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Ina Schmitt

Showing results (31-40 of 40) with videos related to

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Neurobiology of Disease|August 25, 2009
A transgenic mouse model of spinocerebellar ataxia type 3 resembling late disease onset and gender-specific instability of CAG repeatsJana Boy, Thorsten Schmidt, Ulrike Schumann, et al.
European Journal of Human Genetics : EJHG|May 24, 2012
Variants in the 3'UTR of SNCA do not affect miRNA-433 binding and alpha-synuclein expressionIna Schmitt, Ullrich Wüllner, Jan Pierre van Rooyen, et al.
Human Molecular Genetics|December 22, 2005
Rapamycin alleviates toxicity of different aggregate-prone proteinsZdenek Berger, Brinda Ravikumar, Fiona M Menzies, et al.
Brain : a Journal of Neurology|June 10, 2011
N-terminal ataxin-3 causes neurological symptoms with inclusions, endoplasmic reticulum stress and ribosomal dislocationJeannette Hübener, Franz Vauti, Claudia Funke, et al.
Plos Biology|November 17, 2016
The Machado-Joseph Disease Deubiquitinase Ataxin-3 Regulates the Stability and Apoptotic Function of p53Hongmei Liu, Xiaoling Li, Guozhu Ning, et al.
Life Science Alliance|November 21, 2018
LATS1 and LATS2 suppress breast cancer progression by maintaining cell identity and metabolic stateNoa Furth, Ioannis S Pateras, Ron Rotkopf, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|March 7, 2008
Neurodegeneration and motor dysfunction in a conditional model of Parkinson's diseaseSilke Nuber, Elisabeth Petrasch-Parwez, Beate Winner, et al.
Human Molecular Genetics|March 7, 2003
Transgenic rat model of Huntington's diseaseStephan von Hörsten, Ina Schmitt, Huu Phuc Nguyen, et al.
Parkinsonism & Related Disorders|June 21, 2022
Methylation of alpha-synuclein in a Sudanese cohortYousuf Bakhit, Ina Schmitt, Ahlam Hamed, et al.
Brain : a Journal of Neurology|May 2, 2017
Hypomorphic mutations in POLR3A are a frequent cause of sporadic and recessive spastic ataxiaMartina Minnerop, Delia Kurzwelly, Holger Wagner, et al.
Pageof 4

Showing results (31-40 of 40) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 40 results.
Neurobiology of Disease|August 25, 2009
A transgenic mouse model of spinocerebellar ataxia type 3 resembling late disease onset and gender-specific instability of CAG repeatsJana Boy, Thorsten Schmidt, Ulrike Schumann, et al.
European Journal of Human Genetics : EJHG|May 24, 2012
Variants in the 3'UTR of SNCA do not affect miRNA-433 binding and alpha-synuclein expressionIna Schmitt, Ullrich Wüllner, Jan Pierre van Rooyen, et al.
Human Molecular Genetics|December 22, 2005
Rapamycin alleviates toxicity of different aggregate-prone proteinsZdenek Berger, Brinda Ravikumar, Fiona M Menzies, et al.
Brain : a Journal of Neurology|June 10, 2011
N-terminal ataxin-3 causes neurological symptoms with inclusions, endoplasmic reticulum stress and ribosomal dislocationJeannette Hübener, Franz Vauti, Claudia Funke, et al.
Plos Biology|November 17, 2016
The Machado-Joseph Disease Deubiquitinase Ataxin-3 Regulates the Stability and Apoptotic Function of p53Hongmei Liu, Xiaoling Li, Guozhu Ning, et al.
Life Science Alliance|November 21, 2018
LATS1 and LATS2 suppress breast cancer progression by maintaining cell identity and metabolic stateNoa Furth, Ioannis S Pateras, Ron Rotkopf, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|March 7, 2008
Neurodegeneration and motor dysfunction in a conditional model of Parkinson's diseaseSilke Nuber, Elisabeth Petrasch-Parwez, Beate Winner, et al.
Human Molecular Genetics|March 7, 2003
Transgenic rat model of Huntington's diseaseStephan von Hörsten, Ina Schmitt, Huu Phuc Nguyen, et al.
Parkinsonism & Related Disorders|June 21, 2022
Methylation of alpha-synuclein in a Sudanese cohortYousuf Bakhit, Ina Schmitt, Ahlam Hamed, et al.
Brain : a Journal of Neurology|May 2, 2017
Hypomorphic mutations in POLR3A are a frequent cause of sporadic and recessive spastic ataxiaMartina Minnerop, Delia Kurzwelly, Holger Wagner, et al.
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