日期 影响因子
日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:
–

Interactome Analysis of the CC2D1A Scaffold Reveals Novel Neuronal Interactions and a Postsynaptic Role

CC2D1A支架的相互作用组分析揭示了新的神经元相互作用和突触后作用

期刊:Molecular & Cellular Proteomics
影响因子:5.5
doi:10.1016/j.mcpro.2026.101546
Heller, Abigail T; Bhattacharya, Aniket; Li, Haorong; Turkalj, Luka; Thiyagarajan, Shruthi; Suzuki, Emma; Mossa, Adele; Zheng, Haiyan; Hao, Ling; Manzini, M Chiara
神经科学
C2D1A
发表日期：2026
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Computational Analysis of CC2D1A Missense Mutations: Insight into Protein Structure and Interaction Dynamics

CC2D1A错义突变的计算分析：深入了解蛋白质结构和相互作用动力学

期刊:ACS Chemical Neuroscience
影响因子:3.9
doi:10.1021/acschemneuro.4c00570
Abuelrub, Anwar; Erol, Ismail; Nalbant Bingol, Nurdeniz; Ozemri Sag, Sebnem; Temel, Sehime G; Durdağı, Serdar
C2D1A
发表日期：2025
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Characterization, expression, and mutational analysis of endosomal protein lethal giant disc (Lgd/CC2D1A) as a biomarker in patients with T-cell acute lymphoblastic leukemia.

对内体蛋白致死巨盘（Lgd/CC2D1A）作为T细胞急性淋巴细胞白血病患者的生物标志物进行表征、表达和突变分析。

期刊:Discover Oncology
影响因子:2.9
doi:10.1007/s12672-025-03786-4
Pandey Sandeep, Singh Ranjana, Habib Nimra, Kushwaha Rashmi, Mahdi Abbas Ali
白血病
细胞生物学
T细胞
C2D1A
T细胞
发表日期：2025
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Interactome Analysis of the CC2D1A Scaffold Reveals Novel Neuronal Interactions and a Postsynaptic Role

CC2D1A支架的相互作用组分析揭示了新的神经元相互作用和突触后作用

期刊:
影响因子:
doi:10.1101/2025.06.26.661826
Heller, Abigail T; Bhattacharya, Aniket; Li, Haorong; Turkalj, Luka; Thiyagarajan, Shruthi; Suzuki, Emma; Mossa, Adele; Zheng, Haiyan; Hao, Ling; Manzini, M Chiara
C2D1A
神经科学
发表日期：2025
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Autism-Related Cc2d1a Heterozygous Mice: Increased Levels of miRNAs Retained in DNA/RNA Hybrid Profiles (R-Loop)

与自闭症相关的 Cc2d1a 杂合子小鼠：DNA/RNA 杂交谱（R-Loop）中保留的 miRNA 水平升高

期刊:Biomolecules
影响因子:4.8
doi:10.3390/biom14091183.
Elif Funda Sener,Halime Dana,Reyhan Tahtasakal,Serpil Taheri,Minoo Rassoulzadegan
自闭症
C2D1A
miRNA
发表日期：2024
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A nonsense CC2D1A variant is associated with congenital anomalies, motor delay, hypotonia, and slight deformities

CC2D1A无义变异与先天性异常、运动发育迟缓、肌张力低下和轻微畸形有关。

期刊:Heliyon
影响因子:3.6
doi:10.1016/j.heliyon.2024.e27946
Yi, Sheng; Tang, Xianglian; Zhang, Qiang; Liang, Yu; Huang, Jing; Zhang, Shujie; Huang, Limei; Yi, Shang; Huang, Minpan; Qin, Zailong; Luo, Jingsi
C2D1A
发育与干细胞
发表日期：2024
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Identification of a Novel Variant in CC2D1A Gene Linked to Autosomal Recessive Intellectual Disability 3 in an Iranian Family and Investigating the Structure and Pleiotropic Effects of this Gene

在伊朗一个家族中鉴定出与常染色体隐性遗传智力障碍3型相关的CC2D1A基因新变异，并研究该基因的结构和多效性

期刊:Iranian Journal of Child Neurology
影响因子:0.9
doi:10.22037/ijcn.v18i1.42188
Rashvand, Zahra; Najmabadi, Hossein; Kahrizi, Kimia; Mozhdehipanah, Hossein; Moradi, Mohammad; Estaki, Zohreh; Taherkhani, Khadijeh; Nikzat, Nooshin; Najafipour, Reza; Omrani, Mir Davood
C2D1A
发表日期：2024
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Monoallelic Mutations in CC2D1A Suggest a Novel Role in Human Heterotaxy and Ciliary Dysfunction

CC2D1A基因的单等位基因突变提示其在人类异位症和纤毛功能障碍中发挥新作用

期刊:Circulation-Genomic and Precision Medicine
影响因子:5.5
doi:10.1161/CIRCGEN.120.003000
Ma, Alvin Chun Hang; Mak, Christopher Chun Yu; Yeung, Kit San; Pei, Steven Lim Cho; Ying, Dingge; Yu, Mullin Ho Chung; Hasan, Kazi Md Mahmudul; Chen, Xiangke; Chow, Pak Cheong; Cheung, Yiu Fai; Chung, Brian Hon Yin
C2D1A
Human
发表日期：2020
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Gq-mediated Akt translocation to the membrane: a novel PIP3-independent mechanism in platelets

Gq 介导的 Akt 转位至膜：血小板中一种新的 PIP3 独立机制

期刊:Blood
影响因子:21
doi:10.1182/blood-2014-05-576306
Rachit Badolia, Bhanu Kanth Manne, Carol Dangelmaier, Jonathan Chernoff, Satya P Kunapuli
信号转导
血小板
IHC
IP
WB
PI3K/Akt
C2D1A
发表日期：2015
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The Mammalian Orthologs of Drosophila Lgd, CC2D1A and CC2D1B, Function in the Endocytic Pathway, but Their Individual Loss of Function Does Not Affect Notch Signalling

果蝇 Lgd 的哺乳动物直系同源物 CC2D1A 和 CC2D1B 在内吞途径中发挥作用，但它们各自的功能丧失并不影响 Notch 信号传导

期刊:PLoS Genetics
影响因子:
doi:10.1371/journal.pgen.1005749
Nadja Drusenheimer, Bernhard Migdal, Sandra Jäckel, Lena Tveriakhina, Kristina Scheider, Katharina Schulz, Jieny Gröper, Karl Köhrer, Thomas Klein
信号转导
ICC
Notch
Drosophila
C2D1A
发表日期：2015
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