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PRDM12:疼痛研究的新机遇。

PRDM12: New Opportunity in Pain Research.

机构信息

Department of Neurology, Medical University of Vienna, Vienna, Austria.

Department of Neurology, Medical University of Vienna, Vienna, Austria; Ludwig Boltzmann Institute for Rare and Undiagnosed Diseases, Vienna, Austria; CeMM Research Center for Molecular Medicine of the Austrian Academy of Sciences, Vienna, Austria.

出版信息

Trends Mol Med. 2020 Oct;26(10):895-897. doi: 10.1016/j.molmed.2020.07.007. Epub 2020 Aug 20.

DOI:10.1016/j.molmed.2020.07.007
PMID:32828702
Abstract

PRDM12 is a newly identified causative gene for a type of congenital insensitivity to pain disorder, which is characterized by the inability to perceive pain. Here, we discuss the (patho)physiology of PRDM12 function and the opportunities and challenges those data provide for novel therapeutic approaches in various pain disorders.

摘要

PRDM12 是一种新发现的先天性无痛症的致病基因,其特征是无法感知疼痛。在这里,我们讨论了 PRDM12 功能的(病理)生理学,以及这些数据为各种疼痛障碍的新型治疗方法提供的机会和挑战。

相似文献

1
PRDM12: New Opportunity in Pain Research.PRDM12:疼痛研究的新机遇。
Trends Mol Med. 2020 Oct;26(10):895-897. doi: 10.1016/j.molmed.2020.07.007. Epub 2020 Aug 20.
2
Structural and functional annotation of PR/SET Domain (PRDM) protein family: In-silico study elaborating role of PRDM12 mutation in congenital insensitivity to pain.PR/SET 结构域(PRDM)蛋白家族的结构和功能注释:通过计算机模拟研究阐述 PRDM12 突变在先天性无痛症中的作用。
Comput Biol Chem. 2020 Dec;89:107382. doi: 10.1016/j.compbiolchem.2020.107382. Epub 2020 Sep 24.
3
Clinical features for diagnosis and management of patients with PRDM12 congenital insensitivity to pain.PRDM12先天性无痛觉患者诊断与管理的临床特征
J Med Genet. 2016 Aug;53(8):533-5. doi: 10.1136/jmedgenet-2015-103646. Epub 2016 Mar 14.
4
Loss of Prdm12 during development, but not in mature nociceptors, causes defects in pain sensation.在发育过程中丢失 Prdm12,但在成熟的伤害感受器中不丢失,会导致痛觉感觉缺陷。
Cell Rep. 2021 Mar 30;34(13):108913. doi: 10.1016/j.celrep.2021.108913.
5
PRDM12 in Health and Diseases.PRDM12 在健康与疾病中的作用
Int J Mol Sci. 2021 Nov 6;22(21):12030. doi: 10.3390/ijms222112030.
6
Midface toddler excoriation syndrome (MiTES) can be caused by autosomal recessive biallelic mutations in a gene for congenital insensitivity to pain, PRDM12.先天性无痛症相关基因 PRDM12 的常染色体隐性双等位基因突变可导致婴儿中颜面中部擦烂综合征(MiTES)。
Br J Dermatol. 2018 Nov;179(5):1135-1140. doi: 10.1111/bjd.16893. Epub 2018 Sep 16.
7
Transcriptional regulator PRDM12 is essential for human pain perception.转录调节因子PRDM12对人类疼痛感知至关重要。
Nat Genet. 2015 Jul;47(7):803-8. doi: 10.1038/ng.3308. Epub 2015 May 25.
8
Prdm12 modulates pain-related behavior by remodeling gene expression in mature nociceptors.PRDM12 通过重塑成熟伤害感受器中的基因表达来调节疼痛相关行为。
Pain. 2022 Aug 1;163(8):e927-e941. doi: 10.1097/j.pain.0000000000002536. Epub 2021 Dec 24.
9
Ocular manifestations among patients with congenital insensitivity to pain due to variants in PRDM12 and SCN9A genes.PRDM12 和 SCN9A 基因突变导致先天性痛觉缺失症患者的眼部表现。
Am J Med Genet A. 2022 Dec;188(12):3463-3468. doi: 10.1002/ajmg.a.62968. Epub 2022 Sep 16.
10
Midfacial toddler excoriation syndrome (MiTES): case series, diagnostic criteria and evidence for a pathogenic mechanism.婴儿期面中部擦烂综合征(MiTES):病例系列、诊断标准和发病机制的证据。
Br J Dermatol. 2024 Aug 14;191(3):437-446. doi: 10.1093/bjd/ljae151.

引用本文的文献

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Brain-body physiology: Local, reflex, and central communication.脑-体生理学:局部、反射及中枢通讯
Cell. 2024 Oct 17;187(21):5877-5890. doi: 10.1016/j.cell.2024.08.050.
2
Loss of G9a does not phenocopy the requirement for Prdm12 in the development of the nociceptive neuron lineage.G9a 的缺失并不表现出在伤害感受神经元谱系发育中对 Prdm12 的需求。
Neural Dev. 2024 Jan 2;19(1):1. doi: 10.1186/s13064-023-00179-7.
3
Prdm12 represses the expression of the visceral neuron determinants Phox2a/b in developing somatosensory ganglia.
Prdm12在发育中的躯体感觉神经节中抑制内脏神经元决定因子Phox2a/b的表达。
iScience. 2023 Oct 31;26(12):108364. doi: 10.1016/j.isci.2023.108364. eCollection 2023 Dec 15.
4
Developmental exposure to the pesticide malathion enhances expression of Prdm12, a regulator of nociceptor development, in .发育期接触杀虫剂马拉硫磷会增强伤害感受器发育调节因子Prdm12的表达。
MicroPubl Biol. 2023 Mar 20;2023. doi: 10.17912/micropub.biology.000786. eCollection 2023.
5
Congenital insensitivity to pain associated with mutation: Two case reports and a literature review.与突变相关的先天性无痛觉:两例病例报告及文献综述。
Front Genet. 2023 Mar 20;14:1139161. doi: 10.3389/fgene.2023.1139161. eCollection 2023.
6
Transcription factor mesenchyme homeobox protein 2 (MEOX2) modulates nociceptor function.转录因子间充质同源盒蛋白 2(MEOX2)调节伤害感受器功能。
FEBS J. 2022 Jun;289(12):3457-3476. doi: 10.1111/febs.16347. Epub 2022 Feb 16.
7
PRDM12 in Health and Diseases.PRDM12 在健康与疾病中的作用
Int J Mol Sci. 2021 Nov 6;22(21):12030. doi: 10.3390/ijms222112030.
8
Genome-wide association study of problematic opioid prescription use in 132,113 23andMe research participants of European ancestry.全基因组关联研究显示,在欧洲血统的 132113 名 23andMe 研究参与者中,阿片类药物处方的使用存在问题。
Mol Psychiatry. 2021 Nov;26(11):6209-6217. doi: 10.1038/s41380-021-01335-3. Epub 2021 Nov 2.
9
PRDM12 Is Transcriptionally Active and Required for Nociceptor Function Throughout Life.PRDM12具有转录活性,是整个生命周期中伤害感受器功能所必需的。
Front Mol Neurosci. 2021 Sep 27;14:720973. doi: 10.3389/fnmol.2021.720973. eCollection 2021.
10
Loss of Prdm12 during development, but not in mature nociceptors, causes defects in pain sensation.在发育过程中丢失 Prdm12,但在成熟的伤害感受器中不丢失,会导致痛觉感觉缺陷。
Cell Rep. 2021 Mar 30;34(13):108913. doi: 10.1016/j.celrep.2021.108913.