These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
47 related articles for article (PubMed ID: 32567678)
1. A Rare MPIG6B Gene Mutation in a Saudi Adolescent Male With Thrombocytopenia, Anemia, and Myelofibrosis: A Case Report. Alasmari BG; Alpakra M; Saeed S; Rayees S; Elzubair L; Aljunaid A Cureus; 2024 Feb; 16(2):e54042. PubMed ID: 38481905 [TBL] [Abstract][Full Text] [Related]
2. SLFN14 ribosomopathy and platelet dysfunction. Lee K; Poncz M Blood; 2023 May; 141(18):2170-2172. PubMed ID: 37140956 [No Abstract] [Full Text] [Related]
3. MPIG6B Gene-Related Myelofibrosis: A Rare Inherited Disease That Is Frequently Described in Arab Population. Attar LJ; Alelaimat A; Alshorman A; Aladily TN Avicenna J Med; 2024 Jan; 14(1):69-72. PubMed ID: 38694137 [TBL] [Abstract][Full Text] [Related]
4. Treatment of congenital thrombocytopenia and decreased collagen reactivity in G6b-B-deficient mice. Mazharian A; Maître B; Bornert A; Hennequin D; Lourenco-Rodrigues M; Geer MJ; Smith CW; Heising S; Walter M; Montel F; Walker LSK; de la Salle H; Watson SP; Gachet C; Senis YA Blood Adv; 2023 Jan; 7(1):46-59. PubMed ID: 36269841 [TBL] [Abstract][Full Text] [Related]
6. Qu S; Zhang D; Xu Z; Jia Y; Qin T; Pan L; Cai W; Zhang Y; Gale RP; Xiao Z Leuk Res Rep; 2022; 17():100303. PubMed ID: 35330689 [TBL] [Abstract][Full Text] [Related]
7. G6b-B regulates an essential step in megakaryocyte maturation. Becker IC; Nagy Z; Manukjan G; Haffner-Luntzer M; Englert M; Heib T; Vögtle T; Gross C; Bharti R; Dietrich S; Mott K; Heck J; Stegmaier S; Baranowsky A; Schinke T; Schlegel N; Heckel T; Stegner D; Pleines I; Ignatius A; Schulze H; Nieswandt B Blood Adv; 2022 May; 6(10):3155-3161. PubMed ID: 35134123 [TBL] [Abstract][Full Text] [Related]
8. A Deep Dive into the Pathology of Gray Platelet Syndrome: New Insights on Immune Dysregulation. Glembotsky AC; De Luca G; Heller PG J Blood Med; 2021; 12():719-732. PubMed ID: 34408521 [TBL] [Abstract][Full Text] [Related]
9. Hematopoietic transcription factor mutations: important players in inherited platelet defects. Songdej N; Rao AK Blood; 2017 May; 129(21):2873-2881. PubMed ID: 28416505 [TBL] [Abstract][Full Text] [Related]
10. Aetiology and outcomes of secondary myelofibrosis occurring in the context of inherited platelet disorders: A single institutional study of four patients. Saliba AN; Ferrer A; Gangat N; Pruthi RK; Tefferi A; Higgins A; Bezerra ED; Buglioni A; Salama ME; Klee EW; Pinto E Vairo F; Mangaonkar A; Majerus J; Chen D; Patnaik MM Br J Haematol; 2020 Sep; 190(5):e316-e320. PubMed ID: 32567678 [No Abstract] [Full Text] [Related]
11. Congenital macrothrombocytopenia with focal myelofibrosis due to mutations in human G6b-B is rescued in humanized mice. Hofmann I; Geer MJ; Vögtle T; Crispin A; Campagna DR; Barr A; Calicchio ML; Heising S; van Geffen JP; Kuijpers MJE; Heemskerk JWM; Eble JA; Schmitz-Abe K; Obeng EA; Douglas M; Freson K; Pondarré C; Favier R; Jarvis GE; Markianos K; Turro E; Ouwehand WH; Mazharian A; Fleming MD; Senis YA Blood; 2018 Sep; 132(13):1399-1412. PubMed ID: 29898956 [TBL] [Abstract][Full Text] [Related]
14. What to do when you suspect an inherited platelet disorder. Lambert MP Hematology Am Soc Hematol Educ Program; 2011; 2011():377-83. PubMed ID: 22160061 [TBL] [Abstract][Full Text] [Related]