Zobrazeno 1 - 10
of 19
pro vyhledávání: '"Hind A. Elnasri"'
Publikováno v:
Informatics in Medicine Unlocked, Vol 19, Iss , Pp 100337- (2020)
Genetic polymorphisms in the GGCX gene have been associated with many vitamin K-dependent protein disorders including vitamin K-dependent clotting factors deficiency, osteoporosis, vascular calcification disorders, and pseudoxanthoma elasticum syndro
Externí odkaz:
https://doaj.org/article/334717881e9f4a44ac479f1d81fcd8e2
Publikováno v:
International Journal on Food, Agriculture and Natural Resources, Vol 4, Iss 4, Pp 36-40 (2023)
Heavy metals are known for their toxic effects and lead to serious health problems. Fish is widely consumed, and the fish industry is rapidly growing. Heavy metals can accumulate in different parts of the fish from water, feed or sediment and can be
Externí odkaz:
https://doaj.org/article/ad618ae51eee4bc88152744eeec8d311
Determination of Lead and Cadmium level in cattle offals, water and feed in Omdurman locality –Sudan
Publikováno v:
International Journal on Food, Agriculture and Natural Resources, Vol 4, Iss 2, Pp 15-19 (2023)
This study was carried out to determine the level of Cadmiuum (Cd) and Lead (Pb) in cattle meat, offals, water and feed samples. The samples were obtained from Al Muwalih area (Omdurman locality- Sudan). Laboratory analysis was carried out using Atom
Externí odkaz:
https://doaj.org/article/1846a7cd0948404aafeeb61035ee7ca1
Publikováno v:
Asian Journal of Fisheries and Aquatic Research. :15-21
This study aimed to investigate the levels of lead (Pb) and Cadmium (Cd) in water and fish muscle obtained from Elshajara area - Khartoum - Sudan. This area is located near one of the important factories in the country and is also an important fishin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f3810d2d59dd5cc2a1bfe10c239c387e
https://doi.org/10.9734/ajfar/2020/v7i430125
https://doi.org/10.9734/ajfar/2020/v7i430125
Autor:
Mona Abdelrahman Mohamed Khaier, Doaa A. Gassim, Hind Abdelaziz Elnasri, Afraa M. Albakrye, Mozan Osman Hassan
Publikováno v:
Informatics in Medicine Unlocked, Vol 19, Iss, Pp 100337-(2020)
Genetic polymorphisms in the GGCX gene have been associated with many vitamin K-dependent protein disorders including vitamin K-dependent clotting factors deficiency, osteoporosis, vascular calcification disorders, and pseudoxanthoma elasticum syndro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a201f339b887f7b8087a92177a75247b
http://www.sciencedirect.com/science/article/pii/S2352914820300332
http://www.sciencedirect.com/science/article/pii/S2352914820300332
Publikováno v:
International Journal of Current Microbiology and Applied Sciences. 7:592-600
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a5eecfedf0a6a5104d2445ab3bb2cd49
https://doi.org/10.20546/ijcmas.2018.707.072
https://doi.org/10.20546/ijcmas.2018.707.072
Autor:
Abubaker A. El Ayis, Hind A. Elnasri
Publikováno v:
International Journal of Scientific Footprints. 5:24-34
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::604169ddf2347153c20650210754e6b1
https://doi.org/10.22576/ijsf/sf-2017-71
https://doi.org/10.22576/ijsf/sf-2017-71
Publikováno v:
Journal of agricultural, environmental and veterinary sciences. 3
Background: (BMPR2) gene is encoded gene and cause pulmonary arterial hypertension. Also, it has major role in regulating the growth the maturation of cells. A (BMPR2) gene contains only 25 SNPs as deleterious SNPs and was analyzed in this study. Mat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a91a01769c617819310ef767701744e1
https://doi.org/10.26389/ajsrp.m250319
https://doi.org/10.26389/ajsrp.m250319
Autor:
Hind Abdelaziz Elnasri, Howeida Abdullah Mustafa, Mona AbdelRahman Mohammed Khair, Nidal Abdelwahid, Afraa Mohamed Suliman Albkrye, Buthiena Mohamed AbdAlla
Publikováno v:
Clinical and Translational Medicine
Clinical and Translational Medicine, Vol 9, Iss 1, Pp 1-10 (2020)
Clinical and Translational Medicine, Vol 9, Iss 1, Pp 1-10 (2020)
Background The Peroxisome proliferator-activated receptor gamma gene (PPARG), encodes a member of the peroxisome-activated receptor subfamily of nuclear receptors. PPARs form heterodimers with retinoid X receptors (RXRs) which regulate transcription
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::75e5f4d8bcd164d0223f15df0e32c99f
https://pubmed.ncbi.nlm.nih.gov/32064572
https://pubmed.ncbi.nlm.nih.gov/32064572
Autor:
Mona Abdelrahman Mohamed Khaier, Hind Abdelaziz Elnasri, Hadeel Salah Kashan, Afra Mohamed Albkrye
Publikováno v:
Informatics in Medicine Unlocked, Vol 27, Iss, Pp 100808-(2021)
Introduction Dopa responsive dystonia (DRD) is an inherited movement disorder. Mutations in GCH1 gene is the most common root of autosomal dominant, early onset of DRD. This study aimed to analyze the genetic variation that can alter the expression a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::89b33f12ac45d2beeb2202b2fa42b515
https://doi.org/10.1016/j.imu.2021.100808
https://doi.org/10.1016/j.imu.2021.100808