Pages that link to "Q33596076"

The following pages link to A study of the Huntington's disease associated trinucleotide repeat in the Scottish population. (Q33596076):

Displaying 31 items.

• HIP-I: a huntingtin interacting protein isolated by the yeast two-hybrid system (Q24320108) (← links)
• Molecular basis of the common electrophoretic polymorphism (Fu1/Fu2) in human alpha-L-fucosidase (Q24517858) (← links)
• Disease-Associated Polyglutamine Stretches in Monomeric Huntingtin Adopt a Compact Structure (Q27677065) (← links)
• Huntington CAG repeat size does not modify onset age in familial Parkinson's disease: the GenePD study (Q30438950) (← links)
• Evidence for a modifier of onset age in Huntington disease linked to the HD gene in 4p16. (Q30445013) (← links)
• A specific mutation for Huntington's disease (Q33596040) (← links)
• Expanded CAG trinucleotide repeat of Huntington's disease gene in a patient with schizophrenia and normal striatal histology (Q33674835) (← links)
• Study of the Huntington's disease (HD) gene CAG repeats in schizophrenic patients shows overlap of the normal and HD affected ranges but absence of correlation with schizophrenia (Q33674958) (← links)
• Analysis of triplet repeats in the huntingtin gene in Japanese families affected with Huntington's disease (Q33682442) (← links)
• The likelihood of being affected with Huntington disease by a particular age, for a specific CAG size (Q35238524) (← links)
• Family history and DNA analysis in patients with suspected Huntington's disease (Q35458053) (← links)
• Phenotypic characterization of individuals with 30-40 CAG repeats in the Huntington disease (HD) gene reveals HD cases with 36 repeats and apparently normal elderly individuals with 36-39 repeats (Q35882893) (← links)
• Advances in Huntington's disease diagnostics: development of a standard reference material (Q36528887) (← links)
• Factors associated with HD CAG repeat instability in Huntington disease (Q37248874) (← links)
• A Drosophila model of Huntington disease-like 2 exhibits nuclear toxicity and distinct pathogenic mechanisms from Huntington disease (Q39732144) (← links)
• Poly-L-glutamine forms cation channels: relevance to the pathogenesis of the polyglutamine diseases (Q40164617) (← links)
• Examination of Huntington's disease with atypical clinical features in a Bangladeshi family tree (Q40407798) (← links)
• The genetic defect causing Huntington's disease: repeated in other contexts? (Q41456204) (← links)
• Reliability of clinical diagnosis of Huntington's disease (Q41979514) (← links)
• Huntington disease--another chapter rewritten (Q42587589) (← links)
• Mutation analysis in patients with possible but apparently sporadic Huntington's disease (Q45289058) (← links)
• Mutational bias provides a model for the evolution of Huntington's disease and predicts a general increase in disease prevalence. (Q45289187) (← links)
• Trinucleotide (CAG) repeat expansion in chromosomes of Spanish patients with Huntington's disease (Q45289222) (← links)
• Instability of highly expanded CAG repeats in mice transgenic for the Huntington's disease mutation. (Q45293768) (← links)
• Reduced penetrance of the Huntington's disease mutation (Q45294302) (← links)
• Juvenile Huntington disease in the Netherlands (Q45295074) (← links)
• Molecular diagnosis of Huntington disease in Brazilian patients (Q45300182) (← links)
• Comparative sequence analysis of the human and pufferfish Huntington's disease genes (Q45307541) (← links)
• Triplet repeat variability in the signal peptide sequence of the Xmrk receptor tyrosine kinase gene in Xiphophorus fish (Q47990453) (← links)
• Interaction of normal and expanded CAG repeat sizes influences age at onset of Huntington disease (Q57628958) (← links)
• Molecular Genetics of Huntington’s Disease (Q74790223) (← links)