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8 documents found
1: Title: L-GATOR: Genetic Association Testing for a Longitudinally Measured Quantitative Trait in Samples with Related Individuals.
Authors: Wu, Xiaowei, et.al. .
Journal: American journal of human genetics (Am J Hum Genet), Vol. 102 (4): 574-591, 2018 .
Snippet: Of the smallest p values, one-third occur in or near genes that have been previously identified as associated with pulse pressure (such as PIK3CG) and systolic and diastolic blood pressure (such as C10orf107), showing that L-GATOR is able to prioritize relevant loci in a genome screen.
Affiliation: Department of Statistics, The University of Chicago, Chicago, IL 60637, USA. Department of Statistics, The University of Chicago, Chicago, IL 60637, USA; Department of Human Genetics, The University of Chicago, Chicago, IL 60637, USA. Electronic address: mcpeek@uchicago.edu. .
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2: Title: Gene-by-Psychosocial Factor Interactions Influence Diastolic Blood Pressure in European and African Ancestry Populations: Meta-Analysis of Four Cohort Studies.
Authors: Smith, Jennifer A, et.al. .
Journal: International journal of environmental research and public health (Int J Environ Res Public Health), Vol. 14 (12), 2017 .
Snippet: In European ancestry participants, outward/trait anger score had a significant interaction with the C10orf107 genomic region (p = 0.0019).
Affiliation: Department of Epidemiology, School of Public Health, University of Michigan, Ann Arbor, MI 48109, USA. smjenn@umich.edu. Survey Research Center, Institute for Social Research, University of Michigan, Ann Arbor, MI 48104, USA. smjenn@umich.edu. Department of Epidemiology, School of Public Health, University of Michigan, Ann Arbor, MI 48109, USA. zhaowei@umich.edu. Department of Epidemiology, School of Public Health, University of Michigan, Ann Arbor, MI 48109, USA. kyasutak@umich.edu. Department of Epidemiology, School of Public Health, University of Michigan, Ann Arbor, MI 48109, USA. eaugust@umich.edu. Department of Epidemiology, School of Public Health, University of Michigan, Ann Arbor, MI 48109, USA. ratliffs@umich.edu. Survey Research Center, Institute for Social Research, University of Michigan, Ann Arbor, MI 48104, USA. jfaul@umich.edu. Department of Human Genetics and Institute of Molecular Medicine, University of Texas Health Science Center, Houston, TX 77030, USA. eric.boerwinkle@uth.tmc.edu. Center for Complex Disease Genomics, McKusick-Nathans Institute of Genetic Medicine, Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA. aravinda@jhmi.edu. Department of Epidemiology and Biostatistics, Dornsife School of Public Health, Drexel University, Philadelphia, PA 19104, USA. avd37@drexel.edu. Department of Physiology and Biophysics, University of Mississippi Medical Center, Jackson, MS 39216, USA. ygao@umc.edu. Department of Physiology and Biophysics, University of Mississippi Medical Center, Jackson, MS 39216, USA. griswold@umc.edu. Department of Epidemiology, Gillings School of Global Public Health, University of North Carolina, Chapel Hill, NC 27599, USA. gerardo_heiss@unc.edu. Department of Epidemiology, School of Public Health, University of Michigan, Ann Arbor, MI 48109, USA. skardia@umich.edu. Department of Epidemiology, Human Genetics and Environmental Sciences, School of Public Health, University of Texas Health Science Center at Houston, Houston, TX 77030, USA. alanna.c.morrison@uth.tmc.edu. Department of Medicine, University of Mississippi Medical Center, Jackson, MS 39216, USA. smusani@umc.edu. Jackson Heart Study, Jackson State University, Jackson, MS 39213, USA. smwasongwe@umc.edu. Department of Epidemiology, Gillings School of Global Public Health, University of North Carolina, Chapel Hill, NC 27599, USA. kari_north@unc.edu. Department of Epidemiology, Gillings School of Global Public Health, University of North Carolina, Chapel Hill, NC 27599, USA. kathryn_rose@unc.edu. Department of Medicine, University of Mississippi Medical Center, Jackson, MS 39216, USA. msims2@umc.edu. Department of Epidemiology, Rollins School of Public Health, Emory University, Atlanta, GA 30322, USA. yvsun@emory.edu. Survey Research Center, Institute for Social Research, University of Michigan, Ann Arbor, MI 48104, USA. dweir@umich.edu. Department of Epidemiology, School of Public Health, University of Michigan, Ann Arbor, MI 48109, USA. needhamb@umich.edu. .
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3: Title: Molecular characterization of the rare translocation t(3;10)(q26;q21) in an acute myeloid leukemia patient.
Authors: Jancuskova, Tereza, et.al. .
Journal: Molecular cytogenetics (Mol Cytogenet), Vol. 7, 2014 .
Snippet: RESULTS: Using a combination of cytogenetic and molecular approaches, we mapped the t(3;10)(q26;q21) to the single nucleotide level, revealing a fusion of the MECOM gene (3q26.2) and C10orf107 (10q21.2).
Affiliation: Laboratory for Molecular Diagnostics, synlab genetics s.r.o., Evropska 176/16, Prague 6 16000, Czech Republic. Department I of Internal Medicine, University at Cologne, Kerpener Str., Cologne, Germany. Oncological Therapy Center, Buchforststr., Cologne, Germany. Jena University Hospital, Institute of Human Genetics, Kollegiengasse 10, Jena, Germany. .
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4: Title: Proteomic analysis of the follicular fluid of Tianzhu white yak during diestrus.
Authors: Tao, Jinzhong, et.al. .
Journal: International journal of molecular sciences (Int J Mol Sci), Vol. 15 (3): 4481-91, 2014 .
Snippet: Fourteen of these spots were analyzed by MALDI-TOF/TOF-MS and identified as: AS3MT, VDP, ANKRD6, C10orf107 protein, MRP4, MAPKAP1, AGO3, profilin-β-actin, SPT2 homolog, AGP, AR, RNF20, obscurin-like-1, and one unnamed protein.
Affiliation: Agricultural College, Ningxia University, Yinchuan 750021, China. tao_jz@nxu.edu.cn. College of Veterinary Medicine, Gansu Agricultural University, Lanzhou 730070, China. zhaogs111@163.com. College of Veterinary Medicine, Gansu Agricultural University, Lanzhou 730070, China. zhaoxx@gsau.edu.cn. College of Animal Science and Technology, Gansu Agricultural University, Lanzhou 730070, China. lifd@gsau.edu.cn. College of Veterinary Medicine, Gansu Agricultural University, Lanzhou 730070, China. wx.258.h@st.gsau.edu.cn. College of Veterinary Medicine, Gansu Agricultural University, Lanzhou 730070, China. hujj@gsau.edu.cn. College of Veterinary Medicine, Gansu Agricultural University, Lanzhou 730070, China. zhychy@163.com. .
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5: Title: Genetic variation in CYP17A1 is associated with arterial stiffness in diabetic subjects.
Authors: Yang, Soo Jin, et.al. .
Journal: Experimental diabetes research (Exp Diabetes Res), Vol. 2012, 2012 .
Snippet: Out of the 52 SNPs analyzed, four SNPs including rs5326 (DRD1), rs1004467 (CYP17A1), rs2960306 (GRK4), and rs11191548 (near NT5C2) in diabetic subjects and rs1530440 (C10orf107) in prediabetic subjects showed a modest association with hypertension (P = 0.0265, 0.0020, 0.0066, 0.0078, and 0.0015, resp; all were insignificant after Bonferroni correction).
Affiliation: Department of Food and Nutrition, Chonnam National University, Gwangju, Republic of Korea. .
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6: Title: Genetic variations in the CYP17A1 and NT5C2 genes are associated with a reduction in visceral and subcutaneous fat areas in Japanese women.
Authors: Hotta, Kikuko, et.al. .
Journal: Journal of human genetics (J Hum Genet), Vol. 57 (1): 46-51, 2012 .
Snippet: We genotyped 1279 Japanese subjects (556 men and 723 women) who underwent computed tomography for measuring the visceral fat area (VFA) and subcutaneous fat area (SFA) at the following SNPs: FGF5 rs16998073, CACNB2 rs11014166, C10orf107 rs1530440, CYP17A1 rs1004467, NT5C2 rs11191548, PLEKHA7 rs381815, ATP2B1 rs2681472 and rs2681492, ARID3B rs6495112, CSK rs1378942, PLCD3 rs12946454, and ZNF652 rs16948048.
Affiliation: EBM Research Center, Kyoto University Graduate School of Medicine, Yoshida-Konoecho, Sakyo-ku, Kyoto, Japan. kikukoh@kuhp.kyoto-u.ac.jp .
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7: Title: Common variants in or near FGF5, CYP17A1 and MTHFR genes are associated with blood pressure and hypertension in Chinese Hans.
Authors: Liu, Chen, et.al. .
Journal: Journal of hypertension (J Hypertens), Vol. 29 (1): 70-5, 2011 .
Snippet: METHODS: We genotyped eight of these variants (in or near FGF5, CYP17A1, MTHFR, ZNF652, PLCD3, ATP2B1, c10orf107) in a population-based cohort of Chinese Hans (N = 3210).
Affiliation: Key Laboratory of Nutrition and Metabolism, Institute for Nutritional Sciences, Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences and Graduate School of Chinese Academy of Sciences, Shanghai, China. .
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8: Title: Genome-wide association study identifies eight loci associated with blood pressure.
Journal: Nature genetics (Nat Genet), Vol. 41 (6): 666-76, 2009 .
Snippet: We identified association between systolic or diastolic blood pressure and common variants in eight regions near the CYP17A1 (P = 7 × 10(-24)), CYP1A2 (P = 1 × 10(-23)), FGF5 (P = 1 × 10(-21)), SH2B3 (P = 3 × 10(-18)), MTHFR (P = 2 × 10(-13)), c10orf107 (P = 1 × 10(-9)), ZNF652 (P = 5 × 10(-9)) and PLCD3 (P = 1 × 10(-8)) genes.
Affiliation: Center for Human Genetic Research, Massachusetts General Hospital, Boston, Massachusetts, USA. cnewtoncheh@chgr.mgh.harvard.edu .
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