Human Genome Epidemiology Literature Finder
Records 1 - 17 (of 17 Records) |
Query Trace: Syndrome and CTNNB1[original query] |
---|
APC and CTNNB1 mutations are rare in sporadic ependymomas. Cancer genetics and cytogenetics 2006 Jul 168 (2): 158-61. Onilude Olabisi E, Lusher Meryl E, Lindsey Janet C, Pearson Andrew D J, Ellison David W, Clifford Steven |
TP53 mutation is frequently associated with CTNNB1 mutation or MYCN amplification and is compatible with long-term survival in medulloblastoma. Journal of clinical oncology : official journal of the American Society of Clinical Oncology 2010 Dec 28 (35): 5188-96. Pfaff Elke, Remke Marc, Sturm Dominik, Benner Axel, Witt Hendrik, Milde Till, von Bueren André O, Wittmann Andrea, Schöttler Anna, Jorch Norbert, Graf Norbert, Kulozik Andreas E, Witt Olaf, Scheurlen Wolfram, von Deimling Andreas, Rutkowski Stefan, Taylor Michael D, Tabori Uri, Lichter Peter, Korshunov Andrey, Pfister Stefan |
GNAS-activating mutations define a rare subgroup of inflammatory liver tumors characterized by STAT3 activation. Journal of hepatology 2012 Jan 56 (1): 184-91. Nault Jean Charles, Fabre Monique, Couchy Gabrielle, Pilati Camilla, Jeannot Emmanuelle, Tran Van Nhieu Jeanne, Saint-Paul Marie-Christine, De Muret Anne, Redon Marie-José, Buffet Catherine, Salenave Sylvie, Balabaud Charles, Prevot Sophie, Labrune Philippe, Bioulac-Sage Paulette, Scoazec Jean-Yves, Chanson Philippe, Zucman-Rossi Jessi |
ß-catenin (CTNNB1) mutations and clinicopathological features of mesenteric desmoid-type fibromatosis. Histopathology 2013 Jan 62 (2): 294-304. Huss Sebastian, Nehles Julia, Binot Elke, Wardelmann Eva, Mittler Jens, Kleine Michaela Angelika, Künstlinger Helen, Hartmann Wolfgang, Hohenberger Peter, Merkelbach-Bruse Sabine, Buettner Reinhard, Schildhaus Hans-Ulri |
Molecular pathogenesis of endometrial cancers in patients with Lynch syndrome. Cancer 2013 Aug 119 (16): 3027-33. Huang Marilyn, Djordjevic Bojana, Yates Melinda S, Urbauer Diana, Sun Charlotte, Burzawa Jennifer, Daniels Molly, Westin Shannon N, Broaddus Russell, Lu Kar |
PRKACA mutations in cortisol-producing adenomas and adrenal hyperplasia: a single-center study of 60 cases. European journal of endocrinology / European Federation of Endocrine Societies 2015 Mar . Thiel Anne, Reis Anna-Carinna, Haase Matthias, Goh Gerald, Schott Matthias, Willenberg Holger S, Scholl Ute Ingr |
Clinical characteristics of PRKACA mutations in Chinese patients with adrenal lesions: a single-centre study. Clinical endocrinology 2016 Jun . Li Xintao, Wang Baojun, Tang Lu, Lang Bin, Zhang Yu, Zhang Fan, Chen Luyao, Ouyang Jinzhi, Zhang |
Mismatch repair deficiency commonly precedes adenoma formation in Lynch Syndrome-Associated colorectal tumorigenesis. Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc 2017 May . Sekine Shigeki, Mori Taisuke, Ogawa Reiko, Tanaka Masahiro, Yoshida Hiroshi, Taniguchi Hirokazu, Nakajima Takeshi, Sugano Kokichi, Yoshida Teruhiko, Kato Mamoru, Furukawa Eisaku, Ochiai Atsushi, Hiraoka Nobuyos |
Molecular Background of Colorectal Tumors From Patients With Lynch Syndrome Associated With Germline Variants in PMS2. Gastroenterology 2018 5 155 (3): 844-851. Ten Broeke Sanne W, van Bavel Tom C, Jansen Anne M L, Gómez-García Encarnca, Hes Frederik J, van Hest Liselot P, Letteboer Tom G W, Olderode-Berends Maran J W, Ruano Dina, Spruijt Liesbeth, Suerink Manon, Tops Carli M, van Eijk Ronald, Morreau Hans, van Wezel Tom, Nielsen Maart |
Development of new preclinical models to advance adrenocortical carcinoma research. Endocrine-related cancer 2018 1 25 (4): 437-451. Kiseljak-Vassiliades Katja, Zhang Yu, Bagby Stacey M, Kar Adwitiya, Pozdeyev Nikita, Xu Mei, Gowan Katherine, Sharma Vibha, Raeburn Christopher D, Albuja-Cruz Maria, Jones Kenneth L, Fishbein Lauren, Schweppe Rebecca E, Somerset Hilary, Pitts Todd M, Leong Stephen, Wierman Margaret |
Intracholecystic Papillary Neoplasms Are Distinct From Papillary Gallbladder Cancers: A Clinicopathologic and Exome-sequencing Study. The American journal of surgical pathology 2019 2 43 (6): 783-791. Akita Masayuki, Fujikura Kohei, Ajiki Tetsuo, Fukumoto Takumi, Otani Kyoko, Hirose Takanori, Tominaga Masahiro, Itoh Tomoo, Zen Y |
Novel pathogenic alterations in pediatric and adult desmoid-type fibromatosis - A systematic analysis of 204 cases. Scientific reports 2020 Feb 10 (1): 3368. Trautmann Marcel, Rehkämper Jan, Gevensleben Heidrun, Becker Jessica, Wardelmann Eva, Hartmann Wolfgang, Grünewald Inga, Huss Sebasti |
Intratumoral heterogeneity of the tumor cells based on in situ cortisol excess in cortisol-producing adenomas; ?An association among morphometry, genotype and cellular senescence?. The Journal of steroid biochemistry and molecular biology 2020 10 204 105764. Gao Xin, Yamazaki Yuto, Tezuka Yuta, Pieroni Jacopo, Ishii Kae, Atsumi Nanako, Ono Yoshikiyo, Omata Kei, Morimoto Ryo, Nakamura Yasuhiro, Satoh Fumitoshi, Sasano Hirono |
Phase II Trial of Cabozantinib in Recurrent/Metastatic Endometrial Cancer: A Study of the Princess Margaret, Chicago, and California Consortia (NCI9322/PHL86). Clinical cancer research : an official journal of the American Association for Cancer Research 2020 Jan . Dhani Neesha C, Hirte Hal W, Wang Lisa, Burnier Julia V, Jain Angela, Butler Marcus O, Welch Stephen, Fleming Gini F, Hurteau Jean, Matsuo Koji, Matei Daniela, Jimenez Waldo, Johnston Carolyn, Cristea Mihaela, Tonkin Katia, Ghatage Prafull, Lheureux Stephanie, Mehta Anjali, Quintos Judy, Tan Qian, Kamel-Reid Suzanne, Ludkovski Olga, Tsao Ming-Sound, Wright John J, Oza Amit |
Associations of Pathogenic Variants in MLH1, MSH2, and MSH6 With Risk of Colorectal Adenomas and Tumors and With Somatic Mutations in Patients With Lynch Syndrome. Gastroenterology 2020 1 158 (5): 1326-1333. Engel Christoph, Ahadova Aysel, Seppälä Toni T, Aretz Stefan, Bigirwamungu-Bargeman Marloes, Bläker Hendrik, Bucksch Karolin, Büttner Reinhard, de Vos Tot Nederveen Cappel Wouter T, Endris Volker, Holinski-Feder Elke, Holzapfel Stefanie, Hüneburg Robert, Jacobs Maarten A J M, Koornstra Jan J, Langers Alexandra M, Lepistö Anna, Morak Monika, Möslein Gabriela, Peltomäki Päivi, Pylvänäinen Kirsi, Rahner Nils, Renkonen-Sinisalo Laura, Schulmann Karsten, Steinke-Lange Verena, Stenzinger Albrecht, Strassburg Christian P, van de Meeberg Paul C, van Kouwen Mariette, van Leerdam Monique, Vangala Deepak B, Vecht Juda, Verhulst Marie-Louise, von Knebel Doeberitz Magnus, Weitz Jürgen, Zachariae Silke, Loeffler Markus, Mecklin Jukka-Pekka, Kloor Matthias, Vasen Hans F, , |
High Prevalence of DICER1 Mutations and Low Frequency of Gene Fusions in Pediatric Follicular-Patterned Tumors of the Thyroid. Endocrine pathology 2021 7 32 (3): 336-346. Bae Ja-Seong, Jung Seung-Hyun, Hirokawa Mitsuyoshi, Bychkov Andrey, Miyauchi Akira, Lee Sohee, Chung Yeun-Jun, Jung Chan Kw |
Cancer predisposition signaling in Beckwith-Wiedemann Syndrome drives Wilms tumor development. British journal of cancer 2023 12 . Snehal Nirgude, Natali S Sobel Naveh, Sanam L Kavari, Emily M Traxler, Jennifer M Kali |
- Page last reviewed:Feb 1, 2024
- Page last updated:Apr 22, 2024
- Content source: