| Publication |
Sentence |
Publish Date |
Extraction Date |
Species |
| Emmanuelle Dura, Laurent Villard, Jean-Christophe Rou. Expression of methyl CpG binding protein 2 (Mecp2) during the postnatal development of the mouse brainstem. Brain research. vol 1236. 2009-04-16. PMID:18761004. |
mutations in mecp2 lead to a wide range of neurological phenotypes and the better known of these diseases is rett syndrome. |
2009-04-16 |
2023-08-12 |
mouse |
| Jean-Christophe Roux, Emmanuelle Dura, Laurent Villar. Tyrosine hydroxylase deficit in the chemoafferent and the sympathoadrenergic pathways of the Mecp2 deficient mouse. Neuroscience letters. vol 447. issue 1. 2009-04-14. PMID:18834926. |
mutations in the gene encoding the transcriptional methyl-cpg binding protein 2 (mecp2) cause a wide range of neurological disorders and the better known of these diseases is rett syndrome (rs). |
2009-04-14 |
2023-08-12 |
mouse |
| Debra E Weese-Mayer, Steven P Lieske, Christina M Boothby, Anna S Kenny, Heather L Bennett, Jan-Marino Ramire. Autonomic dysregulation in young girls with Rett Syndrome during nighttime in-home recordings. Pediatric pulmonology. vol 43. issue 11. 2009-04-13. PMID:18831533. |
this study was designed to specifically characterize the autonomic phenotype of cardiorespiratory dysregulation during the nighttime in young girls with mecp2 mutation-confirmed rett syndrome (rs), studied in their home environment. |
2009-04-13 |
2023-08-12 |
Not clear |
| Lisa M Monteggia, Ege T Kavalal. Rett syndrome and the impact of MeCP2 associated transcriptional mechanisms on neurotransmission. Biological psychiatry. vol 65. issue 3. 2009-04-10. PMID:19058783. |
rett syndrome and the impact of mecp2 associated transcriptional mechanisms on neurotransmission. |
2009-04-10 |
2023-08-12 |
Not clear |
| Lisa M Monteggia, Ege T Kavalal. Rett syndrome and the impact of MeCP2 associated transcriptional mechanisms on neurotransmission. Biological psychiatry. vol 65. issue 3. 2009-04-10. PMID:19058783. |
rett syndrome, a neurodevelopmental disorder that arises from mutations in the methyl-cpg-binding protein-2 (mecp2) gene, is a salient example for such a disease state in which synaptic transmission-in particular, spontaneous neurotransmission and short-term synaptic plasticity, have been altered. |
2009-04-10 |
2023-08-12 |
Not clear |
| C S Loat, S Curran, C M Lewis, J Duvall, D Geschwind, P Bolton, I W Crai. Methyl-CpG-binding protein 2 polymorphisms and vulnerability to autism. Genes, brain, and behavior. vol 7. issue 7. 2009-04-10. PMID:19125863. |
the methyl-binding protein gene, mecp2, is a candidate for involvement in autism through its implication as a major causative factor in rett syndrome that has similarities to autism. |
2009-04-10 |
2023-08-12 |
Not clear |
| Sabrina Buoni, Raffaella Zannolli, Claudio De Felice, Simona Saponari, Mirella Strambi, Maria Teresa Dotti, Elena Castrucci, Letizia Corbini, Alessandra Orsi, Joseph Haye. Drug-resistant epilepsy and epileptic phenotype-EEG association in MECP2 mutated Rett syndrome. Clinical neurophysiology : official journal of the International Federation of Clinical Neurophysiology. vol 119. issue 11. 2009-04-09. PMID:18842453. |
drug-resistant epilepsy and epileptic phenotype-eeg association in mecp2 mutated rett syndrome. |
2009-04-09 |
2023-08-12 |
Not clear |
| Sabrina Buoni, Raffaella Zannolli, Claudio De Felice, Simona Saponari, Mirella Strambi, Maria Teresa Dotti, Elena Castrucci, Letizia Corbini, Alessandra Orsi, Joseph Haye. Drug-resistant epilepsy and epileptic phenotype-EEG association in MECP2 mutated Rett syndrome. Clinical neurophysiology : official journal of the International Federation of Clinical Neurophysiology. vol 119. issue 11. 2009-04-09. PMID:18842453. |
to determine in mecp2-mutated rett syndrome (rtt [mim 312750]): (1) the prevalence of drug-resistant epilepsy (dre); (2) whether the presence of dre is related to the abnormal eeg patterns or to the particular mecp2 mutant genotype. |
2009-04-09 |
2023-08-12 |
Not clear |
| Bonnie C Ward, Nancy H Kolodny, Nupur Nag, Joanne E Berger-Sweene. Neurochemical changes in a mouse model of Rett syndrome: changes over time and in response to perinatal choline nutritional supplementation. Journal of neurochemistry. vol 108. issue 2. 2009-04-08. PMID:19012748. |
rett syndrome (rtt), the second leading cause of mental retardation in girls, is caused by mutations in the x-linked gene for methyl-cpg-binding protein 2 (mecp2), a transcriptional repressor. |
2009-04-08 |
2023-08-12 |
mouse |
| Jifang Tao, Keping Hu, Qiang Chang, Hao Wu, Nicholas E Sherman, Keri Martinowich, Robert J Klose, Carolyn Schanen, Rudolf Jaenisch, Weidong Wang, Yi Eve Su. Phosphorylation of MeCP2 at Serine 80 regulates its chromatin association and neurological function. Proceedings of the National Academy of Sciences of the United States of America. vol 106. issue 12. 2009-04-08. PMID:19225110. |
mutations of mecp2 (methyl-cpg binding protein 2) cause rett syndrome. |
2009-04-08 |
2023-08-12 |
mouse |
| Eric E J Smeets, Mickey Chenault, Leopold M G Curfs, Connie T R M Schrander-Stumpel, Jean-Pierre Frijn. Rett syndrome and long-term disorder profile. American journal of medical genetics. Part A. vol 149A. issue 2. 2009-04-06. PMID:19133691. |
in a cohort of 103 females clinically diagnosed with rett syndrome (rtt), 91 had a detectable mecp2 mutation. |
2009-04-06 |
2023-08-12 |
Not clear |
| M R Matarazzo, M L De Bonis, M Vacca, F Della Ragione, M D'Esposit. Lessons from two human chromatin diseases, ICF syndrome and Rett syndrome. The international journal of biochemistry & cell biology. vol 41. issue 1. 2009-04-02. PMID:18786650. |
both diseases are caused by defects related to dna methylation machinery, with rett syndrome affecting the transduction of the repressive signal from the methyl cpg binding protein prototype, mecp2, and icf syndrome affecting the genetic control of dna methylation, by the dna methyltransferase dnmt3b. |
2009-04-02 |
2023-08-12 |
human |
| Marc Fischer, Julia Reuter, Florian J Gerich, Belinda Hildebrandt, Sonja Hägele, Dörthe Katschinski, Michael Mülle. Enhanced hypoxia susceptibility in hippocampal slices from a mouse model of rett syndrome. Journal of neurophysiology. vol 101. issue 2. 2009-03-26. PMID:19073793. |
rett syndrome is a neurodevelopmental disorder caused by mutations in the x-chromosomal mecp2 gene encoding for the transcriptional regulator methyl cpg binding protein 2 (mecp2). |
2009-03-26 |
2023-08-12 |
mouse |
| Geneviève P Delcuve, Mojgan Rastegar, James R Davi. Epigenetic control. Journal of cellular physiology. vol 219. issue 2. 2009-03-16. PMID:19127539. |
further, research on rett syndrome has revealed an unforeseen role for methyl-cpg-binding protein 2 (mecp2) in neurons. |
2009-03-16 |
2023-08-12 |
Not clear |
| Nurit Ballas, Daniel T Lioy, Christopher Grunseich, Gail Mande. Non-cell autonomous influence of MeCP2-deficient glia on neuronal dendritic morphology. Nature neuroscience. vol 12. issue 3. 2009-03-16. PMID:19234456. |
the neurodevelopmental disorder rett syndrome (rtt) is caused by sporadic mutations in the transcriptional factor methyl-cpg-binding protein 2 (mecp2). |
2009-03-16 |
2023-08-12 |
mouse |
| Daniela Tropea, Emanuela Giacometti, Nathan R Wilson, Caroline Beard, Cortina McCurry, Dong Dong Fu, Ruth Flannery, Rudolf Jaenisch, Mriganka Su. Partial reversal of Rett Syndrome-like symptoms in MeCP2 mutant mice. Proceedings of the National Academy of Sciences of the United States of America. vol 106. issue 6. 2009-03-10. PMID:19208815. |
rett syndrome (rtt) is a severe form of x-linked mental retardation caused by mutations in the gene coding for methyl cpg-binding protein 2 (mecp2). |
2009-03-10 |
2023-08-12 |
mouse |
| Susan E Swanberg, Raman P Nagarajan, Sailaja Peddada, Dag H Yasui, Janine M LaSall. Reciprocal co-regulation of EGR2 and MECP2 is disrupted in Rett syndrome and autism. Human molecular genetics. vol 18. issue 3. 2009-02-27. PMID:19000991. |
reciprocal co-regulation of egr2 and mecp2 is disrupted in rett syndrome and autism. |
2009-02-27 |
2023-08-12 |
mouse |
| Susan E Swanberg, Raman P Nagarajan, Sailaja Peddada, Dag H Yasui, Janine M LaSall. Reciprocal co-regulation of EGR2 and MECP2 is disrupted in Rett syndrome and autism. Human molecular genetics. vol 18. issue 3. 2009-02-27. PMID:19000991. |
mutations in mecp2, encoding methyl-cpg-binding protein 2 (mecp2), cause the neurodevelopmental disorder rett syndrome (rtt). |
2009-02-27 |
2023-08-12 |
mouse |
| Mário Campos, Cláudia Bueno Abdalla, Adriana Vaz dos Santos, Cristiane Pinheiro Pestana, Jussara Mendonça dos Santos, Cíntia Barros Santos-Rebouças, Márcia Mattos Gonçalves Pimente. A MECP2 mutation in a highly conserved aminoacid causing mental retardation in a male. Brain & development. vol 31. issue 2. 2009-02-09. PMID:18678449. |
mutations in mecp2 gene have been reported as being the major cause of rett syndrome. |
2009-02-09 |
2023-08-12 |
Not clear |
| Nupur Nag, Jennifer M Moriuchi, Cassandra G K Peitzman, Bonnie C Ward, Nancy H Kolodny, Joanne E Berger-Sweene. Environmental enrichment alters locomotor behaviour and ventricular volume in Mecp2 1lox mice. Behavioural brain research. vol 196. issue 1. 2009-02-03. PMID:18687363. |
rett syndrome (rtt) is an autistic spectrum developmental disorder associated with mutations in the x-linked mecp2 gene, and severe behavioural and neuropathological deficits. |
2009-02-03 |
2023-08-12 |
mouse |