Zobrazeno 1 - 10
of 48
pro vyhledávání: '"Kevin P Boyd"'
Publikováno v:
Communications Biology, Vol 7, Iss 1, Pp 1-13 (2024)
Abstract Membrane curvature is essential for many cellular structures and processes, and factors such as leaflet asymmetry, lipid composition, and proteins all play important roles. Cardiolipin is the signature lipid of mitochondrial membranes and is
Externí odkaz:
https://doaj.org/article/4411d732a6384f96a6a980dd9e1bcd18
Autor:
John R. Jones, David A. Cairns, Tom Menzies, Charlotte Pawlyn, Faith E. Davies, Rachel Sigsworth, Annamaria Brioli, Matthew W. Jenner, Martin F. Kaiser, Catherine Olivier, Molly Reed, Mark T. Drayson, Roger G. Owen, Kevin D. Boyd, Gordon Cook, Gareth J. Morgan, Graham H. Jackson
Publikováno v:
EClinicalMedicine, Vol 62, Iss , Pp 102099- (2023)
Summary: Background: Early trials of long-term lenalidomide use reported an increased incidence of second primary malignancy (SPM), including acute myeloid leukaemia and myelodysplastic syndrome. Later, meta-analysis suggested the link to be secondar
Externí odkaz:
https://doaj.org/article/7b401565bf86409c8aca965e1f509a9d
Autor:
Aikaterini Panopoulou, Sandra Easdale, Mark Ethell, Emma Nicholson, Mike Potter, Asterios Giotas, Helena Woods, Tracy Thornton, Charlotte Pawlyn, Kevin D. Boyd, Martin F. Kaiser
Publikováno v:
HemaSphere, Vol 7, Iss 2, p e831 (2023)
Refined prediction of early relapse following standard-of-care (SoC) autologous stem cell transplant (ASCT) in newly diagnosed multiple myeloma (NDMM) could inform real-world risk-stratified post-ASCT strategies. We investigated the impact of double
Externí odkaz:
https://doaj.org/article/6e2bc5ac2d034cf78e663d2ca195209b
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 13, Iss 1, Pp 1-7 (2018)
Abstract Background Neurofibromatosis type 1 (NF1) is a genetic disorder characterized by a predisposition to develop multiple benign tumors. A major feature of NF1 is the development of localized cutaneous neurofibromas. Cutaneous neurofibromas mani
Externí odkaz:
https://doaj.org/article/eb47b134c34d40bc98353fec4e0af402
Publikováno v:
BMC Cancer, Vol 17, Iss 1, Pp 1-6 (2017)
Abstract Background Multiple Myeloma is a cancer of plasma cells associated with significantly reduced survival. Long term survivorship from myeloma is very rare and despite advances in its treatment the disease is generally considered incurable. We
Externí odkaz:
https://doaj.org/article/56d2e2d9d892416fbe85275cd8e1fc88
Autor:
Abigail J, Engwall-Gill, Sherwin S, Chan, Kevin P, Boyd, Jacqueline M, Saito, Mary E, Fallat, Shawn D, St Peter, Stephanie, Bolger-Theut, Eric J, Crotty, Jared R, Green, Rebecca L, Hulett Bowling, Sachin S, Kumbhar, Mantosh S, Rattan, Cody M, Young, Joseph K, Canner, Katherine J, Deans, Samir K, Gadepalli, Michael A, Helmrath, Ronald B, Hirschl, Rashmi, Kabre, Dave R, Lal, Matthew P, Landman, Charles M, Leys, Grace Z, Mak, Peter C, Minneci, Tiffany N, Wright, Shaun M, Kunisaki, Sarah, Fox
Publikováno v:
JAMA network open. 5(6)
The ability of computed tomography (CT) to distinguish between benign congenital lung malformations and malignant cystic pleuropulmonary blastomas (PPBs) is unclear.To assess whether chest CT can detect malignant tumors among postnatally detected lun
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e1f882ba91d3618047f616136b4029b6
https://pubmed.ncbi.nlm.nih.gov/35771580
https://pubmed.ncbi.nlm.nih.gov/35771580
Autor:
Jerry Xiao, Selim Firat, Dave R. Lal, Mariko Suchi, Kevin P. Boyd, Leslie J. Mortland, Kiran K. Turaga, Meghen B. Browning
Publikováno v:
Journal of Pediatric Hematology/Oncology. 43:228-231
Desmoplastic small round cell tumor is a rare sarcoma with 5-year overall survival of 15%. An 8-year-old female presented with diffuse abdominal/pelvic desmoplastic small round cell tumor including numerous liver metastasis. She underwent neoadjuvant
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::afcd875d4b4009e54beb9ad1c77ad8a5
https://doi.org/10.1097/mph.0000000000001861
https://doi.org/10.1097/mph.0000000000001861
Publikováno v:
Dermatologic clinics. 40(1)
Clinical genetic testing enables the detection of specific gene mutations and variants that predispose individuals and their family members to disease. In recent years, tremendous strides have been made in the variety of clinically useful tests. Targ
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::21325b353a1a179034b30edf18a200a3
https://pubmed.ncbi.nlm.nih.gov/34799030
https://pubmed.ncbi.nlm.nih.gov/34799030
Publikováno v:
Frontiers in Bioengineering and Biotechnology, Vol 3 (2015)
Norwalk virus causes severe gastroenteritis for which there is currently no specific anti-viral therapy. A stage of the infection process is uncoating of the protein capsid to expose the viral genome and allow for viral replication. A mechanical char
Externí odkaz:
https://doaj.org/article/17d045ca110f498584f576ddb51c2ad2
Publikováno v:
Harper's Textbook of Pediatric Dermatology. :1823-1836
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2f669d49ae50e278b462cd235647d604
https://doi.org/10.1002/9781119142812.ch142
https://doi.org/10.1002/9781119142812.ch142