找回密碼
 To register

QQ登錄

只需一步,快速開始

掃一掃,訪問微社區(qū)

打印 上一主題 下一主題

Titlebook: Rare Genetic Disorders; Advancements in Diag Muhammad Umair,Misbahuddin Rafeeq,Qamre Alam Book 2024 The Editor(s) (if applicable) and The A

[復(fù)制鏈接]
樓主: 小天使
31#
發(fā)表于 2025-3-27 00:42:59 | 只看該作者
Drug Discovery and Development for Rare Genetic Disorders,ologies for orphan diseases are discussed. Genome and pharmacogenetics studies provide interpretation for the disease etiology and treatment. Regarding the road map of small-molecule drug development, building up a compound library and bioassay development, virtual and experimental screening, hit co
32#
發(fā)表于 2025-3-27 04:07:14 | 只看該作者
Rare Genetic Disorders: Unraveling the Pathophysiology, Gene Mutations, and Therapeutic Advances inre integral components of Fabry disease management. Marfan syndrome is primarily associated with mutations in the FBN1 gene, encoding truncated or nonfunctional fibrillin-1. Altered fibrillin-1 structure disrupts connective tissue homeostasis, resulting in diverse clinical manifestations. Pathophysi
33#
發(fā)表于 2025-3-27 08:45:13 | 只看該作者
Current Insights into the Potential of Gene Therapy to Treat Rare Mitochondrial Diseases,s therapy is still in its early stages, further research is needed to determine its effectiveness and safety. This chapter explores the biology of the mitochondria, mutations, and prospective uses of gene therapy in the future to treat rare mitochondrial diseases.
34#
發(fā)表于 2025-3-27 10:09:13 | 只看該作者
Challenges and Future Opportunities in Rare Genetic Disorders: A Comprehensive Review,pment costs and little commercial potential. Next-generation sequencing (NGS) has greatly shortened diagnosis time. Genome or exome sequencing can discover causative mutations even in rare or undiagnosed illnesses. This technology and global collaborative networks like the Undiagnosed Diseases Netwo
35#
發(fā)表于 2025-3-27 16:03:09 | 只看該作者
36#
發(fā)表于 2025-3-27 18:29:30 | 只看該作者
37#
發(fā)表于 2025-3-28 00:08:43 | 只看該作者
K. Kumaran,Suruthi Abirami,Abna Ajeesh,J. Hemarangan,T. L. Vasanth Kanth,P. Shriya,K. N. Aruljothid behavioral science, are described among the 300 authoritative yet highly readable entries.?Students will find a world of information and insight behind the familiar fa?ade of the social networks in which they978-1-4614-6170-8
38#
發(fā)表于 2025-3-28 05:27:56 | 只看該作者
39#
發(fā)表于 2025-3-28 07:17:15 | 只看該作者
Nithar Ranjan Madhu,Goutam Biswas,Soumosish Paul,Suman Adhikari,Bhanumati Sarkar,Misbahuddin M. Rafed behavioral science, are described among the 300 authoritative yet highly readable entries.?Students will find a world of information and insight behind the familiar fa?ade of the social networks in which they978-1-4614-6170-8
40#
發(fā)表于 2025-3-28 14:23:19 | 只看該作者
he book reviews the current challenges in the diagnosis and treatment of the patients of rare genetic disorders and future opportunities. This book is useful for clinical geneticists, molecular and biochemical 978-981-99-9325-3978-981-99-9323-9
 關(guān)于派博傳思  派博傳思旗下網(wǎng)站  友情鏈接
派博傳思介紹 公司地理位置 論文服務(wù)流程 影響因子官網(wǎng) 吾愛論文網(wǎng) 大講堂 北京大學(xué) Oxford Uni. Harvard Uni.
發(fā)展歷史沿革 期刊點(diǎn)評 投稿經(jīng)驗(yàn)總結(jié) SCIENCEGARD IMPACTFACTOR 派博系數(shù) 清華大學(xué) Yale Uni. Stanford Uni.
QQ|Archiver|手機(jī)版|小黑屋| 派博傳思國際 ( 京公網(wǎng)安備110108008328) GMT+8, 2025-10-5 08:19
Copyright © 2001-2015 派博傳思   京公網(wǎng)安備110108008328 版權(quán)所有 All rights reserved
快速回復(fù) 返回頂部 返回列表
新化县| 开阳县| 昭觉县| 康马县| 泸定县| 阿拉尔市| 青浦区| 扶沟县| 新化县| 苏尼特左旗| 柯坪县| 青河县| 大新县| 准格尔旗| 东至县| 中超| 东阿县| 乐东| 石狮市| 陵川县| 山阴县| 绍兴市| 甘孜县| 花莲县| 利辛县| 荃湾区| 漳平市| 邓州市| 凤山县| 泗水县| 荆州市| 花垣县| 广州市| 宾川县| 法库县| 阿城市| 鄂尔多斯市| 阳西县| 巴林左旗| 富裕县| 沁水县|