Zobrazeno 1 - 10
of 21
pro vyhledávání: '"Momodou W. Jallow"'
Autor:
Richard Sidebottom, Solomon Bizuayehu Wassie, Carla Cerami, Momodou W. Jallow, Shailaja Fennell, Sarah Dalzell
Publikováno v:
Frontiers in Nutrition, Vol 9 (2022)
The Covid pandemic has exposed fissures of inequality through heightened food insecurity and nutritional deficiency for vulnerable social cohorts with limited coping mechanisms. Given the multi-dimensional pathways through which its effects have been
Externí odkaz:
https://doaj.org/article/8dbe9fb80ef24f3381a0efeaa17e84ff
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-9 (2021)
Abstract Genome-wide association studies in Europeans and Asians have identified numerous variants in the transmembrane protease serine 6 (TMPRSS6) and transferrin (TF) genes that are associated with changes in iron status. We sought to investigate t
Externí odkaz:
https://doaj.org/article/4f5d466afd1243188432805331e09794
Formalising recall by genotype as an efficient approach to detailed phenotyping and causal inference
Autor:
Laura J. Corbin, Vanessa Y. Tan, David A. Hughes, Kaitlin H. Wade, Dirk S. Paul, Katherine E. Tansey, Frances Butcher, Frank Dudbridge, Joanna M. Howson, Momodou W. Jallow, Catherine John, Nathalie Kingston, Cecilia M. Lindgren, Michael O’Donavan, Stephen O’Rahilly, Michael J. Owen, Colin N. A. Palmer, Ewan R. Pearson, Robert A. Scott, David A. van Heel, John Whittaker, Tim Frayling, Martin D. Tobin, Louise V. Wain, George Davey Smith, David M. Evans, Fredrik Karpe, Mark I. McCarthy, John Danesh, Paul W. Franks, Nicholas J. Timpson
Publikováno v:
Nature Communications, Vol 9, Iss 1, Pp 1-11 (2018)
Recall-by-Genotype (RbG) is an approach to recall participants from genetic studies based on their specific genotype for further, more extensive phenotyping. Here, the authors discuss examples of RbG as well as practical and ethical considerations an
Externí odkaz:
https://doaj.org/article/4889e7ce60af487a8fa26fd2a38318e8
Autor:
Andrew E. Armitage, Schadrac C. Agbla, Modupeh Betts, Ebrima A. Sise, Momodou W. Jallow, Ellen Sambou, Bakary Darboe, Archibald Worwui, George M. Weinstock, Martin Antonio, Sant-Rayn Pasricha, Andrew M. Prentice, Hal Drakesmith, Momodou K. Darboe, Brenda Anna Kwambana-Adams
Publikováno v:
Haematologica, Vol 104, Iss 8 (2019)
Iron deficiency and iron deficiency anemia are highly prevalent in low-income countries, especially among young children. Hepcidin is the major regulator of systemic iron homeostasis. It controls dietary iron absorption, dictates whether absorbed iro
Externí odkaz:
https://doaj.org/article/12ff59563e9240c595770c350292f7fb
Autor:
Rita Wegmüller, Amat Bah, Lindsay Kendall, Morgan M Goheen, Saikou Sanyang, Ebrima Danso, Ebrima A Sise, Amadou Jallow, Hans Verhoef, Momodou W Jallow, Miriam Wathuo, Andrew E Armitage, Hal Drakesmith, Sant-Rayn Pasricha, James H Cross, Carla Cerami, Andrew M Prentice
Publikováno v:
The Lancet Global Health 11 (2023) 1
The Lancet Global Health, 11(1), e105-e116
The Lancet Global Health, 11(1), e105-e116
Background: Iron deficiency is the most prevalent nutritional disorder worldwide. Iron supplementation has modest efficacy, causes gastrointestinal side-effects that limit compliance, and has been associated with serious adverse outcomes in children
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::710c6c231dd92170140b3cfb90cfec8c
https://research.wur.nl/en/publications/hepcidin-guided-screen-and-treat-interventions-for-young-children
https://research.wur.nl/en/publications/hepcidin-guided-screen-and-treat-interventions-for-young-children
Publikováno v:
Scientific Reports
Scientific Reports, Vol 11, Iss 1, Pp 1-9 (2021)
Scientific Reports, Vol 11, Iss 1, Pp 1-9 (2021)
Genome-wide association studies in Europeans and Asians have identified numerous variants in the transmembrane protease serine 6 (TMPRSS6) and transferrin (TF) genes that are associated with changes in iron status. We sought to investigate the effect
Background: The role of genetic determinants in mediating iron status in Africans is not fully understood. Genome-wide association studies in non-African populations have revealed genetic variants in the transmembrane protease serine 6 gene (TMPRSS6)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6e021bcfa6faf6d77a19ea5b2aaf58e9
Publikováno v:
F1000Research
Background: Oral iron supplementation is commonly used to treat and prevent anaemia. The transmembrane protease serine 6 gene (TMPRSS6), which encodes matriptase 2, is a negative regulator of hepcidin, the key controller of iron homeostasis. Genome-w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4497163b9af294edf1d63f08f0b88326
https://researchonline.lshtm.ac.uk/id/eprint/4659115/1/e8cb783c-a10f-47fe-acd3-2eee06a8d590_19080_-_carla_cerami_v2.pdf
https://researchonline.lshtm.ac.uk/id/eprint/4659115/1/e8cb783c-a10f-47fe-acd3-2eee06a8d590_19080_-_carla_cerami_v2.pdf
Publikováno v:
Current Developments in Nutrition
Background The role of genetic determinants in mediating iron status in Africans is not fully understood. Genome-wide association studies in non-African populations have revealed genetic variants in the transmembrane protease serine 6 gene (TMPRSS6)
Publikováno v:
PLoS ONE, Vol 15, Iss 7, p e0235141 (2020)
PLoS ONE
PLoS ONE
Iron deficiency anaemia is a major health problem affecting approximately 1.2 billion people worldwide. Young children, women of reproductive age and pregnant women living in sub-Saharan Africa are the most vulnerable. It is estimated that iron defic