Human Genome Epidemiology Literature Finder
Records 1 - 13 (of 13 Records) |
Query Trace: HOXA9[original query] |
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Altered transmission of HOX and apoptotic SNPs identify a potential common pathway for clubfoot. American journal of medical genetics. Part A 2009 Dec 149A (12): 2745-52. Ester Audrey R, Weymouth Katelyn S, Burt Amber, Wise Carol A, Scott Allison, Gurnett Christina A, Dobbs Matthew B, Blanton Susan H, Hecht Jacqueline |
Mutation screening of HOXA7 and HOXA9 genes in Chinese women with Müllerian duct abnormalities. Reproductive biomedicine online 2014 Nov 29 (5): 595-9. Chen Xinxia, Mu Yulan, Li Chunyan, Li Guangyu, Zhao Hui, Qin Yingying, Chen Zi-Jia |
JAK3 mutations and HOXA9 expression are important cooperating events in T-cell acute lymphoblastic leukemia. Molecular & cellular oncology 2018 9 5 (3): e1458014. de Bock Charles E, Cools J |
HOXA9 rs3801776 G>A polymorphism increases congenital talipes equinovarus risk in a Chinese population. The journal of gene medicine 2019 Aug e3119. Li Jingchun, Wu Jianping, Liu Yanhan, Li Yiqiang, Xiao Zhilan, Jiang Xiaoling, Tang Yaping, Xu Hongw |
[Characteristics of a patient with myeloid neoplasm and co-existence of t(7;11)(p15;p15) and t(5;12)(q33;p13) translocations]. Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2019 3 36 (3): 249-252. Zhang Xiuwen, Zhou Min, Chao Hongying, Jiang Naike, Lu Xuzhang, Jiang Yu, Zhang |
Genome-wide DNA methylation profile of early-onset endometrial cancer: its correlation with genetic aberrations and comparison with late-onset endometrial cancer. Carcinogenesis 2019 3 40 (5): 611-623. Makabe Takeshi, Arai Eri, Hirano Takuro, Ito Nanako, Fukamachi Yukihiro, Takahashi Yoriko, Hirasawa Akira, Yamagami Wataru, Susumu Nobuyuki, Aoki Daisuke, Kanai Y |
Combining copy number, methylation markers, and mutations as a panel for endometrial cancer detection via intravaginal tampon collection. Gynecologic oncology 2019 12 156 (2): 387-392. Sangtani Ajleeta, Wang Chen, Weaver Amy, Hoppman Nicole L, Kerr Sarah E, Abyzov Alexej, Shridhar Viji, Staub Julie, Kocher Jean-Pierre A, Voss Jesse S, Podratz Karl C, Wentzensen Nicolas, Kisiel John B, Sherman Mark E, Bakkum-Gamez Jamie |
Identifying genetic variants and pathways associated with extreme levels of fetal hemoglobin in sickle cell disease in Tanzania. BMC medical genetics 2020 Jun 21 (1): 125. Nkya Siana, Mwita Liberata, Mgaya Josephine, Kumburu Happiness, van Zwetselaar Marco, Menzel Stephan, Mazandu Gaston Kuzamunu, Sangeda Raphael, Chimusa Emile, Makani Jul |
[Clinical Characteristics and Prognosis of Adult Acute Myeloid Leukemia with NUP98 Gene Rearrangement]. Zhongguo shi yan xue ye xue za zhi 2021 10 29 (5): 1450-1455. Lu Ning, Ding Yi, Wu Yong-Li, Wang Li-Li, Jing Yu, Li Hong-Hua, Li Me |
Chemosensitivity of gastric cancer: analysis of key pathogenic transcription factors. Journal of gastrointestinal oncology 2022 7 13 (3): 977-984. Weng Jianze, Wu Aixiang, Ying Jingw |
Putative regulatory functions of SNPs associated with bronchial asthma, arterial hypertension and their comorbid phenotype. Vavilovskii zhurnal genetiki i selektsii 2021 Dec 25 (8): 855-863. Goncharova I A, Bragina E Yu, Zhalsanova I Zh, Freidin M B, Nazarenko M |
Recruitment of MLL1 complex is essential for SETBP1 to induce myeloid transformation. iScience 2022 1 25 (1): 103679. Nguyen Nhu, Gudmundsson Kristbjorn O, Soltis Anthony R, Oakley Kevin, Roy Kartik R, Han Yufen, Gurnari Carmelo, Maciejewski Jaroslaw P, Crouch Gary, Ernst Patricia, Dalgard Clifton L, Du Ya |
Multigene Panel Sequencing Identifies a Novel Germline Mutation Profile in Male Breast Cancer Patients. International journal of molecular sciences 2023 9 24 (18): . Ayman Al Saati, Pierre Vande Perre, Julien Plenecassagnes, Julia Gilhodes, Nils Monselet, Bastien Cabarrou, Norbert Lignon, Thomas Filleron, Dominique Telly, Emilie Perello-Lestrade, Viviane Feillel, Anne Staub, Mathilde Martinez, Edith Chipoulet, Gaëlle Collet, Fabienne Thomas, Laurence Gladieff, Christine Toul |
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- Page last updated:Mar 25, 2024
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