Rezultati pretrage - Stortchevoi, Alexei

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

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RECQ1 plays a distinct role in cellular response to oxidative DNA damage od 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 od Parvathaneni, Swetha, Stortchevoi, Alexei, Sommers, Joshua A., Brosh, Robert M., Sharma, Sudha

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High-throughput Minitaturized RNA-Seq Library Preparation od 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 od 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 od 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. od 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 od 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 od 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 od 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 od 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 od 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 od 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 od 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 od 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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