-
1
-
-
0021808444
-
A novel brain ATPase with properties expected for the fast axonal transport motor
-
Brady, S. T. (1985). A novel brain ATPase with properties expected for the fast axonal transport motor. Nature 317: 73-75.
-
(1985)
Nature
, vol.317
, pp. 73-75
-
-
Brady, S.T.1
-
2
-
-
0344450710
-
Linkage mapping of the mouse gene, iv, that controls left right asymmetry of the heart and viscera
-
Broeckner, M., D'Eustachio, P., and Horwich, A. L. (1989). Linkage mapping of the mouse gene, iv, that controls left right asymmetry of the heart and viscera. Proc. Natl. Acad. Sci. USA 86: 5035-5038.
-
(1989)
Proc. Natl. Acad. Sci. USA
, vol.86
, pp. 5035-5038
-
-
Broeckner, M.1
D'Eustachio, P.2
Horwich, A.L.3
-
3
-
-
0027755695
-
Cloning and genetic characterization of the human kinesin light chain (KLC) gene
-
Cabeza-Arvelaiz, Y., Shih, L.-C. N., Hardman, N., Asselbergs, F., Bilbe, G., Schmitz, A., White, B., Siciliano, M. J., and Lachman, L. B. (1993). Cloning and genetic characterization of the human kinesin light chain (KLC) gene. DNA Cell Biol. 12: 881-892.
-
(1993)
DNA Cell Biol.
, vol.12
, pp. 881-892
-
-
Cabeza-Arvelaiz, Y.1
Shih, L.-C.N.2
Hardman, N.3
Asselbergs, F.4
Bilbe, G.5
Schmitz, A.6
White, B.7
Siciliano, M.J.8
Lachman, L.B.9
-
4
-
-
0025876059
-
Molecular genetics of kinesin light chains: Generation of isoforms by alternative splicing
-
Cyr, J. L., Pfister, K. K., Bloom, G. S., Slaughter, C. A., and Brady, S. T. (1991). Molecular genetics of kinesin light chains: Generation of isoforms by alternative splicing. Proc. Natl. Acad. Sci. USA 88: 10114-10118.
-
(1991)
Proc. Natl. Acad. Sci. USA
, vol.88
, pp. 10114-10118
-
-
Cyr, J.L.1
Pfister, K.K.2
Bloom, G.S.3
Slaughter, C.A.4
Brady, S.T.5
-
5
-
-
0027058632
-
A gene for usher syndrome type I (USH1A) maps to chromosome 14q
-
Kaplan, J., Gerber, S., Bonneau, D., Rozet, J. M., Delrieu, O., Briard, M. L., Dollfus, H., Ghazi, I., Dufier, J. L., Frézal, J., and Munnich, A. (1992). A gene for Usher syndrome type I (USH1A) maps to chromosome 14q. Genomics 14: 979-987.
-
(1992)
Genomics
, vol.14
, pp. 979-987
-
-
Kaplan, J.1
Gerber, S.2
Bonneau, D.3
Rozet, J.M.4
Delrieu, O.5
Briard, M.L.6
Dollfus, H.7
Ghazi, I.8
Dufier, J.L.9
Frézal, J.10
Munnich, A.11
-
6
-
-
0027965107
-
Localization of the human cytoplasmic dynein heavy chain (DNECL) to 14qter by fluorescence in situ hybridization
-
Narayan, D., Desai, T., Banks, A., Patanjali, S. R., Ravikumar, T. S., and Ward, D. C. (1994). Localization of the human cytoplasmic dynein heavy chain (DNECL) to 14qter by fluorescence in situ hybridization. Genomics 22: 660-661.
-
(1994)
Genomics
, vol.22
, pp. 660-661
-
-
Narayan, D.1
Desai, T.2
Banks, A.3
Patanjali, S.R.4
Ravikumar, T.S.5
Ward, D.C.6
-
7
-
-
0028363485
-
Cloning and localization of a conventional kinesin motor expressed exclusively in neurons
-
Niclar, J., Navone, F., Hom-Booher, N., and Vale, R. D. (1994). Cloning and localization of a conventional kinesin motor expressed exclusively in neurons. Neuron 12: 1059-1072.
-
(1994)
Neuron
, vol.12
, pp. 1059-1072
-
-
Niclar, J.1
Navone, F.2
Hom-Booher, N.3
Vale, R.D.4
-
8
-
-
0022446922
-
Cytogenetic analysis using quantitative, high-sensitivity, fluorescence hybridization
-
Pinkel, D., Straume, T., and Gray, J. W. (1986). Cytogenetic analysis using quantitative, high-sensitivity, fluorescence hybridization. Proc. Natl. Acad. Sci. USA 83: 2934-2938.
-
(1986)
Proc. Natl. Acad. Sci. USA
, vol.83
, pp. 2934-2938
-
-
Pinkel, D.1
Straume, T.2
Gray, J.W.3
-
9
-
-
0022385727
-
Identification of a novel force-generating protein, kinesin, involved in microtubule-based motility
-
Vale, R. D., Reese, T. S., and Sheetz, M. P. (1985). Identification of a novel force-generating protein, kinesin, involved in microtubule-based motility. Cell 42: 39-50.
-
(1985)
Cell
, vol.42
, pp. 39-50
-
-
Vale, R.D.1
Reese, T.S.2
Sheetz, M.P.3
-
10
-
-
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., Varela, A., Levilliers, J., Weston, M. D., Kelley, P. M., Kimberling, W. J., Wagenaar, M., Levi-Acobas, F., Larget-Piet, D., Munnich, A., Steel, K P., 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
Varela, A.8
Levilliers, J.9
Weston, M.D.10
Kelley, P.M.11
Kimberling, W.J.12
Wagenaar, M.13
Levi-Acobas, F.14
Larget-Piet, D.15
Munnich, A.16
Steel, K.P.17
Brown, S.D.M.18
Petit, C.19
|