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Distribution of PCP4 protein in the forebrain of adult mice.
Renelt M, von Bohlen und Halbach V, von Bohlen und Halbach O. Renelt M, et al. Among authors: von bohlen und halbach v, von bohlen und halbach o. Acta Histochem. 2014 Jul;116(6):1056-61. doi: 10.1016/j.acthis.2014.04.012. Epub 2014 Jun 20. Acta Histochem. 2014. PMID: 24954028
Impact of a deletion of the full-length and short isoform of p75NTR on cholinergic innervation and the population of postmitotic doublecortin positive cells in the dentate gyrus.
Poser R, Dokter M, von Bohlen Und Halbach V, Berger SM, Busch R, Baldus M, Unsicker K, von Bohlen Und Halbach O. Poser R, et al. Among authors: von bohlen und halbach v. Front Neuroanat. 2015 May 27;9:63. doi: 10.3389/fnana.2015.00063. eCollection 2015. Front Neuroanat. 2015. PMID: 26074780 Free PMC article.
BDNF effects on dendritic spine morphology and hippocampal function.
von Bohlen Und Halbach O, von Bohlen Und Halbach V. von Bohlen Und Halbach O, et al. Among authors: von bohlen und halbach v. Cell Tissue Res. 2018 Sep;373(3):729-741. doi: 10.1007/s00441-017-2782-x. Epub 2018 Feb 15. Cell Tissue Res. 2018. PMID: 29450725 Review.
ATP6AP2 over-expression causes morphological alterations in the hippocampus and in hippocampus-related behaviour.
Bracke A, Schäfer S, von Bohlen Und Halbach V, Klempin F, Bente K, Bracke K, Staar D, van den Brandt J, Harzsch S, Bader M, Wenzel UO, Peters J, von Bohlen Und Halbach O. Bracke A, et al. Among authors: von bohlen und halbach v. Brain Struct Funct. 2018 Jun;223(5):2287-2302. doi: 10.1007/s00429-018-1633-1. Epub 2018 Feb 23. Brain Struct Funct. 2018. PMID: 29473106
A patient-specific induced pluripotent stem cell model for West syndrome caused by ST3GAL3 deficiency.
van Diepen L, Buettner FFR, Hoffmann D, Thiesler CT, von Bohlen Und Halbach O, von Bohlen Und Halbach V, Jensen LR, Steinemann D, Edvardson S, Elpeleg O, Schambach A, Gerardy-Schahn R, Kuss AW. van Diepen L, et al. Among authors: von bohlen und halbach v. Eur J Hum Genet. 2018 Dec;26(12):1773-1783. doi: 10.1038/s41431-018-0220-5. Epub 2018 Aug 8. Eur J Hum Genet. 2018. PMID: 30089820 Free PMC article.
A mouse model for intellectual disability caused by mutations in the X-linked 2'‑O‑methyltransferase Ftsj1 gene.
Jensen LR, Garrett L, Hölter SM, Rathkolb B, Rácz I, Adler T, Prehn C, Hans W, Rozman J, Becker L, Aguilar-Pimentel JA, Puk O, Moreth K, Dopatka M, Walther DJ, von Bohlen Und Halbach V, Rath M, Delatycki M, Bert B, Fink H, Blümlein K, Ralser M, Van Dijck A, Kooy F, Stark Z, Müller S, Scherthan H, Gecz J, Wurst W, Wolf E, Zimmer A, Klingenspor M, Graw J, Klopstock T, Busch D, Adamski J, Fuchs H, Gailus-Durner V, de Angelis MH, von Bohlen Und Halbach O, Ropers HH, Kuss AW. Jensen LR, et al. Among authors: von bohlen und halbach v. Biochim Biophys Acta Mol Basis Dis. 2019 Sep 1;1865(9):2083-2093. doi: 10.1016/j.bbadis.2018.12.011. Epub 2018 Dec 14. Biochim Biophys Acta Mol Basis Dis. 2019. PMID: 30557699 Free article.
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