Zobrazeno 1 - 10
of 112
pro vyhledávání: '"Akkad, Denis A."'
Autor:
Rey, Linda K., Wieczorek, Stefan, Akkad, Denis A., Linker, Ralf A., Chan, Andrew, Hoffjan, Sabine
Publikováno v:
In Molecular and Cellular Probes 2011 25(5):255-259
Autor:
Akkad, Denis A.
Publikováno v:
kostenfrei.
Bochum, Univ., Diss., 2009
Externí odkaz:
http://d-nb.info/994860862/34
http://www-brs.ub.ruhr-uni-bochum.de/netahtml/HSS/Diss/AkkadDenisA/diss.pdf
http://www-brs.ub.ruhr-uni-bochum.de/netahtml/HSS/Diss/AkkadDenisA/diss.pdf
Autor:
Kropatsch, Regina, Petrasch-Parwez, Elisabeth, Seelow, Dominik, Schlichting, Annegrit, Gerding, Wanda M., Akkad, Denis A., Epplen, Joerg T., Dekomien, Gabriele
Publikováno v:
In Molecular and Cellular Probes 2010 24(6):357-363
Autor:
Hoffjan, Sabine, Akkad, Denis A.
Publikováno v:
In Molecular and Cellular Probes 2010 24(5):237-243
Autor:
Akkad, Denis A.1 amer.akkad@ruhr-uni-bochum.de, Olischewsky, Alexandra2, Reiner, Franziska2, Hellwig, Kerstin2, Esser, Sarika1, Epplen, Jörg T.1, Curk, Tomaz3, Gold, Ralf2, Haghikia, Aiden2 aiden.haghikia@ruhr-uni-bochum.de
Publikováno v:
PLoS ONE. May2015, Vol. 10 Issue 5, p1-14. 14p.
Autor:
Haghikia Aiden, Wieczorek Stefan, Akkad Denis A, Saft Carsten, Taherzadeh-Fard Elahe, Chan Andrew, Epplen Jörg T, Arning Larissa
Publikováno v:
Molecular Neurodegeneration, Vol 6, Iss 1, p 32 (2011)
Abstract Background Huntington disease (HD) is an inherited neurodegenerative disease caused by an abnormal expansion of a CAG repeat in the huntingtin HTT (HD) gene. The primary genetic determinant of the age at onset (AO) is the length of the HTT C
Externí odkaz:
https://doaj.org/article/4425634951c24054bec1d06e2015d5b5
Publikováno v:
BMC Medical Genetics, Vol 9, Iss 1, p 107 (2008)
Abstract Background Nerve growth factor β (NGFB) is involved in cell proliferation and survival, and it is a mediator of the immune response. ProNGF, the precursor protein of NGFB, has been shown to induce cell death via interaction with the p75 neu
Externí odkaz:
https://doaj.org/article/7356f7720c0d4977b2d80386a4a64ace
Autor:
Kropatsch, Regina, Akkad, Denis A., Frank, Matthias, Rosenhagen, Carsten, Altmüller, Janine, Nürnberg, Peter, Epplen, Jörg T. (Prof. Dr. med.), Dekomien, Gabriele
\(\textbf {Background:}\) Progressive retinal atrophy (PRA) belongs to a group of inherited retinal disorders associated with gradual vision impairment due to degeneration of retinal photoreceptors in various dog breeds. PRA is highly heterogeneous,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3579::b55b9595ad1823e8a710f6e8e0b18cf0
https://hss-opus.ub.ruhr-uni-bochum.de/opus4/frontdoor/index/index/docId/5814
https://hss-opus.ub.ruhr-uni-bochum.de/opus4/frontdoor/index/index/docId/5814
Autor:
Kropatsch, Regina, Akkad, Denis A., Frank, Matthias, Rosenhagen, Carsten, Altmüller, Janine, Nürnberg, Peter, Epplen, Jörg T., Dekomien, Gabriele
Publikováno v:
Canine Genetics and Epidemiology
Background Progressive retinal atrophy (PRA) belongs to a group of inherited retinal disorders associated with gradual vision impairment due to degeneration of retinal photoreceptors in various dog breeds. PRA is highly heterogeneous, with autosomal
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::844b52848217a9af5bd707b0c8db68bd
http://europepmc.org/articles/PMC4938961
http://europepmc.org/articles/PMC4938961
Autor:
Schrewe, Lisa, Salmen, Anke (Dr. med.), Akkad, Denis A., Hoffjan, Sabine (PD Dr. med.), Demir, S., Böhme, A., Gold, Ralf (Prof. Dr. med.), Chan, Andrew (Dr. med.)
\(\textbf {Background:}\) Despite pleiotropic immunomodulatory effects of apolipoprotein E (apoE) \(\textit {in vitro}\), its effects on the clinical course of experimental autoimmune encephalomyelitis (EAE) and multiple sclerosis (MS) are still cont
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3579::22058e077af066cfbfb7cfbd72a6fcd7
https://hss-opus.ub.ruhr-uni-bochum.de/opus4/files/5837/ChanAndrew1.pdf
https://hss-opus.ub.ruhr-uni-bochum.de/opus4/files/5837/ChanAndrew1.pdf