Zobrazeno 1 - 10
of 78
pro vyhledávání: '"P. J., Cozzone"'
Autor:
Nithin R. Iyer, Siew-Pang Chan, Oi Wah Liew, Jenny P.C. Chong, Jennifer A. Bryant, Thu-Thao Le, Chanchal Chandramouli, Patrick J. Cozzone, Frank Eisenhaber, Roger Foo, A. Mark Richards, Carolyn S.P. Lam, Martin Ugander, Calvin W-L. Chin, on behalf of the ATTRaCT investigators
Publikováno v:
BMC Cardiovascular Disorders, Vol 24, Iss 1, Pp 1-13 (2024)
Abstract Background Heart failure (HF) and diabetes are associated with increased incidence and worse prognosis of each other. The prognostic value of global longitudinal strain (GLS) measured by cardiovascular magnetic resonance (CMR) has not been e
Externí odkaz:
https://doaj.org/article/50c9a119501141aaba899532f7f7c77d
Autor:
Christopher J. Charles, Philip Lee, Renee R. Li, Teresa Yeung, Stephane M. Ibraham Mazlan, Zhi Wei Tay, Desiree Abdurrachim, Xing Qi Teo, Wei‐Hsin Wang, Dominique P.V. deKleijn, Patrick J. Cozzone, Carolyn S.P. Lam, A. Mark Richards
Publikováno v:
ESC Heart Failure, Vol 7, Iss 1, Pp 93-103 (2020)
Abstract Aims A significant proportion of heart failure (HF) patients have HF preserved ejection fraction (HFpEF). The lack of effective treatments for HFpEF remains a critical unmet need. A key obstacle to therapeutic innovation in HFpEF is the pauc
Externí odkaz:
https://doaj.org/article/b620b2bfbc6140a1966ee714e67936b8
Autor:
Meriam Koob, Angèle Viola, Yann Le Fur, Patrick Viout, Hélène Ratiney, Sylviane Confort-Gouny, Patrick J Cozzone, Nadine Girard
Publikováno v:
PLoS ONE, Vol 11, Iss 8, p e0160990 (2016)
Preterm birth represents a high risk of neurodevelopmental disabilities when associated with white-matter damage. Recent studies have reported cognitive deficits in children born preterm without brain injury on MRI at term-equivalent age. Understandi
Externí odkaz:
https://doaj.org/article/1871dd1c982b45e3b0e5e858f4f75f8e
Publikováno v:
PLoS ONE, Vol 11, Iss 8, p e0161803 (2016)
We present a pilot study aimed at determining the effects of expression of ATP-binding cassette member B5 (ABCB5), a previously described marker for melanoma-initiating cells, on cellular metabolism. Metabolic profiles for two groups of human G3361 m
Externí odkaz:
https://doaj.org/article/d15fc8a521b9413abbe4251d530c8c8e
Autor:
Alain J Cozzone
Publikováno v:
Emerging Microbes and Infections, Vol 1, Iss 1, Pp 1-3 (2012)
Emerging Microbes & Infections (2012) 1, e38; doi:10.1038/emi.2012.35
Externí odkaz:
https://doaj.org/article/c163c7b1528849769bf56015132ad832
Autor:
Charlotte Gineste, Coen Ottenheijm, Yann Le Fur, Sébastien Banzet, Emilie Pecchi, Christophe Vilmen, Patrick J Cozzone, Nathalie Koulmann, Edna C Hardeman, David Bendahan, Julien Gondin
Publikováno v:
PLoS ONE, Vol 9, Iss 9, p e109066 (2014)
Nemaline myopathy is the most common disease entity among non-dystrophic skeletal muscle congenital diseases. The first disease causing mutation (Met9Arg) was identified in the gene encoding α-tropomyosin slow gene (TPM3). Considering the conflictin
Externí odkaz:
https://doaj.org/article/b32b4c15c7ce415da68396d55d8cb58a
Publikováno v:
PLoS ONE, Vol 8, Iss 2, p e56101 (2013)
Many diseases, including brain disorders, are associated with perturbations of tissue metabolism. However, an often overlooked issue is the impact that inflammations outside the brain may have on brain metabolism. Our main goal was to study similarit
Externí odkaz:
https://doaj.org/article/09ce55bc1ba34f86a2655cf97ef28d55
Autor:
Charlotte Gineste, Yann Le Fur, Christophe Vilmen, Arnaud Le Troter, Emilie Pecchi, Patrick J Cozzone, Edna C Hardeman, David Bendahan, Julien Gondin
Publikováno v:
PLoS ONE, Vol 8, Iss 4, p e61517 (2013)
Nemaline myopathy (NM) is the most common disease entity among non-dystrophic skeletal muscle congenital diseases. Mutations in the skeletal muscle α-actin gene (ACTA1) account for ∼25% of all NM cases and are the most frequent cause of severe for
Externí odkaz:
https://doaj.org/article/15dfb273180c41c6a596155050b68a20
Autor:
Charlotte Gineste, Guillaume Duhamel, Yann Le Fur, Christophe Vilmen, Patrick J Cozzone, Kristen J Nowak, David Bendahan, Julien Gondin
Publikováno v:
PLoS ONE, Vol 8, Iss 8, p e72294 (2013)
Nemaline myopathy (NM), the most common non-dystrophic congenital disease of skeletal muscle, can be caused by mutations in the skeletal muscle α-actin gene (ACTA1) (~25% of all NM cases and up to 50% of severe forms of NM). Muscle function of the r
Externí odkaz:
https://doaj.org/article/adbb7b1661c64ab388f04b42da99d788
Publikováno v:
PLoS ONE, Vol 7, Iss 12, p e53266 (2012)
Cerebral stroke is a worldwide leading cause of disability. The two-pore domain K⁺ channels identified as background channels are involved in many functions in brain under physiological and pathological conditions. We addressed the hypothesis that
Externí odkaz:
https://doaj.org/article/7f1ffef68a5f48fea51efd0ad2205b78