Altered visual function and interneuron survival in Atrx knockout mice: inference for the human syndrome.
ATRX is an SWI/SNF-like chromatin remodeling protein that is mutated in several X-linked mental retardation syndromes, including the ATR-X syndrome. In mice, Atrx expression is widespread and attempts to understand its function in brain development are hampered by the lethality associated with ubiqu...
Main Authors: | Medina, C, Mazerolle, C, Wang, Y, Bérubé, N, Coupland, S, Gibbons, R, Wallace, V, Picketts, D |
---|---|
Format: | Journal article |
Language: | English |
Published: |
2009
|
Similar Items
-
Disruption of ATRX in mouse by conditional knockout.
by: Gibbons, R, et al.
Published: (2002) -
The chromatin-remodeling protein ATRX is critical for neuronal survival during corticogenesis.
by: Bérubé, N, et al.
Published: (2005) -
Identification of mutations in ATRX by RNase mismatch cleavage.
by: Gibbons, R, et al.
Published: (1997) -
Effects of a postnatal Atrx conditional knockout in neurons on autism-like behaviours in male and female mice
by: Nicole Martin-Kenny, et al.
Published: (2020-06-01) -
Comparison of the human and murine ATRX gene identifies highly conserved, functionally important domains.
by: Picketts, D, et al.
Published: (1998)