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The coding and non-coding transcriptional landscape of subependymal giant cell astrocytomas.
Bongaarts A, van Scheppingen J, Korotkov A, Mijnsbergen C, Anink JJ, Jansen FE, Spliet WGM, den Dunnen WFA, Gruber VE, Scholl T, Samueli S, Hainfellner JA, Feucht M, Kotulska K, Jozwiak S, Grajkowska W, Buccoliero AM, Caporalini C, Giordano F, Genitori L, Coras R, Blümcke I, Krsek P, Zamecnik J, Meijer L, Scicluna BP, Schouten-van Meeteren AYN, Mühlebner A, Mills JD, Aronica E. Bongaarts A, et al. Among authors: gruber ve. Brain. 2020 Jan 1;143(1):131-149. doi: 10.1093/brain/awz370. Brain. 2020. PMID: 31834371 Free PMC article.
Dysregulation of the MMP/TIMP Proteolytic System in Subependymal Giant Cell Astrocytomas in Patients With Tuberous Sclerosis Complex: Modulation of MMP by MicroRNA-320d In Vitro.
Bongaarts A, de Jong JM, Broekaart DWM, van Scheppingen J, Anink JJ, Mijnsbergen C, Jansen FE, Spliet WGM, den Dunnen WFA, Gruber VE, Scholl T, Hainfellner JA, Feucht M, Borkowska J, Kotulska K, Jozwiak S, Grajkowska W, Buccoliero AM, Caporalini C, Giordano F, Genitori L, Scicluna BP, Schouten-van Meeteren AYN, van Vliet EA, Mühlebner A, Mills JD, Aronica E. Bongaarts A, et al. Among authors: gruber ve. J Neuropathol Exp Neurol. 2020 Jul 1;79(7):777-790. doi: 10.1093/jnen/nlaa040. J Neuropathol Exp Neurol. 2020. PMID: 32472129 Free PMC article.
Distinct DNA Methylation Patterns of Subependymal Giant Cell Astrocytomas in Tuberous Sclerosis Complex.
Bongaarts A, Mijnsbergen C, Anink JJ, Jansen FE, Spliet WGM, den Dunnen WFA, Coras R, Blümcke I, Paulus W, Gruber VE, Scholl T, Hainfellner JA, Feucht M, Kotulska K, Jozwiak S, Grajkowska W, Buccoliero AM, Caporalini C, Giordano F, Genitori L, Söylemezoğlu F, Pimentel J, Jones DTW, Scicluna BP, Schouten-van Meeteren AYN, Mühlebner A, Mills JD, Aronica E. Bongaarts A, et al. Among authors: gruber ve. Cell Mol Neurobiol. 2022 Nov;42(8):2863-2892. doi: 10.1007/s10571-021-01157-5. Epub 2021 Oct 28. Cell Mol Neurobiol. 2022. PMID: 34709498 Free PMC article.
Impaired oligodendroglial turnover is associated with myelin pathology in focal cortical dysplasia and tuberous sclerosis complex.
Scholl T, Mühlebner A, Ricken G, Gruber V, Fabing A, Samueli S, Gröppel G, Dorfer C, Czech T, Hainfellner JA, Prabowo AS, Reinten RJ, Hoogendijk L, Anink JJ, Aronica E, Feucht M. Scholl T, et al. Brain Pathol. 2017 Nov;27(6):770-780. doi: 10.1111/bpa.12452. Epub 2017 Feb 9. Brain Pathol. 2017. PMID: 27750396 Free PMC article.
Amplification of human interneuron progenitors promotes brain tumors and neurological defects.
Eichmüller OL, Corsini NS, Vértesy Á, Morassut I, Scholl T, Gruber VE, Peer AM, Chu J, Novatchkova M, Hainfellner JA, Paredes MF, Feucht M, Knoblich JA. Eichmüller OL, et al. Among authors: gruber ve. Science. 2022 Jan 28;375(6579):eabf5546. doi: 10.1126/science.abf5546. Epub 2022 Jan 28. Science. 2022. PMID: 35084981 Free PMC article.
Increased expression of complement components in tuberous sclerosis complex and focal cortical dysplasia type 2B brain lesions.
Gruber VE, Luinenburg MJ, Colleselli K, Endmayr V, Anink JJ, Zimmer TS, Jansen F, Gosselaar P, Coras R, Scholl T, Blumcke I, Pimentel J, Hainfellner JA, Höftberger R, Rössler K, Feucht M, van Scheppingen J, Aronica E, Mühlebner A. Gruber VE, et al. Epilepsia. 2022 Feb;63(2):364-374. doi: 10.1111/epi.17139. Epub 2021 Dec 14. Epilepsia. 2022. PMID: 34904712 Free PMC article.
14 results