MeCP2 (protein) (Croatian Wikipedia)

Analysis of information sources in references of the Wikipedia article "MeCP2 (protein)" in Croatian language version.

refsWebsite

Global rank Croatian rank

10nih.gov

4^th place

13^th place

9doi.org

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12^th place

9worldcat.org

5^th place

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1nrcresearchpress.com

low place

1acs.org

1,248^th place

2,676^th place

1mdpi.com

2,912^th place

low place

acs.org

pubs.acs.org

Ghosh, Rajarshi P.; Nikitina, Tatiana; Horowitz-Scherer, Rachel A.; Gierasch, Lila M.; Uversky, Vladimir N.; Hite, Kristopher; Hansen, Jeffrey C.; Woodcock, Christopher L. 25. svibnja 2010. Unique Physical Properties and Interactions of the Domains of Methylated DNA Binding Protein 2. Biochemistry (engleski). 49 (20): 4395–4410. doi:10.1021/bi9019753. ISSN 0006-2960. PMC 2872689. PMID 20405910CS1 održavanje: format PMC-a (link)

doi.org

Bin Akhtar, Ghanan; Buist, Marjorie; Rastegar, Mojgan. Lipanj 2022. MeCP2 and transcriptional control of eukaryotic gene expression. European Journal of Cell Biology. 101 (3): 151237. doi:10.1016/j.ejcb.2022.151237. ISSN 0171-9335
Krausz, C.; Giachini, C.; Xue, Y.; O'Bryan, M. K.; Gromoll, J.; Rajpert-de Meyts, E.; Oliva, R.; Aknin-Seifer, I.; Erdei, E.; Jorgensen, N.; Simoni, M. Siječanj 2009. Phenotypic variation within European carriers of the Y-chromosomal gr/gr deletion is independent of Y-chromosomal background. Journal of Medical Genetics. 46 (1): 21–31. doi:10.1136/jmg.2008.059915. ISSN 1468-6244. PMC 2698292. PMID 18782837
Chahrour, Maria; Zoghbi, Huda Y. 8. studenoga 2007. The story of Rett syndrome: from clinic to neurobiology. Neuron. 56 (3): 422–437. doi:10.1016/j.neuron.2007.10.001. ISSN 0896-6273. PMID 17988628
Adkins, Nicholas L.; Georgel, Philippe T. Veljača 2011. MeCP2: structure and functionThis paper is one of a selection of papers published in a Special Issue entitled 31st Annual International Asilomar Chromatin and Chromosomes Conference, and has undergone the Journal’s usual peer review process. Biochemistry and Cell Biology (engleski). 89 (1): 1–11. doi:10.1139/O10-112. ISSN 0829-8211
Ghosh, Rajarshi P.; Nikitina, Tatiana; Horowitz-Scherer, Rachel A.; Gierasch, Lila M.; Uversky, Vladimir N.; Hite, Kristopher; Hansen, Jeffrey C.; Woodcock, Christopher L. 25. svibnja 2010. Unique Physical Properties and Interactions of the Domains of Methylated DNA Binding Protein 2. Biochemistry (engleski). 49 (20): 4395–4410. doi:10.1021/bi9019753. ISSN 0006-2960. PMC 2872689. PMID 20405910CS1 održavanje: format PMC-a (link)
Schmidt, Annika; Zhang, Hui; Cardoso, M. Cristina. Travanj 2020. MeCP2 and Chromatin Compartmentalization. Cells (engleski). 9 (4): 878. doi:10.3390/cells9040878. ISSN 2073-4409. PMC 7226738. PMID 32260176CS1 održavanje: format PMC-a (link)
Yasui, Dag H.; Xu, Huichun; Dunaway, Keith W.; LaSalle, Janine M.; Jin, Lee-Way; Maezawa, Izumi. 25. siječnja 2013. MeCP2 modulates gene expression pathways in astrocytes. Molecular Autism. 4 (1): 3. doi:10.1186/2040-2392-4-3. ISSN 2040-2392
Amir, R. E.; Van den Veyver, I. B.; Wan, M.; Tran, C. Q.; Francke, U.; Zoghbi, H. Y. Listopad 1999. Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2. Nature Genetics. 23 (2): 185–188. doi:10.1038/13810. ISSN 1061-4036. PMID 10508514
Krausz, C.; Giachini, C.; Xue, Y.; O'Bryan, M. K.; Gromoll, J.; Rajpert-de Meyts, E.; Oliva, R.; Aknin-Seifer, I.; Erdei, E.; Jorgensen, N.; Simoni, M. Siječanj 2009. Phenotypic variation within European carriers of the Y-chromosomal gr/gr deletion is independent of Y-chromosomal background. Journal of Medical Genetics. 46 (1): 21–31. doi:10.1136/jmg.2008.059915. ISSN 1468-6244. PMC 2698292. PMID 18782837

mdpi.com

Schmidt, Annika; Zhang, Hui; Cardoso, M. Cristina. Travanj 2020. MeCP2 and Chromatin Compartmentalization. Cells (engleski). 9 (4): 878. doi:10.3390/cells9040878. ISSN 2073-4409. PMC 7226738. PMID 32260176CS1 održavanje: format PMC-a (link)

nih.gov

pubmed.ncbi.nlm.nih.gov

Krausz, C.; Giachini, C.; Xue, Y.; O'Bryan, M. K.; Gromoll, J.; Rajpert-de Meyts, E.; Oliva, R.; Aknin-Seifer, I.; Erdei, E.; Jorgensen, N.; Simoni, M. Siječanj 2009. Phenotypic variation within European carriers of the Y-chromosomal gr/gr deletion is independent of Y-chromosomal background. Journal of Medical Genetics. 46 (1): 21–31. doi:10.1136/jmg.2008.059915. ISSN 1468-6244. PMC 2698292. PMID 18782837
Chahrour, Maria; Zoghbi, Huda Y. 8. studenoga 2007. The story of Rett syndrome: from clinic to neurobiology. Neuron. 56 (3): 422–437. doi:10.1016/j.neuron.2007.10.001. ISSN 0896-6273. PMID 17988628
Ghosh, Rajarshi P.; Nikitina, Tatiana; Horowitz-Scherer, Rachel A.; Gierasch, Lila M.; Uversky, Vladimir N.; Hite, Kristopher; Hansen, Jeffrey C.; Woodcock, Christopher L. 25. svibnja 2010. Unique Physical Properties and Interactions of the Domains of Methylated DNA Binding Protein 2. Biochemistry (engleski). 49 (20): 4395–4410. doi:10.1021/bi9019753. ISSN 0006-2960. PMC 2872689. PMID 20405910CS1 održavanje: format PMC-a (link)
Schmidt, Annika; Zhang, Hui; Cardoso, M. Cristina. Travanj 2020. MeCP2 and Chromatin Compartmentalization. Cells (engleski). 9 (4): 878. doi:10.3390/cells9040878. ISSN 2073-4409. PMC 7226738. PMID 32260176CS1 održavanje: format PMC-a (link)
Amir, R. E.; Van den Veyver, I. B.; Wan, M.; Tran, C. Q.; Francke, U.; Zoghbi, H. Y. Listopad 1999. Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2. Nature Genetics. 23 (2): 185–188. doi:10.1038/13810. ISSN 1061-4036. PMID 10508514
Krausz, C.; Giachini, C.; Xue, Y.; O'Bryan, M. K.; Gromoll, J.; Rajpert-de Meyts, E.; Oliva, R.; Aknin-Seifer, I.; Erdei, E.; Jorgensen, N.; Simoni, M. Siječanj 2009. Phenotypic variation within European carriers of the Y-chromosomal gr/gr deletion is independent of Y-chromosomal background. Journal of Medical Genetics. 46 (1): 21–31. doi:10.1136/jmg.2008.059915. ISSN 1468-6244. PMC 2698292. PMID 18782837

ncbi.nlm.nih.gov

Krausz, C.; Giachini, C.; Xue, Y.; O'Bryan, M. K.; Gromoll, J.; Rajpert-de Meyts, E.; Oliva, R.; Aknin-Seifer, I.; Erdei, E.; Jorgensen, N.; Simoni, M. Siječanj 2009. Phenotypic variation within European carriers of the Y-chromosomal gr/gr deletion is independent of Y-chromosomal background. Journal of Medical Genetics. 46 (1): 21–31. doi:10.1136/jmg.2008.059915. ISSN 1468-6244. PMC 2698292. PMID 18782837
Ghosh, Rajarshi P.; Nikitina, Tatiana; Horowitz-Scherer, Rachel A.; Gierasch, Lila M.; Uversky, Vladimir N.; Hite, Kristopher; Hansen, Jeffrey C.; Woodcock, Christopher L. 25. svibnja 2010. Unique Physical Properties and Interactions of the Domains of Methylated DNA Binding Protein 2. Biochemistry (engleski). 49 (20): 4395–4410. doi:10.1021/bi9019753. ISSN 0006-2960. PMC 2872689. PMID 20405910CS1 održavanje: format PMC-a (link)
Schmidt, Annika; Zhang, Hui; Cardoso, M. Cristina. Travanj 2020. MeCP2 and Chromatin Compartmentalization. Cells (engleski). 9 (4): 878. doi:10.3390/cells9040878. ISSN 2073-4409. PMC 7226738. PMID 32260176CS1 održavanje: format PMC-a (link)
Krausz, C.; Giachini, C.; Xue, Y.; O'Bryan, M. K.; Gromoll, J.; Rajpert-de Meyts, E.; Oliva, R.; Aknin-Seifer, I.; Erdei, E.; Jorgensen, N.; Simoni, M. Siječanj 2009. Phenotypic variation within European carriers of the Y-chromosomal gr/gr deletion is independent of Y-chromosomal background. Journal of Medical Genetics. 46 (1): 21–31. doi:10.1136/jmg.2008.059915. ISSN 1468-6244. PMC 2698292. PMID 18782837

nrcresearchpress.com

Adkins, Nicholas L.; Georgel, Philippe T. Veljača 2011. MeCP2: structure and functionThis paper is one of a selection of papers published in a Special Issue entitled 31st Annual International Asilomar Chromatin and Chromosomes Conference, and has undergone the Journal’s usual peer review process. Biochemistry and Cell Biology (engleski). 89 (1): 1–11. doi:10.1139/O10-112. ISSN 0829-8211

worldcat.org

Bin Akhtar, Ghanan; Buist, Marjorie; Rastegar, Mojgan. Lipanj 2022. MeCP2 and transcriptional control of eukaryotic gene expression. European Journal of Cell Biology. 101 (3): 151237. doi:10.1016/j.ejcb.2022.151237. ISSN 0171-9335
Krausz, C.; Giachini, C.; Xue, Y.; O'Bryan, M. K.; Gromoll, J.; Rajpert-de Meyts, E.; Oliva, R.; Aknin-Seifer, I.; Erdei, E.; Jorgensen, N.; Simoni, M. Siječanj 2009. Phenotypic variation within European carriers of the Y-chromosomal gr/gr deletion is independent of Y-chromosomal background. Journal of Medical Genetics. 46 (1): 21–31. doi:10.1136/jmg.2008.059915. ISSN 1468-6244. PMC 2698292. PMID 18782837
Chahrour, Maria; Zoghbi, Huda Y. 8. studenoga 2007. The story of Rett syndrome: from clinic to neurobiology. Neuron. 56 (3): 422–437. doi:10.1016/j.neuron.2007.10.001. ISSN 0896-6273. PMID 17988628
Adkins, Nicholas L.; Georgel, Philippe T. Veljača 2011. MeCP2: structure and functionThis paper is one of a selection of papers published in a Special Issue entitled 31st Annual International Asilomar Chromatin and Chromosomes Conference, and has undergone the Journal’s usual peer review process. Biochemistry and Cell Biology (engleski). 89 (1): 1–11. doi:10.1139/O10-112. ISSN 0829-8211
Ghosh, Rajarshi P.; Nikitina, Tatiana; Horowitz-Scherer, Rachel A.; Gierasch, Lila M.; Uversky, Vladimir N.; Hite, Kristopher; Hansen, Jeffrey C.; Woodcock, Christopher L. 25. svibnja 2010. Unique Physical Properties and Interactions of the Domains of Methylated DNA Binding Protein 2. Biochemistry (engleski). 49 (20): 4395–4410. doi:10.1021/bi9019753. ISSN 0006-2960. PMC 2872689. PMID 20405910CS1 održavanje: format PMC-a (link)
Schmidt, Annika; Zhang, Hui; Cardoso, M. Cristina. Travanj 2020. MeCP2 and Chromatin Compartmentalization. Cells (engleski). 9 (4): 878. doi:10.3390/cells9040878. ISSN 2073-4409. PMC 7226738. PMID 32260176CS1 održavanje: format PMC-a (link)
Yasui, Dag H.; Xu, Huichun; Dunaway, Keith W.; LaSalle, Janine M.; Jin, Lee-Way; Maezawa, Izumi. 25. siječnja 2013. MeCP2 modulates gene expression pathways in astrocytes. Molecular Autism. 4 (1): 3. doi:10.1186/2040-2392-4-3. ISSN 2040-2392
Amir, R. E.; Van den Veyver, I. B.; Wan, M.; Tran, C. Q.; Francke, U.; Zoghbi, H. Y. Listopad 1999. Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2. Nature Genetics. 23 (2): 185–188. doi:10.1038/13810. ISSN 1061-4036. PMID 10508514
Krausz, C.; Giachini, C.; Xue, Y.; O'Bryan, M. K.; Gromoll, J.; Rajpert-de Meyts, E.; Oliva, R.; Aknin-Seifer, I.; Erdei, E.; Jorgensen, N.; Simoni, M. Siječanj 2009. Phenotypic variation within European carriers of the Y-chromosomal gr/gr deletion is independent of Y-chromosomal background. Journal of Medical Genetics. 46 (1): 21–31. doi:10.1136/jmg.2008.059915. ISSN 1468-6244. PMC 2698292. PMID 18782837