Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 36 Records) |
Query Trace: PBX1[original query] |
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Analysis of PBX1 mutations in 192 Chinese women with Müllerian duct abnormalities. Fertility and sterility 2011 Jun 95 (8): 2615-7. Ma Jinlong, Qin Yingying, Liu Wen, Duan Hua, Xia Mingdi, Chen Zi-Jia |
Homeobox genes in obsessive-compulsive disorder. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2012 Jan 159B (1): 53-60. Nestadt G, Wang Y, Grados M A, Riddle M A, Greenberg B D, Knowles J A, Fyer A J, McCracken J T, Rauch S L, Murphy D L, Rasmussen S A, Cullen B, Piacentini J, Geller D, Pauls D, Bienvenu O J, Chen Y, Liang K Y, Goes F S, Maher B, Pulver A E, Shugart Y Y, Valle D, Samuels J F, Chang Y |
Non-synonymous variants in pre-B cell leukemia homeobox (PBX) genes are associated with congenital heart defects. European journal of medical genetics 2012 Apr 55 (4): 235-7. Arrington Cammon B, Dowse Benjamin R, Bleyl Steven B, Bowles Neil |
Detection of E2A-PBX1 fusion transcripts in human non-small-cell lung cancer. Journal of experimental & clinical cancer research : CR 2013 32 29. Mo Min-Li, Chen Zhao, Zhou Hai-Meng, Li Hui, Hirata Tomomi, Jablons David M, He Bi |
Identification of inherited genetic variations influencing prognosis in early-onset breast cancer.
Cancer research 2013 Mar 73 (6): 1883-91. Rafiq Sajjad, Tapper William, Collins Andrew, Khan Sofia, Politopoulos Ioannis, Gerty Sue, Blomqvist Carl, Couch Fergus J, Nevanlinna Heli, Liu Jianjun, Eccles Dia |
Analysis of KRAS and NRAS Gene Mutations in Arab Asian Children With Acute Leukemia: High Frequency of RAS Mutations in Acute Lymphoblastic Leukemia. Pediatric blood & cancer 2015 Jul . Al-Kzayer Lika'a Fasih Y, Sakashita Kazuo, Al-Jadiry Mazin Faisal, Al-Hadad Salma Abbas, Ghali Hasanein Habeeb, Uyen Le T N, Liu Tingting, Matsuda Kazuyuki, Abdulkadhim Jaafar M H, Al-Shujairi Tariq Abadi, Matti Zead Ismael I K, Sughayer Maher A, Rihani Rawad, Madanat Faris F, Inoshita Toshi, Kamata Minoru, Koike Kenic |
Associations of Polymorphisms in WNT9B and PBX1 with Mayer-Rokitansky-Küster-Hauser Syndrome in Chinese Han. PloS one 2015 10 (6): e0130202. Ma Wenqing, Li Ya, Wang Man, Li Haixia, Su Tiefen, Li Yan, Wang Shixu |
Mutational status of NRAS, KRAS, and PTPN11 genes is associated with genetic/cytogenetic features in children with B-precursor acute lymphoblastic leukemia. Pediatric blood & cancer 2017 Aug . Liang Der-Cherng, Chen Shih-Hsiang, Liu Hsi-Che, Yang Chao-Ping, Yeh Ting-Chi, Jaing Tang-Her, Hung Iou-Jih, Hou Jen-Yin, Lin Tung-Huei, Lin Chun-Hui, Shih Lee-Yu |
Targeted Exome Sequencing Identifies PBX1 as Involved in Monogenic Congenital Anomalies of the Kidney and Urinary Tract. Journal of the American Society of Nephrology : JASN 2017 May . Heidet Laurence, Morinière Vincent, Henry Charline, De Tomasi Lara, Reilly Madeline Louise, Humbert Camille, Alibeu Olivier, Fourrage Cécile, Bole-Feysot Christine, Nitschké Patrick, Tores Frédéric, Bras Marc, Jeanpierre Marc, Pietrement Christine, Gaillard Dominique, Gonzales Marie, Novo Robert, Schaefer Elise, Roume Joëlle, Martinovic Jelena, Malan Valérie, Salomon Rémi, Saunier Sophie, Antignac Corinne, Jeanpierre Céci |
Copy number alterations determined by single nucleotide polymorphism array testing in the clinical laboratory are indicative of gene fusions in pediatric cancer patients. Genes, chromosomes & cancer 2017 Jun . Busse Tracy M, Roth Jacquelyn J, Wilmoth Donna, Wainwright Luanne, Tooke Laura, Biegel Jaclyn |
Genetic profile of isolated congenital diaphragmatic hernia revealed by targeted next-generation sequencing. Prenatal diagnosis 2018 Jul . Kammoun Molka, Souche Erika, Brady Paul, Ding Jia, Cosemans Nele, Gratacos Eduard, Devriendt Koen, Eixarch Elisenda, Deprest Jan, Vermeesch Joris Robe |
Novel susceptibility variants at the ERG locus for childhood acute lymphoblastic leukemia in Hispanics. Blood 2019 Feb 133 (7): 724-729. Qian Maoxiang, Xu Heng, Perez-Andreu Virginia, Roberts Kathryn G, Zhang Hui, Yang Wenjian, Zhang Shouyue, Zhao Xujie, Smith Colton, Devidas Meenakshi, Gastier-Foster Julie M, Raetz Elizabeth, Larsen Eric, Burchard Esteban G, Winick Naomi, Bowman W Paul, Martin Paul L, Borowitz Michael, Wood Brent, Antillon-Klussmann Federico, Pui Ching-Hon, Mullighan Charles G, Evans William E, Hunger Stephen P, Relling Mary V, Loh Mignon L, Yang Jun |
Polymorphism in the PBX1 gene is related to cystinuria in Brazilian families. Journal of cellular and molecular medicine 2019 Feb 23 (2): 1593-1597. Reis Sabrina T, Leite Katia R M, Marchini Giovanni S, Guimarães Ronaldo M, Viana Nayara I, Pimenta Ruan C A, Torricelli Fabio C, Danilovic Alexandre, Vicentini Fábio Carvalho, Nahas William Carlos, Srougi Miguel, Mazzucchi Eduar |
Gene variations in PBX1, LMX1A and SLITRK1 are associated with obsessive-compulsive disorder and its clinical features. Journal of clinical neuroscience : official journal of the Neurosurgical Society of Australasia 2019 Mar 61 180-185. Melo-Felippe Fernanda B, Fontenelle Leonardo F, Kohlrausch Fabiana |
PBX-WNT-P63-IRF6 pathway in nonsyndromic cleft lip and palate. Birth defects research 2019 Dec . Maili Lorena, Letra Ariadne, Silva Renato, Buchanan Edward P, Mulliken John B, Greives Matthew R, Teichgraeber John F, Blackwell Steven J, Ummer Rohit, Weber Ryan, Chiquet Brett, Blanton Susan H, Hecht Jacqueline |
Genome-Wide Association Study of Susceptibility Loci for TCF3-PBX1 Acute Lymphoblastic Leukemia in Children.
Journal of the National Cancer Institute 2020 9 113 (7): 933-937. Lee Shawn H R, Qian Maoxiang, Yang Wentao, Diedrich Jonathan D, Raetz Elizabeth, Yang Wenjian, Dong Qian, Devidas Meenakshi, Pei Deqing, Yeoh Allen, Cheng Cheng, Pui Ching-Hon, Evans William E, Mullighan Charles G, Hunger Stephen P, Savic Daniel, Relling Mary V, Loh Mignon L, Yang Jun |
Landscape of driver mutations and their clinical impacts in pediatric B-cell precursor acute lymphoblastic leukemia. Blood advances 2020 Oct 4 (20): 5165-5173. Ueno Hiroo, Yoshida Kenichi, Shiozawa Yusuke, Nannya Yasuhito, Iijima-Yamashita Yuka, Kiyokawa Nobutaka, Shiraishi Yuichi, Chiba Kenichi, Tanaka Hiroko, Isobe Tomoya, Seki Masafumi, Kimura Shunsuke, Makishima Hideki, Nakagawa Masahiro M, Kakiuchi Nobuyuki, Kataoka Keisuke, Yoshizato Tetsuichi, Nishijima Dai, Deguchi Takao, Ohki Kentaro, Sato Atsushi, Takahashi Hiroyuki, Hashii Yoshiko, Tokimasa Sadao, Hara Junichi, Kosaka Yoshiyuki, Kato Koji, Inukai Takeshi, Takita Junko, Imamura Toshihiko, Miyano Satoru, Manabe Atsushi, Horibe Keizo, Ogawa Seishi, Sanada Masas |
Exon sequencing reveals that missense mutation of PBX1 gene may increase the risk of non-syndromic cleft lip/palate. International journal of clinical and experimental pathology 2020 1 12 (7): 2691-2698. Ma Jian, Yin Bin, Shi Jia-Yu, Lin Yan-Song, Duan Shi-Jun, Shi Bing, Jia Zhong-L |
Genetic features of B-cell lymphoblastic lymphoma with TCF3-PBX1. Cancer reports (Hoboken, N.J.) 2021 9 5 (9): e1559. Shirai Ryota, Osumi Tomoo, Sato-Otsubo Aiko, Nakabayashi Kazuhiko, Mori Takeshi, Yoshida Masanori, Yoshida Kaoru, Kohri Mika, Ishihara Takashi, Yasue Shiho, Imamura Toshihiko, Endo Mikiya, Miyamoto Satoshi, Ohki Kentaro, Sanada Masashi, Kiyokawa Nobutaka, Ogawa Seishi, Yoshioka Takako, Hata Kenichiro, Takagi Masatoshi, Kato Motohi |
Efficacy and safety of induction chemotherapy with daunorubicin or idarubicin in the treatment of an adult with acute lymphoblastic leukemia. Tumori 2021 7 108 (2): 182-188. Zhang Qi, Zhang Chun-Hong, Wang Zhen-Dong, Wang Do |
Clinical features and prognostic impact of TCF3-PBX1 in childhood acute lymphoblastic leukemia: A single-center retrospective study of 837 patients from China. Current problems in cancer 2021 5 45 (6): 100758. Jia Ming, Hu Bo-Fei, Xu Xiao-Jun, Zhang Jing-Ying, Li Si-Si, Tang Yong-M |
Molecular classification improves risk assessment in adult BCR-ABL1-negative B-ALL. Blood 2021 4 138 (11): 948-958. Paietta Elisabeth, Roberts Kathryn G, Wang Victoria, Gu Zhaohui, Buck Georgina A N, Pei Deqing, Cheng Cheng, Levine Ross L, Abdel-Wahab Omar, Cheng Zhongshan, Wu Gang, Qu Chunxu, Shi Lei, Pounds Stanley, Willman Cheryl L, Harvey Richard, Racevskis Janis, Barinka Jan, Zhang Yanming, Dewald Gordon W, Ketterling Rhett P, Alejos David, Lazarus Hillard M, Luger Selina M, Foroni Letizia, Patel Bela, Fielding Adele K, Melnick Ari, Marks David I, Moorman Anthony V, Wiernik Peter H, Rowe Jacob M, Tallman Martin S, Goldstone Anthony H, Mullighan Charles G, Litzow Mark |
Genomic landscape of B-other acute lymphoblastic leukemia in an adult retrospective cohort with a focus on BCR-ABL1-like subtype. Acta oncologica (Stockholm, Sweden) 2021 3 60 (6): 760-770. Hrabovsky Stepan, Vrzalova Zuzana, Stika Jiri, Jelinkova Hana, Jarosova Marie, Navrkalova Veronika, Martenek Jiri, Folber Frantisek, Salek Cyril, Horacek Jan M, Pospisilova Sarka, Mayer Jiri, Doubek Micha |
rs6426881 in the 3'-UTR of PBX1 is involved in breast and gastric cancers via altering the binding potential of miR-522-3p. Molecular biology reports 2021 10 48 (11): 7405-7414. Mohammadi Maryam, Salehzadeh Ali, Talesh Sasani Soheila, Tarang Alire |
The Clinical Outcomes and Genomic Landscapes of Acute Lymphoblastic Leukemia Patients with E2A-PBX1: A 10-year Retrospective Study. American journal of hematology 2021 Aug . Zhou Biqi, Chu Xinran, Tian Hong, Liu Tianhui, Liu Hong, Gao Wei, Chen Suning, Hu Shaoyan, Wu Depei, Xu Ya |
Evaluate the effects of serum urate level on bone mineral density: a genome-wide gene-environment interaction analysis in UK Biobank cohort.
Endocrine 2021 5 73 (3): 702-711. Yao Yao, Chu Xiaomeng, Ma Mei, Ye Jing, Wen Yan, Li Ping, Cheng Bolun, Cheng Shiqiang, Zhang Lu, Liu Li, Qi Xin, Liang Chujun, Kafle Om Prakash, Wu Cuiyan, Wang Sen, Wang Xi, Ning Yujie, Zhang Fe |
Genetic Variants Associated with Supernormal Coronary Arteries. Journal of atherosclerosis and thrombosis 2022 Jul . Kim Beomsu, Lee Chan Joo, Won Hong-Hee, Lee Sang-H |
Comprehensive genetic analyses of childhood acute leukemia in Iraq using next-generation sequencing. Translational pediatrics 2023 6 12 (5): 827-844. Lika'a Fasih Y Al-Kzayer, Raghad M Saeed, Hasanein Habeeb Ghali, Miyuki Tanaka, Mazin F Al-Jadiry, Safa A Faraj, Salma A Al-Hadad, Hussam M Salih Al Abdullah, Athar A Majeed, Ali Omer Qadir, Dana Ahmed Abdullah, Kani Dlawar Noori, Zheyan Mohammed Hama, Abdulrahman A Muhsin, Adnan Anwer Al-Doski, Yasir S Al-Agele, Abduladheem H Malallah, Khalid S Al-Badrani, Asmaa M A Khaleel, Minoru Kamata, Motoharu Hamada, Seiji Kojima, Yozo Nakazawa, Yusuke Oku |
Prognostic factors of childhood acute lymphoblastic leukemia with TCF3::PBX1 in CCCG-ALL-2015: A multicenter study. Cancer 2023 3 . Zhang Honghong, Wan Yang, Wang Hongsheng, Cai Jiaoyang, Yu Jie, Hu Shaoyan, Fang Yongjun, Gao Ju, Jiang Hua, Yang Minghua, Liang Changda, Jin Runming, Tian Xin, Ju Xiuli, Hu Qun, Jiang Hui, Li Zhifan, Wang Ningling, Sun Lirong, Leung Alex W K, Wu Xuedong, Qian Xiaowen, Qian Maoxiang, Li Chi-Kong, Yang Jun, Tang Jingyan, Zhu Xiaofan, Shen Shuhong, Zhang Li, Pui Ching-Hon, Zhai Xiaow |
Prognostic significance of steroid response in pediatric acute lymphoblastic leukemia: The CCCG-ALL-2015 study. Frontiers in oncology 2023 1 12 1062065. Chu Jinhua, Cai Huaju, Cai Jiaoyang, Bian Xinni, Cheng Yumei, Guan Xianmin, Chen Xiaoqian, Jiang Hua, Zhai Xiaowen, Fang Yongjun, Zhang Lei, Tian Xin, Zhou Fen, Wang Yaqin, Wang Lingzhen, Li Hong, Kwan Alex Leung Wing, Yang Minghua, Yang Hanfang, Zhan Aijun, Wang Ningling, Hu Shaoy |
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- Page last updated:Apr 22, 2024
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