Zobrazeno 1 - 10
of 115
pro vyhledávání: '"Emily, Hansen"'
Publikováno v:
Scientific Reports, Vol 14, Iss 1, Pp 1-15 (2024)
Abstract During metastasis, cancer cells traverse the vasculature by squeezing through very small gaps in the endothelium. Thus, nuclei in metastatic cancer cells must become more malleable to move through these gaps. Our lab showed invasive breast c
Externí odkaz:
https://doaj.org/article/8fd52e3b1a9048d4b6daa6ed984a17e7
Publikováno v:
BMC Health Services Research, Vol 24, Iss 1, Pp 1-18 (2024)
Abstract Background Incorporating perspectives of health consumers, healthcare workers, policy makers and stakeholders through co-design is essential to design services that are fit for purpose. However, the experiences of co-design participants are
Externí odkaz:
https://doaj.org/article/39cdf3480da643f48904d21da9ade33d
Autor:
Priyanka Mishra, Anusha Sivakumar, Avalon Johnson, Carla Pernaci, Anna S. Warden, Lilas Rony El-Hachem, Emily Hansen, Rafael A. Badell-Grau, Veenita Khare, Gabriela Ramirez, Sydney Gillette, Angelyn B. Solis, Peng Guo, Nicole Coufal, Stephanie Cherqui
Publikováno v:
Frontiers in Pharmacology, Vol 15 (2024)
Friedreich ataxia (FRDA) is a multisystemic, autosomal recessive disorder caused by homozygous GAA expansion mutation in the first intron of frataxin (FXN) gene. FXN is a mitochondrial protein critical for iron-sulfur cluster biosynthesis and deficie
Externí odkaz:
https://doaj.org/article/8ba3275eff2a4b498782c624404a638b
Publikováno v:
Archives of Plastic Surgery, Vol 49, Iss 04, Pp 517-522 (2022)
Adams-Oliver syndrome is a well-recognized autosomal dominant disorder for which mutations in six genes are etiologic, but account for only one-third of the cases. We report a patient with two genetic disorders; Adams-Oliver and Xp22.33 deletion synd
Externí odkaz:
https://doaj.org/article/9355d642559b42869d3fe39aa20f37c2
Autor:
Catherine Louise Taylor, Daniel Christensen, Alison Venn, David Preen, Joel Stafford, Emily Hansen, Kim Jose, Stephen Zubrick
Publikováno v:
International Journal of Population Data Science, Vol 6, Iss 3 (2022)
Background In Australia, the health and education sectors provide universal early childhood services for the same population of children. Therefore, there is a strong imperative to view service use and outcomes through a cross-sectoral lens to better
Externí odkaz:
https://doaj.org/article/fc51260cb8924632b860b4343e496ece
Autor:
Laura Sutton, Kim Jose, Alana Betzold, Emily Hansen, Laura Laslett, Jennifer Makin, Tania Winzenberg, Saliu Balogun, Dawn Aitken
Publikováno v:
Osteoarthritis and Cartilage Open, Vol 3, Iss 4, Pp 100218- (2021)
Objective: Using a qualitative design this study aimed to 1) explore the attitudes towards and understanding of osteoarthritis (OA) held by Tasmanian general practitioners (GPs) and orthopaedic surgeons, 2) gain a deeper understanding of conservative
Externí odkaz:
https://doaj.org/article/1a2fd9f3f29c42b2bcb44fb296c696fa
Autor:
Kim Jose, Catherine L. Taylor, Rachael Jones, Susan Banks, Joel Stafford, Stephen R. Zubrick, M’Lynda Stubbs, David B. Preen, Alison Venn, Emily Hansen
Publikováno v:
International Journal of Integrated Care, Vol 21, Iss 2 (2021)
Introduction: There is a global trend towards place-based initiatives (PBIs) to break the cycle of disadvantage and promote positive child development. Co-location is a common element of these initiatives and is intended to deliver more coordinated s
Externí odkaz:
https://doaj.org/article/8a8c6e380a87460fb86fbae19fc927f0
Autor:
Emily Hansen, James M. Holaska
Publikováno v:
Oncotarget. 14:317-320
Publikováno v:
BMC Pregnancy and Childbirth, Vol 18, Iss 1, Pp 1-7 (2018)
Abstract Background Fathers’ attitudes and actions can positively or negatively affect mothers’ intentions to breastfeed, breastfeeding duration and exclusivity. In-depth information about fathers’ perspectives on breastfeeding are largely abse
Externí odkaz:
https://doaj.org/article/69b0679e8d024152973f0f347f2d2e06
Autor:
Kristen Arredondo, Cortlandt Myers, Emily Hansen-Kiss, Mariam T. Mathew, Vijayakumar Jayaraman, Amy Siemon, Dennis Bartholomew, Gail E. Herman, Mari Mori
Publikováno v:
Journal of Child Neurology. 37:517-523
Background and Purpose Mutations in KCNQ3 have classically been associated with benign familial neonatal and infantile seizures and more recently identified in patients with neurodevelopmental disorders and abnormal electroencephalogram (EEG) finding