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2002 1
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2010 1
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2017 1
2018 1
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Page 1
Abnormalities of neural stem cells in Lesch-Nyhan disease.
Dinasarapu AR, Sutcliffe DJ, Seifar F, Visser JE, Jinnah HA. Dinasarapu AR, et al. Among authors: visser je. J Neurogenet. 2022 Mar-Jun;36(2-3):81-87. doi: 10.1080/01677063.2022.2129632. Epub 2022 Oct 13. J Neurogenet. 2022. PMID: 36226509 Free PMC article.
Induced pluripotent stem cells from subjects with Lesch-Nyhan disease.
Sutcliffe DJ, Dinasarapu AR, Visser JE, Hoed JD, Seifar F, Joshi P, Ceballos-Picot I, Sardar T, Hess EJ, Sun YV, Wen Z, Zwick ME, Jinnah HA. Sutcliffe DJ, et al. Among authors: visser je. Sci Rep. 2021 Apr 19;11(1):8523. doi: 10.1038/s41598-021-87955-9. Sci Rep. 2021. PMID: 33875724 Free PMC article.
Haploinsufficiency of MeCP2-interacting transcriptional co-repressor SIN3A causes mild intellectual disability by affecting the development of cortical integrity.
Witteveen JS, Willemsen MH, Dombroski TC, van Bakel NH, Nillesen WM, van Hulten JA, Jansen EJ, Verkaik D, Veenstra-Knol HE, van Ravenswaaij-Arts CM, Wassink-Ruiter JS, Vincent M, David A, Le Caignec C, Schieving J, Gilissen C, Foulds N, Rump P, Strom T, Cremer K, Zink AM, Engels H, de Munnik SA, Visser JE, Brunner HG, Martens GJ, Pfundt R, Kleefstra T, Kolk SM. Witteveen JS, et al. Among authors: visser je. Nat Genet. 2016 Aug;48(8):877-87. doi: 10.1038/ng.3619. Epub 2016 Jul 11. Nat Genet. 2016. PMID: 27399968
Loss of dopamine phenotype among midbrain neurons in Lesch-Nyhan disease.
Göttle M, Prudente CN, Fu R, Sutcliffe D, Pang H, Cooper D, Veledar E, Glass JD, Gearing M, Visser JE, Jinnah HA. Göttle M, et al. Among authors: visser je. Ann Neurol. 2014 Jul;76(1):95-107. doi: 10.1002/ana.24191. Epub 2014 Jun 20. Ann Neurol. 2014. PMID: 24891139 Free PMC article.
25 results