Characterization of the Mammalian YAP (Yes-associated Protein) Gene and Its Role in Defining a Novel Protein Module, the WW Domain (*)
暂无分享,去创建一个
P. Bork | M. Negrini | K. Huebner | M. Sudol | T. Druck | K. Kastury | D. Lehman | A. Einbond
[1] M. Scheffner,et al. A family of proteins structurally and functionally related to the E6-AP ubiquitin-protein ligase. , 1995, Proceedings of the National Academy of Sciences of the United States of America.
[2] S. Altschul,et al. Detection of conserved segments in proteins: iterative scanning of sequence databases with alignment blocks. , 1994, Proceedings of the National Academy of Sciences of the United States of America.
[3] P. Bork,et al. The WW domain: a signalling site in dystrophin? , 1994, Trends in biochemical sciences.
[4] P. Hajduk,et al. Pleckstrin homology domains bind to phosphatidylinositol-4,5-bisphosphate , 1994, Nature.
[5] K. Davies,et al. Increasing complexity of the dystrophin-associated protein complex. , 1994, Proceedings of the National Academy of Sciences of the United States of America.
[6] M. Sudol,et al. Yes-associated protein (YAP65) is a proline-rich phosphoprotein that binds to the SH3 domain of the Yes proto-oncogene product. , 1994, Oncogene.
[7] B. Rost,et al. Combining evolutionary information and neural networks to predict protein secondary structure , 1994, Proteins.
[8] C. Sander,et al. Yeast chromosome III: new gene functions. , 1994, The EMBO journal.
[9] M Bobrow,et al. Searching for the 1 in 2,400,000: A review of dystrophin gene point mutations , 1994, Human mutation.
[10] M. Saraste,et al. Structure and function of the SH3 domain. , 1994, Progress in biophysics and molecular biology.
[11] Mark S. Boguski,et al. Proteins regulating Ras and its relatives , 1993, Nature.
[12] R. Birge,et al. Closing in on SH2 specificity. , 1993, Science.
[13] M. Scheffner,et al. The HPV-16 E6 and E6-AP complex functions as a ubiquitin-protein ligase in the ubiquitination of p53 , 1993, Cell.
[14] T. Pawson,et al. The v-Src SH3 domain binds phosphatidylinositol 3'-kinase , 1993, Molecular and cellular biology.
[15] J. Brugge,et al. Detection of Src homology 3-binding proteins, including paxillin, in normal and v-Src-transformed Balb/c 3T3 cells. , 1993, The Journal of biological chemistry.
[16] T Pawson,et al. SH2 and SH3 domains , 1993, Current Biology.
[17] M. Saraste,et al. Crystal structure of the SH3 domain in human Fyn; comparison of the three‐dimensional structures of SH3 domains in tyrosine kinases and spectrin. , 1993, The EMBO journal.
[18] B. Hemmings,et al. Pleckstrin domain homology , 1993, Nature.
[19] I. Campbell,et al. Solution structure and ligand-binding site of the SH3 domain of the p85α subunit of phosphatidylinositol 3-kinase , 1993, Cell.
[20] D. Baltimore,et al. A putative modular domain present in diverse signaling proteins , 1993, Cell.
[21] Nanxin Li,et al. Guanine-nucleotide-releasing factor hSos1 binds to Grb2 and links receptor tyrosine kinases to Ras signalling , 1993, Nature.
[22] T. Pawson,et al. The SH2 and SH3 domains of mammalian Grb2 couple the EGF receptor to the Ras activator mSos1 , 1993, Nature.
[23] C. Croce,et al. Characterization of human bone marrow‐derived closed circular DNA clones , 1993, Genes, chromosomes & cancer.
[24] K. Irie,et al. MKK1 and MKK2, which encode Saccharomyces cerevisiae mitogen-activated protein kinase-kinase homologs, function in the pathway mediated by protein kinase C , 1993, Molecular and cellular biology.
[25] Peer Bork,et al. A fast, sensitive pattern-matching approach for protein sequences , 1993, Comput. Appl. Biosci..
[26] L. Kunkel,et al. The structural and functional diversity of dystrophin , 1993, Nature Genetics.
[27] Stuart L. Schreiber,et al. Structure of the Pl3K SH3 domain and analysis of the SH3 family , 1993, Cell.
[28] D. Baltimore,et al. Signalling through SH2 and SH3 domains. , 1993, Trends in cell biology.
[29] S. Schreiber,et al. Solution structure of the SH3 domain of Src and identification of its ligand-binding site. , 1992, Science.
[30] T. Pawson,et al. SH2 and SH3 domains: From structure to function , 1992, Cell.
[31] Andrea Musacchio,et al. Crystal structure of a Src-homology 3 (SH3) domain , 1992, Nature.
[32] D. Baltimore,et al. Identification of a protein that binds to the SH3 region of Abl and is similar to Bcr and GAP-rho. , 1992, Science.
[33] Andrea Musacchio,et al. SH3 — an abundant protein domain in search of a function , 1992, FEBS letters.
[34] J. W. Rooney,et al. SPT3 interacts with TFIID to allow normal transcription in Saccharomyces cerevisiae. , 1992, Genes & development.
[35] S. Kumar,et al. Identification of a set of genes with developmentally down-regulated expression in the mouse brain. , 1992, Biochemical and biophysical research communications.
[36] J. Brugge,et al. Effects of SH2 and SH3 deletions on the functional activities of wild-type and transforming variants of c-Src , 1992, Molecular and cellular biology.
[37] H. Horvitz,et al. C. elegans cell-signalling gene sem-5 encodes a protein with SH2 and SH3 domains , 1992, Nature.
[38] Y. Nakamura,et al. Fine-scale mapping of the gene responsible for multiple endocrine neoplasia type 1 (MEN 1). , 1992, American journal of human genetics.
[39] R. Myers,et al. A radiation hybrid map of the proximal long arm of human chromosome 11 containing the multiple endocrine neoplasia type 1 (MEN-1) and bcl-1 disease loci. , 1991, American journal of human genetics.
[40] D. Shalloway,et al. Selective binding of activated pp60c-src by an immobilized synthetic phosphopeptide modeled on the carboxyl terminus of pp60c-src. , 1991, Proceedings of the National Academy of Sciences of the United States of America.
[41] P. Bork. Shuffled domains in extracellular proteins , 1991, FEBS letters.
[42] J. Parsons,et al. The SH2 and SH3 domains of pp60src direct stable association with tyrosine phosphorylated proteins p130 and p110. , 1991, The EMBO journal.
[43] C. Croce,et al. Twenty-seven nonoverlapping zinc finger cDNAs from human T cells map to nine different chromosomes with apparent clustering. , 1991, American journal of human genetics.
[44] H. Varmus,et al. Site-directed mutagenesis of the SH2- and SH3-coding domains of c-src produces varied phenotypes, including oncogenic activation of p60c-src , 1990, Molecular and cellular biology.
[45] D. Mead,et al. Phage lambda cDNA cloning vectors for subtractive hybridization, fusion-protein synthesis and Cre-loxP automatic plasmid subcloning. , 1990, Gene.
[46] C. Larsson,et al. Localization of the MEN1 gene to a small region within chromosome 11q13 by deletion mapping in tumors. , 1990, Proceedings of the National Academy of Sciences of the United States of America.
[47] C. Hall,et al. Novel human brain cDNA encoding a 34,000 Mr protein n-chimaerin, related to both the regulatory domain of protein kinase C and BCR, the product of the breakpoint cluster region gene. , 1990, Journal of molecular biology.
[48] S. Aaronson,et al. An efficient directional cloning system to construct cDNA libraries containing full-length inserts at high frequency. , 1989, Gene.
[49] P. O'Connell,et al. Localization of the genetic defect in multiple endocrine neoplasia type 1 within a small region of chromosome 11. , 1989, American journal of human genetics.
[50] J. Brugge,et al. Deletions within the amino-terminal half of the c-src gene product that alter the functional activity of the protein , 1989, Molecular and cellular biology.
[51] R. Heilig,et al. The chicken dystrophin cDNA: striking conservation of the C‐terminal coding and 3′ untranslated regions between man and chicken. , 1988, The EMBO journal.
[52] C. Larsson,et al. Multiple endocrine neoplasia type 1 gene maps to chromosome 11 and is lost in insulinoma , 1988, Nature.
[53] J. Parsons,et al. Activation of pp60c-src transforming potential by mutations altering the structure of an amino terminal domain containing residues 90-95. , 1988, Oncogene research.
[54] A. D. McLachlan,et al. Profile analysis: detection of distantly related proteins. , 1987, Proceedings of the National Academy of Sciences of the United States of America.
[55] H. Iba,et al. Amino acid substitutions sufficient to convert the nontransforming p60c-src protein to a transforming protein , 1986, Molecular and cellular biology.
[56] C. Croce,et al. The human c-ros gene (ROS) is located at chromosome region 6q16----6q22. , 1986, Proceedings of the National Academy of Sciences of the United States of America.
[57] R. Schimke. Multiple Endocrine Neoplasia , 1986 .
[58] F. Sanger,et al. DNA sequencing with chain-terminating inhibitors. , 1977, Proceedings of the National Academy of Sciences of the United States of America.