PubMed for id: 5236

Year	Number of Results
1973	1
1985	1
1991	1
1992	2
1993	4
1995	1
1996	2
1999	1
2001	1
2002	3
2003	1
2004	3
2005	1
2006	1
2007	2
2008	4
2009	3
2010	5
2011	4
2012	3
2013	2
2014	5
2015	6
2016	2
2017	2
2018	7
2019	9
2020	10
2021	5
2022	8
2023	3
2024	0

1

Knock-down of PGM1 inhibits cell viability, glycolysis, and oxidative phosphorylation in glioma under low glucose condition via the Myc signaling pathway.

Liu S, Deng Y, Yu Y, Xia X. Liu S, et al. Biochem Biophys Res Commun. 2023 May 14;656:38-45. doi: 10.1016/j.bbrc.2023.03.034. Epub 2023 Mar 14. Biochem Biophys Res Commun. 2023. PMID: 36947965

2

Effects of the T337M and G391V disease-related variants on human phosphoglucomutase 1: structural disruptions large and small.

Stiers KM, Owuocha LF, Beamer LJ. Stiers KM, et al. Acta Crystallogr F Struct Biol Commun. 2022 May 1;78(Pt 5):200-209. doi: 10.1107/S2053230X22004174. Epub 2022 Apr 25. Acta Crystallogr F Struct Biol Commun. 2022. PMID: 35506765 Free PMC article.

3

Phosphoglucomutase-1 deficiency: Early presentation, metabolic management and detection in neonatal blood spots.

Conte F, Morava E, Bakar NA, Wortmann SB, Poerink AJ, Grunewald S, Crushell E, Al-Gazali L, de Vries MC, Mørkrid L, Hertecant J, Brocke Holmefjord KS, Kronn D, Feigenbaum A, Fingerhut R, Wong SY, van Scherpenzeel M, Voermans NC, Lefeber DJ. Conte F, et al. Mol Genet Metab. 2020 Sep-Oct;131(1-2):135-146. doi: 10.1016/j.ymgme.2020.08.003. Epub 2020 Sep 17. Mol Genet Metab. 2020. PMID: 33342467 Free article.

4

Enzyme dysfunction at atomic resolution: Disease-associated variants of human phosphoglucomutase-1.

Beamer LJ. Beamer LJ. Biochimie. 2021 Apr;183:44-48. doi: 10.1016/j.biochi.2020.08.017. Epub 2020 Sep 6. Biochimie. 2021. PMID: 32898648 Review.

5

Structural basis for substrate and product recognition in human phosphoglucomutase-1 (PGM1) isoform 2, a member of the α-D-phosphohexomutase superfamily.

Backe PH, Laerdahl JK, Kittelsen LS, Dalhus B, Mørkrid L, Bjørås M. Backe PH, et al. Sci Rep. 2020 Mar 27;10(1):5656. doi: 10.1038/s41598-020-62548-0. Sci Rep. 2020. PMID: 32221390 Free PMC article.

6

A missense variant remote from the active site impairs stability of human phosphoglucomutase 1.

Stiers KM, Hansen RP, Daghlas BA, Mason KN, Zhu JS, Jakeman DL, Beamer LJ. Stiers KM, et al. J Inherit Metab Dis. 2020 Jul;43(4):861-870. doi: 10.1002/jimd.12222. Epub 2020 Feb 18. J Inherit Metab Dis. 2020. PMID: 32057119

7

The congenital disorder of glycosylation in PGM1 (PGM1-CDG) can cause severe cardiomyopathy and unexpected sudden cardiac death in childhood.

Fernlund E, Andersson O, Ellegård R, Årstrand HK, Green H, Olsson H, Gunnarsson C. Fernlund E, et al. Forensic Sci Int Genet. 2019 Nov;43:102111. doi: 10.1016/j.fsigen.2019.06.012. Epub 2019 Jun 17. Forensic Sci Int Genet. 2019. PMID: 31563034

8

Congenital disorder of glycosylation type 1T with a novel truncated homozygous mutation in PGM1 gene and literature review.

Tian WT, Luan XH, Zhou HY, Zhang C, Huang XJ, Liu XL, Chen SD, Tang HD, Cao L. Tian WT, et al. Neuromuscul Disord. 2019 Apr;29(4):282-289. doi: 10.1016/j.nmd.2019.01.001. Epub 2019 Jan 6. Neuromuscul Disord. 2019. PMID: 30737079 Review.

9

Phosphoglucomutase 1 inhibits hepatocellular carcinoma progression by regulating glucose trafficking.

Jin GZ, Zhang Y, Cong WM, Wu X, Wang X, Wu S, Wang S, Zhou W, Yuan S, Gao H, Yu G, Yang W. Jin GZ, et al. PLoS Biol. 2018 Oct 18;16(10):e2006483. doi: 10.1371/journal.pbio.2006483. eCollection 2018 Oct. PLoS Biol. 2018. PMID: 30335765 Free PMC article.

10

Central nervous involvement is common in PGM1-CDG.

Radenkovic S, Witters P, Morava E. Radenkovic S, et al. Mol Genet Metab. 2018 Nov;125(3):200-204. doi: 10.1016/j.ymgme.2018.08.008. Epub 2018 Aug 21. Mol Genet Metab. 2018. PMID: 30262252 Review.

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