Tom Hall Stevens
Affiliations: | 1983- | University of Oregon, Eugene, OR, United States |
Website:
http://molbio.uoregon.edu/facres/stevens.htmlGoogle:
"Tom Hall Stevens"Bio:
https://chemistry.uoregon.edu/profile/tstevens/
https://books.google.com/books?id=-qAvAQAAIAAJ
https://link.springer.com/chapter/10.1007/978-94-009-7049-6_27
Mean distance: (not calculated yet) | S | N | B | C | P |
Cross-listing: Cell Biology Tree
Parents
Sign in to add mentor| Sunney I. Chan | grad student | 1981 | Caltech | |
| (The structure of the metal centers in cytochrome c oxidase.) | ||||
| Randy W. Schekman | post-doc | 1980-1983 | UC Berkeley | |
Children
Sign in to add trainee| Robert Piper | grad student | (Cell Biology Tree) | |
| Joel H. Rothman | grad student | University of Oregon (Cell Biology Tree) | |
| Andrew R. Flannery | grad student | 2005 | University of Oregon (Cell Biology Tree) |
| Mark A. Compton | grad student | 2006 | University of Oregon (Cell Biology Tree) |
| Jillian M. Lottridge | grad student | 2006 | University of Oregon (Cell Biology Tree) |
| Eric N. Senning | grad student | 2009 | University of Oregon (Cell Biology Tree) |
| Nicholas Robert Smith | grad student | 2010 | University of Oregon (Cell Biology Tree) |
| Glen E. Cronan | grad student | 2011 | University of Oregon (Cell Biology Tree) |
| Ryan L. Frei | grad student | 2012 | University of Oregon (Cell Biology Tree) |
| Amy A. Connolly | grad student | 2014 | University of Oregon (Cell Biology Tree) |
| Patricia M. Kane | post-doc | 1988-1991 | University of Oregon |
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Publications
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| Cannata Serio M, Graham LA, Ashikov A, et al. (2020) sMutations in the V-ATPase assembly factor VMA21 cause a congenital disorder of glycosylation with autophagic liver disease. Hepatology (Baltimore, Md.) |
| Guida MC, Hermle T, Graham LA, et al. (2018) ATP6AP2 functions as a V-ATPase assembly factor in the endoplasmic reticulum. Molecular Biology of the Cell. mbcE18040234 |
| Jansen EJ, Timal S, Ryan M, et al. (2016) ATP6AP1 deficiency causes an immunodeficiency with hepatopathy, cognitive impairment and abnormal protein glycosylation. Nature Communications. 7: 11600 |
| Coonrod EM, Graham LA, Carpp LN, et al. (2013) Homotypic vacuole fusion in yeast requires organelle acidification and not the V-ATPase membrane domain. Developmental Cell. 27: 462-8 |
| Finnigan GC, Cronan GE, Park HJ, et al. (2012) Sorting of the yeast vacuolar-type, proton-translocating ATPase enzyme complex (V-ATPase): identification of a necessary and sufficient Golgi/endosomal retention signal in Stv1p. The Journal of Biological Chemistry. 287: 19487-500 |
| Finnigan GC, Hanson-Smith V, Stevens TH, et al. (2012) Evolution of increased complexity in a molecular machine. Nature. 481: 360-4 |
| Finnigan GC, Hanson-Smith V, Houser BD, et al. (2011) The reconstructed ancestral subunit a functions as both V-ATPase isoforms Vph1p and Stv1p in Saccharomyces cerevisiae. Molecular Biology of the Cell. 22: 3176-91 |
| Finnigan GC, Ryan M, Stevens TH. (2011) A genome-wide enhancer screen implicates sphingolipid composition in vacuolar ATPase function in Saccharomyces cerevisiae. Genetics. 187: 771-83 |
| Coonrod EM, Stevens TH. (2010) The yeast vps class E mutants: the beginning of the molecular genetic analysis of multivesicular body biogenesis. Molecular Biology of the Cell. 21: 4057-60 |
| Ryan M, Graham LA, Stevens TH. (2008) Voa1p functions in V-ATPase assembly in the yeast endoplasmic reticulum. Molecular Biology of the Cell. 19: 5131-42 |