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T Gasser

Showing results (291-300 of 316) with videos related to

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American Journal of Human Genetics|February 17, 2001
Origin of the mutations in the parkin gene in Europe: exon rearrangements are independent recurrent events, whereas point mutations may result from Founder effectsM Periquet, C Lücking, J Vaughan, et al.
Cell Death and Differentiation|November 30, 2010
Parkin is transcriptionally regulated by ATF4: evidence for an interconnection between mitochondrial stress and ER stressL Bouman, A Schlierf, A K Lutz, et al.
European Journal of Neurology|May 27, 2010
EFNS guidelines for the molecular diagnosis of neurogenetic disorders: motoneuron, peripheral nerve and muscle disordersJ-M Burgunder, L Schöls, J Baets, et al.
European Journal of Neurology|January 7, 2010
EFNS guidelines on the molecular diagnosis of ataxias and spastic paraplegiasT Gasser, J Finsterer, J Baets, et al.
European Journal of Neurology|December 2, 2009
EFNS guidelines on the molecular diagnosis of mitochondrial disordersJ Finsterer, H F Harbo, J Baets, et al.
Biorxiv : the Preprint Server for Biology|May 19, 2023
Common Analysis of Direct RNA SequencinG CUrrently Leads to Misidentification of 5-Methylcytosine Modifications at GCU MotifsKaylee J Watson, Robin E Bromley, Benjamin C Sparklin, et al.
Neurogenetics|August 29, 2001
Novel mutation in the TOR1A (DYT1) gene in atypical early onset dystonia and polymorphisms in dystonia and early onset parkinsonismJ C Leung, C Klein, J Friedman, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|January 28, 2003
PARK6 is a common cause of familial parkinsonismE M Valente, F Brancati, V Caputo, et al.
Cancer Research|June 5, 2001
High-throughput tissue microarray analysis of 3p25 (RAF1) and 8p12 (FGFR1) copy number alterations in urinary bladder cancerR Simon, J Richter, U Wagner, et al.
Life Science Alliance|November 29, 2023
Common analysis of direct RNA sequencinG CUrrently leads to misidentification of m<sup>5</sup>C at GCU motifsKaylee J Watson, Robin E Bromley, Benjamin C Sparklin, et al.
Pageof 32

Showing results (291-300 of 316) with videos related to

Sort By:
Pageof 32
American Journal of Human Genetics|February 17, 2001
Origin of the mutations in the parkin gene in Europe: exon rearrangements are independent recurrent events, whereas point mutations may result from Founder effectsM Periquet, C Lücking, J Vaughan, et al.
Cell Death and Differentiation|November 30, 2010
Parkin is transcriptionally regulated by ATF4: evidence for an interconnection between mitochondrial stress and ER stressL Bouman, A Schlierf, A K Lutz, et al.
European Journal of Neurology|May 27, 2010
EFNS guidelines for the molecular diagnosis of neurogenetic disorders: motoneuron, peripheral nerve and muscle disordersJ-M Burgunder, L Schöls, J Baets, et al.
European Journal of Neurology|January 7, 2010
EFNS guidelines on the molecular diagnosis of ataxias and spastic paraplegiasT Gasser, J Finsterer, J Baets, et al.
European Journal of Neurology|December 2, 2009
EFNS guidelines on the molecular diagnosis of mitochondrial disordersJ Finsterer, H F Harbo, J Baets, et al.
Biorxiv : the Preprint Server for Biology|May 19, 2023
Common Analysis of Direct RNA SequencinG CUrrently Leads to Misidentification of 5-Methylcytosine Modifications at GCU MotifsKaylee J Watson, Robin E Bromley, Benjamin C Sparklin, et al.
Neurogenetics|August 29, 2001
Novel mutation in the TOR1A (DYT1) gene in atypical early onset dystonia and polymorphisms in dystonia and early onset parkinsonismJ C Leung, C Klein, J Friedman, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|January 28, 2003
PARK6 is a common cause of familial parkinsonismE M Valente, F Brancati, V Caputo, et al.
Cancer Research|June 5, 2001
High-throughput tissue microarray analysis of 3p25 (RAF1) and 8p12 (FGFR1) copy number alterations in urinary bladder cancerR Simon, J Richter, U Wagner, et al.
Life Science Alliance|November 29, 2023
Common analysis of direct RNA sequencinG CUrrently leads to misidentification of m<sup>5</sup>C at GCU motifsKaylee J Watson, Robin E Bromley, Benjamin C Sparklin, et al.
Pageof 32