1 - 25 of
112
results
for author:"Kucherlapati R."
in Literature Citations
| A role for the CHC22 clathrin heavy-chain isoform in human glucose metabolism. Vassilopoulos S., Esk C., Hoshino S., Funke B.H., Chen C.Y., Plocik A.M., Wright W.E., Kucherlapati R., Brodsky F.M. Science 324:1192-1196(2009) · Mapped (4) |
| Apc inhibition of Wnt signaling regulates supernumerary tooth formation during embryogenesis and throughout adulthood. Wang X.P., O'Connell D.J., Lund J.J., Saadi I., Kuraguchi M., Turbe-Doan A., Cavallesco R., Kim H., Park P.J., Harada H. et al. Development 136:1939-1949(2009) · Mapped (32) |
| Lack of lymphatic vessel phenotype in LYVE-1/CD44 double knockout mice. Luong M.X., Tam J., Lin Q., Hagendoorn J., Moore K.J., Padera T.P., Seed B., Fukumura D., Kucherlapati R., Jain R.K. J. Cell. Physiol. 219:430-437(2009) · Mapped (12) |
| Loss of Rb1 in the gastrointestinal tract of Apc1638N mice promotes tumors of the cecum and proximal colon. Kucherlapati M.H., Yang K., Fan K., Kuraguchi M., Sonkin D., Rosulek A., Lipkin M., Bronson R.T., Aronow B.J., Kucherlapati R. Proc. Natl. Acad. Sci. U.S.A. 105:15493-15498(2008) · Mapped (13) |
| Obesity enhances gastrointestinal tumorigenesis in Apc-mutant mice. Gravaghi C., Bo J., Laperle K.M., Quimby F., Kucherlapati R., Edelmann W., Lamprecht S.A. Int J Obes (Lond) 32:1716-1719(2008) · Mapped (10) |
| Dietary calcium and cholecalciferol modulate cyclin D1 expression, apoptosis, and tumorigenesis in intestine of adenomatous polyposis coli1638N/+ mice. Yang K., Lamprecht S.A., Shinozaki H., Fan K., Yang W., Newmark H.L., Kopelovich L., Edelmann W., Jin B., Gravaghi C. et al. J. Nutr. 138:1658-1663(2008) · Mapped (11) |
| Novel roles for MLH3 deficiency and TLE6-like amplification in DNA mismatch repair-deficient gastrointestinal tumorigenesis and progression. Chen P.C., Kuraguchi M., Velasquez J., Wang Y., Yang K., Edwards R., Gillen D., Edelmann W., Kucherlapati R., Lipkin S.M. PLoS Genet. 4:e1000092-e1000092(2008) · Mapped (30) |
| Role of the mismatch repair gene, Msh6, in suppressing genome instability and radiation-induced mutations. Barrera-Oro J., Liu T.Y., Gorden E., Kucherlapati R., Shao C., Tischfield J.A. Mutat. Res. 642:74-79(2008) · Mapped (9) |
| Shared genetic causes of cardiac hypertrophy in children and adults. Morita H., Rehm H.L., Menesses A., McDonough B., Roberts A.E., Kucherlapati R., Towbin J.A., Seidman J.G., Seidman C.E. N. Engl. J. Med. 358:1899-1908(2008) · UniProtKB (3) · Mapped (53) |
| Mutation frequencies and spectra in DNA polymerase eta-deficient mice. Busuttil R.A., Lin Q., Stambrook P.J., Kucherlapati R., Vijg J. Cancer Res. 68:2081-2084(2008) · Mapped (1) |
| Distinct effects of the recurrent Mlh1G67R mutation on MMR functions, cancer, and meiosis. Avdievich E., Reiss C., Scherer S.J., Zhang Y., Maier S.M., Jin B., Hou H. Jr., Rosenwald A., Riedmiller H., Kucherlapati R. et al. Proc. Natl. Acad. Sci. U.S.A. 105:4247-4252(2008) · Mapped (5) |
| Runs of homozygosity reveal highly penetrant recessive loci in schizophrenia. Lencz T., Lambert C., DeRosse P., Burdick K.E., Morgan T.V., Kane J.M., Kucherlapati R., Malhotra A.K. Proc. Natl. Acad. Sci. U.S.A. 104:19942-19947(2007) · Mapped (27) |
| SOS1 mutations are rare in human malignancies: implications for Noonan Syndrome patients. Swanson K.D., Winter J.M., Reis M., Bentires-Alj M., Greulich H., Grewal R., Hruban R.H., Yeo C.J., Yassin Y., Iartchouk O. et al. Genes Chromosomes Cancer 47:253-259(2008) · Mapped (6) |
| Analysis of TBX1 variation in patients with psychotic and affective disorders. Funke B.H., Lencz T., Finn C.T., DeRosse P., Poznik G.D., Plocik A.M., Kane J., Rogus J., Malhotra A.K., Kucherlapati R. Mol. Med. 13:407-414(2007) · Mapped (4) |
| COMT genotype increases risk for bipolar I disorder and influences neurocognitive performance. Burdick K.E., Funke B., Goldberg J.F., Bates J.A., Jaeger J., Kucherlapati R., Malhotra A.K. Bipolar Disord 9:370-376(2007) · Mapped (8) |
| Converging evidence for a pseudoautosomal cytokine receptor gene locus in schizophrenia. Lencz T., Morgan T.V., Athanasiou M., Dain B., Reed C.R., Kane J.M., Kucherlapati R., Malhotra A.K. Mol. Psychiatry 12:572-580(2007) · Mapped (7) |
| Tumor progression in Apc(1638N) mice with Exo1 and Fen1 deficiencies. Kucherlapati M., Nguyen A., Kuraguchi M., Yang K., Fan K., Bronson R., Wei K., Lipkin M., Edelmann W., Kucherlapati R. Oncogene 26:6297-6306(2007) · Mapped (15) |
| Mutation analysis of Son of Sevenless in juvenile myelomonocytic leukemia. Kratz C.P., Niemeyer C.M., Thomas C., Bauhuber S., Matejas V., Bergstrasser E., Flotho C., Flores N.J., Haas O., Hasle H. et al. Leukemia 21:1108-1109(2007) · Mapped (6) |
| Response to treatment and survival of patients with non-small cell lung cancer undergoing somatic EGFR mutation testing. Sequist L.V., Joshi V.A., Janne P.A., Muzikansky A., Fidias P., Meyerson M., Haber D.A., Kucherlapati R., Johnson B.E., Lynch T.J. Oncologist 12:90-98(2007) · Mapped (15) |
| Germline gain-of-function mutations in SOS1 cause Noonan syndrome. Roberts A.E., Araki T., Swanson K.D., Montgomery K.T., Schiripo T.A., Joshi V.A., Li L., Yassin Y., Tamburino A.M., Neel B.G. et al. |
| Participation of mouse DNA polymerase iota in strand-biased mutagenic bypass of UV photoproducts and suppression of skin cancer. Dumstorf C.A., Clark A.B., Lin Q., Kissling G.E., Yuan T., Kucherlapati R., McGregor W.G., Kunkel T.A. Proc. Natl. Acad. Sci. U.S.A. 103:18083-18088(2006) · Mapped (7) |
| DTNBP1 genotype influences cognitive decline in schizophrenia. Burdick K.E., Goldberg T.E., Funke B., Bates J.A., Lencz T., Kucherlapati R., Malhotra A.K. Schizophr. Res. 89:169-172(2007) · Mapped (2) |
| Genomic analysis reveals that Pseudomonas aeruginosa virulence is combinatorial. Lee D.G., Urbach J.M., Wu G., Liberati N.T., Feinbaum R.L., Miyata S., Diggins L.T., He J., Saucier M., Deziel E. et al. Genome Biol. 7:R90.1-R90.14(2006) · UniProtKB (5,886) |
| Adenomatous polyposis coli (APC) is required for normal development of skin and thymus. Kuraguchi M., Wang X.P., Bronson R.T., Rothenberg R., Ohene-Baah N.Y., Lund J.J., Kucherlapati M., Maas R.L., Kucherlapati R. PLoS Genet. 2:e146-e146(2006) · Mapped (18) |
| COMT genotype and manic symptoms in schizophrenia. DeRosse P., Funke B., Burdick K.E., Lencz T., Goldberg T.E., Kane J.M., Kucherlapati R., Malhotra A.K. Schizophr. Res. 87:28-31(2006) · Mapped (8) |
