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Results for

""Fragile X Mental Retardation Protein""[mesh_terms]

24 Results

Searching titles within these results

Multifarious Functions of the Fragile X Mental Retardation Protein.

Kendal Broadie, Jenna K Davis

Trends in genetics : TIG 2018;33(10):703-714

Mitochondrial dysfunction in Fragile X syndrome and Fragile X-associated tremor/ataxia syndrome: prospect use of antioxidants and mitochondrial nutrients.

Federico V Pallardó, Adriana Zatterale, Luca Tiano, Giovanni Pagano, Marco Trifuoggi, Alex Lyakhovich

Molecular biology reports 2024;51(1):480

Generation and Characterization of Human Induced Pluripotent Stem Cell-derived Astrocytes Lacking Fragile X Messenger Ribonucleoprotein.

Rakhi Pal, Sumantra Chattarji, Nikhita Annaiyappa, Bharath Kumar Reddy, Aditi Bhattacharya

Journal of visualized experiments : JoVE 2025

Advances in understanding fragile X syndrome and related disorders.

Liesbeth Rooms, R Frank Kooy

Current opinion in pediatrics 2012;23(6):601-6

Fragile X-associated tremor/ataxia syndrome: pathophysiology and management.

Paul Hagerman, Randi Hagerman

Current opinion in neurology 2021;34(4):541-546

The role of G-quadruplex in RNA metabolism: involvement of FMRP and FMR2P.

Barbara Bardoni, Mireille Melko

Biochimie 2010;92(8):919-26

Clinical, molecular, and pharmacological aspects of FMR1 related disorders.

L Santa María, M A Alliende, M I Peña, P Bravo, P Soto, I Salas, S Aliaga, B Curotto, V Faundes, A Pugin

Neurologia (Barcelona, Spain) 2017;32(4):241-252

Whole exome sequencing in a cohort of familial premature ovarian insufficiency cases reveals a broad array of pathogenic or likely pathogenic variants in 50% of families.

Anne Gompel, Yves Reznik, Sophie Catteau-Jonard, Brigitte Delemer, Véronique Kerlan, Eli Rogers, Alexandre Rouen, Isabelle Cedrin, Sophie Christin-Maitre, Philippe Touraine, Jean-Pierre Siffroi, Esther Kott, Tabassome Simon, Alexandra Rousseau, Sandra Chantot-Bastaraud, Anne Bachelot, Catherine Pienkowski, Thierry Brue, Virginie Grouthier, Anne-Marie Guedj

Fertility and sterility 2022;117(4):843-853

Bioinformatics identification and experimental validation of m6A-related diagnostic biomarkers in the subtype classification of blood monocytes from postmenopausal osteoporosis patients.

De Liang, Xiaobing Jiang, Hui Ren, Zhixiang Liu, Jianchao Cui, Jingjing Tang, Fuyong Yu, Guifeng Chen, Guangye Zhu, Zhida Zhang, Xiang Yu, Gengyang Shen, Jiahui He, Qi Shang, Wenhua Zhao, Bin Xie, Honglin Chen, Peng Zhang

Frontiers in endocrinology 2023;14():990078

Overlapping Molecular Pathways Leading to Autism Spectrum Disorders, Fragile X Syndrome, and Targeted Treatments.

Courtney Jessica Clark, Ruchi Harendra Punatar, Ana Maria Cabal-Herrera, Maria Jimena Salcedo-Arellano, Christopher Allen Romney, Randi J Hagerman

Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics 2021;18(1):265-283

Unravelling the link between neurodevelopmental disorders and short tandem CGG-repeat expansions.

R Frank Kooy, Dale J Annear

Emerging topics in life sciences 2023;7(3):265-275

Polysomnographic Findings in Fragile X Syndrome Children with EEG Abnormalities.

Marco Carotenuto, Michele Roccella, Francesco Pisani, Sara Matricardi, Alberto Verrotti, Giovanni Farello, Francesca Felicia Operto, Ilaria Bitetti, Francesco Precenzano, Giovanni Messina, Maria Ruberto, Cristiana Ciunfrini, Mariagrazia Riccardi, Eugenio Merolla, Grazia Maria Giovanna Pastorino, Anna Nunzia Polito, Rosa Marotta

Behavioural neurology 2020;2019():5202808

Treatments for fragile X syndrome: a closer look at the data.

Scott S Hall

Developmental disabilities research reviews 2010;15(4):353-60

Mechanisms of Genome Instability in the Fragile X-Related Disorders.

Karen Usdin, Bruce E Hayward

Genes 2022;12(10):1633

Arginines of the RGG box regulate FMRP association with polyribosomes and mRNA.

Ernest Blackwell, Xing Zhang, Stephanie Ceman

Human molecular genetics 2010;19(7):1314-23

Results: 1 – 15 / 24

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