CYFIP1 Coordinates mRNA Translation and Cytoskeleton Remodeling to Ensure Proper Dendritic Spine Formation

Cited by (296)

Items 101–200 of 296

1. Dysregulation of the Synaptic Cytoskeleton in the PFC Drives Neural Circuit Pathology, Leading to Social Dysfunction
   Il Hwan Kim, Namsoo Kim, Sunwhi Kim, Koji Toda, Christina M. Catavero, Jamie L. Courtland, Henry H. Yin, Scott H. Soderling · 2020 · Cell Reports
2. An Intellectual Disability-Related Missense Mutation in Rac1 Prevents LTP Induction
   Chen Tian, Yuni Kay, Anastasiia Sadybekov, Sadhna Rao, Vsevolod Katritch, Bruce E. Herring · 2018 · Frontiers in Molecular Neuroscience
3. Reciprocal White Matter Changes Associated With Copy Number Variation at 15q11.2 BP1-BP2: A Diffusion Tensor Imaging Study
   Silva, Ana I., Ulfarsson, Magnus O., Stefansson, Hreinn, Gustafsson, Omar, Walters, G. Bragi, Linden, David E.J., Wilkinson, Lawrence S., Drakesmith, Mark, Owen, Michael J., Hall, Jeremy et al. · 2019 · Biological Psychiatry
4. A Common CYFIP1 Variant at the 15q11.2 Disease Locus Is Associated with Structural Variation at the Language-Related Left Supramarginal Gyrus
   Young Jae Woo, Tao Wang, Tulio M. Guadalupe, Rebecca A. Nebel, Arianna Vino, Victor A. Del Bene, Sophie Molholm, Lars A. Ross, Marcel P. Zwiers, Simon E. Fisher et al. · 2016 · PLoS ONE
5. Tiam1 is Critical for Glutamatergic Synapse Structure and Function in the Hippocampus
   Rao, Sadhna, Kay, Yuni, Herring, Bruce E. · 2019 · The Journal of Neuroscience
6. Nebulized inhalation of LPAE-HDAC10 inhibits acetylation-mediated ROS/NF-κB pathway for silicosis treatment
   Yunze Tian, Hongyang Shi, Danjie Zhang, Chenfei Wang, Feng Zhao, Liang Li, Zhengshui Xu, Jiantao Jiang, Jianzhong Li · 2023 · Journal of Controlled Release
7. Synaptic Synthesis, Dephosphorylation, and Degradation
   Paolo La Montanara, Laura Rusconi, Albina Locarno, Lia Forti, Isabella Barbiero, Marco Tramarin, Chetan Chandola, Charlotte Kilstrup‐Nielsen, Nicoletta Landsberger · 2015 · Journal of Biological Chemistry
8. Reduced CYFIP1 in Human Neural Progenitors Results in Dysregulation of Schizophrenia and Epilepsy Gene Networks
   Rebecca A. Nebel, Dejian Zhao, Erika Pedrosa, Jill Kirschen, Herbert M. Lachman, Deyou Zheng, Brett S. Abrahams · 2016 · PLoS ONE
9. Synapse-Enriched m6A-Modified Malat1 Interacts with the Novel m6A Reader, DPYSL2, and Is Required for Fear-Extinction Memory
   Sachithrani U. Madugalle, Wei‐Siang Liau, Qiongyi Zhao, Xiang Li, Hao Gong, Paul Robert Marshall, Ambika Periyakaruppiah, Esmi Lau Zajaczkowski, Laura Jane Leighton, Haobin Ren et al. · 2023 · Journal of Neuroscience
10. MD and Docking Studies Reveal That the Functional Switch of CYFIP1 is Mediated by a Butterfly-like Motion
    Daniele Di Marino, Giovanni Chillemi, Silvia De Rubeis, Anna Luna Tramontano, Tilmann Achsel, Claudia Bagni · 2015 · Journal of Chemical Theory and Computation
11. Phylogenetic and Molecular Analyses Identify SNORD116 Targets Involved in the Prader–Willi Syndrome
    Laeya Baldini, A. Edwards Robert, Bruno Charpentier, Stéphane Labialle · 2021 · Molecular Biology and Evolution
12. Transcriptomics reveals amygdala neuron regulation by fasting and ghrelin thereby promoting feeding
    Christian Peters, Songwei He, Federica Fermani, Hansol Lim, Wenyu Ding, Christian Mayer, Rüdiger Klein · 2023 · Science Advances
13. Loss of interleukin 1 signaling causes impairment of microglia- mediated synapse elimination and autistic-like behaviour in mice
    Antonella Borreca, Cristina Mantovani, Genni Desiato, Irene Corradini, Fabia Filipello, Chiara Elia, Francesca D’Autilia, Giulia Santamaria, Cecília Garlanda, Raffaella Morini et al. · 2024 · Brain Behavior and Immunity
14. Contribution of induced pluripotent stem cell technologies to the understanding of cellular phenotypes in schizophrenia
    Shabeesh Balan, Manabu Toyoshima, Takeo Yoshikawa · 2018 · Neurobiology of Disease
15. SMN affects membrane remodelling and anchoring of the protein synthesis machinery
    Francesca Gabanella, Cinzia Pisani, Antonella Borreca, Farioli-Vecchioli Stefano, Ciotti Maria Teresa, Ingegnere Tiziano, Annalisa Onori, Martine Ammassari‐Teule, Nicoletta Corbi, Nadia Canu et al. · 2016 · Journal of Cell Science
16. DIXDC1 Phosphorylation and Control of Dendritic Morphology Are Impaired by Rare Genetic Variants
    Vickie Kwan, Durga Praveen Meka, Sean H. White, Claudia Lin-Kar Hung, Nicholas Timothy Holzapfel, Susan Walker, Nadeem Murtaza, Brianna K. Unda, Birgit Schwanke, Ryan K. C. Yuen et al. · 2016 · Cell Reports
17. KIS, a Kinase Associated with Microtubule Regulators, Enhances Translation of AMPA Receptors and Stimulates Dendritic Spine Remodeling
    Neus Pedraza, Raúl Ortiz, Alba Cornadó, Artur Llobet, Martí Aldea, Carme Gallego · 2014 · Journal of Neuroscience
18. The elongation factor eEF1A2 controls translation and actin dynamics in dendritic spines
    Mònica B. Mendoza, Sara Gutierrez, Raúl Ortiz, David F. Moreno, Maria Dermit, Martin Dodel, Elena Rebollo, Miquel Bosch, Faraz K. Mardakheh, Carme Gallego · 2021 · Science Signaling
19. Ablation of ErbB4 from excitatory neurons leads to reduced dendritic spine density in mouse prefrontal cortex
    Margaret A. Cooper, Anthony J. Koleske · 2014 · The Journal of Comparative Neurology
20. Deletion of the KH1 Domain of Fmr1 Leads to Transcriptional Alterations and Attentional Deficits in Rats
    Golden, Carla E M, Breen, Michael S, Koro, Lacin, Sonar, Sankalp, Niblo, Kristi, Browne, Andrew, Burlant, Natalie, Di Marino, Daniele, De Rubeis, Silvia, Baxter, Mark G et al. · 2019 · Cerebral Cortex
21. FMRP and CYFIP1 at the Synapse and Their Role in Psychiatric Vulnerability
    Clifton, Nicholas E., Thomas, Kerrie L., Wilkinson, Lawrence S., Hall, Jeremy, Trent, Simon · 2020 · Complex Psychiatry
22. Epilepsy- and intellectual disability-associated CYFIP2 interacts with both actin regulators and RNA-binding proteins in the neonatal mouse forebrain
    Yeunkum Lee, Yinhua Zhang, Hyojin Kang, Geul Bang, Yoonhee Kim, Hyae Rim Kang, Ruiying Ma, Chunmei Jin, Jin Young Kim, Kihoon Han · 2020 · Biochemical and Biophysical Research Communications
23. Genetic association of FMRP targets with psychiatric disorders
    Nicholas E. Clifton, Elliott Rees, Peter Holmans, Antonio F. Pardiñas, Janet C Harwood, Arianna Di Florio, George Kirov, James Walters, Michael C. O’Donovan, Michael John Owen et al. · 2020 · Molecular Psychiatry
24. Behavioral training rescues motor deficits in Cyfip1 haploinsufficiency mouse model of autism spectrum disorders
    Sven O. Bachmann, Monika Śledziowska, Ellen Cross, Shireene Kalbassi, Sophie Waldron, Fangli Chen, Adam Ranson, Stéphane J. Baudouin · 2019 · Translational Psychiatry
25. FMRP-Driven Neuropathology in Autistic Spectrum Disorder and Alzheimer's disease: A Losing Game
    Louis Bleuzé, Viviana Triaca, Antonella Borreca · 2021 · Frontiers in Molecular Biosciences
26. CYFIP1 overexpression increases fear response in mice but does not affect social or repetitive behavioral phenotypes
    Catherine J. Fricano-Kugler, Aaron Gordon, Grace S. Shin, Kun Gao, Jade Nguyen, Jamee M Berg, Mary Starks, Daniel H. Geschwind · 2019 · Molecular Autism
27. Exploiting aberrant mRNA expression in autism for gene discovery and diagnosis
    Jinting Guan, Ence Yang, Jizhou Yang, Yong Zeng, Guoli Ji, James J. Cai · 2016 · Human Genetics
28. Phosphorylation of CYFIP2, a component of the WAVE-regulatory complex, regulates dendritic spine density and neurite outgrowth in cultured hippocampal neurons potentially by affecting the complex assembly
    Yeunkum Lee, Doyoun Kim, Jae Ryun Ryu, Yinhua Zhang, Shinhyun Kim, Yoonhee Kim, Bokyoung Lee, Woong Sun, Kihoon Han · 2017 · Neuroreport
29. mGlu5-mediated signalling in developing astrocyte and the pathogenesis of autism spectrum disorders
    Francesco Petrelli, Paola Bezzi · 2018 · Current Opinion in Neurobiology
30. Handling FMRP and its molecular partners: Structural insights into Fragile X Syndrome
    Ilda D’Annessa, Francesco Cicconardi, Daniele Di Marino · 2018 · Progress in Biophysics and Molecular Biology
31. Aberrant Rho GTPases signaling and cognitive dysfunction: In vivo evidence for a compelling molecular relationship
    Bianca De Filippis, Emilia Romano, Giovanni Laviola · 2014 · Neuroscience & Biobehavioral Reviews
32. Parental origin impairment of synaptic functions and behaviors in cytoplasmic FMRP interacting protein 1 (Cyfip1) deficient mice
    Leeyup Chung, Xiaoming Wang, Li Zhu, Aaron J. Towers, Xinyu Cao, Il Hwan Kim, Yong‐hui Jiang · 2015 · Brain Research
33. Fragile-X Syndrome Is Associated With NMDA Receptor Hypofunction and Reduced Dendritic Complexity in Mature Dentate Granule Cells
    Suk‐Yu Yau, Luis E.B. Bettio, Jason Chiu, Christine Chiu, Brian R. Christie · 2019 · Frontiers in Molecular Neuroscience
34. A Bright, Nontoxic, and Non-aggregating red Fluorescent Protein for Long-Term Labeling of Fine Structures in Neurons
    Ning Lin, Yang Geng, Matthew Lovett-Barron, Xiaoman Niu, Mengying Deng, Liang Wang, Niloufar Ataie, Alex Sens, Ho Leung Ng, Shoudeng Chen et al. · 2022 · Frontiers in Cell and Developmental Biology
35. A unique binding mode of the eukaryotic translation initiation factor 4E for guiding the design of novel peptide inhibitors
    Daniele Di Marino, Ilda D’Annessa, Holly Tancredi, Claudia Bagni, Emilio Gallicchio · 2015 · Protein Science
36. 11q24.2‐25 micro‐rearrangements in autism spectrum disorders: Relation to brain structures
    Anna Maruani, Guillaume Huguet, Anita Beggiato, Monique Elmaleh, Roberto Toro, Claire S. Leblond, Alexandre Mathieu, Frédérique Amsellem, Nathalie Lemière, Alain Verloès et al. · 2015 · American Journal of Medical Genetics Part A
37. No Escaping the Rat Race: Simulated Night Shift Work Alters the Time-of-Day Variation in BMAL1 Translational Activity in the Prefrontal Cortex
    Andrea R. Marti, Sudarshan S. Patil, Jelena Mrdalj, Peter Meerlo, Silje Skrede, Ståle Pallesen, Torhild Pedersen, Clive R. Bramham, Janne Grønli · 2017 · Frontiers in Neural Circuits
38. Transcriptomics analysis reveals new insights in E171-induced molecular alterations in a mouse model of colon cancer
    Héloïse Proquin, Marlon J. Jetten, Marloes C. M. Jonkhout, Luis G. Garduño-Balderas, Jacob J. Briedé, Theo M. C. M. de Kok, Henk Van Loveren, Yolanda I. Chirino · 2018 · Scientific Reports
39. The integrated stress response effector GADD34 is repurposed by neurons to promote stimulus-induced translation
    Mauricio Martins Oliveira, Muhaned S. Mohamed, Megan K. Elder, Keylin Banegas-Morales, Maggie Mamcarz, Emily H. Lu, Ela N. Golhan, Nishika Navrange, Snehajyoti Chatterjee, Ted G. Abel et al. · 2024 · Cell Reports
40. Dysregulated translational control in brain disorders: from genes to behavior
    Shane A. Wiebe, Anmol Nagpal, Nahum Sonenberg · 2020 · Current Opinion in Genetics & Development
41. The neurobiology of the Prader-Willi phenotype of fragile X syndrome
    Zukhrofi Muzar, Reymundo Lozano, Alexander Kolevzon, Randi Jenssen Hagerman · 2016 · Intractable & Rare Diseases Research
42. Tetraspanin 6: A novel regulator of hippocampal synaptic transmission and long term plasticity
    Isabel H. Salas, Zsuzsanna Callaerts‐Vegh, Amaia M. Arranz, Francesc Xavier Guix, Rudi D’Hooge, Jose Antonio Esteban, Bart De Strooper, Carlos G. Dotti · 2017 · PLoS ONE
43. Making sense of mRNA landscapes: Translation control in neurodevelopment
    Yongkyu Park, Nicholas F. Page, Iva Salamon, Diana Li, Mladen‐Roko Rašin · 2021 · Wiley Interdisciplinary Reviews - RNA
44. Loss of Function in the Neurodevelopmental Disease and Schizophrenia-Associated Gene CYFIP1 in Human Microglia-like Cells Supports a Functional Role in Synaptic Engulfment
    Steven D. Sheridan, Joy E. Horng, Hana Yeh, Liam T. McCrea, Jennifer P Wang, Ting Fu, Roy H. Perlis · 2022 · Biological Psychiatry
45. Children with Autism Spectrum Disorder and Abnormalities of Clinical EEG: A Qualitative Review
    Chiara Bosetti, Luca Ferrini, Anna Rita Ferrari, Emanuele Bartolini, Sara Calderoni · 2024 · Journal of Clinical Medicine
46. Morphoregulatory functions of the RNA-binding motif protein 3 in cell spreading, polarity and migration
    Julie Pilotte, William Bill Kiosses, Stephanie Chan, Helen P. Makarenkova, Esther E. Dupont‐Versteegden, Peter W. Vanderklish · 2018 · Scientific Reports
47. Control of protein synthesis and memory by GluN3A-NMDA receptors through inhibition of GIT1/mTORC1 assembly
    María J. Conde-Dusman, Partha N. Dey, Oscar Elía-Zudaire, Luis G. Rabaneda, Carmen García-Lira, Teddy Grand, Víctor Briz, Eric Raúl Velasco, Raül Andero, Sergio Niñerola et al. · 2021 · eLife
48. Local mRNA translation and cytoskeletal reorganization: Mechanisms that tune neuronal responses
    Nikoletta Triantopoulou, Marina Vidaki · 2022 · Frontiers in Molecular Neuroscience
49. Enhanced Prefrontal Neuronal Activity and Social Dominance Behavior in Postnatal Forebrain Excitatory Neuron-Specific Cyfip2 Knock-Out Mice
    Yinhua Zhang, Rim Kang Hyae, Seung-Hyun Lee, Yoonhee Kim, Ruiying Ma, Chunmei Jin, Ji-Eun Lim, Seoyeon Kim, Yeju Kang, Hyojin Kang et al. · 2020 · Frontiers in Molecular Neuroscience
50. eIF4E phosphorylation recruits β-catenin to mRNA cap and promotes Wnt pathway translation in dentate gyrus LTP maintenance
    Sudarshan S. Patil, K. Chalkiadaki, T. F. Mergiya, Konstanze Krimbacher, Inês S. Amorim, Shreeram Akerkar, C. Gkogkas, C. Bramham · 2023 · iScience
51. Comparing synaptic proteomes across five mouse models for autism reveals converging molecular similarities including deficits in oxidative phosphorylation and Rho GTPase signaling
    Abigail U. Carbonell, Carmen Freire‐Cobo, Ilana V. Deyneko, Saunil Dobariya, Hediye Erdjument‐Bromage, Amy E. Clipperton‐Allen, Damon T. Page, Thomas A. Neubert, Bryen A. Jordan · 2023 · Frontiers in Aging Neuroscience
52. Etiology of Autism the Complexity of Risk Factors in Autism Spectrum Disorder
    Agnes Cristina Fett‐Conte, Ana Luiza Bossolani-Martins, Dante Bruno Avanso Rosan · 2015 · InTech eBooks
53. Xp11.22 deletions encompassing CENPVL1, CENPVL2, MAGED1 and GSPT2 as a cause of syndromic X-linked intellectual disability
    Christina Grau, Molly Starkovich, Mahshid Sababi Azamian, Fan Xia, Sau Wai Cheung, Patricia Evans, Alex Henderson, Seema R. Lalani, Daryl A. Scott · 2017 · PLoS ONE
54. Epigenome-wide association study for perceived discrimination among sub-Saharan African migrants in Europe - the RODAM study
    Loes C. van der Laan, Karlijn A. C. Meeks, Felix Patience Chilunga, Charles O Agyemang, Andrea Venema, Marcel M. A. M. Mannens, Mohammad Hadi Zafarmand, Kerstin Klipstein‐Grobusch, Liam L Smeeth, Adebowale Adeyemo et al. · 2020 · Scientific Reports
55. SREBP modulates the NADP+/NADPH cycle to control night sleep in Drosophila
    Vittoria Mariano, Alexandros K. Kanellopoulos, Giuseppe Aiello, Adrian C. Lo, Eric Legius, Tilmann Achsel, Claudia Bagni · 2023 · Nature Communications
56. Analysis of Diffusion Tensor Imaging Data From the UK Biobank Confirms Dosage Effect of 15q11.2 Copy Number Variation on White Matter and Shows Association With Cognition
    Ana Isabel Silva, George Kirov, Kimberley Marie Kendall, Mathew Bracher-Smith, Lawrence S. Wilkinson, Jérémy Hall, Magnus Orn Ulfarsson, G. Bragi Walters, Hreinn Stefánsson, Kāri Stefánsson et al. · 2021 · Biological Psychiatry
57. Upregulation of eIF4E, but not other translation initiation factors, in dendritic spines during memory formation
    Sofya Gindina, Benjamin W. Botsford, Kiriana K. Cowansage, Joseph E. LeDoux, Eric Klann, Charles A. Hoeffer, Linnaea E. Ostroff · 2021 · The Journal of Comparative Neurology
58. Evidence for a Contribution of the Nlgn3/Cyfip1/Fmr1 Pathway in the Pathophysiology of Autism Spectrum Disorders
    Monika Śledziowska, James Galloway, Stéphane J. Baudouin · 2019 · Neuroscience
59. Persistent Cyfip1 Expression Is Required to Maintain the Adult Subventricular Zone Neurogenic Niche
    Habela, Christa Whelan, Yoon, Ki-Jun, Kim, Nam-Shik, Taga, Arens, Bell, Kassidy, Bergles, Dwight E., Maragakis, Nicholas J., Ming, Guo-li, Song, Hongjun · 2020 · The Journal of Neuroscience
60. Cytoplasmic FMR1 interacting protein (CYFIP) family members and their function in neural development and disorders
    Ísis Venturi Biembengut, Isabelle Leticia Zaboroski Silva, Tatiana de Arruda Campos Brasil de Souza, Patrícia Shigunov · 2021 · Molecular Biology Reports
61. A complex Xp11.22 deletion in a patient with syndromic autism: Exploration of FAM120C as a positional candidate gene for autism
    Veerle De Wolf, An Crepel, Frans C Schuit, Leentje Van Lommel, Berten Ceulemans, Jean G. Steyaert, Eve Seuntjens, Hilde Peeters, Koenraad Devriendt · 2014 · American Journal of Medical Genetics Part A
62. Genetic Causes of Autism Spectrum Disorders
    Guillaume Huguet, Thomas Bourgeron · 2016 · Elsevier eBooks
63. CYFIP1 Dosages Exhibit Divergent Behavioral Impact via Diametric Regulation of NMDA Receptor Complex Translation in Mouse Models of Psychiatric Disorders
    Kim, Nam-Shik, Ringeling, Francisca Rojas, Zhou, Ying, Nguyen, Ha Nam, Temme, Stephanie J., Lin, Yu-Ting, Eacker, Stephen, Dawson, Valina L., Dawson, Ted M., Xiao, Bo et al. · 2022 · Biological Psychiatry
64. Rare copy number variations affecting the synaptic gene DMXL2 in neurodevelopmental disorders
    Gregory Costain, Susan Walker, Bob Argiropoulos, Danielle A. Baribeau, Anne S. Bassett, Erik Boot, Koenraad Devriendt, Barbara Kellam, Christian R. Marshall, Aparna Prasad et al. · 2019 · Journal of Neurodevelopmental Disorders
65. Intellectual Disability and Behavioral Deficits Linked to CYFIP1 Missense Variants Disrupting Actin Polymerization
    Mariano, Vittoria, Kanellopoulos, Alexandros K., Ricci, Carlotta, Di Marino, Daniele, Borrie, Sarah C., Dupraz, Sebastian, Bradke, Frank, Achsel, Tilmann, Legius, Eric, Odent, Sylvie et al. · 2024 · Biological Psychiatry
66. DDX3X syndrome: From clinical phenotypes to biological insights
    Alexa von Mueffling, Marta García-Forn, Silvia De Rubeis · 2024 · Journal of Neurochemistry
67. Sex-specific perturbations of neuronal development caused by mutations in the autism risk gene DDX3X
    Adele Mossa, Lauren Dierdorff, Jerónimo Lukin, Marta García-Forn, Wei Wang, Fatemeh Mamashli, Yeaji Park, Chiara Fiorenzani, Zeynep Akpinar, Janine Kamps et al. · 2025 · Nature Communications
68. Domain-Specific Cognitive Impairments in Humans and Flies With Reduced CYFIP1 Dosage
    Woo, Young Jae, Kanellopoulos, Alexandros K., Hemati, Parisa, Kirschen, Jill, Nebel, Rebecca A., Wang, Tao, Bagni, Claudia, Abrahams, Brett S. · 2019 · Biological Psychiatry
69. Altered presynaptic function and number of mitochondria in the medial prefrontal cortex of adult Cyfip2 heterozygous mice
    Kim, Gyu Hyun, Zhang, Yinhua, Kang, Hyae Rim, Lee, Seung-Hyun, Shin, Jiwon, Lee, Chan Hee, Kang, Hyojin, Ma, Ruiying, Jin, Chunmei, Kim, Yoonhee et al. · 2020 · Molecular Brain
70. Pharmacological Rescue of Hippocampal Fear Learning Deficits in Fragile X Syndrome
    Martinez, Luis A., Tejada-Simon, Maria Victoria · 2018 · Molecular Neurobiology
71. Up-regulated cytoplasmic FMRP-interacting protein 1 in intractable temporal lobe epilepsy patients and a rat model
    Yunyi Huang · 2015 · International Journal of Neuroscience
72. Protein interactome and cell‐type expression analyses reveal that cytoplasmic FMR1 ‐interacting protein 1 ( CYFIP1 ), but not CYFIP2 , associates with astrocytic focal adhesion
    Ruiying Ma, Kaifang Pang, Hyojin Kang, Yinhua Zhang, Geul Bang, Sangwoo Park, Eunha Hwang, Jae Ryun Ryu, Yujin Kwon, Hyae Rim Kang et al. · 2022 · Journal of Neurochemistry
73. Anatomy and Cell Biology of Autism Spectrum Disorder: Lessons from Human Genetics
    Kristel T. E. Kleijer, Guillaume Huguet, Julie Tastet, Thomas Bourgeron, J. Peter H. Burbach · 2017 · Advances in anatomy, embryology and cell biology
74. Translation from the Ribosome to the Clinic: Implication in Neurological Disorders and New Perspectives from Recent Advances
    Kelvin K. Hui, YiKai Chen, Ryo Endo, Motomasa Tanaka · 2019 · Biomolecules
75. Increased Training Intensity Induces Proper Membrane Localization of Actin Remodeling Proteins in the Hippocampus Preventing Cognitive Deficits: Implications for Fragile X Syndrome
    Martinez, L. A., Tejada-Simon, Maria Victoria · 2018 · Molecular Neurobiology
76. A blueprint for research on Shankopathies: A view from research on autism spectrum disorder
    Salvatore Carbonetto · 2013 · Developmental Neurobiology
77. Autocrine insulin pathway signaling regulates actin dynamics in cell wound repair
    Mitsutoshi Nakamura, Jeffrey M. Verboon, Tessa E. Allen, Maria Abreu Blanco, Raymond Liu, Andrew N. M. Dominguez, Jeffrey J. Delrow, Susan M. Parkhurst · 2020 · PLoS Genetics
78. Control of microglial dynamics by Arp2/3 and the autism and schizophrenia-associated protein Cyfip1
    Drew, James, Arancibia-Carcamo, I. Lorena, Jolivet, Renaud, Lopez-Domenech, Guillermo, Attwell, David, Kittler, Josef T. · 2020
79. Effects of copy number variations on brain structure and risk for psychiatric illness: Large-scale studies from the ENIGMA Working Groups on CNVs
    Ida Elken Sønderby, Christopher R. K. Ching, Sophia I. Thomopoulos, Dennis van der Meer, Julio E. Villalón‐Reina, Ingrid Agartz, Katrin Amunts, Celso Arango, Nicola J. Armstrong, Rosa Ayesa‐Arriola et al. · 2021 · PsyArXiv (OSF Preprints)
80. Alteration of synaptic protein composition during developmental synapse maturation
    Takeshi Kaizuka, Toru Takumi · 2024 · European Journal of Neuroscience
81. The role of altered translation in intellectual disability and epilepsy
    Taylor Joseph Malone, Leonard K. Kaczmarek · 2022 · Progress in Neurobiology
82. Complex Interactions between Genes and Social Environment Cause Phenotypes Associated with Autism Spectrum Disorders in Mice
    Monika Śledziowska, Shireene Kalbassi, Stéphane J. Baudouin · 2020 · eNeuro
83. CYFIP1 coordinate with RNMT to induce osteosarcoma cuproptosis via AURKAIP1 m7G modification
    Zili Lin, Ziyi Wu, Yizhe He, Xiang‐Yao Li, Wei Luo · 2025 · Molecular Medicine
84. Investigation of Copy Number Variation in South African Patients With Congenital Heart Defects
    Nicole Saacks, James Eales, Timothy F. Spracklen, Thomas Aldersley, Paul Human, Mark Verryn, John Lawrenson, Blanche J. Cupido, George Comitis, Rik De Decker et al. · 2022 · Circulation Genomic and Precision Medicine
85. FXR1 regulates vascular smooth muscle cell cytoskeleton, VSMC contractility, and blood pressure by multiple mechanisms
    Amanda St. Paul, Cali B. Corbett, Amanda M. Peluzzo, Sheri E. Kelemen, Rachael Okune, Dale S. Haines, Kyle J. Preston, Satoru Eguchi, Michael V. Autieri · 2023 · Cell Reports
86. Microglial phagolysosome dysfunction and altered neural communication amplify phenotypic severity in Prader-Willi Syndrome with larger deletion
    Felipe Corrêa‐da‐Silva, Jenny Carter, Xinyuan Wang, Rui Sun, Ekta Pathak, José Manuel Monroy Kuhn, Sonja Charlotte Schriever, Clarissa M. Maya‐Monteiro, Han Jiao, Martin J. T. Kalsbeek et al. · 2024 · Acta Neuropathologica
87. Identification and characterization of circular RNAs in Longissimus dorsi muscle tissue from two goat breeds using RNA-Seq
    Jiyuan Shen, Huimin Zhen, Lu Li, Yuting Zhang, Jiqing Wang, Jiang Hu, Xiu Liu, Shaobin Li, Zhiyun Hao, Mingna Li et al. · 2022 · Molecular Genetics and Genomics
88. TIAR and FMRP Shape Pro-Survival Nascent Proteome of Leukemia Cells in the Bone Marrow Microenvironment
    Magdalena Wołczyk, Remigiusz Adam Serwa, Agata Kominek, Agata Klejman, Jacek Miłek, Marta Chwałek, Laura Turos-Korgul, Agata Charzyńska, Michał Dąbrowski, Magdalena Dziembowska et al. · 2022 · iScience
89. The WAVE complex in developmental and adulthood brain disorders
    Kim, Hyung-Goo, Berdasco, Clara, Nairn, Angus C., Kim, Yong · 2025 · Experimental & Molecular Medicine
90. Integrated machine learning-driven disulfidptosis profiling: CYFIP1 and EMILIN1 as therapeutic nodes in neuroblastoma
    Zhang Mengzhen, Hou Xinwei, Tan Zeheng, Nan Li, Yang Yang, Yang Huirong, Fan Kaisi, Xiaoting Ding, Yang Liucheng, Kai Wu · 2024 · Journal of Cancer Research and Clinical Oncology
91. Neurodevelopmental disorder-associated CYFIP2 regulates membraneless organelles and eIF2α phosphorylation via protein interactors and actin cytoskeleton
    Yinhua Zhang, Hyae Rim Kang, Yukyung Jun, Hyojin Kang, Geul Bang, Ruiying Ma, Sungjin Ju, Da Eun Yoon, Yoonhee Kim, Kyoungmi Kim et al. · 2024 · Human Molecular Genetics
92. Recent advances in CYFIP2-associated neurodevelopmental disorders: From human genetics to molecular mechanisms and mouse models
    Ruiying Ma, U Suk Kim, Yousun Chung, Hyae Rim Kang, Yinhua Zhang, Kihoon Han · 2024 · Brain and Development
93. Dendrites in Autism Spectrum Disorders
    Verónica Martínez‐Cerdeño, Izumi Maezawa, Lee‐Way Jin · 2016 · Springer eBooks
94. Cyfip1 Regulates SynGAP1 at Hippocampal Synapses
    Abhishek Sahasrabudhe, Fatema Begum, Christopher A. Guevara, Chenel Morrison, Kuangfu Hsiao, Nebojsa Kezunovic, Ozlem Bozdagi-Gunal, Deanna L. Benson · 2021 · Frontiers in Synaptic Neuroscience
95. Elucidating the mechanisms of transcription regulation during heart development by next-generation sequencing
    Keisuke Nimura, Yasufumi Kaneda · 2015 · Journal of Human Genetics
96. Cell-autonomous reduction of CYFIP2 is insufficient to induce Alzheimer's disease-like pathologies in the hippocampal CA1 pyramidal neurons of aged mice
    Ma, Ruiying, Zhang, Yinhua, Li, Huiling, Kang, Hyae Rim, Kim, Yoonhee, Han, Kihoon · 2023 · Animal Cells and Systems
97. The translation initiating factor eIF4E and arginine methylation underlie G3BP1 function in dendritic spine development of neurons
    Rui Dong, Xuejun Li, Angelo D. Flores, Kwok‐On Lai · 2023 · Journal of Biological Chemistry
98. Lipid‐correlated alterations in the transcriptome are enriched in several specific pathways in the postmortem prefrontal cortex of Japanese patients with schizophrenia
    Wataru Arihisa, Takeshi Kondo, Katsushi Yamaguchi, Junya Matsumoto, Hiroki Nakanishi, Yasuto Kunii, Hiroyasu Akatsu, Mizuki Hino, Yoshio Hashizume, Shumpei Sato et al. · 2023 · Neuropsychopharmacology Reports
99. Linking haploinsufficiency of the autism- and schizophrenia-associated gene Cyfip1 with striatal-limbic-cortical network dysfunction and cognitive inflexibility
    Haddon, Josephine E., Titherage, Daniel, Heckenast, Julia R., Carter, Jennifer, Owen, Michael J., Hall, Jeremy, Wilkinson, Lawrence S., Jones, Matthew W. · 2024 · Translational Psychiatry
100. BDNF-dependent nano-organization of Neogenin and the WAVE regulatory complex promotes actin remodeling in dendritic spines
     Belal Shohayeb, Kai Sempert, Tristan P. Wallis, Frédéric A. Meunier, Nela Durisic, Elizabeth A. O’Brien, Cecilia Flores, Helen M. Cooper · 2024 · iScience