Publications
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“Correlation of CYP1A1 and GSTM1 gene polymorphisms and environmental factors to familial aggregation of esophageal cancer among the Kazakh ethnic group in Xinjiang”, vol. 14, pp. 19102-19109, 2015.
, “Effects of the Zhikang capsule on healing of the flap after radical breast cancer surgery”, vol. 14, pp. 5127-5131, 2015.
, , “Meta-analysis of association of common variants in the KCNJ11-ABCC8 region with type 2 diabetes”, vol. 12, pp. 2990-3002, 2013.
, “Combined genetic and imaging diagnosis for two large Chinese families affected with Pelizaeus-Merzbacher disease”, vol. 11, pp. 2035-2044, 2012.
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Bonnet-Dupeyron MN, Combes P, Santander P, Cailloux F, et al. (2008). PLP1 splicing abnormalities identified in Pelizaeus-Merzbacher disease and SPG2 fibroblasts are associated with different types of mutations. Hum. Mutat. 29: 1028-1036.
http://dx.doi.org/10.1002/humu.20758
PMid:18470932
Edgar JM, McLaughlin M, Barrie JA, McCulloch MC, et al. (2004). Age-related axonal and myelin changes in the rumpshaker mutation of the PLP gene. Acta Neuropathol. 107: 331-335.
http://dx.doi.org/10.1007/s00401-003-0808-9
PMid:14745569
Inoue K (2005). PLP1-related inherited dysmyelinating disorders: Pelizaeus-Merzbacher disease and spastic paraplegia type 2. Neurogenetics 6: 1-16.
http://dx.doi.org/10.1007/s10048-004-0207-y
PMid:15627202
Inoue K, Kanai M, Tanabe Y, Kubota T, et al. (2001). Prenatal interphase FISH diagnosis of PLP1 duplication associated with Pelizaeus-Merzbacher disease. Prenat. Diagn. 21: 1133-1136.
http://dx.doi.org/10.1002/pd.186
PMid:11787038
Inoue K, Osaka H, Thurston VC, Clarke JT, et al. (2002). Genomic rearrangements resulting in PLP1 deletion occur by nonhomologous end joining and cause different dysmyelinating phenotypes in males and females. Am. J. Hum. Genet. 71: 838-853.
http://dx.doi.org/10.1086/342728
PMid:12297985 PMCid:378540
Krämer-Albers EM, Gehrig-Burger K, Thiele C, Trotter J, et al. (2006). Perturbed interactions of mutant proteolipid protein/DM20 with cholesterol and lipid rafts in oligodendroglia: implications for dysmyelination in spastic paraplegia. J. Neurosci. 26: 11743-11752.
http://dx.doi.org/10.1523/JNEUROSCI.3581-06.2006
PMid:17093095
Mattei MG, Alliel PM, Dautigny A, Passage E, et al. (1986). The gene encoding for the major brain proteolipid (PLP) maps on the q-22 band of the human X chromosome. Hum. Genet. 72: 352-353.
http://dx.doi.org/10.1007/BF00290964
PMid:3457761
Willard HF and Riordan JR (1985). Assignment of the gene for myelin proteolipid protein to the X chromosome: implications for X-linked myelin disorders. Science 230: 940-942.
http://dx.doi.org/10.1126/science.3840606
PMid:3840606