Zobrazeno 1 - 10
of 66
pro vyhledávání: '"Adadey P"'
Autor:
Dillon Strepay, Rafal T. Olszewski, Sydney Nixon, Soumya Korrapati, Samuel Adadey, Andrew J. Griffith, Yijun Su, Jiamin Liu, Harshad Vishwasrao, Shoujun Gu, Thomas Saunders, Isabelle Roux, Michael Hoa
Publikováno v:
Scientific Reports, Vol 14, Iss 1, Pp 1-14 (2024)
Abstract The stria vascularis (SV) is a stratified epithelium in the lateral wall of the mammalian cochlea, responsible for both endolymphatic ion homeostasis and generation of the endocochlear potential (EP) critical for normal hearing. The SV has t
Externí odkaz:
https://doaj.org/article/bb8c7c0b6df341d3a917073f881c322a
Autor:
Aniefiok John Udoakang, Nora Nghochuzie Nganyewo, Alexandra Lindsey Djomkam Zune, Charles Ochieng' Olwal, Nsikak-Abasi Aniefiok Etim, Mary Aigbiremo Oboh, Kesego Tapela, Francis Dzabeng, Samuel Mawuli Adadey, Agnes Udoh, Mazo Koné, Joe Kimanthi Mutungi, Peter Kojo Quashie, Gordon Akanzuwine Awandare, Lily Paemka
Publikováno v:
PLoS ONE, Vol 19, Iss 2, p e0281342 (2024)
Coronavirus disease 2019 (COVID-19) pandemic, caused by the Severe Acute Coronavirus 2 (SARS-CoV-2), is a global health threat with extensive misinformation and conspiracy theories. Therefore, this study investigated the knowledge, attitude and perce
Externí odkaz:
https://doaj.org/article/15839f536cf24e7cb5f83f1bd7cb1e73
Autor:
Samuel Mawuli Adadey, Elvis Twumasi Aboagye, Kevin Esoh, Anushree Acharya, Thashi Bharadwaj, Nicole S. Lin, Lucas Amenga-Etego, Gordon A. Awandare, Isabelle Schrauwen, Suzanne M. Leal, Ambroise Wonkam
Publikováno v:
BMC Medical Genomics, Vol 15, Iss 1, Pp 1-10 (2022)
Abstract Background Childhood hearing impairment (HI) is genetically heterogeneous with many implicated genes, however, only a few of these genes are reported in African populations. Methods This study used exome and Sanger sequencing to resolve the
Externí odkaz:
https://doaj.org/article/c26c36b2c8bc4f9cbf88d7ad662a1b90
Autor:
Oluwafemi Gabriel Oluwole, Chandre Oosterwyk, Dominique Anderson, Samuel Mawuli Adadey, Khuthala Mnika, Noluthando Manyisa, Abdoulaye Yalcouye, Edmond T. Wonkam, Elvis Twumasi Aboagye, Yacouba Dia, Esther Uwibambe, Mario Jonas, Roy Priestley, Kalinka Popel, Thumeka Manyashe, Carmen de Cock, Victoria Nembaware, Ambroise Wonkam
Publikováno v:
Journal of Molecular Pathology, Vol 3, Iss 4, Pp 262-272 (2022)
This study describes the roles of laboratory information management systems (LIMS) in multi-site genetics studies in Africa. We used the HiGeneS Africa project as a case study. The study participants were recruited in six African countries between 20
Externí odkaz:
https://doaj.org/article/f4257a1950c549faab6728a11061298e
Autor:
Ambroise Wonkam, Samuel Mawuli Adadey, Isabelle Schrauwen, Elvis Twumasi Aboagye, Edmond Wonkam-Tingang, Kevin Esoh, Kalinka Popel, Noluthando Manyisa, Mario Jonas, Carmen deKock, Victoria Nembaware, Diana M. Cornejo Sanchez, Thashi Bharadwaj, Abdul Nasir, Jenna L. Everard, Magda K. Kadlubowska, Liz M. Nouel-Saied, Anushree Acharya, Osbourne Quaye, Geoffrey K. Amedofu, Gordon A. Awandare, Suzanne M. Leal
Publikováno v:
Communications Biology, Vol 5, Iss 1, Pp 1-16 (2022)
Whole-exome sequencing for 51 families in Ghana reveals 7 candidate genes associated with hearing impairment, 6 of which have previously been demonstrated to be expressed in the mouse inner ear.
Externí odkaz:
https://doaj.org/article/d54deff9f373468982ff9b09bed87e3a
Autor:
Samuel Mawuli Adadey, Edmond Wonkam-Tingang, Leonardo Alves de Souza Rios, Elvis Twumasi Aboagye, Kevin Esoh, Noluthando Manyisa, Carmen De Kock, Gordon A. Awandare, Shaheen Mowla, Ambroise Wonkam
Publikováno v:
Frontiers in Genetics, Vol 13 (2022)
We have previously reported CLIC5A and SLC12A2 variants in two families from Cameroon and Ghana, segregating non-syndromic hearing impairment (NSHI). In this study, biological assays were performed to further functionally investigate the pathogenicit
Externí odkaz:
https://doaj.org/article/c30eeef92166471a8d715fdaa6992a3d
Autor:
Abdoulaye Yalcouyé, Oumou Traoré, Salimata Diarra, Isabelle Schrauwen, Kevin Esoh, Magda Kamila Kadlubowska, Thashi Bharadwaj, Samuel Mawuli Adadey, Mohamed Kéita, Cheick O. Guinto, Suzanne M. Leal, Guida Landouré, Ambroise Wonkam
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 10, Iss 7, Pp n/a-n/a (2022)
Abstract Background Branchio‐otic syndrome (BO) is one of the most common types of syndromic hearing impairment (HI) with an incidence of 1/40,000 globally. It is an autosomal dominant disorder typically characterized by the coexistence of branchia
Externí odkaz:
https://doaj.org/article/ca03eeb61eff4b5fbd4945c6bd94d3c1
Akademický článek
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Akademický článek
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Autor:
Samuel C. B. Stubbs, Osbourne Quaye, Maame Ekua Acquah, Samuel Mawuli Adadey, Iain R. L. Kean, Srishti Gupta, Barbara A. Blacklaws
Publikováno v:
BMC Veterinary Research, Vol 16, Iss 1, Pp 1-18 (2020)
Abstract Background The introduction of rotavirus A vaccination across the developing world has not proved to be as efficacious as first hoped. One cause of vaccine failure may be infection by zoonotic rotaviruses that are very variable antigenically
Externí odkaz:
https://doaj.org/article/7a8bf4181a4a42f794caca8eaa210a25