Human Genome Epidemiology Literature Finder
Records 1 - 23 (of 23 Records) |
Query Trace: PROM1[original query] |
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CRTC2 and PROM1 expression in non-small cell lung cancer: analysis by Western blot and immunohistochemistry. Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine 2014 Dec 35 (12): 11719-26. Li Yalun, He Yanqi, Qiu Zhixin, Zhou Bin, Shi Shaoqin, Zhang Kui, Luo Yangkun, Huang Qian, Li Weim |
Mutation screening of retinal dystrophy patients by targeted capture from tagged pooled DNAs and next generation sequencing. PloS one 2014 9 (8): e104281. Watson Christopher M, El-Asrag Mohammed, Parry David A, Morgan Joanne E, Logan Clare V, Carr Ian M, Sheridan Eamonn, Charlton Ruth, Johnson Colin A, Taylor Graham, Toomes Carmel, McKibbin Martin, Inglehearn Chris F, Ali Man |
[Endometrial cancer in young women--clinical and molecular aspects]. Ginekologia polska 2014 12 85 (10): 754-9. Lapi?ska-Szumczyk Sylwia, Supernat Anna, ?aczek Anna J, Majewska Hanna, Gulczy?ski Jacek, Sawicki Sambor, Biernat Wojciech, Wydra Dariu |
Next-generation sequencing-based comprehensive molecular analysis of 43 Japanese patients with cone and cone-rod dystrophies. Molecular vision 2016 22 150-60. Oishi Maho, Oishi Akio, Gotoh Norimoto, Ogino Ken, Higasa Koichiro, Iida Kei, Makiyama Yukiko, Morooka Satoshi, Matsuda Fumihiko, Yoshimura Nagahi |
Cancer Stem Cell Gene Variants Predict Disease Recurrence in Patients Treated with Radical Prostatectomy for Prostate Cancer. International journal of medical sciences 2017 11 14 (12): 1301-1306. Lin Victor C, Huang Shu-Pin, Huang Chao-Yuan, Yu Chia-Cheng, Yin Hsin-Ling, Huang Tsung-Yi, Lee Cheng-Hsueh, Lu Te-Ling, Bao Bo-Yi |
[Molecular genetic diagnosis of Stargardt disease]. Vestnik oftalmologii 2017 133 (4): 4-11. Sheremet N L, Zhorzholadze N V, Ronzina I A, Grushke I G, Kurbatov S A, Chukhrova A L, Loginova A N, Shcherbakova P O, Tanas A S, Polyakov A V, Strel'nikov V |
PROM1 gene variations in Brazilian patients with macular dystrophy. Ophthalmic genetics 2017 1 38 (1): 39-42. Salles Mariana Vallim, Motta Fabiana Louise, Dias da Silva Elton, Varela Lima Teixeira Patricia, Antunes Costa Kárita, Filippelli-Silva Rafael, Martin Renan, Pesquero João Bosco, Ferraz Sallum Juliana Mar |
Mutations in Splicing Factor Genes Are a Major Cause of Autosomal Dominant Retinitis Pigmentosa in Belgian Families. PloS one 2017 1 12 (1): e0170038. Van Cauwenbergh Caroline, Coppieters Frauke, Roels Dimitri, De Jaegere Sarah, Flipts Helena, De Zaeytijd Julie, Walraedt Sophie, Claes Charlotte, Fransen Erik, Van Camp Guy, Depasse Fanny, Casteels Ingele, de Ravel Thomy, Leroy Bart P, De Baere Elfri |
Clinical and Genetic Characteristics Analysis of Korean Patients with Stargardt Disease Using Targeted Exome Sequencing. Ophthalmologica. Journal international d'ophtalmologie. International journal of ophthalmology. Zeitschrift fur Augenheilkunde 2018 Jul 1-11. Sung Youngje, Choi Seung Woo, Shim Sung Han, Song Won Kyu |
PROM1 and PROM2 expression differentially modulates clinical prognosis of cancer: a multiomics analysis. Cancer gene therapy 2019 6 27 (3-4): 147-167. Saha Subbroto Kumar, Islam S M Riazul, Kwak Kyung-Sup, Rahman Md Shahedur, Cho Ssang-G |
Clinical and genetic characteristics of 10 Japanese patients with PROM1-associated retinal disorder: A report of the phenotype spectrum and a literature review in the Japanese population. American journal of medical genetics. Part C, Seminars in medical genetics 2020 8 184 (3): 656-674. Fujinami Kaoru, Oishi Akio, Yang Lizhu, Arno Gavin, Pontikos Nikolas, Yoshitake Kazutoshi, Fujinami-Yokokawa Yu, Liu Xiao, Hayashi Takaaki, Katagiri Satoshi, Mizobuchi Kei, Mizota Atsushi, Shinoda Kei, Nakamura Natsuko, Kurihara Toshihide, Tsubota Kazuo, Miyake Yozo, Iwata Takeshi, Tsujikawa Akitaka, Tsunoda Kazushige, |
Novel variants associated with Stargardt disease in Chinese patients. Gene 2020 6 754 144890. Hu Fangyuan, Gao Fengjuan, Li Jiankang, Xu Ping, Wang Dandan, Chen Fang, Zhang Shenghai, Wu Jiho |
Targeted next-generation sequencing identifies ABCA4 mutations in Chinese families with childhood-onset and adult-onset Stargardt disease. Bioscience reports 2021 5 41 (6): . Qu Ling-Hui, Jin Xin, Zeng Chao, Zhou Nian-Gou, Liu Yan-Hong, Lin |
Whole exome sequencing analysis identifies novel Stargardt disease-related gene mutations in Chinese Stargardt disease and retinitis pigmentosa patients. Eye (London, England) 2021 4 36 (4): 749-759. Ng Tsz Kin, Cao Yingjie, Yuan Xiang-Ling, Chen Shaowan, Xu Yanxuan, Chen Shao-Lang, Zheng Yuqian, Chen Hao |
Clinical and Genetic Spectrum of Stargardt Disease in Argentinean Patients. Frontiers in genetics 2021 4 12 646058. Mena Marcela D, Moresco Angélica A, Vidal Sofía H, Aguilar-Cortes Diana, Obregon María G, Fandiño Adriana C, Sendoya Juan M, Llera Andrea S, Podhajcer Osvaldo |
Acquired mutations and transcriptional remodeling in long-term estrogen-deprived locoregional breast cancer recurrences. Breast cancer research : BCR 2021 1 23 (1): 1. Priedigkeit Nolan, Ding Kai, Horne William, Kolls Jay K, Du Tian, Lucas Peter C, Blohmer Jens-Uwe, Denkert Carsten, Machleidt Anna, Ingold-Heppner Barbara, Oesterreich Steffi, Lee Adrian |
PROM1, CXCL8, RUNX1, NAV1 and TP73 genes as independent markers predictive of prognosis or response to treatment in two cohorts of high-grade serous ovarian cancer patients. PloS one 2022 17 (7): e0271539. Dansonka-Mieszkowska Agnieszka, Szafron Laura Aleksandra, Kulesza Magdalena, Stachurska Anna, Leszczynski Pawel, Tomczyk-Szatkowska Agnieszka, Sobiczewski Piotr, Parada Joanna, Kulinczak Mariusz, Moes-Sosnowska Joanna, Pienkowska-Grela Barbara, Kupryjanczyk Jolanta, Chechlinska Magdalena, Szafron Lukasz Mich |
Polygenic Risk Score and Rare Variant Burden Identified by Targeted Sequencing in a Group of Patients with Pigment Epithelial Detachment in Age-Related Macular Degeneration. Genes 2023 9 14 (9): . Anna W?sowska, Adam Sendecki, Anna Boguszewska-Chachulska, S?awomir Tep |
Identification of Prominent Genes between 3D Glioblastoma Models and Clinical Samples via GEO/TCGA/CGGA Data Analysis. Biology 2023 5 12 (5): . Brandon Wee Siang Phon, Saatheeyavaane Bhuvanendran, Qasim Ayub, Ammu Kutty Radhakrishnan, Muhamad Noor Alfarizal Kamarud |
Nationwide genetic analysis of more than 600 families with inherited eye diseases in Argentina. NPJ genomic medicine 2023 5 8 (1): 8. Patricio G Schlottmann, José D Luna, Natalia Labat, María Belén Yadarola, Silvina Bainttein, Evangelina Esposito, Agustina Ibañez, Evangelina Ivón Barbaro, Alejandro Álvarez Mendiara, Carolina P Picotti, Andrea Chirino Misisian, Luciana Andreussi, Julieta Gras, Luciana Capalbo, Mauro Visotto, José E Dipierri, Emilio Alcoba, Laura Fernández Gabrielli, Silvia Ávila, María Emilia Aucar, Daniel M Martin, Gerardo Juan Ormaechea, M Eugenia Inga, Aníbal A Francone, Martin Charles, Tamara Zompa, Pablo Javier Pérez, Vanesa Lotersztein, Pedro J Nuova, Ivana B Canonero, Omar A Mahroo, Michel Michaelides, Gavin Arno, Malena Daich Vare |
Relationship between genotype, phenotype, and refractive status in patients of inherited retinal degeneration. Eye (London, England) 2024 8 . Wan-Chen Tsai, Yao-Lin Liu, Tzu-Hsun Tsai, Ying-Ju Lai, Chang-Hao Yang, Chung-May Yang, Tzyy-Chang Ho, Chang-Ping Lin, Yi-Ting Hsieh, Po-Ting Yeh, Chao-Wen Lin, Tso-Ting Lai, Pei-Lung Chen, Ta-Ching Ch |
Sex Distributions in Non-ABCA4 Autosomal Macular Dystrophies. Investigative ophthalmology & visual science 2024 5 65 (5): 9. Amit V Mishra, Sandra Vermeirsch, Siying Lin, Maria P Martin-Gutierrez, Mark Simcoe, Nikolas Pontikos, Elena Schiff, Thales A C de Guimarães, Pirro G Hysi, Michel Michaelides, Gavin Arno, Andrew R Webster, Omar A Mahr |
GLI1 polymorphisms influence remission rate and prognosis of young de novo acute myeloid leukemia patients treated with cytarabine-based chemotherapy. Annals of hematology 2024 4 . Yanfeng Liu, Yi Liu, Peng Chen, Ge Chen, Xiaoping Ch |
- Page last reviewed:Feb 1, 2024
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