Zobrazeno 1 - 10
of 272
pro vyhledávání: '"P. ten Hoopen"'
Publikováno v:
Earth System Science Data, Vol 15, Pp 211-224 (2023)
We present a database from substantial collections of macronutrient data made on 20 oceanographic cruises, primarily from around the island of South Georgia and the Scotia Sea. This sector of the Southern Ocean was studied comprehensively during the
Externí odkaz:
https://doaj.org/article/1ff14d7b7ca04b7f9e5e1d607e552cfc
Akademický článek
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Autor:
Praneeth R. Kuninty, Karin Binnemars-Postma, Ahmed Jarray, Kunal P. Pednekar, Marcel A. Heinrich, Helen J. Pijffers, Hetty ten Hoopen, Gert Storm, Peter van Hoogevest, Wouter K. den Otter, Jai Prakash
Publikováno v:
Nature Communications, Vol 13, Iss 1, Pp 1-17 (2022)
Tumor-associated macrophages are mostly pro-tumorigenic, due to their re-programming by the tumor microenvironment. Here authors show that nanoliposomes, incorporating phospholipids with a flipping-tail chain, are engulfed specifically by intratumora
Externí odkaz:
https://doaj.org/article/c7139cc6942449fc878247554c64ac93
Autor:
Philip S. Robinson, Laura E. Thomas, Federico Abascal, Hyunchul Jung, Luke M. R. Harvey, Hannah D. West, Sigurgeir Olafsson, Bernard C. H. Lee, Tim H. H. Coorens, Henry Lee-Six, Laura Butlin, Nicola Lander, Rebekah Truscott, Mathijs A. Sanders, Stefanie V. Lensing, Simon J. A. Buczacki, Rogier ten Hoopen, Nicholas Coleman, Roxanne Brunton-Sim, Simon Rushbrook, Kourosh Saeb-Parsy, Fiona Lalloo, Peter J. Campbell, Iñigo Martincorena, Julian R. Sampson, Michael R. Stratton
Publikováno v:
Nature Communications, Vol 13, Iss 1, Pp 1-12 (2022)
Inherited mutations in MUTYH have been shown to predispose patients to colorectal cancers. Here, the authors show that MUTYH mutations lead to an increased somatic base substitution mutation rate in normal intestinal epithelial cells, which is the li
Externí odkaz:
https://doaj.org/article/c14b563faf084d9f9abf9b953d1b62bf
Akademický článek
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Akademický článek
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Publikováno v:
Frontiers in Agronomy, Vol 4 (2022)
The vascular disease Verticillium wilt of cacao (Theobroma cacao), caused by the soilborne fungus Verticillium dahliae, is often qualified as a “minor” disease. However, it can cause severe losses locally, for example, in western Uganda and north
Externí odkaz:
https://doaj.org/article/91ec5d80979742d59bfffeb1fb474e87
Autor:
Seong Keat Cheah, Chad Ramese Bisambar, Deborah Pitfield, Olivier Giger, Rogier ten Hoopen, Jose-Ezequiel Martin, Graeme R Clark, Soo-Mi Park, Craig Parkinson, Benjamin G Challis, Ruth T Casey
Publikováno v:
Endocrinology, Diabetes & Metabolism Case Reports, Vol 1, Iss 1, Pp 1-7 (2021)
A 38-year-old female was identified as carrying a heterozygous pathogenic MEN1 variant (c.1304delG) through predictive genetic testing, following a diagnosis of familial hyperparathyroidism. Routine screening for parathyroid and pituitary disease was
Externí odkaz:
https://doaj.org/article/c9f0caffde984c3cbe47f04d220f4b90
Autor:
Luigi Aloj, Olivier Giger, Iosif A. Mendichovszky, Ben G. Challis, Meytar Ronel, Ines Harper, Heok Cheow, Rogier ten Hoopen, Deborah Pitfield, Ferdia A. Gallagher, Bala Attili, Mary McLean, Robin L. Jones, Palma Dileo, Venkata Ramesh Bulusu, Eamonn R. Maher, Ruth T. Casey
Publikováno v:
EJNMMI Research, Vol 11, Iss 1, Pp 1-10 (2021)
Abstract Background [68 Ga]Ga-DOTATATE PET/CT is now recognised as the most sensitive functional imaging modality for the diagnosis of well-differentiated neuroendocrine tumours (NET) and can inform treatment with peptide receptor radionuclide therap
Externí odkaz:
https://doaj.org/article/3128c75f9b434cb5bedd12ba6834b549
Autor:
Kyra Lubbers, Eefje M. Stijl, Bram Dierckx, Doesjka A. Hagenaar, Leontine W. ten Hoopen, Jeroen S. Legerstee, Pieter F. A. de Nijs, André B. Rietman, Kirstin Greaves-Lord, Manon H. J. Hillegers, Gwendolyn C. Dieleman, Sabine E. Mous, ENCORE Expertise Center, Rianne Oostenbrink, Karen C.G.B. Bindels-de Heus, Marie-Claire Y. de Wit, Henriëtte A. Mol, Ype Elgersma
Publikováno v:
Frontiers in Psychiatry, Vol 13 (2022)
ObjectiveThe etiology of autism spectrum disorder (ASD) remains unclear, due to genetic heterogeneity and heterogeneity in symptoms across individuals. This study compares ASD symptomatology between monogenetic syndromes with a high ASD prevalence, i
Externí odkaz:
https://doaj.org/article/202fd10196a84dc78ef4070ab5f15967