Human Genome Epidemiology Literature Finder
Records 1 - 8 (of 8 Records) |
Query Trace: PRKCD[original query] |
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DGKH genetic risk variant influences gene expression in bipolar affective disorder. Journal of affective disorders 2016 Jul 198 148-57. Kittel-Schneider Sarah, Lorenz Carina, Auer Joyce, Weißflog Lena, Reif Andre |
Genetic alterations and their clinical implications in gastric cancer peritoneal carcinomatosis revealed by whole-exome sequencing of malignant ascites. Oncotarget 2016 Jan . Lim Byungho, Kim Chan, Kim Jeong-Hwan, Kwon Woo Sun, Lee Won Seok, Kim Jeong Min, Park Jun Yong, Kim Hyo Song, Park Kyu Hyun, Kim Tae Soo, Park Jong-Lyul, Chung Hyun Cheol, Rha Sun Young, Kim Seon-You |
Significant alterations of the novel 15 gene signature identified from macrophage-tumor interactions in breast cancer. Biochimica et biophysica acta. General subjects 2017 12 1862 (3): 669-683. Singh Rajshri, Dagar Priya, Pal Shyama, Basu Bhakti, Shankar Bhavani |
De novo mutations implicate novel genes in systemic lupus erythematosus. Human molecular genetics 2017 11 27 (3): 421-429. Pullabhatla Venu, Roberts Amy L, Lewis Myles J, Mauro Daniele, Morris David L, Odhams Christopher A, Tombleson Philip, Liljedahl Ulrika, Vyse Simon, Simpson Michael A, Sauer Sascha, de Rinaldis Emanuele, Syvänen Ann-Christine, Vyse Timothy |
Genetic variants of PDGF signaling pathway genes predict cutaneous melanoma survival. Oncotarget 2017 Sep 8 (43): 74595-74606. Li Hong, Wang Yanru, Liu Hongliang, Shi Qiong, Li Hongyu, Wu Wenting, Zhu Dakai, Amos Christopher I, Fang Shenying, Lee Jeffrey E, Li Yi, Han Jiali, Wei Qing |
Evaluating the Genetics of Common Variable Immunodeficiency: Monogenetic Model and Beyond. Frontiers in immunology 2018 6 9 636. de Valles-Ibáñez Guillem, Esteve-Solé Ana, Piquer Mònica, González-Navarro E Azucena, Hernandez-Rodriguez Jessica, Laayouni Hafid, González-Roca Eva, Plaza-Martin Ana María, Deyà-Martínez Ángela, Martín-Nalda Andrea, Martínez-Gallo Mónica, García-Prat Marina, Del Pino-Molina Lucía, Cuscó Ivón, Codina-Solà Marta, Batlle-Masó Laura, Solís-Moruno Manuel, Marquès-Bonet Tomàs, Bosch Elena, López-Granados Eduardo, Aróstegui Juan Ignacio, Soler-Palacín Pere, Colobran Roger, Yagüe Jordi, Alsina Laia, Juan Manel, Casals Ferr |
99-Case Study of Sporadic Aortic Dissection by Whole Exome Sequencing Indicated Novel Disease-Associated Genes and Variants in Chinese Population. BioMed research international 2020 2020 7857043. Wang Zanxin, Zhuang Xianmian, Chen Bailang, Wen Junmin, Peng Fang, Liu Xiling, Wei Minx |
Genetic association of PRKCD and CARD9 polymorphisms with Vogt-Koyanagi-Harada disease in the Chinese Han population. Human genomics 2023 2 17 (1): 9. Zhou Chunya, Cai Shiya, Xie Yuhong, Zeng Zhen, Zhang Jun, Su Guannan, Wu Qiuying, Ye Xingsheng, Cao Qingfeng, Yang Peizeng, Hu Jianm |
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- Page last updated:Apr 29, 2024
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