| Publication |
Sentence |
Publish Date |
Extraction Date |
Species |
| A R Carter, R A Sega. Rett syndrome model suggests MECP2 gives neurons the quiet they need to think. Nature neuroscience. vol 4. issue 4. 2001-05-03. PMID:11276217. |
rett syndrome model suggests mecp2 gives neurons the quiet they need to think. |
2001-05-03 |
2023-08-12 |
Not clear |
| b' M Auranen, R Vanhala, M Vosman, M Levander, T Varilo, M Hietala, R Riikonen, L Peltonen, I J\\xc3\\xa4rvel\\xc3\\xa. MECP2 gene analysis in classical Rett syndrome and in patients with Rett-like features. Neurology. vol 56. issue 5. 2001-04-19. PMID:11245712.' |
mecp2 gene analysis in classical rett syndrome and in patients with rett-like features. |
2001-04-19 |
2023-08-12 |
Not clear |
| b' M Auranen, R Vanhala, M Vosman, M Levander, T Varilo, M Hietala, R Riikonen, L Peltonen, I J\\xc3\\xa4rvel\\xc3\\xa. MECP2 gene analysis in classical Rett syndrome and in patients with Rett-like features. Neurology. vol 56. issue 5. 2001-04-19. PMID:11245712.' |
to discuss the diagnostic criteria for rett syndrome based on mutational screening of the methyl-cpg-binding protein 2 gene ( mecp2 ) in patients with classic rett syndrome and patients with rett-like features. |
2001-04-19 |
2023-08-12 |
Not clear |
| R Z Chen, S Akbarian, M Tudor, R Jaenisc. Deficiency of methyl-CpG binding protein-2 in CNS neurons results in a Rett-like phenotype in mice. Nature genetics. vol 27. issue 3. 2001-04-12. PMID:11242118. |
consistent with this notion is the recent demonstration that mecp2 mutations cause rett syndrome (rtt, mim 312750), a childhood neurological disorder that represents one of the most common causes of mental retardation in females. |
2001-04-12 |
2023-08-12 |
mouse |
| R Z Chen, S Akbarian, M Tudor, R Jaenisc. Deficiency of methyl-CpG binding protein-2 in CNS neurons results in a Rett-like phenotype in mice. Nature genetics. vol 27. issue 3. 2001-04-12. PMID:11242118. |
mecp2 deficiency in these neurons is sufficient to cause neuronal dysfunction with symptomatic manifestation similar to rett syndrome. |
2001-04-12 |
2023-08-12 |
mouse |
| V Bourdon, C Philippe, O Labrune, D Amsallem, C Arnould, P Jonveau. A detailed analysis of the MECP2 gene: prevalence of recurrent mutations and gross DNA rearrangements in Rett syndrome patients. Human genetics. vol 108. issue 1. 2001-03-15. PMID:11214906. |
a detailed analysis of the mecp2 gene: prevalence of recurrent mutations and gross dna rearrangements in rett syndrome patients. |
2001-03-15 |
2023-08-12 |
Not clear |
| V Bourdon, C Philippe, O Labrune, D Amsallem, C Arnould, P Jonveau. A detailed analysis of the MECP2 gene: prevalence of recurrent mutations and gross DNA rearrangements in Rett syndrome patients. Human genetics. vol 108. issue 1. 2001-03-15. PMID:11214906. |
mutations in the x-linked methyl-cpg-binding protein 2 gene (mecp2) have been found to be a cause of rett syndrome (rtt). |
2001-03-15 |
2023-08-12 |
Not clear |
| C W Lam, W L Yeung, C H Ko, P M Poon, S F Tong, K Y Chan, I F Lo, L Y Chan, J Hui, V Wong, C P Pang, Y M Lo, T F Fo. Spectrum of mutations in the MECP2 gene in patients with infantile autism and Rett syndrome. Journal of medical genetics. vol 37. issue 12. 2001-01-25. PMID:11106359. |
spectrum of mutations in the mecp2 gene in patients with infantile autism and rett syndrome. |
2001-01-25 |
2023-08-12 |
Not clear |
| I M Buyse, P Fang, K T Hoon, R E Amir, H Y Zoghbi, B B Ro. Diagnostic testing for Rett syndrome by DHPLC and direct sequencing analysis of the MECP2 gene: identification of several novel mutations and polymorphisms. American journal of human genetics. vol 67. issue 6. 2001-01-18. PMID:11055898. |
diagnostic testing for rett syndrome by dhplc and direct sequencing analysis of the mecp2 gene: identification of several novel mutations and polymorphisms. |
2001-01-18 |
2023-08-12 |
Not clear |
| J Dragich, I Houwink-Manville, C Schane. Rett syndrome: a surprising result of mutation in MECP2. Human molecular genetics. vol 9. issue 16. 2000-11-30. PMID:11005791. |
rett syndrome: a surprising result of mutation in mecp2. |
2000-11-30 |
2023-08-12 |
Not clear |
| J Dragich, I Houwink-Manville, C Schane. Rett syndrome: a surprising result of mutation in MECP2. Human molecular genetics. vol 9. issue 16. 2000-11-30. PMID:11005791. |
the identification of mutations in the gene encoding methyl cpg binding protein 2 (mecp2) in rett syndrome represents a major advance in the field. |
2000-11-30 |
2023-08-12 |
Not clear |
| J Dragich, I Houwink-Manville, C Schane. Rett syndrome: a surprising result of mutation in MECP2. Human molecular genetics. vol 9. issue 16. 2000-11-30. PMID:11005791. |
although much is known about the biochemical function of mecp2, the phenotype of rett syndrome suggests that it plays an unexplored but critical role in development and maintenance of the nervous system. |
2000-11-30 |
2023-08-12 |
Not clear |
| T H Besto. The DNA methyltransferases of mammals. Human molecular genetics. vol 9. issue 16. 2000-11-30. PMID:11005794. |
a second human disorder (rett syndrome) has been found to result from mutations in the mecp2 gene, which encodes a protein that binds to methylated dna. |
2000-11-30 |
2023-08-12 |
mouse |
| T M Yusufzai, A P Wolff. Functional consequences of Rett syndrome mutations on human MeCP2. Nucleic acids research. vol 28. issue 21. 2000-11-16. PMID:11058114. |
functional consequences of rett syndrome mutations on human mecp2. |
2000-11-16 |
2023-08-12 |
human |
| T M Yusufzai, A P Wolff. Functional consequences of Rett syndrome mutations on human MeCP2. Nucleic acids research. vol 28. issue 21. 2000-11-16. PMID:11058114. |
the neurodevelopmental disorder known as rett syndrome has recently been linked to the methyl-cpg-binding transcriptional repressor, mecp2. |
2000-11-16 |
2023-08-12 |
human |
| T M Yusufzai, A P Wolff. Functional consequences of Rett syndrome mutations on human MeCP2. Nucleic acids research. vol 28. issue 21. 2000-11-16. PMID:11058114. |
together, these results provide evidence of how rett syndrome mutations can affect distinct functions of mecp2 and give insight into these mutations that may contribute to the disease. |
2000-11-16 |
2023-08-12 |
human |
| I Meloni, M Bruttini, I Longo, F Mari, F Rizzolio, P D'Adamo, K Denvriendt, J P Fryns, D Toniolo, A Renier. A mutation in the rett syndrome gene, MECP2, causes X-linked mental retardation and progressive spasticity in males. American journal of human genetics. vol 67. issue 4. 2000-10-31. PMID:10986043. |
a mutation in the rett syndrome gene, mecp2, causes x-linked mental retardation and progressive spasticity in males. |
2000-10-31 |
2023-08-12 |
Not clear |
| I Meloni, M Bruttini, I Longo, F Mari, F Rizzolio, P D'Adamo, K Denvriendt, J P Fryns, D Toniolo, A Renier. A mutation in the rett syndrome gene, MECP2, causes X-linked mental retardation and progressive spasticity in males. American journal of human genetics. vol 67. issue 4. 2000-10-31. PMID:10986043. |
heterozygous mutations in the x-linked mecp2 gene cause rett syndrome, a severe neurodevelopmental disorder of young females. |
2000-10-31 |
2023-08-12 |
Not clear |
| C De Bona, M Zappella, G Hayek, I Meloni, F Vitelli, M Bruttini, R Cusano, P Loffredo, I Longo, A Renier. Preserved speech variant is allelic of classic Rett syndrome. European journal of human genetics : EJHG. vol 8. issue 5. 2000-09-18. PMID:10854091. |
here we explore the spectrum of mutations affecting the mecp2 gene in a group of 25 classic rett syndrome girls and in three patients with the preserved speech variant. |
2000-09-18 |
2023-08-12 |
Not clear |
| K Obata, T Matsuishi, Y Yamashita, T Fukuda, K Kuwajima, I Horiuchi, S Nagamitsu, R Iwanaga, A Kimura, I Omori, S Endo, K Mori, I Kond. Mutation analysis of the methyl-CpG binding protein 2 gene (MECP2) in patients with Rett syndrome. Journal of medical genetics. vol 37. issue 8. 2000-09-12. PMID:10991688. |
mutation analysis of the methyl-cpg binding protein 2 gene (mecp2) in patients with rett syndrome. |
2000-09-12 |
2023-08-12 |
Not clear |