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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Oct 4, 2023. (Total: 221739Documents)
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Records 1 - 8 (of 8 Records)

Query Trace: Sarcoma and Hras[original query]
Absence of oncogenic mutations of RAS family genes in soft tissue sarcomas of 100 Japanese patients.
Anticancer research 2010 Jan 30 (1): 245-51.
Jin Yonghui, Shima Yasuko, Furu Moritoshi, Aoyama Tomoki, Nakamata Takeharu, Nakayama Tomitaka, Nakamura Takashi, Toguchida Jun
Mutations in FGFR3 and PIK3CA, singly or combined with RAS and AKT1, are associated with AKT but not with MAPK pathway activation in urothelial bladder cancer.
Human pathology 2012 Oct 43 (10): 1573-82.
Juanpere Nuria, Agell Laia, Lorenzo Marta, de Muga Silvia, López-Vilaró Laura, Murillo Raquel, Mojal Sergi, Serrano Sergio, Lorente José A, Lloreta Josep, Hernández Silv
Comprehensive survey of HRAS, KRAS, and NRAS mutations in proliferative thyroid lesions from an ethnically diverse population.
Anticancer research 2013 Nov 33 (11): 4779-84.
Schulten Hans-Juergen, Salama Sherine, Al-Ahmadi Alaa, Al-Mansouri Zuhoor, Mirza Zeenat, Al-Ghamdi Khalid, Al-Hamour Osman Abdel, Huwait Etimad, Gari Mamdooh, Al-Qahtani Mohammad Hussain, Al-Maghrabi Jaud
Subsets of salivary duct carcinoma defined by morphologic evidence of pleomorphic adenoma, PLAG1 or HMGA2 rearrangements, and common genetic alterations.
Cancer 2016 Jul .
Chiosea Simion I, Thompson Lester D R, Weinreb Ilan, Bauman Julie E, Mahaffey Alyssa M, Miller Caitlyn, Ferris Robert L, Gooding William
PREDICTIVE VALUE OF SOMATIC MUTATIONS FOR THE DEVELOPMENT OF MALIGNANCY IN THYROID NODULES BY CYTOPATHOLOGY.
Endocrine practice : official journal of the American College of Endocrinology and the American Association of Clinical Endocrinologists 2016 May .
Halászlaki Csaba, Tóbiás Bálint, Balla Bernadett, Kósa János P, Horányi János, Bölöny Eszter, Nagy Zsolt, Speer Gábor, Járay Balázs, Székely Eszter, Istók Roland, Székely Tamás, Putz Zsuzsanna, Dank Magdolna, Lakatos Péter, Takács Istv
Frequent HRAS Mutations in Malignant Ectomesenchymoma: Overlapping Genetic Abnormalities With Embryonal Rhabdomyosarcoma.
The American journal of surgical pathology 2016 Feb .
Huang Shih-Chiang, Alaggio Rita, Sung Yun-Shao, Chen Chun-Liang, Zhang Lei, Kao Yu-Chien, Agaram Narasimhan P, Wexler Leonard H, Antonescu Cristina
GNA14, GNA11, and GNAQ Mutations Are Frequent in Benign but Not Malignant Cutaneous Vascular Tumors.
Frontiers in genetics 2021 5 12 663272.
Jansen Philipp, Müller Hansgeorg, Lodde Georg C, Zaremba Anne, Möller Inga, Sucker Antje, Paschen Annette, Esser Stefan, Schaller Jörg, Gunzer Matthias, Standl Fabian, Bauer Sebastian, Schadendorf Dirk, Mentzel Thomas, Hadaschik Eva, Griewank Klaus
Genetic profile of thymic epithelial tumors in the Japanese population: an exploratory study examining potential therapeutic targets.
Translational lung cancer research 2023 5 12 (4): 707-718.
Midori Shimada, Hirokazu Taniguchi, Hiroyuki Yamaguchi, Hiroshi Gyotoku, Daisuke Sasaki, Norihito Kaku, Chikako Senju, Hiroaki Senju, Erika Imamura, Shinnosuke Takemoto, Kazuko Yamamoto, Noriho Sakamoto, Yasushi Obase, Tomoshi Tsuchiya, Minoru Fukuda, Hiroshi Soda, Kazuto Ashizawa, Junya Fukuoka, Takeshi Nagayasu, Katsunori Yanagihara, Hiroshi Muk
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