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Frontiers in Genetics
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March 28, 2019
Opportunities and Challenges for Molecular Understanding of Ciliopathies-The 100,000 Genomes Project
Gabrielle Wheway, Hannah M Mitchison,
Ultrastructural Pathology
|
September 20, 2017
Motile cilia defects in diseases other than primary ciliary dyskinesia: The contemporary diagnostic and research role for transmission electron microscopy
Hannah M Mitchison, Amelia Shoemark
Frontiers in Genetics
|
October 2, 2019
Corrigendum: Opportunities and Challenges for Molecular Understanding of Ciliopathies-The 100,000 Genomes Project
Gabrielle Wheway, , Hannah M Mitchison
The Journal of Pathology
|
November 19, 2016
Motile and non-motile cilia in human pathology: from function to phenotypes
Hannah M Mitchison, Enza Maria Valente
Biochimica Et Biophysica Acta
|
October 7, 2006
Progress towards understanding disease mechanisms in small vertebrate models of neuronal ceroid lipofuscinosis
Jonathan D Cooper, Claire Russell, Hannah M Mitchison
Seminars in Cell & Developmental Biology
|
December 6, 2020
Motile cilia and airway disease
Marie Legendre, Laure-Emmanuelle Zaragosi, Hannah M Mitchison
Human Molecular Genetics
|
August 6, 2008
Transcript and in silico analysis of CLN3 in juvenile neuronal ceroid lipofuscinosis and associated mouse models
Chun-Hung Chan, Hannah M Mitchison, David A Pearce
Brain Pathology (Zurich, Switzerland)
|
March 5, 2004
Selectivity and types of cell death in the neuronal ceroid lipofuscinoses
Hannah M Mitchison, Ming J Lim, Jonathan D Cooper
Biochimica Et Biophysica Acta
|
January 1, 2013
Bioinformatic perspectives in the neuronal ceroid lipofuscinoses
Stanislav Kmoch, Viktor Stránecký, Richard D Emes, et al.
Journal of Health Psychology
|
January 29, 2024
'Don't let it hold you back' - The experience of transition to adulthood in young people with primary ciliary dyskinesia: An interpretative phenomenological analysis
Rhys Dore, Isabella E Nizza, Hannah M Mitchison, et al.
Page
of 9
Search research articles
Search
Showing results (1-10 of 84) with videos related to
Sort By:
Page
of 9
Frontiers in Genetics
|
March 28, 2019
Opportunities and Challenges for Molecular Understanding of Ciliopathies-The 100,000 Genomes Project
Gabrielle Wheway, Hannah M Mitchison,
Ultrastructural Pathology
|
September 20, 2017
Motile cilia defects in diseases other than primary ciliary dyskinesia: The contemporary diagnostic and research role for transmission electron microscopy
Hannah M Mitchison, Amelia Shoemark
Frontiers in Genetics
|
October 2, 2019
Corrigendum: Opportunities and Challenges for Molecular Understanding of Ciliopathies-The 100,000 Genomes Project
Gabrielle Wheway, , Hannah M Mitchison
The Journal of Pathology
|
November 19, 2016
Motile and non-motile cilia in human pathology: from function to phenotypes
Hannah M Mitchison, Enza Maria Valente
Biochimica Et Biophysica Acta
|
October 7, 2006
Progress towards understanding disease mechanisms in small vertebrate models of neuronal ceroid lipofuscinosis
Jonathan D Cooper, Claire Russell, Hannah M Mitchison
Seminars in Cell & Developmental Biology
|
December 6, 2020
Motile cilia and airway disease
Marie Legendre, Laure-Emmanuelle Zaragosi, Hannah M Mitchison
Human Molecular Genetics
|
August 6, 2008
Transcript and in silico analysis of CLN3 in juvenile neuronal ceroid lipofuscinosis and associated mouse models
Chun-Hung Chan, Hannah M Mitchison, David A Pearce
Brain Pathology (Zurich, Switzerland)
|
March 5, 2004
Selectivity and types of cell death in the neuronal ceroid lipofuscinoses
Hannah M Mitchison, Ming J Lim, Jonathan D Cooper
Biochimica Et Biophysica Acta
|
January 1, 2013
Bioinformatic perspectives in the neuronal ceroid lipofuscinoses
Stanislav Kmoch, Viktor Stránecký, Richard D Emes, et al.
Journal of Health Psychology
|
January 29, 2024
'Don't let it hold you back' - The experience of transition to adulthood in young people with primary ciliary dyskinesia: An interpretative phenomenological analysis
Rhys Dore, Isabella E Nizza, Hannah M Mitchison, et al.
Page
of 9