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PRKAR1B mutation associated with a new neurodegenerative disorder with unique pathology.
Wong TH, Chiu WZ, Breedveld GJ, Li KW, Verkerk AJ, Hondius D, Hukema RK, Seelaar H, Frick P, Severijnen LA, Lammers GJ, Lebbink JH, van Duinen SG, Kamphorst W, Rozemuller AJ; Netherlands Brain Bank; Bakker EB; International Parkinsonism Genetics Network; Neumann M, Willemsen R, Bonifati V, Smit AB, van Swieten J. Wong TH, et al. Among authors: lebbink jh. Brain. 2014 May;137(Pt 5):1361-73. doi: 10.1093/brain/awu067. Epub 2014 Apr 9. Brain. 2014. PMID: 24722252
Binding of carboxypeptidase N to fibrinogen and fibrin.
Talens S, Lebbink JH, Malfliet JJ, Demmers JA, Uitte de Willige S, Leebeek FW, Rijken DC. Talens S, et al. Among authors: lebbink jh. Biochem Biophys Res Commun. 2012 Oct 19;427(2):421-5. doi: 10.1016/j.bbrc.2012.09.081. Epub 2012 Sep 21. Biochem Biophys Res Commun. 2012. PMID: 23000409
Dual daughter strand incision is processive and increases the efficiency of DNA mismatch repair.
Hermans N, Laffeber C, Cristovão M, Artola-Borán M, Mardenborough Y, Ikpa P, Jaddoe A, Winterwerp HH, Wyman C, Jiricny J, Kanaar R, Friedhoff P, Lebbink JH. Hermans N, et al. Among authors: lebbink jh. Nucleic Acids Res. 2016 Aug 19;44(14):6770-86. doi: 10.1093/nar/gkw411. Epub 2016 May 12. Nucleic Acids Res. 2016. PMID: 27174933 Free PMC article.
Biallelic PAX5 mutations cause hypogammaglobulinemia, sensorimotor deficits, and autism spectrum disorder.
Kaiser FMP, Gruenbacher S, Oyaga MR, Nio E, Jaritz M, Sun Q, van der Zwaag W, Kreidl E, Zopf LM, Dalm VASH, Pel J, Gaiser C, van der Vliet R, Wahl L, Rietman A, Hill L, Leca I, Driessen G, Laffeber C, Brooks A, Katsikis PD, Lebbink JHG, Tachibana K, van der Burg M, De Zeeuw CI, Badura A, Busslinger M. Kaiser FMP, et al. Among authors: lebbink jhg. J Exp Med. 2022 Sep 5;219(9):e20220498. doi: 10.1084/jem.20220498. Epub 2022 Aug 10. J Exp Med. 2022. PMID: 35947077 Free PMC article.
55 results