Zobrazeno 1 - 10
of 66
pro vyhledávání: '"G Devito"'
Autor:
Liani G. Devito, Eugénie S. Lim, Samuel M. O’Toole, Scott T.C. Shepherd, Daqi Deng, Hugang Feng, Taja Barber, William M. Drake, Samra Turajlic, Lyn Healy
Publikováno v:
Stem Cell Research, Vol 81, Iss , Pp 103611- (2024)
VHL disease is an inherited and autosomal dominant disorder affecting 1 in 36,0000 individuals worldwide. It is caused by von Hippel-Lindau (VHL) gene mutations and can affect both genders and all ethnic backgrounds (Nordstrom-O’Brien et al., 2009;
Externí odkaz:
https://doaj.org/article/a5c182d7d32646be97ee01377b0b973f
Autor:
Jessica Pawly, MD, Rachel H. Park, MD, Graham Grogan, Robert G. DeVito, MD, Brittany J. Behar, MD, John T. Stranix, MD
Publikováno v:
Plastic and Reconstructive Surgery, Global Open, Vol 12, Iss S6, Pp 7-8 (2024)
Externí odkaz:
https://doaj.org/article/8ae183f7ee6445e480db506051e2c36f
Autor:
Polliana Mendes Candia Scaffa, Alexander Kendall, Marcelo Yudi Icimoto, Ana Paula Piovezan Fugolin, Matthew G. Logan, Andre G. DeVito-Moraes, Steven H. Lewis, Hua Zhang, Hui Wu, Carmem S. Pfeifer
Publikováno v:
Scientific Reports, Vol 13, Iss 1, Pp 1-12 (2023)
Abstract Streptococcus mutans is the primary oral caries-forming bacteria, adept at producing “sticky” biofilms via the synthesis of insoluble extracellular polysaccharides (EPS), catalyzed by glucosyltransferases (GTFs). To circumvent the use of
Externí odkaz:
https://doaj.org/article/e5e55e63186740e78688ad3b0c9cf8b2
Autor:
Robert G. DeVito, MD, Benjamin G. Ke, BA;, Kristen L. Stephens, MD, Jesse Chou, MD;, Scott T. Hollenbeck, MD;, Chris A. Campbell, MD;, John T. Stranix, MD
Publikováno v:
Plastic and Reconstructive Surgery, Global Open, Vol 12, Iss S6, Pp 3-3 (2024)
Externí odkaz:
https://doaj.org/article/e16d7a9200a64d509546655c8add35d1
Autor:
Liani G. Devito, Zeinab Shadman Zanjani, James R. Evans, Annarita Scardamaglia, Henry Houlden, Sonia Gandhi, Lyn Healy
Publikováno v:
Stem Cell Research, Vol 71, Iss , Pp 103134- (2023)
Mutations or multiplications of the SNCA (Synuclein Alpha) gene cause rare autosomal dominant Parkinson’s disease (PD). The SNCA G51D missense mutation is associated with a synucleinopathy that shares PD and multiple system atrophy (MSA) characteri
Externí odkaz:
https://doaj.org/article/109104c721ef4032ad486c5484466892
Autor:
Rachel H. Park, MD, Robert G. Devito, MD, Jesse Chou, MD, Chris A. Campbell, MD, John T. Stranix, MD
Publikováno v:
Plastic and Reconstructive Surgery, Global Open, Vol 12, Iss 1S1, Pp 10-10 (2024)
Externí odkaz:
https://doaj.org/article/4e9c3be6d1194743bf5fed19c5c7254e
Publikováno v:
Plastic and Reconstructive Surgery, Global Open, Vol 12, Iss 1S1, Pp 8-8 (2024)
Externí odkaz:
https://doaj.org/article/90ac7c73fd684a65bf7bc76662b7ecef
Autor:
Robert G. Devito, MD, Kristen L. Stephens, MD, Scott Hollenbeck, MD, Chris A. Campbell, MD, John T. Stranix, MD
Publikováno v:
Plastic and Reconstructive Surgery, Global Open, Vol 12, Iss 1S1, Pp 29-29 (2024)
Externí odkaz:
https://doaj.org/article/f4fe0de3cbd84bc88c5bd634c1509804
Autor:
Liani G. Devito, Valentina M. Lionello, Francesco Muntoni, Francesco Saverio Tedesco, Lyn Healy
Publikováno v:
Stem Cell Research, Vol 69, Iss , Pp 103079- (2023)
Centronuclear myopathies (CNMs) are a group of inherited rare muscle disorders characterised by the abnormal position of the nucleus in the center of the muscle fiber. One of CNM is the X-Linked Myotubular Myopathy, caused by mutations in the myotubu
Externí odkaz:
https://doaj.org/article/cfaa9962540c4c82827e55ec27efcc0e
Publikováno v:
Plastic and Reconstructive Surgery, Global Open, Vol 11, Iss 4S, Pp 9-10 (2023)
Externí odkaz:
https://doaj.org/article/0ba1197d937543f3ab42f37b854be2d0