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The Profile of Articles on Mutations, Oligodontia, and Ethical Statements in Dental Research.关于基因突变、少牙症和牙科研究中伦理声明的文章概况。
J Empir Res Hum Res Ethics. 2022 Oct;17(4):412-425. doi: 10.1177/15562646221116801. Epub 2022 Jul 25.
2
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Novel missense mutations in the AXIN2 gene associated with non-syndromic oligodontia.与非综合征性少牙症相关的AXIN2基因中的新型错义突变。
Arch Oral Biol. 2014 Mar;59(3):349-53. doi: 10.1016/j.archoralbio.2013.12.009. Epub 2013 Dec 31.
4
A Novel AXIN2 Missense Mutation Is Associated with Non-Syndromic Oligodontia.一种新的AXIN2错义突变与非综合征性少牙症相关。
PLoS One. 2015 Sep 25;10(9):e0138221. doi: 10.1371/journal.pone.0138221. eCollection 2015.
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Nonsyndromic oligodontia : Does the Tooth Agenesis Code (TAC) enable prediction of the causative mutation?非综合征性少牙症:牙齿发育不全编码(TAC)能否预测致病突变?
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本文引用的文献

1
Authors submission guidelines, a survey of pediatric dentistry journals regarding ethical issues.作者投稿指南,对儿科学杂志的调查,关于伦理问题。
PLoS One. 2022 Jan 19;17(1):e0261881. doi: 10.1371/journal.pone.0261881. eCollection 2022.
2
Familial colorectal cancer and tooth agenesis caused by an AXIN2 variant: how do we detect families with rare cancer predisposition syndromes?AXIN2 变异导致的家族性结直肠癌和牙齿缺失:我们如何检测具有罕见癌症易感性综合征的家族?
Fam Cancer. 2022 Jul;21(3):325-332. doi: 10.1007/s10689-021-00280-y. Epub 2021 Oct 12.
3
Analyses of oligodontia phenotypes and genetic etiologies.少牙畸形表型与遗传病因分析。
Int J Oral Sci. 2021 Sep 30;13(1):32. doi: 10.1038/s41368-021-00135-3.
4
Reasons for and time to retraction of genetics articles published between 1970 and 2018.1970 年至 2018 年间发表的遗传学文章被撤稿的原因和时间。
J Med Genet. 2019 Nov;56(11):734-740. doi: 10.1136/jmedgenet-2019-106137. Epub 2019 Jul 12.
5
Phenotypic confirmation of oligodontia, colorectal polyposis and cancer in a family carrying an exon 7 nonsense variant in the AXIN2 gene.携带 AXIN2 基因外显子 7 无义变异的家族中,表现型确认少牙症、结直肠息肉和癌症。
Fam Cancer. 2019 Jul;18(3):311-315. doi: 10.1007/s10689-019-00120-0.
6
Exploring PubMed as a reliable resource for scholarly communications services.探索将PubMed作为学术交流服务的可靠资源。
J Med Libr Assoc. 2019 Jan;107(1):16-29. doi: 10.5195/jmla.2019.433. Epub 2019 Jan 1.
7
Nonsyndromic oligodontia : Does the Tooth Agenesis Code (TAC) enable prediction of the causative mutation?非综合征性少牙症:牙齿发育不全编码(TAC)能否预测致病突变?
J Orofac Orthop. 2017 Mar;78(2):112-120. doi: 10.1007/s00056-016-0056-y. Epub 2017 Feb 15.
8
Ethical Process Reporting in Indian Dental Journals.印度牙科期刊中的伦理过程报告
Account Res. 2016;23(3):163-177. doi: 10.1080/08989621.2015.1100540.
9
A Novel AXIN2 Missense Mutation Is Associated with Non-Syndromic Oligodontia.一种新的AXIN2错义突变与非综合征性少牙症相关。
PLoS One. 2015 Sep 25;10(9):e0138221. doi: 10.1371/journal.pone.0138221. eCollection 2015.
10
Novel missense mutations in the AXIN2 gene associated with non-syndromic oligodontia.与非综合征性少牙症相关的AXIN2基因中的新型错义突变。
Arch Oral Biol. 2014 Mar;59(3):349-53. doi: 10.1016/j.archoralbio.2013.12.009. Epub 2013 Dec 31.

关于基因突变、少牙症和牙科研究中伦理声明的文章概况。

The Profile of Articles on Mutations, Oligodontia, and Ethical Statements in Dental Research.

机构信息

Department of Dental Public Health and Professional Practice, School of Dentistry, West Virginia University, 104a Health Sciences Addition, PO Box 9415, Morgantown, WV 26506, USA.

出版信息

J Empir Res Hum Res Ethics. 2022 Oct;17(4):412-425. doi: 10.1177/15562646221116801. Epub 2022 Jul 25.

DOI:10.1177/15562646221116801
PMID:35876356
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9502021/
Abstract

PURPOSE

Editors often require ethical statements in research publications. This is particularly important with genetic data where discrimination may occur upon data disclosures. The purpose of this research is to determine if there was a positive trend of publishing ethical statements in dental genetic research. The study is limited to AXIN2 mutations which may be associated with oligodontia and cancer.

METHODS

A MEDLINE search of 2011-2021 articles concerning AXIN2, oligodontia, and ethical statements was conducted. Reviews, nonhuman subject research, abstracts, and articles not written nor translated into English were excluded.

RESULTS

Forty-four studies were found; 10 excluded. There were 25 (75.8%) with ethical statements, and 25 (75.8%) with participant consent statements. There was no significant difference by year in ethical statements over the ten years (p = 0.094).

CONCLUSION

There is a need to encourage more ethical statements in publications especially for genetically sensitive topics to reassure readers of ethical practices.

摘要

目的

编辑人员通常要求在研究出版物中包含伦理声明。对于可能会因数据披露而引发歧视的遗传数据来说,这一点尤为重要。本研究旨在确定在牙科遗传研究中发表伦理声明是否存在积极趋势。该研究仅限于可能与少牙症和癌症相关的 AXIN2 突变。

方法

对 2011 年至 2021 年期间有关 AXIN2、少牙症和伦理声明的 MEDLINE 文章进行了搜索。排除了综述、非人体研究、摘要以及未用英文撰写或翻译的文章。

结果

共发现 44 项研究,其中 10 项被排除。有 25 项(75.8%)包含伦理声明,25 项(75.8%)包含参与者同意声明。在这十年中,伦理声明的发表在年份上没有显著差异(p=0.094)。

结论

需要鼓励出版物中包含更多的伦理声明,特别是对于遗传敏感主题,以向读者保证伦理实践。