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Quasar Saleem

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Methods in Cell Biology|September 7, 2010
Autosomal dominant leukodystrophy caused by lamin B1 duplications a clinical and molecular case study of altered nuclear function and diseaseQuasar Saleem Padiath, Ying-Hui Fu
BMC Research Notes|August 4, 2023
Enhanced differentiation of the mouse oli-neu oligodendroglial cell line using optimized culture conditionsGuillermo Rodriguez Bey, Quasar Saleem Padiath
Chronobiology International|May 8, 2004
Glycogen synthase kinase 3beta as a likely target for the action of lithium on circadian clocksQuasar Saleem Padiath, Dhanashree Paranjpe, Sanjeev Jain, et al.
Biological Psychiatry|January 21, 2004
A nonsense mutation in the synaptogyrin 1 gene in a family with schizophreniaRanjana Verma, Chitra Chauhan, Quasar Saleem, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|October 1, 2004
Identification of a novel 45 repeat unstable allele associated with a disease phenotype at the MJD1/SCA3 locusQuasar Saleem Padiath, Achal Kumar Srivastava, Sanghmitra Roy, et al.
Gigascience|April 30, 2022
scMAPA: Identification of cell-type-specific alternative polyadenylation in complex tissuesYulong Bai, Yidi Qin, Zhenjiang Fan, et al.
Brain : a Journal of Neurology|August 11, 2022
Variants in the zinc transporter TMEM163 cause a hypomyelinating leukodystrophyMichelle C do Rosario, Guillermo Rodriguez Bey, Bruce Nmezi, et al.
Brain : a Journal of Neurology|September 18, 2024
Biallelic EPB41L3 variants underlie a developmental disorder with seizures and myelination defectsElizabeth A Werren, Guillermo Rodriguez Bey, Purvi Majethia, et al.
Human Mutation|May 8, 2013
Analysis of LMNB1 duplications in autosomal dominant leukodystrophy provides insights into duplication mechanisms and allele-specific expressionElisa Giorgio, Harshvardhan Rolyan, Laura Kropp, et al.
Pageof 1

Showing results (1-10 of 9) with videos related to

Sort By:
Pageof 1
Methods in Cell Biology|September 7, 2010
Autosomal dominant leukodystrophy caused by lamin B1 duplications a clinical and molecular case study of altered nuclear function and diseaseQuasar Saleem Padiath, Ying-Hui Fu
BMC Research Notes|August 4, 2023
Enhanced differentiation of the mouse oli-neu oligodendroglial cell line using optimized culture conditionsGuillermo Rodriguez Bey, Quasar Saleem Padiath
Chronobiology International|May 8, 2004
Glycogen synthase kinase 3beta as a likely target for the action of lithium on circadian clocksQuasar Saleem Padiath, Dhanashree Paranjpe, Sanjeev Jain, et al.
Biological Psychiatry|January 21, 2004
A nonsense mutation in the synaptogyrin 1 gene in a family with schizophreniaRanjana Verma, Chitra Chauhan, Quasar Saleem, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|October 1, 2004
Identification of a novel 45 repeat unstable allele associated with a disease phenotype at the MJD1/SCA3 locusQuasar Saleem Padiath, Achal Kumar Srivastava, Sanghmitra Roy, et al.
Gigascience|April 30, 2022
scMAPA: Identification of cell-type-specific alternative polyadenylation in complex tissuesYulong Bai, Yidi Qin, Zhenjiang Fan, et al.
Brain : a Journal of Neurology|August 11, 2022
Variants in the zinc transporter TMEM163 cause a hypomyelinating leukodystrophyMichelle C do Rosario, Guillermo Rodriguez Bey, Bruce Nmezi, et al.
Brain : a Journal of Neurology|September 18, 2024
Biallelic EPB41L3 variants underlie a developmental disorder with seizures and myelination defectsElizabeth A Werren, Guillermo Rodriguez Bey, Purvi Majethia, et al.
Human Mutation|May 8, 2013
Analysis of LMNB1 duplications in autosomal dominant leukodystrophy provides insights into duplication mechanisms and allele-specific expressionElisa Giorgio, Harshvardhan Rolyan, Laura Kropp, et al.
Pageof 1