Human Genome Epidemiology Literature Finder
Records 1 - 10 (of 10 Records) |
Query Trace: COL4A6[original query] |
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Phenotypic and genotypic features of Alport syndrome in Chinese children. Pediatric nephrology (Berlin, Germany) 2002 Dec 17 (12): 1013-20. Wang Fang, Ding Jie, Guo Shunhua, Yang Jiy |
Characterization of uterine leiomyomas by whole-genome sequencing. The New England journal of medicine 2013 Jul 369 (1): 43-53. Mehine Miika, Kaasinen Eevi, Mäkinen Netta, Katainen Riku, Kämpjärvi Kati, Pitkänen Esa, Heinonen Hanna-Riikka, Bützow Ralf, Kilpivaara Outi, Kuosmanen Anna, Ristolainen Heikki, Gentile Massimiliano, Sjöberg Jari, Vahteristo Pia, Aaltonen Lauri |
Highly heterogeneous genomic landscape of uterine leiomyomas by whole exome sequencing and genome-wide arrays. Fertility and sterility 2017 02 107 (2): 457-466.e9. Yatsenko Svetlana A, Mittal Priya, Wood-Trageser Michelle A, Jones Mirka W, Surti Urvashi, Edwards Robert P, Sood Anil K, Rajkovic Aleksand |
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 |
Missense mutations in COL4A5 or COL4A6 genes may cause cerebrovascular fibromuscular dysplasia: Case report and literature review. Medicine 2018 7 97 (30): e11538. Wang Xiaojuan, Li Wei, Wei Ke, Xiao Rui, Wang Juntao, Ma Haichang, Qin Lingzhi, Shao Wenjun, Li Chunya |
Novel immune-related signature for risk stratification and prognosis in prostatic adenocarcinoma. Cancer science 2021 7 112 (10): 4365-4376. Zhao Hai-Bo, Zeng Yan-Ru, Han Zhao-Dong, Zhuo Yang-Jia, Liang Ying-Ke, Hon Chi Tin, Wan Song, Wu Shulin, Dahl Douglas, Zhong Wei-De, Wu Chin-L |
The GWAS Analysis of Body Size and Population Verification of Related SNPs in Hu Sheep. Frontiers in genetics 2021 6 12 642552. Jiang Junfang, Cao Yuhao, Shan Huili, Wu Jianliang, Song Xuemei, Jiang Yongqi |
Analysis of chronic kidney disease patients by targeted next-generation sequencing identifies novel variants in kidney-related genes. Frontiers in genetics 2022 8 13 886038. Alaamery Manal, Alghamdi Jahad, Massadeh Salam, Alsawaji Mona, Aljawini Nora, Albesher Nour, Alghamdi Bader, Almutairi Mansour, Hejaili Fayez, Alfadhel Majid, Baz Batoul, Almuzzaini Bader, Almutairi Adel F, Abdullah Mubarak, Quintana Francisco J, Sayyari Abdull |
Prevalence and clinical significance of co-existing mutations in MED12 and FH in uterine fibroids of Australian women. Frontiers in reproductive health 2023 4 5 1081092. M Fairuz B Jamaluddin, Prathima B Nagendra, Yi-An Ko, Preety Bajwa, Rodney J Scott, Pravin Nahar, Pradeep S Tanw |
A mutational signature and significantly mutated driver genes associated with immune checkpoint inhibitor response across multiple cancers. International immunopharmacology 2023 2 116 109821. Wang Qinghua, Zhang Wenjing, Guo Yuxian, Shi Fuyan, Li Yuting, Kong Yujia, Lyu Juncheng, Wang Suzh |
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- Page last updated:Mar 25, 2024
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