237 related articles for article (PubMed ID: 19859664)
1. Spermine synthase.
Pegg AE; Michael AJ
Cell Mol Life Sci; 2010 Jan; 67(1):113-21. PubMed ID: 19859664
[TBL] [Abstract][Full Text] [Related]
2. Difluoromethylornithine rebalances aberrant polyamine ratios in Snyder-Robinson syndrome.
Stewart TM; Foley JR; Holbert CE; Khomutov M; Rastkari N; Tao X; Khomutov AR; Zhai RG; Casero RA
EMBO Mol Med; 2023 Nov; 15(11):e17833. PubMed ID: 37702369
[TBL] [Abstract][Full Text] [Related]
3. Enhancing human spermine synthase activity by engineered mutations.
Zhang Z; Zheng Y; Petukh M; Pegg A; Ikeguchi Y; Alexov E
PLoS Comput Biol; 2013; 9(2):e1002924. PubMed ID: 23468611
[TBL] [Abstract][Full Text] [Related]
4. Crystal structure of human spermine synthase: implications of substrate binding and catalytic mechanism.
Wu H; Min J; Zeng H; McCloskey DE; Ikeguchi Y; Loppnau P; Michael AJ; Pegg AE; Plotnikov AN
J Biol Chem; 2008 Jun; 283(23):16135-46. PubMed ID: 18367445
[TBL] [Abstract][Full Text] [Related]
5. Spermine synthase deficiency resulting in X-linked intellectual disability (Snyder-Robinson syndrome).
Schwartz CE; Wang X; Stevenson RE; Pegg AE
Methods Mol Biol; 2011; 720():437-45. PubMed ID: 21318891
[TBL] [Abstract][Full Text] [Related]
6. Spermine synthase activity affects the content of decarboxylated S-adenosylmethionine.
Pegg AE; Wang X; Schwartz CE; McCloskey DE
Biochem J; 2011 Jan; 433(1):139-44. PubMed ID: 20950271
[TBL] [Abstract][Full Text] [Related]
7. (
Murray Stewart T; Khomutov M; Foley JR; Guo X; Holbert CE; Dunston TT; Schwartz CE; Gabrielson K; Khomutov A; Casero RA
J Biol Chem; 2020 Mar; 295(10):3247-3256. PubMed ID: 31996374
[TBL] [Abstract][Full Text] [Related]
8. Use of (Gyro) Gy and spermine synthase transgenic mice to study functions of spermine.
Wang X; Pegg AE
Methods Mol Biol; 2011; 720():159-70. PubMed ID: 21318872
[TBL] [Abstract][Full Text] [Related]
9. Spermine synthase overexpression in vivo does not increase susceptibility to DMBA/TPA skin carcinogenesis or Min-Apc intestinal tumorigenesis.
Welsh PA; Sass-Kuhn S; Prakashagowda C; McCloskey D; Feith D
Cancer Biol Ther; 2012 Apr; 13(6):358-68. PubMed ID: 22258329
[TBL] [Abstract][Full Text] [Related]
10. A Y328C missense mutation in spermine synthase causes a mild form of Snyder-Robinson syndrome.
Zhang Z; Norris J; Kalscheuer V; Wood T; Wang L; Schwartz C; Alexov E; Van Esch H
Hum Mol Genet; 2013 Sep; 22(18):3789-97. PubMed ID: 23696453
[TBL] [Abstract][Full Text] [Related]
11. The function of spermine.
Pegg AE
IUBMB Life; 2014 Jan; 66(1):8-18. PubMed ID: 24395705
[TBL] [Abstract][Full Text] [Related]
12. Impaired osteoblast and osteoclast function characterize the osteoporosis of Snyder - Robinson syndrome.
Albert JS; Bhattacharyya N; Wolfe LA; Bone WP; Maduro V; Accardi J; Adams DR; Schwartz CE; Norris J; Wood T; Gafni RI; Collins MT; Tosi LL; Markello TC; Gahl WA; Boerkoel CF
Orphanet J Rare Dis; 2015 Mar; 10():27. PubMed ID: 25888122
[TBL] [Abstract][Full Text] [Related]
13. Effects of Spermine Synthase Deficiency in Mesenchymal Stromal Cells Are Rescued by Upstream Inhibition of Ornithine Decarboxylase.
Cressman A; Morales D; Zhang Z; Le B; Foley J; Murray-Stewart T; Genetos DC; Fierro FA
Int J Mol Sci; 2024 Feb; 25(5):. PubMed ID: 38473716
[TBL] [Abstract][Full Text] [Related]
14. In silico and in vitro investigations of the mutability of disease-causing missense mutation sites in spermine synthase.
Zhang Z; Norris J; Schwartz C; Alexov E
PLoS One; 2011; 6(5):e20373. PubMed ID: 21647366
[TBL] [Abstract][Full Text] [Related]
15. Diagnostic screening for spermine synthase deficiency by liquid chromatography tandem mass spectrometry.
Sowell J; Norris J; Jones K; Schwartz C; Wood T
Clin Chim Acta; 2011 Mar; 412(7-8):655-60. PubMed ID: 21219895
[TBL] [Abstract][Full Text] [Related]
16. X-linked spermine synthase gene (SMS) defect: the first polyamine deficiency syndrome.
Cason AL; Ikeguchi Y; Skinner C; Wood TC; Holden KR; Lubs HA; Martinez F; Simensen RJ; Stevenson RE; Pegg AE; Schwartz CE
Eur J Hum Genet; 2003 Dec; 11(12):937-44. PubMed ID: 14508504
[TBL] [Abstract][Full Text] [Related]
17. New SMS mutation leads to a striking reduction in spermine synthase protein function and a severe form of Snyder-Robinson X-linked recessive mental retardation syndrome.
de Alencastro G; McCloskey DE; Kliemann SE; Maranduba CM; Pegg AE; Wang X; Bertola DR; Schwartz CE; Passos-Bueno MR; Sertié AL
J Med Genet; 2008 Aug; 45(8):539-43. PubMed ID: 18550699
[TBL] [Abstract][Full Text] [Related]
18. Aminopropyltransferases: function, structure and genetics.
Ikeguchi Y; Bewley MC; Pegg AE
J Biochem; 2006 Jan; 139(1):1-9. PubMed ID: 16428313
[TBL] [Abstract][Full Text] [Related]
19. Spermine deficiency in Gy mice caused by deletion of the spermine synthase gene.
Lorenz B; Francis F; Gempel K; Böddrich A; Josten M; Schmahl W; Schmidt J; Lehrach H; Meitinger T; Strom TM
Hum Mol Genet; 1998 Mar; 7(3):541-7. PubMed ID: 9467015
[TBL] [Abstract][Full Text] [Related]
20. Impaired polyamine metabolism causes behavioral and neuroanatomical defects in a mouse model of Snyder-Robinson syndrome.
Akinyele O; Munir A; Johnson MA; Perez MS; Gao Y; Foley JR; Nwafor A; Wu Y; Murray-Stewart T; Casero RA; Bayir H; Kemaladewi DU
Dis Model Mech; 2024 Jun; 17(6):. PubMed ID: 38463005
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
