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Amanat Ali
Amanat Ali
Postdoctoral Scientist, AECOM
Verified email at einsteinmed.edu
Title
Cited by
Cited by
Year
Dynamics of the ACE2–SARS-CoV-2/SARS-CoV spike protein interface reveal unique mechanisms
A Ali, R Vijayan
Scientific reports 10 (1), 14214, 2020
2392020
From desert to medicine: a review of camel genomics and therapeutic products
A Ali, B Baby, R Vijayan
Frontiers in genetics 10, 426751, 2019
842019
Molecular insights into the interaction of hemorphin and its targets
A Ali, B Baby, SS Soman, R Vijayan
Scientific reports 9 (1), 14747, 2019
282019
Molecular basis of the therapeutic properties of hemorphins
A Ali, SAR Alzeyoudi, SA Almutawa, AN Alnajjar, R Vijayan
Pharmacological Research 158, 104855, 2020
222020
Positive modulation of angiotensin II type 1 receptor–mediated signaling by LVV–hemorphin-7
A Ali, A Palakkott, A Ashraf, I Al Zamel, B Baby, R Vijayan, MA Ayoub
Frontiers in Pharmacology 10, 1258, 2019
142019
Dynamics of camel and human hemoglobin revealed by molecular simulations
A Ali, SS Soman, R Vijayan
Scientific reports 12 (1), 122, 2022
132022
Camel hemorphins exhibit a more potent angiotensin-I converting enzyme inhibitory activity than other mammalian hemorphins: An in silico and in vitro study
A Ali, SAR Alzeyoudi, SA Almutawa, AN Alnajjar, Y Al Dhaheri, R Vijayan
Biomolecules 10 (3), 486, 2020
132020
Characterization of ETFDH and PHGDH Mutations in a Patient with Mild Glutaric Aciduria Type II and Serine Deficiency
A Ali, NA Dhahouri, FSA Almesmari, WM Fathalla, FA Jasmi
Genes 12 (5), 703, 2021
62021
Bi‐allelic null variant in matrix metalloproteinase‐15, causes congenital cardiac defect, cholestasis jaundice, and failure to thrive
HA Abdelrahman, N Akawi, AM Al‐Shamsi, A Ali, F Al‐Jasmi, A John, ...
Clinical Genetics 101 (4), 403-410, 2022
52022
Clinical, biochemical, and genetic heterogeneity in glutaric aciduria type ii patients
A Ali, FSA Almesmari, NA Dhahouri, AM Saleh Ali, MAAMA Aldhanhani, ...
Genes 12 (9), 1334, 2021
52021
Characterization of ACE2 naturally occurring missense variants: impact on subcellular localization and trafficking
S Badawi, FE Mohamed, NR Alkhofash, A John, A Ali, BR Ali
Human Genomics 16 (1), 35, 2022
42022
Insights into the interaction of LVV-Hemorphin-7 with angiotensin II type 1 receptor
A Ali, EKM Johnstone, B Baby, HB See, A Song, KJ Rosengren, ...
International journal of molecular sciences 22 (1), 209, 2020
42020
A Type 3 Gaucher-Like Disease Due To Saposin C Deficiency in Two Emirati Families Caused by a Novel Splice Site Variant in the PSAP Gene
FE Mohamed, A Ali, A Al-Tenaiji, A Al-Jasmi, F Al-Jasmi
Journal of Molecular Neuroscience 72 (6), 1322-1333, 2022
32022
Case Report: Reinterpretation and Reclassification of ARSB:p.Arg159Cys Variant Identified in an Emirati Patient With Hearing Loss Caused by a Pathogenic Variant in the …
N Al Dhahouri, A Ali, J Hertecant, F Al-Jasmi
Frontiers in Pediatrics 9, 803732, 2022
12022
Polypharmacological potential of natural compounds against prostate cancer explored using molecular docking and molecular dynamics simulations
P Antony, B Baby, ZA Homedi, WA Halabi, A Ali, R Vijayan
International Journal of Computational Biology and Drug Design 13 (2), 181-199, 2020
12020
Spectrum of Genetic Variants in Bilateral Sensorineural Hearing Loss
A Amanat, T Mohammed, K Praseetha, B Ibrahim, A Mushal, J Anne, ...
Frontiers in Genetics 15, 2024
2024
Interaction of Glutathione with MMACHC Arginine-Rich Pocket Variants Associated with Cobalamin C Disease: Insights from Molecular Modeling
P Antony, B Baby, A Ali, R Vijayan, F Al Jasmi
Biomedicines 11 (12), 3217, 2023
2023
Lupus nephritis: A focus on the United Arab Emirates and the potential role of genetics
M Tabouni, A Ali, N Aljaberi, H Alblooshi
Lupus 31 (12), 1415-1422, 2022
2022
Identification of potential anti-obesity drug scaffolds using molecular modelling
A Jobe, B Baby, A Ali, R Vijayan
International Journal of Computational Biology and Drug Design 14 (2), 103-129, 2021
2021
EVALUATION OF THE GENETIC AND STRUCTURAL VARIATIONS OF CAMEL HEMOGLOBIN
A Ali
2020
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