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5. Mpl Baltimore: a thrombopoietin receptor polymorphism associated with thrombocytosis. Moliterno AR; Williams DM; Gutierrez-Alamillo LI; Salvatori R; Ingersoll RG; Spivak JL Proc Natl Acad Sci U S A; 2004 Aug; 101(31):11444-7. PubMed ID: 15269348 [TBL] [Abstract][Full Text] [Related]
6. Identification of Bellanné-Chantelot C; Mosca M; Marty C; Favier R; Vainchenker W; Plo I Front Endocrinol (Lausanne); 2017; 8():235. PubMed ID: 28979237 [TBL] [Abstract][Full Text] [Related]
7. Evidence for a founder effect of the MPL-S505N mutation in eight Italian pedigrees with hereditary thrombocythemia. Liu K; Martini M; Rocca B; Amos CI; Teofili L; Giona F; Ding J; Komatsu H; Larocca LM; Skoda RC Haematologica; 2009 Oct; 94(10):1368-74. PubMed ID: 19608689 [TBL] [Abstract][Full Text] [Related]
8. Unexplained thrombocytosis: association of Baltimore polymorphism with germline MPL nonsense mutation. Verger E; Teillet F; Conejero C; Letort G; Chomienne C; Giraudier S; Cassinat B Br J Haematol; 2016 Oct; 175(1):167-9. PubMed ID: 26568271 [No Abstract] [Full Text] [Related]
9. Germ-line JAK2 mutations in the kinase domain are responsible for hereditary thrombocytosis and are resistant to JAK2 and HSP90 inhibitors. Marty C; Saint-Martin C; Pecquet C; Grosjean S; Saliba J; Mouton C; Leroy E; Harutyunyan AS; Abgrall JF; Favier R; Toussaint A; Solary E; Kralovics R; Constantinescu SN; Najman A; Vainchenker W; Plo I; Bellanné-Chantelot C Blood; 2014 Feb; 123(9):1372-83. PubMed ID: 24398328 [TBL] [Abstract][Full Text] [Related]
10. An incomplete trafficking defect to the cell-surface leads to paradoxical thrombocytosis for human and murine MPL P106L. Favale F; Messaoudi K; Varghese LN; Boukour S; Pecquet C; Gryshkova V; Defour JP; Albu RI; Bluteau O; Ballerini P; Leverger G; Plo I; Debili N; Raslova H; Favier R; Constantinescu SN; Vainchenker W Blood; 2016 Dec; 128(26):3146-3158. PubMed ID: 28034873 [TBL] [Abstract][Full Text] [Related]
11. Clinical course of myeloproliferative leukaemia virus oncogene (MPL) mutation-associated familial thrombocytosis: a review of 64 paediatric and adult patients. Al-Harbi T; Al-Zahrani M; Al-Balwi M; Al-Hazmi A; Alsuhaibani A; Aljafn N; Alsumari F; Aleshaiwi L; Alsuhibani A; Alqasim O; Ahmad N Br J Haematol; 2021 Sep; 194(5):893-898. PubMed ID: 34131895 [TBL] [Abstract][Full Text] [Related]
12. A family with hereditary thrombocythaemia and normal genes for thrombopoietin and c-Mpl. Tecuceanu N; Dardik R; Rabizadeh E; Raanani P; Inbal A Br J Haematol; 2006 Nov; 135(3):348-51. PubMed ID: 16995886 [TBL] [Abstract][Full Text] [Related]
13. Hereditary thrombocytosis caused by MPLSer505Asn is associated with a high thrombotic risk, splenomegaly and progression to bone marrow fibrosis. Teofili L; Giona F; Torti L; Cenci T; Ricerca BM; Rumi C; Nunes V; Foà R; Leone G; Martini M; Larocca LM Haematologica; 2010 Jan; 95(1):65-70. PubMed ID: 19713221 [TBL] [Abstract][Full Text] [Related]
14. Hereditary erythrocytosis, thrombocytosis and neutrophilia. Hong WJ; Gotlib J Best Pract Res Clin Haematol; 2014 Jun; 27(2):95-106. PubMed ID: 25189721 [TBL] [Abstract][Full Text] [Related]
15. Compound heterozygous c-Mpl mutations in a child with congenital amegakaryocytic thrombocytopenia: functional characterization and a review of the literature. Fox NE; Chen R; Hitchcock I; Keates-Baleeiro J; Frangoul H; Geddis AE Exp Hematol; 2009 Apr; 37(4):495-503. PubMed ID: 19302922 [TBL] [Abstract][Full Text] [Related]
18. Rapid detection of MPL Baltimore using LightCycler technology and melting curve analysis. Standen G; Clench T Br J Haematol; 2008 Mar; 140(6):714-6. PubMed ID: 18302717 [No Abstract] [Full Text] [Related]
19. A de novo splice donor mutation in the thrombopoietin gene causes hereditary thrombocythemia in a Polish family. Liu K; Kralovics R; Rudzki Z; Grabowska B; Buser AS; Olcaydu D; Gisslinger H; Tiedt R; Frank P; Okoñ K; van der Maas AP; Skoda RC Haematologica; 2008 May; 93(5):706-14. PubMed ID: 18367486 [TBL] [Abstract][Full Text] [Related]
20. MPL Baltimore mutation and thrombocytosis: case report and literature review. Shkalim-Zemer V; Dgany O; Krasnov T; Yacobovich J; Tamary H J Pediatr Hematol Oncol; 2013 Apr; 35(3):e112-4. PubMed ID: 23511495 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]