-
1
-
-
0024655185
-
Chromosomal localization of zinc finger protein genes in man and mouse
-
Ashworth, A., Williams, B. P., Buchberg, A. M., Goodfellow, P. N., Solomon, E., Potter, J., and Willison, K. R. (1989). Chromosomal localization of zinc finger protein genes in man and mouse. Genomics 4: 323-327.
-
(1989)
Genomics
, vol.4
, pp. 323-327
-
-
Ashworth, A.1
Williams, B.P.2
Buchberg, A.M.3
Goodfellow, P.N.4
Solomon, E.5
Potter, J.6
Willison, K.R.7
-
2
-
-
0028803112
-
The mouse Snell's waltzer deafness gene encodes an unconventional myosin required for structural integrity of inner hair cells
-
Avraham, K. B., Hasson, T., Steel, K. P., Kingsley, D. M., Russell, L. B., Mooseker, M. S., Copeland, N. G., and Jenkins, N. A. (1995). The mouse Snell's waltzer deafness gene encodes an unconventional myosin required for structural integrity of inner hair cells. Nature Genet. 11: 369-374.
-
(1995)
Nature Genet.
, vol.11
, pp. 369-374
-
-
Avraham, K.B.1
Hasson, T.2
Steel, K.P.3
Kingsley, D.M.4
Russell, L.B.5
Mooseker, M.S.6
Copeland, N.G.7
Jenkins, N.A.8
-
3
-
-
0028231886
-
Identification and overlapping expression of multiple unconventional myosin genes in vertebrate cell types
-
Bement, W. M., Hasson, T., Wirth, J. A., Cheney, R. E., and Mooseker, M. S. (1994a). Identification and overlapping expression of multiple unconventional myosin genes in vertebrate cell types. Proc. Natl Acad. Sci. USA 91: 6549-6553.
-
(1994)
Proc. Natl Acad. Sci. USA
, vol.91
, pp. 6549-6553
-
-
Bement, W.M.1
Hasson, T.2
Wirth, J.A.3
Cheney, R.E.4
Mooseker, M.S.5
-
4
-
-
0028061489
-
Cloning and mRNA expression of human unconventional myosin-IC: A homologue of amoeboid myosins-I with a single IQ motif and an SH3 domain
-
Bement, W. M., Wirth, J. A., and Mooseker, M. A. (1994b). Cloning and mRNA expression of human unconventional myosin-IC: A homologue of amoeboid myosins-I with a single IQ motif and an SH3 domain. J. Mol. Biol. 243: 356-363.
-
(1994)
J. Mol. Biol.
, vol.243
, pp. 356-363
-
-
Bement, W.M.1
Wirth, J.A.2
Mooseker, M.A.3
-
5
-
-
0025237394
-
Hereditary motor system diseases (chronic juvenile amyotrophic lateral sclerosis). Conditions combining a bilateral pyramidal syndrome with limb and bulbar amyotrophy
-
Ben Hamida, M., Hentati, F., and Ben Hamida, C. (1990). Hereditary motor system diseases (chronic juvenile amyotrophic lateral sclerosis). Conditions combining a bilateral pyramidal syndrome with limb and bulbar amyotrophy. Brain 113: 347-363.
-
(1990)
Brain
, vol.113
, pp. 347-363
-
-
Ben Hamida, M.1
Hentati, F.2
Ben Hamida, C.3
-
6
-
-
0026545453
-
Close linkage of the olfactory marker protein gene to the mouse deafness mutation shaker-1
-
Brown, K. A., Sutcliffe, M. J., Steel, K. P., and Brown, S. D. M. (1992). Close linkage of the olfactory marker protein gene to the mouse deafness mutation shaker-1. Genomics 13: 189-193.
-
(1992)
Genomics
, vol.13
, pp. 189-193
-
-
Brown, K.A.1
Sutcliffe, M.J.2
Steel, K.P.3
Brown, S.D.M.4
-
7
-
-
0024518749
-
A comprehensive genetic map of murine chromosome 11 reveals extensive linkage conservation between mouse and human
-
Buchberg, A. M., Brownell, E., Nagata, S., Jenkins, N. A., and Copeland, N. G. (1989). A comprehensive genetic map of murine chromosome 11 reveals extensive linkage conservation between mouse and human. Genetics 122: 153-161.
-
(1989)
Genetics
, vol.122
, pp. 153-161
-
-
Buchberg, A.M.1
Brownell, E.2
Nagata, S.3
Jenkins, N.A.4
Copeland, N.G.5
-
9
-
-
0014880803
-
Family studies of early childhood deafness ascertained through the Clarke School for the Deaf
-
Chung, C. S., and Brown, K. S. (1970). Family studies of early childhood deafness ascertained through the Clarke School for the Deaf. Am. J. Hum. Genet. 22: 630-644.
-
(1970)
Am. J. Hum. Genet.
, vol.22
, pp. 630-644
-
-
Chung, C.S.1
Brown, K.S.2
-
10
-
-
0029157421
-
Distribution of the mammalian Stat gene family in mouse chromosomes
-
Copeland, N. G., Gilbert, D. J., Schindler, C., Zhong, Z., Wen, Z., Darnell, J. E., Jr., Mui, A. L.-F., Miyajima, A., Quelle, F. W., Ihle, J. N., and Jenkins, N. A. (1995). Distribution of the mammalian Stat gene family in mouse chromosomes. Genomics 29: 225-228.
-
(1995)
Genomics
, vol.29
, pp. 225-228
-
-
Copeland, N.G.1
Gilbert, D.J.2
Schindler, C.3
Zhong, Z.4
Wen, Z.5
Darnell J.E., Jr.6
Mui, A.L.-F.7
Miyajima, A.8
Quelle, F.W.9
Ihle, J.N.10
Jenkins, N.A.11
-
11
-
-
0026032128
-
Development and applications of a molecular genetic linkage map of the mouse genome
-
Copeland, N. G., and Jenkins, N. A. (1991). Development and applications of a molecular genetic linkage map of the mouse genome. Trends Genet. 7: 113-118.
-
(1991)
Trends Genet.
, vol.7
, pp. 113-118
-
-
Copeland, N.G.1
Jenkins, N.A.2
-
12
-
-
0018368963
-
Mutations affecting pigmentation in man: I. Neuroectodermal melanolysosomal disease
-
Elejalde, B. R., Holguin, J., Valencia, A., Gilbert, E. F., Molina, J., Marin, G., and Arango, L. A. (1979). Mutations affecting pigmentation in man: I. Neuroectodermal melanolysosomal disease. Am. J. Med. Genet. 3: 65-80.
-
(1979)
Am. J. Med. Genet.
, vol.3
, pp. 65-80
-
-
Elejalde, B.R.1
Holguin, J.2
Valencia, A.3
Gilbert, E.F.4
Molina, J.5
Marin, G.6
Arango, L.A.7
-
13
-
-
0028219183
-
Cloning, analysis, and chromosomal localization of myoxin (MYH12), the human homologue to the mouse dilute gene
-
Engle, L. J., and Kennet, R. H. (1994). Cloning, analysis, and chromosomal localization of myoxin (MYH12), the human homologue to the mouse dilute gene. Genomics 19: 407-416.
-
(1994)
Genomics
, vol.19
, pp. 407-416
-
-
Engle, L.J.1
Kennet, R.H.2
-
14
-
-
0028140230
-
Genotypes-phenotype correlations in hypertrophic cardiomyopathy. Insights provided by comparisons of kindreds with distinct and identical β-myosin heavy chain gene mutations
-
Fananapazir, L., and Epstein, N. C. (1994). Genotypes-phenotype correlations in hypertrophic cardiomyopathy. Insights provided by comparisons of kindreds with distinct and identical β-myosin heavy chain gene mutations. Circulation 89: 22-32.
-
(1994)
Circulation
, vol.89
, pp. 22-32
-
-
Fananapazir, L.1
Epstein, N.C.2
-
15
-
-
0028836920
-
A gene for congenital, recessive deafness DFNB3 maps to the pericentromeric region of chromosome 17
-
Friedman, T. B., Liang, Y., Weber, J. L., Hinnant, J. T., Barber, T. D., Winata, S., Arhya, I. N., and Asher, J. H. (1995). A gene for congenital, recessive deafness DFNB3 maps to the pericentromeric region of chromosome 17. Nature Genet. 9: 86-91.
-
(1995)
Nature Genet.
, vol.9
, pp. 86-91
-
-
Friedman, T.B.1
Liang, Y.2
Weber, J.L.3
Hinnant, J.T.4
Barber, T.D.5
Winata, S.6
Arhya, I.N.7
Asher, J.H.8
-
16
-
-
0028860302
-
The shaker-1 mouse deafness mutation encodes a myosin-VII motor
-
Gibson, F., Walsh, J., Mburu, P., Varela, A., Brown, K. A., Antonio, M., Beisel, K., Steel, K. P., and Brown, S. D. M. (1995). The shaker-1 mouse deafness mutation encodes a myosin-VII motor. Nature 374: 62-64.
-
(1995)
Nature
, vol.374
, pp. 62-64
-
-
Gibson, F.1
Walsh, J.2
Mburu, P.3
Varela, A.4
Brown, K.A.5
Antonio, M.6
Beisel, K.7
Steel, K.P.8
Brown, S.D.M.9
-
17
-
-
0029151750
-
The orphan nuclear receptor RORα (RORA) maps to a conserved region of homology on human chromosome 15q21-q22 and mouse chromosome 9
-
Giguère, V., Beatty, B., Squire, J., Copeland, N. G., and Jenkins, N. A. (1995). The orphan nuclear receptor RORα (RORA) maps to a conserved region of homology on human chromosome 15q21-q22 and mouse chromosome 9. Genomics 28: 595-598.
-
(1995)
Genomics
, vol.28
, pp. 595-598
-
-
Giguère, V.1
Beatty, B.2
Squire, J.3
Copeland, N.G.4
Jenkins, N.A.5
-
18
-
-
0027439124
-
Identification of a 120kd hair-bundle myosin located near stereociliary tips
-
Gillespie, P. G., Wagner, M. C., and Hudspeth, A. J. (1993). Identification of a 120kd hair-bundle myosin located near stereociliary tips. Neuron 11: 581-594.
-
(1993)
Neuron
, vol.11
, pp. 581-594
-
-
Gillespie, P.G.1
Wagner, M.C.2
Hudspeth, A.J.3
-
20
-
-
0002780546
-
Catalog of mutant genes and polymorphic loci
-
(M. F. Lyon and A. G. Searle, eds.). Oxford University Press, Oxford, England
-
Green, M. C. (1989). Catalog of mutant genes and polymorphic loci. In "Genetic Variants and Strains of the Laboratory Mouse." (M. F. Lyon and A. G. Searle, eds.), pp. 12-403. Oxford University Press, Oxford, England.
-
(1989)
Genetic Variants and Strains of the Laboratory Mouse
, pp. 12-403
-
-
Green, M.C.1
-
21
-
-
0018086099
-
A syndrome associating partial albinism and immunodeficiency
-
Griscelli, C., Durandy, A., Guy-Grand, D., Daguillard, F., Herzog, C., and Prunieras, M. (1978). A syndrome associating partial albinism and immunodeficiency. Am. J. Med. 65: 691-702.
-
(1978)
Am. J. Med.
, vol.65
, pp. 691-702
-
-
Griscelli, C.1
Durandy, A.2
Guy-Grand, D.3
Daguillard, F.4
Herzog, C.5
Prunieras, M.6
-
22
-
-
0027993176
-
Porcine myosin-VI: Characterization of a new mammalian unconventional myosin
-
Hasson, T., and Mooseker, M. S. (1994). Porcine myosin-VI: Characterization of a new mammalian unconventional myosin. J. Cell Biol. 127: 425-440.
-
(1994)
J. Cell Biol.
, vol.127
, pp. 425-440
-
-
Hasson, T.1
Mooseker, M.S.2
-
23
-
-
0028787263
-
Expression in cochlea and retina of myosin VIIa, the gene product defective in Usher syndrome type 1B
-
Hasson, T., Heintzelman, M. B., Santos-Sacchi, J., Corey, D. P., and Mooseker, M. S. (1995). Expression in cochlea and retina of myosin VIIa, the gene product defective in Usher syndrome type 1B. Proc. Natl. Acad. Sci. USA 92: 9815-9819.
-
(1995)
Proc. Natl. Acad. Sci. USA
, vol.92
, pp. 9815-9819
-
-
Hasson, T.1
Heintzelman, M.B.2
Santos-Sacchi, J.3
Corey, D.P.4
Mooseker, M.S.5
-
24
-
-
0026667606
-
High resolution mapping of mammalian genes by in situ hybridization to free chromatin
-
Heng, H. H. Q., Squire, J., and Tsui, L.-C. (1992). High resolution mapping of mammalian genes by in situ hybridization to free chromatin. Proc. Natl. Acad. Sci. USA 89: 9509-9513.
-
(1992)
Proc. Natl. Acad. Sci. USA
, vol.89
, pp. 9509-9513
-
-
Heng, H.H.Q.1
Squire, J.2
Tsui, L.-C.3
-
25
-
-
0027225483
-
Modes of DAPI banding and simultaneous in situ hybridization
-
Heng, H. H. Q., and Tsui, L.-C. (1993). Modes of DAPI banding and simultaneous in situ hybridization. Chromosoma 102: 325-332.
-
(1993)
Chromosoma
, vol.102
, pp. 325-332
-
-
Heng, H.H.Q.1
Tsui, L.-C.2
-
26
-
-
0028702948
-
FISH detection on DAPI banded chromosomes
-
(K. H. A. Choo, Eds.), Humana Press, Clifton, NJ
-
Heng, H. H. Q., and Tsui, L.-C. (1994). FISH detection on DAPI banded chromosomes. In "Methods in Molecular Biology: In situ Hybridization Protocols" (K. H. A. Choo, Eds.), Vol. 33, pp. 35-49, Humana Press, Clifton, NJ.
-
(1994)
Methods in Molecular Biology: In Situ Hybridization Protocols
, vol.33
, pp. 35-49
-
-
Heng, H.H.Q.1
Tsui, L.-C.2
-
27
-
-
0028098186
-
Genes encoding general initiation factors for RNA polymerase II transcription are dispersed in the human genome
-
Heng, H. H. Q., Xiao, H., Shi, X.-M., Greenblatt, J., and Tsui, L.-C. (1994). Genes encoding general initiation factors for RNA polymerase II transcription are dispersed in the human genome. Hum. Mol. Genet. 3: 61-64.
-
(1994)
Hum. Mol. Genet.
, vol.3
, pp. 61-64
-
-
Heng, H.H.Q.1
Xiao, H.2
Shi, X.-M.3
Greenblatt, J.4
Tsui, L.-C.5
-
28
-
-
0028334717
-
Linkage of recessive familial amyotrophic lateral sclerosis to chromosomes 2q33-q35
-
Hentati, A., Bejaoui, K., Pericak-Vance, M. A., Hentati, F., Speer, M. C., Hung, W.-Y., Figlewicz, D. A., Haines, J., Rimmler, J., Ben Hamida, C., Ben Hamida, M., Brown, R. H., Jr., and Siddique, T. (1994). Linkage of recessive familial amyotrophic lateral sclerosis to chromosomes 2q33-q35. Nature Genet. 7: 425-428.
-
(1994)
Nature Genet.
, vol.7
, pp. 425-428
-
-
Hentati, A.1
Bejaoui, K.2
Pericak-Vance, M.A.3
Hentati, F.4
Speer, M.C.5
Hung, W.-Y.6
Figlewicz, D.A.7
Haines, J.8
Rimmler, J.9
Ben Hamida, C.10
Ben Hamida, M.11
Brown R.H., Jr.12
Siddique, T.13
-
29
-
-
0023665165
-
Identification of a new type of mammalian myosin heavy chain by molecular cloning
-
Hoshimaru, M., and Nakanishi, S. (1987). Identification of a new type of mammalian myosin heavy chain by molecular cloning. J. Biol. Chem. 262: 14625-14632.
-
(1987)
J. Biol. Chem.
, vol.262
, pp. 14625-14632
-
-
Hoshimaru, M.1
Nakanishi, S.2
-
30
-
-
0027161476
-
A kindred with Griscelli disease: Spectrum of neurological involvement
-
Hurvitz, H., Gillis, R., Klaus, S., Klar, A., Gross-Kieselstein, F., and Okon, E. (1993). A kindred with Griscelli disease: Spectrum of neurological involvement. Eur. J. Pediatr. 152: 402-405.
-
(1993)
Eur. J. Pediatr.
, vol.152
, pp. 402-405
-
-
Hurvitz, H.1
Gillis, R.2
Klaus, S.3
Klar, A.4
Gross-Kieselstein, F.5
Okon, E.6
-
31
-
-
0019949189
-
Organization, distribution, and stability of endogenous ecotropic murine leukemia virus DNA sequences in chromosomes of Mus musculus
-
Jenkins, N. A., Copeland, N. G., Taylor, B. A., and Lee, B. K. (1982). Organization, distribution, and stability of endogenous ecotropic murine leukemia virus DNA sequences in chromosomes of Mus musculus. J. Virol. 43: 26-36.
-
(1982)
J. Virol.
, vol.43
, pp. 26-36
-
-
Jenkins, N.A.1
Copeland, N.G.2
Taylor, B.A.3
Lee, B.K.4
-
32
-
-
0026674407
-
A molecular genetic linkage map of mouse chromosome 18 reveals extensive linkage conservation with human chromosomes 5 and 18
-
Justice, M. J., Gilbert, D. J., Kinzler, K. W., Vogelstein, B., Buchberg, A. M., Ceci, J. D., Matsuda, Y., Chapman, V. M., Patriotis, C., Makris, A., Tsichlis, P. N., Jenkins, N. A., and Copeland, N. G. (1992). A molecular genetic linkage map of mouse chromosome 18 reveals extensive linkage conservation with human chromosomes 5 and 18. Genomics 13: 1281-1288.
-
(1992)
Genomics
, vol.13
, pp. 1281-1288
-
-
Justice, M.J.1
Gilbert, D.J.2
Kinzler, K.W.3
Vogelstein, B.4
Buchberg, A.M.5
Ceci, J.D.6
Matsuda, Y.7
Chapman, V.M.8
Patriotis, C.9
Makris, A.10
Tsichlis, P.N.11
Jenkins, N.A.12
Copeland, N.G.13
-
33
-
-
0025288966
-
A genetic linkage map of mouse chromosome 10: Localization of eighteen molecular markers using a single interspecific backcross
-
Justice, M. J., Siracusa, L. D., Gilbert, D. J., Heisterkamp, N., Groffen, J., Chada, K., Silan, C. M., Copeland, N. G., and Jenkins, N. A. (1990). A genetic linkage map of mouse chromosome 10: Localization of eighteen molecular markers using a single interspecific backcross. Genetics 125: 855-866.
-
(1990)
Genetics
, vol.125
, pp. 855-866
-
-
Justice, M.J.1
Siracusa, L.D.2
Gilbert, D.J.3
Heisterkamp, N.4
Groffen, J.5
Chada, K.6
Silan, C.M.7
Copeland, N.G.8
Jenkins, N.A.9
-
34
-
-
0024461491
-
A molecular genetic linkage map of mouse chromosome 9 with regional localizations for the Gsta, T3g, Ets-1 and Ldlr loci
-
Kingsley, D. M., Jenkins, N. A., and Copeland, N. G. (1989). A molecular genetic linkage map of mouse chromosome 9 with regional localizations for the Gsta, T3g, Ets-1 and Ldlr loci. Genetics 123: 165-172.
-
(1989)
Genetics
, vol.123
, pp. 165-172
-
-
Kingsley, D.M.1
Jenkins, N.A.2
Copeland, N.G.3
-
35
-
-
0028032845
-
Partial albinism with immunodeficiency (Griscelli syndrome)
-
Klein, C., Philippe, N., Le Deist, F., Fraitag, S., Prost, C., Durandy, A., Fischer, A., and Griscelli, C. (1994). Partial albinism with immunodeficiency (Griscelli syndrome). J. Pediatr. 125: 886-895.
-
(1994)
J. Pediatr.
, vol.125
, pp. 886-895
-
-
Klein, C.1
Philippe, N.2
Le Deist, F.3
Fraitag, S.4
Prost, C.5
Durandy, A.6
Fischer, A.7
Griscelli, C.8
-
36
-
-
0027278759
-
A myosin-like protein from a higher plant
-
Knight, A. E., and Kendrick-Jones, J. (1993). A myosin-like protein from a higher plant. J. Mol. Biol. 231: 148-154.
-
(1993)
J. Mol. Biol.
, vol.231
, pp. 148-154
-
-
Knight, A.E.1
Kendrick-Jones, J.2
-
37
-
-
0018816959
-
Structure and evolution of calcium-modulated proteins
-
Kretsinger, R. H. (1980). Structure and evolution of calcium-modulated proteins. CRC Crit. Rev. Biochem. 8: 119-174.
-
(1980)
CRC Crit. Rev. Biochem.
, vol.8
, pp. 119-174
-
-
Kretsinger, R.H.1
-
38
-
-
0026939706
-
Oligonucleotide probes for the analysis of specific repetitive DNA sequences by fluorescence in situ hybridization
-
Matera, G., and Ward, D. C. (1992). Oligonucleotide probes for the analysis of specific repetitive DNA sequences by fluorescence in situ hybridization. Hum. Mol. Genet. 1: 535-539.
-
(1992)
Hum. Mol. Genet.
, vol.1
, pp. 535-539
-
-
Matera, G.1
Ward, D.C.2
-
39
-
-
0025967015
-
Novel myosin heavy chain encoded by murine dilute coat colour locus
-
Mercer, J. A., Seperack, P. K., Strobel, M. C., Copeland, N. G., and Jenkins, N. A. (1991). Novel myosin heavy chain encoded by murine dilute coat colour locus. Nature 349: 709-713.
-
(1991)
Nature
, vol.349
, pp. 709-713
-
-
Mercer, J.A.1
Seperack, P.K.2
Strobel, M.C.3
Copeland, N.G.4
Jenkins, N.A.5
-
40
-
-
0028836490
-
Cloning and regional assignment of the human myosin heavy chain 12 (MYH12) gene to chromosomal band 15q21
-
Moore, K. J., Testa, J. R., Francke, U., Milatovich, A., Copeland, N. G., and Jenkins, N. A. (1995). Cloning and regional assignment of the human myosin heavy chain 12 (MYH12) gene to chromosomal band 15q21. Cytogenet. Cell Genet. 69: 53-58.
-
(1995)
Cytogenet. Cell Genet.
, vol.69
, pp. 53-58
-
-
Moore, K.J.1
Testa, J.R.2
Francke, U.3
Milatovich, A.4
Copeland, N.G.5
Jenkins, N.A.6
-
42
-
-
0026410464
-
Genetic epidemiology of hearing impairment
-
Morton, N. E. (1991). Genetic epidemiology of hearing impairment. Ann. NY Acad. Sci. 630: 16-31.
-
(1991)
Ann. NY Acad. Sci.
, vol.630
, pp. 16-31
-
-
Morton, N.E.1
-
43
-
-
0029935463
-
Mouse chromosomal location of three epithelial sodium channel subunit genes and an apical sodium-chloride cotransporter gene
-
Pathak, B. G., Shaughnessy, J. D., Jr., Meneton, P., Greeb, J., Shull, G. E., Jenkins, N. A., and Copeland, N. G. (1996a). Mouse chromosomal location of three epithelial sodium channel subunit genes and an apical sodium-chloride cotransporter gene. Genomics 33: 124-127.
-
(1996)
Genomics
, vol.33
, pp. 124-127
-
-
Pathak, B.G.1
Shaughnessy J.D., Jr.2
Meneton, P.3
Greeb, J.4
Shull, G.E.5
Jenkins, N.A.6
Copeland, N.G.7
-
44
-
-
0030065288
-
Mouse chromosomal location of four Na/H exchanger isoform genes
-
Pathak, B. G., Shull, G. E., Jenkins, N. A., and Copeland, N. G. (1996b). Mouse chromosomal location of four Na/H exchanger isoform genes. Genomics 31: 261-263.
-
(1996)
Genomics
, vol.31
, pp. 261-263
-
-
Pathak, B.G.1
Shull, G.E.2
Jenkins, N.A.3
Copeland, N.G.4
-
45
-
-
0030200746
-
Identification and chromosomal localization of Atm, the mouse homolog of the ataxiatelangiectasia gene
-
Pecker, I., Avraham, K. B., Gilbert, D. J., Savitsky, K., Rotman, G., Harnik, R., Fukao, T., Schröck, E., Hirotsune, S., Tagle, D. A., Collins, F. S., Wynshaw-Boris, A., Ried, T., Copeland, N. G., Jenkins, N. A., Shiloh, Y., and Ziv, Y. (1996). Identification and chromosomal localization of Atm, the mouse homolog of the ataxiatelangiectasia gene. Genomics 35: 39-45.
-
(1996)
Genomics
, vol.35
, pp. 39-45
-
-
Pecker, I.1
Avraham, K.B.2
Gilbert, D.J.3
Savitsky, K.4
Rotman, G.5
Harnik, R.6
Fukao, T.7
Schröck, E.8
Hirotsune, S.9
Tagle, D.A.10
Collins, F.S.11
Wynshaw-Boris, A.12
Ried, T.13
Copeland, N.G.14
Jenkins, N.A.15
Shiloh, Y.16
Ziv, Y.17
-
46
-
-
4243558634
-
MYR6, an unconventional myosin closely related to Dilute
-
Abstract
-
Provance, D. W., Zhao, L. P., Bahler, M., Reinhard, J., Koslovsky, J. S., and Mercer, J. A. (1994). MYR6, an unconventional myosin closely related to Dilute. Mol. Biol. Cell Suppl. 5: 276a. [Abstract]
-
(1994)
Mol. Biol. Cell Suppl.
, vol.5
-
-
Provance, D.W.1
Zhao, L.P.2
Bahler, M.3
Reinhard, J.4
Koslovsky, J.S.5
Mercer, J.A.6
-
47
-
-
0026604579
-
Simultaneous visualization of seven different DNA probes by in situ hybridization using combinatorial fluorescence and digital imaging microscopy
-
Reid, T., Baldini, A., Rand, P. C., and Ward, D. C. (1992). Simultaneous visualization of seven different DNA probes by in situ hybridization using combinatorial fluorescence and digital imaging microscopy. Proc. Natl. Acad. Sci. USA 89: 1388-1392.
-
(1992)
Proc. Natl. Acad. Sci. USA
, vol.89
, pp. 1388-1392
-
-
Reid, T.1
Baldini, A.2
Rand, P.C.3
Ward, D.C.4
-
48
-
-
0027499951
-
Identification, characterization and cloning of myr1, a mammalian myosin-I
-
Rüppert, C., Kroschewski, R., and Bähler, M. (1993). Identification, characterization and cloning of myr1, a mammalian myosin-I. J. Cell Biol. 120: 1393-1403.
-
(1993)
J. Cell Biol.
, vol.120
, pp. 1393-1403
-
-
Rüppert, C.1
Kroschewski, R.2
Bähler, M.3
-
49
-
-
49049127142
-
The pattern of sensorineural degeneration in the cochlea of the deaf shaker-1 mouse: Ultrastructural observations
-
Schnerson, A., Lenoir, M., Van de Water, T. R., and Pujol, R. (1983). The pattern of sensorineural degeneration in the cochlea of the deaf shaker-1 mouse: Ultrastructural observations. Dev. Brain Res. 9: 305-315.
-
(1983)
Dev. Brain Res.
, vol.9
, pp. 305-315
-
-
Schnerson, A.1
Lenoir, M.2
Van De Water, T.R.3
Pujol, R.4
-
50
-
-
0027479904
-
Mammalian myosin Iα, Iβ, and Iγ: New widely expressed genes of the myosin I family
-
Sherr, E. H., Joyce, M. P., and Greene, L. A. (1993). Mammalian myosin Iα, Iβ, and Iγ: New widely expressed genes of the myosin I family. J. Cell Biol. 120: 1405-1416.
-
(1993)
J. Cell Biol.
, vol.120
, pp. 1405-1416
-
-
Sherr, E.H.1
Joyce, M.P.2
Greene, L.A.3
-
51
-
-
0001850991
-
Dilute and Leaden, the p-locus, Ruby-Eye, and Ruby-Eye-2
-
(W. K. Silvers, Ed.), Springer Verlag, New York
-
Silvers, W. K. (1979). Dilute and Leaden, the p-locus, Ruby-Eye, and Ruby-Eye-2. In "Coat Colors of Mice: A Model for Mammalian Gene Action and Interaction" (W. K. Silvers, Ed.), pp. 83-89, 104-107, Springer Verlag, New York.
-
(1979)
Coat Colors of Mice: A Model for Mammalian Gene Action and Interaction
, pp. 83-89
-
-
Silvers, W.K.1
-
52
-
-
0025939498
-
Chromosomal location of the octamer transcription factors, Otf-1, Otf-2, and Otf-3, defines multiple Otf-3-related sequences dispersed in the mouse genome
-
Siracusa, L. D., Rosner, M. H., Vigano, M. A., Gilbert, D. J., Staudt, L. M., Copeland, N. G., and Jenkins, N. A. (1991). Chromosomal location of the octamer transcription factors, Otf-1, Otf-2, and Otf-3, defines multiple Otf-3-related sequences dispersed in the mouse genome. Genomics 10: 313-326.
-
(1991)
Genomics
, vol.10
, pp. 313-326
-
-
Siracusa, L.D.1
Rosner, M.H.2
Vigano, M.A.3
Gilbert, D.J.4
Staudt, L.M.5
Copeland, N.G.6
Jenkins, N.A.7
-
53
-
-
0011731015
-
The initial characterization of human brush border myosin-I
-
Abstract
-
Skowron, J. F., Bement, W. B., and Mooseker, M. S. (1994). The initial characterization of human brush border myosin-I. Mol. Biol. Cell Suppl. 5: 275a [Abstract].
-
(1994)
Mol. Biol. Cell Suppl.
, vol.5
-
-
Skowron, J.F.1
Bement, W.B.2
Mooseker, M.S.3
-
54
-
-
0028306478
-
Mapping of the syndecan genes in the mouse: Linkage with members of the Myc gene family
-
Spring, J., Goldberger, O. A., Jenkins, N. A., Gilbert, D. J., Copeland, N. G., and Bernfield, M. (1994). Mapping of the syndecan genes in the mouse: Linkage with members of the Myc gene family. Genomics 21: 597-601.
-
(1994)
Genomics
, vol.21
, pp. 597-601
-
-
Spring, J.1
Goldberger, O.A.2
Jenkins, N.A.3
Gilbert, D.J.4
Copeland, N.G.5
Bernfield, M.6
-
55
-
-
0029125948
-
Murine chromosomal location of five bHLH-Zip transcription factor genes
-
Steingrímsson, E., Sawadogo, M., Gilbert, D. J., Zervos, A. S., Brent, R., Blanar, M. A., Fisher, D. E., Copeland, N. G., and Jenkins, N. A. (1995). Murine chromosomal location of five bHLH-Zip transcription factor genes. Genomics 28: 179-183.
-
(1995)
Genomics
, vol.28
, pp. 179-183
-
-
Steingrímsson, E.1
Sawadogo, M.2
Gilbert, D.J.3
Zervos, A.S.4
Brent, R.5
Blanar, M.A.6
Fisher, D.E.7
Copeland, N.G.8
Jenkins, N.A.9
-
56
-
-
0028019596
-
Structural organization of the mouse glycophorin A gene
-
Terajima, M., Matsui, Y., Copeland, N. G., Gilbert, D. J., Jenkins, N. A., and Obinata, M. (1994). Structural organization of the mouse glycophorin A gene. J. Biochem. 116: 1105-1110.
-
(1994)
J. Biochem.
, vol.116
, pp. 1105-1110
-
-
Terajima, M.1
Matsui, Y.2
Copeland, N.G.3
Gilbert, D.J.4
Jenkins, N.A.5
Obinata, M.6
-
57
-
-
0028926834
-
Mammalian antioxidant protein complements alkylhydroperoxide reductase (ahpC) mutation in Escherichia coli
-
Tsuji, K., Copeland, N. G., Jenkins, N. A., and Obinata, M. (1995). Mammalian antioxidant protein complements alkylhydroperoxide reductase (ahpC) mutation in Escherichia coli. Biochem. J. 307: 377-381.
-
(1995)
Biochem. J.
, vol.307
, pp. 377-381
-
-
Tsuji, K.1
Copeland, N.G.2
Jenkins, N.A.3
Obinata, M.4
-
58
-
-
0030046902
-
Contractile protein mutations and heart disease
-
Vikstrom, K. L., and Leinwand, L. A. (1996). Contractile protein mutations and heart disease. Curr. Opin. Cell Biol. 8: 97-105.
-
(1996)
Curr. Opin. Cell Biol.
, vol.8
, pp. 97-105
-
-
Vikstrom, K.L.1
Leinwand, L.A.2
-
59
-
-
0030068938
-
A large family of putative transmembrane receptors homologous to the product of the Drosophila tissue polarity gene frizzled
-
Wang, Y., Macke, J. P., Abella, B., Andreasson, K., Worley, P., Gilbert, D. J., Copeland, N. G., Jenkins, N. A., and Nathans, J. (1996). A large family of putative transmembrane receptors homologous to the product of the Drosophila tissue polarity gene frizzled. J. Biol. Chem. 271: 4468-4476.
-
(1996)
J. Biol. Chem.
, vol.271
, pp. 4468-4476
-
-
Wang, Y.1
Macke, J.P.2
Abella, B.3
Andreasson, K.4
Worley, P.5
Gilbert, D.J.6
Copeland, N.G.7
Jenkins, N.A.8
Nathans, J.9
-
60
-
-
0023484279
-
Myosin structure and function in cell motility
-
Warrick, H. M., and Spudich, J. A. (1987). Myosin structure and function in cell motility. Annu. Rev. Cell Biol. 3: 379-421.
-
(1987)
Annu. Rev. Cell Biol.
, vol.3
, pp. 379-421
-
-
Warrick, H.M.1
Spudich, J.A.2
-
61
-
-
0028815440
-
Defective myosin-VIIA gene responsible for Usher syndrome type 1B
-
Weil, D., Blanchard, S., Kaplan, J., Guilford, P., Gibson, F., Walsh, J., Mburu, P., Valera, A., Levilliers, J., Weston, M. D., Kelley, P. M., Levi-Acobas, F., Larget-Piet, D., Munnich, A., Steel, K. P., Kimberling, W. J., Brown, S. D. M., and Petit, C. (1995). Defective myosin-VIIA gene responsible for Usher syndrome type 1B. Nature 374: 60-61.
-
(1995)
Nature
, vol.374
, pp. 60-61
-
-
Weil, D.1
Blanchard, S.2
Kaplan, J.3
Guilford, P.4
Gibson, F.5
Walsh, J.6
Mburu, P.7
Valera, A.8
Levilliers, J.9
Weston, M.D.10
Kelley, P.M.11
Levi-Acobas, F.12
Larget-Piet, D.13
Munnich, A.14
Steel, K.P.15
Kimberling, W.J.16
Brown, S.D.M.17
Petit, C.18
-
62
-
-
0029991890
-
Human myosin-IXB, an unconventional myosin with a chimerin-like rho/rac GTPase-activating protein domain in its tail
-
Wirth, J. A., Jensen, K. A., Post, P. L., Bement, W. M., and Mooseker, M. S. (1996). Human myosin-IXB, an unconventional myosin with a chimerin-like rho/rac GTPase-activating protein domain in its tail. J. Cell Sci. 109: 653-661.
-
(1996)
J. Cell Sci.
, vol.109
, pp. 653-661
-
-
Wirth, J.A.1
Jensen, K.A.2
Post, P.L.3
Bement, W.M.4
Mooseker, M.S.5
-
63
-
-
0029077317
-
A novel chemokine, macrophage inflammatory protein-related protein-2, inhibits colony formation of bone marrow myeloid progenitors
-
Youn, B.-S., Jang, I.-K., Broxmeyer, H. E., Cooper, S., Jenkins, N. A., Gilbert, D. J., Copeland, N. G., Elick, T. E., Fraser, M. J., Jr., and Kwon, B. S. (1995). A novel chemokine, macrophage inflammatory protein-related protein-2, inhibits colony formation of bone marrow myeloid progenitors. J. Immunol. 155: 2661-2667.
-
(1995)
J. Immunol.
, vol.155
, pp. 2661-2667
-
-
Youn, B.-S.1
Jang, I.-K.2
Broxmeyer, H.E.3
Cooper, S.4
Jenkins, N.A.5
Gilbert, D.J.6
Copeland, N.G.7
Elick, T.E.8
Fraser M.J., Jr.9
Kwon, B.S.10
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