Zobrazeno 1 - 10
of 37
pro vyhledávání: '"Erik R. Vossenaar"'
Publikováno v:
Autoimmunity. Jun2004, Vol. 37 Issue 4, p295-299. 5p.
Autor:
Albert J.W. Zendman, Ger J. M. Pruijn, Erik R. Vossenaar, Jan W. Drijfhout, Walther J. van Venrooij
Publikováno v:
Current Rheumatology Reviews. 1:1-7
Rheumatoid arthritis (RA) is a common systemic autoimmune disease with a prevalence of about 1% worldwide [1]. The American College of Rheumatology (ACR) criteria for the classification of RA [2] are not very well suited to diagnose RA at an early st
Autor:
S Nijenhuis, Ger J. M. Pruijn, Albert J.W. Zendman, Erik R. Vossenaar, Walther J. vanVenrooij
Publikováno v:
Clinica Chimica Acta, 350, 17-34
Clinica Chimica Acta, 350, 1-2, pp. 17-34
Clinica Chimica Acta, 350, 1-2, pp. 17-34
Contains fulltext : 58385.pdf (Publisher’s version ) (Closed access) Rheumatoid arthritis (RA) is a common, systemic autoimmune disease of which the exact etiology is not known. In the past 10 years, substantial progress has been made in the identi
Publikováno v:
Clinical and Applied Immunology Reviews. 4:239-262
Rheumatoid arthritis (RA) is a chronic, destructive autoimmune disease affecting the joints. With more sophisticated and effective therapies becoming available and with the understanding that early intervention is crucial in preventing irreversible j
Autor:
J. Graveline, H. Heilbronner, Rick A. Friedman, J.T. den Dunnen, Lorne S. Parnes, P. Thorpe, F. P. M. Cremers, Erik R. Vossenaar, Ling Jia Hu, Niklas Dahl, H.H. Ropers, H.-J. Pander, Didier Lacombe, Cor W. R. J. Cremers, Y.J.M. de Kok, Han G. Brunner, M. Bitner-Glindzicz, Nathan Fischel-Ghodsian, Jocelyn Laporte
Publikováno v:
Human Molecular Genetics, 5, 1229-1235
Human Molecular Genetics, 5, 9, pp. 1229-1235
Human Molecular Genetics
Human Molecular Genetics, 1996, 5 (9), pp.1229-1235. ⟨10.1093/hmg/5.9.1229⟩
Human Molecular Genetics, 5, 9, pp. 1229-1235
Human Molecular Genetics
Human Molecular Genetics, 1996, 5 (9), pp.1229-1235. ⟨10.1093/hmg/5.9.1229⟩
Small mutations in the POU domain gene POU3F4 were recently shown to cause X-linked deafness type 3 (DFN3) in nine unrelated males. The POU3F4 gene was found to be located outside four of five deletions associated with DFN3. Two of these deletions we
Autor:
Marcos López‐Hoyoz, Erik R. Vossenaar, Jesús Merino, Martinus A.M. van Boekel, Ramón Merino, Leo A. B. Joosten, Walther J. van Venrooij
Publikováno v:
Arthritis & Rheumatism. 50:2370-2372
Publikováno v:
Arthritis and rheumatism, 46(10), 2824-2826. John Wiley and Sons Inc.
Autor:
Ger J. M. Pruijn, Jan W. Drijfhout, Reinout Raijmakers, Renato G.S. Chirivi, Jos M.H. Raats, Marloes van den Tillaart, Albert J.W. Zendman, Erik R. Vossenaar, Walther J. van Venrooij, S Nijenhuis
Publikováno v:
Analytical Biochemistry, 369, 2, pp. 232-240
Analytical Biochemistry, 369, 232-240
Analytical Biochemistry, 369, 232-240
Members of the family of peptidylarginine deiminases (PADs, EC 3.5.3.15) catalyze the posttranslational modification of peptidylarginine into peptidylcitrulline. Citrulline-containing epitopes have been shown to be major and specific targets of autoa
Autor:
Ger J. M. Pruijn, Claudia Soede-Huijbregts, Jan W. Drijfhout, Wilma Vree Egberts, Floris P. J. T. Rutjes, Reinout Raijmakers, Peter A. van Veelen, Albert J.W. Zendman, Erik R. Vossenaar, Jos M.H. Raats
Publikováno v:
Journal of Molecular Biology, 367, 1118-1129
Journal of Molecular Biology, 367, 4, pp. 1118-1129
Journal of Molecular Biology, 367, 4, pp. 1118-1129
Peptidylarginine deiminase (PAD) enzymes catalyze the conversion of arginine residues in proteins to citrulline residues. Citrulline is a non-standard amino acid that is not incorporated in proteins during translation, but can be generated post-trans
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d742744a9ac397555dca81219c0d60b9
http://hdl.handle.net/2066/34477
http://hdl.handle.net/2066/34477
Publikováno v:
Autoimmunity, 37, 295-9
Autoimmunity, 37, 4, pp. 295-9
Autoimmunity, 37, 4, pp. 295-9
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