Mineralocorticoid Receptor Phosphorylation Regulates Ligand Binding and Renal Response to Volume Depletion and Hyperkalemia von Shibata, Shigeru, Rinehart, Jesse, Zhang, Junhui, Moeckel, Gilbert, Castañeda-Bueno, María, Stiegler, Amy L., Boggon, Titus J., Gamba, Gerardo, Lifton, Richard P.

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Exome sequencing identifies recurrent mutations in NF1 and RASopathy genes in sun-exposed melanomas von Krauthammer, Michael, Kong, Yong, Bacchiocchi, Antonella, Evans, Perry, Pornputtapong, Natapol, Wu, Cen, McCusker, Jamie P, Ma, Shuangge, Cheng, Elaine, Straub, Robert, Serin, Merdan, Bosenberg, Marcus, Ariyan, Stephan, Narayan, Deepak, Sznol, Mario, Kluger, Harriet M, Mane, Shrikant, Schlessinger, Joseph, Lifton, Richard P, Halaban, Ruth

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Kelch-like 3 and Cullin 3 regulate electrolyte homeostasis via ubiquitination and degradation of WNK4 von Shibata, Shigeru, Zhang, Junhui, Puthumana, Jeremy, Stone, Kathryn L., Lifton, Richard P.

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Mutation of NLRC4 causes a syndrome of enterocolitis and autoinflammation von Romberg, Neil, Al Moussawi, Khatoun, Nelson-Williams, Carol, Stiegler, Amy L, Loring, Erin, Choi, Murim, Overton, John, Meffre, Eric, Khokha, Mustafa K, Huttner, Anita J, West, Brian, Podoltsev, Nikolai A, Boggon, Titus J, Kazmierczak, Barbara I, Lifton, Richard P

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Early and multiple origins of metastatic lineages within primary tumors von Zhao, Zi-Ming, Zhao, Bixiao, Bai, Yalai, Iamarino, Atila, Gaffney, Stephen G., Schlessinger, Joseph, Lifton, Richard P., Rimm, David L., Townsend, Jeffrey P.

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Calcineurin dephosphorylates Kelch-like 3, reversing phosphorylation by angiotensin II and regulating renal electrolyte handling von Ishizawa, Kenichi, Wang, Qin, Li, Jinping, Yamazaki, Osamu, Tamura, Yoshifuru, Fujigaki, Yoshihide, Uchida, Shunya, Lifton, Richard P., Shibata, Shigeru

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Exome Sequencing Identifies Biallelic MSH3 Germline Mutations as a Recessive Subtype of Colorectal Adenomatous Polyposis von Adam, Ronja, Spier, Isabel, Zhao, Bixiao, Kloth, Michael, Marquez, Jonathan, Hinrichsen, Inga, Kirfel, Jutta, Tafazzoli, Aylar, Horpaopan, Sukanya, Uhlhaas, Siegfried, Stienen, Dietlinde, Friedrichs, Nicolaus, Altmüller, Janine, Laner, Andreas, Holzapfel, Stefanie, Peters, Sophia, Kayser, Katrin, Thiele, Holger, Holinski-Feder, Elke, Marra, Giancarlo, Kristiansen, Glen, Nöthen, Markus M., Büttner, Reinhard, Möslein, Gabriela, Betz, Regina C., Brieger, Angela, Lifton, Richard P., Aretz, Stefan

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Predictors of Chemosensitivity in Triple Negative Breast Cancer: An Integrated Genomic Analysis von Jiang, Tingting, Shi, Weiwei, Wali, Vikram B, Pongor, Lőrinc S, Li, Charles, Lau, Rosanna, Győrffy, Balázs, Lifton, Richard P, Symmans, William F, Pusztai, Lajos, Hatzis, Christos

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K⁺ Channel Mutations in Adrenal Aldosterone-Producing Adenomas and Hereditary Hypertension von Choi, Murim, Scholl, Ute I, Yue, Peng, Björklund, Peyman, Zhao, Bixiao, Nelson-Williams, Carol, Ji, Weizhen, Cho, Yoonsang, Patel, Aniruddh, Men, Clara J, Lolis, Elias, Wisgerhof, Max V, Geller, David S, Mane, Shrikant, Hellman, Per, Westin, Gunnar, Åkerström, Göran, Wang, Wenhui, Carling, Tobias, Lifton, Richard P

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Isolated polycystic liver disease genes define effectors of polycystin-1 function von Besse, Whitney, Dong, Ke, Choi, Jungmin, Punia, Sohan, Fedeles, Sorin V, Choi, Murim, Gallagher, Anna-Rachel, Huang, Emily B, Gulati, Ashima, Knight, James, Mane, Shrikant, Tahvanainen, Esa, Tahvanainen, Pia, Sanna-Cherchi, Simone, Lifton, Richard P, Watnick, Terry, Pei, York P, Torres, Vicente E, Somlo, Stefan

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Characterization of the mutational landscape of anaplastic thyroid cancer via whole-exome sequencing von Kunstman, John W, Juhlin, C Christofer, Goh, Gerald, Brown, Taylor C, Stenman, Adam, Healy, James M, Rubinstein, Jill C, Choi, Murim, Kiss, Nimrod, Nelson-Williams, Carol, Mane, Shrikant, Rimm, David L, Prasad, Manju L, Höög, Anders, Zedenius, Jan, Larsson, Catharina, Korah, Reju, Lifton, Richard P, Carling, Tobias

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Genetic diagnosis by whole exome capture and massively parallel DNA sequencing von Choi, Murim, Scholl, Ute I, Ji, Weizhen, Liu, Tiewen, Tikhonova, Irina R, Zumbo, Paul, Nayir, Ahmet, Bakkaloğlu, Aysin, Özen, Seza, Sanjad, Sami, Nelson-Williams, Carol, Farhi, Anita, Mane, Shrikant, Lifton, Richard P

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Genetic landscape of metastatic and recurrent head and neck squamous cell carcinoma von Hedberg, Matthew L, Goh, Gerald, Chiosea, Simion I, Bauman, Julie E, Freilino, Maria L, Zeng, Yan, Wang, Lin, Diergaarde, Brenda B, Gooding, William E, Lui, Vivian W Y, Herbst, Roy S, Lifton, Richard P, Grandis, Jennifer R

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KCNJ10 determines the expression of the apical Na-Cl cotransporter (NCC) in the early distal convoluted tubule (DCT1) von Zhang, Chengbiao, Wang, Lijun, Zhang, Junhui, Su, Xiao-Tong, Lin, Dao-Hong, Scholl, Ute I., Giebisch, Gerhard, Lifton, Richard P., Wang, Wen-Hui

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Phosphoregulation of the Na–K–2Cl and K–Cl cotransporters by the WNK kinases von Kahle, Kristopher T., Rinehart, Jesse, Lifton, Richard P.

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The Congenital Heart Disease Genetic Network Study: Cohort description von Hoang, Thanh T, Goldmuntz, Elizabeth, Roberts, Amy E, Chung, Wendy K, Kline, Jennie K, Deanfield, John E, Giardini, Alessandro, Aleman, Adolfo, Gelb, Bruce D, Mac Neal, Meghan, Porter, Jr, George A, Kim, Richard, Brueckner, Martina, Lifton, Richard P, Edman, Sharon, Woyciechowski, Stacy, Mitchell, Laura E, Agopian, A J

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CARD14-associated papulosquamous eruption: A spectrum including features of psoriasis and pityriasis rubra pilaris von Craiglow, Brittany G., Boyden, Lynn M., Hu, Ronghua, Virtanen, Marie, Su, John, Rodriguez, Gabriela, McCarthy, Catherine, Luna, Paula, Larralde, Margarita, Humphrey, Stephen, Holland, Kristen E., Hogeling, Marcia, Hidalgo-Matlock, Benjamin, Ferrari, Bruno, Fernandez-Faith, Esteban, Drolet, Beth, Cordoro, Kelly M., Bowcock, Anne M., Antaya, Richard J., Ashack, Kurt, Ashack, Richard J., Lifton, Richard P., Milstone, Leonard M., Paller, Amy S., Choate, Keith A.

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Recurrent activating mutation in PRKACA in cortisol-producing adrenal tumors von Goh, Gerald, Scholl, Ute I, Healy, James M, Choi, Murim, Prasad, Manju L, Nelson-Williams, Carol, Kunstman, John W, Korah, Reju, Suttorp, Anna-Carinna, Dietrich, Dimo, Haase, Matthias, Willenberg, Holger S, Stålberg, Peter, Hellman, Per, Åkerström, Göran, Björklund, Peyman, Carling, Tobias, Lifton, Richard P

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De novo mutations in inhibitors of Wnt, BMP, and Ras/ERK signaling pathways in non-syndromic midline craniosynostosis von Timberlake, Andrew T., Furey, Charuta G., Choi, Jungmin, Nelson-Williams, Carol, Loring, Erin, Galm, Amy, Kahle, Kristopher T., Steinbacher, Derek M., Larysz, Dawid, Persing, John A., Lifton, Richard P.

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Developmentally regulated KCC2 phosphorylation is essential for dynamic GABA-mediated inhibition and survival von Watanabe, Miho, Zhang, Jinwei, Mansuri, M Shahid, Duan, Jingjing, Karimy, Jason K, Delpire, Eric, Alper, Seth L, Lifton, Richard P, Fukuda, Atsuo, Kahle, Kristopher T

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