| Publication |
Sentence |
Publish Date |
Extraction Date |
Species |
| Fatima Banine, Valerie Matagne, Larry S Sherman, Sergio R Ojed. Brain region-specific expression of Fxyd1, an Mecp2 target gene, is regulated by epigenetic mechanisms. Journal of neuroscience research. vol 89. issue 6. 2011-08-23. PMID:21394759. |
consistently with these observations, fxyd1 mrna abundance is increased in the fc of rett syndrome (rtt) patients with mecp2 mutations. |
2011-08-23 |
2023-08-12 |
mouse |
| Rodney C Samaco, Jeffrey L Neu. Complexities of Rett syndrome and MeCP2. The Journal of neuroscience : the official journal of the Society for Neuroscience. vol 31. issue 22. 2011-08-23. PMID:21632916. |
complexities of rett syndrome and mecp2. |
2011-08-23 |
2023-08-12 |
Not clear |
| Richard D Smrt, Rebecca L Pfeiffer, Xinyu Zha. Age-dependent expression of MeCP2 in a heterozygous mosaic mouse model. Human molecular genetics. vol 20. issue 9. 2011-08-15. PMID:21330301. |
functional deficiency of the x-linked methyl-cpg binding protein 2 (mecp2) leads to the neurodevelopmental disorder rett syndrome (rtt). |
2011-08-15 |
2023-08-12 |
mouse |
| Chenghua Yang, Mark J van der Woerd, Uma M Muthurajan, Jeffrey C Hansen, Karolin Luge. Biophysical analysis and small-angle X-ray scattering-derived structures of MeCP2-nucleosome complexes. Nucleic acids research. vol 39. issue 10. 2011-08-09. PMID:21278419. |
mutations in mecp2 are associated with rett syndrome, the main cause of mental retardation in girls. |
2011-08-09 |
2023-08-12 |
Not clear |
| Nicolas Voituron, Gérard Hilair. The benzodiazepine Midazolam mitigates the breathing defects of Mecp2-deficient mice. Respiratory physiology & neurobiology. vol 177. issue 1. 2011-08-08. PMID:21315849. |
rett syndrome is a severe neurodevelopmental disease caused by mutations of the transcriptional repressor methyl-cpg-binding protein 2 (mecp2) that induce complex, disabling symptoms, including breathing symptoms. |
2011-08-08 |
2023-08-12 |
mouse |
| Nourhene Fendri-Kriaa, Ines Hsairi, Chamseddine Kifagi, Emna Ellouze, Emna Mkaouar-Rebai, Chahnez Triki, Faiza Fakhfak. A case of a Tunisian Rett patient with a novel double-mutation of the MECP2 gene. Biochemical and biophysical research communications. vol 409. issue 2. 2011-08-08. PMID:21575601. |
rett syndrome is an x-linked dominant disorder caused frequently by mutations in the methyl-cpg-binding protein 2 gene (mecp2). |
2011-08-08 |
2023-08-12 |
Not clear |
| Elisa S Na, Lisa M Monteggi. The role of MeCP2 in CNS development and function. Hormones and behavior. vol 59. issue 3. 2011-08-05. PMID:20515694. |
rett syndrome is a neurodevelopmental disorder that is a direct consequence of functional mutations in the methyl-cpg-binding protein-2 (mecp2) gene, which has focused attention on epigenetic mechanisms in neurons. |
2011-08-05 |
2023-08-12 |
mouse |
| Elisa S Na, Lisa M Monteggi. The role of MeCP2 in CNS development and function. Hormones and behavior. vol 59. issue 3. 2011-08-05. PMID:20515694. |
this review will discuss the role of mecp2 in cns development and function, as well as a potential important role for mecp2 and epigenetic processes involved in mediating transcriptional repression in rett syndrome. |
2011-08-05 |
2023-08-12 |
mouse |
| S-M Weng, F McLeod, M E S Bailey, S R Cob. Synaptic plasticity deficits in an experimental model of rett syndrome: long-term potentiation saturation and its pharmacological reversal. Neuroscience. vol 180. 2011-08-04. PMID:21296130. |
rett syndrome (rtt), a disorder caused almost exclusively by mutations in the x-linked gene, mecp2, has a phenotype thought to be primarily of neurological origin. |
2011-08-04 |
2023-08-12 |
mouse |
| Christopher M McGraw, Rodney C Samaco, Huda Y Zoghb. Adult neural function requires MeCP2. Science (New York, N.Y.). vol 333. issue 6039. 2011-07-19. PMID:21636743. |
rett syndrome (rtt) is a postnatal neurological disorder caused by mutations in mecp2, encoding the epigenetic regulator methyl-cpg-binding protein 2 (mecp2). |
2011-07-19 |
2023-08-12 |
mouse |
| Lyndon G Rosser, Shane McKee, David S Millar, Hayley Archer, James Hughes, Rachel Butler, Nadia Chuzhanova, David N Cooper, Lazarus P Lazaro. Two sisters with Rett syndrome and non-identical paternally-derived microdeletions in the MECP2 gene. Genomic medicine. vol 2. issue 3-4. 2011-07-14. PMID:18810657. |
two sisters with rett syndrome and non-identical paternally-derived microdeletions in the mecp2 gene. |
2011-07-14 |
2023-08-12 |
Not clear |
| Kimberly Augenstein, Jane B Lane, Antony Horton, Carolyn Schanen, Alan K Perc. Variable phenotypic expression of a MECP2 mutation in a family. Journal of neurodevelopmental disorders. vol 1. issue 4. 2011-07-14. PMID:20151026. |
we report a three generation family in which five members, three females and two males, demonstrate a 44 bp deletion (1164-1207del44) in the mecp2 gene associated with rett syndrome, leading to a truncation of the c-terminus of the protein. |
2011-07-14 |
2023-08-12 |
Not clear |
| Kinga Hadzsiev, Noemi Polgar, Judit Bene, Katalin Komlosi, Judit Karteszi, Katalin Hollody, Gyorgy Kosztolanyi, Alessandra Renieri, Bela Meleg. Analysis of Hungarian patients with Rett syndrome phenotype for MECP2, CDKL5 and FOXG1 gene mutations. Journal of human genetics. vol 56. issue 3. 2011-07-14. PMID:21160487. |
analysis of hungarian patients with rett syndrome phenotype for mecp2, cdkl5 and foxg1 gene mutations. |
2011-07-14 |
2023-08-12 |
human |
| Gang Song, Chung Tin, Emanuela Giacometti, Chi-Sang Poo. Habituation without NMDA Receptor-Dependent Desensitization of Hering-Breuer Apnea Reflex in a Mecp2 Mutant Mouse Model of Rett Syndrome. Frontiers in integrative neuroscience. vol 5. 2011-07-14. PMID:21629824. |
habituation without nmda receptor-dependent desensitization of hering-breuer apnea reflex in a mecp2 mutant mouse model of rett syndrome. |
2011-07-14 |
2023-08-12 |
mouse |
| Gang Song, Chung Tin, Emanuela Giacometti, Chi-Sang Poo. Habituation without NMDA Receptor-Dependent Desensitization of Hering-Breuer Apnea Reflex in a Mecp2 Mutant Mouse Model of Rett Syndrome. Frontiers in integrative neuroscience. vol 5. 2011-07-14. PMID:21629824. |
here, we show that abnormal non-associative learning of the hbir may underlie the endophenotypic tachypnea in an animal model of rett syndrome (rtt), an autism-spectrum disorder caused by mutations in the x-linked gene encoding methyl-cpg-binding protein 2 (mecp2). |
2011-07-14 |
2023-08-12 |
mouse |
| Nicholas J Neill, Blake C Ballif, Allen N Lamb, Sumit Parikh, J Britt Ravnan, Roger A Schultz, Beth S Torchia, Jill A Rosenfeld, Lisa G Shaffe. Recurrence, submicroscopic complexity, and potential clinical relevance of copy gains detected by array CGH that are shown to be unbalanced insertions by FISH. Genome research. vol 21. issue 4. 2011-07-13. PMID:21383316. |
using fish, linear amplification, and array cgh, we identified a 126-kb duplicated region from 19p13.3 inserted into mecp2 at xq28 in a patient with symptoms of rett syndrome. |
2011-07-13 |
2023-08-12 |
Not clear |
| Rajni Khajuria, Neerja Gupta, Savita Sapra, Sheffali Gulati, Manju Ghosh, Veena Kalra, Madhulika Kabr. A novel MECP2 change in an indian boy with variant rett phenotype and congenital blindness: implications for genetic counseling and prenatal diagnosis. Journal of child neurology. vol 26. issue 2. 2011-06-30. PMID:21285040. |
mutations in mecp2 gene are the primary cause of rett syndrome, a neurodevelopmental disorder that primarily affects girls, and affect 90% to 95% patients with classical rett syndrome. |
2011-06-30 |
2023-08-12 |
Not clear |
| Rocio G Urdinguio, Agustin F Fernandez, Pilar Lopez-Nieva, Simona Rossi, Dori Huertas, Marta Kulis, Chang-Gong Liu, Carlo M Croce, George A Calin, Manel Estelle. Disrupted microRNA expression caused by Mecp2 loss in a mouse model of Rett syndrome. Epigenetics. vol 5. issue 7. 2011-06-28. PMID:20716963. |
disrupted microrna expression caused by mecp2 loss in a mouse model of rett syndrome. |
2011-06-28 |
2023-08-12 |
mouse |
| Rocio G Urdinguio, Agustin F Fernandez, Pilar Lopez-Nieva, Simona Rossi, Dori Huertas, Marta Kulis, Chang-Gong Liu, Carlo M Croce, George A Calin, Manel Estelle. Disrupted microRNA expression caused by Mecp2 loss in a mouse model of Rett syndrome. Epigenetics. vol 5. issue 7. 2011-06-28. PMID:20716963. |
rett syndrome is a complex neurological disorder that has been associated with mutations in the gene coding for mecp2. |
2011-06-28 |
2023-08-12 |
mouse |
| Rocio G Urdinguio, Agustin F Fernandez, Pilar Lopez-Nieva, Simona Rossi, Dori Huertas, Marta Kulis, Chang-Gong Liu, Carlo M Croce, George A Calin, Manel Estelle. Disrupted microRNA expression caused by Mecp2 loss in a mouse model of Rett syndrome. Epigenetics. vol 5. issue 7. 2011-06-28. PMID:20716963. |
thus, we examined the possible mirna misregulation caused by mecp2 absence in a mouse model of rett syndrome. |
2011-06-28 |
2023-08-12 |
mouse |