Literature DB >> 35167650

Genetics of inherited thrombocytopenias.

Julia T Warren1, Jorge Di Paola1.   

Abstract

The inherited thrombocytopenia syndromes are a group of disorders characterized primarily by quantitative defects in platelet number, though with a variety demonstrating qualitative defects and/or extrahematopoietic findings. Through collaborative international efforts applying next-generation sequencing approaches, the list of genetic syndromes that cause thrombocytopenia has expanded significantly in recent years, now with over 40 genes implicated. In this review, we focus on what is known about the genetic etiology of inherited thrombocytopenia syndromes and how the field has worked to validate new genetic discoveries. We highlight the important role for the clinician in identifying a germline genetic diagnosis and strategies for identifying novel causes through research-based endeavors.
© 2022 by The American Society of Hematology.

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Year:  2022        PMID: 35167650      PMCID: PMC9164741          DOI: 10.1182/blood.2020009300

Source DB:  PubMed          Journal:  Blood        ISSN: 0006-4971            Impact factor:   25.476


  161 in total

1.  A Child With Dyserythropoietic Anemia and Megakaryocyte Dysplasia Due to a Novel 5'UTR GATA1s Splice Mutation.

Authors:  Jacob Zucker; Constance Temm; Magdalena Czader; Grzegorz Nalepa
Journal:  Pediatr Blood Cancer       Date:  2015-12-29       Impact factor: 3.167

2.  c-mpl mutations are the cause of congenital amegakaryocytic thrombocytopenia.

Authors:  M Ballmaier; M Germeshausen; H Schulze; K Cherkaoui; S Lang; A Gaudig; S Krukemeier; M Eilers; G Strauss; K Welte
Journal:  Blood       Date:  2001-01-01       Impact factor: 22.113

Review 3.  Inherited thrombocytopenias: an updated guide for clinicians.

Authors:  Alessandro Pecci; Carlo L Balduini
Journal:  Blood Rev       Date:  2020-12-01       Impact factor: 8.250

4.  A multiinstitutional survey of the Wiskott-Aldrich syndrome.

Authors:  K E Sullivan; C A Mullen; R M Blaese; J A Winkelstein
Journal:  J Pediatr       Date:  1994-12       Impact factor: 4.406

5.  A nonsynonymous SNP in the ITGB3 gene disrupts the conserved membrane-proximal cytoplasmic salt bridge in the alphaIIbbeta3 integrin and cosegregates dominantly with abnormal proplatelet formation and macrothrombocytopenia.

Authors:  Cedric Ghevaert; Alexandre Salsmann; Nicholas A Watkins; Elisabeth Schaffner-Reckinger; Angela Rankin; Stephen F Garner; Jonathan Stephens; Graham A Smith; Najet Debili; William Vainchenker; Philip G de Groot; James A Huntington; Mike Laffan; Nelly Kieffer; Willem H Ouwehand
Journal:  Blood       Date:  2007-12-07       Impact factor: 22.113

6.  Expanding Use of Clinical Genome Sequencing and the Need for More Data on Implementation.

Authors:  Kathryn A Phillips; Michael P Douglas; Deborah A Marshall
Journal:  JAMA       Date:  2020-11-24       Impact factor: 56.272

7.  Mutation in GNE is associated with severe congenital thrombocytopenia.

Authors:  Jane Futterer; Amanda Dalby; Gillian C Lowe; Ben Johnson; Michael A Simpson; Jayashree Motwani; Mike Williams; Steve P Watson; Neil V Morgan
Journal:  Blood       Date:  2018-06-25       Impact factor: 22.113

8.  Altered translation of GATA1 in Diamond-Blackfan anemia.

Authors:  Leif S Ludwig; Hanna T Gazda; Jennifer C Eng; Stephen W Eichhorn; Prathapan Thiru; Roxanne Ghazvinian; Tracy I George; Jason R Gotlib; Alan H Beggs; Colin A Sieff; Harvey F Lodish; Eric S Lander; Vijay G Sankaran
Journal:  Nat Med       Date:  2014-06-22       Impact factor: 53.440

9.  Sphingolipid dysregulation due to lack of functional KDSR impairs proplatelet formation causing thrombocytopenia.

Authors:  Tadbir K Bariana; Veerle Labarque; Jessica Heremans; Chantal Thys; Mara De Reys; Daniel Greene; Benjamin Jenkins; Luigi Grassi; Denis Seyres; Frances Burden; Deborah Whitehorn; Olga Shamardina; Sofia Papadia; Keith Gomez; Nihr BioResource; Chris Van Geet; Albert Koulman; Willem H Ouwehand; Cedric Ghevaert; Mattia Frontini; Ernest Turro; Kathleen Freson
Journal:  Haematologica       Date:  2018-11-22       Impact factor: 9.941

10.  Defects in TRPM7 channel function deregulate thrombopoiesis through altered cellular Mg(2+) homeostasis and cytoskeletal architecture.

Authors:  Simon Stritt; Paquita Nurden; Remi Favier; Marie Favier; Silvia Ferioli; Sanjeev K Gotru; Judith M M van Eeuwijk; Harald Schulze; Alan T Nurden; Michele P Lambert; Ernest Turro; Stephanie Burger-Stritt; Masayuki Matsushita; Lorenz Mittermeier; Paola Ballerini; Susanna Zierler; Michael A Laffan; Vladimir Chubanov; Thomas Gudermann; Bernhard Nieswandt; Attila Braun
Journal:  Nat Commun       Date:  2016-03-29       Impact factor: 14.919

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