Zobrazeno 1 - 10
of 118
pro vyhledávání: '"M.G. Byers"'
Autor:
Vicki L. Schweickart, Carol J. Raport, M.G. Byers, Ronald Godiska, Thomas B. Shows, Patrick W. Gray, Roger L. Eddy
Publikováno v:
Genomics. 23:643-650
A lymphoid-specific member of the G-protein-coupled receptor family has been identified by PCR with degenerate oligonucleotides. We have determined that this receptor, also reported as the Epstein-Barr-induced cDNA EBI1, is expressed in normal lympho
Autor:
Robert B. Schreiber, Larry W. Tjoelker, Patrick W. Gray, Christine E. Seyfried, Thomas B. Shows, Jesus Calderon, Roger L. Eddy, M.G. Byers
Publikováno v:
Biochemistry. 33:3229-3236
Calnexin is a 90-kDa integral membrane protein of the endoplasmic reticulum (ER). Calnexin binds Ca2+ and may function as a chaperone in the transition of proteins from the ER to the outer cellular membrane. We have purified human calnexin in associa
Publikováno v:
Genomics. 13:62-69
Lysyl hydroxylase (EC 1.14.11.4), an alpha 2 dimer, catalyzes the formation of hydroxylysine in collagens by the hydroxylation of lysine residues in peptide linkages. A deficiency in this enzyme activity is known to exist in patients with the type VI
Autor:
Tucker Collins, Parvez Sultan, Michael A. Gimbrone, Amy J. Williams, Roger L. Eddy, Jochen W.U. Fries, M.G. Byers, Thomas B. Shows, Myron I. Cybulsky
Publikováno v:
Proceedings of the National Academy of Sciences. 88:7859-7863
Vascular cell adhesion molecule 1 (VCAM-1) is a cell surface glycoprotein adhesive for certain blood leukocytes and tumor cells, which is expressed by activated endothelium in a variety of pathologic conditions including atherosclerosis. Genomic clon
Autor:
A. Kumamoto, Rosalyn Slater, A. Geurts van Kessel, J.W. Wessels, B.M. Cattanach, E.J. Dreef, R.E. Kibbelaar, G. Otulakowski, Charles E. Schwartz, S. Parikh, G.J. den Ottolander, J. George, I. Hansmann, U. Francke, G.M. Greig, H. Nakai, M.G. Byers, F. Yang, S. Boularand, Roger E. Stevenson, N.S.-F. Ma, J. Hayakawa, L.-C. Tsui, D.W. Threadgill, S. Kubota, D.H. Ledbetter, J. Spencer, I.A. Noordermeer, D.B. Farber, T.B. Nesterova, J.E. Womack, C.A. Kozak, L. Shi, C. Collet, M.C. Phelan, M. Vercruyssen, W.E. Fibbe, J. Mallet, H.F. Willard, E.P. Evans, C. Hanson, R.G. Taylor, N.B. Rubtsov, L.T. Williams, Andries Westerveld, R.G. Lafreniere, S. Navankasattusas, C. Szpirer, C.-L. Hsieh, C. Rasberry, E. Solomon, M.A. Abruzzo, M. Rivière, D.S. Gerhard, J.A. Escobedo, S.I. Radjabli, S.W. Scherer, D. Sheer, I.V. Nikitina, R.H. Brakenhoff, J.A. Miller, T.A. Jones, K.I. Kivirikko, T.J.M. Hulsebos, R.R. Mclnnes, T. Koizumi, M.C. Darmon, A. Goddard, P. Stanislovitis, S.P. Craig, N.J. Nowak, V.E. Powers, M.C. Simmler, S.M. Zakian, Y. Nakai, A.C.B. Peters, M. Kimura, J. Szpirer, M. Danciger, L. Dandolo, M. Westerman, M. van der Ploeg, L. Pajunen, E.P.J. Arnoldus, A.K. Raap, G.C. Beverstock, S. Schnittger, M. Katsuki, V.G. Matveeva, T. Shinohara, J. García-Heras, S.C. Bock, T.B. Shows, K. Klinger, A.P. Jackson, H. van Kamp, Franki Speleman, D.S. Gallagher, P.M. Kluin, A. Kuwano, T. Kajii, H.A. Taylor, B. Redeker, P. Van Oostveldt, T. Pihlajaniemi, JG Leroy, G.N. Hendy, Marcel M.A.M. Mannens, I.W. Craig, P. Avner, T. Abe, B.H. Robinson, V.L. Singer, P. Parham, E.K. Bijlsma, G. Levan, S. Kohno, S.J. Sadler, V.V.N.G. Rao
Publikováno v:
Cytogenetic and Genome Research. 56:217-230
Autor:
G. Levan, S.P. Craig, I.W. Craig, I.V. Nikitina, N.J. Nowak, T. Pihlajaniemi, C.A. Kozak, M.C. Simmler, H.A. Taylor, C. Collet, G.N. Hendy, C.-L. Hsieh, P. Van Oostveldt, R.G. Taylor, J.A. Miller, M.C. Darmon, A.C.B. Peters, J.W. Wessels, E. Solomon, M.A. Abruzzo, T. Abe, S.M. Zakian, M. Kimura, Y. Nakai, D. Sheer, B.M. Cattanach, Rosalyn Slater, Franki Speleman, P.M. Kluin, A. Kuwano, M. Westerman, S. Kohno, S.J. Sadler, N.S.-F. Ma, D.S. Gallagher, V.E. Powers, T.B. Shows, J. George, M. Van der Ploeg, K. Klinger, G.M. Greig, G. Otulakowski, M.C. Phelan, V.L. Singer, J. Szpirer, A.K. Raap, A. Geurts van Kessel, W.E. Fibbe, V.V.N.G. Rao, M. Vercruyssen, E.P. Evans, E.P.J. Arnoldus, E.J. Dreef, L.-C. Tsui, P. Parham, I. Hansmann, S. Parikh, L. Shi, L.T. Williams, R.E. Kibbelaar, J. Hayakawa, T. Kajii, M. Rivière, T. Shinohara, D.S. Gerhard, E.K. Bijlsma, M.G. Byers, A.P. Jackson, S.W. Scherer, S. Boularand, F. Yang, J. Mallet, J.A. Escobedo, Andries Westerveld, H.F. Willard, Roger E. Stevenson, R.R. Mclnnes, P. Stanislovitis, H. van Kamp, D.W. Threadgill, T. Koizumi, T.B. Nesterova, J.E. Womack, N.B. Rubtsov, T.A. Jones, T.J.M. Hulsebos, M. Danciger, S. Kubota, M. Katsuki, D.H. Ledbetter, S. Navankasattusas, C. Szpirer, V.G. Matveeva, S.I. Radjabli, L. Pajunen, R.H. Brakenhoff, J. García-Heras, G.C. Beverstock, S.C. Bock, Charles E. Schwartz, L. Dandolo, S. Schnittger, I.A. Noordermeer, C. Hanson, B.H. Robinson, A. Kumamoto, D.B. Farber, C. Rasberry, B. Redeker, K.I. Kivirikko, G.J. den Ottolander, H. Nakai, JG Leroy, Marcel M.A.M. Mannens, P. Avner, U. Francke, J. Spencer, R.G. Lafreniere, A. Goddard
Publikováno v:
Cytogenetic and Genome Research. 56:I-IV
Autor:
A K Sinclair, Thomas B. Shows, M.G. Byers, Roger L. Eddy, S L Osborne-Lawrence, A D Duby, R N Jenkins
Publikováno v:
Journal of Biological Chemistry. 265:19624-19631
Cartilage matrix protein (CMP) is a major component of the extracellular matrix of nonarticular cartilage. The structure and chromosomal location of the human gene encoding CMP was determined by molecular cloning analysis. We used a partial chicken C
Publikováno v:
Genomics. 6:554-559
The complete amino acid sequence of the human type IV collagenase preproenzyme was determined from cDNA and genomic clones. Primer extension and S1 nuclease analyses as well as nucleotide sequencing of a genomic clone indicate that the first exon has
Autor:
S. Warter, B. Brun, T.A. Donlon, S. Chamberlain, N. Shimizu, S. Minoshima, G.T. O’Neill, P. Mollevanger, T.B. Shows, C. Morris, M. Hauwy, S. Speirs, T.R. Tiersch, J.W. Wessels, P. Devilee, J.C. Winkelmann, P.C. Watkins, D. Nakamura, J.W. Oosterhuis, J. Koch, C. García de la Vega, M. Douglass, Y. Fukushima, J.M. Martínez Zapater, M.G. Byers, N. Heisterkamp, C.J. Cornelisse, R. Fukuyama, A.J. Driesel, C. Clayberger, R.W. Chandler, Q.L. Hao, J. Gosálvez, A.M. Krensky, Y. Shimizu, J. Shaw, P.B. Moens, T. Ashley, V.T.H.B.M. Smit, J. Groffen, N. Tommerup, V. Goyanes, R. Mezzanotte, B.G. Forget, P. Lichter, M.H. Kaufman, S. Ohno, Y. Rumpler, J.R. Testa, R.E. Pearlman, R. Williamson, L.B. Andersen, L.H.J. Looijenga, S. Ohmi-Imajohs, C. López-Fernández, N.L.A. Cacheiro, K. Suzuki, J. Kudoh
Publikováno v:
Cytogenetic and Genome Research. 53:I-IV
Autor:
Hisashi Hagiwara, Kaoru Takeda, Keiya Tada, M.G. Byers, Thomas B. Shows, Hiroshi Nakai, Rachel Myerowitz
Publikováno v:
The Tohoku Journal of Experimental Medicine. 160:203-211
Tay-Sachs disease results from mutation in the gene encoding beta-hexosaminidase A alpha-subunit. Although some reports have suggested the locus on 15q, we tried to determine the finer gene locus using high resolution in situ hybridization. cDNA prob