Suzanne Schubbert, Ph.D.
Affiliations: | 2007 | Biomedical Sciences | University of California, San Francisco, San Francisco, CA |
Area:
Cell Biology, Molecular BiologyGoogle:
"Suzanne Schubbert"Parents
Sign in to add mentor| Kevin M. Shannon | grad student | 2007 | UCSF | |
| (Biochemical and functional analysis of Ras pathway mutations in myeloid leukemia and developmental disorders.) | ||||
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Publications
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| Rauen KA, Schoyer L, McCormick F, et al. (2010) Proceedings from the 2009 genetic syndromes of the Ras/MAPK pathway: From bedside to bench and back. American Journal of Medical Genetics. Part A. 152: 4-24 |
| Søvik O, Schubbert S, Houge G, et al. (2009) De novo HRAS and KRAS mutations in two siblings with short stature and neuro-cardio-facio-cutaneous features. Bmj Case Reports. 2009 |
| Denayer E, Parret A, Chmara M, et al. (2008) Mutation analysis in Costello syndrome: functional and structural characterization of the HRAS p.Lys117Arg mutation. Human Mutation. 29: 232-9 |
| Schubbert S, Bollag G, Lyubynska N, et al. (2007) Biochemical and functional characterization of germ line KRAS mutations. Molecular and Cellular Biology. 27: 7765-70 |
| Søvik O, Schubbert S, Houge G, et al. (2007) De novo HRAS and KRAS mutations in two siblings with short stature and neuro-cardio-facio-cutaneous features. Journal of Medical Genetics. 44: e84 |
| Schubbert S, Shannon K, Bollag G. (2007) Hyperactive Ras in developmental disorders and cancer Nature Reviews Cancer. 7: 295-308 |
| Schubbert S, Bollag G, Shannon K. (2007) Deregulated Ras signaling in developmental disorders: new tricks for an old dog Current Opinion in Genetics and Development. 17: 15-22 |
| Schubbert S, Shannon K, Bollag G. (2007) Erratum: Hyperactive Ras in developmental disorders and cancer Nature Reviews Cancer. 7: 564-564 |
| Kratz CP, Schubbert S, Bollag G, et al. (2006) Germline mutations in components of the Ras signaling pathway in Noonan syndrome and related disorders. Cell Cycle (Georgetown, Tex.). 5: 1607-11 |
| Schubbert S, Zenker M, Rowe SL, et al. (2006) Germline KRAS mutations cause Noonan syndrome. Nature Genetics. 38: 331-6 |