Результаты поиска - Parant, John M.
- Отображение 1 - 15 результаты of 15
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Human transcription factors responsive to initial reprogramming predominantly undergo legitimate reprogramming during fibroblast conversion to iPSCs по Cevallos, Ricardo R., Edwards, Yvonne J. K., Parant, John M., Yoder, Bradley K., Hu, Kejin
Опубликовано 2020Текст -
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Variations in dysfunction of sister chromatid cohesion in esco2 mutant zebrafish reflect the phenotypic diversity of Roberts syndrome по Percival, Stefanie M., Thomas, Holly R., Amsterdam, Adam, Carroll, Andrew J., Lees, Jacqueline A., Yost, H. Joseph, Parant, John M.
Опубликовано 2015Текст -
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Inhibition of SULT4A1 Expression Induces Up-Regulation of Phototransduction Gene Expression in 72-Hour Postfertilization Zebrafish Larvae по Crittenden, Frank, Thomas, Holly, Ethen, Cheryl M., Wu, Zhengliang L., Chen, Dongquan, Kraft, Timothy W., Parant, John M., Falany, Charles N.
Опубликовано 2014Текст -
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Puma, noxa, p53, and p63 differentially mediate stress pathway induced apoptosis по Wang, Jun, Thomas, Holly R., Li, Zhang, Yeo, Nan Cher (Florence), Scott, Hannah E., Dang, Nghi, Hossain, Mohammed Iqbal, Andrabi, Shaida A., Parant, John M.
Опубликовано 2021Текст -
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Evolutionarily conserved genetic interactions between nphp-4 and bbs-5 mutations exacerbate ciliopathy phenotypes по Bentley-Ford, Melissa R, LaBonty, Melissa, Thomas, Holly R, Haycraft, Courtney J, Scott, Mikyla, LaFayette, Cameron, Croyle, Mandy J, Andersen, Reagan S, Parant, John M, Yoder, Bradley K
Опубликовано 2021Текст -
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Truncating PKHD1 and PKD2 mutations alter energy metabolism по Chumley, Phillip, Zhou, Juling, Mrug, Sylvie, Chacko, Balu, Parant, John M., Challa, Anil K., Wilson, Landon S., Berryhill, Taylor F., Barnes, Stephen, Kesterson, Robert A., Bell, P. Darwin, Darley-Usmar, Victor M., Yoder, Bradley K., Mrug, Michal
Опубликовано 2019Текст -
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Mutation of Growth Arrest Specific 8 Reveals a Role in Motile Cilia Function and Human Disease по Lewis, Wesley R., Malarkey, Erik B., Tritschler, Douglas, Bower, Raqual, Pasek, Raymond C., Porath, Jonathan D., Birket, Susan E., Saunier, Sophie, Antignac, Corinne, Knowles, Michael R., Leigh, Margaret W., Zariwala, Maimoona A., Challa, Anil K., Kesterson, Robert A., Rowe, Steven M., Drummond, Iain A., Parant, John M., Hildebrandt, Friedhelm, Porter, Mary E., Yoder, Bradley K., Berbari, Nicolas F.
Опубликовано 2016Текст -
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Genotype–phenotype correlations and novel molecular insights into the DHX30-associated neurodevelopmental disorders по Mannucci, Ilaria, Dang, Nghi D. P., Huber, Hannes, Murry, Jaclyn B., Abramson, Jeff, Althoff, Thorsten, Banka, Siddharth, Baynam, Gareth, Bearden, David, Beleza-Meireles, Ana, Benke, Paul J., Berland, Siren, Bierhals, Tatjana, Bilan, Frederic, Bindoff, Laurence A., Braathen, Geir Julius, Busk, Øyvind L., Chenbhanich, Jirat, Denecke, Jonas, Escobar, Luis F., Estes, Caroline, Fleischer, Julie, Groepper, Daniel, Haaxma, Charlotte A., Hempel, Maja, Holler-Managan, Yolanda, Houge, Gunnar, Jackson, Adam, Kellogg, Laura, Keren, Boris, Kiraly-Borri, Catherine, Kraus, Cornelia, Kubisch, Christian, Le Guyader, Gwenael, Ljungblad, Ulf W., Brenman, Leslie Manace, Martinez-Agosto, Julian A., Might, Matthew, Miller, David T., Minks, Kelly Q., Moghaddam, Billur, Nava, Caroline, Nelson, Stanley F., Parant, John M., Prescott, Trine, Rajabi, Farrah, Randrianaivo, Hanitra, Reiter, Simone F., Schuurs-Hoeijmakers, Janneke, Shieh, Perry B., Slavotinek, Anne, Smithson, Sarah, Stegmann, Alexander P. A., Tomczak, Kinga, Tveten, Kristian, Wang, Jun, Whitlock, Jordan H., Zweier, Christiane, McWalter, Kirsty, Juusola, Jane, Quintero-Rivera, Fabiola, Fischer, Utz, Yeo, Nan Cher, Kreienkamp, Hans-Jürgen, Lessel, Davor
Опубликовано 2021Текст