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B E Becker

Showing results (101-110 of 114) with videos related to

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Neuron|February 5, 2016
A Transient Translaminar GABAergic Interneuron Circuit Connects Thalamocortical Recipient Layers in Neonatal Somatosensory CortexAndre Marques-Smith, Daniel Lyngholm, Anna-Kristin Kaufmann, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|February 17, 2012
Contactin-associated protein-2 antibodies in non-paraneoplastic cerebellar ataxiaEsther B E Becker, Luigi Zuliani, Rosemary Pettingill, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 9, 2009
A point mutation in TRPC3 causes abnormal Purkinje cell development and cerebellar ataxia in moonwalker miceEsther B E Becker, Peter L Oliver, Maike D Glitsch, et al.
Acta Neuropathologica Communications|September 26, 2018
Neurodegeneration in SCA14 is associated with increased PKCγ kinase activity, mislocalization and aggregationMaggie M K Wong, Stephanie D Hoekstra, Jane Vowles, et al.
Cell|June 6, 2006
A conserved MST-FOXO signaling pathway mediates oxidative-stress responses and extends life spanMaria K Lehtinen, Zengqiang Yuan, Peter R Boag, et al.
Brain : a Journal of Neurology|January 12, 2026
Enhanced mGluR1 function causes motor deficits and region-specific Purkinje cell dysfunctionMohamed F Ibrahim, Sevda Boyanova, Yin Chun Cheng, et al.
American Journal of Human Genetics|November 4, 2017
Dominant Mutations in GRM1 Cause Spinocerebellar Ataxia Type 44Lauren M Watson, Elizabeth Bamber, Ricardo Parolin Schnekenberg, et al.
American Journal of Human Genetics|September 9, 2017
Dominant Mutations in GRM1 Cause Spinocerebellar Ataxia Type 44Lauren M Watson, Elizabeth Bamber, Ricardo Parolin Schnekenberg, et al.
American Journal of Human Genetics|October 7, 2017
Dominant Mutations in GRM1 Cause Spinocerebellar Ataxia Type 44Lauren M Watson, Elizabeth Bamber, Ricardo Parolin Schnekenberg, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|April 1, 2018
Genotype-phenotype correlations, dystonia and disease progression in spinocerebellar ataxia type 14Viorica Chelban, Sarah Wiethoff, Bjørn K Fabian-Jessing, et al.
Pageof 12

Showing results (101-110 of 114) with videos related to

Sort By:
Pageof 12
Neuron|February 5, 2016
A Transient Translaminar GABAergic Interneuron Circuit Connects Thalamocortical Recipient Layers in Neonatal Somatosensory CortexAndre Marques-Smith, Daniel Lyngholm, Anna-Kristin Kaufmann, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|February 17, 2012
Contactin-associated protein-2 antibodies in non-paraneoplastic cerebellar ataxiaEsther B E Becker, Luigi Zuliani, Rosemary Pettingill, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 9, 2009
A point mutation in TRPC3 causes abnormal Purkinje cell development and cerebellar ataxia in moonwalker miceEsther B E Becker, Peter L Oliver, Maike D Glitsch, et al.
Acta Neuropathologica Communications|September 26, 2018
Neurodegeneration in SCA14 is associated with increased PKCγ kinase activity, mislocalization and aggregationMaggie M K Wong, Stephanie D Hoekstra, Jane Vowles, et al.
Cell|June 6, 2006
A conserved MST-FOXO signaling pathway mediates oxidative-stress responses and extends life spanMaria K Lehtinen, Zengqiang Yuan, Peter R Boag, et al.
Brain : a Journal of Neurology|January 12, 2026
Enhanced mGluR1 function causes motor deficits and region-specific Purkinje cell dysfunctionMohamed F Ibrahim, Sevda Boyanova, Yin Chun Cheng, et al.
American Journal of Human Genetics|November 4, 2017
Dominant Mutations in GRM1 Cause Spinocerebellar Ataxia Type 44Lauren M Watson, Elizabeth Bamber, Ricardo Parolin Schnekenberg, et al.
American Journal of Human Genetics|September 9, 2017
Dominant Mutations in GRM1 Cause Spinocerebellar Ataxia Type 44Lauren M Watson, Elizabeth Bamber, Ricardo Parolin Schnekenberg, et al.
American Journal of Human Genetics|October 7, 2017
Dominant Mutations in GRM1 Cause Spinocerebellar Ataxia Type 44Lauren M Watson, Elizabeth Bamber, Ricardo Parolin Schnekenberg, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|April 1, 2018
Genotype-phenotype correlations, dystonia and disease progression in spinocerebellar ataxia type 14Viorica Chelban, Sarah Wiethoff, Bjørn K Fabian-Jessing, et al.
Pageof 12