Hasil Pencarian - Marisa S. Bartolomei

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  1. 1
    Modeling human epigenetic disorders in mice: Beckwith-Wiedemann syndrome and Silver-Russell syndrome

    Modeling human epigenetic disorders in mice: Beckwith-Wiedemann syndrome and Silver-Russell syndrome oleh Suhee Chang, Marisa S. Bartolomei

    Diterbitkan 2020-05-01
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  2. 2
    Imprinted genes … and the number is?

    Imprinted genes … and the number is? oleh Gavin Kelsey, Marisa S Bartolomei

    Diterbitkan 2012-01-01
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  3. 3
    Genomic imprinting: An epigenetic regulatory system.

    Genomic imprinting: An epigenetic regulatory system. oleh Marisa S Bartolomei, Rebecca J Oakey, Anton Wutz

    Diterbitkan 2020-08-01
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  4. 4
    Bisphenol a exposure disrupts genomic imprinting in the mouse.

    Bisphenol a exposure disrupts genomic imprinting in the mouse. oleh Martha Susiarjo, Isaac Sasson, Clementina Mesaros, Marisa S Bartolomei

    Diterbitkan 2013-04-01
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  5. 5
    Differential methylation of genes associated with cell adhesion in preeclamptic placentas.

    Differential methylation of genes associated with cell adhesion in preeclamptic placentas. oleh Lauren Anton, Amy G Brown, Marisa S Bartolomei, Michal A Elovitz

    Diterbitkan 2014-01-01
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  6. 6
    A DNMT3A2-HDAC2 Complex Is Essential for Genomic Imprinting and Genome Integrity in Mouse Oocytes

    A DNMT3A2-HDAC2 Complex Is Essential for Genomic Imprinting and Genome Integrity in Mouse Oocytes oleh Pengpeng Ma, Eric de Waal, Jamie R. Weaver, Marisa S. Bartolomei, Richard M. Schultz

    Diterbitkan 2015-11-01
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  7. 7
    Maintenance of paternal methylation and repression of the imprinted H19 gene requires MBD3.

    Maintenance of paternal methylation and repression of the imprinted H19 gene requires MBD3. oleh Kimberly J Reese, Shu Lin, Raluca I Verona, Richard M Schultz, Marisa S Bartolomei

    Diterbitkan 2007-08-01
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  8. 8
    H19 is not hypomethylated or upregulated with age or sex in the aortic valves of mice

    H19 is not hypomethylated or upregulated with age or sex in the aortic valves of mice oleh Mark Vander Roest, Christopher Krapp, Joanne L. Thorvaldsen, Marisa S. Bartolomei, W. David Merryman

    Diterbitkan 2019-10-01
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  9. 9
    A Hox-Embedded Long Noncoding RNA: Is It All Hot Air?

    A Hox-Embedded Long Noncoding RNA: Is It All Hot Air? oleh Licia Selleri, Marisa S Bartolomei, Wendy A Bickmore, Lin He, Lisa Stubbs, Wolf Reik, Gregory S Barsh

    Diterbitkan 2016-12-01
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  10. 10
    Allele-specific RNA imaging shows that allelic imbalances can arise in tissues through transcriptional bursting.

    Allele-specific RNA imaging shows that allelic imbalances can arise in tissues through transcriptional bursting. oleh Orsolya Symmons, Marcello Chang, Ian A Mellis, Jennifer M Kalish, Jihwan Park, Katalin Suszták, Marisa S Bartolomei, Arjun Raj

    Diterbitkan 2019-01-01
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  11. 11
    TET1 displays catalytic and non-catalytic functions in the adult mouse cortex

    TET1 displays catalytic and non-catalytic functions in the adult mouse cortex oleh Yee Hoon Foong, Blake Caldwell, Joanne L. Thorvaldsen, Christopher Krapp, Clementina A. Mesaros, Wanding Zhou, Rahul M. Kohli, Marisa S. Bartolomei

    Diterbitkan 2024-12-01
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  12. 12
    Placental Abnormalities are Associated With Specific Windows of Embryo Culture in a Mouse Model

    Placental Abnormalities are Associated With Specific Windows of Embryo Culture in a Mouse Model oleh Lisa A. Vrooman, Lisa A. Vrooman, Eric A. Rhon-Calderon, Kashviya V. Suri, Asha K. Dahiya, Yemin Lan, Richard M. Schultz, Marisa S. Bartolomei

    Diterbitkan 2022-04-01
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  13. 13
    Rapamycin-independent IGF2 expression in Tsc2-null mouse embryo fibroblasts and human lymphangioleiomyomatosis cells.

    Rapamycin-independent IGF2 expression in Tsc2-null mouse embryo fibroblasts and human lymphangioleiomyomatosis cells. oleh Blanca E Himes, Kseniya Obraztsova, Lurong Lian, Maya Shumyatcher, Ryan Rue, Elena N Atochina-Vasserman, Stella K Hur, Marisa S Bartolomei, Jilly F Evans, Vera P Krymskaya

    Diterbitkan 2018-01-01
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  14. 14
    Loss of DNMT1o disrupts imprinted X chromosome inactivation and accentuates placental defects in females.

    Loss of DNMT1o disrupts imprinted X chromosome inactivation and accentuates placental defects in females. oleh Serge McGraw, Christopher C Oakes, Josée Martel, M Cecilia Cirio, Pauline de Zeeuw, Winifred Mak, Christoph Plass, Marisa S Bartolomei, J Richard Chaillet, Jacquetta M Trasler

    Diterbitkan 2013-11-01
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  15. 15
    Derivation and investigation of the first human cell-based model of Beckwith-Wiedemann syndrome

    Derivation and investigation of the first human cell-based model of Beckwith-Wiedemann syndrome oleh Suhee Chang, Stella K. Hur, Natali S. Sobel Naveh, Joanne L. Thorvaldsen, Deborah L. French, Alyssa L Gagne, Chintan D. Jobaliya, Montserrat C. Anguera, Marisa S. Bartolomei, Jennifer M Kalish

    Diterbitkan 2021-12-01
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  16. 16
    Dysregulated H19/Igf2 expression disrupts cardiac-placental axis during development of Silver-Russell syndrome-like mouse models

    Dysregulated H19/Igf2 expression disrupts cardiac-placental axis during development of Silver-Russell syndrome-like mouse models oleh Suhee Chang, Diana Fulmer, Stella K Hur, Joanne L Thorvaldsen, Li Li, Yemin Lan, Eric A Rhon-Calderon, Nicolae Adrian Leu, Xiaowen Chen, Jonathan A Epstein, Marisa S Bartolomei

    Diterbitkan 2022-11-01
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  17. 17
    Tissue-specific and mosaic imprinting defects underlie opposite congenital growth disorders in mice.

    Tissue-specific and mosaic imprinting defects underlie opposite congenital growth disorders in mice. oleh Andrea Freschi, Stella K Hur, Federica Maria Valente, Folami Y Ideraabdullah, Angela Sparago, Maria Teresa Gentile, Andrea Oneglia, Diego Di Nucci, Luca Colucci-D'Amato, Joanne L Thorvaldsen, Marisa S Bartolomei, Andrea Riccio, Flavia Cerrato

    Diterbitkan 2018-02-01
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