spermidine has been researched along with Mental Retardation, X-Linked in 8 studies
Mental Retardation, X-Linked: A class of genetic disorders resulting in INTELLECTUAL DISABILITY that is associated either with mutations of GENES located on the X CHROMOSOME or aberrations in the structure of the X chromosome (SEX CHROMOSOME ABERRATIONS).
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 5 (62.50) | 24.3611 |
| 2020's | 3 (37.50) | 2.80 |
| Authors | Studies |
|---|---|
| Tao, X | 1 |
| Zhu, Y | 2 |
| Diaz-Perez, Z | 2 |
| Yu, SH | 1 |
| Foley, JR | 2 |
| Stewart, TM | 1 |
| Casero, RA | 2 |
| Steet, R | 1 |
| Zhai, RG | 2 |
| Murray Stewart, T | 1 |
| Khomutov, M | 1 |
| Guo, X | 1 |
| Holbert, CE | 1 |
| Dunston, TT | 1 |
| Schwartz, CE | 4 |
| Gabrielson, K | 1 |
| Khomutov, A | 1 |
| Dontaine, P | 1 |
| Kottos, E | 1 |
| Dassonville, M | 1 |
| Balasel, O | 1 |
| Catros, V | 1 |
| Soblet, J | 1 |
| Perlot, P | 1 |
| Vilain, C | 1 |
| Li, C | 1 |
| Brazill, JM | 1 |
| Liu, S | 1 |
| Bello, C | 1 |
| Morimoto, M | 1 |
| Cascio, L | 1 |
| Pauly, R | 1 |
| Malicdan, MCV | 1 |
| Wang, H | 1 |
| Boccuto, L | 1 |
| Gahl, WA | 2 |
| Boerkoel, CF | 2 |
| Timson, DJ | 1 |
| Albert, JS | 1 |
| Bhattacharyya, N | 1 |
| Wolfe, LA | 1 |
| Bone, WP | 1 |
| Maduro, V | 1 |
| Accardi, J | 1 |
| Adams, DR | 1 |
| Norris, J | 1 |
| Wood, T | 1 |
| Gafni, RI | 1 |
| Collins, MT | 1 |
| Tosi, LL | 1 |
| Markello, TC | 1 |
| Abela, L | 1 |
| Simmons, L | 1 |
| Steindl, K | 1 |
| Schmitt, B | 1 |
| Mastrangelo, M | 1 |
| Joset, P | 1 |
| Papuc, M | 1 |
| Sticht, H | 1 |
| Baumer, A | 1 |
| Crowther, LM | 1 |
| Mathis, D | 1 |
| Rauch, A | 1 |
| Plecko, B | 1 |
| Wang, X | 1 |
| Stevenson, RE | 1 |
| Pegg, AE | 1 |
8 other studies available for spermidine and Mental Retardation, X-Linked
| Article | Year |
|---|---|
Phenylbutyrate modulates polyamine acetylase and ameliorates Snyder-Robinson syndrome in a Drosophila model and patient cells.
Topics: Acetyl Coenzyme A; Acetylesterase; Acetyltransferases; Animals; Drosophila; Mental Retardation, X-Li | 2022 |
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Topics: Acetyltransferases; Animals; Brain; Chromatography, High Pressure Liquid; Fibroblasts; Humans; Male; | 2020 |
Digestive involvement in a severe form of Snyder-Robinson syndrome: Possible expansion of the phenotype.
Topics: Child, Preschool; Failure to Thrive; Humans; Infant; Jejunum; Male; Mental Retardation, X-Linked; Mu | 2021 |
Spermine synthase deficiency causes lysosomal dysfunction and oxidative stress in models of Snyder-Robinson syndrome.
Topics: Animals; Animals, Genetically Modified; Antioxidants; Autophagy; Brain; Disease Models, Animal; Dros | 2017 |
Myosin Va and spermine synthase: partners in exosome transport.
Topics: Animals; Exosomes; Humans; Mental Retardation, X-Linked; Spermidine; Spermine; Spermine Synthase | 2019 |
Impaired osteoblast and osteoclast function characterize the osteoporosis of Snyder - Robinson syndrome.
Topics: Fibroblasts; Humans; Male; Mental Retardation, X-Linked; Mesenchymal Stem Cells; Mutation; Osteoblas | 2015 |
N(8)-acetylspermidine as a potential plasma biomarker for Snyder-Robinson syndrome identified by clinical metabolomics.
Topics: Adolescent; Biomarkers; Case-Control Studies; Child; Child, Preschool; Exome; Female; Humans; Infant | 2016 |
Spermine synthase deficiency resulting in X-linked intellectual disability (Snyder-Robinson syndrome).
Topics: Enzyme Assays; Female; Genes, X-Linked; Humans; Intellectual Disability; Male; Mental Retardation, X | 2011 |