Zobrazeno 1 - 10
of 4 241
pro vyhledávání: '"D. Calder"'
Corrigendum: HPLC for at-line reaction monitoring and purification improves yield and purity of tRNA
Autor:
Polona Megušar, Ewen D. D. Calder, Tina Vodopivec Seravalli, Sergeja Lebar, Louise J. Walport, Rok Sekirnik
Publikováno v:
Frontiers in Molecular Biosciences, Vol 11 (2024)
Externí odkaz:
https://doaj.org/article/5162f5b8cb7b4c169967c77223525909
Autor:
Polona Megušar, Ewen D. D. Calder, Tina Vodopivec Seravalli, Sergeja Lebar, Louise J. Walport, Rok Sekirnik
Publikováno v:
Frontiers in Molecular Biosciences, Vol 11 (2024)
Engineered transfer RNA is an emerging therapeutic modality, particularly suited to treatment of diseases caused by genetic disorders based on premature termination codons, frameshifts, or missense mutations. It is also extensively used in reprogramm
Externí odkaz:
https://doaj.org/article/779c136fa8384102820cf3811c0f1c73
Autor:
Ryan S. D. Calder, Amina T. Schartup
Publikováno v:
GeoHealth, Vol 7, Iss 9, Pp n/a-n/a (2023)
Abstract Interest in health implications of Earth science research has significantly increased. Articles frequently dispense policy advice, for example, to reduce human contaminant exposures. Recommendations such as fish consumption advisories rarely
Externí odkaz:
https://doaj.org/article/3acede82bee14290b2a47f5a2ed2e3be
Publikováno v:
Environmental Research: Infrastructure and Sustainability, Vol 4, Iss 4, p 045005 (2024)
Environmental impact assessment (EIA), life cycle analysis (LCA), and cost benefit analysis (CBA) embed crucial but subjective judgments over the extent of system boundaries and the range of impacts to consider as causally connected to an interventio
Externí odkaz:
https://doaj.org/article/0cae319125034cb998ae844a6fa40907
Publikováno v:
Environmental Research: Infrastructure and Sustainability, Vol 4, Iss 3, p 033002 (2024)
The renewable energy transition is leading to increased electricity trade between the United States and Canada, with Canadian hydropower providing firm lower-carbon power and buffering variability of wind and solar generation in the U.S. However, lon
Externí odkaz:
https://doaj.org/article/4d7285ab78c242c9a90268a6527a7342
Autor:
John Kostanoski
Publikováno v:
Journal of Security Education. 1:129-148
This new column will introduce readers to those educators and trainers whose contributions and scholarly outputs have an enduring quality, and are or promise to be part of the discipline's literature. The column will take the reader on a tour of the
Publikováno v:
Scientific Reports, Vol 12, Iss 1, Pp 1-12 (2022)
Abstract The BoneXpert method for automated determination of bone age from hand X-rays was introduced in 2009 and is currently running in over 200 hospitals. The aim of this work is to present version 3 of the method and validate its accuracy and sel
Externí odkaz:
https://doaj.org/article/0d1299e747ad494cbd8d9c9adc2d5800
Autor:
Christopher M. Orton, Henry E. Symons, Benjamin Moseley, Justice Archer, Natalie A. Watson, Keir E. J. Philip, Sadiyah Sheikh, Brian Saccente-Kennedy, Declan Costello, William J. Browne, James D. Calder, Bryan R. Bzdek, James H. Hull, Jonathan P. Reid, Pallav L. Shah
Publikováno v:
Communications Medicine, Vol 2, Iss 1, Pp 1-9 (2022)
Orton and Symons et al. compare respiratory particle sizes and emission rates by sampling exhalates from participants at rest, and while speaking or exercising. They find that vocalisation produces larger particles and that while emission rates are s
Externí odkaz:
https://doaj.org/article/5f2f9083c7854a6bb237513b87deeffe
Autor:
Ataf H. Sabir, Elizabeth Morley, Jameela Sheikh, Alistair D. Calder, Ana Beleza-Meireles, Moira S. Cheung, Alessandra Cocca, Mattias Jansson, Suzanne Lillis, Yogen Patel, Shu Yau, Christine M. Hall, Amaka C. Offiah, Melita Irving
Publikováno v:
BMC Medical Genomics, Vol 14, Iss 1, Pp 1-14 (2021)
Abstract Background Skeletal dysplasia (SD) conditions are rare genetic diseases of the skeleton, encompassing a heterogeneous group of over 400 disorders, and represent approximately 5% of all congenital anomalies. Developments in genetic and treatm
Externí odkaz:
https://doaj.org/article/2ba7db3ffb1d4355907a9d8ece8ef189
Autor:
Chaofan Zhang, Angad Jolly, Brian J. Shayota, Juliana F. Mazzeu, Haowei Du, Moez Dawood, Patricia Celestino Soper, Ariadne Ramalho de Lima, Bárbara Merfort Ferreira, Zeynep Coban-Akdemir, Janson White, Deborah Shears, Fraser Robert Thomson, Sarah Louise Douglas, Andrew Wainwright, Kathryn Bailey, Paul Wordsworth, Mike Oldridge, Tracy Lester, Alistair D. Calder, Katja Dumic, Siddharth Banka, Dian Donnai, Shalini N. Jhangiani, Lorraine Potocki, Wendy K. Chung, Sara Mora, Hope Northrup, Myla Ashfaq, Jill A. Rosenfeld, Kati Mason, Lynda C. Pollack, Allyn McConkie-Rosell, Wei Kelly, Marie McDonald, Natalie S. Hauser, Peter Leahy, Cynthia M. Powell, Raquel Boy, Rachel Sayuri Honjo, Fernando Kok, Lucia R. Martelli, Vicente Odone Filho, Genomics England Research Consortium, Donna M. Muzny, Richard A. Gibbs, Jennifer E. Posey, Pengfei Liu, James R. Lupski, V. Reid Sutton, Claudia M.B. Carvalho
Publikováno v:
HGG Advances, Vol 3, Iss 1, Pp 100074- (2022)
Summary: Robinow syndrome (RS) is a genetically heterogeneous disorder with six genes that converge on the WNT/planar cell polarity (PCP) signaling pathway implicated (DVL1, DVL3, FZD2, NXN, ROR2, and WNT5A). RS is characterized by skeletal dysplasia
Externí odkaz:
https://doaj.org/article/111938d44884445f92d7831c96a453cf