Targeted Deletion in Astrocyte Intermediate Filament (Gfap) Alters Neuronal Physiology von McCall, M. A., Gregg, R. G., Behringer, R. R., Brenner, M., Delaney, C. L., Galbreath, E. J., Zhang, C. L., Pearce, R. A., Chiu, S. Y., Messing, A.

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Analysis of the Zebrafish perplexed Mutation Reveals Tissue-Specific Roles for de Novo Pyrimidine Synthesis During Development von Willer, G. B, Lee, V. M, Gregg, R. G, Link, B. A

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A role for nyctalopin, a small leucine-rich repeat protein, in localizing the TRP melastatin 1 channel to retinal depolarizing bipolar cell dendrites von Pearring, Jillian N, Bojang, Jr, Pasano, Shen, Yin, Koike, Chieko, Furukawa, Takahisa, Nawy, Scott, Gregg, Ronald G

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A naturally occurring mouse model of X-linked congenital stationary night blindness von Pardue, MT, McCall, MA, LaVail, MM, Gregg, RG, Peachey, NS

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pigk Mutation underlies macho behavior and affects Rohon-Beard cell excitability von Carmean, V, Yonkers, M A, Tellez, M B, Willer, J R, Willer, G B, Gregg, R G, Geisler, R, Neuhauss, S C, Ribera, A B

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Cardiac Troponin I Gene Knockout: A Mouse Model of Myocardial Troponin I Deficiency von Huang, XuPei, Pi, YeQing, Lee, Kevin J, Henkel, Anne S, Gregg, Ronald G, Powers, Patricia A, Walker, Jeffery W

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Newborn Screening for Cystic Fibrosis in Wisconsin: Comparison of Biochemical and Molecular Methods von Gregg, Ronald G, Simantel, Amy, Farrell, Philip M, Koscik, Rebecca, Kosorok, Michael R, Laxova, Anita, Laessig, Ronald, Hoffman, Gary, Hassemer, David, Mischler, Elaine H, Splaingard, Mark

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A calcium channel mutation causing hypokalemic periodic paralysis von Jurkat-Rott, Karln, Lehmann-Horn, Frank, Elbaz, Alexis, Heine, Roland, Gregg, Ronald G., Hogan, Kirk, Powers, Patricia A., Laple, Pascale, Vale-Santos, José E., Weissenbach, Jean, Fontaine, Bertrand

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Genetic localization of an autosomal dominant leukodystrophy mimicking chronic progressive multiple sclerosis to chromosome 5q31 von COFFEEN, C. M, MCKENNA, C. E, FU, Y.-H, KOEPPEN, A. H, PLASTER, N. M, MARAGAKIS, N, MIHALOPOULOS, J, SCHWANKHAUS, J. D, FLANIGAN, K. M, GREGG, R. G, PTACEK, L. J

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Genetic heterogeneity in families with hereditary multiple exostoses von COOK, A, RASKIND, W, WIJSMAN, E, HECHT, J. T, WELLS, D, WAGNER, M. J, BLANTON, S. H, PAULI, R. M, GREGG, R. G, FRANCOMANO, C. A, PUFFENBERGER, E, CONRAD, U, SCHMALE, G, SCHELLENBERG, G

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Morphological and Physiological Consequences of the Selective Elimination of Rod Photoreceptors in Transgenic Mice von McCALL, M.A., GREGG, R.G., MERRIMAN, K., GOTO, Y., PEACHEY, N.S., STANFORD, L.R.

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Skeletal muscle and brain isoforms of a beta-subunit of human voltage-dependent calcium channels are encoded by a single gene von POWERS, PA, LIU, SY, HOGAN, K, GREGG, RG

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Positional Cloning of the young Mutation Identifies an Essential Role for the Brahma Chromatin Remodeling Complex in Mediating Retinal Cell Differentiation von Gregg, Ronald G., Willer, Gregory B., Fadool, James M., Dowling, John E., Link, Brian A.

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Application of DNA analysis in a population-screening program for neonatal diagnosis of cystic fibrosis (CF) : comparison of screening protocols von GREGG, R. G, WILFOND, B. S, FARRELL, P. M, LAXOVA, A, HASSEMER, D, MISCHLER, E. H

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Regulatory Elements in the Introns of the Human HPRT Gene are Necessary for Its Expression in Embryonic Stem Cells von Reid, Laura H., Gregg, Ronald G., Smithies, Oliver, Koller, Beverly H.

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Localization of the Mouse nob (no b-wave) Gene to the Centromeric Region of the X Chromosome von Candille, Sophie I, Pardue, Machelle T, McCall, Maureen A, Peachey, Neal S, Gregg, Ronald G

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Molecular characterization of the gene encoding the gamma subunit of the human skeletal muscle 1,4-dihydropyridine-sensitive Ca2+ channel (CACNLG), cDNA sequence, gene structure, a... von POWERS, P. A, SHUYING LIU, HOGAN, K, GREGG, R. G

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Localization of a Non-Specific X-linked Mental Retardation Gene, MRX23, to Xq23–q24 von Gregg, Ronald G., Palmer, Christina, Kirkpatrick, Susan, Simantel, Amy

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A Cysteine-for-Arginine Substitution (R614C) in the Human Skeletal Muscle Calcium Release Channel Cosegregates With Malignant Hyperthermia von Hogan, Kirk, Couch, Fergus, Powers, Pat A., Gregg, Ron G.

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Refined genetic localization for central core disease von MULLEY, J. C, KOZMAN, H. M, HAAN, E. A, PHILLIPS, H. A, GEDEON, A. K, MCCURE, J. A, ILES, D. E, GREGG, R. G, HOGAN, K, COUCH, F. J, MACLENNAN, D. H

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