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David J Picketts

Showing results (31-40 of 60) with videos related to

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BMC Medical Genetics|February 28, 2008
Characterization of novel isoforms and evaluation of SNF2L/SMARCA1 as a candidate gene for X-linked mental retardation in 12 families linked to Xq25-26Maribeth A Lazzaro, Matthew A M Todd, Paul Lavigne, et al.
The Journal of Biological Chemistry|March 3, 2004
A novel transcription regulatory complex containing death domain-associated protein and the ATR-X syndrome proteinJun Tang, Shaobo Wu, Hongtu Liu, et al.
Molecular and Cellular Biology|December 31, 2005
Inhibitor of apoptosis protein cIAP2 is essential for lipopolysaccharide-induced macrophage survivalDamiano Conte, Martin Holcik, Charles A Lefebvre, et al.
Neuroscience|November 16, 2020
Sensory Experience Modulates Atrx-mediated Neuronal Integrity in the Mouse RetinaPamela S Lagali, Brandon Y H Zhao, Keqin Yan, et al.
Human Molecular Genetics|December 18, 2008
Altered visual function and interneuron survival in Atrx knockout mice: inference for the human syndromeChantal F Medina, Chantal Mazerolle, Yaping Wang, et al.
Nature Communications|December 1, 2025
Interferon dependent immune memory during HSV-1 neuronal latency via increased H3K9me3 and restriction by ATRXAbigail L Whitford, Gaelle Auguste, Alison K Francois, et al.
The Journal of Clinical Investigation|November 2, 2012
Compromised genomic integrity impedes muscle growth after Atrx inactivationMichael S Huh, Tina Price O'Dea, Dahmane Ouazia, et al.
Scientific Reports|July 18, 2025
SMARCA5 is required for the development of granule cell neuron precursors and Sonic Hedgehog Medulloblastoma growthFoteini Tsiami, Layla Drwesh, Surender Surender, et al.
The Journal of Clinical Investigation|January 26, 2005
The chromatin-remodeling protein ATRX is critical for neuronal survival during corticogenesisNathalie G Bérubé, Marie Mangelsdorf, Magdalena Jagla, et al.
Pediatric Blood & Cancer|September 1, 2010
T-cell acute lymphoblastic leukemia in association with Börjeson-Forssman-Lehmann syndrome due to a mutation in PHF6Mwe Mwe Chao, Matthew A Todd, Udo Kontny, et al.
Pageof 6

Showing results (31-40 of 60) with videos related to

Sort By:
Pageof 6
BMC Medical Genetics|February 28, 2008
Characterization of novel isoforms and evaluation of SNF2L/SMARCA1 as a candidate gene for X-linked mental retardation in 12 families linked to Xq25-26Maribeth A Lazzaro, Matthew A M Todd, Paul Lavigne, et al.
The Journal of Biological Chemistry|March 3, 2004
A novel transcription regulatory complex containing death domain-associated protein and the ATR-X syndrome proteinJun Tang, Shaobo Wu, Hongtu Liu, et al.
Molecular and Cellular Biology|December 31, 2005
Inhibitor of apoptosis protein cIAP2 is essential for lipopolysaccharide-induced macrophage survivalDamiano Conte, Martin Holcik, Charles A Lefebvre, et al.
Neuroscience|November 16, 2020
Sensory Experience Modulates Atrx-mediated Neuronal Integrity in the Mouse RetinaPamela S Lagali, Brandon Y H Zhao, Keqin Yan, et al.
Human Molecular Genetics|December 18, 2008
Altered visual function and interneuron survival in Atrx knockout mice: inference for the human syndromeChantal F Medina, Chantal Mazerolle, Yaping Wang, et al.
Nature Communications|December 1, 2025
Interferon dependent immune memory during HSV-1 neuronal latency via increased H3K9me3 and restriction by ATRXAbigail L Whitford, Gaelle Auguste, Alison K Francois, et al.
The Journal of Clinical Investigation|November 2, 2012
Compromised genomic integrity impedes muscle growth after Atrx inactivationMichael S Huh, Tina Price O'Dea, Dahmane Ouazia, et al.
Scientific Reports|July 18, 2025
SMARCA5 is required for the development of granule cell neuron precursors and Sonic Hedgehog Medulloblastoma growthFoteini Tsiami, Layla Drwesh, Surender Surender, et al.
The Journal of Clinical Investigation|January 26, 2005
The chromatin-remodeling protein ATRX is critical for neuronal survival during corticogenesisNathalie G Bérubé, Marie Mangelsdorf, Magdalena Jagla, et al.
Pediatric Blood & Cancer|September 1, 2010
T-cell acute lymphoblastic leukemia in association with Börjeson-Forssman-Lehmann syndrome due to a mutation in PHF6Mwe Mwe Chao, Matthew A Todd, Udo Kontny, et al.
Pageof 6