| Publication |
Sentence |
Publish Date |
Extraction Date |
Species |
| Alessandra Pecorelli, Guido Leoni, Franco Cervellati, Raffaella Canali, Cinzia Signorini, Silvia Leoncini, Alessio Cortelazzo, Claudio De Felice, Lucia Ciccoli, Joussef Hayek, Giuseppe Valacch. Genes related to mitochondrial functions, protein degradation, and chromatin folding are differentially expressed in lymphomonocytes of Rett syndrome patients. Mediators of inflammation. vol 2013. 2014-10-14. PMID:24453408. |
rett syndrome (rtt) is mainly caused by mutations in the x-linked methyl-cpg binding protein (mecp2) gene. |
2014-10-14 |
2023-08-12 |
human |
| Alessio Cortelazzo, Roberto Guerranti, Claudio De Felice, Cinzia Signorini, Silvia Leoncini, Alessandra Pecorelli, Claudia Landi, Luca Bini, Barbara Montomoli, Claudia Sticozzi, Lucia Ciccoli, Giuseppe Valacchi, Joussef Haye. A plasma proteomic approach in Rett syndrome: classical versus preserved speech variant. Mediators of inflammation. vol 2013. 2014-10-14. PMID:24453418. |
rett syndrome (rtt) is a progressive neurodevelopmental disorder mainly caused by mutations in the gene encoding the methyl-cpg-binding protein 2 (mecp2). |
2014-10-14 |
2023-08-12 |
Not clear |
| Jennifer Larimore, Pearl V Ryder, Kun-Yong Kim, L Alex Ambrose, Christopher Chapleau, Gaston Calfa, Christina Gross, Gary J Bassell, Lucas Pozzo-Miller, Yoland Smith, Konrad Talbot, In-Hyun Park, Victor Faunde. MeCP2 regulates the synaptic expression of a Dysbindin-BLOC-1 network component in mouse brain and human induced pluripotent stem cell-derived neurons. PloS one. vol 8. issue 6. 2014-09-29. PMID:23750231. |
we tested this hypothesis by asking if mutations in the asd gene mecp2 which cause rett syndrome affect the expression of genes encoding the schizophrenia risk factor dysbindin, a subunit of the biogenesis of lysosome-related organelles complex-1 (bloc-1), and associated interacting proteins. |
2014-09-29 |
2023-08-12 |
mouse |
| Takeo Kubot. [Epigenome: what we learned from Rett syndrome, a neurological disease caused by mutation of a methyl-CpG binding protein]. Rinsho shinkeigaku = Clinical neurology. vol 53. issue 11. 2014-09-19. PMID:24291980. |
we recently reported that neurological symptoms of rett syndrome, which is an autistic disorder caused by mutations in methyl-cpg binding protein 2 (mecp2), was associated with failure of epigenomic gene regulation in neuronal cells, and that clinical differences in the identical twins with rett syndrome in the differences in dna methylation in neuronal genes, but not caused by dna sequence differences. |
2014-09-19 |
2023-08-12 |
Not clear |
| Jenny Downs, Stephanie Parkinson, Sonia Ranelli, Helen Leonard, Pamela Diener, Meir Lota. Perspectives on hand function in girls and women with Rett syndrome. Developmental neurorehabilitation. vol 17. issue 3. 2014-09-18. PMID:23869872. |
rett syndrome is a rare neurodevelopmental disorder that is usually associated with a mutation on the x-linked mecp2 gene. |
2014-09-18 |
2023-08-12 |
Not clear |
| Scott S Maxwell, Gregory J Pelka, Patrick Pl Tam, Assam El-Ost. Chromatin context and ncRNA highlight targets of MeCP2 in brain. RNA biology. vol 10. issue 11. 2014-09-16. PMID:24270455. |
the discovery that rett syndrome (rtt) is caused by mutation of the methyl-cpg-binding-protein mecp2 provided a major breakthrough in understanding the neurodevelopmental disorder and accelerated mecp2 research. |
2014-09-16 |
2023-08-12 |
Not clear |
| Paul R van Urk, Mariëll P van den Berg, Barend J van Royen, Eric E J Smeets, Leopold M G Curf. [Rett syndrome]. Nederlands tijdschrift voor geneeskunde. vol 158. issue 3. 2014-09-16. PMID:24423488. |
rett syndrome is caused by mutations in the x-linked mecp2 gene, encoding mecp2 protein. |
2014-09-16 |
2023-08-12 |
Not clear |
| Nikolaos Mellios, Jonathan Woodson, Rodrigo I Garcia, Benjamin Crawford, Jitendra Sharma, Steven D Sheridan, Stephen J Haggarty, Mriganka Su. β2-Adrenergic receptor agonist ameliorates phenotypes and corrects microRNA-mediated IGF1 deficits in a mouse model of Rett syndrome. Proceedings of the National Academy of Sciences of the United States of America. vol 111. issue 27. 2014-09-15. PMID:24958851. |
rett syndrome is a severe childhood onset neurodevelopmental disorder caused by mutations in methyl-cpg-binding protein 2 (mecp2), with known disturbances in catecholamine synthesis. |
2014-09-15 |
2023-08-13 |
mouse |
| Chaoran Li, Shan Jiang, Si-Qi Liu, Erik Lykken, Lin-tao Zhao, Jose Sevilla, Bo Zhu, Qi-Jing L. MeCP2 enforces Foxp3 expression to promote regulatory T cells' resilience to inflammation. Proceedings of the National Academy of Sciences of the United States of America. vol 111. issue 27. 2014-09-15. PMID:24958888. |
here, we demonstrate that methyl-cpg binding protein 2 (mecp2), an eminent epigenetic regulator known primarily as the etiological factor of rett syndrome, is critical to sustain foxp3 expression in tregs during inflammation. |
2014-09-15 |
2023-08-13 |
mouse |
| Jorge Castro, Rodrigo I Garcia, Showming Kwok, Abhishek Banerjee, Jeremy Petravicz, Jonathan Woodson, Nikolaos Mellios, Daniela Tropea, Mriganka Su. Functional recovery with recombinant human IGF1 treatment in a mouse model of Rett Syndrome. Proceedings of the National Academy of Sciences of the United States of America. vol 111. issue 27. 2014-09-15. PMID:24958891. |
rett syndrome is a neurodevelopmental disorder that arises from mutations in the x-linked gene methyl-cpg binding protein 2 (mecp2). |
2014-09-15 |
2023-08-13 |
mouse |
| Wenxu Yang, Hong Pa. Regulation mechanism and research progress of MeCP2 in Rett syndrome. Yi chuan = Hereditas. vol 36. issue 7. 2014-09-11. PMID:25076025. |
regulation mechanism and research progress of mecp2 in rett syndrome. |
2014-09-11 |
2023-08-13 |
Not clear |
| Grazia Della Sala, Tommaso Pizzoruss. Synaptic plasticity and signaling in Rett syndrome. Developmental neurobiology. vol 74. issue 2. 2014-09-03. PMID:23908158. |
rett syndrome (rtt) is a disorder that is caused in the majority of cases by mutations in the gene methyl-cpg-binding protein-2 (mecp2). |
2014-09-03 |
2023-08-12 |
Not clear |
| Elisa Bellini, Giulio Pavesi, Isabella Barbiero, Anna Bergo, Chetan Chandola, Mohammad S Nawaz, Laura Rusconi, Gilda Stefanelli, Marta Strollo, Maria M Valente, Charlotte Kilstrup-Nielsen, Nicoletta Landsberge. MeCP2 post-translational modifications: a mechanism to control its involvement in synaptic plasticity and homeostasis? Frontiers in cellular neuroscience. vol 8. 2014-08-28. PMID:25165434. |
although rett syndrome (rtt) represents one of the most frequent forms of severe intellectual disability in females worldwide, we still have an inadequate knowledge of the many roles played by mecp2 (whose mutations are responsible for most cases of rtt) and their relevance for rtt pathobiology. |
2014-08-28 |
2023-08-13 |
mouse |
| D M Kat. Brain-derived neurotrophic factor and Rett syndrome. Handbook of experimental pharmacology. vol 220. 2014-08-26. PMID:24668484. |
rett syndrome (rtt) is a devastating neurodevelopmental disorder with autistic features caused by loss-of-function mutations in the gene encoding methyl-cpg-binding protein 2 (mecp2), a transcriptional regulatory protein. |
2014-08-26 |
2023-08-12 |
mouse |
| Pei-Wei Zhao, Xue-Lian He, Jun Lin, Ge-Fei Wu, Xin Yue, Bo Bi, Jia-Sheng Hu, Zhi-Sheng Li. [Clinical features and MECP2 mutations in children with Rett syndrome]. Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics. vol 16. issue 4. 2014-08-26. PMID:24750837. |
[clinical features and mecp2 mutations in children with rett syndrome]. |
2014-08-26 |
2023-08-13 |
Not clear |
| Pei-Wei Zhao, Xue-Lian He, Jun Lin, Ge-Fei Wu, Xin Yue, Bo Bi, Jia-Sheng Hu, Zhi-Sheng Li. [Clinical features and MECP2 mutations in children with Rett syndrome]. Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics. vol 16. issue 4. 2014-08-26. PMID:24750837. |
to study the clinical features and mutations in methyl-cpg-binding protein 2 (mecp2) gene among children with classical rett syndrome in china. |
2014-08-26 |
2023-08-13 |
Not clear |
| Erica S Levitt, Barbara J Hunnicutt, Sharon J Knopp, John T Williams, John M Bissonnett. A selective 5-HT1a receptor agonist improves respiration in a mouse model of Rett syndrome. Journal of applied physiology (Bethesda, Md. : 1985). vol 115. issue 11. 2014-08-25. PMID:24092697. |
rett syndrome is a neurological disorder caused by loss of function mutations in the gene that encodes the dna binding protein methyl-cpg-binding protein 2 (mecp2). |
2014-08-25 |
2023-08-12 |
mouse |
| Robin M Forbes-Lorman, Joseph R Kurian, Anthony P Auge. MeCP2 regulates GFAP expression within the developing brain. Brain research. vol 1543. 2014-08-18. PMID:24269336. |
mutations in mecp2 cause rett syndrome (rtt), an x-linked neurodevelopmental disorder that primarily affects females. |
2014-08-18 |
2023-08-12 |
rat |
| Veysel Nijat Baş, Semra Çetinkaya, Sebahat Yılmaz Ağladıoğlu, Ayşe Aksoy, Başak Gülpınar, Zehra Ayca. Report of the first case of precocious puberty in Rett syndrome. Journal of pediatric endocrinology & metabolism : JPEM. vol 26. issue 9-10. 2014-08-13. PMID:23612537. |
rett syndrome is an x-linked dominant disorder frequently caused by the mutations in the methyl-cpg-binding protein 2 gene (mecp2). |
2014-08-13 |
2023-08-12 |
Not clear |
| Min Lang, Robert G Wither, Sinisa Colic, Chiping Wu, Philippe P Monnier, Berj L Bardakjian, Liang Zhang, James H Eubank. Rescue of behavioral and EEG deficits in male and female Mecp2-deficient mice by delayed Mecp2 gene reactivation. Human molecular genetics. vol 23. issue 2. 2014-08-05. PMID:24009314. |
mutations of the x-linked gene encoding methyl cpg binding protein type 2 (mecp2) are the predominant cause of rett syndrome, a severe neurodevelopmental condition that affects primarily females. |
2014-08-05 |
2023-08-12 |
mouse |