Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Manoo Bhakta"'
Publikováno v:
Biotechnology Progress. 36
We propose an integrated structural approach to search potential aptamer molecules for targeting cancer receptor proteins. We used the outer cellular domain of the B-lymphocyte antigen, CD19, as the target for this study. First, using available prote
Publikováno v:
Journal of pediatric hematology/oncology. 42(4)
Phosphoglycerate kinase (PGK) is glycolytic enzyme critical in the creation of adenosine triphosphate. Mutations in the gene for this enzyme, PGK1, are associated with PGK deficiency, which is characterized by neurologic symptoms, nonhereditary spher
Publikováno v:
Journal of Blood Disorders & Transfusion.
Autor:
D. Ashley Hill, Arie Perry, Christine E. Fuller, Lars M. Wagner, Jeffrey S. Dome, Márcia Pedrosa, Manoo Bhakta
Publikováno v:
Journal of Pediatric Hematology/Oncology. 24:385-388
Metastatic rhabdoid tumor of the kidney (RTK) is a highly lethal malignancy; only one survivor with stage 4 disease has been reported. The authors reviewed the cases of two patients with metastatic RTK who had excellent responses to therapy. Both pat
Autor:
Susan M. Colman, Anthony M. Ford, Elisabeth R. van Wering, Richard Hain, Lyndal Kearney, Bryan D. Young, Christine J. Harrison, Tracy Chaplin, Tim Eden, Manoo Bhakta, Caroline M. Bateman, Philip Ancliff, Eric J. Gratias, Giovanni Cazzaniga, Mel Greaves
Chimeric fusion genes are highly prevalent in childhood acute lymphoblastic leukemia (ALL) and are mostly prenatal, early genetic events in the evolutionary trajectory of this cancer. ETV6-RUNX1–positive ALL also has multiple (∼ 6 per case) copy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e2423697aa4d745e47a3cec6c062d8c8
http://hdl.handle.net/10281/299717
http://hdl.handle.net/10281/299717
Publikováno v:
Journal of pediatric hematology/oncology. 24(9)
A 13-year-old boy and a 16-year-old girl both presented with headaches and nausea after they were diagnosed with severe acquired aplastic anemia. Both patients had symptoms and signs consistent with the clinical syndrome of pseudotumor cerebri includ
Publikováno v:
Blood. 112:597-597
DNA methylation as a source for epigenetic variability has been implicated in a variety of different cancer types. Often these studies are confounded by inter-individual differences in the epigenetic profiles. The pattern of epigenetic marks can be a