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Benefits of Exome Sequencing in Children with Suspected Isolated Hearing Loss.
Genes (Basel). 2021 Aug 20;12(8):1277. doi: 10.3390/genes12081277.
Genes (Basel). 2021.
PMID: 34440452
Free PMC article.
Autosomal recessive cerebellar ataxia of adult onset due to STUB1 mutations.
Depondt C, Donatello S, Simonis N, Rai M, van Heurck R, Abramowicz M, D'Hooghe M, Pandolfo M.
Depondt C, et al. Among authors: van heurck r.
Neurology. 2014 May 13;82(19):1749-50. doi: 10.1212/WNL.0000000000000416. Epub 2014 Apr 9.
Neurology. 2014.
PMID: 24719489
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Bimodal modulation of tau protein phosphorylation and conformation by extracellular Zn2+ in human-tau transfected cells.
Boom A, Authelet M, Dedecker R, Frédérick C, Van Heurck R, Daubie V, Leroy K, Pochet R, Brion JP.
Boom A, et al. Among authors: van heurck r.
Biochim Biophys Acta. 2009 Jun;1793(6):1058-67. doi: 10.1016/j.bbamcr.2008.11.011. Epub 2008 Dec 8.
Biochim Biophys Acta. 2009.
PMID: 19111579
Free article.
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Human-Specific NOTCH2NL Genes Expand Cortical Neurogenesis through Delta/Notch Regulation.
Suzuki IK, Gacquer D, Van Heurck R, Kumar D, Wojno M, Bilheu A, Herpoel A, Lambert N, Cheron J, Polleux F, Detours V, Vanderhaeghen P.
Suzuki IK, et al. Among authors: van heurck r.
Cell. 2018 May 31;173(6):1370-1384.e16. doi: 10.1016/j.cell.2018.03.067. Epub 2018 May 31.
Cell. 2018.
PMID: 29856955
Free PMC article.
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CROCCP2 acts as a human-specific modifier of cilia dynamics and mTOR signaling to promote expansion of cortical progenitors.
Van Heurck R, Bonnefont J, Wojno M, Suzuki IK, Velez-Bravo FD, Erkol E, Nguyen DT, Herpoel A, Bilheu A, Beckers S, Ledent C, Vanderhaeghen P.
Van Heurck R, et al.
Neuron. 2023 Jan 4;111(1):65-80.e6. doi: 10.1016/j.neuron.2022.10.018. Epub 2022 Nov 4.
Neuron. 2023.
PMID: 36334595
Free PMC article.
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Epidemiology of MDR-TB in a Belgian infectious diseases unit: a 15 years review.
van Heurck R, Payen MC, De Wit S, Clumeck N.
van Heurck R, et al.
Acta Clin Belg. 2013 Sep-Oct;68(5):321-4. doi: 10.2143/ACB.3269.
Acta Clin Belg. 2013.
PMID: 24579238
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