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J Buckle

Showing results (111-120 of 137) with videos related to

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Journal of Neuroimaging : Official Journal of the American Society of Neuroimaging|February 5, 2009
Deep gray matter involvement on brain MRI scans is associated with clinical progression in multiple sclerosisMohit Neema, Ashish Arora, Brian C Healy, et al.
Journal of Immunology (Baltimore, Md. : 1950)|February 11, 1999
Direct analysis of viral-specific CD8+ T cells with soluble HLA-A2/Tax11-19 tetramer complexes in patients with human T cell lymphotropic virus-associated myelopathyK Bieganowska, P Höllsberg, G J Buckle, et al.
Journal of Medical Genetics|February 2, 2020
ATR-16 syndrome: mechanisms linking monosomy to phenotypeChristian Babbs, Jill Brown, Sharon W Horsley, et al.
Blood|March 3, 2011
Codanin-1 mutations in congenital dyserythropoietic anemia type 1 affect HP1{alpha} localization in erythroblastsRaffaele Renella, Nigel A Roberts, Jill M Brown, et al.
Nucleic Acids Research|September 26, 2025
Coordinated control of genome-nuclear lamina interactions by topoisomerase 2B and lamin B receptorTom van Schaik, Mikhail Magnitov, Marcel de Haas, et al.
Journal of the Neurological Sciences|May 12, 2009
Incidence and factors associated with treatment failure in the CLIMB multiple sclerosis cohort studyS A Gauthier, B I Glanz, M Mandel, et al.
Blood|January 29, 2011
Global gene expression analysis of human erythroid progenitorsAlison T Merryweather-Clarke, Ann Atzberger, Shamit Soneji, et al.
Nature Communications|September 23, 2018
A tissue-specific self-interacting chromatin domain forms independently of enhancer-promoter interactionsJill M Brown, Nigel A Roberts, Bryony Graham, et al.
Science (New York, N.Y.)|May 27, 2006
A regulatory SNP causes a human genetic disease by creating a new transcriptional promoterMarco De Gobbi, Vip Viprakasit, Jim R Hughes, et al.
Haematologica|May 30, 2013
Homozygous mutations in a predicted endonuclease are a novel cause of congenital dyserythropoietic anemia type IChristian Babbs, Nigel A Roberts, Luis Sanchez-Pulido, et al.
Pageof 14

Showing results (111-120 of 137) with videos related to

Sort By:
Pageof 14
Journal of Neuroimaging : Official Journal of the American Society of Neuroimaging|February 5, 2009
Deep gray matter involvement on brain MRI scans is associated with clinical progression in multiple sclerosisMohit Neema, Ashish Arora, Brian C Healy, et al.
Journal of Immunology (Baltimore, Md. : 1950)|February 11, 1999
Direct analysis of viral-specific CD8+ T cells with soluble HLA-A2/Tax11-19 tetramer complexes in patients with human T cell lymphotropic virus-associated myelopathyK Bieganowska, P Höllsberg, G J Buckle, et al.
Journal of Medical Genetics|February 2, 2020
ATR-16 syndrome: mechanisms linking monosomy to phenotypeChristian Babbs, Jill Brown, Sharon W Horsley, et al.
Blood|March 3, 2011
Codanin-1 mutations in congenital dyserythropoietic anemia type 1 affect HP1{alpha} localization in erythroblastsRaffaele Renella, Nigel A Roberts, Jill M Brown, et al.
Nucleic Acids Research|September 26, 2025
Coordinated control of genome-nuclear lamina interactions by topoisomerase 2B and lamin B receptorTom van Schaik, Mikhail Magnitov, Marcel de Haas, et al.
Journal of the Neurological Sciences|May 12, 2009
Incidence and factors associated with treatment failure in the CLIMB multiple sclerosis cohort studyS A Gauthier, B I Glanz, M Mandel, et al.
Blood|January 29, 2011
Global gene expression analysis of human erythroid progenitorsAlison T Merryweather-Clarke, Ann Atzberger, Shamit Soneji, et al.
Nature Communications|September 23, 2018
A tissue-specific self-interacting chromatin domain forms independently of enhancer-promoter interactionsJill M Brown, Nigel A Roberts, Bryony Graham, et al.
Science (New York, N.Y.)|May 27, 2006
A regulatory SNP causes a human genetic disease by creating a new transcriptional promoterMarco De Gobbi, Vip Viprakasit, Jim R Hughes, et al.
Haematologica|May 30, 2013
Homozygous mutations in a predicted endonuclease are a novel cause of congenital dyserythropoietic anemia type IChristian Babbs, Nigel A Roberts, Luis Sanchez-Pulido, et al.
Pageof 14