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	41.	Markov chain Monte Carlo analysis of human Y-chromosome microsatellites provides evidence of biased mutation. [electronic resource] by Cooper, G Burroughs, N J Rand, D A Rubinsztein, D C Amos, W Producer: 19991124 In: Proceedings of the National Academy of Sciences of the United States of America vol. 96 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	42.	A locus for autosomal dominant "pure" hereditary spastic paraplegia maps to chromosome 19q13. [electronic resource] by Reid, E Dearlove, A M Osborn, O Rogers, M T Rubinsztein, D C Producer: 20000330 In: American journal of human genetics vol. 66 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	43.	Subclinical cognitive impairment in autosomal dominant "pure" hereditary spastic paraplegia. [electronic resource] by Reid, E Grayson, C Rubinsztein, D C Rogers, M T Rubinsztein, J S Producer: 19991119 In: Journal of medical genetics vol. 36 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	44.	Wild-type but not mutant huntingtin modulates the transcriptional activity of liver X receptors. [electronic resource] by Futter, M Diekmann, H Schoenmakers, E Sadiq, O Chatterjee, K Rubinsztein, D C Producer: 20090923 In: Journal of medical genetics vol. 46 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	45.	The molecular biology of Huntington's disease. [electronic resource] by Ho, L W Carmichael, J Swartz, J Wyttenbach, A Rankin, J Rubinsztein, D C Producer: 20010329 In: Psychological medicine vol. 31 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	46.	Genetic association between monoamine oxidase A microsatellite and RFLP alleles and bipolar affective disorder: analysis and meta-analysis. [electronic resource] by Rubinsztein, D C Leggo, J Goodburn, S Walsh, C Jain, S Paykel, E S Producer: 19961205 In: Human molecular genetics vol. 5 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	47.	Mild myotonic dystrophy is associated with memory impairment in the context of normal general intelligence. [electronic resource] by Rubinsztein, J S Rubinsztein, D C McKenna, P J Goodburn, S Holland, A J Producer: 19970430 In: Journal of medical genetics vol. 34 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	48.	Myotonic dystrophy CTG repeats and the associated insertion/deletion polymorphism in human and primate populations. [electronic resource] by Rubinsztein, D C Leggo, J Amos, W Barton, D E Ferguson-Smith, M A Producer: 19950404 In: Human molecular genetics vol. 3 Availability: No items available. Save to lists Add to cart (remove)
	49.	Bacterial and yeast chaperones reduce both aggregate formation and cell death in mammalian cell models of Huntington's disease. [electronic resource] by Carmichael, J Chatellier, J Woolfson, A Milstein, C Fersht, A R Rubinsztein, D C Producer: 20000919 In: Proceedings of the National Academy of Sciences of the United States of America vol. 97 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	50.	Normal CAG and CCG repeats in the Huntington's disease genes of Parkinson's disease patients. [electronic resource] by Rubinsztein, D C Leggo, J Goodburn, S Barton, D E Ferguson-Smith, M A Producer: 19951215 In: American journal of medical genetics vol. 60 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	51.	Haplotype analysis of the delta 2642 and (CAG)n polymorphisms in the Huntington's disease (HD) gene provides an explanation for an apparent 'founder' HD haplotype. [electronic resource] by Rubinsztein, D C Leggo, J Goodburn, S Barton, D E Ferguson-Smith, M A Producer: 19950629 In: Human molecular genetics vol. 4 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	52.	Identification of two new LDL-receptor mutations causing homozygous familial hypercholesterolemia in a South African of Indian origin. [electronic resource] by Rubinsztein, D C Jialal, I Leitersdorf, E Coetzee, G A van der Westhuyzen, D R Producer: 19930915 In: Biochimica et biophysica acta vol. 1182 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	53.	Genotypes at the GluR6 kainate receptor locus are associated with variation in the age of onset of Huntington disease. [electronic resource] by Rubinsztein, D C Leggo, J Chiano, M Dodge, A Norbury, G Rosser, E Craufurd, D Producer: 19970522 In: Proceedings of the National Academy of Sciences of the United States of America vol. 94 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	54.	The ACE I allele is associated with increased risk for ruptured intracranial aneurysms. [electronic resource] by Keramatipour, M McConnell, R S Kirkpatrick, P Tebbs, S Furlong, R A Rubinsztein, D C Producer: 20000828 In: Journal of medical genetics vol. 37 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	55.	Analysis of the monoamine oxidase A (MAOA) gene in bipolar affective disorder by association studies, meta-analyses, and sequencing of the promoter. [electronic resource] by Furlong, R A Ho, L Rubinsztein, J S Walsh, C Paykel, E S Rubinsztein, D C Producer: 19991101 In: American journal of medical genetics vol. 88 Availability: No items available. Save to lists Add to cart (remove)
	56.	Familial defective apolipoprotein-B is rare in hypercholesterolaemic South African Afrikaners, coloureds and Indians. [electronic resource] by Rubinsztein, D C Coetzee, G A van der Westhuyzen, D R Langenhoven, E Kotze, M J Producer: 19950908 In: South African medical journal = Suid-Afrikaanse tydskrif vir geneeskunde vol. 85 Availability: No items available. Save to lists Add to cart (remove)
	57.	No association of the tryptophan hydroxylase gene with bipolar affective disorder, unipolar affective disorder, or suicidal behaviour in major affective disorder. [electronic resource] by Furlong, R A Ho, L Rubinsztein, J S Walsh, C Paykel, E S Rubinsztein, D C Producer: 19980624 In: American journal of medical genetics vol. 81 Availability: No items available. Save to lists Add to cart (remove)
	58.	Instability of normal (CTG)n alleles in the DM kinase gene. [electronic resource] by Dow, D J Rubinsztein, D C Yates, J R Barton, D E Ferguson-Smith, M A Producer: 19971209 In: Journal of medical genetics vol. 34 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	59.	Stop signal response inhibition is not modulated by tryptophan depletion or the serotonin transporter polymorphism in healthy volunteers: implications for the 5-HT theory of impulsivity. [electronic resource] by Clark, L Roiser, J P Cools, R Rubinsztein, D C Sahakian, B J Robbins, T W Producer: 20060214 In: Psychopharmacology vol. 182 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	60.	Effects of heat shock, heat shock protein 40 (HDJ-2), and proteasome inhibition on protein aggregation in cellular models of Huntington's disease. [electronic resource] by Wyttenbach, A Carmichael, J Swartz, J Furlong, R A Narain, Y Rankin, J Rubinsztein, D C Producer: 20000425 In: Proceedings of the National Academy of Sciences of the United States of America vol. 97 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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Your search returned 124 results.