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Manuela Neumann

Showing results (51-60 of 175) with videos related to

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The Lancet. Neurology|January 25, 2025
Amyotrophic lateral sclerosis caused by FUS mutations: advances with broad implicationsThomas G Moens, Sandrine Da Cruz, Manuela Neumann, et al.
Archives of Neurology|December 17, 2009
Transactive response DNA-binding protein 43 burden in familial Alzheimer disease and Down syndromeCarol F Lippa, Andrea L Rosso, Lauren D Stutzbach, et al.
Nephrology (Carlton, Vic.)|July 22, 2015
Novel COL4A3 gene mutations in a consanguineous family with autosomal recessive Alport syndromeNirmala D Sirisena, Shenal Thalgahagoda, Asiri Abeyagunawardena, et al.
Nature Communications|May 18, 2017
Temporal dynamics of gene expression and histone marks at the Arabidopsis shoot meristem during floweringYuan You, Aneta Sawikowska, Manuela Neumann, et al.
Genetics|December 6, 2018
Fine-Grained Analysis of Spontaneous Mutation Spectrum and Frequency in <i>Arabidopsis thaliana</i>Mao-Lun Weng, Claude Becker, Julia Hildebrandt, et al.
Journal of Cancer Research and Clinical Oncology|January 6, 2019
High frequency of H3 K27M mutations in adult midline gliomasAzadeh Ebrahimi, Marco Skardelly, Martin U Schuhmann, et al.
Acta Neuropathologica|May 27, 2011
Neuropathological background of phenotypical variability in frontotemporal dementiaKeith A Josephs, John R Hodges, Julie S Snowden, et al.
Brain : a Journal of Neurology|November 22, 2014
Reply: PRKAR1B mutations are a rare cause of FUS negative neuronal intermediate filament inclusion diseaseTsz Hang Wong, Annemieke J M H Verkerk, Annemieke J Rozemuller, et al.
Rapid Communications in Mass Spectrometry : RCM|June 18, 2003
The amyloid-beta (Abeta) peptide pattern in cerebrospinal fluid in Alzheimer's disease: evidence of a novel carboxyterminally elongated Abeta peptidePiotr Lewczuk, Hermann Esselmann, Markus Meyer, et al.
Journal of Neurology|July 8, 2008
Dopaminergic midbrain neurons are the prime target for mitochondrial DNA deletionsAndreas Bender, Rachel-Maria Schwarzkopf, Anja McMillan, et al.
Pageof 18

Showing results (51-60 of 175) with videos related to

Sort By:
Pageof 18
The Lancet. Neurology|January 25, 2025
Amyotrophic lateral sclerosis caused by FUS mutations: advances with broad implicationsThomas G Moens, Sandrine Da Cruz, Manuela Neumann, et al.
Archives of Neurology|December 17, 2009
Transactive response DNA-binding protein 43 burden in familial Alzheimer disease and Down syndromeCarol F Lippa, Andrea L Rosso, Lauren D Stutzbach, et al.
Nephrology (Carlton, Vic.)|July 22, 2015
Novel COL4A3 gene mutations in a consanguineous family with autosomal recessive Alport syndromeNirmala D Sirisena, Shenal Thalgahagoda, Asiri Abeyagunawardena, et al.
Nature Communications|May 18, 2017
Temporal dynamics of gene expression and histone marks at the Arabidopsis shoot meristem during floweringYuan You, Aneta Sawikowska, Manuela Neumann, et al.
Genetics|December 6, 2018
Fine-Grained Analysis of Spontaneous Mutation Spectrum and Frequency in <i>Arabidopsis thaliana</i>Mao-Lun Weng, Claude Becker, Julia Hildebrandt, et al.
Journal of Cancer Research and Clinical Oncology|January 6, 2019
High frequency of H3 K27M mutations in adult midline gliomasAzadeh Ebrahimi, Marco Skardelly, Martin U Schuhmann, et al.
Acta Neuropathologica|May 27, 2011
Neuropathological background of phenotypical variability in frontotemporal dementiaKeith A Josephs, John R Hodges, Julie S Snowden, et al.
Brain : a Journal of Neurology|November 22, 2014
Reply: PRKAR1B mutations are a rare cause of FUS negative neuronal intermediate filament inclusion diseaseTsz Hang Wong, Annemieke J M H Verkerk, Annemieke J Rozemuller, et al.
Rapid Communications in Mass Spectrometry : RCM|June 18, 2003
The amyloid-beta (Abeta) peptide pattern in cerebrospinal fluid in Alzheimer's disease: evidence of a novel carboxyterminally elongated Abeta peptidePiotr Lewczuk, Hermann Esselmann, Markus Meyer, et al.
Journal of Neurology|July 8, 2008
Dopaminergic midbrain neurons are the prime target for mitochondrial DNA deletionsAndreas Bender, Rachel-Maria Schwarzkopf, Anja McMillan, et al.
Pageof 18