Results for &quot;&quot;Chromosomes, Human, Pair 12&quot;&quot;[mesh_terms]

What are the frequency, distribution, and functional effects of vitamin D receptor polymorphisms as related to cancer risk?

Richard C Strange, Nicholas J Rukin

Nutrition reviews 2007;65(8 Pt 2):S96-101

Variable Phenotypes of Epilepsy, Intellectual Disability, and Schizophrenia Caused by 12p13.33-p13.32 Terminal Microdeletion in a Korean Family: A Case Report and Literature Review.

Ji Yoon Han, Joonhong Park

Genes 2022;12(7):1001

GWAS of habitual coffee consumption reveals a sex difference in the genetic effect of the 12q24 locus in the Japanese population.

Huijuan Jia, Shun Nogawa, Kaoru Kawafune, Tsuyoshi Hachiya, Shoko Takahashi, Maki Igarashi, Kenji Saito, Hisanori Kato

BMC genetics 2020;20(1):61

Pleiotropic QTL on chromosome 12q23-q24 influences triglyceride and high-density lipoprotein cholesterol levels: the HERITAGE family study.

Mary E Feitosa, Treva Rice, Ingrid B Borecki, Tuomo Rankinen, Arthur S Leon, James S Skinner, Jean-Pierre Després, John Blangero, Claude Bouchard, D C Rao

Human biology 2007;78(3):317-27

Four children with postnatally diagnosed mosaic trisomy 12: Clinical features, literature review, and current diagnostic capabilities of genetic testing.

Jie Hu, Zhishuo Ou, Urvashi Surti, Sally Kochmar, Lori Hoffner, Suneeta Madan-Khetarpal, Georgianne L Arnold, Leslie Walsh, Roxanne Acquaro, Jessica Sebastian, Svetlana A Yatsenko

American journal of medical genetics. Part A 2021;182(4):813-822

Chromosome-centric human proteome project: deciphering proteins associated with glioma and neurodegenerative disorders on chromosome 12.

Akhilesh Pandey, Visith Thongboonkerd, Manoj Kumar Gupta, Savita Jayaram, Anil K Madugundu, Sandip Chavan, Jayshree Advani, Ravi Sirdeshmukh

Journal of proteome research 2015;13(7):3178-90

Strong association between the 12q24 locus and sweet taste preference in the Japanese population revealed by genome-wide meta-analysis.

Kaoru Kawafune, Tsuyoshi Hachiya, Shun Nogawa, Shoko Takahashi, Huijuan Jia, Kenji Saito, Hisanori Kato

Journal of human genetics 2021;65(11):939-947

Analysis of a positional candidate gene for inflammatory bowel disease: NRAMP2.

S J van Deventer, G N Tytgat, P H Reitsma, P C Stokkers, K Huibregtse, A C Leegwater

Inflammatory bowel diseases 2000;6(2):92-8

Acute myeloid leukemia with NUP98::RARG rearrangement: a case report and review of the relevant literature.

Ritsuro Suzuki, Takeshi Taketani, Junki Inamura, Miho Mochida, Tsukimi Goto, Sho Igarashi, Nodoka Tsukada, Masayo Yamamoto, Motohiro Shindo, Kazuya Sato

International journal of hematology 2025;121(2):265-271

Novel single-base deletional mutation in major intrinsic protein (MIP) in autosomal dominant cataract.

David D Geyer, M Anne Spence, Meriam Johannes, Pamela Flodman, Kevin P Clancy, Rebecca Berry, Robert S Sparkes, Matthew D Jonsen, Sherwin J Isenberg, J Bronwyn Bateman

American journal of ophthalmology 2006;141(4):761-3

First insights into the molecular basis of pleomorphic adenomas of the salivary glands.

M L Voz, W J Van de Ven, K Kas

Advances in dental research 2002;14():81-3

Association of Genetic Variant at Chromosome 12q23.1 With Neuropathic Pain Susceptibility.

Abirami Veluchamy, Harry L Hébert, Natalie R van Zuydam, Ewan R Pearson, Archie Campbell, Caroline Hayward, Weihua Meng, Mark I McCarthy, David L H Bennett, Colin N A Palmer, Blair H Smith

JAMA network open 2022;4(12):e2136560

Plain Language Summary

Fusion of the NUP98 gene and the homeobox gene HOXC13 in acute myeloid leukemia with t(11;12)(p15;q13).

Ioannis Panagopoulos, Margareth Isaksson, Rolf Billström, Bodil Strömbeck, Felix Mitelman, Bertil Johansson

Genes, chromosomes & cancer 2003;36(1):107-12

Meta-analysis of genome-wide association studies identifies multiple lung cancer susceptibility loci in never-smoking Asian women.

Zhaoming Wang, Wei Jie Seow, Kouya Shiraishi, Chao A Hsiung, Keitaro Matsuo, Jie Liu, Kexin Chen, Taiki Yamji, Yang Yang, I-Shou Chang, Chen Wu, Yun-Chul Hong, Laurie Burdett, Kathleen Wyatt, Charles C Chung, Shengchao A Li, Meredith Yeager, Amy Hutchinson, Wei Hu, Neil Caporaso, Maria T Landi, Nilanjan Chatterjee, Minsun Song, Joseph F Fraumeni, Takashi Kohno, Jun Yokota, Hideo Kunitoh, Kyota Ashikawa, Yukihide Momozawa, Yataro Daigo, Tetsuya Mitsudomi, Yasushi Yatabe, Toyoaki Hida, Zhibin Hu, Juncheng Dai, Hongxia Ma, Guangfu Jin, Bao Song, Zhehai Wang, Sensen Cheng, Zhihua Yin, Xuelian Li, Yangwu Ren, Peng Guan, Jiang Chang, Wen Tan, Chien-Jen Chen, Gee-Chen Chang, Ying-Huang Tsai, Wu-Chou Su, Kuan-Yu Chen, Ming-Shyan Huang, Yuh-Min Chen, Hong Zheng, Haixin Li, Ping Cui, Huan Guo, Ping Xu, Li Liu, Motoki Iwasaki, Taichi Shimazu, Shoichiro Tsugane, Junjie Zhu, Gening Jiang, Ke Fei, Jae Yong Park, Yeul Hong Kim, Jae Sook Sung, Kyong Hwa Park, Young Tae Kim, Yoo Jin Jung, Chang Hyun Kang, In Kyu Park, Hee Nam Kim, Hyo-Sung Jeon, Jin Eun Choi, Yi Young Choi, Jin Hee Kim, In-Jae Oh, Young-Chul Kim, Sook Whan Sung, Jun Suk Kim, Ho-Il Yoon, Sun-Seog Kweon, Min-Ho Shin, Adeline Seow, Ying Chen, Wei-Yen Lim, Jianjun Liu, Maria Pik Wong, Victor Ho Fun Lee, Bryan A Bassig, Margaret Tucker, Sonja I Berndt, Wong-Ho Chow, Bu-Tian Ji, Junwen Wang, Jun Xu, Alan Dart Loon Sihoe, James C M Ho, John K C Chan, Jiu-Cun Wang, Daru Lu, Xueying Zhao, Zhenhong Zhao, Junjie Wu, Hongyan Chen, Li Jin, Fusheng Wei, Guoping Wu, She-Juan An, Xu-Chao Zhang, Jian Su, Yi-Long Wu, Yu-Tang Gao, Yong-Bing Xiang, Xingzhou He, Jihua Li, Wei Zheng, Xiao-Ou Shu, Qiuyin Cai, Robert Klein, William Pao, Charles Lawrence, H Dean Hosgood, Chin-Fu Hsiao, Li-Hsin Chien, Ying-Hsiang Chen, Chung-Hsing Chen, Wen-Chang Wang, Chih-Yi Chen, Chih-Liang Wang, Chong-Jen Yu, Hui-Ling Chen, Yu-Chun Su, Fang-Yu Tsai, Yi-Song Chen, Yao-Jen Li, Tsung-Ying Yang, Chien-Chung Lin, Pan-Chyr Yang, Tangchun Wu, Dongxin Lin, Baosen Zhou, Jinming Yu, Hongbing Shen, Michiaki Kubo, Stephen J Chanock, Nathaniel Rothman, Qing Lan

Human molecular genetics 2016;25(3):620-9