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Role of sphingolipid metabolism in neurodegeneration

Journal of neurochemistry, 2021-07, Vol.158 (1), p.25-35

2021

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Development of Epirubicin-Loaded Biocompatible Polymer PLA-PEG-PLA Nanoparticles: Synthesis, Characterization, Stability, and In Vitro Anticancerous Assessment

Polymers, 2021-04, Vol.13 (8), p.1212

2021

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A Novel Homozygous Non-sense Mutation in the Catalytic Domain of MTHFR Causes Severe 5,10-Methylenetetrahydrofolate Reductase Deficiency

Frontiers in neurology, 2019-04, Vol.10, p.411

2019

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Consanguinity and Congenital Heart Disease Susceptibility: Insights into Rare Genetic Variations in Saudi Arabia

Genes, 2022-02, Vol.13 (2), p.354

2022

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Association between human leukocyte antigen alleles and COVID-19 disease severity

Journal of infection and public health, 2024-09, Vol.17 (9), p.102498, Article 102498

2024

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A cell-based drug delivery platform for treating central nervous system inflammation

Journal of molecular medicine (Berlin, Germany), 2021-05, Vol.99 (5), p.663-671

2021

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Fast-Dissolving Nifedipine and Atorvastatin Calcium Electrospun Nanofibers as a Potential Buccal Delivery System

Pharmaceutics, 2022-02, Vol.14 (2), p.358

2022

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Tween 80-Based Self-Assembled Mixed Micelles Boost Valsartan Transdermal Delivery

Pharmaceuticals (Basel, Switzerland), 2023-12, Vol.17 (1), p.19

2023

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Novel Autosomal Recessive Splice-Altering Variant in PRKD1 Is Associated with Congenital Heart Disease

Genes, 2021-04, Vol.12 (5), p.612

2021

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Optimized Polyethylene Glycolylated Polymer–Lipid Hybrid Nanoparticles as a Potential Breast Cancer Treatment

Pharmaceutics, 2020-07, Vol.12 (7), p.666

2020

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Analysis of chronic kidney disease patients by targeted next-generation sequencing identifies novel variants in kidney-related genes

Frontiers in genetics, 2022-08, Vol.13, p.886038-886038

2022

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The Role of the Disrupted Podosome Adaptor Protein (SH3PXD2B) in Frank-Ter Haar Syndrome

Genes, 2022-01, Vol.13 (2), p.236

2022

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Development of a Colorimetric Tool for SARS-CoV-2 and Other Respiratory Viruses Detection Using Sialic Acid Fabricated Gold Nanoparticles

Pharmaceutics, 2021-04, Vol.13 (4), p.502

2021

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Reply to Zandi, M.; Soltani, S. Comment on “Alfassam et al. Development of a Colorimetric Tool for SARS-CoV-2 and Other Respiratory Viruses Detection Using Sialic Acid Fabricated Gold Nanoparticles. Pharmaceutics 2021, 13, 502”

Pharmaceutics, 2022-09, Vol.14 (9), p.1878

2022

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TGFBR1 Variants Can Associate with Non-Syndromic Congenital Heart Disease without Aortopathy

Journal of cardiovascular development and disease, 2023-11, Vol.10 (11), p.455

2023

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InP/ZnS Nanocrystals as Fluorescent Probes for the Detection of ATP

Nanomaterials and Nanotechnology, 2014, Vol.4 (Godište 2014), p.1

2014

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Association of KIR gene polymorphisms with COVID-19 disease

Clinical immunology (Orlando, Fla.), 2022-01, Vol.234, p.108911-108911, Article 108911

2022

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A missense mutation in the CRBN gene that segregates with intellectual disability and self-mutilating behaviour in a consanguineous Saudi family

Journal of medical genetics, 2017-04, Vol.54 (4), p.236-240

2017

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Interferon-induced transmembrane protein-3 genetic variant rs12252 is associated with COVID-19 mortality

Genomics (San Diego, Calif.), 2021-07, Vol.113 (4), p.1733-1741

2021

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Correlation between ABO Blood Group Phenotype and the Risk of COVID-19 Infection and Severity of Disease in a Saudi Arabian Cohort

Journal of Epidemiology and Global Health, 2022-03, Vol.12 (1), p.85-91

2022

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PDCD6IP, encoding a regulator of the ESCRT complex, is mutated in microcephaly

Clinical genetics, 2020-07, Vol.98 (1), p.80-85

2020

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Enhancement of ciprofloxacin activity by incorporating it in solid lipid nanoparticles

Tropical journal of pharmaceutical research, 2020-05, Vol.19 (5), p.909-918

2020

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Preparation of anastrozole loaded PEG-PLA nanoparticles: evaluation of apoptotic response of breast cancer cell lines

International journal of nanomedicine, 2018-01, Vol.13, p.199-208

2018

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ADAMTS19‐associated heart valve defects: Novel genetic variants consolidating a recognizable cardiac phenotype

Clinical genetics, 2020-07, Vol.98 (1), p.56-63

2020

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Electrophoretic properties of BSA-coated quantum dots

Analytical and bioanalytical chemistry, 2010-02, Vol.396 (3), p.1087-1094

2010

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Role of sphingolipid metabolism in neurodegeneration

Development of Epirubicin-Loaded Biocompatible Polymer PLA-PEG-PLA Nanoparticles: Synthesis, Characterization, Stability, and In Vitro Anticancerous Assessment

A Novel Homozygous Non-sense Mutation in the Catalytic Domain of MTHFR Causes Severe 5,10-Methylenetetrahydrofolate Reductase Deficiency

Consanguinity and Congenital Heart Disease Susceptibility: Insights into Rare Genetic Variations in Saudi Arabia

Association between human leukocyte antigen alleles and COVID-19 disease severity

A cell-based drug delivery platform for treating central nervous system inflammation

Fast-Dissolving Nifedipine and Atorvastatin Calcium Electrospun Nanofibers as a Potential Buccal Delivery System

Tween 80-Based Self-Assembled Mixed Micelles Boost Valsartan Transdermal Delivery

Novel Autosomal Recessive Splice-Altering Variant in PRKD1 Is Associated with Congenital Heart Disease

Optimized Polyethylene Glycolylated Polymer–Lipid Hybrid Nanoparticles as a Potential Breast Cancer Treatment

Analysis of chronic kidney disease patients by targeted next-generation sequencing identifies novel variants in kidney-related genes

The Role of the Disrupted Podosome Adaptor Protein (SH3PXD2B) in Frank-Ter Haar Syndrome

Development of a Colorimetric Tool for SARS-CoV-2 and Other Respiratory Viruses Detection Using Sialic Acid Fabricated Gold Nanoparticles

Reply to Zandi, M.; Soltani, S. Comment on “Alfassam et al. Development of a Colorimetric Tool for SARS-CoV-2 and Other Respiratory Viruses Detection Using Sialic Acid Fabricated Gold Nanoparticles. Pharmaceutics 2021, 13, 502”

TGFBR1 Variants Can Associate with Non-Syndromic Congenital Heart Disease without Aortopathy

InP/ZnS Nanocrystals as Fluorescent Probes for the Detection of ATP

Association of KIR gene polymorphisms with COVID-19 disease

A missense mutation in the CRBN gene that segregates with intellectual disability and self-mutilating behaviour in a consanguineous Saudi family

Interferon-induced transmembrane protein-3 genetic variant rs12252 is associated with COVID-19 mortality

Correlation between ABO Blood Group Phenotype and the Risk of COVID-19 Infection and Severity of Disease in a Saudi Arabian Cohort

PDCD6IP, encoding a regulator of the ESCRT complex, is mutated in microcephaly

Enhancement of ciprofloxacin activity by incorporating it in solid lipid nanoparticles

Preparation of anastrozole loaded PEG-PLA nanoparticles: evaluation of apoptotic response of breast cancer cell lines

ADAMTS19‐associated heart valve defects: Novel genetic variants consolidating a recognizable cardiac phenotype

Electrophoretic properties of BSA-coated quantum dots

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