Zobrazeno 1 - 10
of 25
pro vyhledávání: '"Faizeh Al- Quobaili"'
Publikováno v:
Middle East Fertility Society Journal, Vol 22, Iss 2, Pp 101-104 (2017)
Introduction: Insulin like growth factor-1 (IGF-1) has been found to stimulate follicular development, estrogen and progesterone production and oocyte maturation. This study aims to detect the changes in the follicular fluid IGF-1 levels in normo-ovu
Externí odkaz:
https://doaj.org/article/d28451e30e0f4b3685c254b551d51a66
Publikováno v:
BMC Medical Genetics, Vol 20, Iss 1, Pp 1-6 (2019)
Abstract Background Type 2 diabetes mellitus is believed to be a polygenic disorder that develops as a result of a complex interaction between multiple genes and environmental factors. KCNJ11 gene encodes a Kir6.2 protein which forms the inner sectio
Externí odkaz:
https://doaj.org/article/6ed933cf661d4de1ba354c036ba8d52d
Publikováno v:
Research Journal of Pharmacy and Technology. :3595-3602
Objectives: Endocrine disorders continue to affect the health of thalassemia patients, foremost of which is hypogonadism being the most frequent endocrine complication that involves 70-80% of beta-thalassemia major (β-TM) patients. Actually, the rol
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d9d01a2dbca57d64f4d871ab9ecc125b
https://doi.org/10.52711/0974-360x.2021.00622
https://doi.org/10.52711/0974-360x.2021.00622
Publikováno v:
Hemoglobin. 44:42-46
β-Thalassemia (β-thal) is an inherited blood disorder caused by reduced or absent synthesis of β-globin chains leading to imbalance of globin chain synthesis. β0-Thalassemia (β0-thal), refers to the complete absence of β-globin chain production
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::19d56b705ada3d1f11819380c2264731
https://doi.org/10.1080/03630269.2019.1709207
https://doi.org/10.1080/03630269.2019.1709207
Publikováno v:
BMC Medical Genetics, Vol 20, Iss 1, Pp 1-6 (2019)
BMC Medical Genetics
BMC Medical Genetics
Background Type 2 diabetes mellitus is believed to be a polygenic disorder that develops as a result of a complex interaction between multiple genes and environmental factors. KCNJ11 gene encodes a Kir6.2 protein which forms the inner section of the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dc6bb86bc0aa8e1a0051ce14bfa75f0c
http://link.springer.com/article/10.1186/s12881-019-0846-3
http://link.springer.com/article/10.1186/s12881-019-0846-3
Publikováno v:
Medical Journal of the Islamic Republic of Iran
Background: The pathogenesis of Alzheimer’s disease (AD) is believed to be occurred by the production of neurotic plaques of the beta-amyloid peptide (Aβ) and deposition of them. Therefore, biomarkers of abnormal Aβ processing may represent befor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::02775fbbef58f31c7eeb868785236c26
https://doi.org/10.47176/mjiri.35.19
https://doi.org/10.47176/mjiri.35.19
Publikováno v:
Hemoglobin. 43:283-285
β-Thalassemia (β-thal) is a hereditary and heterogeneous group of disorders caused by mutations on the β-globin gene that result in the reduced or non production of β-globin chains. We report a rare β-globin mutation, IVS-II-848 (C>A) (HBB: c.31
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a459ba2b2f91adb162a01f32cec48e4c
https://doi.org/10.1080/03630269.2019.1670206
https://doi.org/10.1080/03630269.2019.1670206
Publikováno v:
The Open Public Health Journal. 10:132-139
Background: Obestatin is a novel hormone derived from preproghrelin, which was reported to inhibit appetite and gastric motility. Study Aim: This study aimed to investigate plasma obestatin levels in obese patients with T2D patients, which had not be
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::85544346756b9cc3f3a8e69b6463bef1
https://doi.org/10.2174/1874944501710010132
https://doi.org/10.2174/1874944501710010132
Publikováno v:
Middle East Fertility Society Journal, Vol 22, Iss 2, Pp 101-104 (2017)
Introduction: Insulin like growth factor-1 (IGF-1) has been found to stimulate follicular development, estrogen and progesterone production and oocyte maturation. This study aims to detect the changes in the follicular fluid IGF-1 levels in normo-ovu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1c388444a016716bb318ce88993162aa
https://doi.org/10.1016/j.mefs.2017.01.002
https://doi.org/10.1016/j.mefs.2017.01.002
Publikováno v:
Hemoglobin. 43(4-5)
β-Thalassemia (β-thal) is a hereditary and heterogeneous group of disorders caused by mutations on the β-globin gene that result in the reduced or non production of β-globin chains. We report a rare β-globin mutation, IVS-II-848 (CA) (
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::c086b2c63c66340f96467063b96622e2
https://pubmed.ncbi.nlm.nih.gov/31718331
https://pubmed.ncbi.nlm.nih.gov/31718331