Mutations in NPC1 Highlight a Conserved NPC1-Specific Cysteine-Rich Domain von Greer, WL, Dobson, MJ, Girouard, GS, Byers, DM, Riddell, DC, Neumann, PE

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Altered Sensory Processing in the Somatosensory Cortex of the Mouse Mutant Barrelless von Welker, E., Armstrong-James, M., Bronchti, G., Ourednik, W., Gheorghita-Baechler, F., Dubois, R., Guernsey, D. L., Van der Loos, H., Neumann, P. E.

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Linkage of Niemann-Pick Disease Type D to the Same Region of Human Chromosome 18 as Niemann-Pick Disease Type C von Greer, W.L., Riddell, D.C., Byers, D.M., Welch, J.P., Girouard, G.S., Sparrow, S.M., Gillan, T.L., Neumann, P.E.

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Familial essential thrombocythemia with spontaneous megakaryocyte colony formation and acquired JAK2 mutations von Higgs, J R, Sadek, I, Neumann, P E, Ing, V W, Renault, N K, Berman, J N, Greer, W L

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Maternal Behavior in Female C57BL/6J and DBA/2J Inbred Mice von Brown, Richard E, Mathieson, W.Bruce, Stapleton, Jennifer, Neumann, Paul E

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Loss of adenylyl cyclase I activity disrupts patterning of mouse somatosensory cortex von Schalkwyk, Leonard C, Neumann, Paul E, Guernsey, Duane L, Smallman, Donald S, Wong, Scott T, Storm, Daniel R, Fine, Alan, Leong, Wey L, Abdel-Majid, Raja M, Dobson, Melanie J

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The Nova Scotia (type D) form of Niemann-Pick disease is caused by a G3097→T transversion in NPC1 von GREER, W. L, RIDDELL, D. C, GILLAN, T. L, GIROUARD, G. S, SPARROW, S. M, BYERS, D. M, DOBSON, M. J, NEUMANN, P. E

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Genetic Dissection of Susceptibility to Audiogenic Seizures in Inbred Mice von Neumann, Paul E., Collins, Robert L.

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Rocker Is a New Variant of the Voltage-Dependent Calcium Channel Gene Cacna1a von Zwingman, Theresa A, Neumann, Paul E, Noebels, Jeffrey L, Herrup, Karl

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Adenylyl cyclase I regulates AMPA receptor trafficking during mouse cortical 'barrel' map development von Lu, Hui-Chen, Crair, Michael C, She, Wei-Chi, Plas, Daniel T, Neumann, Paul E, Janz, Roger

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Genotype/phenotype correlations in aniridia von Gupta, Sanjoy K, De Becker, Inge, Tremblay, François, Guernsey, Duane L, Neumann, Paul E

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Multifactorial inheritance of neural tube defects: localization of the major gene and recognition of modifiers in ct mutant mice von Neumann, Paul E, Frankel, Wayne N, Letts, Verity A, Coffin, John M, Copp, Andrew J, Bernfield, Merton

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Two-Locus Linkage Analysis Using Recombinant Inbred Strains and Bayes' Theorem von Neumann, P. E

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Susceptibility of AKXD recombinant inbred mouse strains to lymphomas von GILBERT, D. J, NEUMANN, P. E, TAYLOR, B. A, JENKINS, N. A, COPELAND, N. G

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Organization and promoter activity of the mouse syndecan-1 gene von Hinkes, M.T., Goldberger, O.A., Neumann, P.E., Kokenyesi, R., Bernfield, M.

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Effects of PAX6 mutations on retinal function: an electroretinographic study von Tremblay, François, Gupta, Sanjoy K, De Becker, Inge, Guernsey, Duane L, Neumann, Paul E

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INFERENCE IN LINKAGE ANALYSIS OF MULTIFACTORIAL TRAITS USING RECOMBINANT INBRED STRAINS OF MICE von NEUMANN, PE

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Three-Locus Linkage Analysis Using Recombinant Inbred Strains and Bayes' Theorem von Neumann, P. E

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Linkage disequilibrium mapping of the Nova Scotia variant of Niemann-Pick disease von Greer, WL, Riddell, DC, Murty, S, Gillan, TL, Girouard, GS, Sparrow, SM, Tatlidil, C, Dobson, MJ, Neumann, PE

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Insertional Mutation in a Transgenic Mouse Allelic with Purkinje Cell Degeneration von Krulewski, Thomas F., Neumann, Paul E., Gordon, Jon W.

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