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M E Cheetham

Showing results (21-30 of 35) with videos related to

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Cytogenetics and Cell Genetics|October 12, 1999
Assignment of the neuronal cochaperone, HSJ1, to human chromosome bands 2q32-->q34 between D2S295 and D2S339 by in situ hybridization and somatic cell and radiation hybridsJ P Chapple, A J Hardcastle, U Kurzik-Dumke, et al.
FEBS Letters|December 21, 1987
Isolation of cDNAs coding for epitopes shared by microtubule-associated proteins and neurofibrillary tangle in Alzheimer's diseaseJ P Brion, M E Cheetham, P A Robinson, et al.
Journal of Medical Genetics|February 5, 2002
In vitro analysis of aminoglycoside therapy for the Arg120stop nonsense mutation in RP2 patientsC Grayson, J P Chapple, K R Willison, et al.
Eye (London, England)|December 16, 2017
A novel missense mutation in HSF4 causes autosomal-dominant congenital lamellar cataract in a British familyV Berry, N Pontikos, A Moore, et al.
Human Molecular Genetics|August 15, 2000
Mutations in the N-terminus of the X-linked retinitis pigmentosa protein RP2 interfere with the normal targeting of the protein to the plasma membraneJ P Chapple, A J Hardcastle, C Grayson, et al.
Trends in Molecular Medicine|September 1, 2001
Unfolding retinal dystrophies: a role for molecular chaperones?J P Chapple, C Grayson, A J Hardcastle, et al.
Clinical Neuropathology|October 1, 2009
Homocysteine-induced endoplasmic reticulum protein (herp) is up-regulated in parkinsonian substantia nigra and present in the core of Lewy bodiesH Slodzinski, L B Moran, G J Michael, et al.
Biorxiv : the Preprint Server for Biology|May 19, 2023
Eupatilin improves cilia defects in human CEP290 ciliopathy modelsJ C Corral-Serrano, P E Sladen, D Ottaviani, et al.
Journal of Neuroscience Research|August 20, 2008
DnaJB6 is present in the core of Lewy bodies and is highly up-regulated in parkinsonian astrocytesP F Durrenberger, M D Filiou, L B Moran, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|February 10, 2017
Hsp40 Molecules That Target to the Ubiquitin-proteasome System Decrease Inclusion Formation in Models of Polyglutamine DiseaseJ L Howarth, S Kelly, M P Keasey, et al.
Pageof 4

Showing results (21-30 of 35) with videos related to

Sort By:
Pageof 4
Cytogenetics and Cell Genetics|October 12, 1999
Assignment of the neuronal cochaperone, HSJ1, to human chromosome bands 2q32-->q34 between D2S295 and D2S339 by in situ hybridization and somatic cell and radiation hybridsJ P Chapple, A J Hardcastle, U Kurzik-Dumke, et al.
FEBS Letters|December 21, 1987
Isolation of cDNAs coding for epitopes shared by microtubule-associated proteins and neurofibrillary tangle in Alzheimer's diseaseJ P Brion, M E Cheetham, P A Robinson, et al.
Journal of Medical Genetics|February 5, 2002
In vitro analysis of aminoglycoside therapy for the Arg120stop nonsense mutation in RP2 patientsC Grayson, J P Chapple, K R Willison, et al.
Eye (London, England)|December 16, 2017
A novel missense mutation in HSF4 causes autosomal-dominant congenital lamellar cataract in a British familyV Berry, N Pontikos, A Moore, et al.
Human Molecular Genetics|August 15, 2000
Mutations in the N-terminus of the X-linked retinitis pigmentosa protein RP2 interfere with the normal targeting of the protein to the plasma membraneJ P Chapple, A J Hardcastle, C Grayson, et al.
Trends in Molecular Medicine|September 1, 2001
Unfolding retinal dystrophies: a role for molecular chaperones?J P Chapple, C Grayson, A J Hardcastle, et al.
Clinical Neuropathology|October 1, 2009
Homocysteine-induced endoplasmic reticulum protein (herp) is up-regulated in parkinsonian substantia nigra and present in the core of Lewy bodiesH Slodzinski, L B Moran, G J Michael, et al.
Biorxiv : the Preprint Server for Biology|May 19, 2023
Eupatilin improves cilia defects in human CEP290 ciliopathy modelsJ C Corral-Serrano, P E Sladen, D Ottaviani, et al.
Journal of Neuroscience Research|August 20, 2008
DnaJB6 is present in the core of Lewy bodies and is highly up-regulated in parkinsonian astrocytesP F Durrenberger, M D Filiou, L B Moran, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|February 10, 2017
Hsp40 Molecules That Target to the Ubiquitin-proteasome System Decrease Inclusion Formation in Models of Polyglutamine DiseaseJ L Howarth, S Kelly, M P Keasey, et al.
Pageof 4