Human Genome Epidemiology Literature Finder
Records 1 - 10 (of 10 Records) |
Query Trace: CRIM1[original query] |
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Genome-wide association study of anthropometric traits in Korcula Island, Croatia.
Croatian medical journal 2009 Feb 50 (1): 7-16. Polasek Ozren, Marusi? Ana, Rotim Kresimir, Hayward Caroline, Vitart Veronique, Huffman Jennifer, Campbell Susan, Jankovi? Stipan, Boban Mladen, Biloglav Zrinka, Kolci? Ivana, Krzelj Vjekoslav, Terzi? Janos, Matec Lana, Tometi? Gordan, Nonkovi? Dijana, Nincevi? Jasna, Pehli? Marina, Zedelj Jurica, Velagi? Vedran, Jurici? Danica, Kirac Iva, Belak Kovacevi? Sanja, Wright Alan F, Campbell Harry, Rudan Ig |
A genome-wide association study of total serum and mite-specific IgEs in asthma patients.
PloS one 2013 8 (8): e71958. Kim Jeong-Hyun, Cheong Hyun Sub, Park Jong Sook, Jang An-Soo, Uh Soo-Taek, Kim Yong-Hoon, Kim Mi-Kyeong, Choi Inseon S, Cho Sang Heon, Choi Byoung Whui, Bae Joon Seol, Park Choon-Sik, Shin Hyoung D |
Circular RNA circCRIM1 inhibits invasion and metastasis in lung adenocarcinoma through the microRNA (miR)-182/miR-93-leukemia inhibitory factor receptor pathway. Cancer science 2019 7 110 (9): 2960-2972. Wang Lin, Liang Yingkuan, Mao Qixing, Xia Wenjie, Chen Bing, Shen Hongyu, Xu Lin, Jiang Feng, Dong Gaoch |
New Genetic Loci Associated With Chronic Kidney Disease in an Indigenous Australian Population. Frontiers in genetics 2019 5 10 330. Thomson Russell J, McMorran Brendan, Hoy Wendy, Jose Matthew, Whittock Lucy, Thornton Tim, Burgio Gaétan, Mathews John Duncan, Foote Sim |
Homozygote CRIM1 variant is associated with thiopurine-induced neutropenia in leukemic patients with both wildtype NUDT15 and TPMT. Journal of translational medicine 2020 Jul 18 (1): 265. Park Yoomi, Kim Hyery, Seo Heewon, Choi Jung Yoon, Ma Youngeun, Yun Sunmin, Min Byung-Joo, Seo Myung-Eui, Yoo Keon Hee, Kang Hyoung Jin, Im Ho Joon, Kim Ju H |
Interplay between IL6 and CRIM1 in thiopurine intolerance due to hematological toxicity in leukemic patients with wild-type NUDT15 and TPMT. Scientific reports 2021 5 11 (1): 9676. Kim Hyery, You Seungwon, Park Yoomi, Choi Jung Yoon, Ma Youngeun, Hong Kyung Tak, Koh Kyung-Nam, Yun Sunmin, Lee Kye Hwa, Shin Hee Young, Lee Suehyun, Yoo Keon Hee, Im Ho Joon, Kang Hyoung Jin, Kim Ju H |
Whole Exome Sequencing in Coloboma/Microphthalmia: Identification of Novel and Recurrent Variants in Seven Genes. Genes 2021 1 12 (1): . Haug Patricia, Koller Samuel, Maggi Jordi, Lang Elena, Feil Silke, Wlodarczyk Agnès, Bähr Luzy, Steindl Katharina, Rohrbach Marianne, Gerth-Kahlert Christina, Berger Wolfga |
Bioinformatics analysis reveals three key genes and four survival genes associated with youth-onset NSCLC. Open medicine (Warsaw, Poland) 2022 7 17 (1): 1123-1133. Han Xuan, Ren Peng, Ma Shaoh |
Genetic Variants Associated with Adverse Events after Angiotensin-Converting Enzyme Inhibitor Use: Replication after GWAS-Based Discovery. Yonsei medical journal 2022 3 63 (4): 342-348. Lee Chan Joo, Choi Bogeum, Pak Hayeon, Park Jung Mi, Lee Ji Hyun, Lee Sang-H |
Identification of a cuproptosis-related lncRNA prognostic signature in lung adenocarcinoma. Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico 2023 1 . Chen Ran, Luo Haichao, Chen Qitian, Wang Changyi |
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