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426 related items for PubMed ID: 17692293
41. Serum levels and genetic variation of TGF-beta1 are not associated with Alzheimer's disease. Rodríguez-Rodríguez E, Sánchez-Juan P, Mateo I, Llorca J, Infante J, García-Gorostiaga I, Berciano J, Combarros O. Acta Neurol Scand; 2007 Dec; 116(6):409-12. PubMed ID: 17986101 [Abstract] [Full Text] [Related]
42. Effect of IL-6 polymorphism on risk of Alzheimer disease: genotype-phenotype association study in Japanese cases. Shibata N, Ohnuma T, Takahashi T, Baba H, Ishizuka T, Ohtsuka M, Ueki A, Nagao M, Arai H. Am J Med Genet; 2002 May 08; 114(4):436-9. PubMed ID: 11992567 [Abstract] [Full Text] [Related]
43. Association of a functional NOS1 promoter repeat with Alzheimer's disease in the VITA cohort. Reif A, Grünblatt E, Herterich S, Wichart I, Rainer MK, Jungwirth S, Danielczyk W, Deckert J, Tragl KH, Riederer P, Fischer P. J Alzheimers Dis; 2011 May 08; 23(2):327-33. PubMed ID: 21098972 [Abstract] [Full Text] [Related]
44. Association analysis of the functional MAOA gene promoter and MAOB gene intron 13 polymorphisms in tension type headache patients. Edgnülü TG, Özge A, Erdal N, Kuru O, Erdal ME. Adv Clin Exp Med; 2014 May 08; 23(6):901-6. PubMed ID: 25618115 [Abstract] [Full Text] [Related]
45. MAO A VNTR polymorphism and variation in human morphology: a VBM study. Cerasa A, Gioia MC, Labate A, Lanza P, Magariello A, Muglia M, Quattrone A. Neuroreport; 2008 Jul 16; 19(11):1107-10. PubMed ID: 18596609 [Abstract] [Full Text] [Related]
46. Association study and meta-analysis of Alzheimer's disease risk and presenilin-1 intronic polymorphism. Rodríguez-Manotas M, Amorín-Díaz M, Cañizares-Hernández F, Ruíz-Espejo F, Martínez-Vidal S, González-Sarmiento R, Martínez-Hernández P, Cabezas-Herrera J. Brain Res; 2007 Sep 19; 1170():119-28. PubMed ID: 17719017 [Abstract] [Full Text] [Related]
47. Gene-gene interaction between MAOA and COMT in suicidal behavior: analysis in schizophrenia. De Luca V, Tharmalingam S, Müller DJ, Wong G, de Bartolomeis A, Kennedy JL. Brain Res; 2006 Jun 30; 1097(1):26-30. PubMed ID: 16725119 [Abstract] [Full Text] [Related]
48. MAOA genotype, family relations and sexual abuse in relation to adolescent alcohol consumption. Nilsson KW, Comasco E, Åslund C, Nordquist N, Leppert J, Oreland L. Addict Biol; 2011 Apr 30; 16(2):347-55. PubMed ID: 20731636 [Abstract] [Full Text] [Related]
49. Relationship of the Ubiquilin 1 gene with Alzheimer's and Parkinson's disease and cognitive function. Arias-Vásquez A, de Lau L, Pardo L, Liu F, Feng BJ, Bertoli-Avella A, Isaacs A, Aulchenko Y, Hofman A, Oostra B, Breteler M, van Duijn C. Neurosci Lett; 2007 Aug 31; 424(1):1-5. PubMed ID: 17709205 [Abstract] [Full Text] [Related]
50. Genetically increased risk of sleep disruption in Alzheimer's disease. Craig D, Hart DJ, Passmore AP. Sleep; 2006 Aug 31; 29(8):1003-7. PubMed ID: 16944667 [Abstract] [Full Text] [Related]
51. The PPAR-alpha gene in Alzheimer's disease: lack of replication of earlier association. Sjölander A, Minthon L, Bogdanovic N, Wallin A, Zetterberg H, Blennow K. Neurobiol Aging; 2009 Apr 31; 30(4):666-8. PubMed ID: 17850927 [Abstract] [Full Text] [Related]
52. P-selectin glycoprotein ligand-1 variable number of tandem repeats (VNTR) polymorphism in patients with multiple sclerosis. Scalabrini D, Galimberti D, Fenoglio C, Comi C, De Riz M, Venturelli E, Castelli L, Piccio L, Ronzoni M, Lovati C, Mariani C, Monaco F, Bresolin N, Scarpini E. Neurosci Lett; 2005 Nov 18; 388(3):149-52. PubMed ID: 16039046 [Abstract] [Full Text] [Related]
53. Detection and analysis of four polymorphic markers at the human monoamine oxidase (MAO) gene in Japanese controls and patients with Parkinson's disease. Nakatome M, Tun Z, Shimada S, Honda K. Biochem Biophys Res Commun; 1998 Jun 18; 247(2):452-6. PubMed ID: 9642149 [Abstract] [Full Text] [Related]
54. ACE gene is associated with Alzheimer's disease and atrophy of hippocampus and amygdala. Sleegers K, den Heijer T, van Dijk EJ, Hofman A, Bertoli-Avella AM, Koudstaal PJ, Breteler MM, van Duijn CM. Neurobiol Aging; 2005 Jun 18; 26(8):1153-9. PubMed ID: 15917098 [Abstract] [Full Text] [Related]
55. Case-control study of vascular endothelial growth factor (VEGF) genetic variability in Alzheimer's disease. Mateo I, Llorca J, Infante J, Rodríguez-Rodríguez E, Sánchez-Quintana C, Sánchez-Juan P, Berciano J, Combarros O. Neurosci Lett; 2006 Jun 19; 401(1-2):171-3. PubMed ID: 16569480 [Abstract] [Full Text] [Related]
56. A functional polymorphism in the promoter region of MAOA gene is associated with daytime sleepiness in healthy subjects. Ojeda DA, Niño CL, López-León S, Camargo A, Adan A, Forero DA. J Neurol Sci; 2014 Feb 15; 337(1-2):176-9. PubMed ID: 24360188 [Abstract] [Full Text] [Related]
57. A regulatory polymorphism of the monoamine oxidase-A gene may be associated with variability in aggression, impulsivity, and central nervous system serotonergic responsivity. Manuck SB, Flory JD, Ferrell RE, Mann JJ, Muldoon MF. Psychiatry Res; 2000 Jul 24; 95(1):9-23. PubMed ID: 10904119 [Abstract] [Full Text] [Related]
58. Association study between antipsychotic-induced restless legs syndrome and polymorphisms of monoamine oxidase genes in schizophrenia. Kang SG, Park YM, Choi JE, Lim SW, Lee HJ, Lee SH, Kim YK, Kim SH, Cho SN, Kim L. Hum Psychopharmacol; 2010 Jul 24; 25(5):397-403. PubMed ID: 20589923 [Abstract] [Full Text] [Related]
59. Gene-gene interaction between MAOA and COMT in suicidal behavior. De Luca V, Tharmalingam S, Sicard T, Kennedy JL. Neurosci Lett; 2010 Jul 24; 383(1-2):151-4. PubMed ID: 15936529 [Abstract] [Full Text] [Related]
60. MAOA gene polymorphisms and response to mirtazapine in major depression. Tzeng DS, Chien CC, Lung FW, Yang CY. Hum Psychopharmacol; 2009 Jun 24; 24(4):293-300. PubMed ID: 19382113 [Abstract] [Full Text] [Related] Page: [Previous] [Next] [New Search]