Your selections:
A high-throughput protocol for mutation scanning of the BRCA1 and BRCA2 genes
- Hondow, Heather L., Fox, Stephen B., Mitchell, Gillian, Scott, Rodney J., Beshay, Victoria, Wong, Stephen Q., kConFab Investigators,, Dobrovic, Alexander
An in vivo tumor model exploiting metabolic response as a biomarker for targeted drug development
- Cullinane, C., Dorow, D. S., Kansara, M., Conus, N., Binns, D., Hicks, R. J., Ashman, Leonie K., McArthur, G. A., Thomas, D. M.
- Vilain, R., Braye, S. G., Ashman, L., Scott, R. J.
- Cotton, Richard G. H., Al Aqeel , Aida I., Patrinos, George P., Qi, Ming, Ramesar, Rajkumar S., Scott, Rodney J., Sijmons, Rolf H., Sobrido, Maria-Jesus, Vihinen, Mauno, Al-Mulla, Fahd, Carrera, Paola, Claustres, Mireille, Ekong, Rosemary, Hyland, Valentine J., Macrae, Finlay A., Marafie, Makia J., Paalman, Mark H.
- Cahif, Ashley, Parkinson, Gemma M., Dayas, Christopher V., Smith, Doug W.
Clinical, genetic, and enzymatic characterization of P450 oxidoreductase deficiency in four patients
- Sahakitrungruang, Taninee, Huang, Ningwu, Tee, Meng Kian, Agrawal, Vishal, Russell, William E., Crock, Patricia, Murphy, Nuala, Migeon, Claude J., Miller, Walter L.
- Gronwald, J., Jauch, A., Cybulski, C., Schoell, B., Bohm-Steuer, B., Lener, M., Grabowska, E., Gorski, B., Jakubowska, A., Domagala, W., Chosia, M., Scott, Rodney J, Lubinski, J.
Flecainide prevents catecholaminergic polymorphic ventricular tachycardia in mice and humans
- Watanabe, Hiroshi, Chopra, Nagesh, Laver, Derek, Hwang, Hyun Seok, Davies, Sean S., Roach, Daniel E., Duff, Henry J., Roden, Dan M., Wilde, Arthur A. M., Knollmann, Björn C.
Genetic variants in MUTYH are not associated with endometrial cancer risk
- Ashton, Katie A., Proietto, Anthony, Otton, Geoffrey, Symonds, Ian, Scott, Rodney J.
- Frost, Michelle J., Ferrao, Petranel T., Hughes, Timothy P., Ashman, Leonie K.
MSH6 and PMS2 mutation positive Australian Lynch syndrome families: novel mutations, cancer risk and age of diagnosis of colorectal cancer
- Talseth-Palmer, Bente A., McPhillips, Mary, Groombridge, Claire, Spigelman, Allan, Scott, Rodney J.
Mutation of vertex-magic regular graphs
- Kimberley, J. S., MacDougall, J. A.
Occurrence of c-kit+ tumor cells in hepatitis B virus-associated hepatocellular carcinoma
- Lee, Eung Seok, Han, Eun Mee, Kim, Young-Sik, Shin, Bong Kyung, Kim, Chul Hwan, Kim, Han Kyeom, Won, Nam Hee, Yeom, Bon Woo, Kim, Insun, Leong, Anthony S.-Y.
Recognizable cerebellar dysplasia associated with mutations in multiple tubulin genes
- Oegema, Renske, Cushion, Thomas D., Dobyns, William B., Ishak, Gisele E., Rees, Mark I., Doherty, Dan, Phelps, Ian G., Chung, Seo-Kyung, Dempsey, Jennifer C., Collins, Sarah, Mullins, Jonathan G. L., Dudding, Tracy, Gill, Harinder, Green, Andrew J.
- Gilfillan, Gregor D., Selmer, Kaja K., Sjøholm, Hans, Server, Andres, Samuelsson, Lena, Christianson, Arnold, Tarpey, Patrick, Whibley, Annabel, Stratton, Michael R., Futreal, P. Andrew, Teague, Jon, Edkins, Sarah, Roxrud, Ingrid, Gecz, Jozef, Turner, Gillian, Raymond, F. Lucy, Schwartz, Charles, Stevenson, Roger E., Undlien, Dag E., Strømme, Petter, Smith, Raffaella, Kyllerman, Mårten, Eiklid, Kristin, Kroken, Mette, Mattingsdal, Morten, Egeland, Thore, Stenmark, Harald
Vertex-magic labelings: mutations
- Gray, I. D., MacDougall, James A.
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