Zobrazeno 1 - 10
of 82
pro vyhledávání: '"Diane M Dunn"'
Publikováno v:
PLoS ONE, Vol 12, Iss 4, p e0175367 (2017)
Nicotine modulates multiple inflammatory responses in the lung through the nicotinic acetylcholine receptor subtype alpha7 (α7). Previously we reported that α7 modulates both the hematopoietic and epithelium responses in the lung to the bacterial i
Externí odkaz:
https://doaj.org/article/6184f33eb6f34ec1bbc690dc3c8a6092
Autor:
Russell J Butterfield, Diane M Dunn, Ying Hu, Kory Johnson, Carsten G Bönnemann, Robert B Weiss
Publikováno v:
PLoS ONE, Vol 12, Iss 12, p e0189664 (2017)
The collagen VI related muscular dystrophies (COL6-RD), Ullrich congenital muscular dystrophy (UCMD) and Bethlem myopathy (BM) are among the most common congenital muscular dystrophies and are characterized by distal joint laxity and a combination of
Externí odkaz:
https://doaj.org/article/9aa99d0d1f1e4d13b736b141104e6446
Publikováno v:
PLoS ONE, Vol 12, Iss 11, p e0187773 (2017)
Cigarette smoking (CS) is a principal contributor to a spectrum of devastating lung diseases whose occurrence and severity may vary between individuals and not appear for decades after prolonged use. One explanation for the variability and delay in d
Externí odkaz:
https://doaj.org/article/b0fc045f62d24e86b4f4c7e7116b8bf0
Autor:
Martin Kaltenpoth, Patrice Showers Corneli, Diane M Dunn, Robert B Weiss, Erhard Strohm, Jon Seger
Publikováno v:
PLoS ONE, Vol 7, Iss 3, p e32826 (2012)
Mitochondrial genes in animals are especially useful as molecular markers for the reconstruction of phylogenies among closely related taxa, due to the generally high substitution rates. Several insect orders, notably Hymenoptera and Phthiraptera, sho
Externí odkaz:
https://doaj.org/article/057985acbcfa43478ce8e99a0bed5b3f
Autor:
Adam L Clayton, Kelly F Oakeson, Maria Gutin, Arthur Pontes, Diane M Dunn, Andrew C von Niederhausern, Robert B Weiss, Mark Fisher, Colin Dale
Publikováno v:
PLoS Genetics, Vol 8, Iss 11, p e1002990 (2012)
Despite extensive study, little is known about the origins of the mutualistic bacterial endosymbionts that inhabit approximately 10% of the world's insects. In this study, we characterized a novel opportunistic human pathogen, designated "strain HS,"
Externí odkaz:
https://doaj.org/article/f884926eb7494eab953cdb9c02b129ad
Autor:
Robert B Weiss, Timothy B Baker, Dale S Cannon, Andrew von Niederhausern, Diane M Dunn, Nori Matsunami, Nanda A Singh, Lisa Baird, Hilary Coon, William M McMahon, Megan E Piper, Michael C Fiore, Mary Beth Scholand, John E Connett, Richard E Kanner, Lorise C Gahring, Scott W Rogers, John R Hoidal, Mark F Leppert
Publikováno v:
PLoS Genetics, Vol 4, Iss 7, p e1000125 (2008)
People who begin daily smoking at an early age are at greater risk of long-term nicotine addiction. We tested the hypothesis that associations between nicotinic acetylcholine receptor (nAChR) genetic variants and nicotine dependence assessed in adult
Externí odkaz:
https://doaj.org/article/967db3d79cd44178b104b1f07b91bd4b
Publikováno v:
bioRxiv
Fascioscapulohumeral muscular dystrophy (FSHD) is caused by a unique genetic mechanism that relies on contraction and hypomethylation of the D4Z4 macrosatellite array on the chromosome 4q telomere allowing ectopic expression of theDUX4gene in skeleta
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a2f5fb623d8296a2d98f90906076e46d
https://europepmc.org/articles/PMC9949141/
https://europepmc.org/articles/PMC9949141/
Autor:
Megan A. Waldrop, Steven A. Moore, Katherine D. Mathews, Benjamin W. Darbro, Livja Medne, Richard Finkel, Anne M. Connolly, Thomas O. Crawford, Daniel Drachman, Nicolas Wein, Ali A. Habib, Monika A. Krzesniak‐Swinarska, Craig M. Zaidman, James J. Collins, Manu Jokela, Bjarne Udd, John W. Day, Gloria Ortiz‐Guerrero, Jeff Statland, Russell J. Butterfield, Diane M. Dunn, Robert B. Weiss, Kevin M. Flanigan
Publikováno v:
Hum Mutat
Human mutation, vol 43, iss 4
Human mutation, vol 43, iss 4
DMD pathogenic variants for Duchenne and Becker muscular dystrophy are detectable with high sensitivity by standard clinical exome analyses of genomic DNA. However, up to 7% of DMD mutations are deep intronic and analysis of muscle-derived RNA is an
Autor:
Roxane Alles, Veronica J. Vieland, Robert B. Weiss, Megan A. Waldrop, John Burian, Paul T. Martin, Kevin M. Flanigan, Sang-Cheol Seok, Diane M. Dunn, Melissa Moore-Clingenpeel, Lindsay N. Alfano, Tabatha R. Simmons
The major determinant of disease severity in patients with severe Duchenne muscular dystrophy (DMD) or milder Becker muscular dystrophy (BMD) is whether their dystrophin gene (DMD) mutation disrupts the mRNA reading frame or allows expression of a pa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::09b1f6360f4a63fecf3342e07518ca40
https://doi.org/10.1101/2021.11.03.21265887
https://doi.org/10.1101/2021.11.03.21265887
Autor:
John Burian, Lindsay N. Alfano, Tabatha R. Simmons, Roxane Alles, Robert B. Weiss, Melissa Moore-Clingenpeel, Diane M. Dunn, Sang-Cheol Seok, Kevin M. Flanigan, Veronica J. Vieland, Paul T. Martin, Megan A. Waldrop
Although the major determinant of disease severity in patients with severe Duchenne muscular dystrophy (DMD) or milder Becker muscular dystrophy (BMD) is whether their dystrophin gene (DMD) mutation disrupts the mRNA reading frame or allows expressio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1bf8e8ccebe283ed9b7285e320376e61
https://doi.org/10.1101/2021.11.03.21265899
https://doi.org/10.1101/2021.11.03.21265899