Zobrazeno 1 - 10
of 11
pro vyhledávání: '"Lilian Hunt"'
Autor:
Manuel Spitschan, Nayantara Santhi, Amrita Ahluwalia, Dorothee Fischer, Lilian Hunt, Natasha A Karp, Francis Lévi, Inés Pineda-Torra, Parisa Vidafar, Rhiannon White
Publikováno v:
eLife, Vol 11 (2022)
Growing evidence shows that sex differences impact many facets of human biology. Here we review and discuss the impact of sex on human circadian and sleep physiology, and we uncover a data gap in the field investigating the non-visual effects of ligh
Externí odkaz:
https://doaj.org/article/f119125cadf64eb6bf223214de317f6f
Autor:
Robertson, Lilian Hunt Alan
Quantum devices in the Noisy Intermediate-Scale Quantum (NISQ) era are limited by high error rates and short decoherence times. Typically, compiler optimisations have provided solutions at the gate level. Alternatively, we exploit the finest level of
Externí odkaz:
http://arxiv.org/abs/2311.08742
Autor:
Ilaria Dalla Rosa, Yolanda Cámara, Romina Durigon, Chloe F Moss, Sara Vidoni, Gokhan Akman, Lilian Hunt, Mark A Johnson, Sarah Grocott, Liya Wang, David R Thorburn, Michio Hirano, Joanna Poulton, Robert W Taylor, Greg Elgar, Ramon Martí, Peter Voshol, Ian J Holt, Antonella Spinazzola
Publikováno v:
PLoS Genetics, Vol 12, Iss 1, p e1005779 (2016)
MPV17 is a mitochondrial inner membrane protein whose dysfunction causes mitochondrial DNA abnormalities and disease by an unknown mechanism. Perturbations of deoxynucleoside triphosphate (dNTP) pools are a recognized cause of mitochondrial genomic i
Externí odkaz:
https://doaj.org/article/fd0c8fb28a5f40f98a92dee74e9682c6
Publikováno v:
Science. 377:1492-1495
Funding agencies have ample room to improve their policies
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7bbb57dcd82a39e8507001619b002ff6
https://doi.org/10.1126/science.abp9775
https://doi.org/10.1126/science.abp9775
Autor:
Daniël A. Lionarons, Davide Zecchin, Jeffrey R. MacDonald, Wei-Li Di, Hui Chen, Miriam Molina, Stuart Horswell, Gemma Tell, Véronique Bataille, Dale Bryant, Julia Newton-Bishop, Philip Stanier, Gudrun E. Moore, Kiran Parmar, Josep Malvehy, Catherine A. Harwood, Satyamaanasa Polubothu, Cristina Carrera, Jérémie Nsengimana, Veronica A. Kinsler, Julian Downward, Nathan Wlodarchak, Alan Pittman, Susana Puig, Yongna Xing, Neil J. Sebire, Anna C. Thomas, Mark Harland, L. Al-Olabi, Mehdi Zarrei, Michael Howell, Sarah Brand, Paulina Stadnik, Stephen W. Scherer, Lilian Hunt, Eugene Healy, Dale Moulding, Paula Aguilera, J.A. Puig-Butillé, Deborah Morrogh, Vanessa Martins da Silva, Sam Loughlin, Regula Waelchli, Sara Martin Barberan, Greg Elgar, Lionel Larue
Publikováno v:
Genetics in medicine, 23(9), 1636-1647. Lippincott Williams and Wilkins
Genetics in Medicine
Genetics in Medicine
Purpose\ud Much of the heredity of melanoma remains unexplained. We sought predisposing germline copy-number variants using a rare disease approach.\ud \ud Methods\ud Whole-genome copy-number findings in patients with melanoma predisposition syndrome
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1cf020b972091ef0da9c25d686d2a0a5
https://pure.amc.nl/en/publications/inherited-duplications-of-ppp2r3b-predispose-to-nevi-and-melanoma-via-a-c21orf91driven-proliferative-phenotype(c7c1481a-d0e0-4090-8d51-8c03bd58e817).html
https://pure.amc.nl/en/publications/inherited-duplications-of-ppp2r3b-predispose-to-nevi-and-melanoma-via-a-c21orf91driven-proliferative-phenotype(c7c1481a-d0e0-4090-8d51-8c03bd58e817).html
Autor:
Manuel Spitschan, Nayantara Santhi, Amrita Ahluwalia, Dorothee Fischer, Lilian Hunt, Natasha A Karp, Francis Lévi, Inés Pineda-Torra, Parisa Vidafar, Rhiannon White
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e1b543c657dead483e036b802a5f54c3
https://doi.org/10.7554/elife.65419.sa2
https://doi.org/10.7554/elife.65419.sa2
Autor:
Manuel Spitschan, Nayantara Santhi, Amrita Ahluwalia, Dorothee Fischer, Lilian Hunt, Natasha A Karp, Francis Lévi, Inés Pineda-Torra, Parisa Vidafar, Rhiannon White
Publikováno v:
eLife. 11
Growing evidence shows that sex differences impact many facets of human biology. Here we review and discuss the impact of sex on human circadian and sleep physiology, and we uncover a data gap in the field investigating the non-visual effects of ligh
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b6272c758a70b85751bb6694ac88d47f
https://pubmed.ncbi.nlm.nih.gov/35179486
https://pubmed.ncbi.nlm.nih.gov/35179486
Autor:
Gemma Tell, Michael Howell, L. Al-Olabi, Julia Newton-Bishop, Josep Malvehy, Susana Puig, Mark Harland, Lilian Hunt, Yongna Xing, Sam Loughlin, Jérémie Nsengimana, Gudrun E. Moore, Regula Waelchli, Lionel Larue, Veronica A. Kinsler, Wei-Li Di, Julian Downward, Anna C. Thomas, Dale Bryant, Catherine A. Harwood, Daniël A. Lionarons, Dale Moulding, Paula Aguilera, Satyamaanasa Polubothu, Greg Elgar, Sarah Brand, Eugene Healy, Cristina Carrera, Philip L. Beales, Paulina Stadnik, Davide Zecchin, Vanessa Martins da Silva, Mehdi Zarrei, Dagan Jenkins, Neil J. Sebire, Véronique Bataille, Stephen W. Scherer, Alan Pittman, Sara Martin Barberan, Juan-Anton Puig-Butillé, Deborah Morrogh, Nathan Wlodarchak, Philip Stanier, Miriam Molina, Jeffrey R. MacDonald, Stuart Horswell, Hui Chen, Kiran Parmar
The majority of the heredity of melanoma remains unexplained, however inherited copy number changes have not yet been systematically studied. The genetic environment is highly relevant to treatment stratification, and new gene discovery is therefore
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e09f513bc2b8b1d8046d1663a4b98ebd
https://doi.org/10.1101/672576
https://doi.org/10.1101/672576
Autor:
Lilian Hunt
Publikováno v:
Physiology News. :19-19
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7740ee5d7cd64573aa3c4fa3bf232402
https://doi.org/10.36866/pn.117.19
https://doi.org/10.36866/pn.117.19
Autor:
Yolanda Cámara, Ramon Martí, David R. Thorburn, Mark A. Johnson, Liya Wang, Ilaria Dalla Rosa, Antonella Spinazzola, Greg Elgar, Lilian Hunt, Michio Hirano, Peter J. Voshol, Joanna Poulton, Chloe F. Moss, Ian Holt, Romina Durigon, Sara Vidoni, Sarah Grocott, Robert W. Taylor, Gokhan Akman
Publikováno v:
Dipòsit Digital de Documents de la UAB
Universitat Autònoma de Barcelona
PLoS Genetics
PLoS Genetics, Vol 12, Iss 1, p e1005779 (2016)
Universitat Autònoma de Barcelona
PLoS Genetics
PLoS Genetics, Vol 12, Iss 1, p e1005779 (2016)
MPV17 is a mitochondrial inner membrane protein whose dysfunction causes mitochondrial DNA abnormalities and disease by an unknown mechanism. Perturbations of deoxynucleoside triphosphate (dNTP) pools are a recognized cause of mitochondrial genomic i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0e682a0c5067443c57a258ca5789d3fe
https://ddd.uab.cat/record/185761
https://ddd.uab.cat/record/185761