Showing 1 - 20 results of 23 for search 'S. Tehrani Fateh', query time: 0.07s
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Insights into additional lactone-based signaling circuits in Streptomyces: existence of acyl-homoserine lactones and LuxI/LuxR homologs in six Streptomyces species by Amir Salehi-Najafabadi, Amir Salehi-Najafabadi, Sepand Tehrani Fateh, Sepand Tehrani Fateh, Ghasem Amoabediny, Ghasem Amoabediny, Javad Hamedi
Published 2024-02-01
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The Effects of Sesquiterpene Lactones on the Differentiation of Human or Animal Cells Cultured In-Vitro: A Critical Systematic Review by Sepand Tehrani Fateh, Sahand Tehrani Fateh, Faezeh Shekari, Majid Mahdavi, Amir Reza Aref, Amir Reza Aref, Amir Salehi-Najafabadi, Amir Salehi-Najafabadi
Published 2022-04-01
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Covid-19 in Parkinson's Disease treated by drugs or brain stimulation by M. Salari, M. Etemadifar, A. Zali, Z. Aminzade, I. Navalpotro-Gomez, S. Tehrani Fateh
Published 2024-04-01
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Covid-19 in Parkinson's Disease treated by drugs or brain stimulation by M. Salari, M. Etemadifar, A. Zali, Z. Aminzade, I. Navalpotro-Gomez, S. Tehrani Fateh
Published 2024-04-01
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Novel BRAT1 variant associated with neurodevelopmental disorder with cerebellar atrophy and seizure: Case report and a literature review by Mohammad-Reza Ghasemi, Sahand Tehrani Fateh, Farzad Hashemi-Gorji, Morteza Sheikhi Nooshabadi, Sahar Alijanpour, Ali Mardi, Mohammad Miryounesi
Published 2024-01-01
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Expanding genetic and clinical aspects of Schwartz-Jampel syndrome: A report of two cases with literature review by Iman Elahi Vahed, Sahand Tehrani Fateh, Melika Kamali, Farzad Hashemi-Gorji, Zahra Esmaeilzadeh, Hossein Sadeghi, Mohammad Miryounesi, Mohammad-Reza Ghasemi
Published 2024-09-01
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Non-coding RNAs as potential therapeutic targets for receptor tyrosine kinase signaling in solid tumors: current status and future directions by Aysan Moeinafshar, Mohammad Nouri, Nima Shokrollahi, Mahdi Masrour, Amirmohammad Behnam, Sahand Tehrani Fateh, Hossein Sadeghi, Mohammad Miryounesi, Mohammad-Reza Ghasemi
Published 2024-01-01
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Novel TECPR2 variant in two cases of hereditary sensory and autonomic neuropathy type 9: insights from genetic characterization and comprehensive literature review by Aysan Moeinafshar, Sahand Tehrani Fateh, Farzad Hashemi-Gorji, Parvaneh Karimzadeh, Elham Gholibeglou, Masoumeh Rostami, Hossein Sadeghi, Mohammad Miryounesi, Mohammad-Reza Ghasemi
Published 2024-11-01
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Hydrophobic@amphiphilic hybrid nanostructure of iron-oxide and graphene quantum dot surfactant as a theranostic platform by Sepand Tehrani Fateh, Mahdieh Ahmadi Kamalabadi, Azita Aliakbarniya, Saeideh Jafarinejad-Farsangi, Maedeh Koohi, Elham Jafari, Zahra Miri Karam, Fariborz Keyhanfar, Amin Shiralizadeh Dezfuli
Published 2022-03-01
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Expression assay of the COLQ in a family with congenital myasthenic syndrome and symptomatic carriers by Mohammad Farid Mohammadi, Sahand Tehrani Fateh, Hadi Aghajani, Afshin Bahramy, Seyed Mohammad Salar Zaheryani, Javad Behroozi, Seyyed Mohammad Kahani, Pouria Mohammadi, Masoud Garshasbi
Published 2023-10-01
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The effects of hesperidin supplementation on cardiovascular risk factors in adults: a systematic review and dose–response meta-analysis by Atie Sadat Khorasanian, Sahand Tehrani Fateh, Fatemeh Gholami, Niloufar Rasaei, Hadis Gerami, Hadis Gerami, Sayyed Saeid Khayyatzadeh, Sayyed Saeid Khayyatzadeh, Farideh Shiraseb, Omid Asbaghi, Omid Asbaghi
Published 2023-07-01
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Clinical Features and Genetic Characteristics of XLID Patients With KDM5C Gene Mutations: Insights on Phenotype–Genotype Correlations From 175 Previous Cases and Identification of... by Mohammad‐Reza Ghasemi, Zahra Esmaeilizadeh, Sahand Tehrani Fateh, Hossein Sadeghi, Saman Bagheri, Farzad Hashemi‐Gorji, Morteza Sheikhi Nooshabadi, Rasoul Madannezhad, Toktam Sadat Tavabe Ghavami, Reza Mirfakhraie, Mohammad Miryounesi
Published 2025-01-01
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Comprehensive review and expanding the genetic landscape of Cornelia-de-Lange spectrum: insights from novel mutations and skin biopsy in exome-negative cases by Sahand Tehrani Fateh, Nadia Mohammad Zadeh, Shadab Salehpour, Farzad Hashemi-Gorji, Ashkan Omidi, Hossein Sadeghi, Reza Mirfakhraie, Parinaz Moghimi, Sepideh Keyvanfar, Sepideh Mohammadi Sarvaleh, Mohammad Miryounesi, Mohammad-Reza Ghasemi
Published 2024-01-01
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Identification of novel mutations in TPK1 and SLC19A3 genes in families exhibiting thiamine metabolism dysfunction syndrome by Fatemeh Norouzi Rostami, Hossein Sadeghi, Farzad Hashemi-Gorji, Sahand Tehrani Fateh, Reza Mirfakhraie, Parvaneh Karimzadeh, Milad Davarpanah, Sanaz Jamshidi, Rasoul Madannejad, Parinaz Moghimi, Mahdis Ekrami, Mohammad Miryounesi, Mohammad-Reza Ghasemi
Published 2024-03-01
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