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 ...
★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