| Publication |
Sentence |
Publish Date |
Extraction Date |
Species |
| Sarika U Peters, Reyna L Gordon, Alexandra P Ke. Induced gamma oscillations differentiate familiar and novel voices in children with MECP2 duplication and Rett syndromes. Journal of child neurology. vol 30. issue 2. 2015-09-25. PMID:24776956. |
it was hypothesized that children with mecp2 duplication (overexpression of mecp2) and rett syndrome (underexpression of mecp2) would exhibit distinct electroencephalographic (eeg) indices of auditory stimulus discrimination. |
2015-09-25 |
2023-08-13 |
Not clear |
| Sarika U Peters, Reyna L Gordon, Alexandra P Ke. Induced gamma oscillations differentiate familiar and novel voices in children with MECP2 duplication and Rett syndromes. Journal of child neurology. vol 30. issue 2. 2015-09-25. PMID:24776956. |
in this study, gamma-band oscillatory responses to familiar and novel voices were examined and related to social functioning in 17 children (3-11 years old) with mecp2 duplication (n = 12) and rett syndrome (n = 5). |
2015-09-25 |
2023-08-13 |
Not clear |
| Sarika U Peters, Reyna L Gordon, Alexandra P Ke. Induced gamma oscillations differentiate familiar and novel voices in children with MECP2 duplication and Rett syndromes. Journal of child neurology. vol 30. issue 2. 2015-09-25. PMID:24776956. |
relative to the stranger's voice, gamma activity in response to the mother's voice was increased in mecp2 duplication but decreased in rett syndrome. |
2015-09-25 |
2023-08-13 |
Not clear |
| Gaston Calfa, Wei Li, John M Rutherford, Lucas Pozzo-Mille. Excitation/inhibition imbalance and impaired synaptic inhibition in hippocampal area CA3 of Mecp2 knockout mice. Hippocampus. vol 25. issue 2. 2015-09-16. PMID:25209930. |
rett syndrome (rtt) is a neurodevelopment disorder associated with intellectual disabilities and caused by loss-of-function mutations in the gene encoding the transcriptional regulator methyl-cpg-binding protein-2 (mecp2). |
2015-09-16 |
2023-08-13 |
mouse |
| Anna Urbanowicz, Jenny Downs, Sonya Girdler, Natalie Ciccone, Helen Leonar. Aspects of speech-language abilities are influenced by MECP2 mutation type in girls with Rett syndrome. American journal of medical genetics. Part A. vol 167A. issue 2. 2015-09-16. PMID:25428820. |
aspects of speech-language abilities are influenced by mecp2 mutation type in girls with rett syndrome. |
2015-09-16 |
2023-08-13 |
Not clear |
| Anna Urbanowicz, Jenny Downs, Sonya Girdler, Natalie Ciccone, Helen Leonar. Aspects of speech-language abilities are influenced by MECP2 mutation type in girls with Rett syndrome. American journal of medical genetics. Part A. vol 167A. issue 2. 2015-09-16. PMID:25428820. |
this study investigates relationships between methyl-cpg-binding protein 2 gene (mecp2) mutation type and speech-language abilities in girls with rett syndrome. |
2015-09-16 |
2023-08-13 |
Not clear |
| W A Gold, T A Lacina, L C Cantrill, John Christodoulo. MeCP2 deficiency is associated with reduced levels of tubulin acetylation and can be restored using HDAC6 inhibitors. Journal of molecular medicine (Berlin, Germany). vol 93. issue 1. 2015-09-08. PMID:25209898. |
rett syndrome (rtt) is a severe neurodevelopmental disorder, predominantly caused by loss of function mutations in the x-linked methyl-cpg-binding protein 2 (mecp2) gene. |
2015-09-08 |
2023-08-13 |
mouse |
| Fang-Chi Kao, San-Hua Su, Gregory C Carlson, Wenlin Lia. MeCP2-mediated alterations of striatal features accompany psychomotor deficits in a mouse model of Rett syndrome. Brain structure & function. vol 220. issue 1. 2015-08-28. PMID:24218106. |
rett syndrome (rtt) is a neurodevelopmental disorder caused by mutations in the methyl-cpg-binding protein 2 (mecp2) gene. |
2015-08-28 |
2023-08-12 |
mouse |
| Eike Wegener, Cornelia Brendel, Andre Fischer, Swen Hülsmann, Jutta Gärtner, Peter Huppk. Characterization of the MeCP2R168X knockin mouse model for Rett syndrome. PloS one. vol 9. issue 12. 2015-08-27. PMID:25541993. |
rett syndrome, one of the most common causes of mental retardation in females, is caused by mutations in the x chromosomal gene mecp2. |
2015-08-27 |
2023-08-13 |
mouse |
| Eike Wegener, Cornelia Brendel, Andre Fischer, Swen Hülsmann, Jutta Gärtner, Peter Huppk. Characterization of the MeCP2R168X knockin mouse model for Rett syndrome. PloS one. vol 9. issue 12. 2015-08-27. PMID:25541993. |
mice deficient for mecp2 recapitulate some of the symptoms seen in patients with rett syndrome. |
2015-08-27 |
2023-08-13 |
mouse |
| Francesco Bedogni, Riccardo L Rossi, Francesco Galli, Clementina Cobolli Gigli, Anna Gandaglia, Charlotte Kilstrup-Nielsen, Nicoletta Landsberge. Rett syndrome and the urge of novel approaches to study MeCP2 functions and mechanisms of action. Neuroscience and biobehavioral reviews. vol 46 Pt 2. 2015-08-11. PMID:24594195. |
rett syndrome and the urge of novel approaches to study mecp2 functions and mechanisms of action. |
2015-08-11 |
2023-08-12 |
Not clear |
| Lin Chen, Kaifu Chen, Laura A Lavery, Steven Andrew Baker, Chad A Shaw, Wei Li, Huda Y Zoghb. MeCP2 binds to non-CG methylated DNA as neurons mature, influencing transcription and the timing of onset for Rett syndrome. Proceedings of the National Academy of Sciences of the United States of America. vol 112. issue 17. 2015-07-29. PMID:25870282. |
mecp2 binds to non-cg methylated dna as neurons mature, influencing transcription and the timing of onset for rett syndrome. |
2015-07-29 |
2023-08-13 |
mouse |
| Lin Chen, Kaifu Chen, Laura A Lavery, Steven Andrew Baker, Chad A Shaw, Wei Li, Huda Y Zoghb. MeCP2 binds to non-CG methylated DNA as neurons mature, influencing transcription and the timing of onset for Rett syndrome. Proceedings of the National Academy of Sciences of the United States of America. vol 112. issue 17. 2015-07-29. PMID:25870282. |
a prime example involving epigenetic dysfunction is the postnatal neurodevelopmental disorder rett syndrome (rtt), which is caused by mutations in the gene encoding methyl-cpg binding protein 2 (mecp2). |
2015-07-29 |
2023-08-13 |
mouse |
| Laura Dean Heckman, Maria H Chahrour, Huda Y Zoghb. Rett-causing mutations reveal two domains critical for MeCP2 function and for toxicity in MECP2 duplication syndrome mice. eLife. vol 3. 2015-07-28. PMID:24970834. |
loss of function of the x-linked gene encoding methyl-cpg binding protein 2 (mecp2) causes the progressive neurological disorder rett syndrome (rtt). |
2015-07-28 |
2023-08-13 |
mouse |
| Karolina Szczesna, Olga de la Caridad, Paolo Petazzi, Marta Soler, Laura Roa, Mauricio A Saez, Stéphane Fourcade, Aurora Pujol, Rafael Artuch-Iriberri, Marta Molero-Luis, August Vidal, Dori Huertas, Manel Estelle. Improvement of the Rett syndrome phenotype in a MeCP2 mouse model upon treatment with levodopa and a dopa-decarboxylase inhibitor. Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology. vol 39. issue 12. 2015-07-10. PMID:24917201. |
improvement of the rett syndrome phenotype in a mecp2 mouse model upon treatment with levodopa and a dopa-decarboxylase inhibitor. |
2015-07-10 |
2023-08-13 |
mouse |
| Karolina Szczesna, Olga de la Caridad, Paolo Petazzi, Marta Soler, Laura Roa, Mauricio A Saez, Stéphane Fourcade, Aurora Pujol, Rafael Artuch-Iriberri, Marta Molero-Luis, August Vidal, Dori Huertas, Manel Estelle. Improvement of the Rett syndrome phenotype in a MeCP2 mouse model upon treatment with levodopa and a dopa-decarboxylase inhibitor. Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology. vol 39. issue 12. 2015-07-10. PMID:24917201. |
rett syndrome is a neurodevelopmental autism spectrum disorder caused by mutations in the gene coding for methyl cpg-binding protein (mecp2). |
2015-07-10 |
2023-08-13 |
mouse |
| Mark J Zylka, Jeremy M Simon, Benjamin D Philpo. Gene length matters in neurons. Neuron. vol 86. issue 2. 2015-06-26. PMID:25905808. |
(2015) found that mecp2, the gene mutated in rett syndrome, represses long (> 100 kb) genes associated with neuronal physiology and connectivity by binding to methylated ca sites in dna. |
2015-06-26 |
2023-08-13 |
Not clear |
| Harrison W Gabel, Benyam Kinde, Hume Stroud, Caitlin S Gilbert, David A Harmin, Nathaniel R Kastan, Martin Hemberg, Daniel H Ebert, Michael E Greenber. Disruption of DNA-methylation-dependent long gene repression in Rett syndrome. Nature. vol 522. issue 7554. 2015-06-25. PMID:25762136. |
disruption of the mecp2 gene leads to rett syndrome (rtt), a severe neurological disorder with features of autism. |
2015-06-25 |
2023-08-13 |
mouse |
| Dorothy P Schafer, Beth Steven. Brains, Blood, and Guts: MeCP2 Regulates Microglia, Monocytes, and Peripheral Macrophages. Immunity. vol 42. issue 4. 2015-06-24. PMID:25902477. |
mutations in methyl-cpg-binding protein 2 (mecp2) underlie most cases of rett syndrome, a neurodevelopmental disorder with neurological and somatic impairments. |
2015-06-24 |
2023-08-13 |
mouse |
| Juan Ausió, Alexia Martínez de Paz, Manel Estelle. MeCP2: the long trip from a chromatin protein to neurological disorders. Trends in molecular medicine. vol 20. issue 9. 2015-06-23. PMID:24766768. |
since the discovery of its fundamental involvement in rett syndrome, methyl cpg binding protein 2 (mecp2) has been the focus of an exhaustive biochemical and functional characterization. |
2015-06-23 |
2023-08-13 |
Not clear |