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Showing "Human Genetics Centre University Oxford Deploys Univa Solutions" PubMed Articles 1–25 of 24,000+

Oxford Specialist Handbooks in Paediatrics - Paediatric Neurology: Rob Forsyth and Richard Newton (eds) : Published by Oxford University Press, UK; Third Edition: 2018; ISBN: 978-0-19-878444-9.

The creation of the International Federation of Human Genetics Societies in 1995-1996.

Activities and initiatives of the renewed European Society of Human Genetics (ESHG) (1992-2017).

The Big Data Revolution and Human Genetics.

Updates offer robust and fair approach to resolving patient safety incidents.

Sam Foster, Chief Nurse, Oxford University Hospitals, welcomes the recommendations emerging from the latest reviews and highlights the importance of investigating systemic, as well as human factors.

Involving the European National Human Genetics Societies.

Cardiac transplantation in systemic sclerosis: single-centre experience of three cases.

Genetic populations and virulence factors of Helicobacter pylori.

Helicobacter pylori is a bacterium that has infected more than half of the human population worldwide. This bacterium is closely associated with serious human diseases, such as gastric cancer, and identifying and understanding factors that predict bacterial virulence is a priority. In addition, this pathogen shows high genetic diversity and co-evolution with human hosts. H. pylori population genetics, therefore, has emerged as a tool to track human demographic history. As the number of genome sequences avai...

University of Wisconsin versus Normal Saline Solutions for Preservation of Blood Vessels of Brain Death Donors; A Histopathological Study.

To compare the cellular changes of harvested arteries which were preserved in normal saline (NS) and the standard and routinely used university of Wisconsin (UW) solution.

Recognition of clinical genetics in Europe.



From Mendel to Medical Genetics.

Tocilizumab in the treatment of severe and/or refractory vasculo-Behçet's disease: a single-centre experience in China.

2017 Curt Stern Award: The Complexity of Simple Genetics.

Procedural complications of endovascular treatment in patients with aneurysmal subarachnoid haemorrhage treated at a single centre.

We present a single-centre experience of procedural complications suffered by patients undergoing endovascular treatment for a ruptured saccular intracranial aneurysm at Tampere University Hospital, Finland, between 2000 and 2014.

Rogers, B. Perception: A Very Short Introduction Rogers B. Perception: A Very Short Introduction . Oxford, England: Oxford University Press, 2017; 184 pp.: ISBN 9780198791003, £7.99 paperback.

Study of manganese binding to the ferroxidase centre of human H-type ferritin.

Ferritins are ubiquitous and conserved proteins endowed with enzymatic ferroxidase activity, that oxidize Fe(II) ions at the dimetal ferroxidase centre to form a mineralized Fe(III) oxide core deposited within the apo-protein shell. Herein, the in vitro formation of a heterodimetal cofactor constituted by Fe and Mn ions has been investigated in human H ferritin (hHFt). Namely, Mn and Fe binding at the hHFt ferroxidase centre and its effects on Fe(II) oxidation have been investigated by UV-Vis ferroxidation ...

Ureteral injuries during different types of hysterecomy: A 7-year series at a single university center.

Accidental ureteral injury with gynaecologic surgery, especially hysterectomy, represents a high risk of patient morbidity. The incidence may vary from centre to centre. As the introduction of new minimally invasive surgical techniques and instruments may have affected the incidence of ureteral injury, we de novo analysed the incidence data for the last seven years.

Correction: The population genetics of human disease: The case of recessive, lethal mutations.

[This corrects the article DOI: 10.1371/journal.pgen.1006915.].

Reply to the Comment Entitled "Association of FTO rs9939609 with Obesity".

The Level of Monocyte Chemoattractant Protein-1 May be Affected by Several Factors.

No Abstract.

Martin Method for Estimation of Low-Density Lipoprotein Cholesterol.

No Abstract.

BrainImageR: Spatiotemporal gene set analysis referencing the human brain.

Neuronal analyses such as transcriptomics, epigenetics, and genome-wide association studies must be assessed in the context of the human brain to generate biologically meaningful inferences. It is often difficult to access primary human brain tissue; therefore, approximations are made using alternative sources such as peripheral tissues or in vitro-derived neurons. Gene sets from these studies are then assessed for their association with the post-mortem human brain. However, most analyses of post-mortem dat...

The European Board of Medical Genetics: development of a professional registration system in Europe.

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