A dormant TIL phenotype defines non-small cell lung carcinomas sensitive to immune checkpoint blockers von Gettinger, S. N., Choi, J., Mani, N., Sanmamed, M. F., Datar, I., Sowell, Ryan, Du, Victor Y., Kaftan, E., Goldberg, S., Dong, W., Zelterman, D., Politi, K., Kavathas, P., Kaech, S., Yu, X., Zhao, H., Schlessinger, J., Lifton, R., Rimm, D. L., Chen, L., Herbst, R. S., Schalper, K. A.

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Whole-exome sequencing and immune profiling of early-stage lung adenocarcinoma with fully annotated clinical follow-up von Kadara, H, Choi, M, Zhang, J., Parra, E.R., Rodriguez-Canales, J., Gaffney, S.G., Zhao, Z., Behrens, C., Fujimoto, J., Chow, C., Yoo, Y., Kalhor, N., Moran, C., Rimm, D., Swisher, S., Gibbons, D.L., Heymach, J., Kaftan, E., Townsend, J.P., Lynch, T.J., Schlessinger, J., Lee, J., Lifton, R.P., Wistuba, I.I., Herbst, R.S.

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Mutation profiles in early-stage lung squamous cell carcinoma with clinical follow-up and correlation with markers of immune function von Choi, M., Kadara, H., Zhang, J., Parra, E.R., Rodriguez-Canales, J., Gaffney, S.G., Zhao, Z., Behrens, C., Fujimoto, J., Chow, C., Kim, K., Kalhor, N., Moran, C., Rimm, D., Swisher, S., Gibbons, D.L., Heymach, J., Kaftan, E., Townsend, J.P., Lynch, T.J., Schlessinger, J., Lee, J., Lifton, R.P., Herbst, R.S., Wistuba, I.I.

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Modeling non-syndromic autism and the impact of TRPC6 disruption in human neurons von Griesi-Oliveira, K, Acab, A, Gupta, A R, Sunaga, D Y, Chailangkarn, T, Nicol, X, Nunez, Y, Walker, M F, Murdoch, J D, Sanders, S J, Fernandez, T V, Ji, W, Lifton, R P, Vadasz, E, Dietrich, A, Pradhan, D, Song, H, Ming, G-l, Gu, X, Haddad, G, Marchetto, M C N, Spitzer, N, Passos-Bueno, M R, State, M W, Muotri, A R

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Human Hypertension Caused by Mutations in WNK Kinases von Wilson, Frederick H., Disse-Nicodème, Sandra, Choate, Keith A., Ishikawa, Kazuhiko, Nelson-Williams, Carol, Desitter, Isabelle, Gunel, Murat, Milford, David V., Lipkin, Graham W., Achard, Jean-Michel, Feely, Morgan P., Dussol, Bertrand, Berland, Yvon, Unwin, Robert J., Mayan, Haim, Simon, David B., Farfel, Zvi, Jeunemaitre, Xavier, Lifton, Richard P.

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Serial exome analysis of disease progression in premalignant gammopathies von Zhao, S, Choi, M, Heuck, C, Mane, S, Barlogie, B, Lifton, R P, Dhodapkar, M V

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Phenotypic spectrum of autosomal recessive congenital ichthyosis due to PNPLA1 mutation von Boyden, L.M., Craiglow, B.G., Hu, R.H., Zhou, J., Browning, J., Eichenfield, L., Lim, Y.L., Luu, M., Randolph, L.M., Ginarte, M., Fachal, L., Rodriguez‐Pazos, L., Vega, A., Kramer, D., Yosipovitch, G., Vahidnezhad, H., Youssefian, L., Uitto, J., Lifton, R.P., Paller, A.S., Milstone, L.M., Choate, K.A.

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Activating Mineralocorticoid Receptor Mutation in Hypertension Exacerbated by Pregnancy von Geller, David S., Farhi, Anita, Pinkerton, Nikki, Fradley, Michael, Moritz, Michael, Spitzer, Adrian, Meinke, Gretchen, Francis T. F. Tsai, Sigler, Paul B., Lifton, Richard P.

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Paracellin-1, a renal tight junction protein required for paracellular Mg2+ resorption von SIMON, D. B, YIN LU, MCCREDIE, D, MILFORD, D, SANJAD, S, LIFTON, R. P, CHOATE, K. A, VELAZQUEZ, H, AL-SABBAN, E, PRAGA, M, CASARI, G, BETTINELLI, A, COLUSSI, G, RODRIGUEZ-SORIANO, J

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Gitelman's syndrome revisited: An evaluation of symptoms and health-related quality of life von Cruz, Dinna N., Shaer, Andrea J., Bia, Margaret J., Lifton, Richard P., Simon, David B.

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Whole-exome sequencing and immune profiling of early-stage lung adenocarcinoma with fully annotated clinical follow-up von Kadara, H., Choi, M., Zhang, J., Parra, E.R., Rodriguez-Canales, J., Gaffney, S.G., Zhao, Z., Behrens, C., Fujimoto, J., Chow, C., Yoo, Y., Kalhor, N., Moran, C., Rimm, D., Swisher, S., Gibbons, D.L., Heymach, J., Kaftan, E., Townsend, J.P., Lynch, T.J., Schlessinger, J., Lee, J., Lifton, R.P., Wistuba, I.I., Herbst, R.S.

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Molecular Mechanisms of Human Hypertension von Lifton, Richard P., Gharavi, Ali G., Geller, David S.

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Additional support for the association of SLITRK1 var321 and Tourette syndrome von O'Roak, B J, Morgan, T M, Fishman, D O, Saus, E, Alonso, P, Gratacòs, M, Estivill, X, Teltsh, O, Kohn, Y, Kidd, K K, Cho, J, Lifton, R P, State, M W

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The yeast AMP-activated protein kinase Snf1 phosphorylates the inositol polyphosphate kinase Kcs1 von Sunder, Sham, Bauman, Joshua S., Decker, Stuart J., Lifton, Alexandra R., Kumar, Anuj

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Molecular Genetics of Human Blood Pressure Variation von Lifton, Richard P.

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Hypertension caused by a truncated epithelial sodium channel gamma subunit: genetic heterogeneity of Liddle syndrome von Hansson, J.H, Nelson-Williams, C, Suzuki, H, Schild, L, Shimkets, R, Lu, Y, Canessa, C, Iwasaki, T, Rossier, B, Lifton, R.P

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Mutations in the gene encoding B1 subunit of H+-ATPase cause renal tubular acidosis with sensorineural deafness von Karet, Fiona E., Finberg, Karin E., Nelson, Raoul D., Nayir, Ahmet, Mocan, Hilal, Sanjad, Sami A., Rodriguez-Soriano, Juan, Santos, Fernando, Cremers, Cor W.R.J., Pietro, Antonio Di, Hoffbrand, Barry I., Winiarski, Jacek, Bakkaloglu, Aysin, Ozen, Seza, Dusunsel, Ruhan, Goodyer, Paul, Hulton, Sally A., Wu, Doris K., Skvorak, Anne B., Morton, Cynthia C., Cunningham, Michael J., Jha, Vivekanand, Lifton, Richard P.

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IgA nephropathy, the most common cause of glomerulonephritis, is linked to 6q22–23 von Gharavi, Ali G., Yan, Yan, Scolari, Francesco, Schena, F. Paolo, Frasca, Giovanni M., Ghiggeri, Gian Marco, Cooper, Kerry, Amoroso, Antonio, Viola, Battista Fabio, Battini, Graziana, Caridi, Gianluca, Canova, Cristina, Farhi, Anita, Subramanian, Vairavan, Nelson-Williams, Carol, Woodford, Sue, Julian, Bruce A., Wyatt, Robert J., Lifton, Richard P.

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Genetic heterogeneity of Bartter's syndrome revealed by mutations in the K+ channel, ROMK von SIMON, D. B, KARET, F. E, RODRIGUEZ-SORIANO, J, HAMDAN, J. H, DIPIETRO, A, TRACHTMAN, H, SANJAD, S. A, LIFTON, R. P

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