NMDA But Not Non-NMDA Excitotoxicity is Mediated by Poly(ADP-Ribose) Polymerase von Mandir, Allen S, Poitras, Marc F, Berliner, Adam R, Herring, William J, Guastella, Daniel B, Feldman, Alicia, Poirier, Guy G, Wang, Zhao-Qi, Dawson, Ted M, Dawson, Valina L

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Preservative-free tafluprost in the treatment of open-angle glaucoma or ocular hypertension in India: a phase III clinical trial von Chabi, A., Baranak, C., Lupinacci, R., Herring, W. J.

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0103 REM SLEEP IS INDUCED BY DUAL AND OREXIN 2 RECEPTOR ANTAGONISTS VIA MECHANISMS BEYOND ALPHA1-NORADRENERGIC SIGNALING von Gotter, AL, Stevens, J, Garson, SL, Fox, SV, Svetnik, V, 
Tannenbaum, PL, Forman, MS, Coleman, PJ, Herring, WJ, 
Renger, JJ, Winrow, CJ

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Orexin receptor antagonism for treatment of insomnia: A randomized clinical trial of suvorexant von HERRING, W. Joseph, SNYDER, Ellen, BUDD, Kerry, HUTZELMANN, Jill, SNAVELY, Duane, LIU, Kenneth, LINES, Christopher, ROTH, Thomas, MICHELSON, David

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A Randomized, Placebo-Controlled, Crossover Pilot Trial of the Oral Selective NR2B Antagonist MK-0657 in Patients With Treatment-Resistant Major Depressive Disorder von IBRAHIM, Lobna, DIAZGRANADOS, Nancy, JOLKOVSKY, Libby, BRUTSCHE, Nancy, LUCKENBAUGH, David A, HERRING, W. Joseph, POTTER, William Z, ZARATE, Carlos A

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Dynamic Regulation of Neuronal NO Synthase Transcription by Calcium Influx through a CREB Family Transcription Factor-Dependent Mechanism von Sasaki, Masayuki, Gonzalez-Zulueta, Mirella, Huang, Hui, Herring, William J., Ahn, Sohyun, Ginty, David D., Dawson, Valina L., Dawson, Ted M.

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Truncated N-Terminal Fragments of Huntingtin with Expanded Glutamine Repeats form Nuclear and Cytoplasmic Aggregates in Cell Culture von Cooper, Jillian K., Schilling, Gabriele, Peters, Matthew F., Herring, William J., Sharp, Alan H., Kaminsky, Zachary, Masone, Jamie, Khan, Farhat A., Delanoy, Michael, Borchelt, David R., Dawson, Valina L., Dawson, Ted M., Ross, Christopher A.

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Rat muscle branched-chain ketoacid dehydrogenase activity and mRNAs increase with extracellular acidemia von England, B. K, Greiber, S, Mitch, W. E, Bowers, B. A, Herring, W. J, McKean, M, Ebb, R. G, Price, S. R, Danner, D. J

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Nuclear Localization of a Non-caspase Truncation Product of Atrophin-1, with an Expanded Polyglutamine Repeat, Increases Cellular Toxicity von Nucifora, Jr, Frederick C, Ellerby, Lisa M, Wellington, Cheryl L, Wood, Jon D, Herring, William J, Sawa, Akira, Hayden, Michael R, Dawson, Valina L, Dawson, Ted M, Ross, Christopher A

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Nuclear Targeting of Mutant Huntingtin Increases Toxicity von Peters, Matthew F., Nucifora, Frederick C., Kushi, Jonathan, Seaman, Holly C., Cooper, Jillian K., Herring, William J., Dawson, Valina L., Dawson, Ted M., Ross, Christopher A.

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Construction and nucleotide sequence of a cDNA encoding the full-length preprotein for human branched chain acyltransferase von Danner, D J, Litwer, S, Herring, W J, Pruckler, J

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Orexin receptor antagonists for the treatment of insomnia and potential treatment of other neuropsychiatric indications von Herring, W. Joseph, Roth, Thomas, Krystal, Andrew D., Michelson, David

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Reversion of the Maple Syrup Urine Disease Phenotype of Impaired Branched Chain α-Ketoacid Dehydrogenase Complex Activity in Fibroblasts from an Affected Child von Litwer, S, Herring, W J, Danner, D J

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Structure of the gene encoding dihydrolipoyl transacylase (E2) component of human branched chain alpha-keto acid dehydrogenase complex and characterization of an E2 pseudogene von LAU, KS, HERRING, WJ, CHUANG, JL, MCKEAN, M, DANNER, DJ, COX, RP, CHUANG, DT

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Sugammadex efficacy for reversal of rocuronium- and vecuronium-induced neuromuscular blockade: A pooled analysis of 26 studies von Herring, William Joseph, Woo, Tiffany, Assaid, Christopher A., Lupinacci, Robert J., Lemmens, Hendrikus J., Blobner, Manfred, Khuenl-Brady, Karin S.

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The complete cDNA sequence for dihydrolipoyl transacylase (E2) of human branched-chain α-keto acid dehydrogenase complex von Lau, Kim S., Chuang, Jacinta L., Joseph Herring, W., Danner, Dean J., Cox, Rody P., Chuang, David T.

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Branched chain acyltransferase absence due to an Alu-based genomic deletion allele and an exon skipping allele in a compound heterozygote proband expressing maple syrup urine disea... von Herring, W.Joseph, McKean, Martha, Dracopoli, Nicolas, Danner, Dean J.

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Thiamin-Responsive Maple Syrup Urine Disease in a Patient Antigenically Missing Dihydrolipoamide Acyltransferase von Ellerine, N.P., Herring, W.J., Elsas, L.J., Mckean, M.C., Klein, P.D., Danner, D.J.

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Molecular Genetic Basis for Inherited Human Disorders of Branched-Chain α-Keto Acid Dehydrogenase Complex von DANNER, DEAN J., LITWER, STUART, HERRING, W. JOSEPH, ELSAS, LOUIS J.

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Molecular genetic basis of maple syrup urine disease in a family with two defective alleles for branched chain acyltransferase and localization of the gene to human chromosome I von HERRING, W. J, LITWER, S, WEBER, J. L, DANNER, D. J

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