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

Bằng Cichon, Magdalena A., Gainullin, Vladimir G., Zhang, Ying, Radisky, Derek C.
Được phát hành 2011

Estimating the burden and economic impact of pediatric genetic disease

Bằng Gonzaludo, Nina, Belmont, John W., Gainullin, Vladimir G., Taft, Ryan J.
Xuất bản năm Genet Med (2018)

Correction: Estimating the burden and economic impact of pediatric genetic disease

Bằng Gonzaludo, Nina, Belmont, John W., Gainullin, Vladimir G., Taft, Ryan J.
Xuất bản năm Genet Med (2019)

Polycystin-1 maturation requires polycystin-2 in a dose-dependent manner

Bằng Gainullin, Vladimir G., Hopp, Katharina, Ward, Christopher J., Hommerding, Cynthia J., Harris, Peter C.
Xuất bản năm J Clin Invest (2015)

Cl(−) and H(+) coupling properties and subcellular localizations of wildtype and disease-associated variants of the voltage-gated Cl(−)/H(+) exchanger ClC-5

Bằng Chang, Min-Hwang, Brown, Matthew R., Liu, Yiran, Gainullin, Vladimir G., Harris, Peter C., Romero, Michael F., Lieske, John C.
Xuất bản năm J Biol Chem (2020)

The Meckel syndrome protein meckelin (TMEM67) is a key regulator of cilia function but is not required for tissue planar polarity

Bằng Leightner, Amanda C., Hommerding, Cynthia J., Peng, Ying, Salisbury, Jeffrey L., Gainullin, Vladimir G., Czarnecki, Peter G., Sussman, Caroline R., Harris, Peter C.
Được phát hành 2013

Functional polycystin-1 dosage governs autosomal dominant polycystic kidney disease severity

Bằng 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.
Được phát hành 2012

Disrupting polycystin-2 EF hand Ca(2+) affinity does not alter channel function or contribute to polycystic kidney disease

Bằng 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.
Xuất bản năm J Cell Sci (2020)

Molecular Diagnostic Yield of Exome Sequencing in Patients With Cerebral Palsy

Bằng 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.
Xuất bản năm JAMA (2021)

Identification of Biomarkers for PKD1 Using Urinary Exosomes

Bằng 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.
Xuất bản năm J Am Soc Nephrol (2015)

ExpansionHunter Denovo: a computational method for locating known and novel repeat expansions in short-read sequencing data

Bằng 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.
Xuất bản năm Genome Biol (2020)

Mutations in GANAB, Encoding the Glucosidase IIα Subunit, Cause Autosomal-Dominant Polycystic Kidney and Liver Disease

Bằng 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.
Xuất bản năm Am J Hum Genet (2016)

Monoallelic Mutations to DNAJB11 Cause Atypical Autosomal-Dominant Polycystic Kidney Disease

Bằng 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.
Xuất bản năm Am J Hum Genet (2018)

Genome sequencing in persistently unsolved white matter disorders

Bằng 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
Xuất bản năm Ann Clin Transl Neurol (2020)