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ACS Sensors|January 20, 2022
Development of a Sub-ppb Resolution Methane Sensor Using a GaSb-Based DFB Diode Laser near 3270 nm for Fugitive Emission MeasurementJalal Norooz Oliaee, Nicaulas A Sabourin, Simon A Festa-Bianchet, et al.
Clinical Physics and Physiological Measurement : an Official Journal of the Hospital Physicists' Association, Deutsche Gesellschaft Fur Medizinische Physik and the European Federation of Organisations for Medical Physics|May 1, 1987
Continuous 24 hour ambulatory monitoring of intragastric pH in manB K Kapur, P J Howlett, N G Kenyon, et al.
International Journal of General Medicine|August 26, 2024
The Path to Diagnosis of Severe Asthma-A Qualitative ExplorationSharon R Davis, Biljana Cvetkovski, Gregory Peter Katsoulotos, et al.
Nature Genetics|June 28, 2011
Dynamic CpG island methylation landscape in oocytes and preimplantation embryosSébastien A Smallwood, Shin-Ichi Tomizawa, Felix Krueger, et al.
Acute Medicine|April 11, 2023
Enhanced Care Units: Guidance on development and implementation within Acute MedicineNicholas Smallwood, Sanjay Krishnamoorthy, Kathleen Bonnici, et al.
Neuroimage|March 31, 2023
Omnipresence of the sensorimotor-association axis topography in the human connectomeKarl-Heinz Nenning, Ting Xu, Alexandre R Franco, et al.
Frontiers in Human Neuroscience|November 28, 2013
The default modes of reading: modulation of posterior cingulate and medial prefrontal cortex connectivity associated with comprehension and task focus while readingJonathan Smallwood, Krzysztof J Gorgolewski, Johannes Golchert, et al.
BMJ Open|September 23, 2021
Influence of COVID-19 on the preventive health behaviours of indigenous peoples of Australia residing in New South Wales: a mixed-method study protocolKim Usher, Navjot Bhullar, David Sibbritt, et al.
Human Molecular Genetics|May 2, 2001
Contrasting effects on HIF-1alpha regulation by disease-causing pVHL mutations correlate with patterns of tumourigenesis in von Hippel-Lindau diseaseS C Clifford, M E Cockman, A C Smallwood, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 1, 1988
Genetic deficiency of the alpha subunit of the guanine nucleotide-binding protein Gs as the molecular basis for Albright hereditary osteodystrophyM A Levine, T G Ahn, S F Klupt, et al.
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