All Relations between Rett Syndrome and Neurodevelopmental Disorders

Publication Sentence Publish Date Extraction Date Species
Tal David Berger, Chen Fogel Berger, Sewar Gara, Bruria Ben-Zeev, Batia Weis. Nutritional and gastrointestinal manifestations in Rett syndrome: long-term follow-up. European journal of pediatrics. 2024-07-03. PMID:38960904. rett syndrome is a rare neurodevelopmental disorder associated with methyl cpg binding protein 2 (mecp2) gene mutations. 2024-07-03 2024-07-10 Not clear
Emilie Audouard, Nicolas Khefif, Béatrix Gillet-Legrand, Fanny Nobilleau, Ouafa Bouazizi, Serena Stanga, Gaëtan Despres, Sandro Alves, Antonin Lamazière, Nathalie Cartier, Françoise Pigue. Modulation of Brain Cholesterol Metabolism through CYP46A1 Overexpression for Rett Syndrome. Pharmaceutics. vol 16. issue 6. 2024-06-27. PMID:38931878. rett syndrome (rtt) is a rare neurodevelopmental disorder caused by mutation in the x-linked gene methyl-cpg-binding protein 2 (mecp2), a ubiquitously expressed transcriptional regulator. 2024-06-27 2024-06-29 Not clear
Hong-Wei Dong, Kelly Weiss, Kathryn Baugh, Mac J Meadows, Colleen M Niswender, Jeffrey L Neu. Potentiation of the muscarinic acetylcholine receptor 1 modulates neurophysiological features in a mouse model of Rett syndrome. Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics. 2024-06-16. PMID:38880672. rett syndrome (rtt) is a neurodevelopmental disorder primarily caused by mutations in the x chromosome-linked gene methyl-cpg binding protein 2 (mecp2). 2024-06-16 2024-06-19 mouse
Kathleen J Motil, Arthur Beisang, Constance Smith-Hicks, Anthony Lembo, Shannon M Standridge, Edwin Li. Recommendations for the management of gastrointestinal comorbidities with or without trofinetide use in rett syndrome. Expert review of gastroenterology & hepatology. 2024-06-13. PMID:38869952. although gastrointestinal (gi) comorbidities are experienced by over 90% of individuals with rett syndrome (rtt), a neurodevelopmental disorder associated with mutations in the mecp2 gene, many neurologists and pediatricians do not rank the management of these comorbidities among the most important treatment goals for rtt. 2024-06-13 2024-06-16 Not clear
Destynie Medeiros, Karen Ayala-Baylon, Hailey Egido-Betancourt, Eric Miller, Christopher Chapleau, Holly Robinson, Mary L Phillips, Tao Yang, Frank M Longo, Wei Li, Lucas Pozzo-Mille. A small-molecule TrkB ligand improves dendritic spine phenotypes and atypical behaviors in female Rett syndrome mice. Disease models & mechanisms. vol 17. issue 6. 2024-05-24. PMID:38785269. rett syndrome (rtt) is a neurodevelopmental disorder caused by mutations in mecp2, which encodes methyl-cpg-binding protein 2, a transcriptional regulator of many genes, including brain-derived neurotrophic factor (bdnf). 2024-05-24 2024-05-27 mouse
Indumathy Jagadeeswaran, Jiyoung Oh, Sarah E Sinnet. Preclinical milestones in MECP2 gene transfer for treating Rett syndrome. Developmental neuroscience. 2024-05-09. PMID:38723617. rett syndrome (rtt) is a neurodevelopmental disorder caused by mutations in the transcriptional regulator methyl-cpg-binding protein 2 (mecp2). 2024-05-09 2024-05-27 mouse
Yi Liu, Anthony Flamier, George W Bell, Annette Jun Diao, Troy W Whitfield, Hao-Che Wang, Yizhe Wu, Fabian Schulte, Max Friesen, Ruisi Guo, Maisam Mitalipova, X Shawn Liu, Seychelle M Vos, Richard A Young, Rudolf Jaenisc. MECP2 directly interacts with RNA polymerase II to modulate transcription in human neurons. Neuron. 2024-05-02. PMID:38697112. mutations in the methyl-dna-binding protein mecp2 cause the neurodevelopmental disorder rett syndrome (rtt). 2024-05-02 2024-05-05 human
Nicholas J Santistevan, Colby T Ford, Cole S Gilsdorf, Yevgenya Grinbla. Behavioral and transcriptomic analyses of mecp2 function in zebrafish. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics. 2024-03-29. PMID:38551133. rett syndrome (rtt), a human neurodevelopmental disorder characterized by severe cognitive and motor impairments, is caused by dysfunction of the conserved transcriptional regulator methyl-cpg-binding protein 2 (mecp2). 2024-03-29 2024-03-31 mouse
Dennis Lebeda, Adrian Fierenz, Lina Werfel, Rina Rosin-Arbesfeld, Julia Hofhuis, Sven Thom. Systematic and quantitative analysis of stop codon readthrough in Rett syndrome nonsense mutations. Journal of molecular medicine (Berlin, Germany). 2024-03-02. PMID:38430393. rett syndrome (rtt) is a neurodevelopmental disorder resulting from genetic mutations in the methyl cpg binding protein 2 (mecp2) gene. 2024-03-02 2024-03-04 Not clear
Breanne J Byiers, Alyssa M Merbler, Chantel C Barney, Kristin A Frenn, Angela Panoskaltsis-Mortari, Michael J Ehrhardt, Timothy J Feyma, Arthur A Beisang, Frank Symon. Evidence of altered salivary cytokine concentrations in Rett syndrome and associations with clinical severity. Brain, behavior, & immunity - health. vol 1. 2024-02-20. PMID:38377412. immune dysregulation may play a role in the development of rett syndrome (rtt), a neurodevelopmental disorder caused by mutations of the mecp2 gene. 2024-02-20 2024-02-23 Not clear
Anastasia Neklyudova, Rabiat Kuramagomedova, Victoria Voinova, Olga Sysoev. Atypical brain responses to 40-Hz click trains in girls with Rett syndrome: Auditory steady-state response and sustained wave. Psychiatry and clinical neurosciences. 2024-02-07. PMID:38321640. the current study aimed to infer neurophysiological mechanisms of auditory processing in children with rett syndrome (rtt)-rare neurodevelopmental disorders caused by mecp2 mutations. 2024-02-07 2024-02-09 Not clear
Ze Cao, Xia Min, Xingxing Xie, Maoqing Huang, Yingying Liu, Weimin Sun, Guifang Xu, Miao He, Kaiwen He, Ying Li, Junying Yua. RIPK1 activation in Mecp2-deficient microglia promotes inflammation and glutamate release in RTT. Proceedings of the National Academy of Sciences of the United States of America. vol 121. issue 6. 2024-01-30. PMID:38289948. rett syndrome (rtt) is a devastating neurodevelopmental disorder primarily caused by mutations in the methyl-cpg binding protein 2 (mecp2) gene. 2024-01-30 2024-02-02 mouse
Priscila Frayre, Karen Ponce-Rubio, Jessica Frayre, Jacquelin Medrano, Elisa Sun N. POMC-specific knockdown of MeCP2 leads to adverse phenotypes in mice chronically exposed to high fat diet. Behavioural brain research. 2024-01-15. PMID:38224819. methyl-cpg binding protein 2 (mecp2) is an epigenetic factor associated with the neurodevelopmental disorders rett syndrome and mecp2 duplication syndrome. 2024-01-15 2024-01-18 mouse
Mohan Gomathi, Venkatesan Dhivya, Vijayakumar Padmavathi, Murugasamy Pradeepkumar, S Robert Wilson, Nachimuthu Senthil Kumar, Vellingiri Balachanda. Genetic Instability and Disease Progression of Indian Rett Syndrome Patients. Molecular neurobiology. 2023-12-26. PMID:38147229. rett syndrome (rtt) is the rare neurodevelopmental disorder caused by mutations in methyl cpg binding protein 2 (mecp2) gene with a prevalence of 1:10,000 worldwide. 2023-12-26 2023-12-28 Not clear
Arianna Pasqui, Vittoria Cicaloni, Laura Tinti, Anna Guiotto, Cristina Tinti, Alessia Mori, Marco Bruttini, Joussef Hayek, Alessandra Pecorelli, Laura Salvini, Giuseppe Valacch. A proteomic approach to investigate the role of the MECP2 gene mutation in Rett syndrome redox regulatory pathways. Archives of biochemistry and biophysics. 2023-12-18. PMID:38110111. mutations in the x-linked methyl-cpg-binding 2 (mecp2) gene lead to rett syndrome (rtt; omim 312750), a devasting neurodevelopmental disorder. 2023-12-18 2023-12-21 Not clear
Santosh R D'Mell. Rett and Rett-related disorders: Common mechanisms for shared symptoms? Experimental biology and medicine (Maywood, N.J.). 2023-12-07. PMID:38057990. rett syndrome is a neurodevelopmental disorder caused by loss-of-function mutations in the methyl-cpg binding protein-2 (mecp2) gene that is characterized by epilepsy, intellectual disability, autistic features, speech deficits, and sleep and breathing abnormalities. 2023-12-07 2023-12-10 Not clear
Santosh R D'Mell. Rett and Rett-related disorders: Common mechanisms for shared symptoms? Experimental biology and medicine (Maywood, N.J.). 2023-12-07. PMID:38057990. the relatively recent realization that cdkl5 deficiency disorder (cdd), foxg1 syndrome, and rett syndrome are distinct neurodevelopmental disorders with some distinctive features have resulted in separate focus being placed on each disorder with the assumption that distinct molecular mechanisms underlie their pathogenesis. 2023-12-07 2023-12-10 Not clear
Azam Asgarihafshejani, Vineeth Andisseryparambi Raveendran, Jessica C Pressey, Melanie A Woodi. LTP is Absent in the CA1 Region of the Hippocampus of Male and Female Rett Syndrome Mouse Models. Neuroscience. 2023-11-30. PMID:38036056. rett syndrome (rtt) is a debilitating neurodevelopmental disorder caused by mutations in the x-linked methyl-cpg-binding protein 2 (mecp2) gene, resulting in severe deficits in learning and memory. 2023-11-30 2023-12-10 mouse
Catarina Miranda-Lourenço, Jéssica Rosa, Nádia Rei, Rita F Belo, Ana Luísa Lopes, Diogo Silva, Cátia Vieira, Teresa Magalhães-Cardoso, Ricardo Viais, Paulo Correia-de-Sá, Ana M Sebastião, Maria J Diógene. Adenosinergic System and BDNF Signaling Changes as a Cross-Sectional Feature of RTT: Characterization of International journal of molecular sciences. vol 24. issue 22. 2023-11-25. PMID:38003438. adenosinergic system and bdnf signaling changes as a cross-sectional feature of rtt: characterization of rett syndrome is an x-linked neurodevelopmental disorder (rtt; omim#312750) associated to 2023-11-25 2023-11-28 Not clear
Destynie Medeiros, Karen Ayala-Baylon, Hailey Egido-Betancourt, Eric Miller, Christopher A Chapleau, Holly A Robinson, Mary L Phillips, Tao Yang, Frank Longo, Wei Li, Lucas Pozzo-Mille. A small-molecule TrkB ligand improves dendritic spine phenotypes and atypical behaviors in female Rett syndrome mice. bioRxiv : the preprint server for biology. 2023-11-21. PMID:37986936. rett syndrome (rtt) is a neurodevelopmental disorder caused by mutations in methyl-cpg-binding protein-2 (mecp2), encoding a transcriptional regulator of many genes, including brain-derived neurotrophic factor (bdnf). 2023-11-21 2023-11-29 mouse