Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Ruud A. Wolterman"'
Autor:
Iliana Michailidou, Aldo Jongejan, Jeroen P. Vreijling, Theodosia Georgakopoulou, Marit B. de Wissel, Ruud A. Wolterman, Patrick Ruizendaal, Ngaisah Klar-Mohamad, Anita E. Grootemaat, Daisy I. Picavet, Vinod Kumar, Cees van Kooten, Trent M. Woodruff, B. Paul Morgan, Nicole N. van der Wel, Valeria Ramaglia, Kees Fluiter, Frank Baas
Publikováno v:
Acta Neuropathologica Communications, Vol 6, Iss 1, Pp 1-17 (2018)
Abstract The complement system is a key driver of neuroinflammation. Activation of complement by all pathways, results in the formation of the anaphylatoxin C5a and the membrane attack complex (MAC). Both initiate pro-inflammatory responses which can
Externí odkaz:
https://doaj.org/article/aa28a418a3c5487a95181f43b8fe2680
Autor:
Tanja Kulkens, Pieter A. Bolhuis, Ruud A. Wolterman, Stephan Kemp, Saskia te Nijenhuis, Linda J. Valentijn, Gerard W. Hensels, Frans G.I. Jennekens, Marianne de Visser, Jessica E. Hoogendijk, Frank Baas
Publikováno v:
Nature genetics, 5(1), 35-39. Nature Publishing Group
Charcot-Marie-Tooth disease type 1B (CMT1B) is genetically linked to chromosome 1q21-23. The major peripheral myelin protein gene, P0, has been cloned and localized to the same chromosomal region. P0 is a 28 kDa glycoprotein involved in the compactio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8c4b4f00c46feb2f287169a2aa0cbb32
https://pure.amc.nl/en/publications/deletion-of-the-serine-34-codon-from-the-major-peripheral-myelin-protein-p0-gene-in-charcotmarietooth-disease-type-1b(6cf1fff1-7aef-4a06-9ec9-cbb112700254).html
https://pure.amc.nl/en/publications/deletion-of-the-serine-34-codon-from-the-major-peripheral-myelin-protein-p0-gene-in-charcotmarietooth-disease-type-1b(6cf1fff1-7aef-4a06-9ec9-cbb112700254).html
Collagen synthesis in cultured myoblasts and myotubes from patients with Duchenne muscular dystrophy
Publikováno v:
Journal of the neurological sciences. 82(1-3)
Collagen synthesis was studied in cultured myoblasts and myotubes from 4 patients with Duchenne muscular dystrophy (DMD) and 4 control persons. Incorporation of [3H]proline into collagen of DMD cells and control cells was not significantly different.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::22bfd37d6aef616b71c97182bbdcce99
https://pubmed.ncbi.nlm.nih.gov/3440869
https://pubmed.ncbi.nlm.nih.gov/3440869
Autor:
Michailidou, Iliana1,2, Jongejan, Aldo3, Vreijling, Jeroen P.2, Georgakopoulou, Theodosia1, de Wissel, Marit B.1, Wolterman, Ruud A.1, Ruizendaal, Patrick1, Klar-Mohamad, Ngaisah4, Grootemaat, Anita E.5, Picavet, Daisy I.5, Kumar, Vinod6, van Kooten, Cees4, Woodruff, Trent M.6, Morgan, B. Paul7, van der Wel, Nicole N.5, Ramaglia, Valeria1,8, Fluiter, Kees2, Baas, Frank2 F.Baas@lumc.nl
Publikováno v:
Acta Neuropathologica Communications. 5/3/2018, Vol. 6 Issue 1, pN.PAG-N.PAG. 1p.
Publikováno v:
Human Genetics; 1990, Vol. 85 Issue 3, p327-329, 3p
Publikováno v:
Neuron Glia Biology; 2007 Supplement, Vol. 3 Issue S1, pS177-S198, 1p