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Page 1
Postmortem Genetic Testing for Cardiac Ion Channelopathies in Stillbirths.
Munroe PB, Addison S, Abrams DJ, Sebire NJ, Cartwright J, Donaldson I, Cohen MM, Mein C, Tinker A, Harmer SC, Aziz Q, Terry A, Struebig M, Warren HR, Vadgama B, Fowler DJ, Peebles D, Taylor AM, Lally PJ, Thayyil S. Munroe PB, et al. Among authors: mein c. Circ Genom Precis Med. 2018 Jan;11(1):e001817. doi: 10.1161/CIRCGEN.117.001817. Epub 2018 Jan 11. Circ Genom Precis Med. 2018. PMID: 29874177 Free article.
High quality genomic DNA extraction from postmortem fetal tissue.
Addison S, Sebire NJ, Taylor AM, Abrams D, Peebles D, Mein C, Munroe PB, Thayyil S. Addison S, et al. Among authors: mein c. J Matern Fetal Neonatal Med. 2012 Nov;25(11):2467-9. doi: 10.3109/14767058.2012.704442. Epub 2012 Jul 5. J Matern Fetal Neonatal Med. 2012. PMID: 22765762 Free article.
Selection of candidate genes in hypertension.
Mein CA, Caulfield MJ, Munroe PB. Mein CA, et al. Methods Mol Med. 2005;108:107-29. doi: 10.1385/1-59259-850-1:107. Methods Mol Med. 2005. PMID: 16028679
Genetics of essential hypertension.
Mein CA, Caulfield MJ, Dobson RJ, Munroe PB. Mein CA, et al. Hum Mol Genet. 2004 Apr 1;13 Spec No 1:R169-75. doi: 10.1093/hmg/ddh078. Epub 2004 Feb 5. Hum Mol Genet. 2004. PMID: 14764624 Review.
Single-Cell Expression Profiling Reveals a Dynamic State of Cardiac Precursor Cells in the Early Mouse Embryo.
Kokkinopoulos I, Ishida H, Saba R, Ruchaya P, Cabrera C, Struebig M, Barnes M, Terry A, Kaneko M, Shintani Y, Coppen S, Shiratori H, Ameen T, Mein C, Hamada H, Suzuki K, Yashiro K. Kokkinopoulos I, et al. Among authors: mein c. PLoS One. 2015 Oct 15;10(10):e0140831. doi: 10.1371/journal.pone.0140831. eCollection 2015. PLoS One. 2015. PMID: 26469858 Free PMC article.
Haplotypes of the WNK1 gene associate with blood pressure variation in a severely hypertensive population from the British Genetics of Hypertension study.
Newhouse SJ, Wallace C, Dobson R, Mein C, Pembroke J, Farrall M, Clayton D, Brown M, Samani N, Dominiczak A, Connell JM, Webster J, Lathrop GM, Caulfield M, Munroe PB. Newhouse SJ, et al. Among authors: mein c. Hum Mol Genet. 2005 Jul 1;14(13):1805-14. doi: 10.1093/hmg/ddi187. Epub 2005 May 11. Hum Mol Genet. 2005. PMID: 15888480
Differences between disease-associated endoplasmic reticulum aminopeptidase 1 (ERAP1) isoforms in cellular expression, interactions with tumour necrosis factor receptor 1 (TNF-R1) and regulation by cytokines.
Yousaf N, Low WY, Onipinla A, Mein C, Caulfield M, Munroe PB, Chernajovsky Y. Yousaf N, et al. Among authors: mein c. Clin Exp Immunol. 2015 May;180(2):289-304. doi: 10.1111/cei.12575. Clin Exp Immunol. 2015. PMID: 25545008 Free PMC article. Clinical Trial.
Increased support for linkage of a novel locus on chromosome 5q13 for essential hypertension in the British Genetics of Hypertension Study.
Munroe PB, Wallace C, Xue MZ, Marçano AC, Dobson RJ, Onipinla AK, Burke B, Gungadoo J, Newhouse SJ, Pembroke J, Brown M, Dominiczak AF, Samani NJ, Lathrop M, Connell J, Webster J, Clayton D, Farrall M, Mein CA, Caulfield M; Medical Research Council British Genetics of Hypertension Study. Munroe PB, et al. Among authors: mein ca. Hypertension. 2006 Jul;48(1):105-11. doi: 10.1161/01.HYP.0000228324.74255.f1. Epub 2006 Jun 5. Hypertension. 2006. PMID: 16754790
Linkage analysis using co-phenotypes in the BRIGHT study reveals novel potential susceptibility loci for hypertension.
Wallace C, Xue MZ, Newhouse SJ, Marcano AC, Onipinla AK, Burke B, Gungadoo J, Dobson RJ, Brown M, Connell JM, Dominiczak A, Lathrop GM, Webster J, Farrall M, Mein C, Samani NJ, Caulfield MJ, Clayton DG, Munroe PB. Wallace C, et al. Among authors: mein c. Am J Hum Genet. 2006 Aug;79(2):323-31. doi: 10.1086/506370. Epub 2006 Jun 19. Am J Hum Genet. 2006. PMID: 16826522 Free PMC article.
156 results