
Health Dictionary
Reliable, easy-to-read patient information on common medical conditions — written in plain language, free of jargon, and grounded in current evidence. Browse the most frequent diagnoses, understand what they mean for everyday life, and learn which steps and questions help you have a focused conversation with your doctor.
KIFC3
Introduction
Kinesin-like protein KIFC3 is a protein that in humans is encoded by the KIFC3 gene.[1][2]
References
References
- ↑ Hoang EH, Whitehead JL, Dose AC, Burnside B (Dec 1998). “Cloning of a novel C-terminal kinesin (KIFC3) that maps to human chromosome 16q13-q21 and thus is a candidate gene for Bardet-Biedl syndrome”. Genomics. 52 (2): 219–22. doi:10.1006/geno.1998.5431. PMID 9782090.
- ↑ “Entrez Gene: KIFC3 kinesin family member C3”.
Further reading
Further reading
- Diu A, Moebius U, Ferradini L, et al. (1993). “Limited T-cell receptor diversity in liver-infiltrating lymphocytes from patients with primary biliary cirrhosis”. J. Autoimmun. 6 (5): 611–9. doi:10.1006/jaut.1993.1050. PMID 8240664.
- Hoang E, Bost-Usinger L, Burnside B (1999). “Characterization of a novel C-kinesin (KIFC3) abundantly expressed in vertebrate retina and RPE”. Exp. Eye Res. 69 (1): 57–68. doi:10.1006/exer.1999.0671. PMID 10375449.
- Noda Y, Okada Y, Saito N, et al. (2001). “KIFC3, a microtubule minus end-directed motor for the apical transport of annexin XIIIb-associated Triton-insoluble membranes”. J. Cell Biol. 155 (1): 77–88. doi:10.1083/jcb.200108042. PMC 2150803. PMID 11581287.
- Xu Y, Takeda S, Nakata T, et al. (2002). “Role of KIFC3 motor protein in Golgi positioning and integration”. J. Cell Biol. 158 (2): 293–303. doi:10.1083/jcb.200202058. PMC 2173137. PMID 12135985.
- Strausberg RL, Feingold EA, Grouse LH, et al. (2003). “Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences”. Proc. Natl. Acad. Sci. U.S.A. 99 (26): 16899–903. doi:10.1073/pnas.242603899. PMC 139241. PMID 12477932.
- Ota T, Suzuki Y, Nishikawa T, et al. (2004). “Complete sequencing and characterization of 21,243 full-length human cDNAs”. Nat. Genet. 36 (1): 40–5. doi:10.1038/ng1285. PMID 14702039.
- Gerhard DS, Wagner L, Feingold EA, et al. (2004). “The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC)”. Genome Res. 14 (10B): 2121–7. doi:10.1101/gr.2596504. PMC 528928. PMID 15489334.
- Roni V, Carpio R, Wissinger B (2007). “Mapping of transcription start sites of human retina expressed genes”. BMC Genomics. 8: 42. doi:10.1186/1471-2164-8-42. PMCÂ 1802077. PMIDÂ 17286855.
