Zobrazeno 1 - 10
of 675
pro vyhledávání: '"Bracken Michael B"'
Autor:
DeWan Andrew T, Egan Kathryn Brigham, Hellenbrand Karen, Sorrentino Keli, Pizzoferrato Nicole, Walsh Kyle M, Bracken Michael B
Publikováno v:
BMC Medical Genetics, Vol 13, Iss 1, p 95 (2012)
Abstract Background Despite the success of genome-wide association studies for asthma, few, if any, definitively causal variants have been identified and there is still a substantial portion of the heritability of the disease yet to be discovered. So
Externí odkaz:
https://doaj.org/article/2ef2cd0b4d93493ab1d1460d65e2dd12
Autor:
Jacobs Daniel I, Bracken Michael B
Publikováno v:
BMC Medical Genetics, Vol 13, Iss 1, p 97 (2012)
Abstract Background The x-ray cross complementing group 1 gene (XRCC1) is crucial to proper repair of DNA damage such as single-strand DNA breaks. A non-synonymous polymorphism in XRCC1, 399 G → A, has been shown to reduce effectiveness of such DNA
Externí odkaz:
https://doaj.org/article/40762fb125794d05ba769873f4c67d8b
Autor:
Zhao Linlu, Triche Elizabeth W, Walsh Kyle M, Bracken Michael B, Saftlas Audrey F, Hoh Josephine, Dewan Andrew T
Publikováno v:
BMC Pregnancy and Childbirth, Vol 12, Iss 1, p 61 (2012)
Abstract Background Specific genetic contributions for preeclampsia (PE) are currently unknown. This genome-wide association study (GWAS) aims to identify maternal single nucleotide polymorphisms (SNPs) and copy-number variants (CNVs) involved in the
Externí odkaz:
https://doaj.org/article/138c3082c6534fcaab2fbbf529a1cdce
Autor:
Sordillo Joanne E, Sharma Sunita, Poon Audrey, Lasky-Su Jessica, Belanger Kathleen, Milton Donald K, Bracken Michael B, Triche Elizabeth W, Leaderer Brian P, Gold Diane R, Litonjua Augusto A
Publikováno v:
BMC Medical Genetics, Vol 12, Iss 1, p 158 (2011)
Abstract Background Polymorphisms in the endotoxin-mediated TLR4 pathway genes have been associated with asthma and atopy. We aimed to examine how genetic polymorphisms in innate immunity pathways interact with endotoxin to influence asthma risk in c
Externí odkaz:
https://doaj.org/article/13574fe7d36f49c29e57f82ee5333afb
Autor:
Bracken Michael B, Zhao Linlu
Publikováno v:
BMC Medical Genetics, Vol 12, Iss 1, p 93 (2011)
Abstract Background Asthma is a phenotypically diverse disease with genetic susceptibility. A single nucleotide polymorphism (SNP) in the CD14 gene at position -260 (also known as -159) C>T has been inconsistently associated with asthma. The aim of t
Externí odkaz:
https://doaj.org/article/a1fd8424421c4cfcaa0059f74b6a8581
Autor:
Bracken Michael B, Holford Theodore R, Belanger Kathleen D, Triche Elizabeth W, Zhu Yong, Gent Janneane F, Pettigrew Melinda M, Leaderer Brian P
Publikováno v:
BMC Medical Genetics, Vol 8, Iss 1, p 15 (2007)
Abstract Background We examined the association between single nucleotide polymorphisms (SNPs) in loci encoding surfactant protein A (SFTPA) and risk of wheeze and persistent cough during the first year of life among a cohort of infants at risk for d
Externí odkaz:
https://doaj.org/article/72b84bf6d9bb47f69f0b83078e9ac96c
Autor:
Bracken Michael B, Holford Theodore R, Belanger Kathleen D, Triche Elizabeth W, Zhu Yong, Gent Janneane F, Pettigrew Melinda M, Leaderer Brian P
Publikováno v:
BMC Medical Genetics, Vol 7, Iss 1, p 68 (2006)
Abstract Background Otitis media is one of the most common infections of early childhood. Surfactant protein A functions as part of the innate immune response, which plays an important role in preventing infections early in life. This prospective stu
Externí odkaz:
https://doaj.org/article/0beba867d06f496c8ddeec5f0853ba1f
Autor:
Wallach, Joshua D, Wang, Kun, Zhang, Audrey D, Cheng, Deanna, Nardini, Holly K Grossetta, Lin, Haiqun, Bracken, Michael B, Desai, Mayur, Krumholz, Harlan M, Ross, Joseph S
Publikováno v:
BMJ: British Medical Journal, 2020 Feb 01. 368, 1-19.
Externí odkaz:
https://www.jstor.org/stable/27232746
Autor:
Gatto, Nicolle M., Bracken, Michael B., Kolitsopoulos, Francesca, Duggan, William T., Koch, Gary G., Wise, Robert A., Jackson, Neville C.
Publikováno v:
In Contemporary Clinical Trials Communications June 2020 18