Paternal imprinting of mouse serotonin receptor 2A gene Htr2 in embryonic eye: a conserved imprinting regulation on the RB/Rb locus.

[1]  M. Sasaki,et al.  Genomic imprinting of the human serotonin-receptor (HTR2) gene involved in development of retinoblastoma. , 1996, American journal of human genetics.

[2]  V. Chapman,et al.  Identification of Grf1 on mouse chromosome 9 as an imprinted gene by RLGS–M , 1996, Nature Genetics.

[3]  R. Duman,et al.  Chronic antidepressant administration increases the expression of cAMP response element binding protein (CREB) in rat hippocampus , 1996, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[4]  K. Ishizaki,et al.  Delayed development of retinoblastoma associated with loss of a maternal allele on chromosome 13 , 1995, International journal of cancer.

[5]  K. Ishizaki,et al.  Mutations in the retinoblastoma gene and their expression in somatic and tumor cells of patients with hereditary retinoblastoma , 1994, Human mutation.

[6]  W. Benedict,et al.  Characterization of intragenic deletions in two sporadic germinal mutation cases of retinoblastoma resulting in abnormal gene expression. , 1991, Oncogene.

[7]  L. Cavalli-Sforza,et al.  The serotonin receptor subtype 2 locusHTR2 is on human chromosome 13 near genes for esterase D and retinoblastoma-1 and on mouse chromosome 14 , 1990, Somatic cell and molecular genetics.

[8]  B. Cattanach,et al.  Autosomal and X-chromosome imprinting. , 1990, Development (Cambridge, England). Supplement.

[9]  T. Jessell,et al.  The 5HT2 receptor defines a family of structurally distinct but functionally conserved serotonin receptors. , 1990, Proceedings of the National Academy of Sciences of the United States of America.

[10]  Stephen H. Friend,et al.  A human DNA segment with properties of the gene that predisposes to retinoblastoma and osteosarcoma , 1986, Nature.