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Results 1-10 of 37 (Search time: 0.002 seconds).
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PreviewIssue DateTitleAuthor(s)
2020Drosophila as a model to understand autophagy deregulation in human disordersDenton, D.; O'Keefe, L.; Kumar, S.; Martinez, A.B.; Galluzzi, L.
2020Molecular patterns of response and treatment failure after frontline venetoclax combinations in older patients with AMLDiNardo, C.D.; Tiong, I.S.; Quaglieri, A.; MacRaild, S.; Loghavi, S.; Brown, F.C.; Thijssen, R.; Pomilio, G.; Ivey, A.; Salmon, J.; Glytsou, C.; Fleming, S.A.; Zhang, Q.; Ma, H.; Patel, K.P.; Kornblau, S.M.; Xu, Z.; Chua, C.C.; Chen, X.; Blombery, P.; et al.
2020Grass-specific EPAD1 is essential for pollen exine patterning in riceLi, H.J.; Kim, Y.J.; Yang, L.; Liu, Z.; Zhang, J.; Shi, H.; Huang, G.; Persson, S.; Zhang, D.; Liang, W.
2023Next-Generation JAK2 Inhibitors for the Treatment of Myeloproliferative Neoplasms: Lessons from Structure-Based Drug Discovery ApproachesNair, P.C.; Piehler, J.; Tvorogov, D.; Ross, D.M.; Lopez, A.F.; Gotlib, J.; Thomas, D.
2021A framework for high-resolution phenotyping of candidate male infertility mutants: from human to mouseHouston, B.J.; Conrad, D.F.; O'Bryan, M.K.
2020Phenotypic characterization and comparison of Phe508del and cystic fibrosis transmembrane conductance regulator (CFTR) knockout rat models of cystic fibrosis generated by CRISPR/Cas9 gene editingMcCarron, A.; Cmielewski, P.; Reyne, N.; McIntyre, C.; Finnie, J.; Craig, F.; Rout-Pitt, N.; Delhove, J.; Schjenken, J.E.; Chan, H.Y.; Boog, B.; Knight, E.; Gilmore, R.C.; O'Neal, W.K.; Boucher, R.C.; Parsons, D.; Donnelley, M.
2020Heterozygous rare genetic variants in non-syndromic early-onset obesitySerra-Juhé, C.; Martos-Moreno, G.; Bou de Pieri, F.; Flores, R.; Chowen, J.A.; Pérez-Jurado, L.A.; Argente, J.
2020Manganese import protects Salmonella enterica serovar Typhimurium against nitrosative stressYousuf, S.; Karlinsey, J.E.; Neville, S.L.; McDevitt, C.A.; Libby, S.J.; Fang, F.C.; Frawley, E.R.
2020RUNX1-mutated families show phenotype heterogeneity and a somatic mutation profile unique to germline predisposed AMLBrown, A.L.; Arts, P.; Carmichael, C.L.; Babic, M.; Dobbins, J.; Chong, C.-E.; Schreiber, A.W.; Feng, J.; Phillips, K.; Wang, P.P.S.; Ha, T.; Homan, C.C.; King-Smith, S.L.; Rawlings, L.; Vakulin, C.; Dubowsky, A.; Burdett, J.; Moore, S.; McKavanagh, G.; Henry, D.; et al.
2021RUNX1 mutations in blast-phase chronic myeloid leukemia associate with distinct phenotypes, transcriptional profiles, and drug responsesAdnan Awad, S.; Dufva, O.; Ianevski, A.; Ghimire, B.; Koski, J.; Maliniemi, P.; Thomson, D.; Schreiber, A.; Heckman, C.A.; Koskenvesa, P.; Korhonen, M.; Porkka, K.; Branford, S.; Aittokallio, T.; Kankainen, M.; Mustjoki, S.