Literature DB >> 30635630

The S505A thrombopoietin receptor mutation in childhood hereditary thrombocytosis and essential thrombocythemia is S505N: single letter amino acid code matters.

Jean-Philippe Defour1,2,3, Gabriel Levy1,2,4, Emilie Leroy1,2, Steven O Smith5, Stefan N Constantinescu6,7.   

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Year:  2019        PMID： 30635630     DOI： 10.1038/s41375-018-0356-x

Source DB:  PubMed          Journal:  Leukemia        ISSN： 0887-6924            Impact factor:   11.528


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  3 in total

Review 1.  In and out: Traffic and dynamics of thrombopoietin receptor.

Authors:  Anita Roy; Saurabh Shrivastva; Saadia Naseer
Journal:  J Cell Mol Med       Date:  2021-08-27       Impact factor: 5.295

2.  Children and Adolescents with Chronic Myeloproliferative Neoplasms: Still an Unmet Biological and Clinical Need?

Authors:  Tariq I Mughal; Michael W Deininger; Nicole Kucine; Giuseppe Saglio; Richard A Van Etten
Journal:  Hemasphere       Date:  2019-08-01

Review 3.  Functional Consequences of Mutations in Myeloproliferative Neoplasms.

Authors:  Stefan N Constantinescu; William Vainchenker; Gabriel Levy; Nicolas Papadopoulos
Journal:  Hemasphere       Date:  2021-06-01
  3 in total

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