
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.
RAB34
Introduction
Ras-related protein Rab-34 is a protein that in humans is encoded by the RAB34 gene.[1][2]
References
References
- ↑ Sun P, Yamamoto H, Suetsugu S, Miki H, Takenawa T, Endo T (Feb 2003). “Small GTPase Rah/Rab34 is associated with membrane ruffles and macropinosomes and promotes macropinosome formation”. J Biol Chem. 278 (6): 4063–71. doi:10.1074/jbc.M208699200. PMID 12446704.
- ↑ “Entrez Gene: RAB34 RAB34, member RAS oncogene family”.
Further reading
Further reading
- Wang T, Hong W (2003). “Interorganellar regulation of lysosome positioning by the Golgi apparatus through Rab34 interaction with Rab-interacting lysosomal protein”. Mol. Biol. Cell. 13 (12): 4317–32. doi:10.1091/mbc.E02-05-0280. PMC 138636. PMID 12475955.
- 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.
- Chen T, Han Y, Yang M, et al. (2003). “Rab39, a novel Golgi-associated Rab GTPase from human dendritic cells involved in cellular endocytosis”. Biochem. Biophys. Res. Commun. 303 (4): 1114–20. doi:10.1016/S0006-291X(03)00482-0. PMID 12684051.
- Wang T, Wong KK, Hong W (2004). “A unique region of RILP distinguishes it from its related proteins in its regulation of lysosomal morphology and interaction with Rab7 and Rab34”. Mol. Biol. Cell. 15 (2): 815–26. doi:10.1091/mbc.E03-06-0413. PMC 329395. PMID 14668488.
- 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.
- Barrios-Rodiles M, Brown KR, Ozdamar B, et al. (2005). “High-throughput mapping of a dynamic signaling network in mammalian cells”. Science. 307 (5715): 1621–5. doi:10.1126/science.1105776. PMID 15761153.
- Colucci AM, Campana MC, Bellopede M, Bucci C (2005). “The Rab-interacting lysosomal protein, a Rab7 and Rab34 effector, is capable of self-interaction”. Biochem. Biophys. Res. Commun. 334 (1): 128–33. doi:10.1016/j.bbrc.2005.06.067. PMID 15996637.
- Speight P, Silverman M (2005). “Diacylglycerol-activated Hmunc13 serves as an effector of the GTPase Rab34”. Traffic. 6 (10): 858–65. doi:10.1111/j.1600-0854.2005.00321.x. PMID 16138900.
- Otsuki T, Ota T, Nishikawa T, et al. (2007). “Signal sequence and keyword trap in silico for selection of full-length human cDNAs encoding secretion or membrane proteins from oligo-capped cDNA libraries”. DNA Res. 12 (2): 117–26. doi:10.1093/dnares/12.2.117. PMID 16303743.
- Coyne CB, Shen L, Turner JR, Bergelson JM (2007). “Coxsackievirus entry across epithelial tight junctions requires occludin and the small GTPases Rab34 and Rab5”. Cell Host Microbe. 2 (3): 181–92. doi:10.1016/j.chom.2007.07.003. PMC 2719558. PMID 18005733.
