-
1
-
-
0028678828
-
Motor proteins. 1. Kinesins
-
Bloom G. S., Endow S. A. Motor proteins. 1. Kinesins. Protein Profile. 1:1995;1059-1116.
-
(1995)
Protein Profile
, vol.1
, pp. 1059-1116
-
-
Bloom, G.S.1
Endow, S.A.2
-
2
-
-
0031149156
-
Multiple kinesin family members expressed in teleost retina and RPE include a novel C-terminal kinesin
-
Bost-Usinger L., Chen R. J., Hillman D., Park P., Burnside B. Multiple kinesin family members expressed in teleost retina and RPE include a novel C-terminal kinesin. Exp. Eye Res. 64:1997;781-794.
-
(1997)
Exp. Eye Res.
, vol.64
, pp. 781-794
-
-
Bost-Usinger, L.1
Chen, R.J.2
Hillman, D.3
Park, P.4
Burnside, B.5
-
3
-
-
0031127101
-
Linkage mapping in 29 Bardet-Biedl syndrome families confirms loci in chromosomal regions 11q13, 15q22.3-q23, and 16q21
-
Bruford E. A., Riise R., Teague P. W., Porter K., Thomson K. L., Moore A. T., Jay M., Warburg M., Schinzel A., Tommerup N., Tornqvist K., Rosenberg T., Patton M., Mansfield D. C., Wright A. F. Linkage mapping in 29 Bardet-Biedl syndrome families confirms loci in chromosomal regions 11q13, 15q22.3-q23, and 16q21. Genomics. 41:1997;93-99.
-
(1997)
Genomics
, vol.41
, pp. 93-99
-
-
Bruford, E.A.1
Riise, R.2
Teague, P.W.3
Porter, K.4
Thomson, K.L.5
Moore, A.T.6
Jay, M.7
Warburg, M.8
Schinzel, A.9
Tommerup, N.10
Tornqvist, K.11
Rosenberg, T.12
Patton, M.13
Mansfield, D.C.14
Wright, A.F.15
-
4
-
-
0029990004
-
Report of the Fourth International Workshop on Human Chromosome 16 Mapping 1995
-
Dogget N. A., Breuning M. H., Callen D. F. Report of the Fourth International Workshop on Human Chromosome 16 Mapping 1995. Cytogenet. Cell Genet. 72:1996;271-293.
-
(1996)
Cytogenet. Cell Genet.
, vol.72
, pp. 271-293
-
-
Dogget, N.A.1
Breuning, M.H.2
Callen, D.F.3
-
5
-
-
0024472754
-
The cardinal manifestations of Bardet-Biedl syndrome, a form of Laurence-Moon-Biedl syndrome
-
Green J. S., Parfrey P. S., Harnett J. D., Farid N. R., Cramer B. C., Johnson G., Heath O., McManamon P. J., O'Leary E., Pryse-Phillips W. The cardinal manifestations of Bardet-Biedl syndrome, a form of Laurence-Moon-Biedl syndrome. N. Engl. J. Med. 321:1989;1002-1009.
-
(1989)
N. Engl. J. Med.
, vol.321
, pp. 1002-1009
-
-
Green, J.S.1
Parfrey, P.S.2
Harnett, J.D.3
Farid, N.R.4
Cramer, B.C.5
Johnson, G.6
Heath, O.7
McManamon, P.J.8
O'Leary, E.9
Pryse-Phillips, W.10
-
7
-
-
0027426195
-
Linkage of Bardet-Biedl syndrome to chromosome 16q and evidence for non-allelic heterogeneity
-
Kwitek-Black A. E., Carmi R., Duyk G. M., Buetow K. H., Elbedour K., Parvari R., Yandava C. N., Stone E. M., Sheffield V. C. Linkage of Bardet-Biedl syndrome to chromosome 16q and evidence for non-allelic heterogeneity. Nat. Genet. 5:1993;392-396.
-
(1993)
Nat. Genet.
, vol.5
, pp. 392-396
-
-
Kwitek-Black, A.E.1
Carmi, R.2
Duyk, G.M.3
Buetow, K.H.4
Elbedour, K.5
Parvari, R.6
Yandava, C.N.7
Stone, E.M.8
Sheffield, V.C.9
-
8
-
-
0030111466
-
Kinesin proteins: A phylum of motors for microtubule-based motility
-
Moore J. D., Endow S. A. Kinesin proteins: A phylum of motors for microtubule-based motility. BioEssays. 18:1996;207-219.
-
(1996)
BioEssays
, vol.18
, pp. 207-219
-
-
Moore, J.D.1
Endow, S.A.2
-
9
-
-
0017119173
-
Inherited retinal dystrophy: Primary defect in pigment epithelium determined with experimental rat chimeras
-
Mullen R. J., LaVail M. M. Inherited retinal dystrophy: Primary defect in pigment epithelium determined with experimental rat chimeras. Science. 192:1976;799-801.
-
(1976)
Science
, vol.192
, pp. 799-801
-
-
Mullen, R.J.1
Lavail, M.M.2
-
10
-
-
0026604808
-
Differential localizations of and requirements for the twoDrosophila
-
Porter J. A., Hick J. L., Williams D. S., Montell C. Differential localizations of and requirements for the twoDrosophila. J. Cell Biol. 116:1992;683-693.
-
(1992)
J. Cell Biol.
, vol.116
, pp. 683-693
-
-
Porter, J.A.1
Hick, J.L.2
Williams, D.S.3
Montell, C.4
-
11
-
-
0030885299
-
Identification and classification of 16 new kinesin superfamily (KIF) proteins in mouse genome
-
Nakagawa T., Tanaka Y., Matsuoka E., Kondo S., Okada Y., Noda Y., Kanai Y., Hirokawa N. Identification and classification of 16 new kinesin superfamily (KIF) proteins in mouse genome. Proc. Natl. Acad. Sci. USA. 94:1997;9654-9659.
-
(1997)
Proc. Natl. Acad. Sci. USA
, vol.94
, pp. 9654-9659
-
-
Nakagawa, T.1
Tanaka, Y.2
Matsuoka, E.3
Kondo, S.4
Okada, Y.5
Noda, Y.6
Kanai, Y.7
Hirokawa, N.8
-
12
-
-
15144342084
-
An STS-based radiation hybrid map of the human genome
-
Stewart E. A., McKusick K. B., Aggarwal A., Bajorek E., Brady S., Chu A., Fang N., Hadley D., Harris M., Hussain S., Lee R., Maratukulam A., O'Connor K., Perkins S., Piercy M., Qin F., Reif T., Sanders C., She X., Sun W.-L., Tabar P., Voyticky S., Cowles S., Fan J.-B., Mader C., Quakenbush J., Myers R. M., Cox D. R. An STS-based radiation hybrid map of the human genome. Genome Res. 7:1997;422-433.
-
(1997)
Genome Res.
, vol.7
, pp. 422-433
-
-
Stewart, E.A.1
McKusick, K.B.2
Aggarwal, A.3
Bajorek, E.4
Brady, S.5
Chu, A.6
Fang, N.7
Hadley, D.8
Harris, M.9
Hussain, S.10
Lee, R.11
Maratukulam, A.12
O'Connor, K.13
Perkins, S.14
Piercy, M.15
Qin, F.16
Reif, T.17
Sanders, C.18
She, X.19
Sun, W.-L.20
Tabar, P.21
Voyticky, S.22
Cowles, S.23
Fan, J.-B.24
Mader, C.25
Quakenbush, J.26
Myers, R.M.27
Cox, D.R.28
more..
-
13
-
-
0025796794
-
Retinitis pigmentosa and its models
-
London.: Pergamon. p. 293-332
-
Voaden M. J. Retinitis pigmentosa and its models. Progress in Retinal Research. 1991;Pergamon, London. p. 293-332.
-
(1991)
Progress in Retinal Research
-
-
Voaden, M.J.1
-
14
-
-
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., Larger-Piet D., Munnich A., Steel K. P., Brown S. D. M., Petit C. Defective myosin VIIA gene responsible for Usher syndrome type 1B. Nature. 374:1995;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
Larger-Piet, D.15
Munnich, A.16
Steel, K.P.17
Brown, S.D.M.18
Petit, C.19
-
15
-
-
0031260399
-
Identification, partial characterization, and genetic mapping of kinesin-like protein genes in mouse
-
Yang Z., Hanlon D. W., Marszalek J. R., Goldstein L. S. B. Identification, partial characterization, and genetic mapping of kinesin-like protein genes in mouse. Genomics. 45:1997;123-131.
-
(1997)
Genomics
, vol.45
, pp. 123-131
-
-
Yang, Z.1
Hanlon, D.W.2
Marszalek, J.R.3
Goldstein, L.S.B.4
|