Human Genome Epidemiology Literature Finder
Records 1 - 12 (of 12 Records) |
Query Trace: C1R[original query] |
---|
A polymorphism in the complement component C1r is not associated with sporadic Alzheimer's disease. Neuroscience letters 2003 Jan 336 (2): 101-4. Rosenmann Hanna, Meiner Zeev, Kahana Esther, Aladjem Zoja, Friedman Gideon, Ben-Yehuda Arie, Grenader Tal, Wertman Eli, Abramsky Od |
Association of the 3' UTR transcription factor LBP-1c/CP2/LSF polymorphism with late-onset Alzheimer's disease. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2003 Feb 117B (1): 114-7. Luedecking-Zimmer Erin, DeKosky Steven T, Nebes Robert, Kamboh M Ily |
Clinical presentations and molecular basis of complement C1r deficiency in a male African-American patient with systemic lupus erythematosus. Lupus 2011 Oct 20 (11): 1126-34. Wu Y L, Brookshire B P, Verani R R, Arnett F C, Yu C |
Brief Report: Functional Interaction of Endoplasmic Reticulum Aminopeptidase 2 and HLA-B27 Activates the Unfolded Protein Response. Arthritis & rheumatology (Hoboken, N.J.) 2016 12 69 (5): 1009-1015. Zhang Zhenbo, Ciccia Francesco, Zeng Fanxing, Guggino Giuliana, Yee Kirby, Abdullah Hasan, Silverberg Mark S, Alessandro Riccardo, Triolo Giovanni, Haroon Nig |
Broad Susceptibility of Nucleolar Proteins and Autoantigens to Complement C1 Protease Degradation. Journal of immunology (Baltimore, Md. : 1950) 2017 12 199 (12): 3981-3990. Cai Yitian, Wee Seng Yin Kelly, Chen Junjie, Teo Boon Heng Dennis, Ng Yee Leng Carol, Leong Khai Pang, Lu Jinh |
Investigation of C1-complex regions reveals new C1Q variants associated with protection from systemic lupus erythematosus, and affect its transcript abundance. Scientific reports 2018 May 8 (1): 8048. Guo Jianping, Gao Yanyan, Wang Yuxuan, Zou Yundong, Du Yan, Luo Cainan, Shi Yamei, Yang Yue, Wu Xinyu, Su Yin, Wu Lijun, Chen Shi, Li Zhang |
Functional DNA variations associated with Saudi female with low VO: a pilot microarray study. American journal of translational research 2019 7 11 (6): 3659-3670. Al Asoom Lubna Ibrahim, Alsuwat Hind Saleh, Rafique Nazish, Al Makhaita Marwah, Alamoudi Widyan, AbdulAzeez Sayed, Borgio Jesu Franc |
Weighted burden analysis of exome-sequenced late-onset Alzheimer's cases and controls provides further evidence for a role for PSEN1 and suggests involvement of the PI3K/Akt/GSK-3? and WNT signalling pathways. Annals of human genetics 2020 Feb . Curtis David, Bakaya Kaushiki, Sharma Leona, Bandyopadhyay Sreej |
Recurrent germline mutations as genetic markers for aortic root dilatation in bicuspid aortic valve patients. Heart and vessels 2020 Oct . Wu Boting, Li Jun, Wang Yongshi, Cheng Yunfeng, Wang Chunsheng, Shu Xianho |
A 44-kb deleted-type copy number variation is associated with decreasing complement component activity and calf mortality in Japanese Black cattle. BMC genomics 2021 2 22 (1): 107. Sasaki Shinji, Miki Youko, Ibi Takayuki, Wakaguri Hiroyuki, Yoshida Yuichi, Sugimoto Yoshikazu, Suzuki Yuta |
Genetic Susceptibility to Enteric Fever in Experimentally Challenged Human Volunteers. Infection and immunity 2022 3 90 (4): e0038921. Barton Amber, Hill Jennifer, Bibi Sagida, Chen Liye, Jones Claire, Jones Elizabeth, Camara Susana, Shrestha Sonu, Jin Celina, Gibani Malick M, Dobinson Hazel, Waddington Claire, Darton Thomas C, Blohmke Christoph J, Pollard Andrew |
The Relationship between Complement Components C1R and C5 Gene Polymorphism and the Values of Blood Indices in Suckling Piglets. Genes 2023 11 14 (11): . Hanna Szyma?ska, Ewa Dzika, Tadeusz Jaros?aw Zabolewicz, Krystyna ?ycz |
- Page last reviewed:Feb 1, 2024
- Page last updated:Apr 22, 2024
- Content source: