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Verbal memory functioning in adolescents and young adults with Costello syndrome: evidence for relative preservation in recognition memory.Costello 综合征青少年和年轻成人的言语记忆功能:在识别记忆中相对保留的证据。
Am J Med Genet A. 2013 Sep;161A(9):2258-65. doi: 10.1002/ajmg.a.36078. Epub 2013 Aug 5.
2
Behavioral phenotype in Costello syndrome with atypical mutation: a case report.伴有非典型突变的科斯特洛综合征的行为表型:一例报告
Am J Med Genet B Neuropsychiatr Genet. 2015 Jan;168B(1):66-71. doi: 10.1002/ajmg.b.32279. Epub 2014 Nov 4.
3
An attenuated phenotype of Costello syndrome in three unrelated individuals with a HRAS c.179G>A (p.Gly60Asp) mutation correlates with uncommon functional consequences.三名携带HRAS基因c.179G>A(p.Gly60Asp)突变的非亲缘个体中出现的科斯特洛综合征减弱型表型与罕见的功能后果相关。
Am J Med Genet A. 2015 Sep;167A(9):2085-97. doi: 10.1002/ajmg.a.37128. Epub 2015 Apr 25.
4
Decreased bone mineral density in Costello syndrome.科斯特洛综合征患者骨矿物质密度降低。
Mol Genet Metab. 2014 Jan;111(1):41-5. doi: 10.1016/j.ymgme.2013.08.007. Epub 2013 Aug 16.
5
Longitudinal course of cognitive, adaptive, and behavioral characteristics in Costello syndrome.Costello 综合征认知、适应和行为特征的纵向病程。
Am J Med Genet A. 2009 Dec;149A(12):2666-72. doi: 10.1002/ajmg.a.33126.
6
Dermatological phenotype in Costello syndrome: consequences of Ras dysregulation in development.Costello 综合征的皮肤表型:Ras 失调对发育的影响。
Br J Dermatol. 2012 Mar;166(3):601-7. doi: 10.1111/j.1365-2133.2011.10744.x.
7
Mechanisms underlying cognitive deficits in a mouse model for Costello Syndrome are distinct from other RASopathy mouse models.在 Costello 综合征的小鼠模型中,认知缺陷的潜在机制有别于其他 RASopathy 小鼠模型。
Sci Rep. 2017 Apr 28;7(1):1256. doi: 10.1038/s41598-017-01218-0.
8
Neurocognitive, adaptive, and behavioral functioning of individuals with Costello syndrome: a review.Costello 综合征个体的神经认知、适应和行为功能:综述。
Am J Med Genet C Semin Med Genet. 2011 May 15;157C(2):115-22. doi: 10.1002/ajmg.c.30299. Epub 2011 Apr 14.
9
Enhanced human brain associative plasticity in Costello syndrome.增强型人类大脑联合可塑性在科斯特洛综合征中的表现。
J Physiol. 2010 Sep 15;588(Pt 18):3445-56. doi: 10.1113/jphysiol.2010.191072. Epub 2010 Jul 26.
10
C4ST-1/CHST11-controlled chondroitin sulfation interferes with oncogenic HRAS signaling in Costello syndrome.C4ST-1/CHST11 调控的软骨素硫酸化干扰角化细胞综合征中的癌基因 HRAS 信号通路。
Eur J Hum Genet. 2012 Aug;20(8):870-7. doi: 10.1038/ejhg.2012.12. Epub 2012 Feb 8.

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Recognition Memory in Noonan Syndrome.努南综合征中的识别记忆
Brain Sci. 2021 Jan 29;11(2):169. doi: 10.3390/brainsci11020169.
2
Costello syndrome: Clinical phenotype, genotype, and management guidelines.考斯特洛综合征:临床表型、基因型及管理指南。
Am J Med Genet A. 2019 Sep;179(9):1725-1744. doi: 10.1002/ajmg.a.61270. Epub 2019 Jun 20.
3
Age-related differences in prevalence of autism spectrum disorder symptoms in children and adolescents with Costello syndrome.患有科斯特洛综合征的儿童和青少年中自闭症谱系障碍症状患病率的年龄相关差异。
Am J Med Genet A. 2017 May;173(5):1294-1300. doi: 10.1002/ajmg.a.38174. Epub 2017 Apr 4.
4
Phenotypic spectrum of Costello syndrome individuals harboring the rare HRAS mutation p.Gly13Asp.携带罕见HRAS突变p.Gly13Asp的科斯特洛综合征患者的表型谱。
Am J Med Genet A. 2017 May;173(5):1309-1318. doi: 10.1002/ajmg.a.38178. Epub 2017 Apr 3.
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A new bioinformatic insight into the associated proteins in psychiatric disorders.对精神疾病相关蛋白质的一种新的生物信息学见解。
Springerplus. 2016 Nov 14;5(1):1967. doi: 10.1186/s40064-016-3655-6. eCollection 2016.

本文引用的文献

1
Prevalence and clinical features of Costello syndrome and cardio-facio-cutaneous syndrome in Japan: findings from a nationwide epidemiological survey.日本全国性流行病学调查中 Costello 综合征和心面 cuts 综合征的患病率和临床特征。
Am J Med Genet A. 2012 May;158A(5):1083-94. doi: 10.1002/ajmg.a.35292. Epub 2012 Apr 11.
2
The recognition heuristic: a review of theory and tests.启发式识别法:理论与测试研究综述。
Front Psychol. 2011 Jul 5;2:147. doi: 10.3389/fpsyg.2011.00147. eCollection 2011.
3
The large-scale structure of semantic networks: statistical analyses and a model of semantic growth.语义网络的大规模结构:统计分析和语义增长模型。
Cogn Sci. 2005 Jan 2;29(1):41-78. doi: 10.1207/s15516709cog2901_3.
4
Neurocognitive, adaptive, and behavioral functioning of individuals with Costello syndrome: a review.Costello 综合征个体的神经认知、适应和行为功能:综述。
Am J Med Genet C Semin Med Genet. 2011 May 15;157C(2):115-22. doi: 10.1002/ajmg.c.30299. Epub 2011 Apr 14.
5
Phenotypic analysis of individuals with Costello syndrome due to HRAS p.G13C.HRAS p.G13C 所致 Costello 综合征患者的表型分析。
Am J Med Genet A. 2011 Apr;155A(4):706-16. doi: 10.1002/ajmg.a.33884. Epub 2011 Mar 15.
6
Long term memory profile of disorders associated with dysregulation of the RAS-MAPK signaling cascade.与 RAS-MAPK 信号级联失调相关的疾病的长期记忆特征。
Behav Genet. 2011 May;41(3):423-9. doi: 10.1007/s10519-011-9446-5. Epub 2011 Jan 28.
7
Disorders of dysregulated signal traffic through the RAS-MAPK pathway: phenotypic spectrum and molecular mechanisms.RAS-MAPK 信号通路失调导致的疾病:表型谱和分子机制。
Ann N Y Acad Sci. 2010 Dec;1214:99-121. doi: 10.1111/j.1749-6632.2010.05790.x. Epub 2010 Oct 19.
8
Enhanced human brain associative plasticity in Costello syndrome.增强型人类大脑联合可塑性在科斯特洛综合征中的表现。
J Physiol. 2010 Sep 15;588(Pt 18):3445-56. doi: 10.1113/jphysiol.2010.191072. Epub 2010 Jul 26.
9
High incidence of progressive postnatal cerebellar enlargement in Costello syndrome: brain overgrowth associated with HRAS mutations as the likely cause of structural brain and spinal cord abnormalities.Costello 综合征患者存在进行性产后小脑增大的高发率:HRAS 突变相关的脑过度生长可能是导致结构性脑和脊髓异常的原因。
Am J Med Genet A. 2010 May;152A(5):1161-8. doi: 10.1002/ajmg.a.33391.
10
Relationship between measures of working memory capacity and the time course of short-term memory retrieval and interference resolution.工作记忆容量测量与短期记忆提取和干扰解决的时间进程之间的关系。
J Exp Psychol Learn Mem Cogn. 2010 Mar;36(2):383-97. doi: 10.1037/a0018029.

Costello 综合征青少年和年轻成人的言语记忆功能:在识别记忆中相对保留的证据。

Verbal memory functioning in adolescents and young adults with Costello syndrome: evidence for relative preservation in recognition memory.

机构信息

Section of Psychology, Department of Pediatrics, Baylor College of Medicine/Texas Children's Hospital, Houston, Texas 77030, USA.

出版信息

Am J Med Genet A. 2013 Sep;161A(9):2258-65. doi: 10.1002/ajmg.a.36078. Epub 2013 Aug 5.

DOI:10.1002/ajmg.a.36078
PMID:23918324
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3745536/
Abstract

Costello syndrome (CS) is a rare genetic disorder caused by germline mutations in the HRAS proto-oncogene which belongs to the family of syndromes called rasopathies. HRAS plays a key role in synaptic long-term potentiation (LTP) and memory formation. Prior research has found impaired recall memory in CS despite enhancement in LTP that would predict memory preservation. Based on findings in other rasopathies, we hypothesized that the memory deficit in CS would be specific to recall, and that recognition memory would show relative preservation. Memory was tested using word-list learning and story memory tasks with both recall and recognition trials, a design that allowed us to examine these processes separately. Participants were 11 adolescents and young adults with molecularly confirmed CS, all of whom fell in the mild to moderate range of intellectual disability. Results indicated a clear dissociation between verbal recall, which was impaired (M = 69 ± 14), and recognition memory, which was relatively intact (M = 86 ± 14). Story recognition was highly correlated with listening comprehension (r = 0.986), which also fell in the low-average range (M = 80 ± 12.9). Performance on other measures of linguistic ability and academic skills was impaired. The findings suggest relatively preserved recognition memory that also provides some support for verbal comprehension. This is the first report of relatively normal performance in a cognitive domain in CS. Further research is needed to better understand the mechanisms by which altered RAS-MAPK signaling affects neuronal plasticity and memory processes in the brain.

摘要

科斯陶尔综合征(CS)是一种罕见的遗传性疾病,由 HRAS 原癌基因的种系突变引起,该基因属于 rasopathy 综合征家族。HRAS 在突触长时程增强(LTP)和记忆形成中发挥关键作用。先前的研究发现,尽管 LTP 增强会预测记忆保存,但 CS 中存在回忆记忆受损的情况。基于其他 rasopathy 的发现,我们假设 CS 中的记忆缺陷将是特定于回忆的,而识别记忆将表现出相对保存。使用单词列表学习和故事记忆任务测试记忆,包括回忆和识别试验,这种设计允许我们分别检查这些过程。参与者是 11 名分子确诊的 CS 青少年和年轻人,他们都处于轻度至中度智力残疾范围内。结果表明,言语回忆明显受损(M = 69 ± 14),而识别记忆相对完整(M = 86 ± 14),两者之间存在明显的分离。故事识别与听力理解高度相关(r = 0.986),后者也处于低平均水平(M = 80 ± 12.9)。其他语言能力和学术技能测试的表现受损。这些发现表明相对保存的识别记忆,也为言语理解提供了一些支持。这是 CS 认知领域相对正常表现的首次报告。需要进一步研究以更好地理解改变的 RAS-MAPK 信号如何影响大脑中的神经元可塑性和记忆过程。