WordNet
- the 14th letter of the Roman alphabet (同)n
PrepTutorEJDIC
- nitrogenの化学記号
- neodymiumの化学記号
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出典(authority):フリー百科事典『ウィキペディア（Wikipedia）』「2016/08/25 21:31:18」(JST)
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- 1. ムコ多糖症：合併症およびマネージメント mucopolysaccharidoses complications and management
- 2. ムコ多糖症：臨床的特徴および診断 mucopolysaccharidoses clinical features and diagnosis
- 3. シェーグレン・ラルソン症候群 sjogren larsson syndrome
- 4. X染色体連鎖劣性魚鱗癬 recessive x linked ichthyosis
- 5. 過期妊娠 postterm pregnancy
English Journal
- Arylsulfatase B (N-acetylgalactosamine-4-sulfatase): potential role as a biomarker in prostate cancer.
- Feferman L, Bhattacharyya S, Deaton R, Gann P, Guzman G, Kajdacsy-Balla A, Tobacman JK.Source1] Department of Medicine, University of Illinois at Chicago, Chicago, IL, USA [2] Jesse Brown VA Medical Center, Chicago, IL, USA.
- Prostate cancer and prostatic diseases.Prostate Cancer Prostatic Dis.2013 Jul 9. doi: 10.1038/pcan.2013.18. [Epub ahead of print]
- Background:The enzyme arylsulfatase B (ARSB; N-acetylgalactosamine-4-sulfatase) degrades chondroitin-4-sulfate (C4S) and is reduced in malignant colonic and mammary tissues but has not previously been evaluated in prostate cancer.Methods:ARSB immunostaining was performed on two tissue microarrays (T
- PMID 23835622
- Mucopolysaccharidosis type VI: a predominantly cardiac phenotype associated with homozygosity for p.R152W mutation in the ARSB gene.
- Jurecka A, Zakharova E, Cimbalistiene L, Gusina N, Kulpanovich A, Golda A, Opoka-Winiarska V, Piotrowska E, Voskoboeva E, Tylki-Szymańska A.SourceDepartment of Molecular Biology, University of Gdańsk, Gdańsk, Poland. ajurecka@gmail.com
- American journal of medical genetics. Part A.Am J Med Genet A.2013 Jun;161(6):1291-9. doi: 10.1002/ajmg.a.35905. Epub 2013 Apr 30.
- Mucopolysaccharidosis type VI (MPS VI) is a rare lysosomal, autosomal recessive storage disorder caused by deficient activity of N-acetylgalactosamine-4-sulfatase (ARSB). Approximately, 140 ARSB gene mutations have been identified; however, most are private mutations making genotype-phenotype correl
- PMID 23633437
- Spondyloepiphyseal Dysplasias and Bilateral Legg-Calvé-Perthes Disease: Diagnostic Considerations for Mucopolysaccharidoses.
- Mendelsohn NJ, Wood T, Olson RA, Temme R, Hale S, Zhang H, Read L, White KK.SourceDepartment of Medical Genetics, Children's Hospitals and Clinics of Minnesota, 2525 Chicago Avenue S., CSC 560, Minneapolis, MN, 55404, USA, nancy.mendelsohn@childrensmn.org.
- JIMD reports.JIMD Rep.2013 May 9. [Epub ahead of print]
- Mucopolysaccharidosis type VI (MPS VI, Maroteaux-Lamy syndrome, MIM 253200 ) is an autosomal recessive lysosomal storage disease (LSD) caused by decreased activity of arylsulfatase B (N-acetylgalactosamine 4-sulfatase) enzyme resulting in dermatan sulfate accumulation; mucopolysaccharidosis type IVA
- PMID 23657977
Japanese Journal
- Maroteaux-Lamy disease (Mucopolysaccharidosis VI), subtype A : deficiency of a N-acetylgalactosamine-4-sulfatase
- O'BRIEN J. F.
- Biochem Biophys Res Comm 60, 1170-1177, 1974
- NAID 80013035310
Related Links
- a relatively high rate of immunotolerance towards recombinant human N-acetylgalactosamine-4-sulfatase can be achieved in MPS-VI cats with a shortcourse ... mucopolysaccharidosis type VI, i.e. MPS VI or Maroteaux-Lamy ...
- 1. Biochim Biophys Acta. 1995 Dec 12;1272(3):129-32. N-acetylgalactosamine-4-sulfatase: identification of four new mutations within the conserved sulfatase region causing mucopolysaccharidosis type VI. Simonaro CM(1 ...
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★リンクテーブル★
| リンク元 | 「N-アセチルガラクトサミン-4-スルファターゼ」 |
| 関連記事 | 「n」「sulfatase」「N」「acetylgalactosamine」「Nd」 |
「N-アセチルガラクトサミン-4-スルファターゼ」
「n」
- n.
- pの前の[n]はmと記載する。synptom→symptom
「sulfatase」
「N」
- アスパラギン asparagine
- 窒素(原子、分子)