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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.
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.
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.
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CACNA1B mutation is linked to unique myoclonus-dystonia syndrome.
Groen JL, Andrade A, Ritz K, Jalalzadeh H, Haagmans M, Bradley TE, Jongejan A, Verbeek DS, Nürnberg P, Denome S, Hennekam RC, Lipscombe D, Baas F, Tijssen MA.
Groen JL, et al. Among authors: bradley te.
Hum Mol Genet. 2015 Feb 15;24(4):987-93. doi: 10.1093/hmg/ddu513. Epub 2014 Oct 8.
Hum Mol Genet. 2015.
PMID: 25296916
Free PMC article.
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Deep sequencing of virus-infected cells reveals HIV-encoded small RNAs.
Schopman NC, Willemsen M, Liu YP, Bradley T, van Kampen A, Baas F, Berkhout B, Haasnoot J.
Schopman NC, et al.
Nucleic Acids Res. 2012 Jan;40(1):414-27. doi: 10.1093/nar/gkr719. Epub 2011 Sep 12.
Nucleic Acids Res. 2012.
PMID: 21911362
Free PMC article.
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Mutations in ZBTB20 cause Primrose syndrome.
Cordeddu V, Redeker B, Stellacci E, Jongejan A, Fragale A, Bradley TE, Anselmi M, Ciolfi A, Cecchetti S, Muto V, Bernardini L, Azage M, Carvalho DR, Espay AJ, Male A, Molin AM, Posmyk R, Battisti C, Casertano A, Melis D, van Kampen A, Baas F, Mannens MM, Bocchinfuso G, Stella L, Tartaglia M, Hennekam RC.
Cordeddu V, et al. Among authors: bradley te.
Nat Genet. 2014 Aug;46(8):815-7. doi: 10.1038/ng.3035. Epub 2014 Jul 13.
Nat Genet. 2014.
PMID: 25017102
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