Comparative analysis of algorithms for identifying amplifications and deletions in array CGH data von Lai, Weil R., Johnson, Mark D., Kucherlapati, Raju, Park, Peter J.

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Converging evidence for a pseudoautosomal cytokine receptor gene locus in schizophrenia von LENCZ, T, MORGAN, T. V, ATHANASIOU, M, DAIN, B, REED, C. R, KANE, J. M, KUCHERLAPATI, R, MAIHOTRA, A. K

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A novel mouse model of cerebral cavernous malformations based on the two-hit mutation hypothesis recapitulates the human disease von MCDONALD, David A, SHENKAR, Robert, MARCHUK, Douglas A, SHI, Changbin, STOCKTON, Rebecca A, AKERS, Amy L, KUCHERLAPATI, Melanie H, KUCHERLAPATI, Raju, BRAINER, James, GINSBERG, Mark H, AWAD, Issam A

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Mutations in PTPN11 , encoding the protein tyrosine phosphatase SHP-2, cause Noonan syndrome von Tartaglia, Marco, Mehler, Ernest L, Goldberg, Rosalie, Zampino, Giuseppe, Brunner, Han G, Kremer, Hannie, van der Burgt, Ineke, Crosby, Andrew H, Ion, Andra, Jeffery, Steve, Kalidas, Kamini, Patton, Michael A, Kucherlapati, Raju S, Gelb, Bruce D

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Reduced fractional anisotropy and axial diffusivity in white matter in 22q11.2 deletion syndrome: A pilot study von Kikinis, Z, Asami, T, Bouix, S, Finn, C.T, Ballinger, T, Tworog-Dube, E, Kucherlapati, R, Kikinis, R, Shenton, M.E, Kubicki, M

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Molecular Definition of 22q11 Deletions in 151 Velo-Cardio-Facial Syndrome Patients von Carlson, C., Sirotkin, H., Pandita, R., Goldberg, R., McKie, J., Wadey, R., Patanjali, S.R., Weissman, S.M., Anyane-Yeboa, K., Warburton, D., Scambler, P., Shprintzen, R., Kucherlapati, R., Morrow, B.E.

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Tumor progression in Apc(1638N) mice with Exo1 and Fen1 deficiencies von Kucherlapati, M, Nguyen, A, Kuraguchi, M, Yang, K, Fan, K, Bronson, R, Wei, K, Lipkin, M, Edelmann, W, Kucherlapati, R

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Over-expression of a human chromosome 22q11.2 segment including TXNRD2, COMT and ARVCF developmentally affects incentive learning and working memory in mice von Suzuki, Go, Harper, Kathryn M., Hiramoto, Takeshi, Funke, Birgit, Lee, MoonSook, Kang, Gina, Buell, Mahalah, Geyer, Mark A., Kucherlapati, Raju, Morrow, Bernice, Männistö, Pekka T., Agatsuma, Soh, Hiroi, Noboru

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Apc1638T: a mouse model delineating critical domains of the adenomatous polyposis coli protein involved in tumorigenesis and development von Smits, R, Kielman, M F, Breukel, C, Zurcher, C, Neufeld, K, Jagmohan-Changur, S, Hofland, N, van Dijk, J, White, R, Edelmann, W, Kucherlapati, R, Khan, P M, Fodde, R

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Mutations in the activin receptor-like kinase 1 gene in hereditary haemorrhagic telangiectasia type 2 von Johnson, D.W, Berg, J.N, Baldwin, M.A, Gallione, C.J, Marondel, I, Yoon, S.-J, Stenzel, T.T, Speer, M, Pericak-Vance, M.A, Diamond, A, Guttmacher, A.E, Jackson, C.E, Attisano, L, Kucherlapati, R, Porteous, M.E.M, Marchuk, D.A

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Mutations in human cause limb and cardiac malformation in Holt-Oram syndrome von Basson1, Craig T, Bachinsky, David R, Lin, Robert C, Levi, Tatjana, Elkins, Jacob A, Soults, Johann, Grayzel, David, Kroumpouzou, Elena, Traill, Thomas A, Leblanc-Straceski, Janine, Renault, Beatrice, Kucherlapati, Raju, J.G, Seidman, Seidman, Christine E

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Obesity enhances gastrointestinal tumorigenesis in Apc-mutant mice von Gravaghi, C, Bo, J, LaPerle, K.M.D, Quimby, F, Kucherlapati, R, Edelmann, W, Lamprecht, S.A

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Cardiovascular disease in Noonan syndrome von Prendiville, Terence W, Gauvreau, Kimberlee, Tworog-Dube, Erica, Patkin, Lynne, Kucherlapati, Raju S, Roberts, Amy E, Lacro, Ronald V

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The Murine N-ras Gene is not Essential for Growth and Development von Umanoff, Heywood, Edelmann, Winfried, Pellicer, Angel, Kucherlapati, Raju

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A mutation in a case of early onset narcolepsy and a generalized absence of hypocretin peptides in human narcoleptic brains von Mignot, Emmanuel, Peyron, Christelle, Faraco, Juliette, Rogers, William, Ripley, Beth, Overeem, Sebastiaan, Charnay, Yves, Nevsimalova, Sona, Aldrich, Michael, Reynolds, David, Albin, Roger, Li, Robin, Hungs, Marcel, Pedrazzoli, Mario, Padigaru, Muralidhara, Kucherlapati, Melanie, Fan, Jun, Maki, Richard, Lammers, Gert Jan, Bouras, Constantin, Kucherlapati, Raju, Nishino, Seiji

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Mutation analysis of Son of Sevenless in juvenile myelomonocytic leukemia von Kratz, C P, Niemeyer, C M, Thomas, C, Bauhuber, S, Matejas, V, Bergsträsser, E, Flotho, C, Flores, N J, Haas, O, Hasle, H, van den Heuvel-Eibrink, M M, Kucherlapati, R S, Lang, P, Roberts, A E, Starý, J, Strahm, B, Swanson, K D, Trebo, M, Zecca, M, Neel, B, Locatelli, F, Loh, M L, Zenker, M

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Experimental autoimmune encephalomyelitis in mice lacking glial fibrillary acidic protein is characterized by a more severe clinical course and an infiltrative central nervous syst... von Liedtke, W, Edelmann, W, Chiu, FC, Kucherlapati, R, Raine, CS

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(ps1) Personalized Medicine: Opportunities and Challenges von Kucherlapati, R.

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Colorectal Cancer in Mice Genetically Deficient in the Mucin Muc2 von Velcich, Anna, Yang, WanCai, Heyer, Joerg, Fragale, Alessandra, Nicholas, Courtney, Viani, Stephanie, Kucherlapati, Raju, Lipkin, Martin, Yang, Kan, Augenlicht, Leonard

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Differential gene expression following early renal ischemia/reperfusion von Supavekin, Suroj, Zhang, Weijia, Kucherlapati, Raju, Kaskel, Frederick J., Moore, Leon C., Devarajan, Prasad

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