Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Joanna Hinks"'
Publikováno v:
The International Technical Meeting of the The Institute of Navigation.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cf717e3d7f8c2bf92d434ada682cde39
https://doi.org/10.33012/2022.18163
https://doi.org/10.33012/2022.18163
Publikováno v:
Proceedings of the 34th International Technical Meeting of the Satellite Division of The Institute of Navigation (ION GNSS+ 2021).
The next generation of GNSS promises new satellite constellation and signal designs that will improve capabilities and performances for all users. In particular, novel signal designs are being explored with different characteristic modulations and ba
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ad0c6a040cbf206a446df90fe9b45db2
https://doi.org/10.33012/2021.18009
https://doi.org/10.33012/2021.18009
Autor:
Martin Schwarz, Livia Budişan, Emma Brownsell, Liviu Pop, I. Popa, M Bulman, Gheorghe Benga, Simona Mosescu, Lucian Frenţescu, Geraldine Malone, Joanna Hinks, Emil Tomescu, Mirela Filip, Helen Shaw
Publikováno v:
Journal of Cystic Fibrosis. 7(5):423-428
Background Cystic fibrosis (CF) is produced by mutations in the Cystic Fibrosis Transmembrane Conductance Regulator Gene (CFTR) gene. Methods One hundred twenty eight patients with CF were analysed for mutations in the CFTR gene in order to establish
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3657829bfbebc4ae7ce87da9542e00f4
Autor:
Anne Goodeve, Türkiz Gürsel, Simon Allen, Joanna Hinks, Joanna L. Blagg, Jørgen Ingerslev, Adel M. Abuzenadah, Martina E. Daly, Ian R. Peake
Publikováno v:
Blood. 96:560-568
In this report we describe the molecular defect underlying partial and severe quantitative von Willebrand factor (VWF) deficiencies in 3 families previously diagnosed with types 1 and 3 Von Willebrand-disease. Analysis of the VWF gene in affected fam
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6f173183931de692e9da149b63f60013
https://doi.org/10.1182/blood.v96.2.560.014k01_560_568
https://doi.org/10.1182/blood.v96.2.560.014k01_560_568
Autor:
Joanna Hinks, Mark Psiaki
Publikováno v:
AIAA Guidance, Navigation, and Control Conference.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8e1e85401ecd610bb1f0ef2a4d28fdc6
https://doi.org/10.2514/6.2012-4758
https://doi.org/10.2514/6.2012-4758
Autor:
Ayesha Irtiza-Ali, Joanna Hinks, T. Roberts, Maurice Super, Anthony M. Heagerty, Martin Schwarz, Stephen A Roberts, Michele Young, Alison Smith
Publikováno v:
Hypertension (Dallas, Tex. : 1979). 44(6)
Individuals homozygous for the autosomal recessive disorder CF are known to have low blood pressure, thought to be caused by greatly increased sweat salt loss. We examined whether carriers of the CF gene also have low blood pressure. Our pilot studie
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f030d9c3ab253915617c5722c817f9b3
https://pubmed.ncbi.nlm.nih.gov/15477385
https://pubmed.ncbi.nlm.nih.gov/15477385