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什么是 'arylsulphatase+-%26%2338463%3b'? 定义 arylsulphatase+-%26%2338463%3B related diagnosis for 'arylsulphatase+-%26%2338463%3b' related procedure for 'arylsulphatase+-%26%2338463%3b'/相关的诊断 related medication for 'arylsulphatase+-%26%2338463%3b'/相关的诊断 以下是类型的医生有关 'arylsulphatase+-%26%2338463%3B'. related types of physicians '' show local physicians 郵政編碼 找到的地方 星級代表沒有相關的專題評價 更多 結果表明，電腦產生的建議，以幫助您找到一個醫生. MEDgle不推薦任何特定類型的醫生或聲稱是完整或準確的供應商和專業建議. 网络搜索结果 'arylsulphatase+-%26%2338463%3b'? 结果 1 - 50 - arylsulphatase+-%26%2338463%3B Arylsulfatase A - Wikipedia, the free encyclopedia [翻译此页] Arylsulfatase A (or cerebroside-sulfatase) is an enzyme that breaks down cerebroside 3 ... "Terminal 22q deletion associated with a partial deficiency of arylsulphatase A. ... http://en.wikipedia.org/wiki/Arylsulfatase_A   en.wikipedia.org - summary Arylsulfatase A - Wikipedia [翻译此页] Een deficiëntie van arylsulfatase A leidt tot metachromatische leukodystrofie. ... Terminal 22q deletion associated with a partial deficiency of arylsulphatase A. ... http://nl.wikipedia.org/wiki/Arylsulfatase_A   nl.wikipedia.org - summary Laboratory diagnosis of lysosomal storage diseases -- Fabry ... [翻译此页] Lysosomal storage diseases (LSDs) represent a heterogeneous group of disorders that all ... glucosidase, ?-hexosaminidase A and arylsulphatase A, and is linked ... http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=fabry&part=A556   www.ncbi.nlm.nih.gov - summary Pseudodeficiency alleles - Wikipedia, the free encyclopedia [翻译此页] One possible cause of false positive results is a pseudodeficiency allele. ... Low arylsulphatase A activity can occur in healthy individuals. ... http://en.wikipedia.org/wiki/Pseudodeficiency_alleles   en.wikipedia.org - summary Restoration of arylsulphatase B activity in human ... [翻译此页] A human ASB cDNA has been subcloned into the retroviral vector pXT1 containing the bacterial neomycin ... Restoration of arylsulphatase A activity in human-metachromatic ... http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1151119   www.ncbi.nlm.nih.gov - summary Complete disease list [翻译此页] alpha 1-antitrypsin indicate a single origin for deficiency allele PI Z ... arylsulfatase A pseudodeficiency. arylsulphatase A pseudodeficiency ... http://geneticassociationdb.nih.gov/diseaselist.html   geneticassociationdb.nih.gov - summary Cyanide binding and inhibition of a purified arylsulphatase ... [翻译此页] Full text is available as a scanned copy of the original print version. ... The arylsulphatase of a strain of Alcaligenes metalcaligenes isolated from intertidal mud. ... http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1187670   www.ncbi.nlm.nih.gov - summary lexsrv3.nlm.nih.gov/SPECIALIST/Projects/lexicon/current/release/... [翻译此页] A|Vit A| E0006085|vit A|Vit A| E0006086|vit. C|Vit C| E0006087|vit. E ... hydrocarbon|arylhydrocarbon| E0010637|arylsulphatase A|arylsulfatase A| E0010637 ... http://lexsrv3.nlm.nih.gov/SPECIALIST/Projects/lexicon/current/release/LEX/LRSPL   lexsrv3.nlm.nih.gov - summary CYB5R3 - Wikipedia, the free encyclopedia [翻译此页] The erythrocyte form is located in a soluble fraction of circulating erythrocytes and is ... "Terminal 22q deletion associated with a partial deficiency of arylsulphatase A. ... http://en.wikipedia.org/wiki/CYB5R3   en.wikipedia.org - summary The functional consequences of mis-sense mutations affecting ... [翻译此页] Metachromatic leukodystrophy is a lysosomal storage disorder caused by the deficiency of arylsulphatase A. We describe the functional consequences ... http://www.ncbi.nlm.nih.gov/pubmed/12086582   www.ncbi.nlm.nih.gov - summary Frequency of arylsulphatase A pseudodeficiency associated ... [翻译此页] Arylsulphatase A (ASA, EC 3.1.6.1) is a lysosomal enzyme that catalyses cerebroside sulphate degradation. ... We report a reliable stratagem for detecting the two PD associated ... http://www.ncbi.nlm.nih.gov/pubmed/7815433   www.ncbi.nlm.nih.gov - summary User:ProteinBoxBot/PBB Log Wiki 11-6-2007 Rerun B-6 ... [翻译此页] { PBB_Summary | section_title = | summary_text = This gene encodes a member of the ADAM (a disintegrin and ... arylsulphatase A pseudodeficiency associated mutations in a healthy ... http://en.wikipedia.org/wiki/User:ProteinBoxBot/PBB_Log_Wiki_11-6-2007_Rerun_B-6   en.wikipedia.org - summary Missense mutations in the arylsulphatase A genes of ... [翻译此页] The first new mutation is a C-->A change at base 884 in exon 5 of the arylsulphatase A (ASA) gene causing a ... A late-infantile MLD patient was found to be homozygous for this ... http://www.ncbi.nlm.nih.gov/pubmed/7906588   www.ncbi.nlm.nih.gov - summary E0000046|A-1|A1| E0000050|A.A.M.D.|AAMD| E0000081|AIDS related ... [翻译此页] A|Vit A| E0006086|vit. C|Vit C| E0006087|vit. E|Vit E| E0006088|vit. G|Vit G| E0006089 ... coxsackie A9 virus| E0019502|Coxsackie A virus|coxsackie A virus| E0019503|Coxsackie ... http://lexsrv2.nlm.nih.gov/SPECIALIST/Projects/lexicon/2004/...   lexsrv2.nlm.nih.gov - summary Prevalence of common mutations in the arylsulphatase A gene ... [翻译此页] 1993 Mar;91(1):73-7. Prevalence of common mutations in the arylsulphatase A gene in metachromatic leukodystrophy patients diagnosed in Britain. ... http://www.ncbi.nlm.nih.gov/pubmed/8095918   www.ncbi.nlm.nih.gov - summary User:ProteinBoxBot/PBB Log Wiki 11-6-2007 B-6 - Wikipedia ... [翻译此页] This gene encodes a nonmuscle, cytoskeletal, alpha actinin isoform and maps to ... associated with a partial deficiency of arylsulphatase A. |journal=J. ... http://en.wikipedia.org/wiki/User:ProteinBoxBot/PBB_Log_Wiki_11-6-2007_B-6   en.wikipedia.org - summary lexsrv3.nlm.nih.gov/SPECIALIST/Projects/lexicon/2003 ... [翻译此页] A|Vit A| E0006086|vit. C|Vit C| E0006087|vit. E|Vit E| E0006088|vit. G|Vit G| E0006089 ... a propos|apropos| E0010157|a propos|apropos| E0010194|aquaeduct|aqueduct ... http://lexsrv3.nlm.nih.gov/SPECIALIST/Projects/lexicon/2003/...   lexsrv3.nlm.nih.gov - summary Arylsulfatase A (ARSA) [翻译此页] Human protein-coding gene ARSA. Represented by 407 ESTs from 177 cDNA libraries. Corresponds to 5 reference sequences (different isoforms). [UniGene 141151 - Hs.88251] http://www.ncbi.nlm.nih.gov/UniGene/clust.cgi?ORG=Hs&MAXEST=999999&CID=88251   www.ncbi.nlm.nih.gov - summary Cellular pathophysiology of lysosomal storage diseases ... [翻译此页] Arylsulphatase A deficiency causes meta-chromatic leukodystrophy, a lipid storage disease. ... P426L-substituted arylsulphatase A is so far the only example of a lysosomal ... http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=fabry&part=A276   www.ncbi.nlm.nih.gov - summary A link between DNA methylation and epigenetic silencing in ... [翻译此页] A link between DNA methylation and epigenetic silencing in transgenic Volvox carteri ... by biolistic bombardment with a foreign arylsulphatase gene (C-ars), the transgene is ... http://www.ncbi.nlm.nih.gov/pmc/articles/PMC29749/   www.ncbi.nlm.nih.gov - summary Diagnosis of Metachromatic Leukodystrophy, Krabbe Disease ... [翻译此页] Full text is available as a scanned copy of the original print version. ... Low arylsulphatase A activity in a family without metachromatic leukodystrophy. ... http://www.ncbi.nlm.nih.gov/pmc/articles/PMC370230/   www.ncbi.nlm.nih.gov - summary Adult metachromatic leukodystrophy: disorganized ... [翻译此页] Restoration of arylsulphatase A activity in human-metachromatic leukodystrophy ... Zhang X, et al. A novel arylsulphatase A protein variant and genotype ... http://www.ncbi.nlm.nih.gov/pmc/articles/PMC543838/   www.ncbi.nlm.nih.gov - summary Novel mutations associated with metachromatic leukodystrophy ... [翻译此页] Their diagnosis was confirmed by determination of the activity of arylsulphatase A in leukocytes and by abnormal urinary excretion of sulphatides. ... http://www.ncbi.nlm.nih.gov/pubmed/15326627   www.ncbi.nlm.nih.gov - summary Arylsulphatase from Alteromonas carrageenovora. [翻译此页] The structural gene of arylsulphatase (atsA) was cloned and sequenced. ... Arylsulphatase was partially purified from cell extracts of both A. carrageenovora and recombinant ... http://www.ncbi.nlm.nih.gov/pubmed/8535517   www.ncbi.nlm.nih.gov - summary A unique familial leukodystrophy with adult onset dementia ... [翻译此页] Numerous lysosomal enzyme assays including leucocyte arylsulphatase A and galactocerebrosidase activities, plasma and fibroblast very long chain ... http://www.ncbi.nlm.nih.gov/pubmed/9703182   www.ncbi.nlm.nih.gov - summary 10196694 - PubMed Result [翻译此页] ... the loss of the single N-glycosylation site in a patient with metachromatic leukodystrophy and normal arylsulphatase A activity. Eur J Hum Genet. ... http://www.ncbi.nlm.nih.gov/pubmed/?term=10196694   www.ncbi.nlm.nih.gov - summary Search Results: Merck Manual Professional [翻译此页] Results for "Arylsulphatase A deficiency" Did you mean Arylsulfatase A deficiency? Pages. containing the term "Arylsulphatase A deficiency" results 1 - 10 of 500 ... http://www.merck.com/mmpe/search.html?qt=Arylsulphatase+A+deficiency   www.merck.com - summary Arylsulfatase A Deficiency -- GeneReviews -- NCBI Bookshelf [翻译此页] GeneReviews designates a molecular genetic test as clinically ... Kurosawa K, Ida H, Eto Y. Prevalence of arylsulphatase A mutations in 11 Japanese patients with metachromatic ... http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=mld   www.ncbi.nlm.nih.gov - summary Human N-acetylgalactosamine-4-sulphate sulphatase ... [翻译此页] The use of a monoclonal antibody linked to a solid support facilitated the purification ... oligosaccharides as substrates for the determination of arylsulphatase B activity. ... http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1148614/   www.ncbi.nlm.nih.gov - summary Studies on the Arylsulphatase and phenol sulphotransferase ... [翻译此页] 3. The arylsulphatase activity of these extracts can be resolved into ... A comparison of the arylsulphatase and cerebroside sulphatase activities of sulphatase A. ... http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1165676   www.ncbi.nlm.nih.gov - summary Identification and characterization of mutations in housefly ... [翻译此页] S B Walsh, T A Dolden, G D Moores, M Kristensen, T Lewis, A L Devonshire, and M S ... Barth ML, Fensom A, Harris A. Missense mutations in the arylsulphatase A genes of ... http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1222133/   www.ncbi.nlm.nih.gov - summary A cDNA clone for human glucosamine-6-sulphatase reveals ... [翻译此页] Department of Chemical Pathology, Adelaide Children's Hospital, South Australia. ... classified as a non-arylsulphatase since, relative to arylsulphatase B, it shows ... http://www.ncbi.nlm.nih.gov/pubmed/1463457   www.ncbi.nlm.nih.gov - summary Late onset MLD with normal nerve conduction associated with ... [翻译此页] Gallo S, Randi D, Bertelli M, Salviati A, Pandolfo M. Istituto BIRD Europe, Vicenza, Italy. ... the arylsulphatase A (ASA) sulphatase and carboxyterminal domains, resulting in ... http://www.ncbi.nlm.nih.gov/pubmed/15026521   www.ncbi.nlm.nih.gov - summary geneticassociationdb.nih.gov/disease.txt [翻译此页] ... arylsulfatase A pseudodeficiency arylsulphatase A pseudodeficiency ... familial amyloid polyneuropathy in a Hungarian family. familial amyloid polyneuropathy. familial amyloid ... http://geneticassociationdb.nih.gov/disease.txt   geneticassociationdb.nih.gov - summary Gene dosage effect in acquired monosomy 7: distinct behaviour ... [翻译此页] A group of 19 patients with similar diseases but with normal ... beta-galactosidase and arylsulphatase A, whose genes are not on chromosome 7, were tested as control enzymes. ... http://www.ncbi.nlm.nih.gov/pubmed/1964582   www.ncbi.nlm.nih.gov - summary "Meikle PJ"[Author] - PubMed Result [翻译此页] Diagnosis of metachromatic leukodystrophy by immune quantification of arylsulphatase A protein and activity in dried blood spots. Clin Chem. ... http://www.ncbi.nlm.nih.gov/pubmed?term="Meikle+PJ"[Author]&...   www.ncbi.nlm.nih.gov - summary Naturally Occurring Genetic Disorders of Glycosylation ... [翻译此页] Nevertheless, a substantial proportion of sites receive a normal Glc3Man9GlcNAc2 ... TBG deficiency, increased serum arylsulphatase A and increased CSF protein: A new syndrome? ... http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=glyco&part=A2361   www.ncbi.nlm.nih.gov - summary Arylsulfatase A Deficiency [翻译此页] MLD) is a disorder of impaired breakdown of sulfatides that occur throughout the body, ... H, Eto Y. Prevalence of arylsulphatase A mutations in 11 Japanese ... http://www.ncbi.nlm.nih.gov/bookshelf/picrender.fcgi?book=ge...   www.ncbi.nlm.nih.gov - summary Genetics and Craniofacial & Dental Anomalies [翻译此页] To provide NIDCR with a set of prioritized recommendations for future ... Further, a number of innovative technological developments. now provide approaches to high ... http://www.nidcr.nih.gov/NR/rdonlyres/392686B3-47E0-448D-A98...   www.nidcr.nih.gov - summary X-linked ichthyosis and X-linked placental sulfatase ... [翻译此页] Full text is available as a scanned copy of the original print version. Get a printable ... of the demonstration of arylsulphatase activity in cryostat sections. ... http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1903491/   www.ncbi.nlm.nih.gov - summary Human eosinophil arylsulfatase B. Structure and activity of ... [翻译此页] Full text is available as a scanned copy of the original print version. Get a printable ... A rapid and sensitive method for the quantitation of microgram quantities of protein ... http://www.ncbi.nlm.nih.gov/pmc/articles/PMC436843/   www.ncbi.nlm.nih.gov - summary Molecular and biochemical characterisation of a novel ... [翻译此页] Northern blot analysis of Arylsulfatase G revealed a ubiquitous expression pattern. ... and p-nitrocatechol sulphate, but no arylsulphatase activity was detectable. ... http://www.ncbi.nlm.nih.gov/pubmed/12461688   www.ncbi.nlm.nih.gov - summary Restoring biochemical activity and bacterial diversity in a ... [翻译此页] Trichloroethylene had a marked negative effect on soil dehydrogenase, beta-glucosidase, urease, phosphatase, and arylsulphatase activities. ... http://www.ncbi.nlm.nih.gov/pubmed/18751749   www.ncbi.nlm.nih.gov - summary Prevalence of arylsulphatase A mutations in 11 Japanese ... [翻译此页] 1998 Oct;21(7):781-2. Prevalence of arylsulphatase A mutations in 11 Japanese patients with metachromatic leukodystrophy: identification of two novel mutations. ... http://www.ncbi.nlm.nih.gov/pubmed/9819708   www.ncbi.nlm.nih.gov - summary Studies on glucosaminidase. 4. The fluorimetric assay of ... [翻译此页] Full text is available as a scanned copy of the original print version. ... A study of the arylsulphatase activity of takadiastase towards some phenolic ... http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1205188   www.ncbi.nlm.nih.gov - summary The hill coefficient for the Ca2+-activation of striated ... [翻译此页] Get a printable copy (PDF file) of the complete article (508K), or click on a page image below to browse page ... deaminase, arylsulphatase, benzylamine oxidase, chymotrypsin, ... http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1435008   www.ncbi.nlm.nih.gov - summary Comparative immunological studies on arylsulfatase in ... [翻译此页] Full text is available as a scanned copy of the original print version. Get a printable ... and induction of arylsulphatase synthesis in Aerobacter aerogenes. ... http://www.ncbi.nlm.nih.gov/pmc/articles/PMC222055/   www.ncbi.nlm.nih.gov - summary Report of a mucopolysaccharidosis occurring in Australian ... [翻译此页] The first 2 reported cases of a mucopolysaccharidosis occurring in an Australian aboriginal family are ... and decreased activity of arylsulphatase B. Thus, they represented ... http://www.ncbi.nlm.nih.gov/pubmed/106124   www.ncbi.nlm.nih.gov - summary Structure and chromosomal localization of the human ... [翻译此页] A genomic GYG2 clone was used to localize the gene to Xp22.3 by fluorescence in-situ hybridization. ... and its 3' end is 34.5 kb from the 3' end of the arylsulphatase gene ARSD. ... http://www.ncbi.nlm.nih.gov/pubmed/10721716   www.ncbi.nlm.nih.gov - summary [Mucopolysaccharidosis: 20-year enzymatic diagnosis in Cuba] [翻译此页] SUBJECTS AND METHODS: A total of 664 patients with a clinical suspicion of some type of ... N-acetylglucosaminidase, beta-galactosidase, arylsulphatase B and beta-glucuronidase ... http://www.ncbi.nlm.nih.gov/pubmed/19859885   www.ncbi.nlm.nih.gov - summary 显示更多 1  2

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