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pro vyhledávání: '"Arning, Larissa (Prof. Dr.)"'
The causative mutation for Huntington disease (HD), an expanded trinucleotide repeat sequence in the first exon of the huntingtin gene \(\it (HTT)\) is naturally polymorphic and inevitably associated with disease symptoms above 39 CAG repeats. Althou
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3579::6ee4e699924ecf07272b627e2c6481c6
https://hss-opus.ub.ruhr-uni-bochum.de/opus4/frontdoor/index/index/docId/8597
https://hss-opus.ub.ruhr-uni-bochum.de/opus4/frontdoor/index/index/docId/8597
Autor:
Schlüter, Caroline (Dr. rer. nat.), Arning, Larissa (Prof. Dr.), Fraenz, Christoph (M. Sc.), Friedrich, Patrick (M. Sc.), Pinnow, Marlies (Dr. rer. nat.), Güntürkün, Onur (Prof. Dr. Dr. h.c.), Beste, Christian (Dr. rer. nat.), Ocklenburg, Sebastian (Prof. Dr. rer. nat.), Genç, Erhan (Dr. rer. nat.)
Although procrastination is a widespread phenomenon with significant influence on our personal and professional life, its genetic foundation is somewhat unknown. An important factor that influences our ability to tackle specific goals directly instea
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3579::6cc5ce3f0e2039cf2688ddcd532be605
https://hss-opus.ub.ruhr-uni-bochum.de/opus4/frontdoor/index/index/docId/7304
https://hss-opus.ub.ruhr-uni-bochum.de/opus4/frontdoor/index/index/docId/7304
Autor:
Aydin, Gülsah, Dekomien, Gabriele, Hoffjan, Sabine (PD Dr. med.), Gerding, Wanda Maria, Epplen, Jörg T. (Prof. Dr. med.), Arning, Larissa (Prof. Dr.)
\(\textbf {Background:}\) Spinocerebellar ataxia (SCA) subtypes are often caused by expansions in non-coding regions of genes like \(\textit {SCA8, SCA10, SCA12}\) and \(\it {SCA36}\). Other ataxias are known to be associated with repeat expansions s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3579::86ee57139893ef162a4e1dc2f06f6647
https://hss-opus.ub.ruhr-uni-bochum.de/opus4/files/6002/ArningLarissa2.pdf
https://hss-opus.ub.ruhr-uni-bochum.de/opus4/files/6002/ArningLarissa2.pdf
Autor:
Arning, Larissa (Prof. Dr.), Ocklenburg, Sebastian (Prof. Dr. rer. nat.), Schulz, Stefanie, Ness, Vanessa, Gerding, Wanda Maria, Hengstler, Jan Georg, Falkenstein, Michael (Prof. em. Dr. med. Dipl.-Psych. Dipl.-Ing.), Epplen, Jörg T. (Prof. Dr. med.), Güntürkün, Onur (Prof. Dr. Dr. h.c.), Beste, Christian (Dr. rer. nat.)
Prenatal androgen exposure has been suggested to be one of the factors influencing handedness, making the androgen receptor gene (AR) a likely candidate gene for individual differences in handedness. Here, we examined the relationship between the len
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3579::5d68a35494fe13a65fe7be7e74f3ff57
https://hss-opus.ub.ruhr-uni-bochum.de/opus4/frontdoor/index/index/docId/5786
https://hss-opus.ub.ruhr-uni-bochum.de/opus4/frontdoor/index/index/docId/5786