Human Genome Epidemiology Literature Finder
Records 1 - 10 (of 10 Records) |
Query Trace: BMP1[original query] |
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Somatic frameshift mutations of bone morphogenic protein receptor 2 gene in gastric and colorectal cancers with microsatellite instability. APMIS : acta pathologica, microbiologica, et immunologica Scandinavica 2010 Nov 118 (11): 824-9. Park Sang Wook, Hur Soo Young, Yoo Nam Jin, Lee Sug Hyu |
Genetic variation in the transforming growth factor-ß signaling pathway and survival after diagnosis with colon and rectal cancer. Cancer 2011 Sep 117 (18): 4175-83. Slattery Martha L, Lundgreen Abbie, Herrick Jennifer S, Wolff Roger K, Caan Bette |
Genetic variation in bone morphogenetic protein and colon and rectal cancer. International journal of cancer. Journal international du cancer 2012 Feb 130 (3): 653-64. Slattery Martha L, Lundgreen Abbie, Herrick Jennifer S, Kadlubar Susan, Caan Bette J, Potter John D, Wolff Roger |
Genetic variation in bone morphogenetic proteins and breast cancer risk in hispanic and non-hispanic white women: The breast cancer health disparities study. International journal of cancer. Journal international du cancer 2012 Nov . Slattery ML, John EM, Torres-Mejia G, Herrick JS, Giuliano AR, Baumgartner KB, Hines LM, Wolff RK |
A Candidate-Pathway Approach to Identify Gene-Environment Interactions: Analyses of Colon Cancer Risk and Survival. Journal of the National Cancer Institute 2015 Sep 107 (9): . Sharafeldin Noha, Slattery Martha L, Liu Qi, Franco-Villalobos Conrado, Caan Bette J, Potter John D, Yasui Yuta |
Integrative functional genomics identifies regulatory mechanisms at coronary artery disease loci. Nature communications 2016 7 12092. Miller Clint L, Pjanic Milos, Wang Ting, Nguyen Trieu, Cohain Ariella, Lee Jonathan D, Perisic Ljubica, Hedin Ulf, Kundu Ramendra K, Majmudar Deshna, Kim Juyong B, Wang Oliver, Betsholtz Christer, Ruusalepp Arno, Franzén Oscar, Assimes Themistocles L, Montgomery Stephen B, Schadt Eric E, Björkegren Johan L M, Quertermous Thom |
BMP1 5'UTR?+?104 T/C gene variation: can be a predictive marker for serum HDL and apoprotein A1 levels in male patients with coronary heart disease. Molecular biology reports 2018 Jul . Akadam-Teker Basak, Ozkara Gulcin, Kurnaz-Gomleksiz Ozlem, Bugra Zehra, Teker Erhan, Ozturk Oguz, Yilmaz-Aydogan Hul |
Genotype-phenotype correlation among Malaysian patients with osteogenesis imperfecta. Clinica chimica acta; international journal of clinical chemistry 2018 5 484 141-147. Mohd Nawawi Nadiah, Selveindran Nalini M, Rasat Rahmah, Chow Yock Ping, Abdul Latiff Zarina, Syed Zakaria Syed Zulkifli, Jamal Rahman, Abdul Murad Nor Azian, Abd Aziz Bilkis Ba |
Diagnostic strategies and genotype-phenotype correlation in a large Indian cohort of osteogenesis imperfecta. Bone 2018 3 110 368-377. Mrosk Julia, Bhavani Gandham SriLakshmi, Shah Hitesh, Hecht Jochen, Krüger Ulrike, Shukla Anju, Kornak Uwe, Girisha Katta Moh |
High bone mass phenotype in a cohort of patients with Osteogenesis Imperfecta caused due to BMP1 and C-propeptide cleavage variants in COL1A1. Bone reports 2021 7 15 101102. Campanini E H, Baker D, Arundel P, Bishop N J, Offiah A C, Keigwin S, Cadden S, Dall'Ara E, Nicolaou N, Giles S, Fernandes J A, Balasubramanian |
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