Comprehensive whole-genome sequencing of an early-stage primary myelofibrosis patient defines low mutational burden and non-recurrent candidate genes

In order to identify novel somatic mutations associated with classic BCR/ABL1-negative myeloproliferative neoplasms, we performed high-coverage genome sequencing of DNA from peripheral blood granulocytes and cultured skin fibroblasts from a patient with MPL W515K-positive primary myelofibrosis. The...

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Hlavní autoři: Merker, Jason D., Roskin, Krishna M., Ng, Dana, Pan, Cuiping, Fisk, Dianna G., King, Jasmine J., Hoh, Ramona, Stadler, Michael, Okumoto, Lawrence M., Abidi, Parveen, Hewitt, Rhonda, Jones, Carol D., Gojenola, Linda, Clark, Michael J., Zhang, Bing, Cherry, Athena M., George, Tracy I., Snyder, Michael, Boyd, Scott D., Zehnder, James L., Fire, Andrew Z., Gotlib, Jason
Médium: Artigo
Jazyk:Inglês
Vydáno: Ferrata Storti Foundation 2013
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On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC3815168/
https://ncbi.nlm.nih.gov/pubmed/23872309
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3324/haematol.2013.092379
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