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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1975 1
1977 1
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1986 2
1987 1
1988 1
1990 2
1991 2
1992 1
1993 3
1994 2
1995 1
1996 1
1998 3
1999 1
2002 1
2003 3
2004 7
2005 1
2006 4
2007 4
2008 4
2009 4
2010 5
2011 5
2012 3
2013 6
2014 5
2015 6
2016 4
2017 5
2018 3
2019 3
2020 1
2021 7
2022 8
2025 0

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Similar articles for PMID: 37590701

95 results

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Page 1
Enzyme assay of protein O-mannosyltransferase (POMT1/2).
Akasaka-Manya K, Manya H, Endo T. Akasaka-Manya K, et al. 2021 Oct 27 [updated 2022 Mar 23]. In: Nishihara S, Angata K, Aoki-Kinoshita KF, Hirabayashi J, editors. Glycoscience Protocols (GlycoPODv2) [Internet]. Saitama (JP): Japan Consortium for Glycobiology and Glycotechnology; 2021–. 2021 Oct 27 [updated 2022 Mar 23]. In: Nishihara S, Angata K, Aoki-Kinoshita KF, Hirabayashi J, editors. Glycoscience Protocols (GlycoPODv2) [Internet]. Saitama (JP): Japan Consortium for Glycobiology and Glycotechnology; 2021–. PMID: 37590701 Free Books & Documents. Review. No abstract available.
O-mannosylation in mammalian cells.
Endo T, Manya H. Endo T, et al. Methods Mol Biol. 2006;347:43-56. doi: 10.1385/1-59745-167-3:43. Methods Mol Biol. 2006. PMID: 17072003
Enzyme assay of protein O-linked-mannose β1,2-N-acetylglucosaminyltransferase 1 and protein O-linked-mannose β1,4-N-acetylglucosaminyltransferase 2 (POMGNT1/2).
Akasaka-Manya K, Manya H, Endo T. Akasaka-Manya K, et al. 2022 Jan 25 [updated 2022 Mar 24]. In: Nishihara S, Angata K, Aoki-Kinoshita KF, Hirabayashi J, editors. Glycoscience Protocols (GlycoPODv2) [Internet]. Saitama (JP): Japan Consortium for Glycobiology and Glycotechnology; 2021–. 2022 Jan 25 [updated 2022 Mar 24]. In: Nishihara S, Angata K, Aoki-Kinoshita KF, Hirabayashi J, editors. Glycoscience Protocols (GlycoPODv2) [Internet]. Saitama (JP): Japan Consortium for Glycobiology and Glycotechnology; 2021–. PMID: 37590579 Free Books & Documents. Review. No abstract available.
Mutations in the O-mannosyltransferase gene POMT1 give rise to the severe neuronal migration disorder Walker-Warburg syndrome.
Beltrán-Valero de Bernabé D, Currier S, Steinbrecher A, Celli J, van Beusekom E, van der Zwaag B, Kayserili H, Merlini L, Chitayat D, Dobyns WB, Cormand B, Lehesjoki AE, Cruces J, Voit T, Walsh CA, van Bokhoven H, Brunner HG. Beltrán-Valero de Bernabé D, et al. Am J Hum Genet. 2002 Nov;71(5):1033-43. doi: 10.1086/342975. Epub 2002 Oct 4. Am J Hum Genet. 2002. PMID: 12369018 Free PMC article.
95 results