Resultados da pesquisa - Stortchevoi, Alexei

SPRI Beads-based Size Selection in the Range of 2-10kb Por Stortchevoi, Alexei, Kamelamela, Noelani, Levine, Stuart S.

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RECQ1 plays a distinct role in cellular response to oxidative DNA damage Por Sharma, Sudha, Phatak, Pornima, Stortchevoi, Alexei, Jasin, Maria, LaRocque, Jeannine R.

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Human RECQ1 Interacts with Ku70/80 and Modulates DNA End-Joining of Double-Strand Breaks Por Parvathaneni, Swetha, Stortchevoi, Alexei, Sommers, Joshua A., Brosh, Robert M., Sharma, Sudha

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High-throughput Minitaturized RNA-Seq Library Preparation Por Mildrum, Samuel, Hendricks, Austin, Stortchevoi, Alexei, Kamelamela, Noelani, Butty, Vincent L., Levine, Stuart S.

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A Novel Microduplication of ARID1B: Clinical, Genetic and Proteomic Findings Por Seabra, Catarina M., Szoko, Nicholas, Erdin, Serkan, Ragavendran, Ashok, Stortchevoi, Alexei, Maciel, Patrícia, Lundberg, Kathleen, Schlatzer, Daniela, Smith, Janice, Talkowski, Michael E., Gusella, James F., Natowicz, Marvin R.

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WNT/β-Catenin Pathway and Epigenetic Mechanisms Regulate the Pitt-Hopkins Syndrome and Schizophrenia Risk Gene TCF4 Por Hennig, Krista M., Fass, Daniel M., Zhao, Wen-Ning, Sheridan, Steven D., Fu, Ting, Erdin, Serkan, Stortchevoi, Alexei, Lucente, Diane, Cody, Jannine D., Sweetser, David, Gusella, James F., Talkowski, Michael E., Haggarty, Stephen J.

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Developmental regulation of neuronal gene expression by Elongator complex protein 1 dosage. Por Morini, Elisabetta, Gao, Dadi, Logan, Emily M., Salani, Monica, Krauson, Aram J., Chekuri, Anil, Chen, Yei-Tsung, Ragavendran, Ashok, Chakravarty, Probir, Erdin, Serkan, Stortchevoi, Alexei, Svejstrup, Jesper Q., Talkowski, Michael E., Slaugenhaupt, Susan A.

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Engineering microdeletions and microduplications by targeting segmental duplications with CRISPR Por Tai, Derek J. C., Ragavendran, Ashok, Manavalan, Poornima, Stortchevoi, Alexei, Seabra, Catarina M., Erdin, Serkan, Collins, Ryan L., Blumenthal, Ian, Chen, Xiaoli, Shen, Yiping, Sahin, Mustafa, Zhang, Chengsheng, Lee, Charles, Gusella, James F., Talkowski, Michael E.

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Histone deacetylase knockouts modify transcription, CAG instability and nuclear pathology in Huntington disease mice Por Kovalenko, Marina, Erdin, Serkan, Andrew, Marissa A, St Claire, Jason, Shaughnessey, Melissa, Hubert, Leroy, Neto, João Luís, Stortchevoi, Alexei, Fass, Daniel M, Mouro Pinto, Ricardo, Haggarty, Stephen J, Wilson, John H, Talkowski, Michael E, Wheeler, Vanessa C

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CHD8 regulates neurodevelopmental pathways associated with autism spectrum disorder in neural progenitors Por Sugathan, Aarathi, Biagioli, Marta, Golzio, Christelle, Erdin, Serkan, Blumenthal, Ian, Manavalan, Poornima, Ragavendran, Ashok, Brand, Harrison, Lucente, Diane, Miles, Judith, Sheridan, Steven D., Stortchevoi, Alexei, Kellis, Manolis, Haggarty, Stephen J., Katsanis, Nicholas, Gusella, James F., Talkowski, Michael E.

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Transcriptional consequences of MBD5 disruption in mouse brain and CRISPR-derived neurons Por Seabra, Catarina M., Aneichyk, Tatsiana, Erdin, Serkan, Tai, Derek J. C., De Esch, Celine E. F., Razaz, Parisa, An, Yu, Manavalan, Poornima, Ragavendran, Ashok, Stortchevoi, Alexei, Abad, Clemer, Young, Juan I., Maciel, Patricia, Talkowski, Michael E., Gusella, James F.

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Efficient ablation of genes in human hematopoietic stem and effector cells using CRISPR/Cas9 Por Mandal, Pankaj K., Ferreira, Leonardo M. R., Collins, Ryan, Meissner, Torsten B., Boutwell, Christian L., Friesen, Max, Vrbanac, Vladimir, Garrison, Brian S., Stortchevoi, Alexei, Bryder, David, Musunuru, Kiran, Brand, Harrison, Tager, Andrew M., Allen, Todd M., Talkowski, Michael E., Rossi, Derrick J., Cowan, Chad A.

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Defining the diverse spectrum of inversions, complex structural variation, and chromothripsis in the morbid human genome Por Collins, Ryan L., Brand, Harrison, Redin, Claire E., Hanscom, Carrie, Antolik, Caroline, Stone, Matthew R., Glessner, Joseph T., Mason, Tamara, Pregno, Giulia, Dorrani, Naghmeh, Mandrile, Giorgia, Giachino, Daniela, Perrin, Danielle, Walsh, Cole, Cipicchio, Michelle, Costello, Maura, Stortchevoi, Alexei, An, Joon-Yong, Currall, Benjamin B., Seabra, Catarina M., Ragavendran, Ashok, Margolin, Lauren, Martinez-Agosto, Julian A., Lucente, Diane, Levy, Brynn, Sanders, Stephan J., Wapner, Ronald J., Quintero-Rivera, Fabiola, Kloosterman, Wigard, Talkowski, Michael E.

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Dissecting the Causal Mechanism of X-Linked Dystonia-Parkinsonism by Integrating Genome and Transcriptome Assembly Por Aneichyk, Tatsiana, Hendriks, William T., Yadav, Rachita, Shin, David, Gao, Dadi, Vaine, Christine A., Collins, Ryan L., Domingo, Aloysius, Currall, Benjamin, Stortchevoi, Alexei, Multhaupt-Buell, Trisha, Penney, Ellen B., Cruz, Lilian, Dhakal, Jyotsna, Brand, Harrison, Hanscom, Carrie, Antolik, Caroline, Dy, Marisela, Ragavendran, Ashok, Underwood, Jason, Cantsilieris, Stuart, Munson, Katherine M., Eichler, Evan E., Acuña, Patrick, Go, Criscely, Jamora, R. Dominic G., Rosales, Raymond L., Church, Deanna M., Williams, Stephen R., Garcia, Sarah, Klein, Christine, Müller, Ulrich, Wilhelmsen, Kirk C., Marc Timmers, H. T., Sapir, Yechiam, Wainger, Brian J., Henderson, Daniel, Ito, Naoto, Weisenfeld, Neil, Jaffe, David, Sharma, Nutan, Breakefield, Xandra O., Ozelius, Laurie J., Bragg, D. Cristopher, Talkowski, Michael E.

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SMCHD1 mutations associated with a rare muscular dystrophy can also cause isolated arhinia and Bosma arhinia microphthalmia syndrome Por Shaw, Natalie D, Brand, Harrison, Kupchinsky, Zachary A, Bengani, Hemant, Plummer, Lacey, Jones, Takako I, Erdin, Serkan, Williamson, Kathleen A, Rainger, Joe, Stortchevoi, Alexei, Samocha, Kaitlin, Currall, Benjamin B, Dunican, Donncha S, Collins, Ryan L, Willer, Jason R, Lek, Angela, Lek, Monkol, Nassan, Malik, Pereira, Shahrin, Kammin, Tammy, Lucente, Diane, Silva, Alexandra, Seabra, Catarina M, Chiang, Colby, An, Yu, Ansari, Morad, Rainger, Jacqueline K, Joss, Shelagh, Smith, Jill Clayton, Lippincott, Margaret F, Singh, Sylvia S, Patel, Nirav, Jing, Jenny W, Law, Jennifer R, Ferraro, Nalton, Verloes, Alain, Rauch, Anita, Steindl, Katharina, Zweier, Markus, Scheer, Ianina, Sato, Daisuke, Okamoto, Nobuhiko, Jacobsen, Christina, Tryggestad, Jeanie, Chernausek, Steven, Schimmenti, Lisa A, Brasseur, Benjamin, Cesaretti, Claudia, García-Ortiz, Jose E, Buitrago, Tatiana Pineda, Silva, Orlando Perez, Hoffman, Jodi D, Mühlbauer, Wolfgang, Ruprecht, Klaus W, Loeys, Bart L, Shino, Masato, Kaindl, Angela M, Cho, Chie-Hee, Morton, Cynthia C, Meehan, Richard R, van Heyningen, Veronica, Liao, Eric C, Balasubramanian, Ravikumar, Hall, Janet E, Seminara, Stephanie B, Macarthur, Daniel, Moore, Steven A, Yoshiura, Koh-ichiro, Gusella, James F, Marsh, Joseph A, Graham, John M, Lin, Angela E, Katsanis, Nicholas, Jones, Peter L, Crowley, William F, Davis, Erica E, FitzPatrick, David R, Talkowski, Michael E

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