A. Michalik

发表

Intraneuronal amyloid β and reduced brain volume in a novel APP T714I mouse model for Alzheimer's disease

Annemie Van der Linden, Samir Kumar-Singh, Christine Van Broeckhoven, 2008, Neurobiology of Aging.

Intraneuronal amyloid beta and reduced brain volume in a novel APP T714I mouse model for Alzheimer's disease.

Samir Kumar-Singh, Christine Van Broeckhoven, Annemie Van der Linden, 2008, Neurobiology of aging.

Ataxin‐7 aggregation and ubiquitination in infantile SCA7 with 180 CAG repeats

C. van Broeckhoven, B. Harding, F. Scaravilli, 2004, Annals of neurology.

Pure Familial Spastic Paraplegia: Clinical and Genetic Analysis of Nine Belgian Pedigrees

J. Weissenbach, C. Broeckhoven, J. Hazan, 1996, European journal of human genetics : EJHG.

Hot-spot residue in small heat-shock protein 22 causes distal motor neuropathy

C. Broeckhoven, W. Robberecht, J. Vandekerckhove, 2004, Nature Genetics.

Spinocerebellar ataxia type 7 associated with pigmentary retinal dystrophy

C. Broeckhoven, A. Michalik, J. Martin, 2004, European Journal of Human Genetics.

Molecular genetic analysis of autosomal dominant cerebellar ataxia with retinal degeneration (ADCA type II) caused by CAG triplet repeat expansion.

J. Theuns, H. Backhovens, A. Wehnert, 1998, Human molecular genetics.

Association of ataxin-7 with the proteasome subunit S4 of the 19S regulatory complex.

C. van Broeckhoven, C. Gorbea, L. Ptáček, 2001, Human molecular genetics.

Pathogenesis of polyglutamine disorders: aggregation revisited.

Christine Van Broeckhoven, C. van Broeckhoven, A. Michalik, 2003, Human molecular genetics.

Isolation of CAG/CTG repeats from within the chromosome 2p21-p24 locus for autosomal dominant spastic paraplegia (SPG4) by YAC fragmentation

C. van Broeckhoven, P. de Jonghe, J. Del-Favero, 1999, Human Genetics.

Genomic organisation of the spinocerebellar ataxia type 7 (SCA7) gene responsible for autosomal dominant cerebellar ataxia with retinal degeneration

C. van Broeckhoven, J. Del-Favero, A. Michalik, 1999, Human Genetics.

Proteasome degrades soluble expanded polyglutamine completely and efficiently

Christine Van Broeckhoven, C. Broeckhoven, A. Michalik, 2004, Neurobiology of Disease.

Genomic organisation of the spinocerebellar ataxia type 7 (SCA7) gene responsible for autosomal dominant cerebellar ataxia with retinal degeneration.

C. Broeckhoven, J. Del-Favero, A. Michalik, 1999 .