Zobrazeno 1 - 10
of 686
pro vyhledávání: '"Fellerer, K"'
Autor:
Fellerer, K. G., Hadas, Moses
Publikováno v:
The Musical Quarterly, 1953 Oct 01. 39(4), 576-594.
Externí odkaz:
https://www.jstor.org/stable/739857
Autor:
Fellerer, K. G.
Publikováno v:
Archiv für Musikwissenschaft, 1924 Dec 01. 6(4), 471-483.
Externí odkaz:
https://www.jstor.org/stable/929637
Autor:
Fellerer, K. G.
Publikováno v:
Studia Musicologica Academiae Scientiarum Hungaricae, 1969 Jan 01. 11(1/4), 159-167.
Externí odkaz:
https://www.jstor.org/stable/901276
Autor:
Fellerer, K. G.
Publikováno v:
Studia Musicologica Academiae Scientiarum Hungaricae, 1962 Jan 01. 3(1/4), 109-115.
Externí odkaz:
https://www.jstor.org/stable/901634
Autor:
Suarez-Calvet, M, Morenas-Rodriguez, E, Kleinberger, G, Schlepckow, K, Caballero, MAA, Franzmeier, N, Capell, A, Fellerer, K, Nuscher, B, Eren, E, Levin, J, Deming, Y, Piccio, L, Karch, CM, Cruchaga, C, Shaw, LM, Trojanowski, JQ, Weiner, M, Ewers, M, Haass, C, Alzheimers Dis Neuroimaging
Publikováno v:
Molecular Neurodegeneration
r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
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r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
instname
BackgroundTREM2 is a transmembrane receptor that is predominantly expressed by microglia in the central nervous system. Rare variants in the TREM2 gene increase the risk for late-onset Alzheimer's disease (AD). Soluble TREM2 (sTREM2) resulting from s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=RECOLECTA___::8cad209e182c55aad6c082f454920ca6
https://iibsantpau.fundanetsuite.com/Publicaciones/ProdCientif/PublicacionFrw.aspx?id=3048
https://iibsantpau.fundanetsuite.com/Publicaciones/ProdCientif/PublicacionFrw.aspx?id=3048
Autor:
Gotzl, J., Colombo, Alessio Vittorio, Mazaheri, Fargol, Smith, S., Fellerer, K., Butovsky, O., Tahirovic, Sabina, Capell, A., Haass, Christian
Publikováno v:
Journal of neurochemistry 138(Supplement 1), 410 (2016).
Heterozygous loss-of-function mutations in the progranulin(GRN) gene result in GRN haploinsufficiency, which is a majorcause for familial frontotemporal lobar degeneration (FTLD) withTAR DNA-binding protein (TDP) -43 and ubiquitin-positiveinclusions
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_____10678::4b6634e911b3a8176aea1f360bdfb8ea
https://pub.dzne.de/record/145519
https://pub.dzne.de/record/145519
Publikováno v:
Journal of neurochemistry 138(Supplement 1), 419 (2016).
Heterozygous loss-of-function mutations in the progranulin(GRN) gene result in GRN haploinsufficiency, which is, besidesthe C9orf72 repeat expansions, the major cause of familialfrontotemporal lobar degeneration (FTLD) with TAR DNA-bindingprotein (T
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_____10678::d6ba0371592a852a64564d881df96101
Autor:
Svenningsson, Anna L.1,2 (AUTHOR) anna.svenningsson@med.lu.se, Bocancea, Diana I.3,4 (AUTHOR), Stomrud, Erik1,2 (AUTHOR), van Loenhoud, Anita3,4 (AUTHOR), Barkhof, Frederik5,6 (AUTHOR), Mattsson-Carlgren, Niklas1,7,8 (AUTHOR), Palmqvist, Sebastian1,2 (AUTHOR), Hansson, Oskar1,2 (AUTHOR), Ossenkoppele, Rik1,3,4 (AUTHOR)
Publikováno v:
Alzheimer's Research & Therapy. 10/12/2024, Vol. 16 Issue 1, p1-17. 17p.
Autor:
Zeng, Xuemei1 (AUTHOR), Lafferty, Tara K.1 (AUTHOR), Sehrawat, Anuradha1 (AUTHOR), Chen, Yijun2 (AUTHOR), Ferreira, Pamela C. L.1 (AUTHOR), Bellaver, Bruna1 (AUTHOR), Povala, Guilherme1 (AUTHOR), Kamboh, M. Ilyas3 (AUTHOR), Klunk, William E.1 (AUTHOR), Cohen, Ann D.1 (AUTHOR), Lopez, Oscar L.4 (AUTHOR), Ikonomovic, Milos D.1,4,5 (AUTHOR), Pascoal, Tharick A.1 (AUTHOR), Ganguli, Mary1,4,6 (AUTHOR), Villemagne, Victor L.1 (AUTHOR), Snitz, Beth E.4 (AUTHOR), Karikari, Thomas K.1 (AUTHOR) Karikaritk@upmc.edu
Publikováno v:
Molecular Neurodegeneration. 10/10/2024, Vol. 19 Issue 1, p1-21. 21p.
Autor:
Werner G; Metabolic Biochemistry, Biomedical Center (BMC), Faculty of Medicine, Ludwig-Maximilians-Universität München, Munich, Germany., Damme M; Institute of Biochemistry, Kiel University, Kiel, Germany., Schludi M; German Center for Neurodegenerative Diseases (DZNE), Munich, Germany., Gnörich J; Department of Nuclear Medicine, University Hospital, Ludwig-Maximilians-Universität München, Munich, Germany., Wind K; Department of Nuclear Medicine, University Hospital, Ludwig-Maximilians-Universität München, Munich, Germany., Fellerer K; Metabolic Biochemistry, Biomedical Center (BMC), Faculty of Medicine, Ludwig-Maximilians-Universität München, Munich, Germany., Wefers B; German Center for Neurodegenerative Diseases (DZNE), Munich, Germany.; Institute of Developmental Genetics, Helmholtz Zentrum München, German Research Center for Environmental Health, Neuherberg, Germany., Wurst W; German Center for Neurodegenerative Diseases (DZNE), Munich, Germany.; Institute of Developmental Genetics, Helmholtz Zentrum München, German Research Center for Environmental Health, Neuherberg, Germany.; Munich Cluster for Systems Neurology (SyNergy), Munich, Germany., Edbauer D; German Center for Neurodegenerative Diseases (DZNE), Munich, Germany., Brendel M; Department of Nuclear Medicine, University Hospital, Ludwig-Maximilians-Universität München, Munich, Germany., Haass C; Metabolic Biochemistry, Biomedical Center (BMC), Faculty of Medicine, Ludwig-Maximilians-Universität München, Munich, Germany.; German Center for Neurodegenerative Diseases (DZNE), Munich, Germany.; Munich Cluster for Systems Neurology (SyNergy), Munich, Germany., Capell A; Metabolic Biochemistry, Biomedical Center (BMC), Faculty of Medicine, Ludwig-Maximilians-Universität München, Munich, Germany.
Publikováno v:
EMBO reports [EMBO Rep] 2020 Oct 05; Vol. 21 (10), pp. e50241. Date of Electronic Publication: 2020 Sep 14.