Human Genome Epidemiology Literature Finder
Rare Diseases
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Records 1 - 26 (of 26 Records) |
| Query Trace: Fibrosarcoma[original query] |
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Genome-wide association scan identifies candidate polymorphisms associated with differential response to anti-TNF treatment in rheumatoid arthritis.
Molecular medicine (Cambridge, Mass.) 0 14 (9-10): 575-81. Liu Chunyu, Batliwalla Franak, Li Wentian, Lee Annette, Roubenoff Ronenn, Beckman Evan, Khalili Houman, Damle Aarti, Kern Marlena, Furie Richard, Dupuis Josée, Plenge Robert M, Coenen Marieke J H, Behrens Timothy W, Carulli John P, Gregersen Peter |
| Association between obesity and polymorphisms in SEC16B, TMEM18, GNPDA2, BDNF, FAIM2 and MC4R in a Japanese population. Journal of human genetics 2009 Dec 54 (12): 727-31. Hotta Kikuko, Nakamura Michihiro, Nakamura Takahiro, Matsuo Tomoaki, Nakata Yoshio, Kamohara Seika, Miyatake Nobuyuki, Kotani Kazuaki, Komatsu Ryoya, Itoh Naoto, Mineo Ikuo, Wada Jun, Masuzaki Hiroaki, Yoneda Masato, Nakajima Atsushi, Funahashi Tohru, Miyazaki Shigeru, Tokunaga Katsuto, Kawamoto Manabu, Ueno Takato, Hamaguchi Kazuyuki, Tanaka Kiyoji, Yamada Kentaro, Hanafusa Toshiaki, Oikawa Shinichi, Yoshimatsu Hironobu, Nakao Kazuwa, Sakata Toshiie, Matsuzawa Yuji, Kamatani Naoyuki, Nakamura Yusu |
| [Association between single nucleotide polymorphisms of v-maf musculoaponeurotic fibrosarcoma oncogene homolog B gene and non-syndromic cleft lip with or without cleft palate]. Zhongguo xiu fu chong jian wai ke za zhi = Zhongguo xiufu chongjian waike zazhi = Chinese journal of reparative and reconstructive surgery 2012 Jul 26 (7): 845-8. Cheng Hongqiu, Huang Enmin, Tang Shijie, Xu Mingyan, Shu Sheny |
| Further evidence of association of the ABCA4 gene with cleft lip/palate. European journal of oral sciences 2012 Dec 120 (6): 6. Fontoura C, Silva RM, Granjeiro JM, Letra A |
| Association study of single nucleotide polymorphisms of MAFB with non-syndromic cleft lip with or without cleft palate in a population in Heilongjiang Province, northern China. The British journal of oral & maxillofacial surgery 2014 Oct 52 (8): 746-50. Mi Na, Hao Yanru, Jiao Xiaohui, Zheng Xudong, Song Tao, Shi Jinna, Dong Ch |
| Copy number alterations and neoplasia-specific mutations in MELK, PDCD1LG2, TLN1, and PAX5 at 9p in different neoplasias. Genes, chromosomes & cancer 2014 Jul 53 (7): 579-88. Sarhadi Virinder Kaur, Lahti Leo, Scheinin Ilari, Ellonen Pekka, Kettunen Eeva, Serra Massimo, Scotlandi Katia, Picci Piero, Knuutila Saka |
| Association of polymorphisms in the MAFB gene and the risk of coronary artery disease and ischemic stroke: a case-control study. Lipids in health and disease 2015 14 (1): 79. Yang Qian, Yin Rui-Xing, Zhou Yi-Jiang, Cao Xiao-Li, Guo Tao, Chen Wu-Xi |
| A rare variant at 11p13 is associated with tuberculosis susceptibility in the Han Chinese population. Scientific reports 2016 6 24016. Chen Cheng, Zhao Qi, Hu Yi, Shao Yan, Li Guoli, Zhu Limei, Lu Wei, Xu Bi |
| Population-level effect of molecular testing and targeted therapy in patients with advanced pulmonary adenocarcinoma: a prospective cohort study. Virchows Archiv : an international journal of pathology 2018 Apr 472 (4): 581-588. Schwegler Christine, Kaufmann Dinu, Pfeiffer David, Aebi Stefan, Diebold Joachim, Gautschi Oliv |
| Breast cancer cases of female patients under 35 years of age in Togo: A series of 158 cases. Molecular and clinical oncology 2017 12 7 (6): 1125-1129. Darré Tchin, Tchaou Mazamaesso, Folligan Koué, Amadou Abdoulatif, N'Timon Bidamin, Sonhaye Lantam, Aboubakari Abdoul-Samadou, Amégbor Koffi, Akpadza Koffi, Napo Koura Ga |
| Impact of phosphoinositide-3-kinase and vitamin D3 nuclear receptor single-nucleotide polymorphisms on the outcome of malignant melanoma patients. Oncotarget 2017 (44): 75914-75923. Morgese Francesca, Soldato Davide, Pagliaretta Silvia, Giampieri Riccardo, Brancorsini Donatella, Torniai Mariangela, Rinaldi Silvia, Savini Agnese, Onofri Azzurra, Scarpelli Marina, Berardi Rossa |
| Survival Outcomes in Patients With RAS Wild Type Metastatic Colorectal Cancer Classified According to Köhne Prognostic Category and BRAF Mutation Status. Clinical colorectal cancer 2017 11 17 (1): 50-57.e8. Siena Salvatore, Rivera Fernando, Taieb Julien, Peeters Marc, Prenen Hans, Koukakis Reija, Demonty Gaston, Köhne Claus-Henni |
| A common variant of MAF/c-MAF, transcriptional factor gene in the kidney, is associated with gout susceptibility. Human cell 2018 Jan 31 (1): 10-13. Higashino Toshihide, Matsuo Hirotaka, Okada Yukinori, Nakashima Hiroshi, Shimizu Seiko, Sakiyama Masayuki, Tadokoro Shin, Nakayama Akiyoshi, Kawaguchi Makoto, Komatsu Mako, Hishida Asahi, Nakatochi Masahiro, Ooyama Hiroshi, Imaki Junko, Shinomiya Nariyos |
| Polymorphic Variants of V-Maf Musculoaponeurotic Fibrosarcoma Oncogene Homolog B (rs13041247 and rs11696257) and Risk of Non-Syndromic Cleft Lip/Palate: Systematic Review and Meta-Analysis. International journal of environmental research and public health 2019 8 16 (15): . Imani Mohammad Moslem, Lopez-Jornet Pia, Pons-Fuster López Eduardo, Sadeghi Maso |
| Clinical, histopathological, and molecular analyses of IDH-wild-type WHO grade II-III gliomas to establish genetic predictors of poor prognosis. Brain tumor pathology 2019 Jul . Kuwahara Kiyonori, Ohba Shigeo, Nakae Shunsuke, Hattori Natsuki, Pareira Eriel Sandika, Yamada Seiji, Sasaki Hikaru, Abe Masato, Hasegawa Mitsuhiro, Hirose Yuic |
| Clinical spectrum of Li-Fraumeni syndrome/Li-Fraumeni-like syndrome in Brazilian individuals with the TP53 p.R337H mutation. The Journal of steroid biochemistry and molecular biology 2019 4 190 250-255. Ferreira Amanda Meneses, Brondani Vania Balderrama, Helena Vanessa Petry, Charchar Helaine Laiz Silva, Zerbini Maria Claudia Nogueira, Leite Luiz Antonio Senna, Hoff Ana Oliveira, Latronico Ana Claudia, Mendonca Berenice Bilharinho, Diz Maria Del Pilar Estevez, de Almeida Madson Queiroz, Fragoso Maria Candida Barisson Villar |
| Radiotherapy-induced malignancies in breast cancer patients with TP53 pathogenic germline variants (Li-Fraumeni syndrome). Familial cancer 2019 Nov . Petry Vanessa, Bonadio Renata Colombo, Cagnacci Allyne Queiroz Carneiro, Senna Luiz Antonio Leite, Campos Roberta do Nascimento Galvão, Cotti Guilherme Cutait, Hoff Paulo M, Fragoso Maria Candida Barisson Villares, Estevez-Diz Maria Del Pil |
| A novel MAF missense mutation leads to congenital nuclear cataract by impacting the transactivation of crystallin and noncrystallin genes. Gene 2019 Jan 692 113-118. Si Nuo, Song Zixun, Meng Xiaolu, Li Xinru, Xiao Wei, Zhang X |
| Association between MAFB rs17820943 and rs6072081 polymorphism and risk of nonsyndromic cleft lip with or without cleft palate: a meta-analysis. The British journal of oral & maxillofacial surgery 2020 Jul . Liang X, Huang L, Ou Y, He Y, Tang |
| Gene-gene interactions between BMP4 and ARHGAP29 among non-syndromic cleft lip only (NSCLO) trios from western Han Chinese population. International journal of clinical and experimental pathology 2020 13 (2): 295-301. Wang Yiru, Shi Jiayu, Zheng Qian, Shi Bing, Jia Zhongl |
| ZNF687 Mutations in an Extended Cohort of Neoplastic Transformations in Paget's Disease of Bone: Implications for Clinical Pathology. Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research 2020 Feb . Scotto di Carlo Federica, Pazzaglia Laura, Mumm Steven, Benassi Maria S, De Chiara Annarosaria, Franchi Alessandro, Parafioriti Antonina, Righi Alberto, Esposito Teresa, Whyte Michael P, Gianfrancesco Fernan |
| Broadening the genotypic and phenotypic spectrum of MAF in three Chinese Han congenital cataracts families. American journal of medical genetics. Part A 2022 9 188 (10): 2888-2898. Wang Qiwei, Qin Tingfeng, Tan Haowen, Ding Xiaoyan, Lin Xiaoshan, Li Jing, Lin Zhuolin, Sun Limei, Lin Haotian, Chen Weiro |
| Association of Single-Nucleotide Polymorphisms of MAFB Gene with Nonsyndromic Cleft Lip with or without Cleft Palate in Kinh Vietnamese Patients. Indian journal of plastic surgery : official publication of the Association of Plastic Surgeons of India 2022 4 55 (1): 70-74. Phan Hoanh Duy Ba, Phuong Lam Hoai, Vu Hoang A |
| BRAF V600E and previously unidentified KRAS G12C mutations in odontogenic tumors may affect MAPK activation differently depending on tumor type. Genes, chromosomes & cancer 2022 3 61 (8): 481-490. Oh Kyu-Young, Kim Ji-Hoon, Cho Sung-Dae, Yoon Hye-Jung, Lee Jae-Il, Hong Seong-D |
| Novel cataract-causing variant c.177dupC in c-MAF regulates the expression of crystallin genes for cell apoptosis via a mitochondria-dependent pathway. Molecular genetics and genomics : MGG 2023 1 298 (2): 495-506. Li Li, Yue Jian-Fei, Kong De-Qian, Sun Miao-Miao, Li Ke, Zheng Guang-Yi |
| GOAT rs10096097 and CREB1 rs6740584 single nucleotide polymorphisms are associated with type 2 diabetes mellitus in Egyptians. Archiv der Pharmazie 2024 5 e2400011. Nancy N Shahin, Olfat G Shaker, Mohamed O Mahmo |
- Page last reviewed:Feb 1, 2024
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