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Hannah M Mitchison

Showing results (31-40 of 84) with videos related to

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Brain Research|September 18, 2004
Late onset neurodegeneration in the Cln3-/- mouse model of juvenile neuronal ceroid lipofuscinosis is preceded by low level glial activationCharlie C Pontikis, Claire V Cella, Nisha Parihar, et al.
Frontiers in Genetics|October 17, 2022
<i>CFAP300</i> mutation causing primary ciliary dyskinesia in FinlandRüdiger Schultz, Varpu Elenius, Mahmoud R Fassad, et al.
Molecular and Cellular Neurosciences|May 4, 2002
Retinal pathology and function in a Cln3 knockout mouse model of juvenile Neuronal Ceroid Lipofuscinosis (batten disease)Gail M Seigel, Andrew Lotery, Ari Kummer, et al.
Journal of Cell Science|October 9, 2025
Characterisation of a primary ciliary dyskinesia model generated from BMI1-transduced basal epithelial cellsMelis T Dalbay, Eriomina Shahaj, Ileana Guerrini, et al.
Cilia|May 15, 2015
The more we know, the more we have to discover: an exciting future for understanding cilia and ciliopathiesAlexandre Benmerah, Bénédicte Durand, Rachel H Giles, et al.
Human Molecular Genetics|November 2, 2014
A founder CEP120 mutation in Jeune asphyxiating thoracic dystrophy expands the role of centriolar proteins in skeletal ciliopathiesRanad Shaheen, Miriam Schmidts, Eissa Faqeih, et al.
Acta Neuropathologica Communications|October 19, 2017
Glial cells are functionally impaired in juvenile neuronal ceroid lipofuscinosis and detrimental to neuronsLotta Parviainen, Sybille Dihanich, Greg W Anderson, et al.
Neurology. Genetics|August 18, 2020
Hydrocephalus and diffuse choroid plexus hyperplasia in primary ciliary dyskinesia-related MCIDAS mutationEvie Alexandra Robson, Luke Dixon, Liam Causon, et al.
American Journal of Human Genetics|March 1, 2008
Genome-wide high-density SNP-based linkage analysis of infantile hypertrophic pyloric stenosis identifies loci on chromosomes 11q14-q22 and Xq23Kate V Everett, Barry A Chioza, Christina Georgoula, et al.
The European Respiratory Journal|February 23, 2018
Primary ciliary dyskinesia with normal ultrastructure: three-dimensional tomography detects absence of DNAH11Amelia Shoemark, Thomas Burgoyne, Robert Kwan, et al.
Pageof 9

Showing results (31-40 of 84) with videos related to

Sort By:
Pageof 9
Brain Research|September 18, 2004
Late onset neurodegeneration in the Cln3-/- mouse model of juvenile neuronal ceroid lipofuscinosis is preceded by low level glial activationCharlie C Pontikis, Claire V Cella, Nisha Parihar, et al.
Frontiers in Genetics|October 17, 2022
<i>CFAP300</i> mutation causing primary ciliary dyskinesia in FinlandRüdiger Schultz, Varpu Elenius, Mahmoud R Fassad, et al.
Molecular and Cellular Neurosciences|May 4, 2002
Retinal pathology and function in a Cln3 knockout mouse model of juvenile Neuronal Ceroid Lipofuscinosis (batten disease)Gail M Seigel, Andrew Lotery, Ari Kummer, et al.
Journal of Cell Science|October 9, 2025
Characterisation of a primary ciliary dyskinesia model generated from BMI1-transduced basal epithelial cellsMelis T Dalbay, Eriomina Shahaj, Ileana Guerrini, et al.
Cilia|May 15, 2015
The more we know, the more we have to discover: an exciting future for understanding cilia and ciliopathiesAlexandre Benmerah, Bénédicte Durand, Rachel H Giles, et al.
Human Molecular Genetics|November 2, 2014
A founder CEP120 mutation in Jeune asphyxiating thoracic dystrophy expands the role of centriolar proteins in skeletal ciliopathiesRanad Shaheen, Miriam Schmidts, Eissa Faqeih, et al.
Acta Neuropathologica Communications|October 19, 2017
Glial cells are functionally impaired in juvenile neuronal ceroid lipofuscinosis and detrimental to neuronsLotta Parviainen, Sybille Dihanich, Greg W Anderson, et al.
Neurology. Genetics|August 18, 2020
Hydrocephalus and diffuse choroid plexus hyperplasia in primary ciliary dyskinesia-related MCIDAS mutationEvie Alexandra Robson, Luke Dixon, Liam Causon, et al.
American Journal of Human Genetics|March 1, 2008
Genome-wide high-density SNP-based linkage analysis of infantile hypertrophic pyloric stenosis identifies loci on chromosomes 11q14-q22 and Xq23Kate V Everett, Barry A Chioza, Christina Georgoula, et al.
The European Respiratory Journal|February 23, 2018
Primary ciliary dyskinesia with normal ultrastructure: three-dimensional tomography detects absence of DNAH11Amelia Shoemark, Thomas Burgoyne, Robert Kwan, et al.
Pageof 9