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Genetic Testing and Molecular Biomarkers|December 16, 2015
NPM1 Mutation Detection in Acute Myeloid Leukemia: A Method Comparison StudyAileen Azari-Yam, Samira Dabbagh Bagheri, Javad Tavakkoly-Bazzaz, et al.
Molecular Biology Reports|June 14, 2024
Unmasking early colorectal cancer clues: in silico and in vitro investigation of downregulated IGF2, SOCS1, MLH1, and CACNA1G in SSA polypsSeyedeh Nasim Mirbahari, Nayeralsadat Fatemi, Sanaz Savabkar, et al.
European Archives of Oto-Rhino-Laryngology : Official Journal of the European Federation of Oto-Rhino-Laryngological Societies (EUFOS) : Affiliated with the German Society for Oto-Rhino-Laryngology - Head and Neck Surgery|July 12, 2014
GJB2 c.-23+1G>A mutation is second most common mutation among Iranian individuals with autosomal recessive hearing lossSirous Zeinali, Elham Davoudi-Dehaghani, Sarah Azadmehr, et al.
Discover Oncology|January 18, 2025
FadA antigen of Fusobacterium nucleatum: implications for ceRNA network in colorectal cancer and adenomatous polyps progressionSama Rezasoltani, Elahe Shams, Moein Piroozkhah, et al.
Medical Oncology (Northwood, London, England)|January 29, 2022
A linkage between effectual genes in progression of CRC through canonical and non-canonical TGF-β signaling pathwaysMarzieh Shirin, Sajedeh Madadi, Noshad Peyravian, et al.
Cancers|June 22, 2023
Principles of Molecular Utility for CMS Classification in Colorectal Cancer ManagementLeili Rejali, Romina Seifollahi Asl, Fatemeh Sanjabi, et al.
Scientific Reports|November 20, 2024
Comprehensive analysis identifies endocrine fibroblast growth factors as promising prognostic markers for colorectal carcinomaLeili Rejali, Moein Piroozkhah, Mana Jahanbin, et al.
Molecular Biology Reports|April 6, 2023
Long non‑coding RNA LINC00460 contributes as a potential prognostic biomarker through its oncogenic role with ANXA2 in colorectal polypsFarzaneh Alsadat Hosseini, Leili Rejali, Mohammad Reza Zabihi, et al.
Gastroenterology and Hepatology From Bed to Bench|September 28, 2023
A novel stop codon mutation in STK11 gene is associated with Peutz-Jeghers Syndrome and elevated cancer risk: a case studyBinazir Khanabadi, Diba Najafgholizadeh Seyfi, Leili Rejali, et al.
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