-
1
-
-
0028141704
-
The cloning of zebrin II reveals its identity with aldolase C
-
Ah A. H., Dziennis S., Hawkes R., Herrup K. The cloning of zebrin II reveals its identity with aldolase C. Development. 120:1994;2081-2090.
-
(1994)
Development
, vol.120
, pp. 2081-2090
-
-
Ah, A.H.1
Dziennis, S.2
Hawkes, R.3
Herrup, K.4
-
3
-
-
0027367333
-
CDNA cloning of the two subunits of human CAAX farnesyltransferase and chromosomal mapping of FNTA and FNTB loci and related sequences
-
Andres D. A., Milatovich A., Ozcelik T., Wenzlau J. M., Brown M. S., Goldstein J. L., Francke U. cDNA cloning of the two subunits of human CAAX farnesyltransferase and chromosomal mapping of FNTA and FNTB loci and related sequences. Genomics. 18:1993;105-112.
-
(1993)
Genomics
, vol.18
, pp. 105-112
-
-
Andres, D.A.1
Milatovich, A.2
Ozcelik, T.3
Wenzlau, J.M.4
Brown, M.S.5
Goldstein, J.L.6
Francke, U.7
-
4
-
-
0027155208
-
Complex patterns of sequence variation and multiple 5′ and 3′ ends are found among transcripts of the erythroid ankyrin gene
-
Birkenmeier C. S., White R. A., Peters L. L., Hall E. J., Lux S. E., Barker J. E. Complex patterns of sequence variation and multiple 5′ and 3′ ends are found among transcripts of the erythroid ankyrin gene. J. Biol. Chem. 268:1993;9533-9540.
-
(1993)
J. Biol. Chem.
, vol.268
, pp. 9533-9540
-
-
Birkenmeier, C.S.1
White, R.A.2
Peters, L.L.3
Hall, E.J.4
Lux, S.E.5
Barker, J.E.6
-
5
-
-
0029835273
-
Analysis of CA repeat polymorphisms places three human gene loci on the 8p linkage map
-
Bruskiewich R., Everson T., Ma L., Chan L., Schertzer M., Giacobino J.-P., Muzzin P., Wood S. Analysis of CA repeat polymorphisms places three human gene loci on the 8p linkage map. Cytogenet. Cell Genet. 73:1996;331-333.
-
(1996)
Cytogenet. Cell Genet.
, vol.73
, pp. 331-333
-
-
Bruskiewich, R.1
Everson, T.2
Ma, L.3
Chan, L.4
Schertzer, M.5
Giacobino, J.-P.6
Muzzin, P.7
Wood, S.8
-
6
-
-
0029870957
-
Chromosomal localization of the neurological mouse mutations tottering (tgpcdnr
-
Campbell D. B., Hess E. J. Chromosomal localization of the neurological mouse mutations tottering (tgpcdnr. Brain Res. Mol. Brain Res. 37:1996;79-84.
-
(1996)
Brain Res. Mol. Brain Res.
, vol.37
, pp. 79-84
-
-
Campbell, D.B.1
Hess, E.J.2
-
7
-
-
0027163830
-
The human C/EBP-delta (CRP3/CELF) gene: Structure and chromosomal localization
-
Cleutjens C. B. J. M., van Eekelen C. C. E. M., van Dekken H., Smit E. M. E., Hagemeijer A., Wagner M. J., Wells D. E., Trapman J. The human C/EBP-delta (CRP3/CELF) gene: Structure and chromosomal localization. Genomics. 16:1993;520-523.
-
(1993)
Genomics
, vol.16
, pp. 520-523
-
-
Cleutjens, C.B.J.M.1
Van Eekelen, C.C.E.M.2
Van Dekken, H.3
Smit, E.M.E.4
Hagemeijer, A.5
Wagner, M.J.6
Wells, D.E.7
Trapman, J.8
-
8
-
-
0027679382
-
Genome maps IV
-
Copeland N. G., Gilbert D. J., Jenkins N. A., Nadeau J. H., Eppig J. T., Maltais L. J., Miller J. C., Dietrich W. F., Steen R. G., Lincoln S. E., Weaver A., Joyce D. C., Merchant M., Wessel M., Katz H., Stein L. D., Reeve M. P., Daly M. J., Dredge R. D., Marquis A., Goodman N., Lander E. S. Genome maps IV. Science. 262:1993;67.
-
(1993)
Science
, vol.262
, pp. 67
-
-
Copeland, N.G.1
Gilbert, D.J.2
Jenkins, N.A.3
Nadeau, J.H.4
Eppig, J.T.5
Maltais, L.J.6
Miller, J.C.7
Dietrich, W.F.8
Steen, R.G.9
Lincoln, S.E.10
Weaver, A.11
Joyce, D.C.12
Merchant, M.13
Wessel, M.14
Katz, H.15
Stein, L.D.16
Reeve, M.P.17
Daly, M.J.18
Dredge, R.D.19
Marquis, A.20
Goodman, N.21
Lander, E.S.22
more..
-
9
-
-
0021342225
-
Regional mapping of clotting factors VII and X to 13q34. Expression of factor VII through chromosome 8
-
de Grouchy J., Dautzenberg M. D., Turleau C., Beguin S., Chavin-Colin F. Regional mapping of clotting factors VII and X to 13q34. Expression of factor VII through chromosome 8. Hum. Genet. 66:1984;230-233.
-
(1984)
Hum. Genet.
, vol.66
, pp. 230-233
-
-
De Grouchy, J.1
Dautzenberg, M.D.2
Turleau, C.3
Beguin, S.4
Chavin-Colin, F.5
-
10
-
-
0028302127
-
A genetic map of the mouse with 4,006 simple sequence length polymorphisms
-
Dietrich W. F., Miller J. C., Steen R. G., Merchant M., Damron D., Nahf R., Gross A., Joyce D. C., Wessel M., Dredge R. D. A genetic map of the mouse with 4,006 simple sequence length polymorphisms. Nature Genet. 7:1994;220-245.
-
(1994)
Nature Genet.
, vol.7
, pp. 220-245
-
-
Dietrich, W.F.1
Miller, J.C.2
Steen, R.G.3
Merchant, M.4
Damron, D.5
Nahf, R.6
Gross, A.7
Joyce, D.C.8
Wessel, M.9
Dredge, R.D.10
-
11
-
-
13344287050
-
A comprehensive genetic map of the mouse genome
-
Dietrich W. F., Miller J., Steen R., Merchant M. A., Damron-Boles D., Husain Z., Dredge R., Daly M. J., Ingalls K. A., O'Conner T. J., Evans C. A., DeAngelis M. M., Levinson D. M., Kruglyak L., Goodman N., Copeland N. G., Jenkins N. A., Hawkins T. L., Stein L. D., Page D. C., Lander E. S. A comprehensive genetic map of the mouse genome. Nature. 380:1996;149-152.
-
(1996)
Nature
, vol.380
, pp. 149-152
-
-
Dietrich, W.F.1
Miller, J.2
Steen, R.3
Merchant, M.A.4
Damron-Boles, D.5
Husain, Z.6
Dredge, R.7
Daly, M.J.8
Ingalls, K.A.9
O'Conner, T.J.10
Evans, C.A.11
Deangelis, M.M.12
Levinson, D.M.13
Kruglyak, L.14
Goodman, N.15
Copeland, N.G.16
Jenkins, N.A.17
Hawkins, T.L.18
Stein, L.D.19
Page, D.C.20
Lander, E.S.21
more..
-
12
-
-
0028259069
-
Effects of nervous mutation on Purkinje cell compartments defined by Zebrin II and 9-O
-
Edwards M. A., Crandall J. E., Leclerc N., Yamamoto M. Effects of nervous mutation on Purkinje cell compartments defined by Zebrin II and 9-O. Neurosci. Res. 19:1994;167-174.
-
(1994)
Neurosci. Res.
, vol.19
, pp. 167-174
-
-
Edwards, M.A.1
Crandall, J.E.2
Leclerc, N.3
Yamamoto, M.4
-
13
-
-
0030253127
-
A comprehensive large-insert yeast artificial chromosome library for physical mapping of the mouse genome
-
Haldi M. L., Strickland C., Lim P., VanBerkel V., Chen X.-N., Noya D., Korenberg J. R., Husain Z., Miller J., Lander E. S. A comprehensive large-insert yeast artificial chromosome library for physical mapping of the mouse genome. Mamm. Genome. 7:1996;767-769.
-
(1996)
Mamm. Genome
, vol.7
, pp. 767-769
-
-
Haldi, M.L.1
Strickland, C.2
Lim, P.3
Vanberkel, V.4
Chen, X.-N.5
Noya, D.6
Korenberg, J.R.7
Husain, Z.8
Miller, J.9
Lander, E.S.10
-
14
-
-
0029929016
-
Probable exclusion of the cortexin-encoding gene as a candidate for mouse neurological mutants: Nervous, tottering and motor neuron degeneration
-
Horvath D. H., Watson J. B., Travis G. H. Probable exclusion of the cortexin-encoding gene as a candidate for mouse neurological mutants: nervous, tottering and motor neuron degeneration. Gene. 171:1996;305-306.
-
(1996)
Gene
, vol.171
, pp. 305-306
-
-
Horvath, D.H.1
Watson, J.B.2
Travis, G.H.3
-
15
-
-
0029148894
-
Mouse chromosomal location of the CCAAT/enhancer binding proteins C/EBP-β (Cebpb), C/EBP-δ (Cebpd), and CRP1 (Cebpe)
-
Jenkins N. A., Gilbert D. J., Cho B. C., Strobel M. C., Williams S. C., Copeland N. G., Johnson P. F. Mouse chromosomal location of the CCAAT/enhancer binding proteins C/EBP-β (Cebpb), C/EBP-δ (Cebpd), and CRP1 (Cebpe). Genomics. 28:1995;333-336.
-
(1995)
Genomics
, vol.28
, pp. 333-336
-
-
Jenkins, N.A.1
Gilbert, D.J.2
Cho, B.C.3
Strobel, M.C.4
Williams, S.C.5
Copeland, N.G.6
Johnson, P.F.7
-
17
-
-
0028090414
-
Genetic dissection of complex traits
-
Lander E., Schork N. J. Genetic dissection of complex traits. Science. 265:1994;2037-2048.
-
(1994)
Science
, vol.265
, pp. 2037-2048
-
-
Lander, E.1
Schork, N.J.2
-
18
-
-
0028877463
-
Genetic dissection of complex traits: Guidelines for interpreting and reporting results
-
Lander E., Kruglyak L. Genetic dissection of complex traits: Guidelines for interpreting and reporting results. Nature Genet. 11:1995;241-247.
-
(1995)
Nature Genet.
, vol.11
, pp. 241-247
-
-
Lander, E.1
Kruglyak, L.2
-
19
-
-
0015810406
-
Granule cell heterotopia in normal and nervous mutant mice of the BALB/c strain
-
Landis S. C. Granule cell heterotopia in normal and nervous mutant mice of the BALB/c strain. Brain Res. 61:1973a;175-189.
-
(1973)
Brain Res.
, vol.61
, pp. 175-189
-
-
Landis, S.C.1
-
20
-
-
0015788232
-
Ultrastructural changes in the mitochondria of cerebellar Purkinje cells of nervous mutant mice
-
Landis S. C. Ultrastructural changes in the mitochondria of cerebellar Purkinje cells of nervous mutant mice. J. Cell Biol. 57:1973b;782-797.
-
(1973)
J. Cell Biol.
, vol.57
, pp. 782-797
-
-
Landis, S.C.1
-
21
-
-
0015737752
-
Changes in neuronal mitochondrial shape in brains of nervous mutant mice
-
Landis S. C. Changes in neuronal mitochondrial shape in brains of nervous mutant mice. J. Hered. 64:1973c;193-196.
-
(1973)
J. Hered.
, vol.64
, pp. 193-196
-
-
Landis, S.C.1
-
22
-
-
0027298826
-
Retinal degeneration in the nervous mutant mouse. I. Light microscopic cytopathology and changes in the interphotoreceptor matrix
-
LaVail M. M., White M. P., Gorrin G. M., Yasumura D., Porrello K. V., Mullen R. J. Retinal degeneration in the nervous mutant mouse. I. Light microscopic cytopathology and changes in the interphotoreceptor matrix. J. Comp. Neurol. 333:1993;168-181.
-
(1993)
J. Comp. Neurol.
, vol.333
, pp. 168-181
-
-
Lavail, M.M.1
White, M.P.2
Gorrin, G.M.3
Yasumura, D.4
Porrello, K.V.5
Mullen, R.J.6
-
23
-
-
0025338725
-
Hereditary spherocytosis associated with deletion of human erythrocyte ankyrin gene on chromosome 8
-
Lux S. E., Tse W. T., Menninger J. C., John K. M., Harris P., Shalev O., Chilcote R. R., Marchesi S. L., Watkins P. C., Bennett V., McIntosh S., Collins F. S., Francke U., Ward D. C., Forget B. G. Hereditary spherocytosis associated with deletion of human erythrocyte ankyrin gene on chromosome 8. Nature. 345:1990;736-739.
-
(1990)
Nature
, vol.345
, pp. 736-739
-
-
Lux, S.E.1
Tse, W.T.2
Menninger, J.C.3
John, K.M.4
Harris, P.5
Shalev, O.6
Chilcote, R.R.7
Marchesi, S.L.8
Watkins, P.C.9
Bennett, V.10
McIntosh, S.11
Collins, F.S.12
Francke, U.13
Ward, D.C.14
Forget, B.G.15
-
24
-
-
0003928476
-
-
Mouse Genome Database, The Jackson Laboratory, Bar Harbor, ME
-
Mouse Genome Database, 1997, Mouse Genome Informatics Project, The Jackson Laboratory, Bar Harbor, ME, http://www.informatics.jax.org/.
-
(1997)
Mouse Genome Informatics Project
-
-
-
25
-
-
0016588264
-
Two new types of retinal degeneration in cerebellar mutant mice
-
Mullen R. J., LaVail M. M. Two new types of retinal degeneration in cerebellar mutant mice. Nature. 258:1975;528-530.
-
(1975)
Nature
, vol.258
, pp. 528-530
-
-
Mullen, R.J.1
Lavail, M.M.2
-
26
-
-
85030331874
-
-
Nusbaum, C. Slonim, D. Harris, K. Miller, J. Birren, B. Stein, L. Devon, K. Castle, A. Wang, V. Haldi, M. Hui, L. Rozen, S. Nahf, R. FitzHugh, W. Wu, X. Steen, R. Anderson, M. Collymore, A. Devine, R. Gray, D. Horton, L. Kouyoumjian, R. Tam, J. Wu, Y. Ye, W. Zemtseva, I. Hudson, T. Lander, E. 1997, 14
-
Nusbaum, C. Slonim, D. Harris, K. Miller, J. Birren, B. Stein, L. Devon, K. Castle, A. Wang, V. Haldi, M. Hui, L. Rozen, S. Nahf, R. FitzHugh, W. Wu, X. Steen, R. Anderson, M. Collymore, A. Devine, R. Gray, D. Horton, L. Kouyoumjian, R. Tam, J. Wu, Y. Ye, W. Zemtseva, I. Hudson, T. Lander, E. 1997, 14, http://www-genome.wi. mit.edu/cgi-bin/mouse/index.
-
-
-
-
28
-
-
0026044081
-
Purkinje cell degeneration associated with erythroid ankyrin deficiency innbnb
-
Peters L. L., Birkenmeier C. S., Bronson R. T., White R. A., Lux S. E., Otto E., Bennett V., Higgins A., Barker J. E. Purkinje cell degeneration associated with erythroid ankyrin deficiency innbnb. J. Cell. Biol. 114:1991;1233-1241.
-
(1991)
J. Cell. Biol.
, vol.114
, pp. 1233-1241
-
-
Peters, L.L.1
Birkenmeier, C.S.2
Bronson, R.T.3
White, R.A.4
Lux, S.E.5
Otto, E.6
Bennett, V.7
Higgins, A.8
Barker, J.E.9
-
29
-
-
1542501542
-
Genetic mapping of farnesyltransferase alpha (Fnta
-
Porter J. C., Messer A. Genetic mapping of farnesyltransferase alpha (Fnta. Mamm. Genome. 7:1996;622-623.
-
(1996)
Mamm. Genome
, vol.7
, pp. 622-623
-
-
Porter, J.C.1
Messer, A.2
-
32
-
-
0018422683
-
Fate of presynaptic afferents to Purkinje cells in the adult nervous mutant mouse: A model to study presynaptic stabilization
-
Sotelo C., Triller A. Fate of presynaptic afferents to Purkinje cells in the adult nervous mutant mouse: A model to study presynaptic stabilization. Brain Res. 175:1979;11-36.
-
(1979)
Brain Res.
, vol.175
, pp. 11-36
-
-
Sotelo, C.1
Triller, A.2
-
33
-
-
85030334628
-
Genomic cloning and chromosomal sublocalization of the human ankyrin gene
-
Tse W. T., Meninger J., Ward D., John K., Lux S. E., Forget B. G. Genomic cloning and chromosomal sublocalization of the human ankyrin gene. Clin. Res. 38:1990;266A.
-
(1990)
Clin. Res.
, vol.38
-
-
Tse, W.T.1
Meninger, J.2
Ward, D.3
John, K.4
Lux, S.E.5
Forget, B.G.6
-
34
-
-
0028168716
-
Mouse chromosomal localization of the cortexin (Ctxn) gene
-
Watson J. B., Coulter P. M., 2nd Xia, Y. R. and Lusis. Mouse chromosomal localization of the cortexin (Ctxn) gene. Genomics. 22:1994;251-252.
-
(1994)
Genomics
, vol.22
, pp. 251-252
-
-
Watson, J.B.1
Coulter P.M. II2
Xia, Y.R.3
Lusis4
-
35
-
-
0027298827
-
Retinal degeneration in the nervous mutant mouse. II. Electron microscopic analysis
-
White M. P., Gorrin G. M., Mullen R. J., LaVail M. M. Retinal degeneration in the nervous mutant mouse. II. Electron microscopic analysis. J. Comp. Neurol. 333:1993;182-198.
-
(1993)
J. Comp. Neurol.
, vol.333
, pp. 182-198
-
-
White, M.P.1
Gorrin, G.M.2
Mullen, R.J.3
Lavail, M.M.4
-
36
-
-
0026343271
-
The gonadotropin-releasing hormone (Gnrh) gene maps to mouse chromosome 14 and identifies a homologous region on human chromosome 8
-
Williamson P., Lang J., Boyd Y. The gonadotropin-releasing hormone (Gnrh) gene maps to mouse chromosome 14 and identifies a homologous region on human chromosome 8. Somatic Cell Mol. Genet. 17:1991;609-615.
-
(1991)
Somatic Cell Mol. Genet.
, vol.17
, pp. 609-615
-
-
Williamson, P.1
Lang, J.2
Boyd, Y.3
-
37
-
-
0022644792
-
Human luteinizing hormone-releasing hormone gene (LHRH) is located on short arm of chromosome 8 (region 8p11.2-p21)
-
Yang-Feng T. L., Seeburg P. H., Francke U. Human luteinizing hormone-releasing hormone gene (LHRH) is located on short arm of chromosome 8 (region 8p11.2-p21). Somatic Cell Mol. Genet. 12:1986;95-100.
-
(1986)
Somatic Cell Mol. Genet.
, vol.12
, pp. 95-100
-
-
Yang-Feng, T.L.1
Seeburg, P.H.2
Francke, U.3
|