Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Lisa X. Yu"'
Autor:
Lisa X. Yu, Alisha R. Elford, Brian J. Nieman, Kevin J. Tracey, Carmen Dominguez-Brauer, Pamela S. Ohashi, Peder S. Olofsson, Maureen A. Cox, Kyle T. Gill, Gordon Duncan, Gloria H. Y. Lin, Jillian Haight, Dirk Brenner, Tak W. Mak, Benjamin E. Steinberg, Shawn P. Kubli, Andrew J. Elia, Thorsten Berger, Luke N. Buckler, Andrew Wakeham
Publikováno v:
Cox, M A, Duncan, G S, Lin, G H Y, Steinberg, B E, Yu, L X, Brenner, D, Buckler, L N, Elia, A J, Wakeham, A C, Nieman, B, Dominguez-Brauer, C, Elford, A R, Gill, K T, Kubli, S P, Haight, J, Berger, T, Ohashi, P S, Tracey, K J, Olofsson, P S & Mak, T W 2019, ' Choline acetyltransferase–expressing T cells are required to control chronic viral infection ', Science, vol. 363, no. 6427, pp. 639-644 . https://doi.org/10.1126/science.aau9072
ChAT-ty T cells fight viral infection The neurotransmitter acetylcholine (ACh) is involved in processes such as muscle contraction, neuron communication, and vasodilation. Along with neurons, a population of immunological T cells and B cells express
Autor:
Julia C. Boughner, Lisa X. Yu, Nasim Rostampour, R. Mark Henkelman, Matthijs C. van Eede, Shoshana Spring
Publikováno v:
Developmental Dynamics. 247:779-787
Background The p63 gene is integral to the development of many body parts including limb, palate, teeth, and urogenital tract. Loss of p63 expression may alter developmental rate, which is crucial to normal morphogenesis. To validate a novel, unbiase
Autor:
Lindsay S. Cahill, Monique Y. Rennie, John G. Sled, Mike Seed, Christopher K. Macgowan, Lisa X. Yu, John Kingdom, Johnathan Hoggarth, Anum Rahman
Publikováno v:
The Journal of Physiology. 596:3285-3297
Key points Chronic fetal hypoxia is one of the most common complications of pregnancy and is known to cause fetal growth restriction. The structural adaptations of the placental vasculature responsible for growth restriction with chronic hypoxia are
Autor:
Andrea Kassner, Gregory M. T. Hare, John G. Sled, Lindsay S. Cahill, Christopher K. Macgowan, Jesper Pilmeyer, Lisa X. Yu, Joe Steinman
Publikováno v:
Ultrasound in Medicine and Biology, 45(12), 3269-3278. Elsevier
Sickle cell disease (SCD) is associated with a high risk of stroke, and affected individuals often have focal brain lesions termed silent cerebral infarcts. The mechanisms leading to these types of injuries are at present poorly understood. Our group
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::af2a0d5c82bdae26f0017bcffd3cf4b7
https://research.tue.nl/nl/publications/94328d13-1e3a-4e1e-baa2-7bfb390a7937
https://research.tue.nl/nl/publications/94328d13-1e3a-4e1e-baa2-7bfb390a7937
Autor:
John G. Sled, Ahmet Baschat, Johnathan Hoggarth, Lindsay S. Cahill, Christopher K. Macgowan, Greg Stortz, John Kingdom, Yu-Qing Zhou, Lena Serghides, Clare Whitehead, Lisa X. Yu, Anum Rahman
Current methods to detect placental vascular pathologies that monitor Doppler ultrasound changes in umbilical artery (UA) pulsatility have only moderate diagnostic utility, particularly in late gestation. In fetal mice, we recently demonstrated that
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::687f5e280ffc84352111e3dbe43b5bda
https://europepmc.org/articles/PMC6425519/
https://europepmc.org/articles/PMC6425519/
Autor:
Julia C, Boughner, Matthijs C, van Eede, Shoshana, Spring, Lisa X, Yu, Nasim, Rostampour, R Mark, Henkelman
Publikováno v:
Developmental dynamics : an official publication of the American Association of Anatomists. 247(5)
The p63 gene is integral to the development of many body parts including limb, palate, teeth, and urogenital tract. Loss of p63 expression may alter developmental rate, which is crucial to normal morphogenesis. To validate a novel, unbiased embryo ph
Autor:
Lisa X. Yu, Mohammed G. Kabir, Brendan A.S. McIntyre, Valentin Sotov, Adrienne Davies, Mark Henkelman, Jaques Belik, Michelle Letarte, Masahiro Enomoto, Nasir W. Husain, Mansoor Husain, Mirjana Jerkic
Publikováno v:
Cardiovascular Research. 92:375-384
Aims Mutations in the ALK1 gene, coding for an endothelial-specific receptor of the transforming growth factor-β superfamily, are the underlying cause of hereditary haemorrhagic telangiectasia type 2, but are also associated with familial pulmonary
Publikováno v:
American Journal of Physiology-Heart and Circulatory Physiology. 298:H1249-H1259
The availability of detailed three-dimensional images of vascular trees from mammalian organs provides a wealth of essential data for understanding the processes and mechanisms of vascular patterning. Using this detailed geometric data requires the a
Autor:
Brendan A.S. McIntyre, Adrienne Davis, Duncan J. Stewart, Mansoor Husain, Yu-Qing Zhou, Mark Henkelman, Yu Jing Wang, Mohammed G. Kabir, Jaques Belik, Mourad Toporsian, Lisa X. Yu, Michelle Letarte, Mirjana Jerkic
Publikováno v:
Arteriosclerosis, Thrombosis, and Vascular Biology. 30:509-517
Objective— Loss-of-function mutations in genes coding for transforming growth factor-β/bone morphogenetic protein receptors and changes in nitric oxide • (NO • ) bioavailability are associated with hereditary hemorrhagic telangiectasia and som
Autor:
Jingyi Pan, Brendan A.S. McIntyre, R. M. Henkelman, Lisa X. Yu, Michelle Letarte, J. Leen, Jaques Belik, Mirjana Jerkic, Mourad Toporsian
Publikováno v:
American Journal of Physiology-Lung Cellular and Molecular Physiology. 297:L1170-L1178
Endoglin is a TGF-β superfamily receptor critical for endothelial cell function. Mutations in this gene are associated with hereditary hemorrhagic telangiectasia type I (HHT1), and clinical signs of disease are generally more evident later in life.