• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

相似文献

1
Special Issue "Genetics and Epigenetics in Endocrine Disorders".特刊:内分泌紊乱的遗传学和表观遗传学
Genes (Basel). 2023 Sep 5;14(9):1763. doi: 10.3390/genes14091763.
2
Search for Novel Mutational Targets in Human Endocrine Diseases.寻找人类内分泌疾病中的新突变靶标。
Endocrinol Metab (Seoul). 2019 Mar;34(1):23-28. doi: 10.3803/EnM.2019.34.1.23.
3
Harnessing the full potential of reproductive genetics and epigenetics for male infertility in the era of "big data".在“大数据”时代,挖掘生殖遗传学和表观遗传学在男性不育症中的全部潜能。
Fertil Steril. 2020 Mar;113(3):478-488. doi: 10.1016/j.fertnstert.2020.01.001. Epub 2020 Feb 20.
4
The emerging field of forensic epigenetics.新兴的法医表观遗传学领域。
Forensic Sci Int. 2018 Sep;290:e24-e25. doi: 10.1016/j.forsciint.2018.07.019. Epub 2018 Jul 26.
5
Editorial: Interaction of endocrine disorders and metabolic associated fatty liver disease: the genetic and epigenetic basis.社论:内分泌紊乱与代谢相关脂肪性肝病的相互作用:遗传和表观遗传基础
Front Endocrinol (Lausanne). 2023 Nov 7;14:1308860. doi: 10.3389/fendo.2023.1308860. eCollection 2023.
6
Basic Concepts of Genetics.遗传学的基本概念
Exp Suppl. 2019;111:3-19. doi: 10.1007/978-3-030-25905-1_1.
7
Osteoarthritis year in review 2023: genetics, genomics, and epigenetics.2023年骨关节炎年度回顾:遗传学、基因组学和表观遗传学
Osteoarthritis Cartilage. 2024 Feb;32(2):128-137. doi: 10.1016/j.joca.2023.11.006. Epub 2023 Nov 17.
8
Epigenetic Approaches in Non-Model Plants.非模式植物中的表观遗传方法。
Methods Mol Biol. 2020;2093:203-215. doi: 10.1007/978-1-0716-0179-2_14.
9
The Contributions of Nursing to Genetics, Epigenetics, Genomics, and Epigenomics: A Word From the Current President of ISONG.护理对遗传学、表观遗传学、基因组学和表观基因组学的贡献:国际护理基因组学学会现任主席的发言
Biol Res Nurs. 2015 Jul;17(4):362-3. doi: 10.1177/1099800415586250.
10
Genomics into Healthcare: the 5th Pan Arab Human Genetics Conference and 2013 Golden Helix Symposium.基因组学融入医疗保健:第五届泛阿拉伯人类遗传学会议暨2013年金色螺旋研讨会
Hum Mutat. 2014 May;35(5):637-40. doi: 10.1002/humu.22530. Epub 2014 Mar 31.

本文引用的文献

1
Expression Profiling of , , and in the Liver and Pancreas of Recovering Streptozotocin-Induced Diabetic Rats.恢复性链脲佐菌素诱导糖尿病大鼠肝脏和胰腺中、和的表达谱。
Genes (Basel). 2022 Sep 10;13(9):1625. doi: 10.3390/genes13091625.
2
Interactome of PTH-Regulated miRNAs and Their Predicted Target Genes for Investigating the Epigenetic Effects of PTH (1-34) in Bone Metabolism.甲状旁腺激素调节的 miRNA 及其预测靶基因的相互作用组,用于研究甲状旁腺激素(1-34)在骨代谢中的表观遗传效应。
Genes (Basel). 2022 Aug 13;13(8):1443. doi: 10.3390/genes13081443.
3
An Adolescent Boy with Klinefelter Syndrome and 47,XXY/46,XX Mosaicism: Case Report and Review of Literature.一名患有克氏综合征和 47,XXY/46,XX 嵌合体的青少年男性:病例报告及文献复习。
Genes (Basel). 2022 Apr 23;13(5):744. doi: 10.3390/genes13050744.
4
Long-Term Follow-Up of Three Family Members with a Novel Pathogenic Variant Causing Primary Adrenal Insufficiency.新型致病性变异导致原发性肾上腺功能不全的三例家系成员的长期随访。
Genes (Basel). 2022 Apr 20;13(5):717. doi: 10.3390/genes13050717.
5
Pathogenesis of Type 1 Diabetes: Established Facts and New Insights.1 型糖尿病的发病机制:既有事实和新见解。
Genes (Basel). 2022 Apr 16;13(4):706. doi: 10.3390/genes13040706.
6
The Role of Epigenetic Modifications in Late Complications in Type 1 Diabetes.表观遗传修饰在 1 型糖尿病晚期并发症中的作用。
Genes (Basel). 2022 Apr 15;13(4):705. doi: 10.3390/genes13040705.
7
A Novel Splice-Site Deletion in the Gene Causes Combined Pituitary Hormone Deficiency in Multiple Sudanese Pedigrees.一个新的剪接位点缺失导致多个苏丹家系的联合垂体激素缺乏症。
Genes (Basel). 2022 Apr 8;13(4):657. doi: 10.3390/genes13040657.
8
Association of Long Non-Coding RNA Growth Arrest-Specific 5 Genetic Variants with Diabetic Retinopathy.长链非编码 RNA 生长停滞特异性 5 基因变异与糖尿病视网膜病变的关联。
Genes (Basel). 2022 Mar 25;13(4):584. doi: 10.3390/genes13040584.
9
Polymorphism and Endocrine Functions in Subjects with Morbid Obesity Undergoing Bariatric Surgery.病态肥胖患者接受减肥手术后的多态性和内分泌功能。
Genes (Basel). 2022 Jan 25;13(2):222. doi: 10.3390/genes13020222.
10
Detection of Del/Dup Inside /PAR1 Region in Children and Young Adults with Idiopathic Short Stature.检测特发性身材矮小儿童和青年人群的 /PAR1 区域内 Del/Dup 情况。
Genes (Basel). 2021 Sep 29;12(10):1546. doi: 10.3390/genes12101546.

特刊:内分泌紊乱的遗传学和表观遗传学

Special Issue "Genetics and Epigenetics in Endocrine Disorders".

机构信息

Laboratory for Translational Medical Biochemistry, Institute of Biochemistry and Molecular Genetics, Faculty of Medicine, University of Ljubljana, Vrazov trg 2, 1000 Ljubljana, Slovenia.

Clinical Institute for Special Laboratory Diagnostics, University Children's Hospital, University Medical Centre Ljubljana, Vrazov trg 1, 1000 Ljubljana, Slovenia.

出版信息

Genes (Basel). 2023 Sep 5;14(9):1763. doi: 10.3390/genes14091763.

DOI:10.3390/genes14091763
PMID:37761903
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10530912/
Abstract

In the last decade, the development of high-throughput sequencing methodologies has significantly improved the gathering of genomic information and consequent under-standing of the genetic and epigenetic background of complex and monogenetic endocrine disorders [...].

摘要

在过去的十年中,高通量测序方法的发展极大地提高了基因组信息的收集能力,从而加深了对复杂和单基因内分泌疾病的遗传和表观遗传背景的理解[... ]。