-
1
-
-
15844397403
-
Identification of the homologous beige and Chediak-Higashi syndrome genes
-
BARBOSA, M. D. F. S., Q. A. NGUYEN, V. T. TCHERNEV, J. A. ASHLEY, J. C. DETTER et al., 1996 Identification of the homologous beige and Chediak-Higashi syndrome genes. Nature 382: 262-265.
-
(1996)
Nature
, vol.382
, pp. 262-265
-
-
Barbosa, M.D.F.S.1
Nguyen, Q.A.2
Tchernev, V.T.3
Ashley, J.A.4
Detter, J.C.5
-
2
-
-
0031028759
-
Mouse models of human disease. Part II: Recent progress and future directions
-
BEDELL, M. A., D. A. LARGAESPADA, N. A. JENKINS and N. G. COPELAND, 1997 Mouse models of human disease. Part II: Recent progress and future directions. Genes Dev. 11: 11-43.
-
(1997)
Genes Dev.
, vol.11
, pp. 11-43
-
-
Bedell, M.A.1
Largaespada, D.A.2
Jenkins, N.A.3
Copeland, N.G.4
-
3
-
-
0027420994
-
Brain myosin-V is a two-headed unconventional myosin with motor activity
-
CHENEY, R. E., M. K. O'SHEA, J. E. HEUSER, M. V. COELHO, J. S. WOLENSKI et al., 1993 Brain myosin-V is a two-headed unconventional myosin with motor activity. Cell 75: 13-23.
-
(1993)
Cell
, vol.75
, pp. 13-23
-
-
Cheney, R.E.1
O'Shea, M.K.2
Heuser, J.E.3
Coelho, M.V.4
Wolenski, J.S.5
-
4
-
-
0026779374
-
In vitro splicing of cardiac troponin T precursors. Exon mutations disrupt splicing of the upstream intron
-
COOPER, T. A., 1992 In vitro splicing of cardiac troponin T precursors. Exon mutations disrupt splicing of the upstream intron. J. Biol. Chem. 267: 5330-5338.
-
(1992)
J. Biol. Chem.
, vol.267
, pp. 5330-5338
-
-
Cooper, T.A.1
-
5
-
-
0024449348
-
Nucleotide substitutions within the cardiac troponin T alternative exon disrupt pre-mRNA alternative splicing
-
COOPER, T. A., and C. P. ORDAHL, 1989 Nucleotide substitutions within the cardiac troponin T alternative exon disrupt pre-mRNA alternative splicing. Nucleic Acids Res. 17: 7905-7921.
-
(1989)
Nucleic Acids Res.
, vol.17
, pp. 7905-7921
-
-
Cooper, T.A.1
Ordahl, C.P.2
-
6
-
-
0029876377
-
Endoplasmic reticulum is missing in dendritic spines of purkinje cells of the ataxic mutant rat
-
DEKKER-OHNO, K., S. HAYASAKA, Y. TAKAGISHI, S. ODA, N. WAKASUGI et al., 1996 Endoplasmic reticulum is missing in dendritic spines of purkinje cells of the ataxic mutant rat. Brain Res. 714: 226-230.
-
(1996)
Brain Res.
, vol.714
, pp. 226-230
-
-
Dekker-Ohno, K.1
Hayasaka, S.2
Takagishi, Y.3
Oda, S.4
Wakasugi, N.5
-
7
-
-
15144342014
-
Neuro-ectodermal melanolysosomal disease: An autosomal recessive pigment mutation in man
-
ELEJALDE, B. R., A. VALENCIA, E. F. GILBERT, G. MARIN, J. MOLINA et al., 1977 Neuro-ectodermal melanolysosomal disease: an autosomal recessive pigment mutation in man. Am. J. Med. Genet. 3: 65-80.
-
(1977)
Am. J. Med. Genet.
, vol.3
, pp. 65-80
-
-
Elejalde, B.R.1
Valencia, A.2
Gilbert, E.F.3
Marin, G.4
Molina, J.5
-
8
-
-
0028219183
-
Cloning, analysis, and chromosomal localization of myoxin (MYH12), the human homologue to the mouse dilute gene
-
ENGLE, L. J., and R. H. KENNETT, 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
Kennett, R.H.2
-
9
-
-
0027068050
-
Primary structure and cellular localization of chicken brain myosin-V (p190), an unconventional myosin with calmodulin light chains
-
ESPREAFICO, E. M., R. E. CHENEY, M. MATTEOLI, A. A. NASCIMENTO, P. V. DE CAMILLI et al., 1992 Primary structure and cellular localization of chicken brain myosin-V (p190), an unconventional myosin with calmodulin light chains. J. Cell. Biol. 119: 1541-1557.
-
(1992)
J. Cell. Biol.
, vol.119
, pp. 1541-1557
-
-
Espreafico, E.M.1
Cheney, R.E.2
Matteoli, M.3
Nascimento, A.A.4
De Camilli, P.V.5
-
10
-
-
0026065612
-
The role of branchpoint and 3′-exon sequences in the control of balanced splicing of avian retrovirus RNA
-
Fu, X. D., R. A. KATZ, A. M. SKALKA and T. MANIATIS, 1991 The role of branchpoint and 3′-exon sequences in the control of balanced splicing of avian retrovirus RNA. Genes Dev 5: 211-220.
-
(1991)
Genes Dev
, vol.5
, pp. 211-220
-
-
Fu, X.D.1
Katz, R.A.2
Skalka, A.M.3
Maniatis, T.4
-
11
-
-
0028860302
-
A type VII myosin encoded by the mouse deafness gene shaker-1
-
GIBSON, F., J. WALSH, P. MBURU, A. VARELA, K. A. BROWN et al., 1995 A type VII myosin encoded by the mouse deafness gene shaker-1. 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
-
12
-
-
0028216280
-
Identification of MYO4, a second class V myosin gene in yeast
-
HAARER, B. K., A. PETZOLD, S. H. LILLIE and S. S. BROWN, 1994 Identification of MYO4, a second class V myosin gene in yeast. J. Cell Sci. 107: 1055-1064.
-
(1994)
J. Cell Sci.
, vol.107
, pp. 1055-1064
-
-
Haarer, B.K.1
Petzold, A.2
Lillie, S.H.3
Brown, S.S.4
-
13
-
-
0025844789
-
Kinesin-related gene unc-104 is required for axonal transport of synaptic vesicles in C. elegans
-
HALL, D. H., and E. M. HEDGECOCK, 1991 Kinesin-related gene unc-104 is required for axonal transport of synaptic vesicles in C. elegans. Cell 65: 837-847.
-
(1991)
Cell
, vol.65
, pp. 837-847
-
-
Hall, D.H.1
Hedgecock, E.M.2
-
14
-
-
0024501943
-
Alternative processing of bovine growth hormone mRNA is influenced by downstream exon sequences
-
HAMPSON, R. K., L. LA FOLLETTE and F. M. ROTTMAN, 1989 Alternative processing of bovine growth hormone mRNA is influenced by downstream exon sequences. Mol. Cell. Biol. 9: 1604-1610.
-
(1989)
Mol. Cell. Biol.
, vol.9
, pp. 1604-1610
-
-
Hampson, R.K.1
Follette, L.L.A.2
Rottman, F.M.3
-
15
-
-
0025727671
-
Griscelli disease with cerebral involvement
-
HARALDSSON, A., C. M. WEEMAES, J. A. BAKKEREN and R. HAPPLE, 1991 Griscelli disease with cerebral involvement. Eur. J. Pediatr. 150: 419-422.
-
(1991)
Eur. J. Pediatr.
, vol.150
, pp. 419-422
-
-
Haraldsson, A.1
Weemaes, C.M.2
Bakkeren, J.A.3
Happle, R.4
-
16
-
-
0029895005
-
Vertebrate unconventional myosins
-
HASSON, T., and M. S. MOOSEKER, 1996 Vertebrate unconventional myosins. J. Biol. Chem. 271: 16431-16434.
-
(1996)
J. Biol. Chem.
, vol.271
, pp. 16431-16434
-
-
Hasson, T.1
Mooseker, M.S.2
-
17
-
-
0030587438
-
Mapping of unconventional myosins in mouse and human
-
HASSON, T., J. F. SKOWRON, D. J. GILBERT, K. B. AVRAHAM, W. L. PERRY et al., 1996 Mapping of unconventional myosins in mouse and human. Genomics 36: 431-439.
-
(1996)
Genomics
, vol.36
, pp. 431-439
-
-
Hasson, T.1
Skowron, J.F.2
Gilbert, D.J.3
Avraham, K.B.4
Perry, W.L.5
-
18
-
-
0024221141
-
Alternative splicing of tropomyosin pre-mRNAs in vitro and in vivo
-
HELFMAN, D. M., W. M. RICCI and L. A. FINN, 1988 Alternative splicing of tropomyosin pre-mRNAs in vitro and in vivo. Genes Dev. 2: 1627-1638.
-
(1988)
Genes Dev.
, vol.2
, pp. 1627-1638
-
-
Helfman, D.M.1
Ricci, W.M.2
Finn, L.A.3
-
19
-
-
0031893562
-
Molecular genetic dissection of mouse unconventional myosin-VA: Head region mutations
-
HUANG, J.-D., M. JAMIE, T. V. COPE, V. MERMALL, M. C. STROBEL et al., 1998 Molecular genetic dissection of mouse unconventional myosin-VA: head region mutations. Genetics 148: 1951-1961.
-
(1998)
Genetics
, vol.148
, pp. 1951-1961
-
-
Huang, J.-D.1
Jamie, M.2
Cope, T.V.3
Mermall, V.4
Strobel, M.C.5
-
20
-
-
0027161476
-
A kindred with Griscelli disease: Spectrum of neurological involvement
-
HURVITZ, H., R. GILLIS, S KLAUS, A. KLAR, F. GROSS-KIESELSTEIN et al, 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
-
21
-
-
0029981258
-
Mother cell-specific HO expression in budding yeast depends on the unconventional myosin myo4p and other cytoplasmic proteins
-
JANSEN, R. P., C. DOWZER, C. MICHAELIS, M. GALOVA and K. NASMYTH, 1996 Mother cell-specific HO expression in budding yeast depends on the unconventional myosin myo4p and other cytoplasmic proteins. Cell 84: 687-697.
-
(1996)
Cell
, vol.84
, pp. 687-697
-
-
Jansen, R.P.1
Dowzer, C.2
Michaelis, C.3
Galova, M.4
Nasmyth, K.5
-
22
-
-
0025801365
-
The Saccharomyces cerevisiae MYO2 gene encodes an essential myosin for vectorial transport of vesicles
-
JOHNSTON, G. C., J. A. PRENDERGAST and R. A. SINGER, 1991 The Saccharomyces cerevisiae MYO2 gene encodes an essential myosin for vectorial transport of vesicles. J. Cell Biol. 113, 539-551.
-
(1991)
J. Cell Biol.
, vol.113
, pp. 539-551
-
-
Johnston, G.C.1
Prendergast, J.A.2
Singer, R.A.3
-
23
-
-
0025156779
-
Control of retroviral RNA splicing through maintenance of suboptimal processing signals
-
KATZ, R. A., and A. M. SKALKA, 1990 Control of retroviral RNA splicing through maintenance of suboptimal processing signals. Mol. Cell. Biol. 10: 696-704.
-
(1990)
Mol. Cell. Biol.
, vol.10
, pp. 696-704
-
-
Katz, R.A.1
Skalka, A.M.2
-
24
-
-
0026794668
-
The mutational spectrum of single base-pair substitutions in mRNA splice Junetions of human genes: Causes and consequences
-
KRAWCZAK, M., J. REISS and D. N. COOPER, 1992 The mutational spectrum of single base-pair substitutions in mRNA splice Junetions of human genes: causes and consequences. Hum. Genet. 90: 41-54.
-
(1992)
Hum. Genet.
, vol.90
, pp. 41-54
-
-
Krawczak, M.1
Reiss, J.2
Cooper, D.N.3
-
25
-
-
0346210139
-
Myosin VIIa gene - Heterogeneity of the mutations responsible for usher syndrome type Ib
-
LEVY, G., F. LEVIACOBAS, S. BLANCHARD, S. GERBER, D. LARGETPIET et al., 1997 Myosin VIIa gene - heterogeneity of the mutations responsible for usher syndrome type Ib. Human Molecular Genetics 6: 111-116.
-
(1997)
Human Molecular Genetics
, vol.6
, pp. 111-116
-
-
Levy, G.1
Leviacobas, F.2
Blanchard, S.3
Gerber, S.4
Largetpiet, D.5
-
26
-
-
0028352176
-
Immunofluorescence localization of the unconventional myosin, Myo2p, and the putative kinesin-related protein, Smy1p, to the same regions of polarized growth in Saccharomyces cerevisiae
-
LILLIE, S. H., and S. S. BROWN, 1994 Immunofluorescence localization of the unconventional myosin, Myo2p, and the putative kinesin-related protein, Smy1p, to the same regions of polarized growth in Saccharomyces cerevisiae. J. Cell Biol. 125: 825-842.
-
(1994)
J. Cell Biol.
, vol.125
, pp. 825-842
-
-
Lillie, S.H.1
Brown, S.S.2
-
27
-
-
0030960855
-
Mutations in the myosin VIIA gene cause non-syndromic recessive deafness
-
LIU, X. Z., J. WALSH, P. MBURU, J. KENDRICK-JONES, M. J. T. V. COPE et al., 1997 Mutations in the myosin VIIA gene cause non-syndromic recessive deafness. Nature Genet. 16: 188-190.
-
(1997)
Nature Genet.
, vol.16
, pp. 188-190
-
-
Liu, X.Z.1
Walsh, J.2
Mburu, P.3
Kendrick-Jones, J.4
Cope, M.J.T.V.5
-
28
-
-
0023652077
-
A role for exon sequences in alternative splicing of the human fibronectin gene
-
MARDON, H. J., G. SEBASTIO and F. E. BARALLE, 1987 A role for exon sequences in alternative splicing of the human fibronectin gene. Nucleic Acids Res. 15: 7725-7733.
-
(1987)
Nucleic Acids Res.
, vol.15
, pp. 7725-7733
-
-
Mardon, H.J.1
Sebastio, G.2
Baralle, F.E.3
-
29
-
-
0031024091
-
Spectrum of Bmp5 mutations from germline mutagenesis experiments in mice
-
MARKER, P. C., K. J. SEUNG, A. E. BLAND, L. B. RUSSELL and D. M. KINGSLEY, 1997 Spectrum of Bmp5 mutations from germline mutagenesis experiments in mice. Genetics 145: 435-443.
-
(1997)
Genetics
, vol.145
, pp. 435-443
-
-
Marker, P.C.1
Seung, K.J.2
Bland, A.E.3
Russell, L.B.4
Kingsley, D.M.5
-
30
-
-
0025967015
-
Novel myosin heavy chain encoded by murine dilute coat colour locus
-
MERCER, J. A., P. K. SEPERACK, M. C. STROBEL, N. G. COPELAND and N. A. JENKINS, 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
-
31
-
-
0028987993
-
Canoe encodes a novel protein containing a GLGF/ DHR motif and functions with Notch and scabrous in common developmental pathways in Drosophila
-
MIYAMOTO, H., I. NIHONMATSU, S. KONDO, R. UEDA, S. TOGASHI et al., 1995 Canoe encodes a novel protein containing a GLGF/ DHR motif and functions with Notch and scabrous in common developmental pathways in Drosophila. Genes Dev. 9: 612-625.
-
(1995)
Genes Dev.
, vol.9
, pp. 612-625
-
-
Miyamoto, H.1
Nihonmatsu, I.2
Kondo, S.3
Ueda, R.4
Togashi, S.5
-
32
-
-
0028836490
-
Cloning and regional assignment of the human myosin heavy chain 12 (MYH12) gene to chromosome band 15q21
-
MOORE, K. J., J. R. TESTA, U. FRANCKE, A. MILATOVICH, N. G. COPELAND et al., 1995 Cloning and regional assignment of the human myosin heavy chain 12 (MYH12) gene to chromosome 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
-
34
-
-
0030293556
-
Identification and mutation analysis of the complete gene for Chediak-Higashi syndrome
-
NAGLE, D. L., M. A. KARIM, E. A. WOOLF, L. HOLMGREN, P. BORK et al., 1996 Identification and mutation analysis of the complete gene for Chediak-Higashi syndrome. Nature Genet. 14: 307-311.
-
(1996)
Nature Genet.
, vol.14
, pp. 307-311
-
-
Nagle, D.L.1
Karim, M.A.2
Woolf, E.A.3
Holmgren, L.4
Bork, P.5
-
35
-
-
0030914460
-
Griscelli disease maps to chromosome 15q21 and is associated with mutations in the Myosin-Va gene
-
PASTURAL, E., F. J. BARRAT, R. DUFOURCQ-LAGELOUSE, S. CERTAIN, O. SANAL et al., 1997 Griscelli disease maps to chromosome 15q21 and is associated with mutations in the Myosin-Va gene. Nature Genet. 16: 289-292.
-
(1997)
Nature Genet.
, vol.16
, pp. 289-292
-
-
Pastural, E.1
Barrat, F.J.2
Dufourcq-Lagelouse, R.3
Certain, S.4
Sanal, O.5
-
36
-
-
0025755453
-
Human pre-mRNA splicing signals
-
PENOTTI, F. E., 1991 Human pre-mRNA splicing signals. J. Theor. Biol. 150: 385-420.
-
(1991)
J. Theor. Biol.
, vol.150
, pp. 385-420
-
-
Penotti, F.E.1
-
37
-
-
0029035839
-
AF-6/cno: Neither a kinesin nor a myosin, but a bit of both
-
PONTING, C. P., 1995 AF-6/cno: neither a kinesin nor a myosin, but a bit of both. Trends Biochem. Sci. 20: 265-266.
-
(1995)
Trends Biochem. Sci.
, vol.20
, pp. 265-266
-
-
Ponting, C.P.1
-
38
-
-
0027373678
-
Cloning of the ALL-1 fusion partner, the AF-6 gene, involved in acute myeloid leukemias with the t(6;11) chromosome translocation
-
PRASAD, R., Y. Gu, H. ALDER, T. NAKAMURA, O. CANAANI et al., 1993 Cloning of the ALL-1 fusion partner, the AF-6 gene, involved in acute myeloid leukemias with the t(6;11) chromosome translocation. Cancer Res. 53: 5624-5628.
-
(1993)
Cancer Res.
, vol.53
, pp. 5624-5628
-
-
Prasad, R.1
Gu, Y.2
Alder, H.3
Nakamura, T.4
Canaani, O.5
-
39
-
-
0029955902
-
Cultured melanocytes from dilute mutant mice exhibit dendritic morphology and altered melanosome distribution
-
PROVANCE, D. W. JR., M. WEI, V. IPE and J. A. MERCER, 1996 Cultured melanocytes from dilute mutant mice exhibit dendritic morphology and altered melanosome distribution. Proc. Natl. Acad. Sci. USA 93: 14554-14558.
-
(1996)
Proc. Natl. Acad. Sci. USA
, vol.93
, pp. 14554-14558
-
-
Provance Jr., D.W.1
Wei, M.2
Ipe, V.3
Mercer, J.A.4
-
40
-
-
0002430532
-
Studies in mammalian radiation genetics
-
RUSSELL, W. L., 1965 Studies in mammalian radiation genetics. Nucleonics 23: 53-56.
-
(1965)
Nucleonics
, vol.23
, pp. 53-56
-
-
Russell, W.L.1
-
41
-
-
0020287684
-
Dose-response curve for ethylnitrosourea-induced specific-locus mutations in mouse spermatogonia
-
RUSSELL, W. L., P. R. HUNSICKER, G. D. RAYMER, M. H. STEELE, K. F. STELZNER et al., 1982 Dose-response curve for ethylnitrosourea-induced specific-locus mutations in mouse spermatogonia. Proc. Natl. Acad. Sci. USA 79: 3589-3591.
-
(1982)
Proc. Natl. Acad. Sci. USA
, vol.79
, pp. 3589-3591
-
-
Russell, W.L.1
Hunsicker, P.R.2
Raymer, G.D.3
Steele, M.H.4
Stelzner, K.F.5
-
42
-
-
0026658159
-
CDNa encoding the chicken ortholog of the mouse dilute gene product. Sequence comparison reveals a myosin I subfamily with conserved C-terminal domains
-
SANDERS, G., B. LICHTE, H. E. MEYER and M. W. KILIMANN, 1992 cDNA encoding the chicken ortholog of the mouse dilute gene product. Sequence comparison reveals a myosin I subfamily with conserved C-terminal domains. FEBS Lett. 311: 295-298.
-
(1992)
FEBS Lett.
, vol.311
, pp. 295-298
-
-
Sanders, G.1
Lichte, B.2
Meyer, H.E.3
Kilimann, M.W.4
-
43
-
-
0029056416
-
Retroviral sequences located within an intron of the dilute gene alter dilute expression in a tissue-specific manner
-
SEPERACK, P. K, J. A. MERCER, M. C. STROBEL, N. G. COPELAND and N. A. JENKINS, 1995 Retroviral sequences located within an intron of the dilute gene alter dilute expression in a tissue-specific manner. EMBO J. 14: 2326-2332.
-
(1995)
EMBO J.
, vol.14
, pp. 2326-2332
-
-
Seperack, P.K.1
Mercer, J.A.2
Strobel, M.C.3
Copeland, N.G.4
Jenkins, N.A.5
-
44
-
-
0026607344
-
Mutations which alter splicing in the human hypoxanthine-guanine phosphoribosyltransferase gene
-
STEINGRIMSDOTTIR, H., G. ROWLEY, G. DORADO, J. COLE and A. R. LEHMANN, 1992 Mutations which alter splicing in the human hypoxanthine-guanine phosphoribosyltransferase gene. Nucleic Acids Res. 20: 1201-1208.
-
(1992)
Nucleic Acids Res.
, vol.20
, pp. 1201-1208
-
-
Steingrimsdottir, H.1
Rowley, G.2
Dorado, G.3
Cole, J.4
Lehmann, A.R.5
-
46
-
-
0027288912
-
The role of exon sequences in splice site selection
-
WATAKABE, A., K. TANAKA and Y. SHIMURA, 1993 The role of exon sequences in splice site selection. Genes Dev. 7: 407-418.
-
(1993)
Genes Dev.
, vol.7
, pp. 407-418
-
-
Watakabe, A.1
Tanaka, K.2
Shimura, Y.3
-
47
-
-
0028815440
-
Defective myosin VIIA gene responsible for Usher syndrome type 1B
-
WEIL, D., S. BLANCHARD, J. KAPLAN, P. GUILFORD, F. GIBSON et al., 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
-
48
-
-
19244362118
-
Myosin VIIA mutation screening in 189 usher syndrome type 1 patients
-
WESTON, M. D., P. M. KELLEY, L. D. OVERBECK, M. WAGENAAR, D. J. ORTEN et al., 1996 Myosin VIIA mutation screening in 189 usher syndrome type 1 patients. Amer. J. Hum. Genet. 59: 1074-1083.
-
(1996)
Amer. J. Hum. Genet.
, vol.59
, pp. 1074-1083
-
-
Weston, M.D.1
Kelley, P.M.2
Overbeck, L.D.3
Wagenaar, M.4
Orten, D.J.5
-
49
-
-
0030964893
-
Myosin V associates with melanosomes in mouse melanocytes -evidence that myosin V is an organelle motor
-
Wu, X. F., B. BOWERS, Q. WEI, B. KOCHER and J. A. HAMMER, 1997 Myosin V associates with melanosomes in mouse melanocytes -evidence that myosin V is an organelle motor. J. Cell Sci. 110: 847-859.
-
(1997)
J. Cell Sci.
, vol.110
, pp. 847-859
-
-
Wu, X.F.1
Bowers, B.2
Wei, Q.3
Kocher, B.4
Hammer, J.A.5
-
50
-
-
0029784469
-
Cloning and characterization of myr 6, an unconventional myosin of the dilute/myosin-V family
-
ZHAO, L. P., J. S. KOSLOVSKY, J. REINHARD, M. BAHLER, A. E. WITT et al., 1996 Cloning and characterization of myr 6, an unconventional myosin of the dilute/myosin-V family. Proc. Natl. Acad. Sci. USA 93: 10826-10831.
-
(1996)
Proc. Natl. Acad. Sci. USA
, vol.93
, pp. 10826-10831
-
-
Zhao, L.P.1
Koslovsky, J.S.2
Reinhard, J.3
Bahler, M.4
Witt, A.E.5
|