關於 dystrophin中文 ，我們在網路上蒐集到這些相關的討論、資訊與評價

#11. Duchenne型肌营养不良基因治疗研究进展 - NCBI

DMD是由DMD基因突变导致其编码的抗肌萎缩蛋白（dystrophin）缺失或功能丧失引起的。Dystrophin蛋白位于肌细胞膜下的胞质内，其通过连接肌动蛋白和dystrophin相关跨膜糖蛋白 ...

#12. 裘馨氏肌肉萎縮症藥物治療進展 - 藥學雜誌電子報130期

... 基因治療、Duchenne muscular dystrophy、dystrophin、gene therapy ... 在肌肉失養蛋白(dystrophin) 有異常的表現，患者肌膜容易破裂，導致血清 ...

#13. 肌肉萎縮蛋白英文，dystrophin中文，心理學名詞 - 三度漢語網

中文 肌肉萎縮蛋白. 英文 dystrophin. 學術領域 心理學名詞. 肌肉萎缩蛋白用英文怎麼說？ dystrophin. 【肌肉萎縮蛋白】相關詞彙中英文 ...

#14. dystrophin的中文意思 - Dict.site 英漢/漢英線上英文字典

dystrophin 中文 意思是什麼. dystrophin 解釋. 肌營養不良蛋白. 例句. Observation of bone marrow reconstitution and dystrophin expression after bone marrow ...

#15. 异体骨髓干细胞移植后假肥大型肌营养不良症模型鼠膈肌 ...

Dystrophin Expression and Pathology of Diaphragm Muscles of Mdx Mice after ... 簡體中文. 假肥大型肌营养不良症 ； mdx鼠 ； 膈肌 ； 骨髓移植 ； 抗肌萎缩蛋白 ...

#16. 建立以濾紙血片檢測裘馨氏肌肉失養症基因的方法

關鍵字: 裘馨氏肌肉失養症,肌肉萎縮蛋白基因,濾紙血片,目標區間外顯子組定序,基因診斷, Duchenne muscular dystrophy,dystrophin gene,DMD,dried blood spots,targeted ...

#17. Anti-Dystrophin antibody, Mouse monoclonal - Sigma-Aldrich

Anti-Dystrophin antibody, Mouse monoclonal clone MANDRA1, purified from hybridoma cell culture; Synonyms: 抗DMD抗体; find Sigma-Aldrich-SAB4200763 MSDS, ...

#18. Mutational profile of the dystrophin gene | TACG - Dove ...

Changes in dystrophin protein synthesis is correlated with clinical manifestations, characterized by progressive muscle necrosis, loss of ...

#19. Utrophin Compensates dystrophin Loss during Mouse ...

Utrophin Compensates dystrophin Loss during Mouse Spermatogenesis. Hung Chih Chen, Yu Feng Chin, David J. Lundy, Chung Tiang Liang, Ya Hui Chi, Paolin Kuo, ...

#20. Dystrophin 释义| 柯林斯英语词典

Dystrophin 释义: a protein , the absence of which is believed to cause muscular dystrophy | 意思、发音、翻译及示例.

#21. dystrophin — 中文翻译- TechDico辞書

包含许多翻译示例按活动分类“dystrophin” – 英语-中文字典和智能翻译助手。 ... is a lethal muscle wasting disease caused by mutations in the dystrophin gene.

#22. Behavioral, Biochemical and Pathological ... - IMSEAR at SEARO

Background Duchenne muscular dystrophy (DMD) is an X-linked inherited neuromuscular disorder due tomutations in the dystrophin gene. Animal models that ...

#23. Anti-Dystrophin抗体(ab15277) - Abcam中文官网

购买Dystrophin兔多克隆抗体(ab15277)，Dystrophin抗体，可与人,小鼠样本反应。308篇文献引用，23个独立用户反馈。中国现货速达。

#24. Anti-dystrophin Antibody (3B7) | SCBT

dystrophin Antibody (3B7) is a mouse monoclonal IgG2a (kappa light chain) provided at 200 µg/ml; raised against recombinant fragment of human dystrophin ...

#25. 02.肌肉疾病的診斷< 認識疾病< 疾病照護 - 中華民國肌萎縮症 ...

目前應用比較廣泛如dystrophin的免疫組織化學染色，對於診斷因dystrophin缺乏所造成的杜顯氏肌肉失養症(Duchenne muscular dystrophy)及貝克氏肌肉失養症(Becker ...

#26. 轉寄 - 博碩士論文行動網

語文別: 中文 ... 致病原因是由於dystrophin基因突變導致肌肉細胞不能正常產生肌縮蛋白，會使鈣離子滲入細胞，使肌纖維壞死，進而導致患者全身肌肉無力。

#27. 認識罕見疾病裘馨氏肌肉萎縮症與物理治療介紹 - 羅東聖母醫院

... 縮寫DMD)又稱裘馨氏肌肉失. 養症或杜顯式肌肉萎縮症。此疾病為性聯遺傳，為進行性疾病。其成因為X. 染色體短臂Xp21.2 變異或病變，影響肌縮蛋白(dystrophin)組成。

#28. p-dystrophin see pukinje cell dystrophin 中文意思是什麼 - TerryL

p-dystrophin see pukinje cell dystrophin 中文意思是什麼 · p: · dystrophin: 肌營養不良蛋白 · see: n 【宗教】主教的職位[權力]；主教的轄區。 · pukinje: 年普金耶 · cell: ...

#29. dystrophin | Example sentences

dystrophin isn't in the Cambridge Dictionary yet. You can help! Add a definition. Intracellularly, -dystroglycan is linked to the actin cytoskeleton by its ...

#30. 最近上傳

正體中文 | 简体中文 | 全文筆數/總筆數: 17488/30367 ... 2009, DYSTROPHIN免疫組織染色在女性呈現非對稱性肌病變與肌痙攣之診斷價值 · 陳泰亨; 黃婉婷; 陳婉姿; ...

#31. eteplirsen | Michigan Medicine

Eteplirsen works by helping the body produce a protein called dystrophin. Dystrophin is a protein that helps stabilize the structure of muscle tissue and is ...

#32. 相关检查

language. 中文(简体) Chinese (Simplified) ... 一旦明确了dystrophin基因上的确切突变，患儿母亲也应该接受基因检测明确自己是否为携带者。这对于患儿母亲家族中的 ...

#33. Prenatal diagnosis of Duchenne muscular dystrophy revealed ...

Duchenne muscular dystrophies (DMDs) are X-linked recessive neuromuscular disorders with malfunction or absence of the Dystrophin protein.

#34. 裘馨氏肌肉萎縮症 - 慧智基因

... 是肌肉萎縮症中最常見的一種，根據歐美統計每十萬新生男嬰中有約20~30人患病，其致病原因是位於X染色體短臂Xp21的Dystrophin基因(DMD gene)有異常 ...

#35. 杜兴氏肌肉营养不良症_百度百科

杜兴氏肌肉营养不良症（ Duchenne Muscular Dystrophy ， DMD ），乃遗传性肌肉萎缩病。它的基因（ Dystrophin gene ）存在于X 性染色体中（ Xp21 ），因此它是透过性连锁 ...

#36. 美国ACCDON公司旗下品牌 - SCI论文修改

推荐同事 机构合作 中文 繁體中文 English 한국어 日本語 Português Español. 美国ACCDON公司旗下品牌 ... 中英对照. 抗肌萎缩蛋白. dystrophin. 学科分类.

#37. 杜興氏肌肉營養不良的診斷與護理(Duchenne Muscular ...

失序，使肌肉不能製造肌營養不良蛋白(Dystrophin)或製造不足，導致肌肉營養不良。肌肉活組 ... 中文翻譯. 解釋. Applied behaviour analysis. 應用行為分析.

#38. 小鼠Dystrophin (DMD) 蛋白, Recombinant - ELISA试剂盒- 抗体

Recombinant Dystrophin (DMD) 蛋白. 宿主: 小鼠. 宿主: 大肠杆菌（E. Coli）. 产品编号ABIN3009210.

#39. Dystrophin Images, Stock Photos & Vectors | Shutterstock

Find dystrophin stock images in HD and millions of other royalty-free stock photos, illustrations and vectors in the Shutterstock collection.

#40. Dystrophin Antibody - DF8748 - affinity_biosciences - Affinity ...

Alternative Names:Expand▽. BMD; CMD3B; DMD; DMD_HUMAN; Duchenne muscular dystrophy protein; Dystrophin; Muscular dystrophy Duchenne and Becker types; ...

#41. 進行性肌肉營養不良 - 中文百科知識

杜興氏肌肉營養不良症（ Duchenne Muscular Dystrophy ， DMD ），乃遺傳性肌肉萎縮病。它的基因（ Dystrophin gene ）存在於X 性染色體中（ Xp21 ），因此它是透過性連鎖 ...

#42. Gene Therapy for Duchenne Muscular Dystrophy - Johns ...

Nance explains that DMD is caused by deletions, duplications, point mutations or premature stop codons in the gene that makes dystrophin, ...

#43. 资源环境科技发展态势分析平台

Genomic analysis identifies frequent deletions of Dystrophin in olfactory neuroblastoma.NATURE COMMUNICATIONS,9. MLA, Gallia, Gary L.,et al."Genomic analysis ...

#44. 中国西南地区170例杜氏/贝氏肌营养不良症dystrophin基因变异 ...

中文 摘要: 目的构建中国西南地区杜氏/贝氏肌营养不良症（DMD/BMD）dystrophin基因变异谱，探讨dystrophin基因型与临床表型之间的关系。方法采用多重连接探针扩增 ...

#45. Combined gene therapy via VEGF and mini-dystrophin ...

We have demonstrated the efficacy of combined rAAV-mediated dystrophin and VEGF treatment of temporalis muscles in a DMD mouse model. 中文 ...

#46. 多重连接依赖的探针扩增技术在Dystrophin 基因外显子拷贝数 ...

方法应用MLPA对70例确诊的Duchenne/Becker肌营养不良(Duchenne/Becker musculardystrophy,DMD/BMD)患者进行Dystrophin基因外显子缺失及扩增的检测.

#47. 限定检索结果 - 北京联合大学

Background: Dystrophin Dp71 is one of the isoforms produced by the DMD gene which is mutated in patients with Duchenne muscular dystrophy (DMD).

#48. 後基因體時代之生物技術 - 陽明大學

independently expressing both full-length dystrophin and β-galactosidase. Proc. Natl. Acad. Sci. ... 流式細胞技術中文教學網站.

#49. 2020 年實驗動物科學（技術篇）

中文 實驗動物科學教科書，期望國內學校能多利用於大學部與研究所的教學， ... 蛋白（dystrophin）基因剔除小鼠就是這種情況，其發展出與人類相似的嚴重肌營.

#50. Duchenne Muscular Dystrophy and Becker Muscular Dystrophy

Diagnosis is suggested clinically and is confirmed by genetic testing or analysis of the protein product (dystrophin) of the mutated gene.

#51. CRISPR/Cas9 Technology in Restoring Dystrophin ... - JoVE

Duchenne muscular dystrophy (DMD) is a severe progressive muscle disease caused by mutations in the dystrophin gene, which ultimately leads to ...

#52. Promising New Approach to Treat Duchenne Muscular ...

Skeletal muscles without dystrophin (column A) and after dystrophin has been restored (column B), using the CRISPR/Cas9 platform developed by UCLA scientists.

#53. dystrophin翻译为：肌萎缩蛋白

dystrophin 的中文意思：肌萎缩蛋白，点击查看详细解释：dystrophin的中文翻译、dystrophin的发音、音标、用法和双语例句等，让你有效掌握dystrophin这个单词。

#54. Duchenne Muscular Dystrophy (for Parents) - Kids Health

So girls can almost always make working dystrophin using the dystrophin gene on their second X chromosome. But girls with a Duchenne MD gene may still have ...

#55. Eteplirsen (Intravenous Route) Description and Brand Names

Eteplirsen injection is used to treat Duchenne muscular dystrophy (DMD) in patients with a confirmed mutation of the dystrophin gene amenable to exon 51 ...

#56. 抗肌萎缩蛋白病（dystrophinopathies） - 中文版GeneReviews

Mildly 受累的 individuals with confirmatory DMD molecular genetic studies and/or dystrophin studies on muscle biopsy have been classified as ...

#57. Discovery of New Dystrophin Protein Paves Way for DMD ...

Duchenne muscular dystrophy, or DMD, is caused by mutations in the gene that encodes dystrophin, which plays a role in stabilizing the membrane ...

#58. Duchenne and Becker Muscular Dystrophies - DynaMed

Definitions · spectrum of muscle disease caused by pathogenic variants of DMD gene that encodes dystrophin protein · mild forms include asymptomatic disease with ...

#59. 完整显示页面 - Ex Libris

Intravenous Infusion of an Antisense Oligonucleotide Results in Exon Skipping in Muscle Dystrophin mRNA of Duchenne Muscular Dystrophy.-article.

#60. 肢帶型進行性肌肉萎縮症診斷要件 - 隨意窩

例如說，貝克型肌萎症(Becker type muscular dystrophy)和肌縮蛋白(dystrophin)變異的表現型帶原者，在作直接基因分析和肌縮蛋白分析前常被診斷為「肢帶型肌萎症」，而 ...

#61. 新的杜氏肌肉萎缩症的药物和新的药物 - TheSocialMedwork

它是由X染色体上的Dystrophin基因突变引起的，导致Dystrophin蛋白的缺失，这种蛋白有助于保持肌肉细胞的完整性。它是最普遍的神经肌肉疾病，在全世界每3600个男婴中就 ...

#62. A novel high-throughput immunofluorescence analysis ... - Gale

Duchenne muscular dystrophy (DMD, MIM 310200) is a severe form of muscular dystrophy caused by mutations in the dystrophin gene (DMD ) that leads to a lack ...

#63. Pharmacologic Treatment of Duchenne Muscular Dystrophy

dystrophin protein levels), to the genetic testing (looking for the defective dystrophin gene). ... 中文 (Chinese):. 本通知有重要的訊息。

#64. Duchenne muscular dystrophy - What is DMD, diagnosis

If genetic tests are unclear, as they sometimes are, your child might need a muscle biopsy to check for dystrophin in the muscle. Duchenne muscular dystrophy is ...

#65. Becker型肌营养不良和X‐连锁扩张型心肌病心脏并发症的干预 ...

抗肌萎缩蛋白（dystrophin）是肌肉正常工作所必需的。DMD，BMD和XLDCM是由于控制dystrophin蛋白生成的基因变化引起的遗传性疾病。

#66. 多重解析地址选择页面 - 中文DOI

Title：, Clinical application of multiplex ligation-dependent probe amplification for the detection exonic copy number alterations in the Dystrophin gene.

#67. Preventing and treating heart complications in Duchenne and ...

The protein dystrophin is essential for muscles to work normally. DMD, BMD and XLDCM are inherited muscle diseases caused by changes in the ...

#68. Muscular dystrophy: Repair the muscles, not the genetic defect

Though these mice did not have the defect in dystrophin, they still developed muscular dystrophy-like muscle characteristics. When researchers ...

#69. Exon Skipping - Graphic - NYTimes.com

The dystrophin. gene. X chromosome. EXPERIMENTAL DRUGS introduce synthetic RNA designed to block exon 51, which creates a shortened but ...

#70. 大连理工大学主页平台管理系统崔昌浩--中文主页--论文成果

Dystrophin conferral using human endothelium expressing HLA-E in the non-immunosuppressive murine model of Duchenne muscular dystrophy.

#71. James Richardson - Executive Director, Global Development ...

Experience · Executive Director, Global Development Team Lead (Micro-dystrophin) · Team Lead Global Medical Affairs Leads · Senior Director Global Medical Affairs.

#72. 基因缺陷與兒童心臟血管疾病 - 馬偕紀念醫院小兒心臟科衛教資訊

因此， dystrophin 和DAG ，以及MLP 的基因突變都可能造成肌細胞死亡，進而導致老鼠和人類的擴張性心肌症。例如性聯遺傳的Duchenne 氏肌營養不良症（ Duchene muscular ...

#73. 神經肌肉病變的整體復健治療 - 臺北榮民總醫院

本病是因為肌肉細胞幾乎完全缺乏dystrophin所致，dystrophin可說是肌肉細胞的骨架之一，可加強肌肉細胞膜的韌度及彈性。在嬰兒時期雖然當時還沒有明顯 ...

#74. 肌肉組織

骨骼肌細胞的. 表面染成褐色. 是含有 dystrophin。 Page 17. Skeletal muscle blood supply. Endothelial cells stain brown with immunohistochemical.

#75. Vyondys 53 (golodirsen) - Wellmark

FDA approval of Vyondys 53 (golodirsen) was based on an increase in a surrogate marker, dystrophin production in skeletal muscle during a single two-part ...

#76. 西湖大学常兴团队利用碱基编辑，在小鼠模型中治愈杜氏肌营养 ...

其发病原因在于DMD基因突变，造成肌营养不良蛋白Dystrophin表达缺失，引发骨骼肌和心肌的严重缺陷。 作为最常见的致死性遗传病之一，估计每3500-5000 ...

#77. ~彰化基督教醫院罕見疾病電子報~ 第三十五期

依據影響的肌肉蛋白不同，可概略分成Dystrophin– glycoprotein complex 的病變(LGMD2C-F,P) 、肌小節(sarcomere) 相關蛋白的病變(LGMD1A; ...

#78. Dystrophin Antibodies - IHC Primary Antibodies - Histology ...

Duchenne Muscular dystrophy (DMD) is the most common of the muscular dystrophies resulting in progressive muscular wasting and death. Dystrophin is the 427kD ...

#79. 诺西那生钠可以应用于所有的肌营养不良症么？不可随意用药！

这是由于该疾病的致病基因十分明确，有且只有一个，就是dystrophin，中文名既可以是肌营养不良蛋白，又可以叫做抗肌萎缩蛋白。

#80. Duchenne and Becker muscular dystrophy - MedlinePlus

The DMD gene provides instructions for making a protein called dystrophin . This protein is located primarily in skeletal and cardiac muscle, where it helps ...

#81. Leiden Muscular Dystrophy Pages

dystrophin, the dystrophin-associated glyco-protein complex (DGC - dystroglycans, sarcoglycans, sarcospan, syntrophins), homologous proteins (utrophin, ...

#82. Becker Muscular Dystrophy (BMD) - Diseases

The dystrophin protein keeps the muscle cell membrane from breaking or tearing when our muscles contract and relax. Because it connects the center of the ...

#83. 利用两种基因编辑策略精确校正DMD外显子缺失突变 - 生物谷

尽管科学家们几十年来已知抗肌萎缩蛋白（dystrophin）编码基因发生让这种蛋白不能表达的突变导致这种疾病，但是迄今为止还没有一种有效的治疗方法存在 ...

#84. What is exon skipping and how does it work? - Muscular ...

In order to explain the concept of exon skipping, it is first necessary to explain how genes work and how mutations in the dystrophin gene can cause both ...

#85. Sarepta Therapeutics Announces FDA Approval of AMONDYS ...

This indication is based on a statistically significant increase in dystrophin production in skeletal muscle observed in patients treated ...

#86. Duchenne muscular dystrophy (DMD) – information for carriers

DMD is caused by a gene change or alteration, called a genetic mutation, in the dystrophin gene on the X chromosome. DMD can occur randomly in a family or ...