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Results: 1-17 |
Results: 17
Mouse models for the Wolf-Hirschhorn deletion syndrome
Authors: Naf, D Wilson, LA Bergstrom, RA Smith, RS Goodwin, NC Verkerk, A van Ommen, GJ Ackerman, SL Frankel, WN Schimenti, JC
Citation: D. Naf et al., Mouse models for the Wolf-Hirschhorn deletion syndrome, HUM MOL GEN, 10(2), 2001, pp. 91-98
A null mutation in inositol polyphosphate 4-phosphatase type I causes selective neuronal loss in weeble mutant mice
Authors: Nystuen, A Legare, ME Shultz, LD Frankel, WN
Citation: A. Nystuen et al., A null mutation in inositol polyphosphate 4-phosphatase type I causes selective neuronal loss in weeble mutant mice, NEURON, 32(2), 2001, pp. 203-212
Electroconvulsive thresholds of inbred mouse strains
Authors: Frankel, WN Taylor, L Beyer, B Tempel, BL White, HS
Citation: Wn. Frankel et al., Electroconvulsive thresholds of inbred mouse strains, GENOMICS, 74(3), 2001, pp. 306-312
High-resolution genetic and physical mapping of modifier-of-deafwaddler (mdfw) and waltzer (Cdh23(v))
Authors: Bryda, EC Kim, HJ Legare, ME Frankel, WN Noben-Trauth, K
Citation: Ec. Bryda et al., High-resolution genetic and physical mapping of modifier-of-deafwaddler (mdfw) and waltzer (Cdh23(v)), GENOMICS, 73(3), 2001, pp. 338-342
Ducky mouse phenotype of epilepsy and ataxia is associated with mutations in the Cacna2d2 gene and decreased calcium channel current in cerebellar Purkinje cells
Authors: Barclay, J Balaguero, N Mione, M Ackerman, SL Letts, VA Brodbeck, J Canti, C Meir, A Page, KM Kusumi, K Perez-Reyes, E Lander, ES Frankel, WN Gardiner, RM Dolphin, AC Rees, M
Citation: J. Barclay et al., Ducky mouse phenotype of epilepsy and ataxia is associated with mutations in the Cacna2d2 gene and decreased calcium channel current in cerebellar Purkinje cells, J NEUROSC, 21(16), 2001, pp. 6095-6104
Of mice and genome sequence
Authors: Hamilton, BA Frankel, WN
Citation: Ba. Hamilton et Wn. Frankel, Of mice and genome sequence, CELL, 107(1), 2001, pp. 13-16
Sequence interpretation - Functional annotation of mouse genome sequences
Authors: Nadeau, JH Balling, R Barsh, G Beier, D Brown, SDM Bucan, M Camper, S Carlson, G Copeland, N Eppig, J Fletcher, C Frankel, WN Ganten, D Goldowitz, D Goodnow, C Guenet, JL Hicks, G de Angelis, MH Jackson, I Jacob, HJ Jenkins, N Johnson, D Justice, M Kay, S Kingsley, D Lehrach, H Magnuson, T Meisler, M Poustka, AM Rinchik, EM Rossant, J Russell, LB Schimenti, J Shiroishi, T Skarnes, WC Soriano, P Stanford, W Takahashi, JS Wurst, W Zimmer, A
Citation: Jh. Nadeau et al., Sequence interpretation - Functional annotation of mouse genome sequences, SCIENCE, 291(5507), 2001, pp. 1251
Biochemical and biophysical evidence for gamma(2) subunit association withneuronal voltage-activated Ca2+ channels
Authors: Kang, MG Chen, CC Felix, R Letts, VA Frankel, WN Mori, Y Campbell, KP
Citation: Mg. Kang et al., Biochemical and biophysical evidence for gamma(2) subunit association withneuronal voltage-activated Ca2+ channels, J BIOL CHEM, 276(35), 2001, pp. 32917-32924
A major effect QTL determined by multiple genes in epileptic EL mice
Authors: Legare, ME Bartlett, FS Frankel, WN
Citation: Me. Legare et al., A major effect QTL determined by multiple genes in epileptic EL mice, GENOME RES, 10(1), 2000, pp. 42-48
The mouse fidgetin gene defines a new role for AAA family proteins in mammalian development
Authors: Cox, GA Mahaffey, CL Nystuen, A Letts, VA Frankel, WN
Citation: Ga. Cox et al., The mouse fidgetin gene defines a new role for AAA family proteins in mammalian development, NAT GENET, 26(2), 2000, pp. 198-202
The roads from phenotypic variation to gene discovery: mutagenesis versus QTLs
Authors: Nadeau, JH Frankel, WN
Citation: Jh. Nadeau et Wn. Frankel, The roads from phenotypic variation to gene discovery: mutagenesis versus QTLs, NAT GENET, 25(4), 2000, pp. 381-384
A new spontaneous mouse mutation in the Kcne1 gene
Authors: Letts, VA Valenzuela, A Dunbar, C Zheng, QY Johnson, KR Frankel, WN
Citation: Va. Letts et al., A new spontaneous mouse mutation in the Kcne1 gene, MAMM GENOME, 11(10), 2000, pp. 831-835
Multiple seizure susceptibility genes on chromosome 7 in SWXL-4 congenic mouse strains
Authors: Legare, ME Frankel, WN
Citation: Me. Legare et Wn. Frankel, Multiple seizure susceptibility genes on chromosome 7 in SWXL-4 congenic mouse strains, GENOMICS, 70(1), 2000, pp. 62-65
Ataxic mouse mutants and molecular mechanisms of absence epilepsy
Authors: Fletcher, CF Frankel, WN
Citation: Cf. Fletcher et Wn. Frankel, Ataxic mouse mutants and molecular mechanisms of absence epilepsy, HUM MOL GEN, 8(10), 1999, pp. 1907-1912
Detecting genes in new and old mouse models for epilepsy: a prospectus through the magnifying glass
Authors: Frankel, WN
Citation: Wn. Frankel, Detecting genes in new and old mouse models for epilepsy: a prospectus through the magnifying glass, EPILEPSY R, 36(2-3), 1999, pp. 97-110
Genetic modifiers of polycystic kidney disease in intersubspecific KAT2J mutants
Authors: Upadhya, P Churchill, G Birkenmeier, EH Barker, JE Frankel, WN
Citation: P. Upadhya et al., Genetic modifiers of polycystic kidney disease in intersubspecific KAT2J mutants, GENOMICS, 58(2), 1999, pp. 129-137
Identification of the mouse neuromuscular degeneration gene and mapping ofa second site suppressor allele
Authors: Cox, GA Mahaffey, CL Frankel, WN
Citation: Ga. Cox et al., Identification of the mouse neuromuscular degeneration gene and mapping ofa second site suppressor allele, NEURON, 21(6), 1998, pp. 1327-1337
Risultati: 1-17 |