Rethinking Oral Health in Aging: Ecosocial Theory and Intersectionality von Slack-Smith, L., Ng, T., Macdonald, M.E., Durey, A.

Volltext

Obstetric conditions and the placental weight ratio von Macdonald, E.M, Natale, R, Regnault, T.R.H, Koval, J.J, Campbell, M.K

Volltext

Loss of Huntingtin-Mediated BDNF Gene Transcription in Huntington's Disease von Zuccato, Chiara, Ciammola, Andrea, Rigamonti, Dorotea, Leavitt, Blair R., Goffredo, Donato, Conti, Luciano, MacDonald, Marcy E., Friedlander, Robert M., Silani, Vincenzo, Hayden, Michael R., Timmusk, Tõnis, Sipione, Simonetta, Cattaneo, Elena

Volltext

Oral health-related stigma: Describing and defining a ubiquitous phenomenon von Doughty, J, Macdonald, M E, Muirhead, V, Freeman, R

Volltext

Factors associated with HD CAG repeat instability in Huntington disease von Wheeler, V C, Persichetti, F, McNeil, S M, Mysore, J S, Mysore, S S, MacDonald, M E, Myers, R H, Gusella, J F, Wexler, N S

Volltext

The quantity and quality of the social networks of young people with early psychosis compared with closely matched controls von Macdonald, E.M, Hayes, R.L, Baglioni, A.J

Volltext

CAG repeat number governs the development rate of pathology in Huntington's disease von Penney Jr, John B., Vonsattel, Jean-Paul, Macdonald, Marcy E., Gusella, James F., Myers, Richard H.

Volltext

Huntingtin Interacts with a Family of WW Domain Proteins von Faber, Peter W., Barnes, Glenn T., Srinidhi, Jayalakshmi, Chen, Jianmin, Gusella, James F., MacDonald, Marcy E.

Volltext

Huntingtin is required for neurogenesis and is not impaired by the Huntington's disease CAG expansion von White, Jacqueline K, Auerbach, Wojtek, Duyao, Mabel P, Vonsattel, Jean-Paul, Gusella, James F, Joyner, Alexandra L, MacDonald, Marcy E

Volltext

Length-Dependent Gametic CAG Repeat Instability in the Huntington's Disease Knock-in Mouse von Wheeler, Vanessa C., Auerbach, Wojtek, White, Jacqueline K., Srinidhi, Jayalakshmi, Auerbach, Anna, Ryan, Angela, Duyao, Mabel P., Vrbanac, Vladimir, Weaver, Meredith, Gusella, James F., Joyner, Alexandra L., MacDonald, Marcy E.

Volltext

Hypogonadotropic hypogonadism and cleft lip and palate caused by a balanced translocation producing haploinsufficiency for FGFR1 von Kim, HG, Herrick, S R, Lemyre, E, Kishikawa, S, Salisz, J A, Seminara, S, MacDonald, M E, Bruns, G A P, Morton, C C, Quade, B J, Gusella, J F

Volltext

Evidence for the GluR6 gene associated with younger onset age of Huntington's disease von MACDONALD, M. E, VONSATTEL, J. P, SHRINIDHI, J, COUROPMITREE, N. N, CUPPLES, L. A, BIRD, E. D, GUSELLA, J. F, MYERS, R. H

Volltext

Herbicide exposure modifies GSTP1 haplotype association to parkinson onset age : The GenePD study von WILK, J. B, TOBIN, J. E, SINGER, C, GROWDON, J. H, LATOURELLE, J. C, SAINT-HILAIRE, M. H, DESTEFANO, A. L, PRAKASH, R, WILLIAMSON, S, BERG, C. J, SUN, M, GOLDWURM, S, SUCHOWERSKY, O, PEZZOLI, G, RACETTE, B. A, PERLMUTTER, J. S, PARSIAN, A, BAKER, K. B, GIROUX, M. L, LITVAN, I, PRAMSTALLER, P. P, NICHOLSON, G, BURN, D. J, SHILL, H. A, CHINNERY, P. F, VIEREGGE, P, SLEVIN, J. T, CAMBI, F, MACDONALD, M. E, GUSELLA, J. F, MYERS, R. H, GOLBE, L. I, KLEIN, C, WOOTEN, G. F, LEW, M. F, MARK, M. H, GUTTMAN, M, WATTS, R. L

Volltext

Interaction of normal and expanded CAG repeat sizes influences age at onset of Huntington disease von Djoussé, L., Knowlton, B., Hayden, M., Almqvist, E.W., Brinkman, R., Ross, C., Margolis, R., Rosenblatt, A., Durr, A., Dode, C., Morrison, P.J., Novelletto, A., Frontali, M., Trent, R.J.A., McCusker, E., Gómez-Tortosa, E., Mayo, D., Jones, R., Zanko, A., Nance, M., Abramson, R., Suchowersky, O., Paulsen, J., Harrison, M., Yang, Q., Cupples, L.A., Gusella, J.F., MacDonald, M.E., Myers, R.H.

Volltext

Clinical and genetic heterogeneity in benign hereditary chorea von BREEDVELD, G. J, PERCY, A. K, MACDONALD, M. E, DE VRIES, B. B. A, YAPIJAKIS, C, DURE, L. S, IPPEL, E. F, SANDKUIJL, L. A, HEUTINK, P, ARTS, W. F. M

Volltext

Molecular genetics: Unmasking polyglutamine triggers in neurodegenerative disease von Gusella, James F, MacDonald, Marcy E

Volltext

Reduced Penetrance of the Huntington's Disease Mutation von McNeil, Sandra M., Novelletto, Andrea, Srinidhi, Jayalakshmi, Barnes, Glenn, Kornbluth, Ira, Altherr, Michael R., Wasmuth, John J., Gusella, James F., MacDonald, Marcy E., Myers, Richard H.

Volltext

Dominant phenotypes produced by the HD mutation in STHdh(Q111) striatal cells von Trettel, F, Rigamonti, D, Hilditch-Maguire, P, Wheeler, V C, Sharp, A H, Persichetti, F, Cattaneo, E, MacDonald, M E

Volltext

De novo expansion of a (CAG) n repeat in sporadic Huntington's disease von Myers, R. H, MacDonald, M. E, Koroshetz, W. J, Duyao, M. P, Ambrose, C. M, Taylor, S. A. M, Barnes, G, Srinidhi, J, Lin, C. S, Whaley, W. L, Lazzarini, A. M, Schwarz, M, Wolff, G, Bird, E. D, Vonsattel, J.-P. G, Gusella, J. F

Volltext

Huntingtin's WW domain partners in Huntington's disease post-mortem brain fulfill genetic criteria for direct involvement in Huntington's disease pathogenesis von PASSANI, L. A, BEDFORD, M. T, FABER, P. W, MCGINNIS, K. M, SHARP, A. H, GUSELLA, J. F, VONSATTEL, J.-P, MACDONALD, M. E

Volltext