Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Philomene, Lopez Sall"'
Autor:
Benjamin Momo Kadia, Stephen Allen, Rebecca Pradeilles, Bharati Kulkarni, Babacar Faye, Alan Walker, Raghu Pullakhandam, Teena Dasi, Ravindranadh Palika, Santosh Kumar Banjara, Ibrahima Diallo, Elaine Ferguson, Paul Haggarty, Joanne P Webster, Claire Heffernan, Umi Fahmida, Min Kyaw Htet, Tiffany C Angelin, Modou Lamin Jobarteh, Hilary Davies-Kershaw, Kiruthika Selvaraj, Nur L Zahra, Dwi Yanti, Dewi Shinta, Radhika Madhari, Sylvia Fernandez Rao, Dharani Pratyusha Palepu, Dinesh Yadev, Saliou Diouf, Philomene Lopez-Sall, Babacar Diallo, Princillia Mouissi, Sally Fall, Aicha Djigal, Tabitha D Van Immerzeel, Fassia Tairou, Assana Diop, Sara Strout, Darius Tetsa Tata
Publikováno v:
BMJ Paediatrics Open, Vol 8, Iss Suppl 1 (2024)
Externí odkaz:
https://doaj.org/article/0d7d49d5263f4dbda0a2982d9263f273
Autor:
Jean Pascal Demba Diop, Andréa Régina Gnilane Sène, Yacouba Dia, Seydi Abdoul Ba, Serigne Saliou Mbacke, Cheikh Ameth Tidiane Ly, Pierre Diaga Sarr, Doudou Diouf, Sidy Ka, Babacar Mbengue, Serigne Modou Kane Gueye, Pape Saloum Diop, Maguette Sylla Niang, Papa Madieye Gueye, Philomene Lopez Sall, Ahmadou Dem, Aynina Cisse, Alioune Dieye, Rokhaya Ndiaye
Publikováno v:
Frontiers in Oncology, Vol 11 (2022)
Founder mutations have been reported in BRCA1 and BCRA2 in different ethnic groups with inherited breast cancer. Testing of targeted mutations in specific populations is important for cancer prevention in mutation carriers. In Sub-Saharan Africa, onl
Externí odkaz:
https://doaj.org/article/3bbd073a2a1f425abbe10b8a4c2e00ad
Autor:
Jean Pascal Demba, Diop, Andréa Régina Gnilane, Sène, Yacouba, Dia, Seydi Abdoul, Ba, Serigne Saliou, Mbacke, Cheikh Ameth Tidiane, Ly, Pierre Diaga, Sarr, Doudou, Diouf, Sidy, Ka, Babacar, Mbengue, Serigne Modou Kane, Gueye, Pape Saloum, Diop, Maguette, Sylla Niang, Papa Madieye, Gueye, Philomene, Lopez Sall, Ahmadou, Dem, Aynina, Cisse, Alioune, Dieye, Rokhaya, Ndiaye
Publikováno v:
Frontiers in Oncology
Founder mutations have been reported in BRCA1 and BCRA2 in different ethnic groups with inherited breast cancer. Testing of targeted mutations in specific populations is important for cancer prevention in mutation carriers. In Sub-Saharan Africa, onl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::867bb3c56de5fc5730bef55085cc613e
https://pubmed.ncbi.nlm.nih.gov/35096615
https://pubmed.ncbi.nlm.nih.gov/35096615
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