Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 88 Records) |
Query Trace: MED12[original query] |
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Genomic characterisation of breast fibroepithelial lesions in an international cohort. The Journal of pathology 2019 Aug . Md Nasir Nur Diyana, Ng Cedric Chuan Young, Rajasegaran Vikneswari, Wong Suet Far, Liu Wei, Ng Gwendolene Xin Pei, Lee Jing Yi, Guan Peiyong, Lim Jing Quan, Thike Aye Aye, Koh Valerie Cui Yun, Loke Benjamin Nathanael, Chang Kenneth Tou En, Gudi Mihir Ananta, Lian Derrick Wen Quan, Madhukumar Preetha, Tan Benita Kiat Tee, Tan Veronique Kiak Mien, Wong Chow Yin, Yong Wei Sean, Ho Gay Hui, Ong Kong Wee, , Tan Patrick, Teh Bin Tean, Tan Puay Ho |
MED12 Exon 1 Mutational Screening in Iranian Patients with Uterine Leiomyoma. Reports of biochemistry & molecular biology 2019 7 8 (1): 21-24. Akbari Mojdeh, Abedin Do Atieh, Yassaee Fakhrolmolouk, Mirfakhraie Re |
Lujan-Fryns Syndrome Phenotype with Autism-Like Behavior and Atypical Psychotic Symptoms: Case Report. Turk psikiyatri dergisi = Turkish journal of psychiatry 2020 9 31 (3): 216-220. Geni? Bahad?r, ?ahin Ferit, Co?ar Behc |
Genomic profiling of primary and recurrent adult granulosa cell tumors of the ovary. Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc 2020 Mar . Da Cruz Paula Arnaud, da Silva Edaise M, Segura Sheila E, Pareja Fresia, Bi Rui, Selenica Pier, Kim Sarah H, Ferrando Lorenzo, Vahdatinia Mahsa, Soslow Robert A, Vidal August, Gatius Sonia, Przybycin Christopher G, Abu-Rustum Nadeem R, Matias-Guiu Xavier, Rubin Brian P, Reis-Filho Jorge S, DeLair Deborah F, Weigelt Brit |
Detection of MED12 mutations in mesenchymal components of uterine adenomyomas. Human pathology 2020 Nov . Kito Masahiko, Maeda Daichi, Kudo-Asabe Yukitsugu, Tamura Daisuke, Makino Kenichi, Sageshima Masato, Nanjo Hiroshi, Terada Yukihiro, Goto Akite |
De novo loss-of-function variants in X-linked MED12 are associated with Hardikar syndrome in females. Genetics in medicine : official journal of the American College of Medical Genetics 2020 11 23 (4): 637-644. Li Dong, Strong Alanna, Shen Kaitlyn M, Cassiman David, Van Dyck Maria, Linhares Natalia Duarte, Valadares Eugenia Ribeiro, Wang Tiancheng, Pena Sergio D J, Jaeken Jaak, Vergano Samantha, Zackai Elaine, Hing Anne, Chow Penny, Ganguly Arupa, Scholz Tasja, Bierhals Tatjana, Philipp Deindl, Hakonarson Hakon, Bhoj Elizabe |
Association of clinico-genomic characteristics with tumor mutational burden in small cell lung cancer patients. Future oncology (London, England) 2020 11 17 (4): 423-433. Kachroo Sumesh, Shao Changxia, Desai Kaushal, He Jinghua, Jin Fan, Sen Shuva |
Predictive significance of selected gene mutations in relapsed and refractory chronic lymphocytic leukemia patients treated with ibrutinib. European journal of haematology 2020 Nov . Machnicki Marcin M, Górniak Patryk, P?pek Monika, Szymczyk Agnieszka, Iskierka-Ja?d?ewska El?bieta, Steckiewicz Pawe?, Bluszcz Aleksandra, Rydzanicz Ma?gorzata, Hus Marek, P?oski Rafa?, Makuch-?asica Hanna, Nowak Gra?yna, Juszczy?ski Przemys?aw, Jamroziak Krzysztof, Stok?osa Tomasz, Pu?a Barto |
Distinct Genomic Alterations in Prostate Tumors Derived from African American Men. Molecular cancer research : MCR 2020 10 18 (12): 1815-1824. Liu Wennuan, Zheng S Lilly, Na Rong, Wei Lin, Sun Jishan, Gallagher Johnie, Wei Jun, Resurreccion W Kyle, Ernst Sarah, Sfanos Karen S, Isaacs William B, Xu Jianfe |
Droplet-digital PCR reveals frequent mutations in TERT promoter region in breast fibroadenomas and phyllodes tumours, irrespective of the presence of MED12 mutations. British journal of cancer 2020 Oct . Otsuji Kazutaka, Sasaki Takeshi, Tanabe Masahiko, Seto Yasuyu |
Intravenous leiomyomatosis: molecular analysis of 17 cases. Pathology 2019 Dec . Lu Bingjian, Liu Qin, Tang Lanlan, Ma Yu, Shi Haiy |
Somatic mutations in benign breast disease tissues and association with breast cancer risk. BMC medical genomics 2021 7 14 (1): 185. Winham Stacey J, Wang Chen, Heinzen Ethan P, Bhagwate Aditya, Liu Yuanhang, McDonough Samantha J, Stallings-Mann Melody L, Frost Marlene H, Vierkant Robert A, Denison Lori A, Carter Jodi M, Sherman Mark E, Radisky Derek C, Degnim Amy C, Cunningham Julie |
Frequency of MED12 Mutation in Relation to Tumor and Patient's Clinical Characteristics: a Meta-analysis. Reproductive sciences (Thousand Oaks, Calif.) 2021 2 29 (2): 357-365. He Chao, Nelson William, Li Hui, Xu Ya-Dong, Dai Xue-Jiao, Wang Ying-Xiong, Ding Yu-Bin, Li Yan-Ping, Li Ti |
MED12 exon 2 and TERT promoter mutations in primary and recurrent breast fibroepithelial lesions. Pathology international 2021 10 71 (12): 814-822. Hu Yanjiao, Li Guangqi, Wang Lili, Zhang Longxiao, Guan Jingjing, Wang Jiga |
A comprehensive analysis of somatic alterations in Chinese ovarian cancer patients. Scientific reports 2021 Jan 11 (1): 387. Zhang Yingli, Shi Xiaoliang, Zhang Jiejie, Chen Xi, Zhang Peng, Liu Angen, Zhu T |
High prevalence of somatic PIK3CA and TP53 pathogenic variants in the normal mammary gland tissue of sporadic breast cancer patients revealed by duplex sequencing. NPJ breast cancer 2022 6 8 (1): 76. Kostecka Anna, Nowikiewicz Tomasz, Olszewski Pawe?, Koczkowska Magdalena, Horbacz Monika, Heinzl Monika, Andreou Maria, Salazar Renato, Mair Theresa, Madanecki Piotr, Gucwa Magdalena, Davies Hanna, Skokowski Jaros?aw, Buckley Patrick G, P?ksa Rafa?, ?rutek Ewa, Szylberg ?ukasz, Hartman Johan, Jankowski Micha?, Zegarski Wojciech, Tiemann-Boege Irene, Dumanski Jan P, Piotrowski Arkadiu |
Analysis of recurrent molecular alterations in phyllodes tumour of breast: insights into prognosis and pathogenesis. Pathology 2022 Jun . Tsang Julia Y, Shao Yan, Poon Ivan K, Ni Yun-Bi, Kwan Johnny S, Chow Chit, Shea Ka-Ho, Tse Gary |
Cyclin-dependent kinase 8 is an independent prognosticator in uterine leiomyosarcoma. Pathology, research and practice 2022 Jul 235 153920. Yasutake Nobuko, Iwasaki Takeshi, Yamamoto Hidetaka, Sonoda Kenzo, Kodama Keisuke, Okugawa Kaoru, Asanoma Kazuo, Yahata Hideaki, Kato Kiyoko, Oda Yoshin |
High prevalence of deleterious mutations in concomitant nonsyndromic cleft and outflow tract heart defects. American journal of medical genetics. Part A 2022 4 188 (7): 2082-2095. Munabi Naikhoba C O, Mikhail Shady, Toubat Omar, Webb Michelle, Auslander Allyn, Sanchez-Lara Pedro A, Manojlovic Zarko, Schmidt Ryan J, Craig David, Magee William P, Kumar Subramanyan R |
Comparison of MED 12 gene mutation and microRNA-124 expression in leiomyoma and myometrium of Turkish patients. Ginekologia polska 2022 4 . Demiroglu Cagdas, Komurcu Karuserci Ozge, Pence Sadrettin, Pence Halime Han?m, Çaykara Burcu, Sucu Seyhun, Ugur Mete Gür |
MED12 mutation as a potential predictive biomarker for immune checkpoint inhibitors in pan-cancer. European journal of medical research 2022 10 27 (1): 225. Zhou Yong, Tan Yuan, Zhang Qin, Duan Qianqian, Chen J |
Genomic Profiling of Aggressive Thyroid Cancer in Association With its Clinicopathological Characteristics. In vivo (Athens, Greece) 2022 1 36 (1): 111-120. Kim Jae-Hui, Jeong Ji Yun, Seo An Na, Park Nora Jee-Young, Kim Moonsik, Park Ji You |
Genomic alterations related to HPV infection status in a cohort of Chinese prostate cancer patients. European journal of medical research 2023 7 28 (1): 239. Bin Lang, Chen Cao, Xiaoxiao Zhao, Yi Wang, Ying Cao, Xueying Zhou, Tong Zhao, Yuyan Wang, Ting Liu, Wenjia Liang, Zheng Hu, Xun Tian, Jingjing Zhang, Yongji Y |
Prevalence and clinical significance of co-existing mutations in MED12 and FH in uterine fibroids of Australian women. Frontiers in reproductive health 2023 4 5 1081092. M Fairuz B Jamaluddin, Prathima B Nagendra, Yi-An Ko, Preety Bajwa, Rodney J Scott, Pravin Nahar, Pradeep S Tanw |
MED12 variants associated with X-linked recessive partial epilepsy without intellectual disability. Seizure 2023 3 . Yang Jie-Hua, Liu Zhi-Gang, Liu Chun-Ling, Zhang Ming-Rui, Jia Yan-Lu, Zhai Qiong-Xiang, He Ming-Feng, He Na, Qiao Jing- |
Frequently mutated genes in predicting the relapse of stage I lung adenocarcinoma. Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico 2023 2 . Rao Wen, Yang Lujie, Dai Nan, Zhang Liang, Liu Jie, Yang Bo, Li Mengxia, Shan Jinlu, Wang Qiushi, Wang Do |
High-Grade Sarcomas with Myogenic Differentiation Harboring Hotspot PDGFRB Mutations. Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc 2023 2 36 (5): 100104. Dermawan Josephine K, Chiang Sarah, Hensley Martee L, Tap William D, Antonescu Cristina |
Inherited mutations affecting the SRCAP complex are central in moderate-penetrance predisposition to uterine leiomyomas. American journal of human genetics 2023 2 110 (3): 460-474. Välimäki Niko, Jokinen Vilja, Cajuso Tatiana, Kuisma Heli, Taira Aurora, Dagnaud Olivia, Ilves Sini, Kaukomaa Jaana, Pasanen Annukka, Palin Kimmo, Heikinheimo Oskari, Bützow Ralf, Aaltonen Lauri A, Karhu Au |
Establishment of Noninvasive Prediction Models for the Diagnosis of Uterine Leiomyoma Subtypes. Obstetrics and gynecology 2023 12 . Tetsuro Tamehisa, Shun Sato, Takahiro Sakai, Ryo Maekawa, Masahiro Tanabe, Katsuyoshi Ito, Norihiro Sugi |
The Effect of Race/Ethnicity and MED12 Mutation on the Expression of Long Non-Coding RNAs in Uterine Leiomyoma and Myometrium. International journal of molecular sciences 2024 1 25 (2): . Tsai-Der Chuang, Nhu Ton, Shawn Rysling, Drake Boos, Omid Khorr |
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- Page last updated:Apr 22, 2024
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