Zobrazeno 1 - 10
of 29
pro vyhledávání: '"ETNK1"'
Publikováno v:
Heliyon, Vol 9, Iss 9, Pp e19544- (2023)
MicroRNAs (miRNAs) are small, evolutionarily conserved, non-coding RNAs playing a role in the proliferation, metastasis, apoptosis, chemo-sensitivity, and chemo-resistance of gastric cancer, as well as the stemness of gastric cancer stem cells. miR-7
Externí odkaz:
https://doaj.org/article/c633a4a8ddef4d17a5e2888b89fa8e4d
Lncrna FEZf1-as1 negatively regulates ETNK1 to promote malignant progression of renal cell carcinoma
Publikováno v:
Journal of Medical Biochemistry, Vol 42, Iss 2, Pp 232-238 (2023)
Background: To explore the role of LncFEZF1-AS1 in renal cell carcinoma (RCC) tissues and cells, and the possible molecular mechanism. Methods: Expressions of LncFEZF1-AS1 in RCC tissues and adjacent ones were detected. The association of LncFEZF1-AS
Externí odkaz:
https://doaj.org/article/906d2a3ff5bf49bab56099e1f80b30d9
Publikováno v:
Frontiers in Oncology, Vol 11 (2021)
Atypical chronic myeloid leukemia is a rare disease whose pathogenesis has long been debated. It currently belongs to the group of myelodysplastic/myeloproliferative disorders. In this review, an overview on the current knowledge about diagnosis, pro
Externí odkaz:
https://doaj.org/article/861bc3225c5d4c17958485b0290ca4f5
Publikováno v:
Molecular & Cellular Oncology, Vol 8, Iss 2 (2021)
Recently we showed that Ethanolamine Kinase 1 (ETNK1) mutations cause a decreased synthesis of phosphoethanolamine, and that phosphoethanolamine is able to modulate mitochondrial activity through competition with succinate for complex II. The decreas
Externí odkaz:
https://doaj.org/article/5033e7c733c14b04a7bdfa03a7dd1b4b
Akademický článek
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Autor:
Clizia Chinello, Giovanni Zambrotta, Francesca Fanelli, Roberta Corti, Mi Jang, Steen Larsen, Carlo Gambacorti-Passerini, Rossella Renso, Rocco Piazza, Barbara Crescenzi, Mattia Docci, Lisa Marie Røst, Mayla Bertagna, Cristina Mecucci, Stefania Citterio, Deborah D'Aliberti, Francesco Mantegazza, Fulvio Magni, Ilaria Crespiatico, Guido Cavaletti, Antonio Niro, Diletta Fontana, Delphine Rea, Valeria Cassina, Mario Mauri, Domenico Salerno, Per Bruheim, M Bossi, Luca Nardo, Luca Massimino
ETNK1 kinase is responsible for the phosphorylation of ethanolamine to phosphoethanolamine (P-Et) (Kennedy, 1956, J Biol Chem). Recurrent somatic mutations occurring on ETNK1 were identified in about 13% of patients affected by atypical chronic myelo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::578629e64fd8f76dcfc678e902a04e43
https://hdl.handle.net/11380/1249547
https://hdl.handle.net/11380/1249547
Integrated Genomic, Functional, and Prognostic Characterization of Atypical Chronic Myeloid Leukemia
Autor:
Emilio Usala, Giovanni Caocci, Daniele Ramazzotti, Alessandra Pirola, Leonardo Campiotti, Alessandro Morotti, Fabio Stagno, Roberto A. Perego, Silvia Bungaro, Cristina Mastini, Fabio Pagni, Silvia Bombelli, Fabio Ciceri, Vera Magistroni, Bruno Martino, Michele Merli, Antonio Niro, Sara Redaelli, Delphine Rea, Luca Mologni, Rocco Piazza, Diletta Fontana, Virginia Brambilla, Elena Maria Elli, Andrea Aroldi, Carlo Gambacorti-Passerini, Marco Bregni, Luca Massimino, Monica Fumagalli, Francesco Onida
Publikováno v:
HemaSphere
HemaSphere, Vol 4, Iss 6, p e497 (2020)
HemaSphere, Vol 4, Iss 6, p e497 (2020)
Supplemental Digital Content is available for this article.
Atypical chronic myeloid leukemia (aCML) is a BCR-ABL1-negative clonal disorder, which belongs to the myelodysplastic/myeloproliferative group. This disease is characterized by recurren
Atypical chronic myeloid leukemia (aCML) is a BCR-ABL1-negative clonal disorder, which belongs to the myelodysplastic/myeloproliferative group. This disease is characterized by recurren
Akademický článek
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Autor:
Fontana, D, Mauri, M, Niro, A, Massimino, L, Bertagna, M, Zambrotta, G, Bossi, M, CITTERIO, STEFANIA, Crescenzi, B, Signore, G, Piazza, V, Mecucci, C, Cavaletti, G, Rea, D, Gambacorti-Passerini, C, Piazza, R
Atypical chronic myeloid leukemia (aCML) is a clonal disorder belonging to the myelodysplastic/myeloproliferative syndromes. About 13% of aCML cases carry somatic mutations in ETNK1 gene, encoding for H243Y, N244S, and G245V substitutions. We previou
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______1299::68e62819e201d4148f58dea112c1706b
http://hdl.handle.net/10281/205010
http://hdl.handle.net/10281/205010