成人型異染性白質ジストロフィー
- 関
- metachromatic leukodystrophy
WordNet
- any mature animal
- a fully developed person from maturity onward (同)grownup
- (of animals) fully developed; "an adult animal"; "a grown woman" (同)big, full-grown, fully grown, grown, grownup
PrepTutorEJDIC
- 『おとなの』,成人した,成熟した / 成人向きの / 『おとな』,成人
UpToDate Contents
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English Journal
- Distribution of C16:0, C18:0, C24:1 and C24:0 sulfatides in CNS lipid rafts by quantitative UHPLC-MS/MS.
- Moyano AL1, Li G2, Lopez-Rosas A1, Månsson JE3, van Breemen RB2, Givogri MI4.
- Analytical biochemistry.Anal Biochem.2014 Sep 6. pii: S0003-2697(14)00388-1. doi: 10.1016/j.ab.2014.08.033. [Epub ahead of print]
- Sulfated galactosylceramides (sulfatides) are glycosphingolipids associated with cholesterol- and sphingolipid-enriched membrane microdomains (lipid rafts) and are highly expressed in brain tissue. While it is known that sulfatide species show heterogeneity in their fatty acid acyl group composition
- PMID 25205652
- Lentivector integration sites in ependymal cells from a model of metachromatic leukodystrophy: non-B DNA as a new factor influencing integration.
- McAllister RG1, Liu J2, Woods MW1, Tom SK1, Rupar CA3, Barr SD1.
- Molecular therapy. Nucleic acids.Mol Ther Nucleic Acids.2014 Aug 26;3:e187. doi: 10.1038/mtna.2014.39.
- The blood-brain barrier controls the passage of molecules from the blood into the central nervous system (CNS) and is a major challenge for treatment of neurological diseases. Metachromatic leukodystrophy is a neurodegenerative lysosomal storage disease caused by loss of arylsulfatase A (ARSA) activ
- PMID 25158091
- Comparative Efficacy and Safety of Multiple Routes of Direct CNS Administration of Adeno-Associated Virus Gene Transfer Vector Serotype rh.10 Expressing the Human Arylsulfatase A cDNA to Nonhuman Primates.
- Rosenberg JB1, Sondhi D, Rubin DG, Monette S, Chen A, Cram S, De BP, Kaminsky SM, Sevin C, Aubourg P, Crystal RG.
- Human gene therapy. Clinical development.Hum Gene Ther Clin Dev.2014 Aug 21. [Epub ahead of print]
- Abstract Metachromatic leukodystrophy (MLD), a fatal disorder caused by deficiency of the lysosomal enzyme arylsulfatase A (ARSA), is associated with an accumulation of sulfatides, causing widespread demyelination in both central and peripheral nervous systems. On the basis of prior studies demonstr
- PMID 25144894
Japanese Journal
- 遺伝性白質脳症とhereditary diffuse leukoencephalopathy with spheroids(HDLS)の分子病態
- 症例 アキレス腱反射減弱を伴った30歳代の認知症例
- 成人型異染性白質ジストロフィーの1同胞例の歯科治療経験
Related Links
- Metachromatic leukodystrophy (MLD) is part of a larger group of lysosomal storage diseases, some of which are progressive, inherited, and neurodegenerative disorders (metachromatic leukodystrophy included). Four ...
- Metachromatic leukodystrophy is an inherited disorder characterized by the accumulation of fats called sulfatides in cells. This accumulation especially affects cells in the nervous system that produce myelin, the ...
Related Pictures
★リンクテーブル★
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- 英
- adult metachromatic leukodystrophy
- 関
- 異染性白質ジストロフィー
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- 関
- adult human、adult type
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異染性白質ジストロフィー
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白質ジストロフィー