Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Aynina, Cisse"'
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:
Moustapha Djite, Philomène Lopez Sall, Ambroise Wonkam, Aynina Cisse, Ibrahima Diagne, Saliou Diop, Papa Madièye Gueye, Rokhaya Ndiaye Diallo, Souleymane Aidara, Sokhna Mara, Younoussa Keita, Aïssatou Toure, El Hadji Malick Ndour, Nènè Oumou kesso Barry, Jean Pascal Demba Diop, Aliou Abdoulaye Ndongo, Hélène Ange Thérèse Sagna-Bassene, Victoria Nembaware, Indou Dème Ly, Moussa Seck, Khuthala Mnika, Gaston Kuzamunu Mazandu, Fatou Guèye Tall, Rokhaya Dione
Publikováno v:
International Journal of Biological and Chemical Sciences; Vol. 15 No. 6 (2021); 2283-2296
La détermination du Débit de Filtration Glomérulaire (DFG) est importante chez les drépanocytaires du fait qu’ils constituent un groupe de patients chez lesquels des atteintes rénales sont fréquemment décrites notamment l’hyperfiltration g
Autor:
El Hadji Malick Ndour, Philomène Lopez Sall, Ndeye Marieme Thioune, Papa Madieye Gueye, Dominique Doupa, Maimouna Ndour Mbaye, Alix Palanga Koboyo, Nènè Oumou Kesso Barry, Michel Assane Ndour, Aynina Cisse, Demba Diedhiou, Pape Matar Kandji, Najah Fatou Gueye Coly, Pape Amadou Diop, Gueye-Tall Fatou, Moustapha Djite
Publikováno v:
African Journal of Biochemistry Research. 15:43-48
The association between hyperuricemia and metabolic syndrome (MS) has been reported in many studies. The authors performed this cross-sectional study to determine the association between hyperuricemia and the MS among diabetic patients in Dakar. Type
Autor:
Alioune Dieye, Seydi Abdoul Ba, Doudou Diouf, Philomène Lopez Sall, Hagay Sobol, Serigne Modou Kane Gueye, Violaine Bourdon-Huguenin, Mamadou Moustapha Dieng, Ahmadou Dem, Babacar Mbengue, Sidy Ka, Oumar Faye, Aynina Cisse, Pape Saloum Diop, Papa Madieye Gueye, Jean Pascal Demba Diop, Maguette Sylla Niang, Ndiaye R, Yacouba Dia, Thiam A, Papa Amadou Diop
Publikováno v:
npj Genomic Medicine, Vol 5, Iss 1, Pp 1-6 (2020)
NPJ Genomic Medicine
NPJ Genomic Medicine
BRCA1 and BRCA2 are the most incriminated genes in inherited breast/ovarian cancers. Several pathogenic variants of these genes conferring genetic predisposition have been described in different populations but rarely in sub-Saharan Africa. The objec
Autor:
Nènè Oumou Kesso Barry, Pape Matar Kandji, Fatou Gueye-Tall, Pape Amadou Diop, Dominique Doupa, Aynina Cisse, Philomène Lopez Sall, Moustapha Djite, Najah Fatou Coly Gueye, Jean Pascal Demba Diop, Rokhaya Ndiaye-Dia, El Hadji Malick Ndour, Papa Madieye Gueye
Publikováno v:
American Journal of Biochemistry and Molecular Biology. 10:1-5
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
Autor:
Ibrahima Diagne, Rokhaya Ndiaye Diallo, Pape Amadou Diop, Papa Madieye Gueye, Fatou Gueye Tall, Aynina Cisse, Cyril Martin, Philippe Connes, Céline Renoux, Philomène Lopez Sall, Indou Deme Ly, Philippe Joly, El Hadji Malick Ndour
Publikováno v:
Pediatric Blood and Cancer
Pediatric Blood and Cancer, Wiley, 2019, 66 (10), pp.e27934. ⟨10.1002/pbc.27934⟩
Pediatric Blood and Cancer, Wiley, 2019, 66 (10), pp.e27934. ⟨10.1002/pbc.27934⟩
International audience; BACKGROUND: Our objective was to investigate the combined and differential effects of alpha-thalassemia -3.7 kb deletion and HbF-promoting quantitative trait loci (HbF-QTL) in Senegalese hydroxyurea (HU)-free children and youn
Autor:
Scott M. Williams, Alioune Dieye, Sidy Ka, Mbacké Sembène, P. Lopez Sall, Rajkumar Ramesar, Branwen J. Hennig, Michèle Ramsay, Melanie J. Newport, Ahmadou Dem, Mamour Gueye, Papa Madieye Gueye, M. Gadji, Alioune Gaye, N. Diop, Charles N. Rotimi, M. Sylla Niang, Jean Pascal Demba Diop, R. Ndiaye Diallo, Oumar Faye, E. Matovu, Ambroise Wonkam, Aynina Cisse
Publikováno v:
Global Health, Epidemiology and Genomics
The 9th meeting of the African Society of Human Genetics, in partnership with the Senegalese Cancer Research and Study Group and the Human Heredity and Health in Africa (H3Africa) Consortium, was held in Dakar, Senegal. The theme wasStrengthening Hum
Autor:
Rokhaya Ndiaye Diallo, Aynina Cisse, El Hadji Malick Ndour, Philomène Lopez Sall, Ibrahima Diagne, Louis Chillotti, Papa Madieye Gueye, Indou Deme Ly, Pape Amadou Diop, Philippe Connes, Philippe Lacan, Cyril Martin, Céline Renoux, Philippe Joly, Fatou Gueye Tall, Nicolas Veyrenche
Publikováno v:
Hemoglobin
Hemoglobin, Informa Healthcare, 2017, 41 (2), pp.89-95. ⟨10.1080/03630269.2017.1339610⟩
Hemoglobin, Informa Healthcare, 2017, 41 (2), pp.89-95. ⟨10.1080/03630269.2017.1339610⟩
Sickle cell disease is a genetic disorder with a large variability in the pattern and severity of clinical manifestations. Different genetic modulators have been identified but very few epidemiologic data are available on these modifier genes in Sene
Autor:
Niama Diop Sall, Sarr Gn, P. Lopez-Sall, S.N. Diop, M. Touré, N. M. Ndour-Mbaye, A. Sarr, A Sarr, O. Diop, Aynina Cisse
Publikováno v:
Médecine des Maladies Métaboliques. 6:238-243
La rarete des travaux sur le syndrome plurimetabolique (SM) en Afrique nous a incites a entreprendre une etude, en vue d’evaluer sa frequence et celle de ses complications dans une population senegalaise, selon les criteres de l’Organisation mond