Determinants of target gene specificity for steroid/thyroid hormone receptors

[1]  R. Evans,et al.  Trans-activation by thyroid hormone receptors: functional parallels with steroid hormone receptors. , 1989, Proceedings of the National Academy of Sciences of the United States of America.

[2]  C. Tabin,et al.  Spatial and temporal expression of the retinoic acid receptor in the regenerating amphibian limb , 1989, Nature.

[3]  R. Evans,et al.  Transcriptional inhibition by a glucocorticoid receptor-β-galactosidase fusion protein , 1988, Cell.

[4]  K. Semba,et al.  Identification of two novel members of erbA superfamily by molecular cloning: the gene products of the two are highly related to each other. , 1988, Nucleic acids research.

[5]  R. Evans,et al.  Multiple and cooperative trans-activation domains of the human glucocorticoid receptor , 1988, Cell.

[6]  H. Jäckle,et al.  Abdominal segmentation of the Drosophila embryo requires a hormone receptor-like protein encoded by the gap gene knirps , 1988, Nature.

[7]  M. Mckeown,et al.  The Drosophila gene knirps-related is a member of the steroid-receptor gene superf amily , 1988, Nature.

[8]  K. Umesono,et al.  Retinoic acid and thyroid hormone induce gene expression through a common responsive element , 1988, Nature.

[9]  P. Chambon,et al.  Nuclear receptors enhance our understanding of transcription regulation. , 1988, Trends in genetics : TIG.

[10]  B. O’Malley,et al.  Molecular interactions of steroid hormone receptor with its enhancer element: Evidence for receptor dimer formation , 1988, Cell.

[11]  P. Chambon,et al.  The estrogen receptor binds tightly to its responsive element as a ligand-induced homodimer , 1988, Cell.

[12]  P. Chambon,et al.  The N‐terminal DNA‐binding ‘zinc finger’ of the oestrogen and glucocorticoid receptors determines target gene specificity. , 1988, The EMBO journal.

[13]  J. Kokontis,et al.  Identification of a new member of the steroid receptor super-family by cloning and sequence analysis. , 1988, Biochemical and biophysical research communications.

[14]  K. Yamamoto,et al.  The function and structure of the metal coordination sites within the glucocorticoid receptor DNA binding domain , 1988, Nature.

[15]  S. Rusconi,et al.  Metal binding ‘finger’ structures in the glucocorticoid receptor defined by site‐directed mutagenesis. , 1988, The EMBO journal.

[16]  C. Glass,et al.  The thyroid hormone receptor binds with opposite transcriptional effects to a common sequence motif in thyroid hormone and estrogen response elements , 1988, Cell.

[17]  P. Webb,et al.  Characterization of response elements for androgens, glucocorticoids and progestins in mouse mammary tumour virus. , 1988, Nucleic acids research.

[18]  R. Evans,et al.  The steroid and thyroid hormone receptor superfamily. , 1988, Science.

[19]  J. Milbrandt.  Nerve growth factor induces a gene homologous to the glucocorticoid receptor gene , 1988, Neuron.

[20]  Chawnshang Chang,et al.  Molecular cloning of human and rat complementary DNA encoding androgen receptors. , 1988, Science.

[21]  H. Willard,et al.  Cloning of human androgen receptor complementary DNA and localization to the X chromosome. , 1988, Science.

[22]  P. Chambon,et al.  Functional domains of the human estrogen receptor , 1987, Cell.

[23]  Pierre Chambon,et al.  A human retinoic acid receptor which belongs to the family of nuclear receptors , 1987, Nature.

[24]  V. Giguère,et al.  Identification of a receptor for the morphogen retinoic acid , 1987, Nature.

[25]  J. Jonklaas,et al.  Domains of the glucocorticoid receptor involved in specific and nonspecific deoxyribonucleic acid binding, hormone activation, and transcriptional enhancement. , 1987, Molecular endocrinology.

[26]  K. Yamamoto,et al.  Two signals mediate hormone‐dependent nuclear localization of the glucocorticoid receptor. , 1987, The EMBO journal.

[27]  G. Schütz,et al.  Oestrogen and glucocorticoid responsive elements are closely related but distinct , 1987, Nature.

[28]  K. Yamamoto,et al.  Functional dissection of the hormone and DNA binding activities of the glucocorticoid receptor. , 1987, EMBO Journal.

[29]  R. Evans,et al.  Colocalization of DNA-binding and transcriptional activation functions in the human glucocorticoid receptor , 1987, Cell.

[30]  K. Wood,et al.  Firefly luciferase gene: structure and expression in mammalian cells , 1987, Molecular and cellular biology.

[31]  R. Evans,et al.  Functional domains of the human glucocorticoid receptor , 1986, Cell.

[32]  I. Pastan,et al.  Promoter region of the human Harvey ras proto-oncogene: similarity to the EGF receptor proto-oncogene promoter. , 1985, Science.

[33]  A Klug,et al.  Repetitive zinc‐binding domains in the protein transcription factor IIIA from Xenopus oocytes. , 1985, The EMBO journal.

[34]  M. Yaniv,et al.  Two distinct enhancers with different cell specificities coexist in the regulatory region of polyoma , 1984, Cell.

[35]  M. Brown-Luedi,et al.  Sequence homologies in the region preceding the transcription initiation site of the liver estrogen-responsive vitellogenin and apo-VLDLII genes. , 1984, Nucleic acids research.

[36]  B. Howard,et al.  Recombinant genomes which express chloramphenicol acetyltransferase in mammalian cells , 1982, Molecular and cellular biology.

[37]  R. Evans,et al.  A single domain of the estrogen receptor confers deoxyribonucleic acid binding and transcriptional activation of the rat prolactin gene. , 1988, Molecular endocrinology.

[38]  P. Chambon,et al.  Oestradiol induction of a glucocorticoid-responsive gene by a chimaeric receptor , 1987, Nature.

[39]  K. Yamamoto,et al.  Steroid receptor regulated transcription of specific genes and gene networks. , 1985, Annual review of genetics.

[40]  Thomas A. Kunkel,et al.  Rapid and efficient site-specific mutagenesis without phenotypic selection. , 1985, Proceedings of the National Academy of Sciences of the United States of America.