Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Claire E P Smith"'
Autor:
Amit Kumar, Claire E P Smith, Elena E Giorgi, Joshua Eudailey, David R Martinez, Karina Yusim, Ayooluwa O Douglas, Lisa Stamper, Erin McGuire, Celia C LaBranche, David C Montefiori, Genevieve G Fouda, Feng Gao, Sallie R Permar
Publikováno v:
PLoS Pathogens, Vol 14, Iss 4, p e1006944 (2018)
Despite extensive genetic diversity of HIV-1 in chronic infection, a single or few maternal virus variants become the founders of an infant's infection. These transmitted/founder (T/F) variants are of particular interest, as a maternal or infant HIV
Externí odkaz:
https://doaj.org/article/1e3c487738a1442f80d4b880441b3f66
Autor:
Benjamin McClinton, Laura A. Crinnion, Martin McKibbin, Rajarshi Mukherjee, James A. Poulter, Claire E. L. Smith, Manir Ali, Christopher M. Watson, Chris F. Inglehearn, Carmel Toomes
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 11, Iss 6, Pp n/a-n/a (2023)
Abstract Background The widespread adoption of exome sequencing has greatly increased the rate of genetic diagnosis for inherited conditions. However, the detection and validation of large deletions remains challenging. While numerous bioinformatics
Externí odkaz:
https://doaj.org/article/30974ac5421d42c3bd08091e0d58f9b9
Publikováno v:
Frontiers in Cell and Developmental Biology, Vol 8 (2020)
Primary cilia are microtubule-based organelles that extend from the apical surface of most mammalian cells, forming when the basal body (derived from the mother centriole) docks at the apical cell membrane. They act as universal cellular “antennae
Externí odkaz:
https://doaj.org/article/92e03e954e614a7cb8fb07af04d86edc
Publikováno v:
Breast Cancer Research and Treatment. 196:215-220
Publikováno v:
Journal of oncology practice. 15(6)
PURPOSE: It is imperative to provide quality end-of-life (EOL) care for patients with cancer. Although rates of hospice use within the Veterans Health Administration have improved, antineoplastic administration and intensive care unit (ICU) admission
Autor:
Elena E. Giorgi, David R. Martinez, Karina Yusim, Erin McGuire, Celia C. LaBranche, Sallie R. Permar, Ayooluwa O. Douglas, Feng Gao, Amit Kumar, Lisa Stamper, David C. Montefiori, Joshua Eudailey, Genevieve G. Fouda, Claire E. P. Smith
Publikováno v:
PLoS Pathogens
PLoS Pathogens, Vol 14, Iss 4, p e1006944 (2018)
PLoS Pathogens, Vol 14, Iss 4, p e1006944 (2018)
Despite extensive genetic diversity of HIV-1 in chronic infection, a single or few maternal virus variants become the founders of an infant’s infection. These transmitted/founder (T/F) variants are of particular interest, as a maternal or infant HI
Publikováno v:
Journal of Clinical Oncology. 36:3-3
3 Background: It is imperative to provide quality end of life (EOL) care for cancer patients. This entails minimizing aggressive measures at the EOL. Although rates of hospice utilization within the Veteran’s Health Administration have improved, ch
Autor:
Claire E. L. Smith, James A. Poulter, Agne Antanaviciute, Jennifer Kirkham, Steven J. Brookes, Chris F. Inglehearn, Alan J. Mighell
Publikováno v:
Frontiers in Physiology, Vol 8 (2017)
Amelogenesis imperfecta (AI) is the name given to a heterogeneous group of conditions characterized by inherited developmental enamel defects. AI enamel is abnormally thin, soft, fragile, pitted and/or badly discolored, with poor function and aesthet
Externí odkaz:
https://doaj.org/article/3507c36431f64b82b87af660f68bfb9a
Autor:
Claire E. L. Smith, Jennifer Kirkham, Peter F. Day, Francesca Soldani, Esther J. McDerra, James A. Poulter, Christopher F. Inglehearn, Alan J. Mighell, Steven J. Brookes
Publikováno v:
Frontiers in Physiology, Vol 8 (2017)
“Amelogenesis imperfecta” (AI) describes a group of genetic conditions that result in defects in tooth enamel formation. Mutations in many genes are known to cause AI, including the gene encoding the serine protease, kallikrein related peptidase
Externí odkaz:
https://doaj.org/article/4257222f3815414781f21f73df6a9d3b
Autor:
Claire E L Smith, Alexia Alexandraki, Sarah F Cordery, Rekha Parmar, David T Bonthron, Elizabeth M A Valleley
Publikováno v:
PLoS ONE, Vol 12, Iss 9, p e0185678 (2017)
The imprinted gene PLAGL1 is an important regulator of apoptosis and cell cycle arrest. Loss of its expression has been implicated in tumorigenesis in a range of different cancers, and overexpression during fetal development causes transient neonatal
Externí odkaz:
https://doaj.org/article/4c5efe9de045428f9b2d5783e8b068b0