Zobrazeno 1 - 3
of 3
pro vyhledávání: '"genetics [Receptors, Androgen]"'
Autor:
Yolande A.L. Pijnenburg, Philip Scheltens, Wiesje M. van der Flier, Iris E. Jansen, Martine J. van Belzen, Merel W. Boogaard, Jacobijn Gussekloo, Stella Trompet, Raymund A.C. Roos, Yvonne J.M. Campman, N. Ahmad Aziz, Aster V.E. Harder, Sarah L. Gardiner
Publikováno v:
Neurobiology of Aging, 73, 230.e9-230.e17. Elsevier Inc.
Neurobiology of aging 73, 230.e9-230.e17 (2019). doi:10.1016/j.neurobiolaging.2018.09.007
Neurobiology of Aging, 73
Gardiner, S L, Harder, A V E, Campman, Y J M, Trompet, S, Gussekloo, J, van Belzen, M J, Boogaard, M W, Roos, R A C, Jansen, I E, Pijnenburg, Y A L, Scheltens, P, van der Flier, W M & Aziz, N A 2019, ' Repeat length variations in ATXN1 and AR modify disease expression in Alzheimer's disease ', Neurobiology of Aging, vol. 73, pp. 230.e9-230.e17 . https://doi.org/10.1016/j.neurobiolaging.2018.09.007
Neurobiology of aging 73, 230.e9-230.e17 (2019). doi:10.1016/j.neurobiolaging.2018.09.007
Neurobiology of Aging, 73
Gardiner, S L, Harder, A V E, Campman, Y J M, Trompet, S, Gussekloo, J, van Belzen, M J, Boogaard, M W, Roos, R A C, Jansen, I E, Pijnenburg, Y A L, Scheltens, P, van der Flier, W M & Aziz, N A 2019, ' Repeat length variations in ATXN1 and AR modify disease expression in Alzheimer's disease ', Neurobiology of Aging, vol. 73, pp. 230.e9-230.e17 . https://doi.org/10.1016/j.neurobiolaging.2018.09.007
Genomewide association studies (GWASs) have contributed greatly to unraveling the genetic basis of Alzheimer's disease (AD). However, a large amount of “missing heritability” remains. In this exploratory study, we investigated the effect of cytos
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6a44af72365ba7bf897e11cefc146843
https://hdl.handle.net/1887/116663
https://hdl.handle.net/1887/116663
Autor:
Dmitriy Drichel, Regina C. Betz, Stefanie Heilmann, K. Dobson, Andrew G. Messenger, Tobias W. Fischer, Natalie Garcia-Bartels, Markus Böhm, Anja Miesel, Roland Kruse, Silke Redler, Sandra Hanneken, Rachid Tazi-Ahnini, Sabrina Wolf, Kathrin A. Giehl, Tim Becker, Gerhard Lutz, Ulrike Blume-Peytavi, Hans Wolff, Markus M. Nöthen, Pattie Birch, Rima Nuwaihyd
Publikováno v:
Archives of dermatological research 306(4), 413-418 (2013). doi:10.1007/s00403-013-1436-4
Female pattern hair loss (FPHL) is a common hair loss disorder in women and has a complex mode of inheritance. The etiopathogenesis of FPHL is largely unknown; however, it is hypothesized that FPHL and male pattern baldness [androgenetic alopecia (AG
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6b81510ea0933cc089a89002a983036d
https://doi.org/10.1007/s00403-013-1436-4
https://doi.org/10.1007/s00403-013-1436-4
Autor:
Fernando Rivadeneira, M. Arfan Ikram, Jens Wiltfang, Frank Hentschel, Monique M.B. Breteler, Frank Jessen, Reinhard Heun, Peter J. Koudstaal, Oliver Peters, Eckart Rüther, Heike Kölsch, Albert Hofman, Johannes Kornhuber, Elisabeth M. C. Schrijvers, Wolfgang Maier, Martin Dichgans, Cornelia M. van Duijn, André G. Uitterlinden, Steffi G. Riedel-Heller, Hendrik van den Bussche, Britta Schürmann
Publikováno v:
Stroke, 43(2), 315-319. Lippincott Williams & Wilkins
Stroke 43(2), 315-319 (2012). doi:10.1161/STROKEAHA.111.628768
Stroke 43(2), 315-319 (2012). doi:10.1161/STROKEAHA.111.628768
Background and Purpose— Most studies investigating the genetics of dementia have focused on Alzheimer disease, but little is known about the genetics of vascular dementia. The aim of our study was to identify new loci associated with vascular demen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::55280d7424ae19920dafdb42ee0893f2
https://pure.eur.nl/en/publications/b39ac087-3f29-4998-bac5-5823ea8e4c0b
https://pure.eur.nl/en/publications/b39ac087-3f29-4998-bac5-5823ea8e4c0b