WordNet
- any of several complex proteins that are produced by cells and act as catalysts in specific biochemical reactions
PrepTutorEJDIC
- 酵素
UpToDate Contents
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- 1. ライソゾーム膜蛋白質2欠損症（糖原病IIb型、ダノン病） lysosome associated membrane protein 2 deficiency glycogen storage disease iib danon disease
- 2. 肥大型心筋症の遺伝学 genetics of hypertrophic cardiomyopathy
- 3. ゴーシェ病：治療 gaucher disease treatment
- 4. リソソーム酸α-グルコシダーゼ欠損症（ポンペ病、糖原病II型、酸マルターゼ欠損症） lysosomal acid alpha glucosidase deficiency pompe disease glycogen storage disease ii acid maltase deficiency
- 5. ゴーシェ病：病因、臨床症状、および診断 gaucher disease pathogenesis clinical manifestations and diagnosis
English Journal
- Pathologic endothelial response and impaired function of circulating angiogenic cells in patients with Fabry disease.
- Lorenzen JM, Dietrich B, Fiedler J, Jazbutyte V, Fleissner F, Karpinski N, Weidemann F, Wanner C, Asan E, Caprio M, Ertl G, Bauersachs J, Thum T.SourceHannover Medical School, Institute of Molecular and Translational Therapeutic Strategies (IMTTS), Carl-Neuberg-Strasse 1, 30625, Hannover, Germany.
- Basic research in cardiology.Basic Res Cardiol.2013 Jan;108(1):311. doi: 10.1007/s00395-012-0311-3. Epub 2012 Nov 20.
- Fabry disease is an X-chromosomal recessive deficiency of the lysosomal hydrolase alpha-galactosidase A (alpha-Gal). This results in an accumulation of globotriaosylceramide (GL-3) in a variety of cells often with subsequent functional impairment. Here, the impact of Fabry disease on the biology of
- PMID 23184391
- High-throughput screening of stem cell therapy for globoid cell leukodystrophy using automated neurophenotyping of twitcher mice.
- Scruggs BA, Bowles AC, Zhang X, Semon JA, Kyzar EJ, Myers L, Kalueff AV, Bunnell BA.SourceCenter for Stem Cell Research and Regenerative Medicine, Tulane University School of Medicine, 1430 Tulane Avenue, SL-99, New Orleans, LA 70112, USA; Department of Pharmacology, Tulane University School of Medicine, 1430 Tulane Avenue, SL-83, New Orleans, LA 70112, USA.
- Behavioural brain research.Behav Brain Res.2013 Jan 1;236(1):35-47. doi: 10.1016/j.bbr.2012.08.020. Epub 2012 Aug 20.
- Globoid cell leukodystrophy (Krabbe's disease) is an autosomal recessive neurodegenerative disorder that results from the deficiency of galactosylceramidase, a lysosomal enzyme involved in active myelination. Due to the progressive, lethal nature of this disease and the limited treatment options ava
- PMID 22951180
Japanese Journal
- Elevation of Serum Acid Sphingomyelinase Activity in Children with Acute Respiratory Syncytial Virus Bronchiolitis
- The Tohoku Journal of Experimental Medicine 243(4), 275-281, 2017
- NAID 130006252135
- Mucopolysaccharidosis type I, II and VI and response to enzyme replacement therapy: Results from a single-center case series study
- Intractable & Rare Diseases Research 6(3), 183-190, 2017
- NAID 130006078832
- The Coexistence of Multiple Myeloma-associated Amyloid Light-chain Amyloidosis and Fabry Disease in a Hemodialysis Patient
- Internal Medicine 56(7), 841-846, 2017
- NAID 130005530178
Related Links
- Research Topics Lysosomal Enzymes Lysosomes are subcellular organelles which perform many important cellular functions. For example, lysosomes digest foreign material and engulfed viruses and bacteria presenting in ...
- To accomplish the tasks associated with digestion, the lysosomes use some 40 different types of lysosomal enzymes, such as glycosidases, protease, acid phosphatases, sulfatases and lipases. Lysosomal enzymes are ...
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★リンクテーブル★
| リンク元 | 「ライソソーム酵素」「ライソゾーム酵素」 |
| 拡張検索 | 「lysosomal enzyme disorder」 |
| 関連記事 | 「lysosomal」 |
「ライソソーム酵素」
「ライソゾーム酵素」
「lysosomal enzyme disorder」
「lysosomal」
- adj.
- リソソームの、ライソソームの
- 関
- lysosome