Publications
Found 15 results
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“Association between a point mutation at the -743-bp region of the transthyretin (TTR) gene and familial vitreous amyloidosis”, vol. 15, p. -, 2016.
, “Association between a point mutation at the -743-bp region of the transthyretin (TTR) gene and familial vitreous amyloidosis”, vol. 15, p. -, 2016.
, “Association between a point mutation at the -743-bp region of the transthyretin (TTR) gene and familial vitreous amyloidosis”, vol. 15, p. -, 2016.
, “Genomic identification, phylogeny, and expression analysis of MLO genes involved in susceptibility to powdery mildew in Fragaria vesca”, vol. 15, p. -, 2016.
, “Genomic identification, phylogeny, and expression analysis of MLO genes involved in susceptibility to powdery mildew in Fragaria vesca”, vol. 15, p. -, 2016.
, , , “IL-17A and IL-17F polymorphisms and gastric cancer risk: a meta-analysis”, vol. 14, pp. 7008-7017, 2015.
, “MicroRNA-215 functions as a tumor suppressor and directly targets ZEB2 in human pancreatic cancer”, vol. 14, pp. 16133-16145, 2015.
, “Mutation analysis of four Chinese families with pure hereditary spastic paraplegia: pseudo- X-linked dominant inheritance and male lethality due to a novel ATL1 mutation”, vol. 14, pp. 14690-14697, 2015.
, “Prenatal diagnosis of Chinese families with phenylketonuria”, vol. 14, pp. 14615-14628, 2015.
, , “Colorectal cancer susceptibility variants alter risk of breast cancer in a Chinese Han population”, vol. 12, pp. 6268-6274, 2013.
, “Effects of various salinities on Na+-K+-ATPase, Hsp70 and Hsp90 expression profiles in juvenile mitten crabs, Eriocheir sinensis”, vol. 11, pp. 978-986, 2012.
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http://dx.doi.org/10.1126/science.2799391
PMid:2799391
Deane EE, Kelly SP, Luk JC and Woo NY (2002). Chronic salinity adaptation modulates hepatic heat shock protein and insulin-like growth factor I expression in black sea bream. Mar. Biotechnol. 4: 193-205.
Ding S, Wang F, Dong S and Gao Q (2009). Effects of salinity fluctuation amplitudes on growth, osmolarity, Na+-K+- ATPase activity and Hsp70 of juvenile Chinese shrimp Fenneropenaeus chinensis Osbeck. Chin. J. Oceanol. Limnol. 27: 723-728.
http://dx.doi.org/10.1007/s00343-009-9185-0
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http://dx.doi.org/10.1146/annurev.physiol.61.1.243
PMid:10099689
Harris RR and Santos MCF (1993). Sodium uptake and transport (Na+ + K+) ATPase changes following Na+ depletion and low salinity acclimation in the mangrove crab Ucides cordatus (L.). Comp. Biochem. Physiol. 105: 35-42.
http://dx.doi.org/10.1016/0300-9629(93)90170-9
Herborg LM, Rushton SP, Clare AS and Bentley MG (2003). Spread of the Chinese mitten crab (Eriocheir sinensis H. Milne Edwards) in Continental Europe: analysis of a historical data set. Hydrobiologia 503: 21-28.
http://dx.doi.org/10.1023/B:HYDR.0000008483.63314.3c
Holliday CW (1985). Salinity-induced changes in gill Na, K-ATPase activity in the mud fiddler crab, Uca pugnax. J. Exp. Zool. 233: 199-208.
http://dx.doi.org/10.1002/jez.1402330206
Kim CH and Hwang SG (1995). The complete larval development of the mitten crab Eriocheir sinensis H. Milne Edwards, 1853 (Decapoda, Brachyura, Grapsidae) reared in the laboratory and a key to the known zoeae of the Varuninae. Crustaceana 68: 793-812.
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http://dx.doi.org/10.1007/BF02367153
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http://dx.doi.org/10.1002/jez.1402110210
Pan F, Zarate JM, Tremblay GC and Bradley TM (2000). Cloning and characterization of salmon hsp90 cDNA: upregulation by thermal and hyperosmotic stress. J. Exp. Zool. 287: 199-212.
http://dx.doi.org/10.1002/1097-010X(20000801)287:3<199::AID-JEZ2>3.0.CO;2-3
Pan LQ and Luan ZH (2005). The effects of salinity on development and Na+/K+-ATPase activity of Marsupenaeus japonicus postlarvae. Acta Hydrobiol. Sin. 29: 699-703.
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Spees JL, Chang SA, Snyder MJ and Chang ES (2002). Osmotic induction of stress-responsive gene expression in the lobster Homarus americanus. Biol. Bull. 203: 331-337.
http://dx.doi.org/10.2307/1543575
PMid:12480723
Torres G, Charmantier-Daures M, Chifflet S and Anger K (2007). Effects of long-term exposure to different salinities on the location and activity of Na+-K+-ATPase in the gills of juvenile mitten crab, Eriocheir sinensis. Comp. Biochem. Physiol. A Mol. Integr. Physiol. 147: 460-465.
http://dx.doi.org/10.1016/j.cbpa.2007.01.020
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“A novel mutation of the MFN2 gene in a Chinese family with Charcot-Marie-Tooth disease”, vol. 11. pp. 1454-1459, 2012.
, Banchs I, Casasnovas C, Montero J, Martinez-Matos JA, et al. (2008). Two Spanish families with Charcot-Marie-Tooth type 2A: clinical, electrophysiological and molecular findings. Neuromuscul. Disord. 18: 974-978.http://dx.doi.org/10.1016/j.nmd.2008.09.006PMid:18996695Barisic N, Claeys KG, Sirotkovic-Skerlev M, Lofgren A, et al. (2008). Charcot-Marie-Tooth disease: a clinico-genetic confrontation. Ann. Hum. Genet. 72: 416-441.http://dx.doi.org/10.1111/j.1469-1809.2007.00412.xPMid:18215208Cartoni R and Martinou JC (2009). Role of mitofusin 2 mutations in the physiopathology of Charcot-Marie-Tooth disease type 2A. Exp. Neurol. 218: 268-273.http://dx.doi.org/10.1016/j.expneurol.2009.05.003PMid:19427854Chung KW, Kim SB, Park KD, Choi KG, et al. (2006). Early onset severe and late-onset mild Charcot-Marie-Tooth disease with mitofusin 2 (MFN2) mutations. Brain 129: 2103-2118.http://dx.doi.org/10.1093/brain/awl174PMid:16835246Engelfried K, Vorgerd M, Hagedorn M, Haas G, et al. (2006). Charcot-Marie-Tooth neuropathy type 2A: novel mutations in the mitofusin 2 gene (MFN2). BMC Med. Genet. 7: 53.http://dx.doi.org/10.1186/1471-2350-7-53PMid:16762064 PMCid:1524942Honda S, Aihara T, Hontani M, Okubo K, et al. (2005). Mutational analysis of action of mitochondrial fusion factor mitofusin-2. J. Cell Sci. 118: 3153-3161.http://dx.doi.org/10.1242/jcs.02449PMid:15985463Kijima K, Numakura C, Izumino H, Umetsu K, et al. (2005). Mitochondrial GTPase mitofusin 2 mutation in Charcot- Marie-Tooth neuropathy type 2A. Hum. Genet. 116: 23-27.http://dx.doi.org/10.1007/s00439-004-1199-2PMid:15549395Koshiba T, Detmer SA, Kaiser JT, Chen H, et al. (2004). Structural basis of mitochondrial tethering by mitofusin complexes. Science 305: 858-862.http://dx.doi.org/10.1126/science.1099793PMid:15297672Nicolaou P, Zamba-Papanicolaou E, Koutsou P, Kleopa KA, et al. (2010). Charcot-Marie-Tooth disease in Cyprus: epidemiological, clinical and genetic characteristics. Neuroepidemiology 35: 171-177.http://dx.doi.org/10.1159/000314351PMid:20571287Rojo M, Legros F, Chateau D and Lombes A (2002). Membrane topology and mitochondrial targeting of mitofusins, ubiquitous mammalian homologs of the transmembrane GTPase Fzo. J. Cell Sci. 115: 1663-1674.PMid:11950885Santel A and Fuller MT (2001). Control of mitochondrial morphology by a human mitofusin. J. Cell Sci. 114: 867-874.PMid:11181170Verhoeven K, Claeys KG, Zuchner S, Schroder JM, et al. (2006). MFN2 mutation distribution and genotype/phenotype correlation in Charcot-Marie-Tooth type 2. Brain 129: 2093-2102.http://dx.doi.org/10.1093/brain/awl126PMid:16714318Züchner S, Mersiyanova IV, Muglia M, Bissar-Tadmouri N, et al. (2004). Mutations in the mitochondrial GTPase mitofusin 2 cause Charcot-Marie-Tooth neuropathy type 2A. Nat. Genet. 36: 449-451.http://dx.doi.org/10.1038/ng1341PMid:15064763