Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Dominic E Fullenkamp"'
Autor:
Dominic E. Fullenkamp, Alexander B. Willis, Jodi L. Curtin, Ansel P. Amaral, Kyle T. Dittloff, Sloane I. Harris, Ivana A. Chychula, Cory W. Holgren, Paul W. Burridge, Brenda Russell, Alexis R. Demonbreun, Elizabeth M. McNally
Publikováno v:
Disease Models & Mechanisms, Vol 17, Iss 6 (2024)
Externí odkaz:
https://doaj.org/article/b52a5eadd7514af8ba2316e6c7190c6b
Autor:
Dominic E Fullenkamp, Alexander B Willis, Jodi L Curtin, Ansel P Amaral, Sloane I Harris, Paul W Burridge, Alexis R Demonbreun, Elizabeth M McNally
Publikováno v:
Circulation Research. 131
Background: Cardiomyopathy in Duchenne muscular dystrophy (DMD) is a significant driver of disease morbidity and mortality. Induced pluripotent stem cell-derived cardiomyocytes (iPSC-CMs) offer the opportunity to study patient-specific mutations in t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c929ce93c157757ca9ef235a9913a72d
https://doi.org/10.1161/res.131.suppl_1.p2107
https://doi.org/10.1161/res.131.suppl_1.p2107
Autor:
Dominic E. Fullenkamp, Alexander B. Willis, Jodi L. Curtin, Ansel P. Amaral, Sloane I. Harris, Paul W. Burridge, Alexis R. Demonbreun, Elizabeth M. McNally
Heart failure is a major source of mortality in Duchenne muscular dystrophy (DMD). DMD arises from mutations that ablate expression of the protein dystrophin, which render the plasma membrane unusually fragile and prone to disruption. In DMD patients
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ad323fe2e09b77ab48e4e7a45ba1faa6
https://doi.org/10.1101/2022.03.09.483528
https://doi.org/10.1101/2022.03.09.483528
Autor:
Sloane I Harris, Paul W. Burridge, Ansel P Amaral, Elizabeth M. McNally, Alexis R. Demonbreun, Jodi L Curtin, Dominic E. Fullenkamp
Publikováno v:
Circulation Research. 129
Heart failure is leading cause of morbidity and mortality in the X-linked disease Duchenne muscular dystrophy (DMD). DMD is due to mutations the gene encoding dystrophin. Dystrophin localizes to the costamere in skeletal and cardiac muscle and is par
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fbafe85ff8cdb642cfe56416d3fd830b
https://doi.org/10.1161/res.129.suppl_1.p343
https://doi.org/10.1161/res.129.suppl_1.p343
Publikováno v:
Eur Heart J
AIMS : Our objective was to better understand the genetic bases of dilated cardiomyopathy (DCM), a leading cause of systolic heart failure. METHODS AND RESULTS : We conducted the largest genome-wide association study performed so far in DCM, with 271
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::39423b5cf0b16e30a972a46652757a9f
https://pubmed.ncbi.nlm.nih.gov/33677556
https://pubmed.ncbi.nlm.nih.gov/33677556
Autor:
Elizabeth M. McNally, Megan J. Puckelwartz, Tess D. Pottinger, Anthony Gacita, Dominic E. Fullenkamp, Joyce C. Ohiri, Marcelo A. Nobrega
Publikováno v:
Circulation
Background: Inherited cardiomyopathy associates with a range of phenotypes, mediated by genetic and nongenetic factors. Noninherited cardiomyopathy also displays varying progression and outcomes. Expression of cardiomyopathy genes is under the regula
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c3ef6196ef3553472af399d7f7e88612
https://pubmed.ncbi.nlm.nih.gov/33542520
https://pubmed.ncbi.nlm.nih.gov/33542520
Autor:
Marcello A Nobrega, Dominic E. Fullenkamp, Joyce C. Ohiri, Tess D. Pottinger, Anthony Gacita, Megan J. Puckelwartz, Elizabeth M. McNally
Publikováno v:
Circulation. 142
Introduction: Inherited cardiomyopathy is caused by mutations in more than 100 genes. A well-recognized clinical feature of genetic cardiomyopathy is varying phenotypic expression. Even with identical primary mutations, there is a range of clinical o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1e3f53d70d62e8d0839d6141db810114
https://doi.org/10.1161/circ.142.suppl_3.14308
https://doi.org/10.1161/circ.142.suppl_3.14308
Autor:
Niels Holten-Andersen, Gareth H. McKinley, Aditya Jaishankar, Lihong He, Genevieve DiMarco, Phillip B. Messersmith, Ka Yee C. Lee, Dominic E. Fullenkamp, Matthew J. Harrington
Publikováno v:
Journal of materials chemistry. B, vol 2, iss 17
MIT web domain
Journal of Materials Chemistry B
MIT web domain
Journal of Materials Chemistry B
Growing evidence supports a critical role of dynamic metal-coordination crosslinking in soft biological material properties such as self-healing and underwater adhesion. Using bio-inspired metal-coordinating polymers, initial efforts to mimic these p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7a25b28d29fb85904d52d1b027831f93
https://doi.org/10.1039/c3tb21374a
https://doi.org/10.1039/c3tb21374a
Autor:
Dominic E. Fullenkamp, Dusty R. Miller, Devin G. Barrett, Phillip B. Messersmith, Josh W. Kurutz
Publikováno v:
RSC Adv.. 4:25127-25134
The mussel byssus is a remarkable attachment structure that is formed by injection molding and rapid in situ hardening of concentrated solutions of proteins enriched in the catecholic amino acid 3,4-dihydroxy-L-phenylalanine (DOPA). Fe3+, found in hi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1dfa19ad796ce5c7004e37ac6d524fe7
https://doi.org/10.1039/c4ra03178d
https://doi.org/10.1039/c4ra03178d
Autor:
Lihong He, Wesley R. Burghardt, Phillip B. Messersmith, Dominic E. Fullenkamp, Devin G. Barrett
Publikováno v:
Macromolecules. 46:1167-1174
Transient network hydrogels cross-linked through histidine-divalent cation coordination bonds were studied by conventional rheologic methods using histidine-modified star poly(ethylene glycol) (PEG) polymers. These materials were inspired by the muss
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ea6e4f2fdf7db1b7e6e61f2069bdb455
https://doi.org/10.1021/ma301791n
https://doi.org/10.1021/ma301791n