Characterization of a Novel C-Kinesin (KIFC3) Abundantly Expressed in Vertebrate Retina and RPE
- 1 July 1999
- journal article
- Published by Elsevier in Experimental Eye Research
- Vol. 69 (1) , 57-68
- https://doi.org/10.1006/exer.1999.0671
Abstract
No abstract availableKeywords
This publication has 48 references indexed in Scilit:
- Cloning of a Novel C-Terminal Kinesin (KIFC3) That Maps to Human Chromosome 16q13–q21 and Thus Is a Candidate Gene for Bardet–Biedl SyndromeGenomics, 1998
- KIFC2 Is a Novel Neuron-Specific C-Terminal Type Kinesin Superfamily Motor for Dendritic Transport of Multivesicular Body-Like OrganellesNeuron, 1997
- Presynaptic bodies (”ribbons"): from ultrastructural observations to molecular perspectivesCell and tissue research, 1997
- Characterization of a Kinesin-Related Gene ATSV, within the Tuberous Sclerosis Locus (TSC1) Candidate Region on Chromosome 9Q34Genomics, 1996
- Cloning and localization of a conventional kinesin motor expressed exclusively in neuronsNeuron, 1994
- Linkage of Bardet–Biedl syndrome to chromosome 16q and evidence for non–allelic genetic heterogeneityNature Genetics, 1993
- Cloning and expression of a human kinesin heavy chain gene: interaction of the COOH-terminal domain with cytoplasmic microtubules in transfected CV-1 cellsThe Journal of cell biology, 1992
- Predicting Coiled Coils from Protein SequencesScience, 1991
- The Cardinal Manifestations of Bardet–Biedl Syndrome, a Form of Laurence–Moon–Biedl SyndromeNew England Journal of Medicine, 1989
- Cleavage of Structural Proteins during the Assembly of the Head of Bacteriophage T4Nature, 1970