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Ciliary neurotrophic factor null alleles are not a risk factor for Charcot-Marie-Tooth disease, hereditary neuropathy with pressure palsies and amyotrophic lateral sclerosis.
Van Vught PW, Van Wijk J, Bradley TE, Plasmans D, Jakobs ME, Veldink JH, de Jong JM, Van den Berg LH, Baas F. Van Vught PW, et al. Among authors: jakobs me. Neuromuscul Disord. 2007 Dec;17(11-12):964-7. doi: 10.1016/j.nmd.2007.06.006. Epub 2007 Jul 24. Neuromuscul Disord. 2007. PMID: 17651970
Dynamic clonal hematopoiesis and functional T-cell immunity in a supercentenarian.
van den Akker EB, Makrodimitris S, Hulsman M, Brugman MH, Nikolic T, Bradley T, Waisfisz Q, Baas F, Jakobs ME, de Jong D, Slagboom PE, Staal FJT, Reinders MJT, Holstege H. van den Akker EB, et al. Among authors: jakobs me. Leukemia. 2021 Jul;35(7):2125-2129. doi: 10.1038/s41375-020-01086-0. Epub 2020 Nov 12. Leukemia. 2021. PMID: 33184493 Free PMC article. No abstract available.
A frameshift mutation in LRSAM1 is responsible for a dominant hereditary polyneuropathy.
Weterman MA, Sorrentino V, Kasher PR, Jakobs ME, van Engelen BG, Fluiter K, de Wissel MB, Sizarov A, Nürnberg G, Nürnberg P, Zelcer N, Schelhaas HJ, Baas F. Weterman MA, et al. Among authors: jakobs me. Hum Mol Genet. 2012 Jan 15;21(2):358-70. doi: 10.1093/hmg/ddr471. Epub 2011 Oct 19. Hum Mol Genet. 2012. PMID: 22012984 Free PMC article.
SMARCB1/INI1 maternal germ line mosaicism in schwannomatosis.
Hulsebos TJ, Kenter SB, Jakobs ME, Baas F, Chong B, Delatycki MB. Hulsebos TJ, et al. Among authors: jakobs me. Clin Genet. 2010 Jan;77(1):86-91. doi: 10.1111/j.1399-0004.2009.01249.x. Epub 2009 Nov 3. Clin Genet. 2010. PMID: 19912265
Human T-cell memory consists mainly of unexpanded clones.
Klarenbeek PL, Tak PP, van Schaik BD, Zwinderman AH, Jakobs ME, Zhang Z, van Kampen AH, van Lier RA, Baas F, de Vries N. Klarenbeek PL, et al. Among authors: jakobs me. Immunol Lett. 2010 Sep 6;133(1):42-8. doi: 10.1016/j.imlet.2010.06.011. Epub 2010 Jul 16. Immunol Lett. 2010. PMID: 20621124
24 results