CTBP1相关文献与解析，生知库 | 链接生命科学的每一步

CtBP1 is essential for epigenetic silencing of μ-opioid receptor genes in the dorsal root ganglion in spinal nerve ligation-induced neuropathic pain

CtBP1对于脊神经结扎诱发的神经性疼痛中背根神经节μ-阿片受体基因的表观遗传沉默至关重要

doi:10.1016/j.neurot.2024.e00493.

Cheng-Yuan Lai,Ming-Chun Hsieh,Chou-Ming Yeh,Tzer-Bin Lin,Dylan Chou,Hsueh-Hsiao Wang,Kuan-Hung Lin,Jen-Kun Cheng,Po-Sheng Yang,Hsien-Yu Peng

Tissue- and Cell-Type-Specific Genetic Regulation of CTBP1 in Breast Cancer: Integrative Analyses with Exploratory Single-Cell and Imaging Data

乳腺癌中CTBP1的组织和细胞类型特异性基因调控：基于探索性单细胞和成像数据的整合分析

期刊:Breast Cancer-Targets and Therapy

影响因子:3.4

doi:10.2147/BCTT.S560038

Hong, Minping; Huang, XiaoWen; Xu, Qin; Ma, Zhenyi; Ling, Keng

Isogenic iPSC-derived CTBP1 mutant neuronal cells exhibit neurodevelopmental defects

同源iPSC衍生的CTBP1突变神经元细胞表现出神经发育缺陷

期刊:Frontiers in Neuroscience

影响因子:3.2

doi:10.3389/fnins.2025.1695464

Lee, Suhjin; Vijayalingam, Selvamani; Klotz, Elliott; Dedert, Cass; Xu, Fenglian; Chinnadurai, Govindaswamy; Ezekiel, Uthayashanker R

Uterine mesenchymal tumour with a novel EWSR1::CTBP1 gene fusion

具有新型 EWSR1::CTBP1 基因融合的子宫间质肿瘤

期刊:Virchows Archiv

影响因子:3.1

doi:10.1007/s00428-025-04205-3

Bode-Lesniewska, Beata; Illigen, Frank; Matter, Matthias S

Hypotonia, Ataxia, Developmental Delay and Tooth Enamel Defect Syndrome (HADDTS) due to a Heterozygous de Novo Missense Variant in CTBP1 Identified via Whole Genome Sequencing

通过全基因组测序鉴定出的CTBP1基因杂合新生错义变异导致肌张力低下、共济失调、发育迟缓和牙釉质缺陷综合征（HADDTS）。

期刊:Case Reports in Pediatrics

影响因子:0.5

doi:10.1155/crpe/3604592

Silvia Beatriz Sanchez Marco; Pardington, Emily; Monaghan, Marie; Spaull, Robert; Fadilah, Ala; Kurian, Kathreena; Vijayakumar, Kayal; Smithson, Sarah; Majumdar, Anirban

Semaphorin7A patterns neural circuitry in the lateral line of the zebrafish

Semaphorin7A 模式化斑马鱼侧线的神经回路

期刊:Elife

影响因子:6.4

doi:10.7554/eLife.89926

Agnik Dasgupta, Caleb C Reagor, Sang Peter Paik, Lauren M Snow, Adrian Jacobo, A J Hudspeth

CTBP1 links metabolic syndrome to polycystic ovary syndrome through interruption of aromatase and SREBP1

CTBP1 通过阻断芳香化酶和 SREBP1 将代谢综合征与多囊卵巢综合征联系起来

期刊:Communications Biology

影响因子:5.2

doi:10.1038/s42003-024-06857-4

Yue Kong #, Guang Yang #, Xu Feng #, Zhaodong Ji, Xiaoling Wang, Yang Shao, Jiao Meng, Guidong Yao, Chunxia Ren, Gong Yang

Clinical significance and biological roles of lncRNA CTBP1-AS in polycystic ovary syndrome

lncRNA CTBP1-AS在多囊卵巢综合征中的临床意义和生物学作用

期刊:Journal of Ovarian Research

影响因子:3.8

doi:10.1186/s13048-024-01571-5

Li Qin #, Chun Tian #, Liying Huang, Xiao Qin, Shaohua Ling, Jingxi Wei, Bingsheng Huang, Lining Li, Xiaoqiong Luo

A novel CTBP1 variant in a Chinese pediatric patient with a phenotype distinct from hypotonia, ataxia, developmental delay, and tooth enamel defect syndrome

中国一名儿童患者携带一种新的CTBP1变异，其表型不同于肌张力低下、共济失调、发育迟缓和牙釉质缺陷综合征。

期刊:Frontiers in Genetics

影响因子:2.8

doi:10.3389/fgene.2024.1344682

Zhang, Qiang; Liu, Yusi; Liu, Xuan; Zhao, Yue; Zhang, Jihong

NAD(H)-dependent corepressor CTBP1 integrates metabolic signals to drive oncogenic programs

NAD(H)依赖性辅阻遏物CTBP1整合代谢信号以驱动致癌程序

CtBP1 is essential for epigenetic silencing of μ-opioid receptor genes in the dorsal root ganglion in spinal nerve ligation-induced neuropathic pain

CtBP1对于脊神经结扎诱发的神经性疼痛中背根神经节μ-阿片受体基因的表观遗传沉默至关重要

Tissue- and Cell-Type-Specific Genetic Regulation of CTBP1 in Breast Cancer: Integrative Analyses with Exploratory Single-Cell and Imaging Data

乳腺癌中CTBP1的组织和细胞类型特异性基因调控：基于探索性单细胞和成像数据的整合分析

Isogenic iPSC-derived CTBP1 mutant neuronal cells exhibit neurodevelopmental defects

同源iPSC衍生的CTBP1突变神经元细胞表现出神经发育缺陷

Uterine mesenchymal tumour with a novel EWSR1::CTBP1 gene fusion

具有新型 EWSR1::CTBP1 基因融合的子宫间质肿瘤

Hypotonia, Ataxia, Developmental Delay and Tooth Enamel Defect Syndrome (HADDTS) due to a Heterozygous de Novo Missense Variant in CTBP1 Identified via Whole Genome Sequencing

通过全基因组测序鉴定出的CTBP1基因杂合新生错义变异导致肌张力低下、共济失调、发育迟缓和牙釉质缺陷综合征（HADDTS）。

Semaphorin7A patterns neural circuitry in the lateral line of the zebrafish

Semaphorin7A 模式化斑马鱼侧线的神经回路

CTBP1 links metabolic syndrome to polycystic ovary syndrome through interruption of aromatase and SREBP1

CTBP1 通过阻断芳香化酶和 SREBP1 将代谢综合征与多囊卵巢综合征联系起来

Clinical significance and biological roles of lncRNA CTBP1-AS in polycystic ovary syndrome

lncRNA CTBP1-AS在多囊卵巢综合征中的临床意义和生物学作用

A novel CTBP1 variant in a Chinese pediatric patient with a phenotype distinct from hypotonia, ataxia, developmental delay, and tooth enamel defect syndrome

中国一名儿童患者携带一种新的CTBP1变异，其表型不同于肌张力低下、共济失调、发育迟缓和牙釉质缺陷综合征。