Результаты поиска - Martina Brueckner

Отмена результатов
  1. 1
    Genetics and Genomics of Congenital Heart Disease

    Genetics and Genomics of Congenital Heart Disease по Samir Zaidi, Martina Brueckner

    Опубликовано 2017
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  2. 2
    NUP98 Sets the Size-Exclusion Diffusion Limit through the Ciliary Base

    NUP98 Sets the Size-Exclusion Diffusion Limit through the Ciliary Base по S. Joseph Endicott, Martina Brueckner

    Опубликовано 2018
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    Artigo
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  3. 3
    The genetics of congenital heart disease… understanding and improving long-term outcomes in congenital heart disease: a review for the general cardiologist and primary care physician

    The genetics of congenital heart disease… understanding and improving long-term outcomes in congenital heart disease: a review for the general cardiologist and primary care physici... по Mark A. Simmons, Martina Brueckner

    Опубликовано 2017
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  4. 4
    Monocilia in the embryonic mouse heart suggest a direct role for cilia in cardiac morphogenesis

    Monocilia in the embryonic mouse heart suggest a direct role for cilia in cardiac morphogenesis по Jennifer Slough, Laura Cooney, Martina Brueckner

    Опубликовано 2008
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    Artigo
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  5. 5
    Congenital heart disease: emerging themes linking genetics and development

    Congenital heart disease: emerging themes linking genetics and development по Shiaulou Yuan, Samir Zaidi, Martina Brueckner

    Опубликовано 2013
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  6. 6
    The Emerging Complexity of the Vertebrate Cilium: New Functional Roles for an Ancient Organelle

    The Emerging Complexity of the Vertebrate Cilium: New Functional Roles for an Ancient Organelle по Erica E. Davis, Martina Brueckner, Nicholas Katsanis

    Опубликовано 2006
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  7. 7
    Linkage mapping of a mouse gene, iv, that controls left-right asymmetry of the heart and viscera.

    Linkage mapping of a mouse gene, iv, that controls left-right asymmetry of the heart and viscera. по Martina Brueckner, Peter D’Eustachio, Arthur L. Horwich

    Опубликовано 1989
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    Artigo
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  8. 8
    Intraciliary Calcium Oscillations Initiate Vertebrate Left-Right Asymmetry

    Intraciliary Calcium Oscillations Initiate Vertebrate Left-Right Asymmetry по Shiaulou Yuan, Lu Zhao, Martina Brueckner, Zhaoxia Sun

    Опубликовано 2015
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    Artigo
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  9. 9
    A change of heart: new roles for cilia in cardiac development and disease

    A change of heart: new roles for cilia in cardiac development and disease по Lydia Djenoune, Kathryn Berg, Martina Brueckner, Shiaulou Yuan

    Опубликовано 2021
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  10. 10
    Mutation of an axonemal dynein affects left–right asymmetry in inversus viscerum mice

    Mutation of an axonemal dynein affects left–right asymmetry in inversus viscerum mice по Dorothy M. Supp, David P. Witte, S. Steven Potter, Martina Brueckner

    Опубликовано 1997
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    Artigo
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  11. 11
    RFX2 is essential in the ciliated organ of asymmetry and an RFX2 transgene identifies a population of ciliated cells sufficient for fluid flow

    RFX2 is essential in the ciliated organ of asymmetry and an RFX2 transgene identifies a population of ciliated cells sufficient for fluid flow по Brent W. Bisgrove, Svetlana Makova, H. Joseph Yost, Martina Brueckner

    Опубликовано 2011
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    Artigo
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  12. 12
    Two Populations of Node Monocilia Initiate Left-Right Asymmetry in the Mouse

    Two Populations of Node Monocilia Initiate Left-Right Asymmetry in the Mouse по James McGrath, Stefan Somlo, Svetlana Makova, Xin Tian, Martina Brueckner

    Опубликовано 2003
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    Artigo
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  13. 13
    Cilia function as calcium-mediated mechanosensors that instruct left-right asymmetry

    Cilia function as calcium-mediated mechanosensors that instruct left-right asymmetry по Lydia Djenoune, Mohammed Mahamdeh, Thai V. Truong, Christopher Nguyen, Scott E. Fraser, Martina Brueckner, Jonathon Howard, Shiaulou Yuan

    Опубликовано 2023
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    Artigo
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  14. 14
    The heterotaxy gene GALNT11 glycosylates Notch to orchestrate cilia type and laterality

    The heterotaxy gene GALNT11 glycosylates Notch to orchestrate cilia type and laterality по Marko T. Boskovski, Shiaulou Yuan, Nis Borbye‐Lorenzen, Christoffer K. Goth, Svetlana Makova, Henrik Clausen, Martina Brueckner, Mustafa K. Khokha

    Опубликовано 2013
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    Artigo
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  15. 15
    De novo damaging variants associated with congenital heart diseases contribute to the connectome

    De novo damaging variants associated with congenital heart diseases contribute to the connectome по Weizhen Ji, Dina Ferdman, Joshua A. Copel, Dustin Scheinost, Veronika Shabanova, Martina Brueckner, Mustafa K. Khokha, Laura R. Ment

    Опубликовано 2020
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    Artigo
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  16. 16
    Molecular Genetics and Complex Inheritance of Congenital Heart Disease

    Molecular Genetics and Complex Inheritance of Congenital Heart Disease по Nicholas S. Diab, Syndi Barish, Weilai Dong, Shujuan Zhao, Garrett Allington, Xiaobing Yu, Kristopher T. Kahle, Martina Brueckner, Sheng Chih Jin

    Опубликовано 2021
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  17. 17
    Rare copy number variations in congenital heart disease patients identify unique genes in left-right patterning

    Rare copy number variations in congenital heart disease patients identify unique genes in left-right patterning по Khalid A. Fakhro, Murim Choi, Stephanie M. Ware, John W. Belmont, Jeffrey A. Towbin, Richard P. Lifton, Mustafa K. Khokha, Martina Brueckner

    Опубликовано 2011
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    Artigo
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  18. 18
    Targeted deletion of the ATP binding domain of left-right dynein confirms its role in specifying development of left-right asymmetries

    Targeted deletion of the ATP binding domain of left-right dynein confirms its role in specifying development of left-right asymmetries по Dorothy M. Supp, Martina Brueckner, Michael R. Kuehn, David P. Witte, Linda A. Lowe, James McGrath, JoMichelle D. Corrales, S. Steven Potter

    Опубликовано 1999
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    Artigo
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  19. 19
    CANOES: detecting rare copy number variants from whole exome sequencing data

    CANOES: detecting rare copy number variants from whole exome sequencing data по Daniel Backenroth, Jason Homsy, Laura Rodriguez Murillo, Joseph Glessner, Edwin Lin, Martina Brueckner, Richard P. Lifton, Elizabeth Goldmuntz, Wendy K. Chung, Yufeng Shen

    Опубликовано 2014
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    Artigo
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  20. 20
    Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility

    Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility по Andrew Robson, Svetlana Makova, Syndi Barish, Samir Zaidi, Sameet Mehta, Jeffrey Drozd, Sheng Chih Jin, Bruce D. Gelb, Christine E. Seidman, Wendy K. Chung, Richard P. Lifton, Mustafa K. Khokha, Martina Brueckner

    Опубликовано 2019
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