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808 related items for PubMed ID: 27481110
21. VEGF polymorphisms and serum VEGF levels in Parkinson's disease. Mihci E, Ozkaynak SS, Sallakci N, Kizilay F, Yavuzer U. Neurosci Lett; 2011 Apr 20; 494(1):1-5. PubMed ID: 21334418 [Abstract] [Full Text] [Related]
22. SNCA polymorphisms, smoking, and sporadic Parkinson's disease in Japanese. Miyake Y, Tanaka K, Fukushima W, Kiyohara C, Sasaki S, Tsuboi Y, Yamada T, Oeda T, Shimada H, Kawamura N, Sakae N, Fukuyama H, Hirota Y, Nagai M, Fukuoka Kinki Parkinson's Disease Study Group. Parkinsonism Relat Disord; 2012 Jun 20; 18(5):557-61. PubMed ID: 22425546 [Abstract] [Full Text] [Related]
23. Association of AQP4 single nucleotide polymorphisms (rs335929 and rs2075575) with Parkinson's disease: A case-control study. Sun X, Tian Q, Yang Z, Liu Y, Li C, Hou B, Xie A. Neurosci Lett; 2023 Feb 16; 797():137062. PubMed ID: 36626962 [Abstract] [Full Text] [Related]
24. Association of PGLYRP2 gene polymorphism and sporadic Parkinson's disease in northern Chinese Han population. Luan M, Jin J, Wang Y, Li X, Xie A. Neurosci Lett; 2022 Apr 01; 775():136547. PubMed ID: 35218888 [Abstract] [Full Text] [Related]
25. Is the +405 G/C single nucleotide polymorphism of the vascular endothelial growth factor (VEGF) gene associated with late-onset vitiligo? Almasi-Nasrabadi M, Amoli MM, Robati RM, Rajabi F, Parichehreh Dizaji S. Int J Immunogenet; 2019 Aug 01; 46(4):241-246. PubMed ID: 31135085 [Abstract] [Full Text] [Related]
26. Association of TLR9 polymorphisms with sporadic Parkinson's disease in Chinese Han population. Zhu K, Teng J, Zhao J, Liu H, Xie A. Int J Neurosci; 2016 Aug 01; 126(7):612-6. PubMed ID: 26000920 [Abstract] [Full Text] [Related]
27. Is the 1254T>C polymorphism in the DMT1 gene associated with Parkinson's disease? Saadat SM, Değirmenci İ, Özkan S, Saydam F, Özdemir Köroğlu Z, Çolak E, Güneş HV. Neurosci Lett; 2015 May 06; 594():51-4. PubMed ID: 25817364 [Abstract] [Full Text] [Related]
28. Vascular endothelial growth factor single nucleotide polymorphisms and haplotypes in pre-eclampsia: A case-control study. Ben Ali Gannoun M, Al-Madhi SA, Zitouni H, Raguema N, Meddeb S, Hachena Ben Ali F, Mahjoub T, Almawi WY. Cytokine; 2017 Sep 06; 97():175-180. PubMed ID: 28651127 [Abstract] [Full Text] [Related]
29. Association of AKT1 gene polymorphisms with sporadic Parkinson's disease in Chinese Han population. Li XY, Teng JJ, Liu Y, Wu YB, Zheng Y, Xie AM. Neurosci Lett; 2016 Aug 26; 629():38-42. PubMed ID: 27353512 [Abstract] [Full Text] [Related]
30. SNCA rs3822086 C>T Polymorphism Increases the Susceptibility to Parkinson's Disease in a Chinese Han Population. Jian CD, Huang JM, Meng LQ, Li XB, Huang RY, Shi SL, Wu Y, Qin C, Chen J, Zhang YM, Wang S, Feng YL, Zhou SN. Genet Test Mol Biomarkers; 2015 Sep 26; 19(9):481-7. PubMed ID: 26203864 [Abstract] [Full Text] [Related]
31. Association between the vascular endothelial growth factor single nucleotide polymorphisms and diabetic retinopathy risk: A meta-analysis. Xie XJ, Yang YM, Jiang JK, Lu YQ. J Diabetes; 2017 Aug 26; 9(8):738-753. PubMed ID: 27613596 [Abstract] [Full Text] [Related]
32. [Association analysis of the parkin gene in patients with sporadic Parkinson's disease from a Han population of Sichuan province]. Peng R, Chen WJ, Wu Y, Liu M, Lai XH, Zhang JH, Yuan GG, Gou YR, Li T, Wang YC. Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2007 Feb 26; 24(1):38-41. PubMed ID: 17285542 [Abstract] [Full Text] [Related]
33. Polymorphism in MIR4697 but not VPS13C, GCH1, or SIPA1L2 is associated with risk of Parkinson's disease in a Han Chinese population. Yang X, Zheng J, An R, Tian S, Zhao Q, Chen Y, Huang H, Ning PP, Song Y, Xu Y. Neurosci Lett; 2017 May 22; 650():8-11. PubMed ID: 28380328 [Abstract] [Full Text] [Related]
34. Association analysis of single-nucleotide polymorphisms of USP24 and USP40 with Parkinson's disease in the Han Chinese population. Zhao B, Song W, Chen YP, Huang R, Chen K, Cao B, Yang Y, Shang HF. Eur Neurol; 2012 May 22; 68(3):181-4. PubMed ID: 22923019 [Abstract] [Full Text] [Related]
35. [Association of polymorphisms of VEGF and VEGFR1 pathways related genes and risk of pre-eclampsia]. Li L, Guo X, Chen B, Gao Z, Liu J, Wang Q. Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2022 Aug 10; 39(8):893-897. PubMed ID: 35929944 [Abstract] [Full Text] [Related]
36. Further evidence for the contribution of the vascular endothelial growth factor gene in coronary artery disease susceptibility. Cui QT, Li Y, Duan CH, Zhang W, Guo XL. Gene; 2013 Jun 01; 521(2):217-21. PubMed ID: 23545315 [Abstract] [Full Text] [Related]
37. Association analysis of polymorphisms in VMAT2 and TMEM106B genes for Parkinson's disease, amyotrophic lateral sclerosis and multiple system atrophy. Hu T, Chen Y, Ou R, Wei Q, Cao B, Zhao B, Wu Y, Song W, Chen X, Shang HF. J Neurol Sci; 2017 Jun 15; 377():65-71. PubMed ID: 28477711 [Abstract] [Full Text] [Related]
38. Vitamin D receptor gene polymorphism and its association with Parkinson's disease in Chinese Han population. Han X, Xue L, Li Y, Chen B, Xie A. Neurosci Lett; 2012 Sep 06; 525(1):29-33. PubMed ID: 22842395 [Abstract] [Full Text] [Related]
39. SNP rs7684318 of the alpha-synuclein gene is associated with Parkinson's disease in the Han Chinese population. Yu L, Xu P, He X, Hu F, Lin Z, Zhu M, Liu Z, He L, Xu Y. Brain Res; 2010 Jul 30; 1346():262-5. PubMed ID: 20513365 [Abstract] [Full Text] [Related]
40. Association of Polymorphism of Neuronal Nitric Oxide Synthase Gene with Risk to Parkinson's Disease. Gupta SP, Kamal R, Mishra SK, Singh MK, Shukla R, Singh MP. Mol Neurobiol; 2016 Jul 30; 53(5):3309-3314. PubMed ID: 26081147 [Abstract] [Full Text] [Related] Page: [Previous] [Next] [New Search]