Sökresultat - Gainullin, Vladimir

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