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BMC Medical Genetics
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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 Xq25-26
Maribeth 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 protein
Jun 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 survival
Damiano Conte, Martin Holcik, Charles A Lefebvre, et al.
Neuroscience
|
November 16, 2020
Sensory Experience Modulates Atrx-mediated Neuronal Integrity in the Mouse Retina
Pamela 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 syndrome
Chantal 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 ATRX
Abigail 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 inactivation
Michael 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 growth
Foteini 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 corticogenesis
Nathalie 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 PHF6
Mwe Mwe Chao, Matthew A Todd, Udo Kontny, et al.
Page
of 6
Search research articles
Search
Showing results (31-40 of 60) with videos related to
Sort By:
Page
of 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 Xq25-26
Maribeth 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 protein
Jun 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 survival
Damiano Conte, Martin Holcik, Charles A Lefebvre, et al.
Neuroscience
|
November 16, 2020
Sensory Experience Modulates Atrx-mediated Neuronal Integrity in the Mouse Retina
Pamela 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 syndrome
Chantal 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 ATRX
Abigail 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 inactivation
Michael 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 growth
Foteini 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 corticogenesis
Nathalie 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 PHF6
Mwe Mwe Chao, Matthew A Todd, Udo Kontny, et al.
Page
of 6