Risultati della ricerca - Gainullin, Vladimir

Growth of lung cancer cells in three-dimensional microenvironments reveals key features of tumor malignancy() di 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 di 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 di 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 di 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 di 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 di 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 di 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 di 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 di 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 di 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 di 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 di 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 di 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 di 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 di 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 di 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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