Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Amy Geard"'
Autor:
Laura Poupon-Bejuit, Amy Geard, Nathan Millicheap, Eridan Rocha-Ferreira, Henrik Hagberg, Claire Thornton, Ahad A Rahim
Publikováno v:
EMBO Molecular Medicine, Vol 16, Iss 6, Pp 1284-1309 (2024)
Abstract Hypoxic-ischaemic encephalopathy (HIE) arises from diminished blood flow and oxygen to the neonatal brain during labor, leading to infant mortality or severe brain damage, with a global incidence of 1.5 per 1000 live births. Glucagon-like Pe
Externí odkaz:
https://doaj.org/article/755beec1f79d489494da254d818c003f
Autor:
Juan Antinao, Diaz, Amy, Geard, Lorna M, FitzPatrick, Juliette M K M, Delhove, Suzanne M K, Buckley, Simon N, Waddington, Tristan R, McKay, Rajvinder, Karda
Publikováno v:
Methods in molecular biology (Clifton, N.J.). 2081
In vivo bioluminescent imaging allows the detection of reporter gene expression in rodents in real time. Here we describe a novel technology whereby we can generate somatotransgenic rodents with the use of a viral vector carrying a luciferase transge
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::0b7ba92a8c7adb5ee42d2c07c2880228
https://pubmed.ncbi.nlm.nih.gov/31721124
https://pubmed.ncbi.nlm.nih.gov/31721124
Autor:
Léon Tshilolo, Mohamed Cherif Rahimy, Jade Hotchkiss, Melek Chaouch, Neil A. Hanchard, Zainab Abimbola Kashim, Ines Tiouiri, Amy Geard, Melissa A. Haendel, Sumir Panji, Kofi A. Anie, Victoria Nembaware, Jemima A. Dennis-Antwi, Karen Kengne Kamga, Marsha Treadwell, Kais Ghedira, Raphael Z. Sangeda, Emile R. Chimusa, Daima Bukini, Solomon F. Ofori-Acquah, Catherine Chunda-Liyoka, Mario Jonas, Adekunle Adekile, Tshepiso Masekoameng, Vivian Paintsil, Liberata Mwita, Kasadhakawo Musa Waiswa, Gaston K. Mazandu, Adijat Ozohu Jimoh, Guida Landouré, Bamidele O. Tayo, Philomene Lopez-Sall, Andrew D. Campbell, Baba Inusa, Clair Ingram, Jennifer Knight-Madden, Khuthala Mnika, Muntaser E. Ibrahim, Ambroise Wonkam, Nicole Vasilevsky, Deogratias Munube, Furahini Tluway, Julie Makani, Nchangwi Syntia Munung, Cherif Ben Hamda, Kwaku Ohene-Frempong, Leonard Malasa, Biobele J. Brown, Vimal K. Derebail, Obiageli E Nnodu, Charmaine D.M. Royal, Simon Jupp, Nicola Mulder, Miriam V Flor-Park, Alex Osei-Akoto
Publikováno v:
Database: The Journal of Biological Databases and Curation
Sickle cell disease (SCD) is one of the most common monogenic diseases in humans with multiple phenotypic expressions that can manifest as both acute and chronic complications. Although described more than a century ago, challenges in comprehensive d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ee4b96362fdb5776338a6b66eb949e49
https://doi.org/10.1093/database/baz118
https://doi.org/10.1093/database/baz118
Autor:
Catherine Chunda-Liyoka, Melissa A. Haendel, Sumir Panji, Kwaku Ohene-Frempong, Marsha Treadwell, Kenneth Opap, Philomene Lopez-Sall, Simon Jupp, Kofi A. Anie, Bamidele O. Tayo, Vimal K. Derebail, Kais Ghedira, Karen Kengne Kamga, Solomon F. Ofori-Acquah, Andrew D. Campbell, Raphael Z. Sangeda, Adekunle Adekile, Furahini Chinenere, Muntaser E. Ibrahim, Neil A. Hanchard, Damian Nirenberg, Deogratias Munube, Carol Hamilton, Nicola Mulder, Mamana Mbiyavanga, Biobele J. Brown, Jennifer Knight-Madden, Léon Tshilolo, Victoria Nembaware, Baba Inusa, Charmaine D.M. Royal, Miriam Park, Obiageli E Nnodu, Wayne Huggins, Ambroise Wonkam, Gift D. Pule, Amy Geard
Publikováno v:
Applied and Translational Genomics, Vol 9, Iss C, Pp 23-29 (2016)
Applied & Translational Genomics
Applied & Translational Genomics, Elsevier, 2016, 9, pp.23-29. ⟨10.1016/j.atg.2016.03.005⟩
Applied & Translational Genomics
Applied & Translational Genomics, Elsevier, 2016, 9, pp.23-29. ⟨10.1016/j.atg.2016.03.005⟩
International audience; Sickle cell disease (SCD) is a debilitating single gene disorder caused by a single point mutation that results in physical deformation (i.e. sickling) of erythrocytes at reduced oxygen tensions. Up to 75% of SCD in newborns w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5c43dd5c6fc8e6156d44e78040e7985c
http://www.sciencedirect.com/science/article/pii/S2212066116300187
http://www.sciencedirect.com/science/article/pii/S2212066116300187
Autor:
Bernard Chetcha Chemegni, Amy Geard, Gift D. Pule, Valentina Josiane Ngo Bitoungui, Emile R. Chimusa, Ambroise Wonkam, Andre Pascal Kengne
Publikováno v:
British journal of haematology. 178(4)
Micro-albuminuria and glomerular hyperfiltration are primary indicators of renal dysfunctions in Sickle Cell Disease (SCD), with more severe manifestations previously associated with variants in APOL1 and HMOX1 among African Americans. We have invest
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c59ac0a77b160220be16f94953a7fafc
https://pubmed.ncbi.nlm.nih.gov/28466968
https://pubmed.ncbi.nlm.nih.gov/28466968
Publikováno v:
Omics : a journal of integrative biology. 20(10)
Sickle cell disease (SCD) vastly impacts the African continent and is associated with cardiovascular diseases. Stroke, kidney disease, and pulmonary hypertension are considered as proxies of severity in SCD with several genomic loci implicated in the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c8b882fba58379f8abad1117f104a9a7
https://pubmed.ncbi.nlm.nih.gov/27726639
https://pubmed.ncbi.nlm.nih.gov/27726639