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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 hybrids
J 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 disease
J 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 patients
C 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 family
V 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 membrane
J 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 bodies
H 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 models
J 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 astrocytes
P 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 Disease
J L Howarth, S Kelly, M P Keasey, et al.
Page
of 4
Search research articles
Search
Showing results (21-30 of 35) with videos related to
Sort By:
Page
of 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 hybrids
J 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 disease
J 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 patients
C 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 family
V 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 membrane
J 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 bodies
H 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 models
J 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 astrocytes
P 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 Disease
J L Howarth, S Kelly, M P Keasey, et al.
Page
of 4