Zobrazeno 1 - 10
of 37
pro vyhledávání: '"Minnie, Jacob"'
Autor:
Lina A. Dahabiyeh, Refat M. Nimer, Khalid M. Sumaily, Mohamad S. Alabdaljabar, Minnie Jacob, Essa M. Sabi, Maged H. Hussein, Anas Abdel Rahman
Publikováno v:
Scientific Reports, Vol 13, Iss 1, Pp 1-11 (2023)
Abstract Chronic kidney disease (CKD) is a serious public health problem characterized by progressive kidney function loss leading to end-stage renal disease (ESRD) that demands dialysis or kidney transplantation. Early detection can prevent or delay
Externí odkaz:
https://doaj.org/article/9ecc2738f9e3452ea995a1ea63c3031c
Autor:
Minnie Jacob, Afshan Masood, Zakiya Shinwari, Mai Abdel Jabbar, Hamoud Al-Mousa, Rand Arnaout, Bandar AlSaud, Majed Dasouki, Ayodele A. Alaiya, Anas M. Abdel Rahman
Publikováno v:
Frontiers in Allergy, Vol 2 (2021)
Dedicator of cytokinesis 8 deficiency is an autosomal recessive primary immune deficiency disease belonging to the group of hyperimmunoglobulinemia E syndrome (HIES). The clinical phenotype of dedicator of cytokinesis 8 (DOCK8) deficiency, characteri
Externí odkaz:
https://doaj.org/article/d1f6d8850f3e45c4a80647f65242f9cb
Autor:
Dalia Sriwi, Mohamad S. Alabdaljabar, Minnie Jacob, Ahmed H. Mujamammi, Xinyun Gu, Essa M. Sabi, Liang Li, Maged H. Hussein, Majed Dasouki, Anas M. Abdel Rahman
Publikováno v:
Biology, Vol 10, Iss 8, p 770 (2021)
Cystic renal disease (CRD) comprises a heterogeneous group of genetic and acquired disorders. The cystic lesions are detected through imaging, either incidentally or after symptoms develop, due to an underlying disease process. In this study, we aim
Externí odkaz:
https://doaj.org/article/f677725434da4639abff162436bfa892
Autor:
Abeer K. Malkawi, Karem H. Alzoubi, Minnie Jacob, Goran Matic, Asmaa Ali, Achraf Al Faraj, Falah Almuhanna, Majed Dasouki, Anas M. Abdel Rahman
Publikováno v:
Frontiers in Pharmacology, Vol 9 (2018)
Dexamethasone (Dex) is a synthetic glucocorticoid that has anti-inflammatory and immunosuppressant effects and is used in several conditions such as asthma and severe allergy. Patients receiving Dex, either at a high dose or for a long time, might de
Externí odkaz:
https://doaj.org/article/ca70f2771b0b4e728da53e6b9fa439b3
Autor:
Minnie Jacob, Refat M. Nimer, Mohamad S. Alabdaljabar, Essa M. Sabi, Mysoon M. Al-Ansari, Maged Housien, Khalid M. Sumaily, Lina A. Dahabiyeh, Anas M. Abdel Rahman
Publikováno v:
International Journal of Molecular Sciences; Volume 23; Issue 20; Pages: 12614
Nephrotic syndrome (NS) is a kidney illness characterized by excessive proteinuria, hypoalbuminemia, edema, and hyperlipidemia, which may lead to kidney failure and necessitate renal transplantation. End-stage renal disease, cardiovascular issues, an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ed6c9beb8bb1f2386e0504e37f69b863
https://pubmed.ncbi.nlm.nih.gov/36293474
https://pubmed.ncbi.nlm.nih.gov/36293474
Autor:
Minnie Jacob, Xinyun Gu, Xian Luo, Hamoud Al-Mousa, Rand Arnaout, Bandar Al-Saud, Andreas L. Lopata, Liang Li, Majed Dasouki, Anas M. Abdel Rahman
Publikováno v:
Metabolites, Vol 9, Iss 11, p 274 (2019)
Bi-allelic mutations in the dedicator of cytokinesis 8 (DOCK8) are responsible for a rare autosomal recessive primary combined immunodeficiency syndrome, characterized by atopic dermatitis, elevated serum Immunoglobulin E (IgE) levels, recurrent seve
Externí odkaz:
https://doaj.org/article/5e633c0178714e0296ccb53a3a93a4dd
Publikováno v:
International Journal of Molecular Sciences. 24:2406
Hyper-IgE Syndrome (HIES) is a heterogeneous group of primary immune-deficiency disorders characterized by elevated levels of IgE, eczema, and recurrent skin and lung infections. HIES that is autosomally dominant in the signal transducer and activato
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6b16008a59162d13156bfa79243a14bb
https://doi.org/10.3390/ijms24032406
https://doi.org/10.3390/ijms24032406
Autor:
Osama Y. Al-Dirbashi, Tomofumi Santa, Mohamed S. Rashed, Zuhair Al-Hassnan, Nobuyuki Shimozawa, Aziza Chedrawi, Minnie Jacob, Manhal Al-Mokhadab
Publikováno v:
Journal of Lipid Research, Vol 49, Iss 8, Pp 1855-1862 (2008)
Quantification of pristanic acid, phytanic acid, and very long chain fatty acids (i.e., hexacosanoic, tetracosanoic, and docosanoic acids) in plasma is the primary method for investigateing a multitude of peroxisomal disorders (PDs). Typically based
Externí odkaz:
https://doaj.org/article/3398154d3dad4069912bc5e45be67fa7
Autor:
Hicham Benabdelkamel, Anas M. Abdel Rahman, Liang Li, Imran Nizami, Afshan Masood, Majed Dasouki, Minnie Jacob, Mai Abdel Jabar, Xinyun Gu
Publikováno v:
Metabolomics. 17
Cystic fibrosis (CF) is a lethal multisystemic disease of a monogenic origin with numerous mutations. Functional defects in the cystic fibrosis transmembrane conductance receptor (CFTR) protein based on these mutations are categorised into distinct c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::51288f65eba7bf2fa98f7e561f216e40
https://doi.org/10.1007/s11306-020-01760-5
https://doi.org/10.1007/s11306-020-01760-5
Autor:
Yumi Mizuno, Yuichi Ninomiya, Yutaka Nakachi, Mioko Iseki, Hiroyasu Iwasa, Masumi Akita, Tohru Tsukui, Nobuyuki Shimozawa, Chizuru Ito, Kiyotaka Toshimori, Megumi Nishimukai, Hiroshi Hara, Ryouta Maeba, Tomoki Okazaki, Ali Nasser Ali Alodaib, Mohammed Al Amoudi, Minnie Jacob, Fowzan S Alkuraya, Yasushi Horai, Mitsuhiro Watanabe, Hiromi Motegi, Shigeharu Wakana, Tetsuo Noda, Igor V Kurochkin, Yosuke Mizuno, Christian Schönbach, Yasushi Okazaki
Publikováno v:
PLoS Genetics, Vol 9, Iss 2, p e1003286 (2013)
Peroxisomes are subcellular organelles involved in lipid metabolic processes, including those of very-long-chain fatty acids and branched-chain fatty acids, among others. Peroxisome matrix proteins are synthesized in the cytoplasm. Targeting signals
Externí odkaz:
https://doaj.org/article/7c0fcabd2f8148dfb02c972a9f888031