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Structural studies of urinary oligosaccharides from patients with mannosidosis.

作者信息

Matsuura F, Nunez H A, Grabowski G A, Sweeley C C

出版信息

Arch Biochem Biophys. 1981 Apr 1;207(2):337-52. doi: 10.1016/0003-9861(81)90041-2.

DOI:10.1016/0003-9861(81)90041-2
PMID:7247408
Abstract
摘要

相似文献

1
Structural studies of urinary oligosaccharides from patients with mannosidosis.甘露糖苷贮积症患者尿中寡糖的结构研究。
Arch Biochem Biophys. 1981 Apr 1;207(2):337-52. doi: 10.1016/0003-9861(81)90041-2.
2
Alpha-mannosidosis: analysis of urinary oligosaccharides with high performance liquid chromatography and diagnosis of a case with unusually mild presentation.α-甘露糖苷贮积症：用高效液相色谱法分析尿寡糖并诊断一例表现异常轻微的病例
Clin Genet. 1984 Mar;25(3):248-55. doi: 10.1111/j.1399-0004.1984.tb01985.x.
3
Improved thin-layer chromatographic method in the diagnosis of mannosidosis.用于诊断甘露糖苷贮积症的改良薄层色谱法。
Clin Chem. 1978 Sep;24(9):1576-7.
4
Structural analysis of the major caprine beta-mannosidosis urinary oligosaccharides.主要山羊β-甘露糖苷贮积症尿寡糖的结构分析
Biochim Biophys Acta. 1983 Aug 23;759(1-2):67-73. doi: 10.1016/0304-4165(83)90190-3.
5
Urinary excretion of a novel hexasaccharide and glycopeptide analogue in fucosidosis.岩藻糖贮积症中一种新型六糖和糖肽类似物的尿排泄情况。
Biochem Biophys Res Commun. 1979 May 28;88(2):696-705. doi: 10.1016/0006-291x(79)92104-1.
6
The catabolism of mammalian glycoproteins. Comparison of the storage products in bovine, feline and human mannosidosis.哺乳动物糖蛋白的分解代谢。牛、猫和人类甘露糖苷贮积症中储存产物的比较。
Biochem J. 1983 Dec 1;215(3):573-9. doi: 10.1042/bj2150573.
7
Urinary oligosaccharide excretion in disorders of glycolipid, glycoprotein and glycogen metabolism. A review of screening for differential diagnosis.糖脂、糖蛋白和糖原代谢紊乱时的尿低聚糖排泄。鉴别诊断筛查综述。
Eur J Pediatr. 1980 Sep;134(3):183-94. doi: 10.1007/BF00441471.
8
Mannosidosis: isolation and comparison of mannose-containing oligosaccharides from gingiva and urine.甘露糖苷贮积症：牙龈和尿液中含甘露糖寡糖的分离与比较
Eur J Biochem. 1981 Feb;114(2):235-7. doi: 10.1111/j.1432-1033.1981.tb05141.x.
9
Characterization of two mannose-containing oligosaccharides isolated from the urine of patients with mannosidosis.从甘露糖苷贮积症患者尿液中分离出的两种含甘露糖寡糖的特性分析。
Biochemistry. 1974 Feb 26;13(5):871-4. doi: 10.1021/bi00702a006.
10
Mannosidosis. Storage material, alpha-mannosidase specificity and diagnostic methods.甘露糖苷贮积症。贮存物质、α-甘露糖苷酶特异性及诊断方法。
Adv Exp Med Biol. 1976;68:301-11.

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1
Natural history of alpha mannosidosis a longitudinal study.α-甘露糖苷贮积症的自然病史：一项纵向研究。
Orphanet J Rare Dis. 2013 Jun 20;8:88. doi: 10.1186/1750-1172-8-88.
2
Analysis of urinary oligosaccharides in lysosomal storage disorders by capillary high-performance anion-exchange chromatography-mass spectrometry.采用毛细管高效阴离子交换色谱-质谱法分析溶酶体贮积症中的尿低聚糖。
Anal Bioanal Chem. 2012 Jun;403(6):1671-83. doi: 10.1007/s00216-012-5968-9. Epub 2012 Apr 20.
3
The core-specific lysosomal alpha(1-6)-mannosidase activity depends on aspartamidohydrolase activity.
核心特异性溶酶体α(1-6)-甘露糖苷酶活性取决于天冬酰胺酶活性。
Biochem J. 1994 Feb 1;297 ( Pt 3)(Pt 3):463-6. doi: 10.1042/bj2970463.
4
Beta-mannosidosis: prenatal biochemical and morphological characteristics.β-甘露糖苷贮积症：产前生化及形态学特征
J Inherit Metab Dis. 1984;7(2):80-5. doi: 10.1007/BF01805811.
5
Effects of swainsonine on rat liver and kidney: biochemical and morphological studies.苦马豆素对大鼠肝脏和肾脏的影响：生化与形态学研究
J Cell Biol. 1985 Aug;101(2):339-49. doi: 10.1083/jcb.101.2.339.
6
Structural analysis of the major urinary oligosaccharides in feline alpha-mannosidosis.猫α-甘露糖苷贮积症中主要尿低聚糖的结构分析
Biochem J. 1986 Feb 1;233(3):899-904. doi: 10.1042/bj2330899.
7
Bone marrow transplantation in the treatment of alpha-mannosidosis.骨髓移植治疗α-甘露糖苷贮积症。
Arch Dis Child. 1987 Oct;62(10):1044-9. doi: 10.1136/adc.62.10.1044.
8
Characterization of alpha-mannosidase in feline mannosidosis.猫甘露糖苷贮积症中α-甘露糖苷酶的特征分析
J Inherit Metab Dis. 1988;11(1):3-16. doi: 10.1007/BF01800052.
9
Human beta-mannosidase deficiency: biochemical findings in plasma, fibroblasts, white cells and urine.人类β-甘露糖苷酶缺乏症：血浆、成纤维细胞、白细胞及尿液中的生化研究结果
J Inherit Metab Dis. 1988;11(1):17-29. doi: 10.1007/BF01800054.
10
Beta-mannosidosis: prenatal detection of caprine allantoic fluid oligosaccharides with thin layer, gel permeation and high performance liquid chromatography.
J Inherit Metab Dis. 1986;9(1):93-8. doi: 10.1007/BF01813910.