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117 related items for PubMed ID: 12811635
1. Modulation of disease risk according to a cathepsin D / apolipoprotein E genotype in Parkinson's disease. Schulte T, Böhringer S, Schöls L, Müller T, Fischer C, Riess O, Przuntek H, Berger K, Epplen JT, Krüger R. J Neural Transm (Vienna); 2003 Jul; 110(7):749-55. PubMed ID: 12811635 [Abstract] [Full Text] [Related]
2. Genetic associations between cathepsin D exon 2 C-->T polymorphism and Alzheimer's disease, and pathological correlations with genotype. Davidson Y, Gibbons L, Pritchard A, Hardicre J, Wren J, Tian J, Shi J, Stopford C, Julien C, Thompson J, Payton A, Thaker U, Hayes AJ, Iwatsubo T, Pickering-Brown SM, Pendleton N, Horan MA, Burns A, Purandare N, Lendon CL, Neary D, Snowden JS, Mann DM. J Neurol Neurosurg Psychiatry; 2006 Apr; 77(4):515-7. PubMed ID: 16543533 [Abstract] [Full Text] [Related]
3. Association study of cathepsin D gene polymorphism in Iranian patients with sporadic late-onset Alzheimer's disease. Sayad A, Noruzinia M, Zamani M, Harirchian MH, Kazemnejad A. Dement Geriatr Cogn Disord; 2014 Apr; 37(5-6):257-64. PubMed ID: 24281128 [Abstract] [Full Text] [Related]
4. The cathepsin D gene exon 2 (C224T) polymorphism and sporadic Alzheimer's disease in European populations. Capurso C, Solfrizzi V, D'Introno A, Colacicco AM, Capurso SA, Mastroianni F, Liaci M, Vendemiale G, Capurso A, Panza F. J Gerontol A Biol Sci Med Sci; 2005 Aug; 60(8):991-6. PubMed ID: 16127101 [Abstract] [Full Text] [Related]
5. Short arm of chromosome 11 and sporadic Alzheimer's disease: catalase and cathepsin D gene polymorphisms. Capurso C, Solfrizzi V, D'Introno A, Colacicco AM, Capurso SA, Bifaro L, Menga R, Santamato A, Seripa D, Pilotto A, Capurso A, Panza F. Neurosci Lett; 2008 Feb 27; 432(3):237-42. PubMed ID: 18248894 [Abstract] [Full Text] [Related]
6. Influence and interactions of cathepsin D, HLA-DRB1 and APOE on cognitive abilities in an older non-demented population. Payton A, van den Boogerd E, Davidson Y, Gibbons L, Ollier W, Rabbitt P, Worthington J, Horan M, Pendleton N. Genes Brain Behav; 2006 Feb 27; 5 Suppl 1():23-31. PubMed ID: 16417614 [Abstract] [Full Text] [Related]
7. Genetic polymorphism in exon 2 of cathepsin D is not associated with vascular dementia. Jeong BH, Lee KH, Lee YJ, Yun J, Park YJ, Kim YH, Cho YS, Choi EK, Carp RI, Kim YS. Acta Neurol Scand; 2011 Jun 27; 123(6):419-23. PubMed ID: 20597865 [Abstract] [Full Text] [Related]
8. Role of Apolipoprotein E, Cathepsin D, and Brain-Derived Neurotrophic Factor in Parkinson's Disease: A Study from Eastern India. Pal P, Sadhukhan T, Chakraborty S, Sadhukhan S, Biswas A, Das SK, Ray K, Ray J. Neuromolecular Med; 2019 Sep 27; 21(3):287-294. PubMed ID: 31134487 [Abstract] [Full Text] [Related]
9. [The C224T polymorphism in the cathepsin D gene is not associated with sporadic Alzheimer's disease in Chinese]. Sun Y, Shi JJ, Zhang SZ, Tang MN, Han HY, Guo YB, Ma C, Liu XH, Li T. Yi Chuan; 2005 Mar 27; 27(2):190-4. PubMed ID: 15843343 [Abstract] [Full Text] [Related]
10. Parkinson's disease and apolipoprotein E: possible association with dementia but not age at onset. Parsian A, Racette B, Goldsmith LJ, Perlmutter JS. Genomics; 2002 Mar 27; 79(3):458-61. PubMed ID: 11863377 [Abstract] [Full Text] [Related]
11. Interaction of CTSD and A2M polymorphisms in the risk for Alzheimer's disease. Mariani E, Seripa D, Ingegni T, Nocentini G, Mangialasche F, Ercolani S, Cherubini A, Metastasio A, Pilotto A, Senin U, Mecocci P. J Neurol Sci; 2006 Sep 25; 247(2):187-91. PubMed ID: 16784755 [Abstract] [Full Text] [Related]
12. Apolipoprotein E epsilon4 allele in familial and sporadic Parkinson's disease. Blázquez L, Otaegui D, Sáenz A, Paisán-Ruiz C, Emparanza JI, Ruiz-Martinez J, Moreno F, Martí-Massó JF, López de Munain A. Neurosci Lett; 2006 Oct 09; 406(3):235-9. PubMed ID: 16904828 [Abstract] [Full Text] [Related]
13. Cathepsin D polymorphism in Italian elderly subjects with sporadic late-onset Alzheimer's disease. Ingegni T, Nocentini G, Mariani E, Spazzafumo L, Polidori MC, Cherubini A, Catani M, Cadini D, Senin U, Mecocci P. Dement Geriatr Cogn Disord; 2003 Oct 09; 16(3):151-5. PubMed ID: 12826741 [Abstract] [Full Text] [Related]
14. Genetic association of a cathepsin D polymorphism and sporadic Creutzfeldt-Jakob disease. Jeong BH, Lee KH, Lee YJ, Yun J, Park YJ, Bae Y, Kim YH, Cho YS, Choi EK, Carp RI, Kim YS. Dement Geriatr Cogn Disord; 2009 Oct 09; 28(4):302-6. PubMed ID: 19828951 [Abstract] [Full Text] [Related]
15. Cathepsin D (C224T) polymorphism in sporadic and genetic Creutzfeldt-Jakob disease. Kovacs GG, Sanchez-Juan P, Ströbel T, Schuur M, Poleggi A, Nocentini S, Giannattasio C, Belay G, Bishop M, Capellari S, Parchi P, Gelpi E, Gal A, Bakos A, Molnar MJ, Heinemann U, Zerr I, Knight RS, Mitrova E, van Duijn C, Budka H. Alzheimer Dis Assoc Disord; 2010 Oct 09; 24(1):104-7. PubMed ID: 19571726 [Abstract] [Full Text] [Related]
16. Genetic study of apolipoprotein E gene, alpha-1 antichymotrypsin gene in sporadic Parkinson disease. Tang G, Xie H, Xu L, Hao Y, Lin D, Ren D. Am J Med Genet; 2002 May 08; 114(4):446-9. PubMed ID: 11992569 [Abstract] [Full Text] [Related]
17. [Association between polymorphism of alpha 1-antichymotrypsin and apolipoprotein E gene and Parkinson's disease in Shanghai Hans]. Hao Y, Xie H, Xu L. Zhonghua Yi Xue Za Zhi; 2001 Oct 08; 81(19):1172-5. PubMed ID: 11769703 [Abstract] [Full Text] [Related]
18. Lack of association of APOE and tau polymorphisms with dementia in Parkinson's disease. Ezquerra M, Campdelacreu J, Gaig C, Compta Y, Muñoz E, Martí MJ, Valldeoriola F, Tolosa E. Neurosci Lett; 2008 Dec 19; 448(1):20-3. PubMed ID: 18930114 [Abstract] [Full Text] [Related]
19. Association of the mitochondrial tRNA(A4336G) mutation with Alzheimer's and Parkinson's diseases. Egensperger R, Kösel S, Schnopp NM, Mehraein P, Graeber MB. Neuropathol Appl Neurobiol; 1997 Aug 19; 23(4):315-21. PubMed ID: 9292870 [Abstract] [Full Text] [Related]
20. Modulation of the age at onset of Parkinson's disease by apolipoprotein E genotypes. Zareparsi S, Kaye J, Camicioli R, Grimslid H, Oken B, Litt M, Nutt J, Bird T, Schellenberg G, Payami H. Ann Neurol; 1997 Oct 19; 42(4):655-8. PubMed ID: 9382478 [Abstract] [Full Text] [Related] Page: [Next] [New Search]