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M E Cheetham

Showing results (31-40 of 35) with videos related to

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The International Journal of Biochemistry & Cell Biology|January 24, 2007
Cytosolic and ER J-domains of mammalian and parasitic origin can functionally interact with DnaKW S Nicoll, M Botha, C McNamara, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|April 12, 2007
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.
The British Journal of Ophthalmology|March 20, 2004
An atypical phenotype of macular and peripapillary retinal atrophy caused by a mutation in the RP2 geneS S Dandekar, N D Ebenezer, C Grayson, et al.
Cell Death & Disease|May 24, 2014
The heat-shock response co-inducer arimoclomol protects against retinal degeneration in rhodopsin retinitis pigmentosaD A Parfitt, M Aguila, C H McCulley, et al.
Journal of Medical Genetics|August 16, 2003
RPGR mutation associated with retinitis pigmentosa, impaired hearing, and sinorespiratory infectionsI Zito, S M Downes, R J Patel, et al.
Pageof 4

Showing results (31-40 of 35) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 35 results.
The International Journal of Biochemistry & Cell Biology|January 24, 2007
Cytosolic and ER J-domains of mammalian and parasitic origin can functionally interact with DnaKW S Nicoll, M Botha, C McNamara, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|April 12, 2007
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.
The British Journal of Ophthalmology|March 20, 2004
An atypical phenotype of macular and peripapillary retinal atrophy caused by a mutation in the RP2 geneS S Dandekar, N D Ebenezer, C Grayson, et al.
Cell Death & Disease|May 24, 2014
The heat-shock response co-inducer arimoclomol protects against retinal degeneration in rhodopsin retinitis pigmentosaD A Parfitt, M Aguila, C H McCulley, et al.
Journal of Medical Genetics|August 16, 2003
RPGR mutation associated with retinitis pigmentosa, impaired hearing, and sinorespiratory infectionsI Zito, S M Downes, R J Patel, et al.
Pageof 4