Results 261 to 270 of about 115,141 (275)

Bidirectional expression of CUG and CAG expansion transcripts and intranuclear polyglutamine inclusions in spinocerebellar ataxia type 8

Nature Genetics, 2006
Tao Zu, Timothy J Ebner, John W Day
exaly  

Treatment of acute leukemia in children with ataxia telangiectasia (A-T).

European Journal of Medical Genetics, 2016
M. Schoenaker, Felipe Suarez, T. Szczepański, N. Mahlaoui, Jan Loeffen   +4 more
semanticscholar   +1 more source

Vascular endothelial growth factor ameliorates the ataxic phenotype in a mouse model of spinocerebellar ataxia type 1

Nature Medicine, 2011
Marija Cvetanovic, Hugo H Marti, Puneet Opal   +2 more
exaly  

Ataxia telangiectasia

The Journal of Pediatrics, 1967
openaire   +3 more sources

Spectrin mutations cause spinocerebellar ataxia type 5

Nature Genetics, 2006
Karen R Armbrust, Giovanni Stevanin, Alexis Brice   +2 more
exaly  

Mutation of TDP1, encoding a topoisomerase I–dependent DNA damage repair enzyme, in spinocerebellar ataxia with axonal neuropathy

Nature Genetics, 2002
Cornelius F Boerkoel
exaly  

Ataxia telangiectasia: more variation at clinical and cellular levels

Clinical Genetics, 2015
A. Taylor, Z. Lam, J. Last, P. Byrd
semanticscholar   +1 more source

Deletion of Pten in mouse brain causes seizures, ataxia and defects in soma size resembling Lhermitte-Duclos disease

Nature Genetics, 2001
Vuk Stambolic, Akira Suzuki, Ming-Sound Tsao   +2 more
exaly  

Ataxia-Telangiectasia

2003
E. Cubo, C.G. Goetz
openaire   +2 more sources

The gene mutated in ataxia-ocular apraxia 1 encodes the new HIT/Zn-finger protein aprataxin

Nature Genetics, 2001
Clara Barbot, Paula Coutinho, Jorge Sequeiros   +2 more
exaly