HuGE Literature Finder
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| Broad spectrum mutational analysis of chromophobe renal cell carcinoma using next-generation sequencing. Pathology, research and practice 2021 Feb 219 153350. Mollica Veronica, Franceschini Tania, Gruppioni Elisa, Rizzo Alessandro, Ricci Costantino, Schiavina Riccardo, Brunocilla Eugenio, Ardizzoni Andrea, Fiorentino Michelangelo, Giunchi Francesca, Massari Frances |
| Genetic analysis of sinonasal undifferentiated carcinoma discovers recurrent SWI/SNF alterations and a novel PGAP3-SRPK1 fusion gene. BMC cancer 2021 5 21 (1): 636. Heft Neal Molly E, Birkeland Andrew C, Bhangale Apurva D, Zhai Jingyi, Kulkarni Aditi, Foltin Susan K, Jewell Brittany M, Ludwig Megan L, Pinatti Lisa, Jiang Hui, McHugh Jonathan B, Marentette Lawence, McKean Erin L, Brenner J Ch |
| Primary cutaneous SMARCB1-deficient carcinoma. Journal of cutaneous pathology 2021 2 48 (8): 1051-1060. Hui Yiang, Cotzia Paolo, Rana Satshil, Kezlarian Brie E, Lin Oscar, Hollmann Travis J, Dogan Snjeza |
| The clinicopathological significance of SWI/SNF alterations in gastric cancer is associated with the molecular subtypes. PloS one 2021 16 (1): e0245356. Huang Shih-Chiang, Ng Kwai-Fong, Chang Ian Yi-Feng, Chang Chee-Jen, Chao Yi-Chun, Chang Shu-Chen, Chen Min-Chi, Yeh Ta-Sen, Chen Tse-Chi |
| Genetic basis of SMARCB1 protein loss in 22 sinonasal carcinomas. Human pathology 2020 8 104 105-116. Dogan Snjezana, Cotzia Paolo, Ptashkin Ryan N, Nanjangud Gouri J, Xu Bin, Momeni Boroujeni Amir, Cohen Marc A, Pfister David G, Prasad Manju L, Antonescu Cristina R, Chen Yingbei, Gounder Mrinal |
| Mammalian SWI/SNF Complex Genomic Alterations and Immune Checkpoint Blockade in Solid Tumors. Cancer immunology research 2020 4 8 (8): 1075-1084. Abou Alaiwi Sarah, Nassar Amin H, Xie Wanling, Bakouny Ziad, Berchuck Jacob E, Braun David A, Baca Sylvan C, Nuzzo Pier Vitale, Flippot Ronan, Mouhieddine Tarek H, Spurr Liam F, Li Yvonne Y, Li Taiwen, Flaifel Abdallah, Steinharter John A, Margolis Claire A, Vokes Natalie I, Du Heng, Shukla Sachet A, Cherniack Andrew D, Sonpavde Guru, Haddad Robert I, Awad Mark M, Giannakis Marios, Hodi F Stephen, Liu X Shirley, Signoretti Sabina, Kadoch Cigall, Freedman Matthew L, Kwiatkowski David J, Van Allen Eliezer M, Choueiri Toni |
| Mutational spectrum of tobacco associated oral squamous carcinoma and its therapeutic significance. World journal of surgical oncology 2019 11 17 (1): 198. Batta Nishant, Pandey Man |
| Analysis of DNA methylation and microRNA expression in NUT (nuclear protein in testis) midline carcinoma of the sinonasal tract: a clinicopathological, immunohistochemical and molecular genetic study. Neoplasma 2018 1 65 (1): 113-123. Laco J, Kovarikova H, Chmelarova M, Vosmikova H, Sieglova K, Bubancova I, Dundr P, Nemejcova K, Michalek J, Celakovsky P, Mottl R, Sirak I, Vosmik M, Marek I, Geryk T, Mejzlik J, Satankova J, Ryska |
| Epithelial-Myoepithelial Carcinoma: Frequent Morphologic and Molecular Evidence of Preexisting Pleomorphic Adenoma, Common HRAS Mutations in PLAG1-intact and HMGA2-intact Cases, and Occasional TP53, FBXW7, and SMARCB1 Alterations in High-grade Cases. The American journal of surgical pathology 2017 Nov . El Hallani Soufiane, Udager Aaron M, Bell Diana, Fonseca Isabel, Thompson Lester D R, Assaad Adel, Agaimy Abbas, Luvison Alyssa M, Miller Caitlyn, Seethala Raja R, Chiosea Simi |
| Frequent IDH2 R172 mutations in undifferentiated and poorly-differentiated sinonasal carcinomas. The Journal of pathology 2017 May . Dogan Snjezana, Chute Deborah J, Xu Bin, Ptashkin Ryan N, Chandramohan Raghu, Casanova-Murphy Jacklyn, Nafa Khedoudja, Bishop Justin A, Chiosea Simion I, Stelow Edward B, Ganly Ian, Pfister David G, Katabi Nora, Ghossein Ronald A, Berger Michael |
| Comprehensive Genomic Sequencing of Urothelial Tumors Identifies Rare SMARCB1 (INI-1)-Deficient Carcinomas of the Urinary System. Clinical genitourinary cancer 2017 10 16 (2): e373-e382. Gupta Sumati, Albertson Daniel, Gaston David, Heilbrun Marta E, Agarwal Neeraj, Boucher Ken, Parnell Timothy J, Liu Ting, Morgans Alicia, Madison Russell, Gowen Kyle, Miller Vincent A, Ross Jeffrey S, Ali Siraj M, Millis Sherri |
| Molecular alterations of coexisting thyroid papillary carcinoma and anaplastic carcinoma: identification of TERT mutation as an independent risk factor for transformation. Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc 2017 11 30 (11): 1527-1537. Oishi Naoki, Kondo Tetsuo, Ebina Aya, Sato Yukiko, Akaishi Junko, Hino Rumi, Yamamoto Noriko, Mochizuki Kunio, Nakazawa Tadao, Yokomichi Hiroshi, Ito Koichi, Ishikawa Yuichi, Katoh Ryoh |
| Genetic variant in SWI/SNF complexes influences hepatocellular carcinoma risk: a new clue for the contribution of chromatin remodeling in carcinogenesis. Scientific reports 2014 4 4147. Zhong Rong, Liu Li, Tian Yao, Wang Ying, Tian Jing, Zhu Bei-bei, Chen Wei, Qian Jia-ming, Zou Li, Xiao Min, Shen Na, Yang Hong, Lou Jiao, Qiu Qian, Ke Jun-tao, Lu Xing-hua, Wang Zhen-ling, Song Wei, Zhang Ti, Li Hui, Wang Li, Miao Xiao-pi |
| SMARCB1 (INI1)-negative rhabdoid carcinomas of the gastrointestinal tract: clinicopathologic and molecular study of a highly aggressive variant with literature review. The American journal of surgical pathology 2014 2 38 (7): 910-20. Agaimy Abbas, Rau Tilman T, Hartmann Arndt, Stoehr Robe |
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- Page last updated:Mar 22, 2023
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