Warren D. Kruger, PhD
Affiliations: | 1995- | Fox Chase Cancer Center |
Area:
Human Genetics and DiseaseWebsite:
http://www.fccc.edu/research/pid/kruger/index.htmlGoogle:
"Warren Kruger"Mean distance: 9.82 | S | N | B | C | P |
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Publications
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| Cal-Kayitmazbatir S, Kulkoyluoglu-Cotul E, Growe J, et al. (2020) CRY1-CBS binding regulates circadian clock function and metabolism. The Febs Journal |
| Gupta S, Gallego-Villar L, Wang L, et al. (2019) Analysis of the Qatari R336C Cystathionine β-Synthase Protein in Mice. Journal of Inherited Metabolic Disease |
| Lee HO, Gallego-Villar L, Grisch-Chan HM, et al. (2019) Treatment of CBS deficiency in mice using a minicircle-based naked DNA vector. Human Gene Therapy |
| Ismail HM, Krishnamoorthy N, Al-Dewik N, et al. (2018) In silico and in vivo models for Qatari-Specific classical homocystinuria as basis for development of novel therapies. Human Mutation |
| Gupta S, Kelow S, Wang L, et al. (2018) Mouse modeling and structural analysis of the p.G307S mutation in human cystathionine β-synthase () reveal effects on CBS activity but not stability. The Journal of Biological Chemistry |
| Lee HO, Wang L, Kuo YM, et al. (2018) S-adenosylhomocysteine hydrolase over-expression does not alter S-adenosylmethionine or S-adenosylhomocysteine levels in CBS deficient mice. Molecular Genetics and Metabolism Reports. 15: 15-21 |
| Tang B, Lee HO, An SS, et al. (2018) Specific targeting of MTAP-deleted tumors with a combination of 2'-fluoroadenine and 5'-methylthioadenosine. Cancer Research |
| Majtan T, Jones W, Krijt J, et al. (2017) Enzyme Replacement Therapy Ameliorates Multiple Symptoms of Murine Homocystinuria. Molecular Therapy : the Journal of the American Society of Gene Therapy |
| Gallego-Villar L, Hannibal L, Häberle J, et al. (2017) Cysteamine revisited: repair of arginine to cysteine mutations. Journal of Inherited Metabolic Disease |
| Kruger WD. (2017) Cystathionine β-synthase deficiency: Of mice and men. Molecular Genetics and Metabolism |