STV1 gene encodes functional homologue of 95-kDa yeast vacuolar H+-ATPase subunit Vph1p von Manolson, M.F, Wu, B, Proteau, D, Taillon, B.E, Roberts, B.T, Hoyt, M.A, Jones, E.W

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BIA/MS of Epitope-Tagged Peptides Directly from E. Coli Lysate:  Multiplex Detection and Protein Identification at Low-Femtomole to Subfemtomole Levels von Nelson, Randall W, Jarvik, Jonathan W, Taillon, Bruce E, Tubbs, Kemmons A

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Detection of low-frequency pretherapy chemokine (CXC motif) receptor 4 (CXCR4)-using HIV-1 with ultra-deep pyrosequencing von ARCHER, John, BRAVERMAN, Michael S, TAILLON, Bruce E, DESANY, Brian, JAMES, Ian, HARRIGAN, P. Richard, LEWIS, Marilyn, ROBERTSON, David L

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Open systems: panoramic views of gene expression von Green, Cynthia D., Simons, Jan Fredrik, Taillon, Bruce E., Lewin, David A.

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regA, a Volvox gene that plays a central role in germ-soma differentiation, encodes a novel regulatory protein von Kirk, M M, Stark, K, Miller, S M, Müller, W, Taillon, B E, Gruber, H, Schmitt, R, Kirk, D L

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Simultaneous gene expression analysis of steady‐state and actively translated mRNA populations from osteosarcoma MG‐63 cells in response to IL‐1α via an open expression analysis pl... von Ju, Jingfang, Huang, Chunli, Minskoff, Stacey A., Mayotte, Jane E., Taillon, Bruce E., Simons, Jan F.

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The complete nucleotide sequence of the ilvGMEDA operon of Escherichia coli K-12 von LAWTHER, R. P, WEK, R. C, LOPES, J. M, PEREIRA, R, TAILLON, B. E, HATFIELD, G. W

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WECHE: A Novel Hematopoietic Regulatory Factor von Ohneda, Osamu, Ohneda, Kinuko, Nomiyama, Hisayuki, Zheng, Zhong, Gold, Steven A, Arai, Fumio, Miyamoto, Takeshi, Taillon, Bruce E, McIndoe, Richard A, Shimkets, Richard A, Lewin, David A, Suda, Toshio, Lasky, Laurence A

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Mutational analysis of centrin: an EF-hand protein associated with three distinct contractile fibers in the basal body apparatus of Chlamydomonas von Taillon, B.E. (Carnegie Mellon University, Pittsburgh, PA), Adler, S.A, Suhan, J.P, Jarvik, J.W

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Central helix mutations in the centrosome-associated EF-hand protein centrin von Taillon, B.E, Jarvik, J.W

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Analysis of the functional domains of biosynthetic threonine deaminase by comparison of the amino acid sequences of three wild-type alleles to the amino acid sequence of biodegrada... von Taillon, Bruce E., Little, Robert, Lawther, Robert P.

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"One plate/three-reporter" assay format for the detection and validation of yeast two-hybrid interactions von Evans, David R.H, Swirsding, Kendra A, Taillon, Bruce E, Simons, Jan F

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STV1 gene encodes functional homologue of 95-kDa yeast vacuolar H super(+)-ATPase subunit Vph1p von Manolson, M F, Wu, Bingruo, Proteau, D, Taillon, B E, Roberts, B T, Hoyt, MA, Jones, E W

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Mutational analyis of centrin : an EF-hand protein associated with three distinct contractile fibers in the basal body apparatus of Chlamydomonas von TAILLON, B. E, ADLER, S. A, SUHAN, J. P, JARVIK, J. W

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Paired-End Mapping Reveals Extensive Structural Variation in the Human Genome von Korbel, Jan O, Urban, Alexander Eckehart, Affourtit, Jason P, Godwin, Brian, Grubert, Fabian, Simons, Jan Fredrik, Kim, Philip M, Palejev, Dean, Carriero, Nicholas J, Du, Lei, Taillon, Bruce E, Chen, Zhoutao, Tanzer, Andrea, Saunders, A.C. Eugenia, Chi, Jianxiang, Yang, Fengtang, Carter, Nigel P, Hurles, Matthew E, Weissman, Sherman M, Harkins, Timothy T, Gerstein, Mark B, Egholm, Michael, Snyder, Michael

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The International HapMap Project von International HapMap Consortium, The International HapMap Consortium

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A haplotype map of the human genome von Gibbs, Richard A, Belmont, John W, Boudreau, Andrew, Leal, Suzanne M

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The Immunogenetics of Smallpox Vaccination von Stanley, Samuel L., Frey, Sharon E., Taillon-Miller, Patricia, Guo, Jianhua, Miller, Raymond D., Koboldt, Daniel C., Elashoff, Michael, Christensen, Ryan, Saccone, Nancy L., Belshe, Robert B.

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The Canadian Neuromuscular Disease Registry 2010–2019: A Decade of Facilitating Clinical Research Througha Nationwide, Pan-NeuromuscularDisease Registry von Hodgkinson, V., Lounsberry, J., M’Dahoma, S., Russell, A., Jewett, G., Benstead, T., Brais, B., Campbell, C., Johnston, W., Lochmüller, H., McCormick, A., Nguyen, C. T., O’Ferrall, E., Oskoui, M., Abrahao, A., Briemberg, H., Bourque, P.R., Botez, S., Cashman, N., Chapman, K., Chrestian, N., Crone, M., Dobrowolski, P., Dojeiji, S., Dowling, J. J., Dupré, N., Genge, A., Gonorazky, H., Grant, I., Hasal, S., Izenberg, A., Kalra, S., Katzberg, H., Krieger, C., Leung, E., Linassi, G., Mackenzie, A., Mah, J. K., Marrero, A., Massie, R., Matte, G., McAdam, L., McMillan, H., Melanson, M., Mezei, M. M., O’Connell, C., Pfeffer, G., Phan, C., Plamondon, S., Poulin, C., Rodrigue, X., Schellenberg, K., Selby, K., Sheriko, J., Shoesmith, C., Smith, R.G., Taillon, M., Taylor, S., Venance, S., Warman-Chardon, J., Worley, S., Zinman, L., Korngut, L.

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A gene deleted in Kallmann's syndrome shares homology with neural cell adhesion and axonal path-finding molecules von Franco, Brunella, Guioli, Silvana, Pragliola, Antonella, Incerti, Barbara, Bardoni, Barbara, Tonlorenzi, Rossana, Carrozzo, Romeo, Maestrini, Elena, Pieretti, Maura, Taillon-Miller, Patricia, Brown, Carolyn J, Willard, Huntington F, Lawrence, Charles, Persico, M. Graziella, Camerino, Giovanna, Ballabio, Andrea

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