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Jacek Majewski

Showing results (171-180 of 333) with videos related to

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Human Molecular Genetics|August 27, 2015
Homozygous mutation in the eukaryotic translation initiation factor 2alpha phosphatase gene, PPP1R15B, is associated with severe microcephaly, short stature and intellectual disabilityKristin D Kernohan, Martine Tétreault, Urszula Liwak-Muir, et al.
Infection and Immunity|December 4, 2019
ZBTB7B (ThPOK) Is Required for Pathogenesis of Cerebral Malaria and Protection against Pulmonary TuberculosisJames M Kennedy, Anna Georges, Angelia V Bassenden, et al.
Infection and Immunity|December 3, 2014
THEMIS is required for pathogenesis of cerebral malaria and protection against pulmonary tuberculosisSabrina Torre, Sebastien P Faucher, Nassima Fodil, et al.
Human Molecular Genetics|April 26, 2015
An N-terminal formyl methionine on COX 1 is required for the assembly of cytochrome c oxidaseReetta Hinttala, Florin Sasarman, Tamiko Nishimura, et al.
Journal of Oral Pathology & Medicine : Official Publication of the International Association of Oral Pathologists and the American Academy of Oral Pathology|December 8, 2020
Whole-exome sequencing reveals novel vacuolar ATPase genes' variants and variants in genes involved in lysosomal biology and autophagosomal formation in oral granular cell tumorsJosiane Alves França, Tenzin Gayden, Eric Bareke, et al.
Human Mutation|June 29, 2016
Inborn Error of Cobalamin Metabolism Associated with the Intracellular Accumulation of Transcobalamin-Bound Cobalamin and Mutations in ZNF143, Which Codes for a Transcriptional ActivatorMihaela Pupavac, David Watkins, Francis Petrella, et al.
Disease Models & Mechanisms|May 20, 2022
Snrpb is required in murine neural crest cells for proper splicing and craniofacial morphogenesisSabrina Shameen Alam, Shruti Kumar, Marie-Claude Beauchamp, et al.
Human Molecular Genetics|June 19, 2015
Homozygous mutations in MFN2 cause multiple symmetric lipomatosis associated with neuropathySarah L Sawyer, Andy Cheuk-Him Ng, A Micheil Innes, et al.
Clinical Infectious Diseases : an Official Publication of the Infectious Diseases Society of America|April 8, 2014
CARD9 deficiency and spontaneous central nervous system candidiasis: complete clinical remission with GM-CSF therapyChristina Gavino, Anthony Cotter, Daniel Lichtenstein, et al.
Cell Reports|November 18, 2020
H3K27M in Gliomas Causes a One-Step Decrease in H3K27 Methylation and Reduced Spreading within the Constraints of H3K36 MethylationAshot S Harutyunyan, Haifen Chen, Tianyuan Lu, et al.
Pageof 34

Showing results (171-180 of 333) with videos related to

Sort By:
Pageof 34
Human Molecular Genetics|August 27, 2015
Homozygous mutation in the eukaryotic translation initiation factor 2alpha phosphatase gene, PPP1R15B, is associated with severe microcephaly, short stature and intellectual disabilityKristin D Kernohan, Martine Tétreault, Urszula Liwak-Muir, et al.
Infection and Immunity|December 4, 2019
ZBTB7B (ThPOK) Is Required for Pathogenesis of Cerebral Malaria and Protection against Pulmonary TuberculosisJames M Kennedy, Anna Georges, Angelia V Bassenden, et al.
Infection and Immunity|December 3, 2014
THEMIS is required for pathogenesis of cerebral malaria and protection against pulmonary tuberculosisSabrina Torre, Sebastien P Faucher, Nassima Fodil, et al.
Human Molecular Genetics|April 26, 2015
An N-terminal formyl methionine on COX 1 is required for the assembly of cytochrome c oxidaseReetta Hinttala, Florin Sasarman, Tamiko Nishimura, et al.
Journal of Oral Pathology & Medicine : Official Publication of the International Association of Oral Pathologists and the American Academy of Oral Pathology|December 8, 2020
Whole-exome sequencing reveals novel vacuolar ATPase genes' variants and variants in genes involved in lysosomal biology and autophagosomal formation in oral granular cell tumorsJosiane Alves França, Tenzin Gayden, Eric Bareke, et al.
Human Mutation|June 29, 2016
Inborn Error of Cobalamin Metabolism Associated with the Intracellular Accumulation of Transcobalamin-Bound Cobalamin and Mutations in ZNF143, Which Codes for a Transcriptional ActivatorMihaela Pupavac, David Watkins, Francis Petrella, et al.
Disease Models & Mechanisms|May 20, 2022
Snrpb is required in murine neural crest cells for proper splicing and craniofacial morphogenesisSabrina Shameen Alam, Shruti Kumar, Marie-Claude Beauchamp, et al.
Human Molecular Genetics|June 19, 2015
Homozygous mutations in MFN2 cause multiple symmetric lipomatosis associated with neuropathySarah L Sawyer, Andy Cheuk-Him Ng, A Micheil Innes, et al.
Clinical Infectious Diseases : an Official Publication of the Infectious Diseases Society of America|April 8, 2014
CARD9 deficiency and spontaneous central nervous system candidiasis: complete clinical remission with GM-CSF therapyChristina Gavino, Anthony Cotter, Daniel Lichtenstein, et al.
Cell Reports|November 18, 2020
H3K27M in Gliomas Causes a One-Step Decrease in H3K27 Methylation and Reduced Spreading within the Constraints of H3K36 MethylationAshot S Harutyunyan, Haifen Chen, Tianyuan Lu, et al.
Pageof 34