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Profile
Asmaa Abu maziad
Assistant Professor, Pediatrics - (Clinical Scholar Track)
Pediatrics
Full Page
Overview
Research
More
Collaboration
(8)
Russell Witte
Mutual work: 2 Proposals
Collaboration Details
Fayez Ghishan
Mutual work: 1 Proposalīš1 Publication
Collaboration Details
Jason Wertheim
Mutual work: 3 Proposals
Collaboration Details
Pawel Kiela
Mutual work: 1 Publication
Collaboration Details
Rick Schnellmann
Mutual work: 2 Proposals
Collaboration Details
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Publications
(7)
Chart
Bar chart with 4 bars.
The chart has 1 X axis displaying Year.
The chart has 1 Y axis displaying values. Data ranges from 1 to 2.
Created with Highcharts 11.4.8
Year
2020
2021
2023
2024
0
0.5
1
1.5
2
2.5
End of interactive chart.
Recent
The multifaceted helical net of amphipathic alpha-helices; the next dimension of the helical peptide wheel
2024
peptide structure,
protein folding,
helical structure,
molecular biology
background- An In Silico Investigation of the Pathogenic G151R G Protein-Gated Inwardly Rectifying K background- background- Channel 4 Variant to Identify Small Molecule Modulators
2024
protein function,
drug discovery,
genetic variant,
computational modeling
Identification of Potential Modulators of a Pathogenic G Protein-Gated Inwardly Rectifying K Channel 4 Mutant: Investigation in the Context of Drug Discovery for Hypertension
2023
drug discovery,
hypertension,
g-protein signaling
Congenital nephrotic syndrome
2021
genetic disorders,
pediatric nephrology,
kidney disease,
novel therapies
De novo TRIM8 variants impair its protein localization to nuclear bodies and cause developmental delay, epilepsy, and focal segmental glomerulosclerosis
2021
genetics,
neuroscience,
nephrology,
developmental biology,
cell biology
De novo truncating TRIM8 variants impair its protein localization to nuclear bodies and cause a pediatric syndrome of developmental delay, epilepsy and focal segmental glomerulosclerosis
2020
genetics,
neurodevelopmental disorders,
epilepsy,
nephrology
The role of novel COQ8B mutations in glomerulopathy and related kidney defects
2020
genetics,
kidney disease,
mutations,
glomerulopathy,
coq8b
