Mutations in a Novel CLN6-Encoded Transmembrane Protein Cause Variant Neuronal Ceroid Lipofuscinosis in Man and Mouse von Gao, Hanlin, Boustany, Rose-Mary N., Espinola, Janice A., Cotman, Susan L., Srinidhi, Lakshmi, Antonellis, Kristen Auger, Gillis, Tammy, Qin, Xuebin, Liu, Shumei, Donahue, Leah R., Bronson, Roderick T., Faust, Jerry R., Stout, Derek, Haines, Jonathan L., Lerner, Terry J., MacDonald, Marcy E.

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Isolation of a novel gene underlying batten disease, CLN3 von Lerner, Terry J, Boustany, Rose-Mary N, Anderson, John W, D'Arigo, Kenneth L, Schlumpf, Karen, Buckler, Alan J, Gusella, James F, Haines, Jonathan L

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Spectrum of Mutations in the Batten Disease Gene, CLN3 von Munroe, Patricia B., Mitchison, Hannah M., O'Rawe, Angela M., Anderson, John W., Boustany, Rose-Mary, Lerner, Terry J., Taschner, Peter E.M., Vos, Nanneke de, Breuning, Martijn H., Gardiner, R. Mark, Mole, Sara E.

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Cln3(Deltaex7/8) knock-in mice with the common JNCL mutation exhibit progressive neurologic disease that begins before birth von Cotman, Susan L, Vrbanac, Vladimir, Lebel, Lori-Anne, Lee, Richard L, Johnson, Kevin A, Donahue, Leah-Rae, Teed, Allison M, Antonellis, Kristen, Bronson, Roderick T, Lerner, Terry J, MacDonald, Marcy E

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Cln3 Δex7/8 knock-in mice with the common JNCL mutation exhibit progressive neurologic disease that begins before birth von Cotman, Susan L., Vrbanac, Vladimir, Lebel, Lori-Anne, Lee, Richard L., Johnson, Kevin A., Donahue, Leah-Rae, Teed, Allison M., Antonellis, Kristen, Bronson, Roderick T., Lerner, Terry J., MacDonald, Marcy E.

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Mutational Analysis of the Defective Protease in Classic Late-Infantile Neuronal Ceroid Lipofuscinosis, a Neurodegenerative Lysosomal Storage Disorder von Sleat, David E., Gin, Rosalie M., Sohar, Istvan, Wisniewski, Krystyna, Sklower-Brooks, Susan, Pullarkat, Raju K., Palmer, David N., Lerner, Terry J., Boustany, Rose-Mary, Uldall, Peter, Siakotos, Aristotle N., Donnelly, Robert J., Lobel, Peter

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Two RFLPs detected by a cosmid at locus D16S144 von Lerner, T J, Arn, E, Anderson, M A, Klinger, K W, Callen, D F, Tanzi, R E

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Genomic Structure and Complete Nucleotide Sequence of the Batten Disease Gene,CLN3 von Mitchison, Hannah M., Munroe, Patricia B., O'Rawe, Angela M., Taschner, Peter E.M., de Vos, Nanneke, Kremmidiotis, Gabriel, Lensink, Ingrid, Munk, A.Christine, D'Arigo, Kenneth L, Anderson, John W., Lerner, Terry J., Moyzis, Robert K., Callen, David F., Breuning, Martijn H., Doggett, Norman A., Gardiner, R.Mark, Mole, Sara E.

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Isolation and chromosomal mapping of a mouse homolog of the batten disease gene CLN3 von LEE, R. L, JOHNSON, K. R, LERNER, T. J

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Linkage disequilibrium between the juvenile neuronal ceroid lipofuscinosis gene and marker loci on chromosome 16p12.1 von LERNER, T. J, BOUSTANY, R.-M. N, MACCORMACK, K, GLEITSMAN, J, SCHLUMPF, K, BREAKEFIELD, X. O, GUSELLA, J. F, HAINES, J. L

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Isolation and Chromosomal Mapping of a Mouse Homolog of the Batten Disease GeneCLN3 von Lee, Richard L., Johnson, Kenneth R., Lerner, Terry J.

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Chromosomal localization of two genes underlying late-infantile neuronal ceroid lipofuscinosis von Haines, J L, Boustany, R M, Alroy, J, Auger, K J, Shook, K S, Terwedow, H, Lerner, T J

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Apparent generation of a segmented mRNA from two separate tandem gene families in Trypanosoma cruzi von Gonzalez, Antonio, Lerner, Terry J., Huecas, Maria, Sosa-Pineda, Beatriz, Nogueira, Nadia, Lizardi, Paul M.

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Strategy for Mutation Detection in CLN3: Characterisation of Two Finnish Mutations von Munroe, Patricia B., O'Rawe, Angela M., Mitchison, Hannah M., Järvelä, Irma E., Santavuori, Pirkko, Lerner, Terry J., Taschner, P. E., Gardiner, R. M., Mole, Sara E.

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Genetic Mapping of the Batten Disease Locus (CLN3) to the Interval D16S288-D16S383 by Analysis of Haplotypes and Allelic Association von Mitchison, Hannah M., Taschner, Peter E.M., O'Rawe, Angela M., de Vos, Nanneke, Phillips, Hilary A., Thompson, Andrew D., Kozman, Helen M., Haines, Jonathan L., Schlumpf, Karen, D'Arigo, Kenneth, Boustany, Rose-Mary N., Callen, David F., Breuning, Martijn H., Gardiner, R.Mark, Mole, Sara E., Lerner, Terry J.

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YAC and Cosmid Contigs Spanning the Batten Disease (CLN3) Region at 16p12.1–p11.2 von JÄRVELÄ, IRMA E., MITCHISON, HANNAH M., O'RAWE, ANGELA M., MUNROE, PATRICIA B., TASCHNER, PETER E.M., DEVOS, NANNEKE, LERNER, TERRY J., D'ARIGO, KEN L., CALLEN, DAVID F., THOMPSON, ANDREW D., KNIGHT, MAREE, MARRONE, BABETTA L., MUNDT, MARK O., MEINCKE, LINDA, BREUNING, MARTIJN H., GARDINER, MARK R., DOGGETT, NORMAN A., MOLE, SARA E.

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The “steady state” of coliphage f1: DNA synthesis late in infection von Lerner, Terry J., Model, Peter

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Sequence analysis of the D7S8 locus von CURRAN, M. E, LANDES, G. M, LEVERONE, B, WHITE, G. A, LERNER, T. J

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Scotland Funds Biotechnology Research Park von Lerner, Terry J.

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Lab Robot Debuts at Zymark

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