People

Profile

Asmaa Abu maziad

Assistant Professor, Pediatrics - (Clinical Scholar Track)

Collaboration(8)

Page 1 of 2

Publications(7)

Recent

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

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

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

People

Profile

Asmaa Abu maziad

Collaboration(8)

Russell Witte

Fayez Ghishan

Jason Wertheim

Pawel Kiela

Rick Schnellmann

Publications(7)

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

The multifaceted helical net of amphipathic alpha-helices; the next dimension of the helical peptide wheel

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

Congenital nephrotic syndrome

De novo TRIM8 variants impair its protein localization to nuclear bodies and cause developmental delay, epilepsy, and focal segmental glomerulosclerosis

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

The role of novel COQ8B mutations in glomerulopathy and related kidney defects

Profile

Asmaa Abu maziad

Collaboration(8)

Russell Witte

Fayez Ghishan

Jason Wertheim

Pawel Kiela

Rick Schnellmann

Publications(7)

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

The multifaceted helical net of amphipathic alpha-helices; the next dimension of the helical peptide wheel

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

Congenital nephrotic syndrome

De novo TRIM8 variants impair its protein localization to nuclear bodies and cause developmental delay, epilepsy, and focal segmental glomerulosclerosis

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

The role of novel COQ8B mutations in glomerulopathy and related kidney defects