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Association between Gene Polymorphisms and the Risk of Diabetic Kidney Disease in a Chinese Han Population with Type 2 Diabetes.
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Polymorphisms in MYH9 are associated with diabetic nephropathy in European Americans.
Nephrol Dial Transplant. 2012 Apr;27(4):1505-11. doi: 10.1093/ndt/gfr522. Epub 2011 Oct 3.
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Differential effects of MYH9 and APOL1 risk variants on FRMD3 Association with Diabetic ESRD in African Americans.
PLoS Genet. 2011 Jun;7(6):e1002150. doi: 10.1371/journal.pgen.1002150. Epub 2011 Jun 16.
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Association of MYH9 Polymorphisms with Hypertension in Patients with Chronic Kidney Disease in China.
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Sickle cell trait is not independently associated with susceptibility to end-stage renal disease in African Americans.
Kidney Int. 2011 Dec;80(12):1339-43. doi: 10.1038/ki.2011.286. Epub 2011 Aug 17.
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Association between a MYH9 polymorphism (rs3752462) and renal function in the Spanish RENASTUR cohort.
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MYH9 gene polymorphisms may be associated with cerebrovascular blood flow in patients with type 2 diabetes.
Genet Mol Res. 2015 Feb 6;14(1):1008-16. doi: 10.4238/2015.February.6.4.

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Bioinformatics Analysis of Next Generation Sequencing Data Identifies Molecular Biomarkers Associated With Type 2 Diabetes Mellitus.
Clin Med Insights Endocrinol Diabetes. 2023 Feb 20;16:11795514231155635. doi: 10.1177/11795514231155635. eCollection 2023.
3
S-Nitrosylation of RhoGAP Myosin9A Is Altered in Advanced Diabetic Kidney Disease.
Front Med (Lausanne). 2021 Jul 14;8:679518. doi: 10.3389/fmed.2021.679518. eCollection 2021.
6
Association between Gene Polymorphisms and the Risk of Diabetic Kidney Disease in a Chinese Han Population with Type 2 Diabetes.
J Diabetes Res. 2020 Jun 30;2020:5424701. doi: 10.1155/2020/5424701. eCollection 2020.
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Non-diabetic end-stage renal disease in Saudis associated with polymorphism of MYH9 gene but not UMOD gene.
Medicine (Baltimore). 2020 Jan;99(3):e18722. doi: 10.1097/MD.0000000000018722.
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The predictive potential of altered spontaneous brain activity patterns in diabetic retinopathy and nephropathy.
EPMA J. 2019 Jul 5;10(3):249-259. doi: 10.1007/s13167-019-00171-4. eCollection 2019 Sep.
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MYH9-related disease: it does exist, may be more frequent than you think and requires specific therapy.
Clin Kidney J. 2019 Aug 1;12(4):488-493. doi: 10.1093/ckj/sfz103. eCollection 2019 Aug.

本文引用的文献

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Clinical and genetic heterogeneity in familial steroid-sensitive nephrotic syndrome.
Pediatr Nephrol. 2018 Mar;33(3):473-483. doi: 10.1007/s00467-017-3819-9. Epub 2017 Oct 23.
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E1841K Mutation Augments Proteinuria and Podocyte Injury and Migration.
J Am Soc Nephrol. 2018 Jan;29(1):155-167. doi: 10.1681/ASN.2015060707. Epub 2017 Oct 9.
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Cellular force assay detects altered contractility caused by a nephritis-associated mutation in nonmuscle myosin IIA.
Dev Growth Differ. 2017 Jun;59(5):423-433. doi: 10.1111/dgd.12379. Epub 2017 Jul 17.
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Septin 7 reduces nonmuscle myosin IIA activity in the SNAP23 complex and hinders GLUT4 storage vesicle docking and fusion.
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Epidemiology of microvascular complications of diabetes in South Asians and comparison with other ethnicities.
J Diabetes. 2016 Jul;8(4):470-82. doi: 10.1111/1753-0407.12378. Epub 2016 Mar 16.
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MYH9 gene polymorphisms may be associated with cerebrovascular blood flow in patients with type 2 diabetes.
Genet Mol Res. 2015 Feb 6;14(1):1008-16. doi: 10.4238/2015.February.6.4.
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Keloids and non-diabetic kidney disease: similarities and the APOL1-MYH9 haplotype as a possible genetic link.
Med Hypotheses. 2013 Nov;81(5):908-10. doi: 10.1016/j.mehy.2013.08.009. Epub 2013 Aug 22.

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