Articles with public access mandates - Ara KaprelyanLearn more
Available somewhere: 4
Autosomal-recessive congenital cerebellar ataxia is caused by mutations in metabotropic glutamate receptor 1
V Guergueltcheva, DN Azmanov, D Angelicheva, KR Smith, T Chamova, ...
The American Journal of Human Genetics 91 (3), 553-564, 2012
Mandates: National Health and Medical Research Council, Australia
Transcriptome-wide effects of a POLR3A gene mutation in patients with an unusual phenotype of striatal involvement
DN Azmanov, SJ Siira, T Chamova, A Kaprelyan, V Guergueltcheva, ...
Human molecular genetics 25 (19), 4302-4314, 2016
Mandates: Australian Research Council, National Health and Medical Research Council …
GNE myopathy in Roma patients homozygous for the p. I618T founder mutation
T Chamova, V Guergueltcheva, M Gospodinova, S Krause, S Cirak, ...
Neuromuscular Disorders 25 (9), 713-718, 2015
Mandates: UK Medical Research Council
Interaction between transcription factors PAX6/PAX6-5a and specific members of miR-183-96-182 cluster, may contribute to glioma progression in glioblastoma cell lines
E Pavlakis, AB Tonchev, A Kaprelyan, Y Enchev, A Stoykova
Oncology Reports 37 (3), 1579-1592, 2017
Mandates: German Research Foundation
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