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International Journal of Nanomedicine|September 5, 2020
The Effects Study of Isoniazid Conjugated Multi-Wall Carbon Nanotubes Nanofluid on Mycobacterium tuberculosisShahab Zomorodbakhsh, Yasamin Abbasian, Maryam Naghinejad, et al.
Molecular Biology Reports|March 6, 2025
Discovering the pathogenesis of a VUS variant in CDH23 associated with sensorineural hearing loss in an Iranian familyMaryam Naghinejad, Sima Mansoori Derakhshan, Sepideh Parvizpour, et al.
Journal of Molecular Neuroscience : MN|October 23, 2024
A Novel Pathogenic Mutation in WNK1 Gene Causing HSAN Type II in Three SiblingsMaryam Naghinejad, Amir Ebrahimi, Mahmoud Shekari Khaniani, et al.
International Journal of Nanomedicine|October 16, 2020
The Applications of Carbon Nanotubes in the Diagnosis and Treatment of Lung Cancer: A Critical ReviewMojgan Sheikhpour, Maryam Naghinejad, Alibakhsh Kasaeian, et al.
Journal of Human Genetics|April 18, 2025
A random forest-based predictive model for classifying BRCA1 missense variants: a novel approach for evaluating the missense mutations effectHamed Ka, Maryam Naghinejad, Akbar Amirfiroozy, et al.
Biochemical Genetics|October 16, 2025
A Deleterious Variant in MBOAT7 Causes Intellectual Disability in an Iranian Family: An Example of Reassignment of Variants of Uncertain SignificanceNaghmeh Saba, Maryam Naghinejad, Mahmoud Shekari Khaniani, et al.
Molecular Biology Reports|January 17, 2025
The known structural variations in hearing loss and their diagnostic approaches: a comprehensive reviewMaryam Naghinejad, Sepideh Parvizpour, Mahmoud Shekari Khaniani, et al.
Molecular Biology Reports|May 13, 2026
Exploring the pathogenesis of a compound heterozygous variant in ATP7B associated with Wilson disease in an Iranian familyElaheh Hasani, Moein Kohkalani, Maryam Naghinejad, et al.
Molecular and Cellular Probes|January 28, 2025
A comprehensive report of the clinical and mutational profiles of 30 Iranian malignant infantile osteopetrosis patientsAkbar Amirfiroozy, Maryam Naghinejad, Azim Rezamand, et al.
Molecular Biology Reports|October 3, 2025
Exploring genotype-phenotype correlation of a novel SHOX gene splicing variant: Langer mesomelic dysplasia or idiopathic short statureMoein Kohkalani, Seyyed Amin Seyyed Rezaei, Maryam Naghinejad, et al.
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