The NuRD/Mi2 chromatin complex is involved in histone modifications and contains a large number of subunits, including the p66 protein. There are two mouse and human p66 paralogs, p66alpha and p66beta. The functions of these genes are not clear, in part because there are no mutants available, except in invertebrate model systems.We made loss of function mutants in the mouse p66alpha gene (mp66alpha, official name Gatad2a, MGI:2384585). We found that mp66alpha is essential for development, as mutant embryos die around day 10 of embryogenesis. The gene is not required for normal blastocyst development or for implantation. The phenotype of mutant embryos and the pattern of gene expression in mutants are consistent with a role of mp66alpha in g...
AbstractDuring development, the mammalian embryo must integrate signals to control growth and prolif...
BACKGROUND: The diagnostic rate of Mendelian disorders in sequencing studies continues to increase, ...
The tumor suppressor p53 is mutated in over 50% of human sporadic tumors originating from diverse ti...
The NuRD/Mi2 chromatin complex is involved in histone modifications and contains a large number of s...
Mammalian embryogenesis is a dynamic process involving rapid cell proliferation and multiple cellula...
The Mi-2/NuRD complex is a multi-subunit protein complex with enzymatic activities involving chroma-...
Congenital abnormalities can be modeled in the mouse using genetic approaches such as phenotype driv...
Mus Musculus was randomly mutagenized using N-ethyl-N-nitrosourea (ENU). Mutations on Chromosome 5 ...
The mouse t haplotype, a variant 20 cM genomic region on Chromosome 17, harbors 16 embryonic control...
<p><b>Copyright information:</b></p><p>Taken from "p66α and p66β of the Mi-2/NuRD complex mediate MB...
Thiel C, Lübke T, Matthijs G, von Figura K, Körner C. Targeted disruption of the mouse phosphomannom...
BACKGROUND: We have used a sensitized ENU mutagenesis screen to produce mouse lines that carry mutat...
Background: We have used a sensitized ENU mutagenesis screen to produce mouse lines that carry mutat...
We have generated a mouse line with a mutant allele of the mouse Bruce/Birc6 gene induced by gene tr...
Smc5-6 is a highly conserved protein complex related to cohesin and condensin involved in the struct...
AbstractDuring development, the mammalian embryo must integrate signals to control growth and prolif...
BACKGROUND: The diagnostic rate of Mendelian disorders in sequencing studies continues to increase, ...
The tumor suppressor p53 is mutated in over 50% of human sporadic tumors originating from diverse ti...
The NuRD/Mi2 chromatin complex is involved in histone modifications and contains a large number of s...
Mammalian embryogenesis is a dynamic process involving rapid cell proliferation and multiple cellula...
The Mi-2/NuRD complex is a multi-subunit protein complex with enzymatic activities involving chroma-...
Congenital abnormalities can be modeled in the mouse using genetic approaches such as phenotype driv...
Mus Musculus was randomly mutagenized using N-ethyl-N-nitrosourea (ENU). Mutations on Chromosome 5 ...
The mouse t haplotype, a variant 20 cM genomic region on Chromosome 17, harbors 16 embryonic control...
<p><b>Copyright information:</b></p><p>Taken from "p66α and p66β of the Mi-2/NuRD complex mediate MB...
Thiel C, Lübke T, Matthijs G, von Figura K, Körner C. Targeted disruption of the mouse phosphomannom...
BACKGROUND: We have used a sensitized ENU mutagenesis screen to produce mouse lines that carry mutat...
Background: We have used a sensitized ENU mutagenesis screen to produce mouse lines that carry mutat...
We have generated a mouse line with a mutant allele of the mouse Bruce/Birc6 gene induced by gene tr...
Smc5-6 is a highly conserved protein complex related to cohesin and condensin involved in the struct...
AbstractDuring development, the mammalian embryo must integrate signals to control growth and prolif...
BACKGROUND: The diagnostic rate of Mendelian disorders in sequencing studies continues to increase, ...
The tumor suppressor p53 is mutated in over 50% of human sporadic tumors originating from diverse ti...