| Publication |
Sentence |
Publish Date |
Extraction Date |
Species |
| S L Mironov, E Skorova, N Hartelt, L A Mironova, M T Hasan, S Kügle. Remodelling of the respiratory network in a mouse model of Rett syndrome depends on brain-derived neurotrophic factor regulated slow calcium buffering. The Journal of physiology. vol 587. issue Pt 11. 2009-08-03. PMID:19359374. |
rett syndrome caused by mecp2 mutations is a devastating neurodevelopmental disorder accompanied by severe breathing irregularities. |
2009-08-03 |
2023-08-12 |
mouse |
| Kristina Jülich, Denise Horn, Peter Burfeind, Thomas Erler, Bernd Aube. A novel MECP2 mutation in a boy with neonatal encephalopathy and facial dysmorphism. The Journal of pediatrics. vol 155. issue 1. 2009-07-22. PMID:19559301. |
methly-cpg-binding protein 2 (mecp2) mutations cause rett syndrome in females. |
2009-07-22 |
2023-08-12 |
Not clear |
| Rajni Khajuria, Savita Sapra, Manju Ghosh, Neerja Gupta, Sheffali Gulati, Veena Kalra, Madhulika Kabr. Rapid detection of deletions in hotspot C-terminal segment region of MECP2 by routine PCR method: report of two classical Rett syndrome patients of Indian origin. Genetic testing and molecular biomarkers. vol 13. issue 2. 2009-07-09. PMID:19371229. |
rapid detection of deletions in hotspot c-terminal segment region of mecp2 by routine pcr method: report of two classical rett syndrome patients of indian origin. |
2009-07-09 |
2023-08-12 |
Not clear |
| Liron Abuhatzira, Ruth Shemer, Aharon Razi. MeCP2 involvement in the regulation of neuronal alpha-tubulin production. Human molecular genetics. vol 18. issue 8. 2009-07-06. PMID:19174478. |
rett syndrome (rtt) is a severe neurodevelopmental disorder caused by a dominant mutation in the x-linked methyl cpg binding protein 2 (mecp2) gene. |
2009-07-06 |
2023-08-12 |
human |
| Liron Abuhatzira, Ruth Shemer, Aharon Razi. MeCP2 involvement in the regulation of neuronal alpha-tubulin production. Human molecular genetics. vol 18. issue 8. 2009-07-06. PMID:19174478. |
this raises hopes for a cure of rett syndrome and related mecp2 deficiency disorders of the autistic spectrum. |
2009-07-06 |
2023-08-12 |
human |
| Carol J Saunders, Berge E Minassian, Eva W C Chow, Weiwei Zhao, John B Vincen. Novel exon 1 mutations in MECP2 implicate isoform MeCP2_e1 in classical Rett syndrome. American journal of medical genetics. Part A. vol 149A. issue 5. 2009-06-18. PMID:19365833. |
novel exon 1 mutations in mecp2 implicate isoform mecp2_e1 in classical rett syndrome. |
2009-06-18 |
2023-08-12 |
Not clear |
| Carol J Saunders, Berge E Minassian, Eva W C Chow, Weiwei Zhao, John B Vincen. Novel exon 1 mutations in MECP2 implicate isoform MeCP2_e1 in classical Rett syndrome. American journal of medical genetics. Part A. vol 149A. issue 5. 2009-06-18. PMID:19365833. |
rett syndrome (rtt) is a neurodevelopmental disorder caused by mutations in the x-linked mecp2 gene. |
2009-06-18 |
2023-08-12 |
Not clear |
| Thomas N Seyfried, Karie A Heinecke, John G Mantis, Christine A Denn. Brain lipid analysis in mice with Rett syndrome. Neurochemical research. vol 34. issue 6. 2009-06-16. PMID:19002580. |
rett syndrome (rs) is an x-linked neurodevelopmental disorder mostly involving mutations in the gene for methyl-cpg-binding protein 2 (mecp2). |
2009-06-16 |
2023-08-12 |
mouse |
| Ibrahim Baris, Esra Battalogl. A multiplexed ARMS-PCR approach for the detection of common MECP2 mutations. Genetic testing and molecular biomarkers. vol 13. issue 1. 2009-06-15. PMID:19309269. |
rett syndrome (rtt), an x-linked dominant neurodevelopmental disorder, is caused mainly by de novo mutations in the methyl-cpg-binding protein 2 gene (mecp2). |
2009-06-15 |
2023-08-12 |
Not clear |
| Nourhène Fendri-Kriaa, Zaineb Abdelkafi, Imen Ben Rebeh, Fatma Kamoun, Chahnez Triki, Faiza Fakhfak. A novel MECP2 gene mutation in a Tunisian patient with Rett syndrome. Genetic testing and molecular biomarkers. vol 13. issue 1. 2009-06-15. PMID:19309283. |
a novel mecp2 gene mutation in a tunisian patient with rett syndrome. |
2009-06-15 |
2023-08-12 |
Not clear |
| Nourhène Fendri-Kriaa, Zaineb Abdelkafi, Imen Ben Rebeh, Fatma Kamoun, Chahnez Triki, Faiza Fakhfak. A novel MECP2 gene mutation in a Tunisian patient with Rett syndrome. Genetic testing and molecular biomarkers. vol 13. issue 1. 2009-06-15. PMID:19309283. |
rett syndrome (rtt) is an x-linked dominant disorder caused frequently by mutations in the methyl-cpg-binding protein 2 gene (mecp2). |
2009-06-15 |
2023-08-12 |
Not clear |
| Kristopher C Hite, Valerie H Adams, Jeffrey C Hanse. Recent advances in MeCP2 structure and function. Biochemistry and cell biology = Biochimie et biologie cellulaire. vol 87. issue 1. 2009-06-08. PMID:19234536. |
mutations in methyl dna binding protein 2 (mecp2) cause the neurodevelopmental disorder rett syndrome (rtt). |
2009-06-08 |
2023-08-12 |
Not clear |
| b' Anita A Thambirajah, James H Eubanks, Juan Ausi\\xc3\\xb. MeCP2 post-translational regulation through PEST domains: two novel hypotheses: potential relevance and implications for Rett syndrome. BioEssays : news and reviews in molecular, cellular and developmental biology. vol 31. issue 5. 2009-06-08. PMID:19319913.' |
mecp2 post-translational regulation through pest domains: two novel hypotheses: potential relevance and implications for rett syndrome. |
2009-06-08 |
2023-08-12 |
Not clear |
| b' Anita A Thambirajah, James H Eubanks, Juan Ausi\\xc3\\xb. MeCP2 post-translational regulation through PEST domains: two novel hypotheses: potential relevance and implications for Rett syndrome. BioEssays : news and reviews in molecular, cellular and developmental biology. vol 31. issue 5. 2009-06-08. PMID:19319913.' |
mutations in the methyl-cpg-binding protein 2 (mecp2) cause rett syndrome, a severe neurodevelopmental disease associated with ataxia and other post-natal symptoms similar to autism. |
2009-06-08 |
2023-08-12 |
Not clear |
| Izumi Maezawa, Susan Swanberg, Danielle Harvey, Janine M LaSalle, Lee-Way Ji. Rett syndrome astrocytes are abnormal and spread MeCP2 deficiency through gap junctions. The Journal of neuroscience : the official journal of the Society for Neuroscience. vol 29. issue 16. 2009-05-22. PMID:19386901. |
rett syndrome astrocytes are abnormal and spread mecp2 deficiency through gap junctions. |
2009-05-22 |
2023-08-12 |
mouse |
| Izumi Maezawa, Susan Swanberg, Danielle Harvey, Janine M LaSalle, Lee-Way Ji. Rett syndrome astrocytes are abnormal and spread MeCP2 deficiency through gap junctions. The Journal of neuroscience : the official journal of the Society for Neuroscience. vol 29. issue 16. 2009-05-22. PMID:19386901. |
mecp2, an x-linked gene encoding the epigenetic factor methyl-cpg-binding protein-2, is mutated in rett syndrome (rtt) and aberrantly expressed in autism. |
2009-05-22 |
2023-08-12 |
mouse |
| Nadia P Belichenko, Pavel V Belichenko, William C Moble. Evidence for both neuronal cell autonomous and nonautonomous effects of methyl-CpG-binding protein 2 in the cerebral cortex of female mice with Mecp2 mutation. Neurobiology of disease. vol 34. issue 1. 2009-05-05. PMID:19167498. |
rett syndrome (rtt) is an x-linked neurodevelopmental disorder caused by mutations in the gene mecp2, encoding methyl-cpg-binding protein 2 (mecp2). |
2009-05-05 |
2023-08-12 |
mouse |
| Pavel V Belichenko, Elena E Wright, Nadia P Belichenko, Eliezer Masliah, Hong Hua Li, William C Mobley, Uta Franck. Widespread changes in dendritic and axonal morphology in Mecp2-mutant mouse models of Rett syndrome: evidence for disruption of neuronal networks. The Journal of comparative neurology. vol 514. issue 3. 2009-04-30. PMID:19296534. |
rett syndrome (rtt) is a neurodevelopmental disorder caused by mutations in the x-linked gene mecp2. |
2009-04-30 |
2023-08-12 |
mouse |
| B Ben Zeev, A Bebbington, G Ho, H Leonard, N de Klerk, E Gak, M Vecsler, M Vecksler, J Christodoulo. The common BDNF polymorphism may be a modifier of disease severity in Rett syndrome. Neurology. vol 72. issue 14. 2009-04-24. PMID:19349604. |
rett syndrome (rtt) is caused by mutations in the transcriptional repressor methyl cpg-binding protein 2 (mecp2). |
2009-04-24 |
2023-08-12 |
Not clear |
| Megumi Adachi, Anita E Autry, Herb E Covington, Lisa M Monteggi. MeCP2-mediated transcription repression in the basolateral amygdala may underlie heightened anxiety in a mouse model of Rett syndrome. The Journal of neuroscience : the official journal of the Society for Neuroscience. vol 29. issue 13. 2009-04-23. PMID:19339616. |
rett syndrome (rtt) is an x-linked neurodevelopmental disorder that results from loss of function mutations in the methyl-cpg binding protein 2 (mecp2) gene. |
2009-04-23 |
2023-08-12 |
mouse |