Bilaketaren emaitzak - Gainullin, Vladimir

Growth of lung cancer cells in three-dimensional microenvironments reveals key features of tumor malignancy() nork Cichon, Magdalena A., Gainullin, Vladimir G., Zhang, Ying, Radisky, Derek C.

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Estimating the burden and economic impact of pediatric genetic disease nork Gonzaludo, Nina, Belmont, John W., Gainullin, Vladimir G., Taft, Ryan J.

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Correction: Estimating the burden and economic impact of pediatric genetic disease nork Gonzaludo, Nina, Belmont, John W., Gainullin, Vladimir G., Taft, Ryan J.

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Polycystin-1 maturation requires polycystin-2 in a dose-dependent manner nork Gainullin, Vladimir G., Hopp, Katharina, Ward, Christopher J., Hommerding, Cynthia J., Harris, Peter C.

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Uniparental disomy in a population of 32,067 clinical exome trios nork Scuffins, Julie, Keller-Ramey, Jennifer, Dyer, Lindsay, Douglas, Ganka, Torene, Rebecca, Gainullin, Vladimir, Juusola, Jane, Meck, Jeanne, Retterer, Kyle

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Cl(−) and H(+) coupling properties and subcellular localizations of wildtype and disease-associated variants of the voltage-gated Cl(−)/H(+) exchanger ClC-5 nork Chang, Min-Hwang, Brown, Matthew R., Liu, Yiran, Gainullin, Vladimir G., Harris, Peter C., Romero, Michael F., Lieske, John C.

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The Meckel syndrome protein meckelin (TMEM67) is a key regulator of cilia function but is not required for tissue planar polarity nork Leightner, Amanda C., Hommerding, Cynthia J., Peng, Ying, Salisbury, Jeffrey L., Gainullin, Vladimir G., Czarnecki, Peter G., Sussman, Caroline R., Harris, Peter C.

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Combinatorial Chemoprevention Reveals a Novel Smoothened Independent Role of GLI1 in Esophageal Carcinogenesis nork Rizvi, Sumera, DeMars, Cathrine J., Comba, Andrea, Gainullin, Vladimir, Rizvi, Zaheer, Almada, Luciana L., Wang, Kenneth, Lomberk, Gwen, Fernández-Zapico, Martin E., Buttar, Navtej S.

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Functional polycystin-1 dosage governs autosomal dominant polycystic kidney disease severity nork Hopp, Katharina, Ward, Christopher J., Hommerding, Cynthia J., Nasr, Samih H., Tuan, Han-Fang, Gainullin, Vladimir G., Rossetti, Sandro, Torres, Vicente E., Harris, Peter C.

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Disrupting polycystin-2 EF hand Ca(2+) affinity does not alter channel function or contribute to polycystic kidney disease nork Vien, Thuy N., Ng, Leo C. T., Smith, Jessica M., Dong, Ke, Krappitz, Matteus, Gainullin, Vladimir G., Fedeles, Sorin, Harris, Peter C., Somlo, Stefan, DeCaen, Paul G.

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Molecular Diagnostic Yield of Exome Sequencing in Patients With Cerebral Palsy nork Moreno-De-Luca, Andrés, Millan, Francisca, Pesacreta, Denis R., Elloumi, Houda Z., Oetjens, Matthew T., Teigen, Claire, Wain, Karen E., Scuffins, Julie, Myers, Scott M., Torene, Rebecca I., Gainullin, Vladimir G., Arvai, Kevin, Kirchner, H. Lester, Ledbetter, David H., Retterer, Kyle, Martin, Christa L.

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Identification of Biomarkers for PKD1 Using Urinary Exosomes nork Hogan, Marie C., Bakeberg, Jason L., Gainullin, Vladimir G., Irazabal, Maria V., Harmon, Amber J., Lieske, John C., Charlesworth, M. Cristine, Johnson, Kenneth L., Madden, Benjamin J., Zenka, Roman M., McCormick, Daniel J., Sundsbak, Jamie L., Heyer, Christina M., Torres, Vicente E., Harris, Peter C., Ward, Christopher J.

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ExpansionHunter Denovo: a computational method for locating known and novel repeat expansions in short-read sequencing data nork Dolzhenko, Egor, Bennett, Mark F., Richmond, Phillip A., Trost, Brett, Chen, Sai, van Vugt, Joke J. F. A., Nguyen, Charlotte, Narzisi, Giuseppe, Gainullin, Vladimir G., Gross, Andrew M., Lajoie, Bryan R., Taft, Ryan J., Wasserman, Wyeth W., Scherer, Stephen W., Veldink, Jan H., Bentley, David R., Yuen, Ryan K. C., Bahlo, Melanie, Eberle, Michael A.

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Mutations in GANAB, Encoding the Glucosidase IIα Subunit, Cause Autosomal-Dominant Polycystic Kidney and Liver Disease nork Porath, Binu, Gainullin, Vladimir G., Cornec-Le Gall, Emilie, Dillinger, Elizabeth K., Heyer, Christina M., Hopp, Katharina, Edwards, Marie E., Madsen, Charles D., Mauritz, Sarah R., Banks, Carly J., Baheti, Saurabh, Reddy, Bharathi, Herrero, José Ignacio, Bañales, Jesús M., Hogan, Marie C., Tasic, Velibor, Watnick, Terry J., Chapman, Arlene B., Vigneau, Cécile, Lavainne, Frédéric, Audrézet, Marie-Pierre, Ferec, Claude, Le Meur, Yannick, Torres, Vicente E., Harris, Peter C.

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Monoallelic Mutations to DNAJB11 Cause Atypical Autosomal-Dominant Polycystic Kidney Disease nork Cornec-Le Gall, Emilie, Olson, Rory J., Besse, Whitney, Heyer, Christina M., Gainullin, Vladimir G., Smith, Jessica M., Audrézet, Marie-Pierre, Hopp, Katharina, Porath, Binu, Shi, Beili, Baheti, Saurabh, Senum, Sarah R., Arroyo, Jennifer, Madsen, Charles D., Férec, Claude, Joly, Dominique, Jouret, François, Fikri-Benbrahim, Oussamah, Charasse, Christophe, Coulibaly, Jean-Marie, Yu, Alan S., Khalili, Korosh, Pei, York, Somlo, Stefan, Le Meur, Yannick, Torres, Vicente E., Harris, Peter C.

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Genome sequencing in persistently unsolved white matter disorders nork Helman, Guy, Lajoie, Bryan R., Crawford, Joanna, Takanohashi, Asako, Walkiewicz, Marzena, Dolzhenko, Egor, Gross, Andrew M., Gainullin, Vladimir G., Bent, Stephen J., Jenkinson, Emma M., Ferdinandusse, Sacha, Waterham, Hans R., Dorboz, Imen, Bertini, Enrico, Miyake, Noriko, Wolf, Nicole I., Abbink, Truus E. M., Kirwin, Susan M., Tan, Christina M., Hobson, Grace M., Guo, Long, Ikegawa, Shiro, Pizzino, Amy, Schmidt, Johanna L., Bernard, Genevieve, Schiffmann, Raphael, van der Knaap, Marjo S., Simons, Cas, Taft, Ryan J., Vanderver, Adeline

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