Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Lucivana P. de Souza Mourão"'
Autor:
Jhemerson F. Paes, Dania G. Torres, Deborah C. Aquino, Emanuela V. B. Alves, Erycka A. Mesquita, Miliane A. Sousa, Nelson Abrahim Fraiji, Leny N. M. Passos, Rosângela S. Abreu, George A. V. Silva, Andréa M. Tarragô, Lucivana P. de Souza Mourão
Publikováno v:
Scientific Reports, Vol 14, Iss 1, Pp 1-10 (2024)
Abstract BCR::ABL1-negative myeloproliferative neoplasms are hematopoietic disorders characterized by panmyelosis. JAK2 V617F is a frequent variant in these diseases and often occurs in the 46/1 haplotype. The G allele of rs10974944 has been shown to
Externí odkaz:
https://doaj.org/article/95614f4076e745c08a357d8364fc9a60
Autor:
Dania G. Torres, Jhemerson Paes, Allyson G. da Costa, Adriana Malheiro, George V. Silva, Lucivana P. de Souza Mourão, Andréa M. Tarragô
Publikováno v:
Biomolecules, Vol 12, Iss 2, p 291 (2022)
The JAK2V617F variant constitutes a genetic alteration of higher frequency in BCR/ABL1 negative chronic myeloproliferative neoplasms, which is caused by a substitution of a G ˃ T at position 1849 and results in the substitution of valine with phenyl
Externí odkaz:
https://doaj.org/article/399b1ff06a8f4b0089f34de4cc2f58c2
Publikováno v:
International journal of molecular sciences. 23(20)
Haplotype 46/1 (GGCC) consists of a set of genetic variations distributed along chromosome 9p.24.1, which extend from the Janus Kinase 2 gene to Insulin like