Cargando…
Nonfamilial, MPL S505N-Mutated Essential Thrombocythaemia
Mutations of MPL are present in a significant proportion of patients with the myeloproliferative neoplasms (MPN), primary myelofibrosis (PMF), and essential thrombocythaemia (ET). The most frequent of these mutations, W515L and W515K, occur in exon 10 of MPL, which encodes the receptor for thrombopo...
Autores principales: | Morrell, Ruth, Langabeer, Stephen E., Smyth, Liam, Perera, Meegahage, Crotty, Gerard |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2013
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3732633/ https://www.ncbi.nlm.nih.gov/pubmed/23970983 http://dx.doi.org/10.1155/2013/729327 |
Ejemplares similares
-
Can post-splenectomy thrombocytosis mask essential thrombocythaemia?
por: Langabeer, Stephen E.
Publicado: (2020) -
MPL S505C enhances driver mutations at W515 in essential thrombocythemia
por: Varghese, Leila N., et al.
Publicado: (2021) -
Headache in essential thrombocythaemia
por: Frewin, R, et al.
Publicado: (2012) -
Unrecognized pseudohyperkalaemia in essential thrombocythaemia
por: Mannu, Gurdeep Singh, et al.
Publicado: (2011) -
MPL exon 10 mutations in Irish patients with a suspected myeloproliferative neoplasm
por: Lee Tokar, Lisa, et al.
Publicado: (2021)