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Neurogenetics

Showing results (441-450 of 1,081) with videos related to

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Neurogenetics|December 15, 2015
Slc20a2 is critical for maintaining a physiologic inorganic phosphate level in cerebrospinal fluidNina Jensen, Jacob Kwasi Autzen, Lene Pedersen
Neurogenetics|July 12, 2014
A novel mutation in the CSF1R gene causes a variable leukoencephalopathy with spheroidsRoberta La Piana, Alina Webber, Marie-Christine Guiot, et al.
Neurogenetics|March 8, 2016
Up-regulation of SNCA gene expression: implications to synucleinopathiesL Tagliafierro, O Chiba-Falek
Neurogenetics|August 27, 2017
X-linked hypomyelination with spondylometaphyseal dysplasia (H-SMD) associated with mutations in AIFM1Noriko Miyake, Nicole I Wolf, Ferdy K Cayami, et al.
Neurogenetics|May 29, 2016
Alzheimer's disease risk genes in wild-type adult zebrafish exhibit gender-specific expression changes during agingJinyoung Lee, Samuel M Peterson, Jennifer L Freeman
Neurogenetics|June 3, 2016
Very mild features of dysequilibrium syndrome associated with a novel VLDLR missense mutationAlessia Micalizzi, Isabella Moroni, Monia Ginevrino, et al.
Neurogenetics|November 1, 2017
GNE missense mutation in recessive familial amyotrophic lateral sclerosisÇiğdem Köroğlu, Rezzak Yılmaz, Mine Hayriye Sorgun, et al.
Neurogenetics|July 15, 2017
Characterization of SNPs in the dopamine-β-hydroxylase gene providing new insights into its structure-function relationshipToyanji Joseph Punchaichira, Sanjay Kumar Dey, Anirban Mukhopadhyay, et al.
Neurogenetics|January 6, 2021
Selective loss of a LAP1 isoform causes a muscle-specific nuclear envelopathyXavière Lornage, Martial Mallaret, Roberto Silva-Rojas, et al.
Neurogenetics|November 30, 2022
Structural variation and eQTL analysis in two experimental populations of chickens divergently selected for feather-pecking behaviorClemens Falker-Gieske, Jörn Bennewitz, Jens Tetens
Pageof 109

Showing results (441-450 of 1,081) with videos related to

Sort By:
Pageof 109
Neurogenetics|December 15, 2015
Slc20a2 is critical for maintaining a physiologic inorganic phosphate level in cerebrospinal fluidNina Jensen, Jacob Kwasi Autzen, Lene Pedersen
Neurogenetics|July 12, 2014
A novel mutation in the CSF1R gene causes a variable leukoencephalopathy with spheroidsRoberta La Piana, Alina Webber, Marie-Christine Guiot, et al.
Neurogenetics|March 8, 2016
Up-regulation of SNCA gene expression: implications to synucleinopathiesL Tagliafierro, O Chiba-Falek
Neurogenetics|August 27, 2017
X-linked hypomyelination with spondylometaphyseal dysplasia (H-SMD) associated with mutations in AIFM1Noriko Miyake, Nicole I Wolf, Ferdy K Cayami, et al.
Neurogenetics|May 29, 2016
Alzheimer's disease risk genes in wild-type adult zebrafish exhibit gender-specific expression changes during agingJinyoung Lee, Samuel M Peterson, Jennifer L Freeman
Neurogenetics|June 3, 2016
Very mild features of dysequilibrium syndrome associated with a novel VLDLR missense mutationAlessia Micalizzi, Isabella Moroni, Monia Ginevrino, et al.
Neurogenetics|November 1, 2017
GNE missense mutation in recessive familial amyotrophic lateral sclerosisÇiğdem Köroğlu, Rezzak Yılmaz, Mine Hayriye Sorgun, et al.
Neurogenetics|July 15, 2017
Characterization of SNPs in the dopamine-β-hydroxylase gene providing new insights into its structure-function relationshipToyanji Joseph Punchaichira, Sanjay Kumar Dey, Anirban Mukhopadhyay, et al.
Neurogenetics|January 6, 2021
Selective loss of a LAP1 isoform causes a muscle-specific nuclear envelopathyXavière Lornage, Martial Mallaret, Roberto Silva-Rojas, et al.
Neurogenetics|November 30, 2022
Structural variation and eQTL analysis in two experimental populations of chickens divergently selected for feather-pecking behaviorClemens Falker-Gieske, Jörn Bennewitz, Jens Tetens
Pageof 109