolfgang Bergmeier. (2020) Platelet transfusion for patients with platelet dysfunction: effectiveness, mechanisms, and unanswered questions. Current Opinion in Hematology 27:6, pages 378-385.
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Julia Körholz, Nadja Lucas, Franziska Boiti, Karina Althaus, Oliver Tiebel, Mingyan Fang, Reinhard Berner, Min Ae Lee-Kirsch & Ralf Knöfler. (2020) Severe Bleeding Diathesis in Siblings with Platelet Dysfunction due to a Novel Nonsense RASGRP2 Mutation. TH Open 04:04, pages e413-e416.
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Muzaddid Sarker, Ardeshir Goliaei, Florence Golesi, Marjorie Poggi, Aaron A. Cook, Mohammad A.I. Khan, Brenda R. Temple, Lucia Stefanini, Matthias Canault, Wolfgang Bergmeier & Sharon L. Campbell. (2020) Subcellular localization of Rap1 GTPase activator CalDAG‐GEFI is orchestrated by interaction of its atypical C1 domain with membrane phosphoinositides. Journal of Thrombosis and Haemostasis 18:3, pages 693-705.
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Georgi Manukjan, Verena A. Wiegering, Tobias Reindl, Gabriele Strauß, Eva Klopocki, Harald Schulze & Oliver Andres. (2019) Novel variants in FERMT3 and RASGRP2 —Genetic linkage in Glanzmann‐like bleeding disorders . Pediatric Blood & Cancer 67:2.
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Robert H. Lee, Raymond PiattAnkita Dhenge, María L. Lozano, Verónica Palma-Barqueros, José Rivera & Wolfgang Bergmeier. (2019) Impaired hemostatic activity of healthy transfused platelets in inherited and acquired platelet disorders: Mechanisms and implications. Science Translational Medicine 11:522.
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