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NMR in Biomedicine
|
October 20, 2022
Ex vivo proton spectroscopy (<sup>1</sup> H-NMR) analysis of inborn errors of metabolism: Automatic and computer-assisted analyses
Claire Cannet, Georg Frauendienst-Egger, Peter Freisinger, et al.
Journal of Translational Medicine
|
February 8, 2018
Immune monitoring and TCR sequencing of CD4 T cells in a long term responsive patient with metastasized pancreatic ductal carcinoma treated with individualized, neoepitope-derived multipeptide vaccines: a case report
Katja Sonntag, Hisayoshi Hashimoto, Matthias Eyrich, et al.
Neuromolecular Medicine
|
April 8, 2019
A Novel Variant (Asn177Asp) in SPTLC2 Causing Hereditary Sensory Autonomic Neuropathy Type 1C
Saranya Suriyanarayanan, Alaa Othman, Bianca Dräger, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
October 14, 2021
Novel CACNA1A Variant p.Cys256Phe Disrupts Disulfide Bonds and Causes Spinocerebellar Ataxia
Yuliia V Nikonishyna, Nadine J Ortner, Teresa Kaserer, et al.
Scientific Reports
|
March 16, 2019
The Parkinson's disease-linked Leucine-rich repeat kinase 2 (LRRK2) is required for insulin-stimulated translocation of GLUT4
Natalja Funk, Marita Munz, Thomas Ott, et al.
Neurobiology of Aging
|
November 16, 2017
Beyond ALS and FTD: the phenotypic spectrum of TBK1 mutations includes PSP-like and cerebellar phenotypes
Carlo Wilke, Jonathan Baets, Jan L De Bleecker, et al.
Plos One
|
April 2, 2015
No dopamine cell loss or changes in cytoskeleton function in transgenic mice expressing physiological levels of wild type or G2019S mutant LRRK2 and in human fibroblasts
Marta Garcia-Miralles, Janaky Coomaraswamy, Karina Häbig, et al.
Journal of Inherited Metabolic Disease
|
June 27, 2021
3-Hydroxyisobutyrate dehydrogenase (HIBADH) deficiency-A novel disorder of valine metabolism
Melanie Meyer, Jana C Hollenbeck, Janine Reunert, et al.
Clinical Genetics
|
December 30, 2021
Di-genic inheritance of germline POLE and PMS2 pathogenic variants causes a unique condition associated with pediatric cancer predisposition
Orli Michaeli, Hagay Ladany, Ayelet Erez, et al.
Journal of Neurogenetics
|
January 10, 2009
The Wuerzburg hybridoma library against Drosophila brain
Alois Hofbauer, Thomas Ebel, Bernhard Waltenspiel, et al.
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Search research articles
Search
Showing results (91-100 of 226) with videos related to
Sort By:
Page
of 23
NMR in Biomedicine
|
October 20, 2022
Ex vivo proton spectroscopy (<sup>1</sup> H-NMR) analysis of inborn errors of metabolism: Automatic and computer-assisted analyses
Claire Cannet, Georg Frauendienst-Egger, Peter Freisinger, et al.
Journal of Translational Medicine
|
February 8, 2018
Immune monitoring and TCR sequencing of CD4 T cells in a long term responsive patient with metastasized pancreatic ductal carcinoma treated with individualized, neoepitope-derived multipeptide vaccines: a case report
Katja Sonntag, Hisayoshi Hashimoto, Matthias Eyrich, et al.
Neuromolecular Medicine
|
April 8, 2019
A Novel Variant (Asn177Asp) in SPTLC2 Causing Hereditary Sensory Autonomic Neuropathy Type 1C
Saranya Suriyanarayanan, Alaa Othman, Bianca Dräger, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
October 14, 2021
Novel CACNA1A Variant p.Cys256Phe Disrupts Disulfide Bonds and Causes Spinocerebellar Ataxia
Yuliia V Nikonishyna, Nadine J Ortner, Teresa Kaserer, et al.
Scientific Reports
|
March 16, 2019
The Parkinson's disease-linked Leucine-rich repeat kinase 2 (LRRK2) is required for insulin-stimulated translocation of GLUT4
Natalja Funk, Marita Munz, Thomas Ott, et al.
Neurobiology of Aging
|
November 16, 2017
Beyond ALS and FTD: the phenotypic spectrum of TBK1 mutations includes PSP-like and cerebellar phenotypes
Carlo Wilke, Jonathan Baets, Jan L De Bleecker, et al.
Plos One
|
April 2, 2015
No dopamine cell loss or changes in cytoskeleton function in transgenic mice expressing physiological levels of wild type or G2019S mutant LRRK2 and in human fibroblasts
Marta Garcia-Miralles, Janaky Coomaraswamy, Karina Häbig, et al.
Journal of Inherited Metabolic Disease
|
June 27, 2021
3-Hydroxyisobutyrate dehydrogenase (HIBADH) deficiency-A novel disorder of valine metabolism
Melanie Meyer, Jana C Hollenbeck, Janine Reunert, et al.
Clinical Genetics
|
December 30, 2021
Di-genic inheritance of germline POLE and PMS2 pathogenic variants causes a unique condition associated with pediatric cancer predisposition
Orli Michaeli, Hagay Ladany, Ayelet Erez, et al.
Journal of Neurogenetics
|
January 10, 2009
The Wuerzburg hybridoma library against Drosophila brain
Alois Hofbauer, Thomas Ebel, Bernhard Waltenspiel, et al.
Page
of 23