Human Genome Epidemiology Literature Finder
Records 1 - 28 (of 28 Records) |
Query Trace: AKT3[original query] |
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Mutational and immunohistochemical study of the PI3K/Akt pathway in papillary thyroid carcinoma in Greece. Endocrine pathology 2010 Jun 21 (2): 90-100. Sozopoulos Elias, Litsiou Helen, Voutsinas Gerassimos, Mitsiades Nikolaos, Anagnostakis Nikolaos, Tseva Thomais, Patsouris Efstratios, Tseleni-Balafouta Sof |
Roles of genetic variants in the PI3K and RAS/RAF pathways in susceptibility to endometrial cancer and clinical outcomes. Journal of cancer research and clinical oncology 2012 Mar 138 (3): 377-85. Wang Li-E, Ma Hongxia, Hale Katherine S, Yin Ming, Meyer Larissa A, Liu Hongliang, Li Jie, Lu Karen H, Hennessy Bryan T, Li Xuesong, Spitz Margaret R, Wei Qingyi, Mills Gordon |
Peripheral blood gene expression as a novel genomic biomarker in complicated sarcoidosis. PloS one 2012 7 (9): e44818. Zhou Tong, Zhang Wei, Sweiss Nadera J, Chen Edward S, Moller David R, Knox Kenneth S, Ma Shwu-Fan, Wade Michael S, Noth Imre, Machado Roberto F, Garcia Joe G |
AKT3, ANGPTL4, eNOS3, and VEGFA associations with high altitude sickness in Han and Tibetan Chinese at the Qinghai-Tibetan Plateau. International journal of hematology 2012 Aug 96 (2): 200-13. Buroker Norman E, Ning Xue-Han, Zhou Zhao-Nian, Li Kui, Cen Wei-Jun, Wu Xiu-Feng, Zhu Wei-Zhong, Scott C Ronald, Chen Shi-H |
Interaction among apoptosis-associated sequence variants and joint effects on aggressive prostate cancer. BMC medical genomics 2012 5 (1): 11. Lavender Nicole A, Rogers Erica N, Yeyeodu Susan, Rudd James, Hu Ting, Zhang Jie, Brock Guy N, Kimbro Kevin S, Moore Jason H, Hein David W, Kidd La Creis |
Energy balance, polymorphisms in the mTOR pathway, and renal cell carcinoma risk. Journal of the National Cancer Institute 2013 Feb . Shu X, Lin J, Wood CG, Tannir NM, Wu X |
Cyclin D1, EGFR, and Akt/mTOR pathway. Potential prognostic markers in localized laryngeal squamous cell carcinoma. Strahlentherapie und Onkologie : Organ der Deutschen Röntgengesellschaft ... [et al] 2013 Mar 189 (3): 202-14. Dionysopoulos D, Pavlakis K, Kotoula V, Fountzilas E, Markou K, Karasmanis I, Angouridakis N, Nikolaou A, Kalogeras K T, Fountzilas |
Targeted Sequencing and Meta-Analysis of Preterm Birth. PloS one 2016 11 (5): e0155021. Uzun Alper, Schuster Jessica, McGonnigal Bethany, Schorl Christoph, Dewan Andrew, Padbury Jam |
A combination of genetic and biochemical analyses for the diagnosis of PI3K-AKT-mTOR pathway-associated megalencephaly. BMC medical genetics 2017 1 18 (1): 4. Negishi Yutaka, Miya Fuyuki, Hattori Ayako, Johmura Yoshikazu, Nakagawa Motoo, Ando Naoki, Hori Ikumi, Togawa Takao, Aoyama Kohei, Ohashi Kei, Fukumura Shinobu, Mizuno Seiji, Umemura Ayako, Kishimoto Yoko, Okamoto Nobuhiko, Kato Mitsuhiro, Tsunoda Tatsuhiko, Yamasaki Mami, Kanemura Yonehiro, Kosaki Kenjiro, Nakanishi Makoto, Saitoh Shin |
Polymicrogyria in association with hypoglycemia points to mutation in the mTOR pathway. European journal of medical genetics 2018 6 61 (12): 738-740. Stutterd Chloe, McGillivray George, Stark Zornitza, Messazos Betty, Cameron Fergus, White Sue, , Mirzaa Ghayda, Leventer Richa |
Characterization of PIK3CA and PIK3R1 somatic mutations in Chinese breast cancer patients. Nature communications 2018 Apr 9 (1): 1357. Chen Li, Yang Liu, Yao Ling, Kuang Xia-Ying, Zuo Wen-Jia, Li Shan, Qiao Feng, Liu Yi-Rong, Cao Zhi-Gang, Zhou Shu-Ling, Zhou Xiao-Yan, Yang Wen-Tao, Shi Jin-Xiu, Huang Wei, Hu Xin, Shao Zhi-Mi |
Study on the association between PI3K/AKT/mTOR signaling pathway gene polymorphism and susceptibility to gastric cancer. Journal of B.U.ON. : official journal of the Balkan Union of Oncology 0 22 (6): 1488-1493. Qi Lei, Sun Kewen, Zhuang Yun, Yang Jing, Chen Jianpi |
Precise detection of low-level somatic mutation in resected epilepsy brain tissue. Acta neuropathologica 2019 Aug . Sim Nam Suk, Ko Ara, Kim Woo Kyeong, Kim Se Hoon, Kim Ju Seong, Shim Kyu-Won, Aronica Eleonora, Mijnsbergen Caroline, Spliet Wim G M, Koh Hyun Yong, Kim Heung Dong, Lee Joon Soo, Kim Dong Seok, Kang Hoon-Chul, Lee Jeong |
Comparison of TCGA and GENIE genomic datasets for the detection of clinically actionable alterations in breast cancer. Scientific reports 2019 2 9 (1): 1482. Kaur Pushpinder, Porras Tania B, Ring Alexander, Carpten John D, Lang Julie |
Response of high-risk MDS to azacitidine and lenalidomide is impacted by baseline and acquired mutations in a cluster of three inositide-specific genes. Leukemia 2019 Feb . Follo Matilde Y, Pellagatti Andrea, Armstrong Richard N, Ratti Stefano, Mongiorgi Sara, De Fanti Sara, Bochicchio Maria Teresa, Russo Domenico, Gobbi Marco, Miglino Maurizio, Parisi Sarah, Martinelli Giovanni, Cavo Michele, Luiselli Donata, McCubrey James A, Suh Pann-Ghill, Manzoli Lucia, Boultwood Jacqueline, Finelli Carlo, Cocco Luc |
Genetic Heterogeneity of Esophageal Squamous Cell Carcinoma with Inherited Family History. OncoTargets and therapy 2020 13 8795-8802. He Wenwu, Leng Xuefeng, Yang Yanyu, Peng Lin, Shao Yang, Li Xue, Han Yongt |
Molecular basis of unilateral condylar hyperplasia? International journal of oral and maxillofacial surgery 2020 5 49 (11): 1397-1401. Nolte J W, Alders M, Karssemakers L H E, Becking A G, Hennekam R C |
Akt1 genetic variants confer increased susceptibility to thyroid cancer. Endocrine connections 2020 Oct . Crezee Thomas, Petrulea Mirela, Piciu Doina, Jaeger Martin, Smit Jan W A, Plantinga Theo S, Georgescu Carmen E, Netea-Maier Roma |
Cutaneous vascular anomalies associated with a mosaic variant of AKT3: Genetic analysis continues to refine the diagnosis, nomenclature, and classification of vascular anomalies. Journal of the American Academy of Dermatology 2021 7 87 (1): 162-164. Davies Olivia M T, Garzon Maria C, Frieden Ilona J, Cottrell Catherine E, Gripp Karen W, Saneto Russell P, Shwayder Tor, Mirzaa Ghayda M, Drolet Beth |
Genetic heterogeneity of disorders with overgrowth and intellectual disability: Experience from a center in North India. American journal of medical genetics. Part A 2021 5 185 (8): 2345-2355. Moirangthem Amita, Mandal Kausik, Saxena Deepti, Srivastava Priyanka, Gambhir Poonam Singh, Agrawal Neha, Shambhavi Arya, Nampoothiri Sheela, Phadke Shubha |
Characterization of AKT Somatic Mutations in Chinese Breast Cancer Patients. Cancer management and research 2021 13 3055-3065. Wen Lingzhu, Zhang Guochun, Ren Chongyang, Li Xuerui, Mok Hsiaopei, Jia Minghan, Wang Yulei, Chen Bo, Li Kai, Cao Li, Li Cheukfai, Xiao Weikai, Lai Jianguo, Lin Jiali, Wei Guangnan, Li Yingzi, Zhang Yuchen, Chen Xiaoqing, Liao Ni |
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 |
AKT inhibition in the central nervous system induces signaling defects resulting in psychiatric symptomatology. Cell & bioscience 2022 5 12 (1): 56. Tsimberidou Apostolia-Maria, Skliris Antonis, Valentine Alan, Shaw Jamie, Hering Ursula, Vo Henry Hiep, Chan Tung On, Armen Roger S, Cottrell Jeffrey R, Pan Jen Q, Tsichlis Philip |
Cholinergic Synapse Pathway Gene Polymorphisms Associated With Late-Phase Responses in Allergic Rhinitis. Frontiers in allergy 2022 4 2 724328. Samra Simranjit K, Rajasekaran Ashwini, Sandford Andrew J, Ellis Anne K, Tebbutt Scott |
Comprehensive transcriptomic profiling and mutational landscape of primary gastric linitis plastica. Gastric cancer : official journal of the International Gastric Cancer Association and the Japanese Gastric Cancer Association 2022 11 . Liu Zhu, Hong Lian-Lian, Zheng Jin-Sen, Ling Zhe-Nan, Zhang Zhi-Long, Qi Ya-Nan, Zhang Xin-Yu, Zhu Tian-Yu, Wang Jiu-Li, Han Jing, Chen Xiang-Liu, Yu Qi-Ming, Wang Shi, Li Pei, Ling Zhi-Qia |
Integrated exome sequencing and microarray analyses detected genetic defects and underlying pathways of hepatocellular carcinoma. Cancer genetics 2023 7 276-277 30-35. Mei Ling Chong, James Knight, Gang Peng, Weizhen Ji, Hongyan Chai, Yufei Lu, Shengming Wu, Peining Li, Qiping |
Detection of brain somatic mutations in focal cortical dysplasia during epilepsy presurgical workup. Brain communications 2023 6 5 (3): fcad174. Rayann Checri, Mathilde Chipaux, Sarah Ferrand-Sorbets, Emmanuel Raffo, Christine Bulteau, Sarah Dominique Rosenberg, Marion Doladilhe, Georg Dorfmüller, Homa Adle-Biassette, Sara Baldassari, Stéphanie Baul |
Detecting Low-Variant Allele Frequency Mosaic Pathogenic Variants of NF1, TSC2, and AKT3 Genes from Blood in Patients with Neurodevelopmental Disorders. The Journal of molecular diagnostics : JMD 2023 4 . Se Hee Kim, Soon Sung Kwon, Mi Ri Park, Hyeon Ah Lee, Ji Hun Kim, JiHoon Cha, Sangwoo Kim, Seung Tae Baek, Se Hoon Kim, Joon Soo Lee, Heung Dong Kim, Jong Rak Choi, Seung-Tae Lee, Hoon-Chul Ka |
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