Human Genome Epidemiology Literature Finder
|
Records 1 - 30 (of 33 Records) |
| Query Trace: Disease and CTSD[original query] |
|---|
| Cathepsin D polymorphism in Italian elderly subjects with sporadic late-onset Alzheimer's disease. Dementia and geriatric cognitive disorders 2003 16 (3): 151-5. Ingegni Tiziana, Nocentini Giuseppe, Mariani Elena, Spazzafumo Liana, Polidori M Cristina, Cherubini Antonio, Catani Marco, Cadini Donatella, Senin Umberto, Mecocci Patriz |
| Modulation of disease risk according to a cathepsin D / apolipoprotein E genotype in Parkinson's disease. Journal of neural transmission (Vienna, Austria : 1996) 2003 Jul 110 (7): 749-55. Schulte T, Böhringer S, Schöls L, Müller T, Fischer C, Riess O, Przuntek H, Berger K, Epplen J T, Krüger |
| Association between cathepsin D polymorphism and Alzheimer's disease in a Chinese Han population. Dementia and geriatric cognitive disorders 2004 18 (2): 115-9. Li Xiao-Qing, Chen Deng, Zhang Zhen-Xin, Qu Qiu-Ming, Zhang Jun- |
| Single nucleotide polymorphisms associated with aggressive periodontitis and severe chronic periodontitis in Japanese. Biochemical and biophysical research communications 2004 May 317 (3): 887-92. Suzuki A, Ji G, Numabe Y, Muramatsu M, Gomi K, Kanazashi M, Ogata Y, Shimizu E, Shibukawa Y, Ito A, Ito T, Sugaya A, Arai T, Yamada S, Deguchi S, Kamoi K |
| Meta-analysis of the association of the cathepsin D Ala224Val gene polymorphism with the risk of Alzheimer's disease: a HuGE gene-disease association review. American journal of epidemiology 2004 Mar 159 (6): 527-36. Ntais C, Polycarpou A, Ioannidis JP |
| The cathepsin D gene exon 2 (C224T) polymorphism and sporadic Alzheimer's disease in European populations. The journals of gerontology. Series A, Biological sciences and medical sciences 2005 Aug 60 (8): 991-6. Capurso C, Solfrizzi V, D'Introno A, Colacicco AM, Capurso SA, Mastroianni F, Liaci M, Vendemiale G, Capurso A, Panza F |
| [The C224T polymorphism in the cathepsin D gene is not associated with sporadic Alzheimer's disease in Chinese]. Yi chuan = Hereditas / Zhongguo yi chuan xue hui bian ji 2005 Mar 27 (2): 190-4. Sun Yan, Shi Jia-Jun, Zhang Si-Zhong, Tang Mu-Ni, Han Hai-Ying, Guo Yang-Bo, Ma Cui, Liu Xie-He, Li T |
| Interaction of CTSD and A2M polymorphisms in the risk for Alzheimer's disease. Journal of the neurological sciences 2006 Sep 247 (2): 187-91. Mariani Elena, Seripa Davide, Ingegni Tiziana, Nocentini Giuseppe, Mangialasche Francesca, Ercolani Sara, Cherubini Antonio, Metastasio Antonio, Pilotto Alberto, Senin Umberto, Mecocci Patriz |
| The cathepsin D rs17571 polymorphism: effects on CSF tau concentrations in Alzheimer disease. Human mutation 2006 Jun 27 (6): 532-7. Riemenschneider Matthias, Blennow Kaj, Wagenpfeil Stefan, Andreasen Niels, Prince Jonathan A, Laws Simon M, Förstl Hans, Kurz Alexand |
| Membership in genetic groups predicts Alzheimer disease. Rejuvenation research 2006 9 (1): 89-93. Corder Elizabeth H, Huang Rong, Cathcart Heather M, Lanham Irene S, Parker Ginny R, Cheng Danny, Smith Suzanne, Poduslo Shirley |
| Genetic associations between cathepsin D exon 2 C-->T polymorphism and Alzheimer's disease, and pathological correlations with genotype. Journal of neurology, neurosurgery, and psychiatry 2006 Apr 77 (4): 515-7. 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 A J, Iwatsubo T, Pickering-Brown S M, Pendleton N, Horan M A, Burns A, Purandare N, Lendon C L, Neary D, Snowden J S, Mann D M |
| Influence and interactions of cathepsin D, HLA-DRB1 and APOE on cognitive abilities in an older non-demented population. Genes, brain, and behavior 2006 5 Suppl 1 (): 23-31. Payton A, van den Boogerd E, Davidson Y, Gibbons L, Ollier W, Rabbitt P, Worthington J, Horan M, Pendleton |
| Cluster analysis of risk factor genetic polymorphisms in Alzheimer's disease. Neurochemical research 2009 Jan 34 (1): 23-8. Randall C N, Strasburger D, Prozonic J, Morris S N, Winkie A D, Parker G R, Cheng D, Fennell E M, Lanham I, Vakil N, Huang J, Cathcart H, Huang R, Poduslo S |
| Short arm of chromosome 11 and sporadic Alzheimer's disease: catalase and cathepsin D gene polymorphisms. Neuroscience letters 2008 Feb 432 (3): 237-42. Capurso Cristiano, Solfrizzi Vincenzo, D'Introno Alessia, Colacicco Anna M, Capurso Sabrina A, Bifaro Luigia, Menga Roberta, Santamato Andrea, Seripa Davide, Pilotto Alberto, Capurso Antonio, Panza Frances |
| Assessment of Alzheimer's disease case-control associations using family-based methods. Neurogenetics 2009 Feb 10 (1): 19-25. Schjeide Brit-Maren M, McQueen Matthew B, Mullin Kristina, DiVito Jason, Hogan Meghan F, Parkinson Michele, Hooli Basavaraj, Lange Christoph, Blacker Deborah, Tanzi Rudolph E, Bertram La |
| Cathepsin D (C224T) polymorphism in sporadic and genetic Creutzfeldt-Jakob disease. Alzheimer disease and associated disorders 0 24 (1): 104-7. Kovacs Gabor G, Sanchez-Juan Pascual, Ströbel Thomas, Schuur Maaike, Poleggi Anna, Nocentini Sara, Giannattasio Claudia, Belay Girma, Bishop Matthew, Capellari Sabina, Parchi Piero, Gelpi Ellen, Gal Aniko, Bakos Agnes, Molnar Maria J, Heinemann Uta, Zerr Inga, Knight Richard S G, Mitrova Eva, van Duijn Cornelia, Budka Herbe |
| Cathepsin D gene and the risk of Alzheimer's disease: a population-based study and meta-analysis. Neurobiology of aging 2011 Sep 32 (9): 1607-14. Schuur M, Ikram M A, van Swieten J C, Isaacs A, Vergeer-Drop J M, Hofman A, Oostra B A, Breteler M M B, van Duijn C |
| Genetic association of a cathepsin D polymorphism and sporadic Creutzfeldt-Jakob disease. Dementia and geriatric cognitive disorders 2009 28 (4): 302-6. Jeong Byung-Hoon, Lee Kyung-Hee, Lee Yun-Jung, Yun Jisuk, Park Young-Jae, Bae Yoonsang, Kim Young-Hoon, Cho Young-Sook, Choi Eun-Kyoung, Carp Richard I, Kim Yong-S |
| Genetic polymorphism in exon 2 of cathepsin D is not associated with vascular dementia. Acta neurologica Scandinavica 2011 Jun 123 (6): 419-23. Jeong B-H, Lee K-H, Lee Y-J, Yun J, Park Y-J, Kim Y-H, Cho Y-S, Choi E-K, Carp R I, Kim Y |
| Most reported genetic associations with general intelligence are probably false positives. Psychological science 2012 23 (11): 1314-23. Chabris Christopher F, Hebert Benjamin M, Benjamin Daniel J, Beauchamp Jonathan, Cesarini David, van der Loos Matthijs, Johannesson Magnus, Magnusson Patrik K E, Lichtenstein Paul, Atwood Craig S, Freese Jeremy, Hauser Taissa S, Hauser Robert M, Christakis Nicholas, Laibson Dav |
| Crohn disease ATG16L1 polymorphism increases susceptibility to infection with Helicobacter pylori in humans. Autophagy 2012 Sep 8 (9): 1387-8. Raju Deepa, Hussey Séamus, Jones Nicola |
| Association study of cathepsin D gene polymorphism in Iranian patients with sporadic late-onset Alzheimer's disease. Dementia and geriatric cognitive disorders 2013 Nov 37 (5-6): 5-6. Sayad A, Noruzinia M, Zamani M, Harirchian MH, Kazemnejad A |
| Positive Association of the Cathepsin D Ala224Val Gene Polymorphism With the Risk of Alzheimer's Disease. The American journal of the medical sciences 2015 Sep . Paz-Y-Miño César, García-Cárdenas Jennyfer M, López-Cortés Andrés, Salazar Carolina, Serrano Marcos, Leone Paola |
| Absence of association of the Ala58Val (rs17571) CTSD gene variant with Parkinson's disease or amyotrophic lateral sclerosis in a Han Chinese population. Neuroscience letters 2017 Sep . Xi Jing, Yang Xinglong, Zhao Quanzhen, Zheng Jinhua, An Ran, Tian Sijia, Huang Hongyan, Hu Fayunn, Ning Pingping, Xu Yanmi |
| Excessive burden of lysosomal storage disorder gene variants in Parkinson's disease. Brain : a journal of neurology 2017 Nov . Robak Laurie A, Jansen Iris E, van Rooij Jeroen, Uitterlinden André G, Kraaij Robert, Jankovic Joseph, , Heutink Peter, Shulman Joshua |
| Cathepsin D Polymorphism C224T in Childhood-Onset Neurodegenerative Disorders: No Impact for Childhood Dementia. Journal of pediatric genetics 2018 Mar 7 (1): 14-18. Kettwig Matthias, Ohlenbusch Andreas, Jung Klaus, Steinfeld Robert, Gärtner Jut |
| Role of Apolipoprotein E, Cathepsin D, and Brain-Derived Neurotrophic Factor in Parkinson's Disease: A Study from Eastern India. Neuromolecular medicine 2019 May . Pal Prosenjit, Sadhukhan Tamal, Chakraborty Subhadip, Sadhukhan Sriparna, Biswas Arindam, Das Shyamal K, Ray Kunal, Ray Jhar |
| Identification of Novel Genomic-Variant Patterns of OR56A5, OR52L1, and CTSD in Retinitis Pigmentosa Patients by Whole-Exome Sequencing. International journal of molecular sciences 2021 6 22 (11): . Lin Ting-Yi, Chang Yun-Chia, Hsiao Yu-Jer, Chien Yueh, Jheng Ying-Chun, Wu Jing-Rong, Ching Lo-Jei, Hwang De-Kuang, Hsu Chih-Chien, Lin Tai-Chi, Chou Yu-Bai, Huang Yi-Ming, Chen Shih-Jen, Yang Yi-Ping, Tsai Ping-Hsi |
| Impact of cathepsin D activity and C224T polymorphism (rs17571) on chronic obstructive pulmonary disease: correlations with oxidative and inflammatory markers. Clinical and experimental medicine 2021 2 21 (3): 457-465. Bchir Sarra, Boumiza Soumaya, Ben Nasr Hela, Garrouch Abdelhamid, Kallel Imen, Tabka Zouhair, Chahed Kar |
| Untangling the Genetic Threads of Alzheimer's: Insights into Risk Factors and Biomarkers. Current gene therapy 2025 1 . Atabak Naiyeri, Amin Moqadami, Mohammad Khalaj-Kondo |
- Page last reviewed:Feb 1, 2024
- Content source: