Zobrazeno 1 - 10
of 35
pro vyhledávání: '"Ronnie Folkesson"'
Autor:
Ghada Al-Kafaji, Mohamed Sabry, Mona Fares, Ronnie Folkesson, Jarrah R. Alabkal, Moustapha Hassan, Mariam Al-Ramadan
Publikováno v:
Frontiers in Neuroanatomy
Frontiers in Neuroanatomy, Vol 10 (2016)
Frontiers in Neuroanatomy, Vol 10 (2016)
We read with great interest the article by Poser et al. (2015). Full-length human/murine P75NTR (FL-p75NTR; ENST00000172229, ENSMUST00000000122, ENSRNOT00000007268) is encoded by six exons. Four cysteine-rich repeats span P75NTR extracellular domain
Autor:
Bengt Winblad, Katarzyna Malkiewicz, Eirikur Benedikz, Ronnie Folkesson, Tatjana Nilsson, Maria Gabrielsson
Publikováno v:
Nilsson, T, Malkiewicz, K, Gabrielsson, M, Folkesson, R, Winblad, B & Benedikz, E 2006, ' Antibody-bound amyloid precursor protein upregulates ornithine decarboxylase expression ', Biochemical and Biophysical Research Communications, vol. 341, no. 4, pp. 1294-9 . https://doi.org/10.1016/j.bbrc.2006.01.096
Alzheimer’s disease is a neurodegenerative disorder characterised by extracellular accumulation of the Aβ peptide, derived from the amyloid precursor protein (APP). The function of APP as a cell surface receptor was examined by ligand-mimicking us
Autor:
Jie Zhu, Yu Zhu, Zhiguo Chen, Chris Albanese, Bengt Winblad, Rui-Sheng Duan, Ronnie Folkesson
Publikováno v:
Journal of Neurochemistry. 92:1281-1284
Cyclins D and E play critical roles during the G1 phase of mammalian cell division. Cyclin D1 expression is high and expected to play an important role during mouse brain development. However, in the present study, we found no difference in CNS morph
Publikováno v:
Current Opinion in Psychiatry. 15:433-439
Purpose of review A number of Alzheimer transgenic mouse models have been generated using a variety of different constructs containing the amyloid precursor protein. Some of the models develop features of Alzheimer's disease, including amyloid pathol
Autor:
Eirikur Benedikz, Maria Eriksson, Åke Seiger, Anna Nilsson, Ronnie Folkesson, Susanne Froelich-Fabre, Erik Sundström, Elisabet Åkesson, Jenny Dunker
Publikováno v:
Eriksson, M, Nilsson, A, Froelich-Fabre, S, Akesson, E, Dunker, J, Seiger, A, Folkesson, R, Benedikz, E & Sundström, E 2002, ' Cloning and expression of the human N-methyl-D-aspartate receptor subunit NR3A ', Neuroscience Letters, vol. 321, no. 3, pp. 177-81 .
Native N-methyl-D-aspartate (NMDA) receptors are heteromeric assemblies of four or five subunits. The NMDA receptor subunits, NR1, NR2A, NR2B, NR2C, and NR2D have been cloned in several species, including man. The NR3A subunit, which in rodents is pr
Autor:
Lars N.G. Nilsson, Ronnie Folkesson
Publikováno v:
FEBS Letters. 401:83-88
Five distinct human somatostatin receptor subtypes have recently been cloned and characterized. Previous studies have suggested that these receptor subtypes might display coexistent localization, based on in situ hybridization or immunoblockage exper
Autor:
Gabrielle Meyersson, Lena Bergström, S. Påhlman, Lars N.G. Nilsson, Ronnie Folkesson, Bengt Winblad
Publikováno v:
FEBS Letters. 372:88-92
We have characterized somatostatinergic phenotype markers of the human neuroblastoma, LA-N-2. A single mRNA-transcript (approximately 850bp) and two cellular somatostatin immunoreactivity forms, a high molecular weight form (M(r) 15,000) and a fragme
Autor:
Laura Mateos, Angel Cedazo-Minguez, Ronnie Folkesson, Maura Heverin, Muhammad-Al-Mustafa Ismail, Francisco-Javier Gil-Bea, Ludger Schöls, Rebecca Schüle, Ingemar Björkhem
Disturbances in cholesterol metabolism have been associated with hypertension and neurodegenerative disorders. Because cholesterol metabolism in the brain is efficiently separated from plasma cholesterol by the blood-brain barrier (BBB), it is an uns
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::eed7ffe1a1fe980deaa24a4421c5ea33
https://hdl.handle.net/10171/19667
https://hdl.handle.net/10171/19667
Autor:
Karen Duff, John Hardy, Abdul H. Mohammed, Dennis Hellgren, Lars Lannfelt, Ronnie Folkesson, Bengt Winblad
Publikováno v:
Behavioural Brain Research. 57:207-213
Disease-causing mutations in the amyloid precursor protein (APP) gene have been found on chromosome 21 during the last 2 years in some early onset Alzheimer's disease (AD) families. Genetic evidence shows that other genes than the APP are also involv
Autor:
Ewa Kloskowska, Bengt Winblad, Jan Torleif Pedersen, Ronnie Folkesson, Therese M. Pham, Lars Østergaard Pedersen, Eirikur Benedikz
Publikováno v:
Alzheimer's & Dementia. 5