• 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

Effect of the deficits of fragile X mental retardation protein on cognitive status of fragile x males and females assessed by robust pedigree analysis.

作者信息

Loesch Danuta Z, Huggins Richard M, Bui Quang M, Epstein Jennifer L, Taylor Annette K, Hagerman Randi Jensen

机构信息

School of Psychological Science, La Trobe University, Melbourne. d.

出版信息

J Dev Behav Pediatr. 2002 Dec;23(6):416-23. doi: 10.1097/00004703-200212000-00004.

DOI:10.1097/00004703-200212000-00004
PMID:12476071
Abstract

The effect of the fragile X mental retardation 1 (FMR1) gene product (fragile X mental retardation protein [FMRP]) deficits on Full-Scale IQ (FSIQ) and FSIQ-adjusted Wechsler subtests and index scores in fragile X disorder were assessed using a robust modification of the maximum likelihood estimators for pedigree data. The results from 144 extended families have demonstrated a linear effect of progressively reduced levels of FMRP on the FSIQ and all subtest and summary scores in either gender. The effect of FMRP in decreasing FSIQ-adjusted subtest scores was highly significant for Digit Span, Symbol Search, Object Assembly, and Picture Arrangement, with a consistent trend in both genders. Heritability for FSIQ and unadjusted subtest scores estimated from the covariance model did not exceed 50% and varied widely from the highest for Verbal score to the lowest for Picture Completion score. Possible mechanisms by which FMRP deficit impacts on specific weaknesses in fragile X are considered on the basis of present data.

摘要

相似文献

1
Effect of the deficits of fragile X mental retardation protein on cognitive status of fragile x males and females assessed by robust pedigree analysis.
J Dev Behav Pediatr. 2002 Dec;23(6):416-23. doi: 10.1097/00004703-200212000-00004.
2
Effect of fragile X status categories and FMRP deficits on cognitive profiles estimated by robust pedigree analysis.
Am J Med Genet A. 2003 Sep 15;122A(1):13-23. doi: 10.1002/ajmg.a.20214.
3
Phenotypic variation and FMRP levels in fragile X.脆性X综合征的表型变异与脆性X智力低下蛋白水平
Ment Retard Dev Disabil Res Rev. 2004;10(1):31-41. doi: 10.1002/mrdd.20006.
4
Relationship of deficits of FMR1 gene specific protein with physical phenotype of fragile X males and females in pedigrees: a new perspective.FMR1基因特异性蛋白缺陷与系谱中脆性X男性和女性身体表型的关系:一个新视角。
Am J Med Genet A. 2003 Apr 15;118A(2):127-34. doi: 10.1002/ajmg.a.10099.
5
Effect of the fragile X status categories and the fragile X mental retardation protein levels on executive functioning in males and females with fragile X.脆性X状态类别及脆性X智力低下蛋白水平对脆性X男性和女性执行功能的影响。
Neuropsychology. 2003 Oct;17(4):646-657. doi: 10.1037/0894-4105.17.4.646.
6
FMRP expression as a potential prognostic indicator in fragile X syndrome.脆性X综合征中FMRP表达作为一种潜在的预后指标
Am J Med Genet. 1999 May 28;84(3):250-61.
7
Evidence that fragile X mental retardation protein is a negative regulator of translation.脆性X智力低下蛋白是翻译负调控因子的证据。
Hum Mol Genet. 2001 Feb 15;10(4):329-38. doi: 10.1093/hmg/10.4.329.
8
Genotype, molecular phenotype, and cognitive phenotype: correlations in fragile X syndrome.基因型、分子表型与认知表型:脆性X综合征中的相关性
Am J Med Genet. 1999 Apr 2;83(4):286-95.
9
Application of robust pedigree analysis in studies of complex genotype-phenotype relationships in fragile X syndrome.
Am J Med Genet. 2002 Jan 15;107(2):136-42. doi: 10.1002/ajmg.10129.
10
Molecular predictors of cognitive involvement in female carriers of fragile X syndrome.脆性X综合征女性携带者认知受累的分子预测指标
JAMA. 1994 Feb 16;271(7):507-14.

引用本文的文献

1
A near normal distribution of IQ in Fragile X Syndrome.脆性 X 综合征患者的智商呈近似正态分布。
Sci Rep. 2024 Oct 4;14(1):23058. doi: 10.1038/s41598-024-73626-y.
2
The feasibility and utility of hair follicle sampling to measure FMRP and FMR1 mRNA in children with or without fragile X syndrome: a pilot study.利用毛囊取样测量脆性 X 综合征患儿或不伴脆性 X 综合征患儿的 FMRP 和 FMR1 mRNA 的可行性和实用性:一项初步研究。
J Neurodev Disord. 2022 Dec 9;14(1):57. doi: 10.1186/s11689-022-09465-7.
3
Expressive language abilities of boys with idiopathic autism spectrum disorder and boys with fragile X syndrome + autism spectrum disorder: Cross-context comparisons.
患有特发性自闭症谱系障碍的男孩与患有脆性X综合征+自闭症谱系障碍的男孩的表达性语言能力:跨情境比较。
Autism Dev Lang Impair. 2020 Mar 24;5:2396941520912118. doi: 10.1177/2396941520912118. eCollection 2020 Jan-Dec.
4
Rates and Predictors of Co-occurring Autism Spectrum Disorder in Boys with Fragile X Syndrome.脆性X综合征男孩中共患自闭症谱系障碍的发生率及预测因素
Autism Dev Lang Impair. 2020 Jan-Dec;5. doi: 10.1177/2396941520905328. Epub 2020 Feb 12.
5
Analysis of a Repetitive Language Coding System: Comparisons between Fragile X Syndrome, Autism, and Down Syndrome.一种重复性语言编码系统的分析:脆性X综合征、自闭症和唐氏综合征之间的比较。
Brain Sci. 2022 Apr 29;12(5):575. doi: 10.3390/brainsci12050575.
6
Optimization, validation and initial clinical implications of a Luminex-based immunoassay for the quantification of Fragile X Protein from dried blood spots.基于 Luminex 的免疫分析法定量检测干血斑中脆性 X 蛋白的优化、验证及初步临床意义。
Sci Rep. 2022 Apr 4;12(1):5617. doi: 10.1038/s41598-022-09633-8.
7
FMRP Levels in Human Peripheral Blood Leukocytes Correlates with Intellectual Disability.人类外周血白细胞中的脆性X智力低下蛋白(FMRP)水平与智力残疾相关。
Diagnostics (Basel). 2021 Sep 28;11(10):1780. doi: 10.3390/diagnostics11101780.
8
Developmental studies in fragile X syndrome.脆性 X 综合征的发育研究。
J Neurodev Disord. 2020 May 2;12(1):13. doi: 10.1186/s11689-020-09310-9.
9
Executive Function in Fragile X Syndrome: A Systematic Review.脆性X综合征中的执行功能:一项系统综述。
Brain Sci. 2019 Jan 16;9(1):15. doi: 10.3390/brainsci9010015.
10
A Multimethod Analysis of Pragmatic Skills in Children and Adolescents With Fragile X Syndrome, Autism Spectrum Disorder, and Down Syndrome.脆性 X 综合征、自闭症谱系障碍和唐氏综合征儿童和青少年语用技能的多方法分析。
J Speech Lang Hear Res. 2018 Dec 10;61(12):3023-3037. doi: 10.1044/2018_JSLHR-L-18-0008.