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Journal of Photochemistry and Photobiology. B, Biology|June 6, 2016
Preparation and characterization of zinc and copper co-doped WO3 nanoparticles: Application in photocatalysis and photobiologySanaz Mohammadi, Maryam Sohrabi, Ahmad Nozad Golikand, et al.Molecular Genetics & Genomic Medicine|February 22, 2026
Novel Mutations in KCNJ10 Gene Associated With SeSAME Syndrome: Rare Disorder With Possible Common MutationShayan Shakeri, Sanaz Mohammadi, Forough Sadeghipour, et al.Human Genome Variation|August 21, 2019
Identification of mutations in HEXA and HEXB in Sandhoff and Tay-Sachs diseases: a new large deletion caused by Alu elements in HEXAHassan Dastsooz, Mohsen Alipour, Sanaz Mohammadi, et al.Journal of Ophthalmic & Vision Research|May 26, 2017
VSX1 and SOD1 Mutation Screening in Patients with Keratoconus in the South of IranMahmood Nejabat, Payam Naghash, Hassan Dastsooz, et al.Frontiers in Dentistry|June 14, 2023
Association of Serum 25-Hydroxyvitamin D and Chronic Periodontitis in Postmenopausal Women after Non-Surgical Periodontal TherapyAdileh Shirmohammadi, Sanaz Mohammadi, Masoumeh Faramarzi, et al.Frontiers in Pediatrics|August 30, 2017
A Novel Mutation in ERCC8 Gene Causing Cockayne SyndromeMaryam Taghdiri, Hassan Dastsooz, Majid Fardaei, et al.Clinical Nutrition ESPEN|January 23, 2025
The combined effects of omega-3 polyunsaturated fatty acid supplementation and exercise training on body composition and cardiometabolic health in adults: A systematic review and meta-analysisMousa Khalafi, Aref Habibi Maleki, Michael E Symonds, et al.Materials Science & Engineering. C, Materials for Biological Applications|October 25, 2016
Iron doped SnO2/Co3O4 nanocomposites synthesized by sol-gel and precipitation method for metronidazole antibiotic degradationShilpi Agarwal, Inderjeet Tyagi, Vinod Kumar Gupta, et al.European Journal of Medical Genetics|May 26, 2022
ZNF142 mutation causes neurodevelopmental disorder with speech impairment and seizures: Novel variants and literature reviewNeda Kamal, Hossein Jafari Khamirani, Sanaz Mohammadi, et al.Human Genome Variation|June 11, 2021
A novel PTRH2 missense mutation causing IMNEPD: a case reportHossein Jafari Khamirani, Sina Zoghi, Mehdi Dianatpour, et al.Pageof 3