CRISPR-Cpf1 mediates efficient homology-directed repair and temperature-controlled genome editing
Moreno-Mateos, Miguel A, Fernandez, Juan P, Rouet, Romain, Vejnar, Charles E, Lane, Maura A, Mis, Emily, Khokha, Mustafa K, Doudna, Jennifer A, Giraldez, Antonio J
Published in Nature communications (08.12.2017)
Published in Nature communications (08.12.2017)
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Congenital Heart Disease Genetics Uncovers Context-Dependent Organization and Function of Nucleoporins at Cilia
del Viso, Florencia, Huang, Fang, Myers, Jordan, Chalfant, Madeleine, Zhang, Yongdeng, Reza, Nooreen, Bewersdorf, Joerg, Lusk, C. Patrick, Khokha, Mustafa K.
Published in Developmental cell (12.09.2016)
Published in Developmental cell (12.09.2016)
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Mutation of NLRC4 causes a syndrome of enterocolitis and autoinflammation
Romberg, Neil, Al Moussawi, Khatoun, Nelson-Williams, Carol, Stiegler, Amy L, Loring, Erin, Choi, Murim, Overton, John, Meffre, Eric, Khokha, Mustafa K, Huttner, Anita J, West, Brian, Podoltsev, Nikolai A, Boggon, Titus J, Kazmierczak, Barbara I, Lifton, Richard P
Published in Nature genetics (01.10.2014)
Published in Nature genetics (01.10.2014)
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Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development
Owens, Nick D.L., Blitz, Ira L., Lane, Maura A., Patrushev, Ilya, Overton, John D., Gilchrist, Michael J., Cho, Ken W.Y., Khokha, Mustafa K.
Published in Cell reports (Cambridge) (26.01.2016)
Published in Cell reports (Cambridge) (26.01.2016)
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WDR5 Stabilizes Actin Architecture to Promote Multiciliated Cell Formation
Kulkarni, Saurabh S., Griffin, John N., Date, Priya P., Liem, Karel F., Khokha, Mustafa K.
Published in Developmental cell (10.09.2018)
Published in Developmental cell (10.09.2018)
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Rare copy number variations in congenital heart disease patients identify unique genes in left-right patterning
Fakhro, Khalid A., Choi, Murim, Ware, Stephanie M., Belmont, John W., Towbin, Jeffrey A., Lifton, Richard P., Khokha, Mustafa K., Brueckner, Martina
Published in Proceedings of the National Academy of Sciences - PNAS (15.02.2011)
Published in Proceedings of the National Academy of Sciences - PNAS (15.02.2011)
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Membrane potential drives the exit from pluripotency and cell fate commitment via calcium and mTOR
Sempou, Emily, Kostiuk, Valentyna, Zhu, Jie, Cecilia Guerra, M, Tyan, Leonid, Hwang, Woong, Camacho-Aguilar, Elena, Caplan, Michael J, Zenisek, David, Warmflash, Aryeh, Owens, Nick D L, Khokha, Mustafa K
Published in Nature communications (05.11.2022)
Published in Nature communications (05.11.2022)
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CRISPR/Cas9 F0 Screening of Congenital Heart Disease Genes in Xenopus tropicalis
Deniz, Engin, Mis, Emily K, Lane, Maura, Khokha, Mustafa K
Published in Methods in molecular biology (Clifton, N.J.) (01.01.2018)
Published in Methods in molecular biology (Clifton, N.J.) (01.01.2018)
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Mechanical stretch scales centriole number to apical area via Piezo1 in multiciliated cells
Kulkarni, Saurabh, Marquez, Jonathan, Date, Priya, Ventrella, Rosa, Mitchell, Brian J, Khokha, Mustafa K
Published in eLife (29.06.2021)
Published in eLife (29.06.2021)
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A chromosome-scale genome assembly and dense genetic map for Xenopus tropicalis
Mitros, Therese, Lyons, Jessica B., Session, Adam M., Jenkins, Jerry, Shu, Shengquiang, Kwon, Taejoon, Lane, Maura, Ng, Connie, Grammer, Timothy C., Khokha, Mustafa K., Grimwood, Jane, Schmutz, Jeremy, Harland, Richard M., Rokhsar, Daniel S.
Published in Developmental biology (01.08.2019)
Published in Developmental biology (01.08.2019)
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Disrupted ER membrane protein complex-mediated topogenesis drives congenital neural crest defects
Marquez, Jonathan, Criscione, June, Charney, Rebekah M, Prasad, Maneeshi S, Hwang, Woong Y, Mis, Emily K, García-Castro, Martín I, Khokha, Mustafa K
Published in The Journal of clinical investigation (01.02.2020)
Published in The Journal of clinical investigation (01.02.2020)
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Author Correction: Membrane potential drives the exit from pluripotency and cell fate commitment via calcium and mTOR
Sempou, Emily, Kostiuk, Valentyna, Zhu, Jie, Cecilia Guerra, M, Tyan, Leonid, Hwang, Woong, Camacho-Aguilar, Elena, Caplan, Michael J, Zenisek, David, Warmflash, Aryeh, Owens, Nick D L, Khokha, Mustafa K
Published in Nature communications (05.06.2023)
Published in Nature communications (05.06.2023)
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Visualizing flow in an intact CSF network using optical coherence tomography: implications for human congenital hydrocephalus
Date, Priya, Ackermann, Pascal, Furey, Charuta, Fink, Ina Berenice, Jonas, Stephan, Khokha, Mustafa K, Kahle, Kristopher T, Deniz, Engin
Published in Scientific reports (17.04.2019)
Published in Scientific reports (17.04.2019)
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De novo pathogenic variants in neuronal differentiation factor 2 (NEUROD2) cause a form of early infantile epileptic encephalopathy
Sega, Annalisa G, Mis, Emily K, Lindstrom, Kristin, Mercimek-Andrews, Saadet, Ji, Weizhen, Cho, Megan T, Juusola, Jane, Konstantino, Monica, Jeffries, Lauren, Khokha, Mustafa K, Lakhani, Saquib Ali
Published in Journal of medical genetics (01.02.2019)
Published in Journal of medical genetics (01.02.2019)
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Conserved chromatin and repetitive patterns reveal slow genome evolution in frogs
Bredeson, Jessen V, Mudd, Austin B, Medina-Ruiz, Sofia, Mitros, Therese, Smith, Owen Kabnick, Miller, Kelly E, Lyons, Jessica B, Batra, Sanjit S, Park, Joseph, Berkoff, Kodiak C, Plott, Christopher, Grimwood, Jane, Schmutz, Jeremy, Aguirre-Figueroa, Guadalupe, Khokha, Mustafa K, Lane, Maura, Philipp, Isabelle, Laslo, Mara, Hanken, James, Kerdivel, Gwenneg, Buisine, Nicolas, Sachs, Laurent M, Buchholz, Daniel R, Kwon, Taejoon, Smith-Parker, Heidi, Gridi-Papp, Marcos, Ryan, Michael J, Denton, Robert D, Malone, John H, Wallingford, John B, Straight, Aaron F, Heald, Rebecca, Hockemeyer, Dirk, Harland, Richard M, Rokhsar, Daniel S
Published in Nature communications (17.01.2024)
Published in Nature communications (17.01.2024)
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DAAM2 Variants Cause Nephrotic Syndrome via Actin Dysregulation
Schneider, Ronen, Deutsch, Konstantin, Hoeprich, Gregory J., Marquez, Jonathan, Hermle, Tobias, Braun, Daniela A., Seltzsam, Steve, Kitzler, Thomas M., Mao, Youying, Buerger, Florian, Majmundar, Amar J., Onuchic-Whitford, Ana C., Kolvenbach, Caroline M., Schierbaum, Luca, Schneider, Sophia, Halawi, Abdul A., Nakayama, Makiko, Mann, Nina, Connaughton, Dervla M., Klämbt, Verena, Wagner, Matias, Riedhammer, Korbinian M., Renders, Lutz, Katsura, Yoshichika, Thumkeo, Dean, Soliman, Neveen A., Mane, Shrikant, Lifton, Richard P., Shril, Shirlee, Khokha, Mustafa K., Hoefele, Julia, Goode, Bruce L., Hildebrandt, Friedhelm
Published in American journal of human genetics (03.12.2020)
Published in American journal of human genetics (03.12.2020)
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