Lysosomal beta-glucosidase (GBA1) and non-lysosomal beta-glucosidase (GBA2): Potential involvement in the pathogenesis of Gaucher disease/Parkinson disease

Burke Derek G.; Heales Simon J.; Vellodi Ashok

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Lysosomal beta-glucosidase (GBA1) and non-lysosomal beta-glucosidase (GBA2): Potential involvement in the pathogenesis of Gaucher disease/Parkinson disease

机译：溶酶体β-葡萄糖苷酶（GBA1）和非溶酶体β-葡萄糖苷酶（GBA2）：潜在参与高雪氏病/帕金森氏病的发病机理

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《Molecular genetics and metabolism》 |2015年第2期|共1页
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Burke Derek G.; Heales Simon J.; Vellodi Ashok;
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正文语种 eng
中图分类内分泌腺疾病及代谢病;
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1. Lysosomal beta-glucosidase (GBA1) and non-lysosomal beta-glucosidase (GBA2): Potential involvement in the pathogenesis of Gaucher disease/Parkinson disease [J] . Burke Derek G., Heales Simon J., Vellodi Ashok Molecular genetics and metabolism . 2015,第2期

机译：溶酶体β-葡萄糖苷酶（GBA1）和非溶酶体β-葡萄糖苷酶（GBA2）：潜在参与高雪氏病/帕金森氏病的发病机理
2. Production of recombinant human acid beta-glucosidase with high mannose-type N-glycans in rice gnt1 mutant for potential treatment of Gaucher disease [J] . Jung Jae-Wan, Choi Hong-Yeol, Nguyen-Xuan Huy, Protein Expression and Purification . 2019,第期

机译：在水稻GNT1突变体中产生重组人酸β-葡糖苷酶的重组人酸β-葡糖苷酶，用于脉冲疾病的潜在治疗
3. N-octyl-beta-valienamine up-regulates activity of F213I mutant beta-glucosidase in cultured cells: a potential chemical chaperone therapy for Gaucher disease [J] . Lin H, Sugimoto Y, Ohsaki Y, Biochimica et biophysica acta. Molecular basis of disease: BBA . 2004,第3期

机译：N-辛基-β-缬氨酸胺上调培养细胞中F213I突变体β-葡萄糖苷酶的活性：一种针对高雪氏病的潜在化学伴侣疗法
4. Qualitative and Quantitative Analysis of Novel Synphilin-1 Interactors Involved in Aggresome Formation and Parkinson Disease Pathogenesis Using Tandem Affinity Purification and Mass Spectrometry [C] . Xiaobin Xu, Anatoli B. Meriin, Nancy Leymarie, American Society for Mass Spectrometry Conference on Mass Spectrometry and Allied Topics . 2011

机译：用串联亲和纯化和质谱法，富含藻形成和帕金森病作用的新型傻瓜-1交互式的定性和定量分析
5. Patients' opinions on genetic counseling on the increased risk of Parkinson's disease among Gaucher disease carriers [D] . Mulhern, Maureen 2015

机译：患者对高彻病携带者中帕金森氏病风险增加的遗传咨询意见
6. Posttranslational processing of human lysosomal acid beta-glucosidase: a continuum of defects in Gaucher disease type 1 and type 2 fibroblasts. [O] . J E Bergmann, G A Grabowski 1989

机译：人溶酶体酸β-葡萄糖苷酶的翻译后加工：高雪氏病1型和2型成纤维细胞的连续缺陷。
7. Identification of a feedback loop involving beta-glucosidase 2 and its product sphingosine sheds light on the molecular mechanisms in Gaucher disease [O] . Schonauer, S., Körschen, H., Penno, A., 2017

机译：鉴定涉及β-葡糖苷酶2及其产物鞘氨醇的反馈环路揭示了戈谢病的分子机制

Lysosomal beta-glucosidase (GBA1) and non-lysosomal beta-glucosidase (GBA2): Potential involvement in the pathogenesis of Gaucher disease/Parkinson disease

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