scholarly journals Isabella Helen Mary Muir CBE. 20 August 1920—28 November 2005

2018 ◽  
Vol 65 ◽  
pp. 283-298
Author(s):  
Tim Hardingham

Helen Muir was a leader in British biomedical research over many years. She trained as a chemist at Oxford and, having started her research on the structure of penicillin, she moved progressively into biomedical research. Helen's major achievements were in research on joint diseases, particularly osteoarthritis, which affects 8 million sufferers in the UK. She identified the molecular basis of the key load-bearing properties of cartilage in our joints and helped to establish that osteoarthritis was driven by active processes and not just wear and tear. This revolutionized research approaches at the time and the consequences are important to this day. Her careful research analysis laid the foundation for molecular cellular research approaches to degenerative joint diseases. She was Division Head and then Director at the Kennedy Institute for Rheumatology in Hammersmith, London. Helen was highly regarded and was appointed the first woman member of the Medical Research Council and later a Trustee of the Wellcome Trust. She was respected for her opinions, which she expressed in a forthright manner. She was very much without prejudice and judged people on their merits. She could not stand pomposity and, although she became a grand lady, she always had a wry sense of humour and liked a good laugh.

2020 ◽  
Vol 4 (Supplement_2) ◽  
pp. 805-805
Author(s):  
Ebrima Bah ◽  
Frank Michelangeli

Abstract Objectives To find out the overlapping and correlating relationships between serum haptoglobin level, haptoglobin genotype and phenotype, blood haemoglobin level and zinc protoporphyrin (measured in washed RBCs) in association to prevalence of anaemia. It will focus on comparing all the mention components in contrast to each other. The study will also look for the frequency distribution of the major HP alleles. Methods 1278 participants were randomly selected. Blood samples collected by trained nurses. Data generation was done at the Medical research council (keneba field station) research site. Data Analysis was conducted at the university of Chester with the assistance of the computer department team. Results P = 0.000 indicating anaemia prevalence with HP 1 allele. P > 0.05 when ID, IDA and AI relates with HP genotype. Positive correlation between ZnPP and HP serum level, but negative between ZnPP and Hb. P = 0.000 between ZnPP and IDA. P = 0.024 between HP genotype and Hb level. P = 0.013 between HP genotype and HP serum. P = 0.100 between HP genotype and ZnPP. P = 0.000 between ZnPP and IDA. P = 0.024 between HP genotype and Hb. ZnPP shared a positive correlation with HP serum level, and a negative correlation with Hb level. The correlation significant = 0.01 level (2-tailed) P = 0.01. The correlation between HP genotype and HP serum level was significant with P = 0.013, but the correlation between HP genotype and ZnPP was not significant with P = 0.100. Conclusions HP genotype had association with anaemia prevalence and more occurrence was observed in carriers of the type ‘1’ allele. It had no association with ID, IDA and AI. HP genotype had association with HP serum level and Hb level but had no association with ZnPP level. ZnPP level was observed to have had association with HP serum level, Hb level and IDA; but had no association with ID and AI in the region. Funding Sources All the resources used in this study were from MRC Keneba (International Nutrition Group) which is supported by funds from the UK Medical Research Council (MRC) and the UK Department for International Development (DFID) under the MRC/DFID Concordat agreement (Hennig et al., 2015).


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