Human Genome Epidemiology Literature Finder
Primary Immune Deficiency Diseases
Records 1 - 30 (of 38 Records) |
Query Trace: Nijmegen Breakage Syndrome[original query] |
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Increased risk of gastrointestinal lymphoma in carriers of the 657del5 NBS1 gene mutation. International journal of cancer. Journal international du cancer 2006 Dec 119 (12): 2970-3. Steffen Jan, Maneva Galina, Pop?awska Lidia, Varon Raymonda, Mioduszewska Olga, Sperling Ka |
Regional distribution of heterozygous 657del5 mutation carriers of the NBS1 gene in Wielkopolska province (Poland). Journal of applied genetics 2006 47 (3): 269-72. Zió?kowska Iwona, Mosor Maria, Nowak Jer |
Polymorphisms and haplotypes of the NBS1 gene are associated with risk of sporadic breast cancer in non-Hispanic white women <or=55 years. Carcinogenesis 2006 Nov 27 (11): 2209-16. Lu Jiachun, Wei Qingyi, Bondy Melissa L, Li Donghui, Brewster Abenaa, Shete Sanjay, Yu Tse-Kuan, Sahin Aysegul, Meric-Bernstam Funda, Hunt Kelly K, Singletary S Eva, Ross Merrick I, Wang Li |
I171V germline mutation in the NBS1 gene significantly increases risk of breast cancer. Breast cancer research and treatment 2008 Jul 110 (2): 343-8. Roznowski Krzysztof, Januszkiewicz-Lewandowska Danuta, Mosor Maria, Pernak Monika, Litwiniuk Maria, Nowak Jer |
Role of MTHFR (677, 1298) haplotype in the risk of developing secondary leukemia after treatment of breast cancer and hematological malignancies. Leukemia 2007 Jul 21 (7): 1413-22. Guillem V M, Collado M, Terol M J, Calasanz M J, Esteve J, Gonzalez M, Sanzo C, Nomdedeu J, Bolufer P, Lluch A, Tormo |
Cancer risk of heterozygotes with the NBN founder mutation. Journal of the National Cancer Institute 2007 Dec 99 (24): 1875-80. Seemanová Eva, Jarolim Petr, Seeman Pavel, Varon Raymonda, Digweed Martin, Swift Michael, Sperling Ka |
Nijmegen Breakage Syndrome mutations and risk of breast cancer. International journal of cancer. Journal international du cancer 2008 Feb 122 (4): 802-6. Bogdanova Natalia, Feshchenko Sergei, Schürmann Peter, Waltes Regina, Wieland Britta, Hillemanns Peter, Rogov Yuri I, Dammann Olaf, Bremer Michael, Karstens Johann H, Sohn Christof, Varon Raymonda, Dörk Thi |
Mutations in the Nijmegen breakage syndrome gene in medulloblastomas. Clinical cancer research : an official journal of the American Association for Cancer Research 2008 Jul 14 (13): 4053-8. Huang Jian, Grotzer Michael A, Watanabe Takuya, Hewer Ekkehard, Pietsch Torsten, Rutkowski Stefan, Ohgaki Hiro |
Heterozygous carriers of the I171V mutation of the NBS1 gene have a significantly increased risk of solid malignant tumours. European journal of cancer (Oxford, England : 1990) 2008 Mar 44 (4): 627-30. Nowak Jerzy, Mosor Maria, Zió?kowska Iwona, Wierzbicka Malgorzta, Pernak-Schwarz Monika, Przyborska Marta, Roznowski Krzysztof, P?awski Andrzej, S?omski Ryszard, Januszkiewicz Danu |
Variations in the NBN/NBS1 gene and the risk of breast cancer in non-BRCA1/2 French Canadian families with high risk of breast cancer. BMC cancer 2009 9 (1): 181. Desjardins Sylvie, Beauparlant Joly Charles, Labrie Yvan, Ouellette Geneviève, Durocher Francine, |
NBN 657del5 heterozygous mutations and colorectal cancer risk in the Czech Republic. Mutation research 2009 Jun 666 (1-2): 64-7. Pardini Barbara, Naccarati Alessio, Polakova Veronika, Smerhovsky Zdenek, Hlavata Ivona, Soucek Pavel, Novotny Jan, Vodickova Ludmila, Tomanova Vera, Landi Stefano, Vodicka Pav |
Heterozygous germ-line mutations in the NBN gene predispose to medulloblastoma in pediatric patients. Acta neuropathologica 2010 Mar 119 (3): 325-34. Ciara El?bieta, Piekutowska-Abramczuk Dorota, Popowska Ewa, Grajkowska Wies?awa, Barszcz S?awomir, Perek Danuta, Dembowska-Bagi?ska Bo?enna, Perek-Polnik Marta, Kowalewska Ewa, Czaj?ska Aneta, Syczewska Ma?gorzata, Czornak Kamila, Krajewska-Walasek Ma?gorzata, Roszkowski Marcin, Chrzanowska Krystyna |
Mutational inactivation of the nijmegen breakage syndrome gene (NBS1) in glioblastomas is associated with multiple TP53 mutations. Journal of neuropathology and experimental neurology 2009 Feb 68 (2): 210-5. Watanabe Takuya, Nobusawa Sumihito, Lu Shengqing, Huang Jian, Mittelbronn Michel, Ohgaki Hiro |
High prevalence of the NBN gene mutation c.657-661del5 in Southeast Germany. Journal of applied genetics 2010 51 (2): 211-4. Maurer M H, Hoffmann K, Sperling K, Varon |
Role of 657del5 NBN mutation and 7p12.2 (IKZF1), 9p21 (CDKN2A), 10q21.2 (ARID5B) and 14q11.2 (CEBPE) variation and risk of childhood ALL in the Polish population. Leukemia research 2011 Nov 35 (11): 1534-6. Pastorczak Agata, Górniak Patryk, Sherborne Amy, Hosking Fay, Treli?ska Joanna, Lejman Monika, Szczepa?ski Tomasz, Borowiec Maciej, Fendler Wojciech, Kowalczyk Jerzy, Houlston Richard S, M?ynarski Wojcie |
[Heterozygous carriers of Slavic mutation 657del5 of NBN gene in patients with colorectal cancer]. Casopís lékar?? c?eských 2011 150 (2): 97-9. Seemanová Eva, Hoch Jirí, Seeman Pav |
Neonatal screening for severe primary immunodeficiency diseases using high-throughput triplex real-time PCR. Blood 2012 Mar 119 (11): 2552-5. Borte Stephan, von Döbeln Ulrika, Fasth Anders, Wang Ning, Janzi Magdalena, Winiarski Jacek, Sack Ulrich, Pan-Hammarström Qiang, Borte Michael, Hammarström Lenna |
[Study on the association between DNA double-strand break repair gene NBS1 polymorphisms and susceptibility on lung cancer]. Zhonghua liu xing bing xue za zhi = Zhonghua liuxingbingxue zazhi 2010 Feb 31 (2): 213-7. Fan Li-hui, Chen Jun-lei, Cai L |
Identification of a novel NBN truncating mutation in a family with hereditary prostate cancer. Familial cancer 2012 Aug . Zuhlke KA, Johnson AM, Okoth LA, Stoffel EM, Robbins CM, Tembe WA, Salinas CA, Zheng SL, Xu J, Carpten JD, Lange EM, Isaacs WB, Cooney KA |
Significant association between Nijmegen breakage syndrome 1 657del5 polymorphism and breast cancer risk. Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine 2013 Oct 34 (5): 2753-7. Zhang Guofeng, Zeng Yu, Liu Zhongyan, Wei Weiw |
Association between the NBS1 Glu185Gln polymorphism and breast cancer risk: a meta-analysis. Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine 2013 Feb . Yao F, Fang Y, Chen B, Jin F, Wang S |
Functional variants in NBS1 and cancer risk: evidence from a meta-analysis of 60 publications with 111 individual studies. Mutagenesis 2013 Nov 28 (6): 683-97. Gao Ping, Ma Ning, Li Man, Tian Qing-Bao, Liu Dian- |
Current evidence on the relationship between two polymorphisms in the NBS1 gene and breast cancer risk: a meta-analysis. Asian Pacific journal of cancer prevention : APJCP 2012 13 (11): 5375-9. Zhang Zhi-Hua, Yang Lin-Sheng, Huang Fen, Hao Jia-Hu, Su Pu-Yu, Sun Ye-Hu |
Association between the NBS1 Glu185Gln polymorphism and lung cancer risk: a systemic review and meta-analysis. Molecular biology reports 2013 Mar 40 (3): 2711-5. Wang Lixin, Cheng Jinsong, Gao Jinyu, Wang Jipeng, Liu Xiaoning, Xiong Liw |
Contribution of Double-strand Break Repair Gene Nijmegen Breakage Syndrome 1 Genotypes, Gender Difference and Smoking Status to Taiwanese Lung Cancer. Anticancer research 2017 05 37 (5): 2417-2423. Chuang Chin-Liang, Wang Chung-Hsing, Hsu Chang-Hsien, Hsiao Chieh-Lun, Chen Guan-Liang, Yen Shiou-Ting, Li Hsin-Ting, Chang Wen-Shin, Tsai Chia-Wen, Wang Shou-Cheng, Bau DA-Ti |
A non-synonymous polymorphism in NBS1 is associated with progression from chronic hepatitis B virus infection to hepatocellular carcinoma in a Chinese population. OncoTargets and therapy 2018 11 563-569. Zhen Ya'nan, Xiao Ruixue, Chen Xing, Yuan Changjin, Sun Yanlai, Li J |
NBS1 rs2735383 polymorphism is associated with an increased risk of laryngeal carcinoma. BMC cancer 2018 02 18 (1): 175. Hu Xinmei, Liao Juan, Zhao Huiliu, Chen Feng, Zhu Xuefeng, Li Jiangheng, Nong Qingqi |
Association of Single-Nucleotide Polymorphisms in Monoubiquitinated FANCD2-DNA Damage Repair Pathway Genes With Breast Cancer in the Chinese Population. Technology in cancer research & treatment 2018 Jan 17 1533033818819841. Chen Fei-Yu, Wang Hao, Li Hui, Hu Xue-Li, Dai Xu, Wang Shou-Man, Yan Guo-Jiao, Jiang Ping-Lan, Hu Yuan-Ping, Huang Juan, Tang Li- |
Association of Nijmegen Breakage Syndrome 1 Genotypes With Bladder Cancer Risk. Anticancer research 2020 Apr 40 (4): 2011-2017. Chen Meng, Chang Wen-Shin, Shen Te-Chun, Gong Chi-Li, Lin Meng-Liang, Wang Zhi-Hong, Wang Yun-Chi, Chen Chao-Hsuan, Wu Hsi-Chin, Bau DA-Tian, Tsai Chia-W |
Germline Genetic NBN Variation and Predisposition to B-cell Acute Lymphoblastic Leukemia in Children. Research square 2023 7 . Jun Yang, Carolin Escherich, Wenan Chen, Yizhen Li, Wenjian Yang, Rina Nishii, Zhenhua Li, Elizabeth Raetz, Meenakshi Devidas, Gang Wu, Kim Nichols, Hiroto Inaba, Ching-Hon Pui, Sima Jeha, Bruce Camitta, Eric Larsen, Stephen Hunger, Mignon L |
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- Page last updated:May 13, 2024
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