Functions of site-specific histone acetylation and deacetylation von Shahbazian, Mona D, Grunstein, Michael

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Histone H2B Ubiquitylation Controls Processive Methylation but Not Monomethylation by Dot1 and Set1 von Shahbazian, Mona D., Zhang, Kangling, Grunstein, Michael

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Mice with Truncated MeCP2 Recapitulate Many Rett Syndrome Features and Display Hyperacetylation of Histone H3 von Shahbazian, Mona D., Young, Juan I., Yuva-Paylor, Lisa A., Spencer, Corinne M., Antalffy, Barbara A., Noebels, Jeffrey L., Armstrong, Dawna L., Paylor, Richard, Zoghbi, Huda Y.

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Insight into Rett syndrome: MeCP2 levels display tissue- and cell-specific differences and correlate with neuronal maturation von SHAHBAZIAN, Mona D, ANTALFFY, Barbara, ARMSTRONG, Dawna L, ZOGHBI, Huda Y

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Rett Syndrome and MeCP2: Linking Epigenetics and Neuronal Function von Shahbazian, Mona D., Zoghbi, Huda Y.

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A Commutable Cytomegalovirus Calibrator Is Required to Improve the Agreement of Viral Load Values between Laboratories von Caliendo, Angela M, Shahbazian, Mona D, Schaper, Carl, Ingersoll, Jessica, Abdul-Ali, Deborah, Boonyaratanakornkit, Jerry, Pang, Xiao-Li, Fox, Julie, Preiksaitis, Jutta, Schonbrunner, E. Ralf

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Abstract 4648: Development of a rapid, precise, and sensitive molecular assay for ALK fusion detection von Shahbazian, Mona D., Shang, Yulei, Jamba, Maidar, Powell, Michael J.

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Reduction of Purkinje Cell Pathology in SCA1 Transgenic Mice by p53 Deletion von Shahbazian, Mona D., Orr, Harry T., Zoghbi, Huda Y.

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Monitoring next-generation sequencing (NGS) workflows in oncology research using AcroMetrix sequencing controls von Nataraj, Nakul, Norman, Kara, Lau, Aron, Shahbazian, Mona D

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Abstract 4900: A highly multiplexed control material to satisfy the complex needs of targeted next generation sequencing (NGS) oncology assays von Nataraj, Nakul, Shahbazian, Mona D., Lau, Aron, Yucekul, Mahjabeen, Chiang, Patty, Le, Suzy Van, Norman, Kara

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Reduced proportion of Purkinje cells expressing paternally derived mutant Mecp2308 allele in female mouse cerebellum is not due to a skewed primary pattern of X-chromosome inactiva... von Watson, Catherine M., Pelka, Gregory J., Radziewic, Tatiana, Shahbazian, Mona D., Christodoulou, John, Williamson, Sarah L., Tam, Patrick P.L.

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Molecular genetics of Rett syndrome and clinical spectrum of MECP2 mutations von Shahbazian, M D, Zoghbi, H Y

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Identification of MeCP2 mutations in a series of females with autistic disorder von Carney, Regina M., Wolpert, Chantelle M., Ravan, Sarah A., Shahbazian, Mona, Ashley-Koch, Allison, Cuccaro, Michael L., Vance, Jeffery M., Pericak-Vance, Margaret A.

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Implementation of Formalin-Fixed, Paraffin-Embedded Cell Line Pellets as High-Quality Process Controls in Quality Assessment Programs for KRAS Mutation Analysis von Dijkstra, Jeroen R, Opdam, Frank J.M, Boonyaratanakornkit, Jerry, Schönbrunner, E. Ralf, Shahbazian, Mona, Edsjö, Anders, Hoefler, Gerald, Jung, Andreas, Kotsinas, Athanassios, Gorgoulis, Vassilis G, López-Ríos, Fernando, de Stricker, Karin, Rouleau, Etienne, Biesmans, Bart, van Krieken, J. Han J.M

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Do Pre-Analytical Parameters Explain KRAS Test Sensitivity Disparities? von Labourier, Emmanuel, Dijkstra, Jeroen R, van Krieken, J. Han J.M, Opdam, Frank J.M, Boonyaratanakornkit, Jerry, Schönbrunner, E. Ralf, Shahbazian, Mona, Edsjö, Anders, Hoefler, Gerald, Jung, Andreas, Kotsinas, Athanassios, Gorgoulis, Vassilis G, López-Ríos, Fernando, de Stricker, Karin, Rouleau, Etienne, Biesmans, Bart

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Do Pre-Analytical Parameters Explain KRAS Test Sensitivity Disparities? Reply von Dijkstra, Jeroen R., van Krieken, J. Han J. M., Opdam, Frank J. M., Boonyaratanakornkit, Jerry, Schoenbrunner, E. Ralf, Shahbazian, Mona, Edsjö, Anders, Hoefler, Gerald, Jung, Andreas, Kotsinas, Athanassios, Gorgoulis, Vassilis G., Lopez-Rios, Fernando, de Stricker, Karin, Rouleau, Etienne, Biesmans, Bart

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Balanced X chromosome inactivation patterns in the Rett syndrome brain von Shahbazian, Mona D., Sun, Yaling, Zoghbi, Huda Y.

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Infantile hypotonia as a presentation of rett syndrome von Heilstedt, Heidi A., Shahbazian, Mona D., Lee, Brendan

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Reduced proportion of Purkinje cells expressing paternally derived mutant Mecp2 super(308) allele in female mouse cerebellum is not due to a skewed primary pattern of X-chromosome... von Watson, Catherine M, Pelka, Gregory J, Radziewic, Tatiana, Shahbazian, Mona D, Christodoulou, John, Williamson, Sarah L, Tam, Patrick PL

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METHOD FOR PREPARING FFPE QUALITY CONTROL MATERIAL WITH BULKING AGENT von SHAHBAZIAN, Mona, SCHOENBRUNNER, Erhard, LAU, Aron

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