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1
Mutations in a novel gene, NHS, cause the pleiotropic effects of Nance-Horan syndrome, including severe congenital cataract, dental anomalies, and mental retardation.一种新基因NHS的突变会导致南斯-霍兰综合征的多种效应,包括严重先天性白内障、牙齿异常和智力迟钝。
Am J Hum Genet. 2003 Nov;73(5):1120-30. doi: 10.1086/379381. Epub 2003 Oct 16.
2
A novel Xp22.13 microdeletion in Nance-Horan syndrome.Xp22.13 区域新发缺失导致 Nance-Horan 综合征
Birth Defects Res. 2017 Jul 3;109(11):866-868. doi: 10.1002/bdr2.1032. Epub 2017 May 2.
3
Identification of the gene for Nance-Horan syndrome (NHS).南斯-霍兰综合征(NHS)基因的鉴定。
J Med Genet. 2004 Oct;41(10):768-71. doi: 10.1136/jmg.2004.022517.
4
A novel NHS mutation causes Nance-Horan Syndrome in a Chinese family.一种新的NHS突变在中国一个家族中导致了南斯-霍兰综合征。
BMC Med Genet. 2017 Jan 7;18(1):2. doi: 10.1186/s12881-016-0360-9.
5
Identification of a novel mutation in a Chinese family with Nance-Horan syndrome by whole exome sequencing.通过全外显子组测序鉴定一个患有南斯-霍兰综合征的中国家系中的新突变。
J Zhejiang Univ Sci B. 2014 Aug;15(8):727-34. doi: 10.1631/jzus.B1300321.
6
Nance-Horan syndrome in females due to a balanced X;1 translocation that disrupts the NHS gene: Familial case report and review of the literature.女性因X;1平衡易位破坏NHS基因所致的南斯-霍兰综合征:家族病例报告及文献复习
Ophthalmic Genet. 2018 Jan-Feb;39(1):56-62. doi: 10.1080/13816810.2017.1363245. Epub 2017 Sep 18.
7
A Turkish family with Nance-Horan Syndrome due to a novel mutation.一个土耳其家系患 Nance-Horan 综合征,致病原因为一种新的突变。
Gene. 2013 Aug 1;525(1):141-5. doi: 10.1016/j.gene.2013.03.094. Epub 2013 Apr 6.
8
The first missense mutation of NHS gene in a Tunisian family with clinical features of NHS syndrome including cardiac anomaly.NHS 基因在一个具有 NHS 综合征临床特征(包括心脏异常)的突尼斯家族中的首个错义突变。
Eur J Hum Genet. 2011 Aug;19(8):851-6. doi: 10.1038/ejhg.2011.52. Epub 2011 May 11.
9
Identification of three novel NHS mutations in families with Nance-Horan syndrome.在患有南斯-霍兰综合征的家族中鉴定出三种新的NHS突变。
Mol Vis. 2007 Mar 27;13:470-4.
10
[Clinical and genetic characterization of three families with Nance-Horan syndrome caused by NHS gene mutations].[NHS基因突变导致的三例南斯-霍兰综合征家系的临床与遗传学特征]
Zhonghua Yan Ke Za Zhi. 2024 Sep 11;60(9):757-765. doi: 10.3760/cma.j.cn112142-20231113-00230.

引用本文的文献

1
Genetic Landscape of Congenital Cataracts in a Swiss Cohort: Addressing Diagnostic Oversights in Nance-Horan Syndrome.瑞士队列中先天性白内障的遗传图谱:解决南斯-霍兰综合征的诊断疏漏
Biomedicines. 2025 Aug 2;13(8):1883. doi: 10.3390/biomedicines13081883.
2
Epilepsy in NHS actin remodeling regulator gene (NHS) and genotype-phenotype correlations.NHS肌动蛋白重塑调节基因(NHS)中的癫痫及基因型-表型相关性。
Pediatr Res. 2025 Aug 15. doi: 10.1038/s41390-025-04335-z.
3
The NHSL1-A complex interacts with the Arp2/3 complex and controls cell migration efficiency and chemotaxis.NHSL1-A复合物与Arp2/3复合物相互作用,并控制细胞迁移效率和趋化性。
bioRxiv. 2025 Mar 13:2025.03.13.643034. doi: 10.1101/2025.03.13.643034.
4
Nance-Horan-syndrome-like 1b controls mesodermal cell migration by regulating protrusion and actin dynamics during zebrafish gastrulation.南斯-霍兰综合征样1b通过在斑马鱼原肠胚形成过程中调节突起和肌动蛋白动力学来控制中胚层细胞迁移。
Commun Biol. 2025 Feb 28;8(1):328. doi: 10.1038/s42003-025-07689-6.
5
Identification of a novel single nucleotide deletion in the NHS causing Nance-Horan syndrome.在NHS中鉴定出导致南斯-霍兰综合征的一种新型单核苷酸缺失。
BMC Ophthalmol. 2025 Feb 24;25(1):92. doi: 10.1186/s12886-025-03933-z.
6
Genotype-Phenotype Correlations of Nance-Horan Syndrome in Male and Female Carriers of a Novel Variant.一种新型变异的男性和女性携带者中Nance-Horan综合征的基因型-表型相关性
Genes (Basel). 2025 Jan 16;16(1):91. doi: 10.3390/genes16010091.
7
NHSL3 controls single and collective cell migration through two distinct mechanisms.NHSL3 通过两种不同机制控制单个细胞和集体细胞迁移。
Nat Commun. 2025 Jan 2;16(1):205. doi: 10.1038/s41467-024-55647-3.
8
Spotlight on Hemorrhagic Destruction of the Brain, Subependymal Calcification, and Congenital Cataracts (HDBSCC).聚焦脑内出血性破坏、室管膜下钙化和先天性白内障(HDBSCC)。
Eye Brain. 2024 Oct 23;16:55-63. doi: 10.2147/EB.S419663. eCollection 2024.
9
Through the Gateway: A Brief History of Cataract Genetics.穿越门户:白内障遗传学简史。
Genes (Basel). 2024 Jun 14;15(6):785. doi: 10.3390/genes15060785.
10
Nance-Horan Syndrome: characterization of dental, clinical and molecular features in three new families.纳尔逊-霍兰综合征:三新家族的牙齿、临床和分子特征的描述。
BMC Oral Health. 2023 May 23;23(1):314. doi: 10.1186/s12903-023-03029-4.

本文引用的文献

1
Online Mendelian Inheritance in Man 'OMIM'.《人类孟德尔遗传在线》(OMIM)。
Indian J Dermatol Venereol Leprol. 2003 Nov-Dec;69(6):423-4.
2
Refinement of the NHS locus on chromosome Xp22.13 and analysis of five candidate genes.Xp22.13染色体上NHS基因座的细化及五个候选基因的分析
Eur J Hum Genet. 2002 Sep;10(9):516-20. doi: 10.1038/sj.ejhg.5200846.
3
A locus for isolated cataract on human Xp.人类X染色体短臂上的一个孤立性白内障基因座。
J Med Genet. 2002 Feb;39(2):105-9. doi: 10.1136/jmg.39.2.105.
4
Domain disruption and mutation of the bZIP transcription factor, MAF, associated with cataract, ocular anterior segment dysgenesis and coloboma.与白内障、眼前节发育异常和缺损相关的bZIP转录因子MAF的结构域破坏和突变。
Hum Mol Genet. 2002 Jan 1;11(1):33-42. doi: 10.1093/hmg/11.1.33.
5
Application of a time-delay neural network to promoter annotation in the Drosophila melanogaster genome.时延神经网络在黑腹果蝇基因组启动子注释中的应用。
Comput Chem. 2001 Dec;26(1):51-6. doi: 10.1016/s0097-8485(01)00099-7.
6
Monogenic causes of X-linked mental retardation.X连锁智力障碍的单基因病因。
Nat Rev Genet. 2001 Sep;2(9):669-80. doi: 10.1038/35088558.
7
Querkopf, a MYST family histone acetyltransferase, is required for normal cerebral cortex development.Querkopf是一种MYST家族组蛋白乙酰转移酶,是正常大脑皮层发育所必需的。
Development. 2000 Jun;127(12):2537-48. doi: 10.1242/dev.127.12.2537.
8
Missense mutations in the most ancient residues of the PAX6 paired domain underlie a spectrum of human congenital eye malformations.PAX6配对结构域最古老残基中的错义突变是一系列人类先天性眼部畸形的基础。
Hum Mol Genet. 1999 Feb;8(2):165-72. doi: 10.1093/hmg/8.2.165.
9
Efficiency assessment of the gene trap approach.基因捕获方法的效率评估。
Dev Dyn. 1998 Jun;212(2):171-80. doi: 10.1002/(SICI)1097-0177(199806)212:2<171::AID-AJA3>3.0.CO;2-E.
10
A novel homeobox gene PITX3 is mutated in families with autosomal-dominant cataracts and ASMD.一种新型同源盒基因PITX3在常染色体显性白内障和ASMD家系中发生突变。
Nat Genet. 1998 Jun;19(2):167-70. doi: 10.1038/527.

一种新基因NHS的突变会导致南斯-霍兰综合征的多种效应,包括严重先天性白内障、牙齿异常和智力迟钝。

Mutations in a novel gene, NHS, cause the pleiotropic effects of Nance-Horan syndrome, including severe congenital cataract, dental anomalies, and mental retardation.

作者信息

Burdon Kathryn P, McKay James D, Sale Michèle M, Russell-Eggitt Isabelle M, Mackey David A, Wirth M Gabriela, Elder James E, Nicoll Alan, Clarke Michael P, FitzGerald Liesel M, Stankovich James M, Shaw Marie A, Sharma Shiwani, Gajovic Srecko, Gruss Peter, Ross Shelley, Thomas Paul, Voss Anne K, Thomas Tim, Gécz Jozef, Craig Jamie E

机构信息

Menzies Centre for Population Health Research, University of Tasmania, Hobart, Australia.

出版信息

Am J Hum Genet. 2003 Nov;73(5):1120-30. doi: 10.1086/379381. Epub 2003 Oct 16.

DOI:10.1086/379381
PMID:14564667
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1180491/
Abstract

Nance-Horan syndrome (NHS) is an X-linked disorder characterized by congenital cataracts, dental anomalies, dysmorphic features, and, in some cases, mental retardation. NHS has been mapped to a 1.3-Mb interval on Xp22.13. We have confirmed the same localization in the original, extended Australian family with NHS and have identified protein-truncating mutations in a novel gene, which we have called "NHS," in five families. The NHS gene encompasses approximately 650 kb of genomic DNA, coding for a 1,630-amino acid putative nuclear protein. NHS orthologs were found in other vertebrates, but no sequence similarity to known genes was identified. The murine developmental expression profile of the NHS gene was studied using in situ hybridization and a mouse line containing a lacZ reporter-gene insertion in the Nhs locus. We found a complex pattern of temporally and spatially regulated expression, which, together with the pleiotropic features of NHS, suggests that this gene has key functions in the regulation of eye, tooth, brain, and craniofacial development.

摘要

南斯-霍兰综合征(NHS)是一种X连锁疾病,其特征为先天性白内障、牙齿异常、畸形特征,在某些情况下还伴有智力发育迟缓。NHS已被定位到Xp22.13上一个1.3兆碱基的区间。我们在最初那个患有NHS的澳大利亚大家庭中证实了相同的定位,并在五个家庭中鉴定出一个新基因(我们称之为“NHS基因”)中的蛋白质截短突变。NHS基因包含约650千碱基对的基因组DNA,编码一种含1630个氨基酸的假定核蛋白。在其他脊椎动物中发现了NHS直系同源基因,但未鉴定出与已知基因的序列相似性。利用原位杂交技术和一个在Nhs基因座插入了lacZ报告基因的小鼠品系,研究了NHS基因在小鼠中的发育表达谱。我们发现了一种复杂的时空调节表达模式,这与NHS的多效性特征一起表明,该基因在眼睛、牙齿、大脑和颅面发育的调节中具有关键功能。