N. C. Cheng

Knockout mouse model for Fxr2: a model for mental retardation (2002)

Bontekoe, C.J., Kirkpatrick, L., Bakker, C.E., Hoogeveen, A.T., McAninch, R., Merriweather, M., ...

Fragile X syndrome is a common form of mental retardation caused by the absence of the FMR1 protein, FMRP. Fmr1 knockout mice exhibit a phenotype with some similarities to humans, such as...

Cloning and characterization of the Drosophila homolog of the xeroderma pigmentosum complementation group B correcting gene, ERCC3. (1992)

Koken, M.H.M., Vreeken, C., Mol, S.A.M., Cheng, N.C., Jaspers-Dekker, I., Hoeijmakers, J.H.J., ...

Previously the human nucleotide excision repair gene ERCC3 was shown to be responsible for a rare combination of the autosomal recessive DNA repair disorders xeroderma pigmentosum (complementation...

Cloning and characterization of the Drosophila homolog of the xeroderma pigmentosum complementation-group B correcting gene, ERCC3.

Koken, M H, Vreeken, C, Bol, S A, Cheng, N C, Jaspers-Dekker, I, Hoeijmakers, J H, ...

Previously the human nucleotide excision repair gene ERCC3 was shown to be responsible for a rare combination of the autosomal recessive DNA repair disorders xeroderma pigmentosum (complementation...

Cloning and characterization of the Drosophila homolog of the xeroderma pigmentosum complementation-group B correcting gene, ERCC3.

Koken, M H, Vreeken, C, Bol, S A, Cheng, N C, Jaspers-Dekker, I, Hoeijmakers, J H, ...

Previously the human nucleotide excision repair gene ERCC3 was shown to be responsible for a rare combination of the autosomal recessive DNA repair disorders xeroderma pigmentosum (complementation...