Your search returned 34 results.

Results
	21.	Isolation of cDNAs coding for epitopes shared by microtubule-associated proteins and neurofibrillary tangle in Alzheimer's disease. [electronic resource] by Brion, J P Cheetham, M E Robinson, P A Couck, A M Anderton, B H Producer: 19880127 In: FEBS letters vol. 226 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	22.	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. [electronic resource] by Chapple, J P Hardcastle, A J Kurzik-Dumke, U Collier, D A Cheetham, M E Producer: 19991027 In: Cytogenetics and cell genetics vol. 86 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	23.	A novel missense mutation in HSF4 causes autosomal-dominant congenital lamellar cataract in a British family. [electronic resource] by Berry, V Pontikos, N Moore, A Ionides, A C W Plagnol, V Cheetham, M E Michaelides, M Producer: 20181211 In: Eye (London, England) vol. 32 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	24.	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. [electronic resource] by Chapple, J P Hardcastle, A J Grayson, C Spackman, L A Willison, K R Cheetham, M E Producer: 20001012 In: Human molecular genetics vol. 9 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	25.	In vitro analysis of aminoglycoside therapy for the Arg120stop nonsense mutation in RP2 patients. [electronic resource] by Grayson, C Chapple, J P Willison, K R Webster, A R Hardcastle, A J Cheetham, M E Producer: 20020312 In: Journal of medical genetics vol. 39 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	26.	Unfolding retinal dystrophies: a role for molecular chaperones? [electronic resource] by Chapple, J P Grayson, C Hardcastle, A J Saliba, R S van der Spuy, J Cheetham, M E Producer: 20011101 In: Trends in molecular medicine vol. 7 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	27.	Homocysteine-induced endoplasmic reticulum protein (herp) is up-regulated in parkinsonian substantia nigra and present in the core of Lewy bodies. [electronic resource] by Slodzinski, H Moran, L B Michael, G J Wang, B Novoselov, S Cheetham, M E Pearce, R K B Graeber, M B Producer: 20091020 In: Clinical neuropathology vol. 28 Availability: No items available. Save to lists Add to cart (remove)
	28.	DnaJB6 is present in the core of Lewy bodies and is highly up-regulated in parkinsonian astrocytes. [electronic resource] by Durrenberger, P F Filiou, M D Moran, L B Michael, G J Novoselov, S Cheetham, M E Clark, P Pearce, R K B Graeber, M B Producer: 20090408 In: Journal of neuroscience research vol. 87 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	29.	Hsp40 Molecules That Target to the Ubiquitin-proteasome System Decrease Inclusion Formation in Models of Polyglutamine Disease. [electronic resource] by Howarth, J L Kelly, S Keasey, M P Glover, Cpj Lee, Y-B Mitrophanous, K Chapple, J P Gallo, J M Cheetham, M E Uney, J B Publication details: Molecular therapy : the journal of the American Society of Gene Therapy Jun 2007 In: Molecular therapy : the journal of the American Society of Gene Therapy vol. 15 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	30.	Cytosolic and ER J-domains of mammalian and parasitic origin can functionally interact with DnaK. [electronic resource] by Nicoll, W S Botha, M McNamara, C Schlange, M Pesce, E-R Boshoff, A Ludewig, M H Zimmermann, R Cheetham, M E Chapple, J P Blatch, G L Producer: 20070611 In: The international journal of biochemistry & cell biology vol. 39 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	31.	Hsp40 molecules that target to the ubiquitin-proteasome system decrease inclusion formation in models of polyglutamine disease. [electronic resource] by Howarth, J L Kelly, S Keasey, M P Glover, C P J Lee, Y-B Mitrophanous, K Chapple, J P Gallo, J M Cheetham, M E Uney, J B Producer: 20070925 In: Molecular therapy : the journal of the American Society of Gene Therapy vol. 15 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	32.	An atypical phenotype of macular and peripapillary retinal atrophy caused by a mutation in the RP2 gene. [electronic resource] by Dandekar, S S Ebenezer, N D Grayson, C Chapple, J P Egan, C A Holder, G E Jenkins, S A Fitzke, F W Cheetham, M E Webster, A R Hardcastle, A J Producer: 20040511 In: The British journal of ophthalmology vol. 88 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	33.	The heat-shock response co-inducer arimoclomol protects against retinal degeneration in rhodopsin retinitis pigmentosa. [electronic resource] by Parfitt, D A Aguila, M McCulley, C H Bevilacqua, D Mendes, H F Athanasiou, D Novoselov, S S Kanuga, N Munro, P M Coffey, P J Kalmar, B Greensmith, L Cheetham, M E Producer: 20141021 In: Cell death & disease vol. 5 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	34.	RPGR mutation associated with retinitis pigmentosa, impaired hearing, and sinorespiratory infections. [electronic resource] by Zito, I Downes, S M Patel, R J Cheetham, M E Ebenezer, N D Jenkins, S A Bhattacharya, S S Webster, A R Holder, G E Bird, A C Bamiou, D E Hardcastle, A J Producer: 20031103 In: Journal of medical genetics vol. 40 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)