Mutations in a Novel CLN6-Encoded Transmembrane Protein Cause Variant Neuronal Ceroid Lipofuscinosis in Man and Mouse by 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 by 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 by 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 by 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 by 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 by 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 by 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 by 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 by 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 by 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 by Lee, Richard L., Johnson, Kenneth R., Lerner, Terry J.

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Chromosomal localization of two genes underlying late-infantile neuronal ceroid lipofuscinosis by 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 by Gonzalez, Antonio, Lerner, Terry J., Huecas, Maria, Sosa-Pineda, Beatriz, Nogueira, Nadia, Lizardi, Paul M.

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YAC and Cosmid Contigs Spanning the Batten Disease (CLN3) Region at 16p12.1–p11.2 by 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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Sequence analysis of the D7S8 locus by CURRAN, M. E, LANDES, G. M, LEVERONE, B, WHITE, G. A, LERNER, T. J

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TDP-43 loss and ALS-risk SNPs drive mis-splicing and depletion of UNC13A by Brown, Anna-Leigh, Wilkins, Oscar G., Keuss, Matthew J., Hill, Sarah E., Zanovello, Matteo, Lee, Weaverly Colleen, Bampton, Alexander, Lee, Flora C. Y., Masino, Laura, Qi, Yue A., Bryce-Smith, Sam, Gatt, Ariana, Hallegger, Martina, Fagegaltier, Delphine, Phatnani, Hemali, Newcombe, Jia, Gustavsson, Emil K., Seddighi, Sahba, Reyes, Joel F., Coon, Steven L., Ramos, Daniel, Schiavo, Giampietro, Fisher, Elizabeth M. C., Raj, Towfique, Secrier, Maria, Lashley, Tammaryn, Ule, Jernej, Buratti, Emanuele, Humphrey, Jack, Ward, Michael E., Fratta, Pietro

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The rise of affectivism by Dukes, Daniel, Abrams, Kathryn, Adolphs, Ralph, Ahmed, Mohammed E., Beatty, Andrew, Berridge, Kent C., Broomhall, Susan, Brosch, Tobias, Campos, Joseph J., Clay, Zanna, Clément, Fabrice, Cunningham, William A., Damasio, Antonio, Damasio, Hanna, D’Arms, Justin, Davidson, Jane W., de Gelder, Beatrice, Deonna, Julien, de Sousa, Ronnie, Ekman, Paul, Ellsworth, Phoebe C., Fehr, Ernst, Fischer, Agneta, Foolen, Ad, Frevert, Ute, Grandjean, Didier, Gratch, Jonathan, Greenberg, Leslie, Greenspan, Patricia, Gross, James J., Halperin, Eran, Kappas, Arvid, Keltner, Dacher, Knutson, Brian, Konstan, David, Kret, Mariska E., LeDoux, Joseph E., Lerner, Jennifer S., Levenson, Robert W., Loewenstein, George, Manstead, Antony S. R., Maroney, Terry A., Moors, Agnes, Niedenthal, Paula, Parkinson, Brian, Pavlidis, Ioannis, Pelachaud, Catherine, Pollak, Seth D., Pourtois, Gilles, Roettger-Roessler, Birgitt, Russell, James A., Sauter, Disa, Scarantino, Andrea, Scherer, Klaus R., Stearns, Peter, Stets, Jan E., Tappolet, Christine, Teroni, Fabrice, Tsai, Jeanne, Turner, Jonathan, Reekum, Carien Van, Vuilleumier, Patrik, Wharton, Tim, Sander, David

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Quantitation of cannabinoid CB1 receptors in healthy human brain using positron emission tomography and an inverse agonist radioligand by Terry, Garth E., Liow, Jeih-San, Zoghbi, Sami S., Hirvonen, Jussi, Farris, Amanda G., Lerner, Alicja, Tauscher, Johannes T., Schaus, John M., Phebus, Lee, Felder, Christian C., Morse, Cheryl L., Hong, Jinsoo S., Pike, Victor W., Halldin, Christer, Innis, Robert B.

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Retromer dysfunction in amyotrophic lateral sclerosis by Pérez-Torres, Eduardo J, Utkina-Sosunova, Irina, Mishra, Vartika, Barbuti, Peter, De Planell-Saguer, Mariangels, Dermentzaki, Georgia, Geiger, Heather, Basile, Anna O, Robine, Nicolas, Fagegaltier, Delphine, Politi, Kristin A, Rinchetti, Paola, Jackson-Lewis, Vernice, Harms, Matthew, Phatnani, Hemali, Lotti, Francesco, Przedborski, Serge

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Addressing Early Childhood Emotional and Behavioral Problems by Gleason, Mary Margaret, Goldson, Edward, Yogman, Michael W

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