De-repressing LncRNA-Targeted Genes to Upregulate Gene Expression: Focus on Small Molecule Therapeutics by Roya Pedram Fatemi, Dmitry Velmeshev, Mohammad Ali Faghihi

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Transcriptome Analysis May Be Beneficial for Identification of Specific Pathways in Host Cell-Leishmania major Interactions(letter to editor) by Khodaberdi Kalavi, Mohammad Ali Faghihi, Ogholniaz Jorjani, Zolikha Tatari

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Case Report: Expanding the Genetic and Phenotypic Spectrum of Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay by Parham Habibzadeh, Zahra Tabatabaei, Soroor Inaloo, Muhammad Mahdi Nashatizadeh, Matthis Synofzik, Matthis Synofzik, Vahid Reza Ostovan, Mohammad Ali Faghihi, Mohammad Ali Faghihi

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Genetic Testing in Various Neurodevelopmental Disorders Which Manifest as Cerebral Palsy: A Case Study From Iran by Marzieh Nejabat, Soroor Inaloo, Afsaneh Taghipour Sheshdeh, Shima Bahramjahan, Fatima Masoomi Sarvestani, Pegah Katibeh, Hamid Nemati, Hamid Nemati, Seyed Mohammad Bagher Tabei, Mohammad Ali Faghihi, Mohammad Ali Faghihi

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Novel mutations in PANK2 and PLA2G6 genes in patients with neurodegenerative disorders: two case reports by Hassan Dastsooz, Hamid Nemati, Mohammad Ali Farazi Fard, Majid Fardaei, Mohammad Ali Faghihi

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A novel RNA transcript with antiapoptotic function is silenced in fragile X syndrome. by Ahmad M Khalil, Mohammad Ali Faghihi, Farzaneh Modarresi, Shaun P Brothers, Claes Wahlestedt

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A Novel TTC19 Mutation in a Patient With Neurological, Psychological, and Gastrointestinal Impairment by Parham Habibzadeh, Parham Habibzadeh, Soroor Inaloo, Mohammad Silawi, Hassan Dastsooz, Hassan Dastsooz, Mohammad Ali Farazi Fard, Forough Sadeghipour, Zahra Faghihi, Mohaddeseh Rezaeian, Majid Yavarian, Johann Böhm, Mohammad Ali Faghihi, Mohammad Ali Faghihi

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A novel stop-gain mutation in DPYS gene causing Dihidropyrimidinase deficiency, a case report by Malihe Mirzaei, Arghavan Kavosi, Mahboobeh Sharifzadeh, Ghazale Mahjoub, Mohammad Ali Faghihi, Parham Habibzadeh, Majid Yavarian

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A case report of novel mutation in PRF1 gene, which causes familial autosomal recessive hemophagocytic lymphohistiocytosis by Mohammad Reza Bordbar, Farzaneh Modarresi, Mohammad Ali Farazi Fard, Hassan Dastsooz, Nader Shakib Azad, Mohammad Ali Faghihi

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Molecular mechanisms of long non-coding RNAs in anaplastic thyroid cancer: a systematic review by Hilda Samimi, Sayed Mahmoud Sajjadi-Jazi, Soroush Seifirad, Rasha Atlasi, Habibollah Mahmoodzadeh, Mohammad Ali Faghihi, Vahid Haghpanah

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Splicing defect in FKBP10 gene causes autosomal recessive osteogenesis imperfecta disease: a case report by Fatemeh Maghami, Seyed Mohammad Bagher Tabei, Hossein Moravej, Hassan Dastsooz, Farzaneh Modarresi, Mohammad Silawi, Mohammad Ali Faghihi

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Pre-Implantation Genetic Testing for Monogenic Disorders (PGT-M) in A Family with A Novel Mutation in DPAGT1 Gene by Zahra Tabatabaei, Khadijeh Karbalaie, Parham Habibzadeh, Mohammad Ali Farazi Fard, Mohammad Ali Faghihi, Mohammad-Hossein Nasr Esfahani

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An immunocompetent patient with a nonsense mutation in NHEJ1 gene by Hossein Esmaeilzadeh, Mohammad Reza Bordbar, Zahra Hojaji, Parham Habibzadeh, Dorna Afshinfar, Mohammad Miryounesi, Majid Fardaei, Mohammad Ali Faghihi

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A novel frame-shift deletion in FANCF gene causing autosomal recessive Fanconi anemia: a case report by Soheila Zareifar, Hassan Dastsooz, Mahdi Shahriari, Mohammad Ali Faghihi, Golsa Shekarkhar, Mohammadreza Bordbar, Omid Reza Zekavat, Nader Shakibazad

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AICAR and nicotinamide treatment synergistically augment the proliferation and attenuate senescence-associated changes in mesenchymal stromal cells by Mohammadhossein Khorraminejad-Shirazi, Mahsa Sani, Tahereh Talaei-Khozani, Mohammadreza Dorvash, Malihe Mirzaei, Mohammad Ali Faghihi, Ahmad Monabati, Armin Attar

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Case reports of juvenile GM1 gangliosidosisis type II caused by mutation in GLB1 gene by Parvaneh Karimzadeh, Samaneh Naderi, Farzaneh Modarresi, Hassan Dastsooz, Hamid Nemati, Tayebeh Farokhashtiani, Bibi Shahin Shamsian, Soroor Inaloo, Mohammad Ali Faghihi

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Viral metagenomic analysis of fecal samples reveals an enteric virome signature in irritable bowel syndrome by Mina Hojat Ansari, Mehregan Ebrahimi, Mohammad Reza Fattahi, Michael G. Gardner, Ali Reza Safarpour, Mohammad Ali Faghihi, Kamran Bagheri Lankarani

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The First Case of a Small Supernumerary Marker Chromosome 18 in a Klinefelter Fetus: A Case Report by Jamileh Saberzadeh, Mohammad Reza Miri, Mehdi Dianatpour, Abbas Behzad Behbahani, Mohammad Bagher Tabei, Mohsen Alipour, Mohammad Ali Faghihi, Majid Fardaei

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Clinical and molecular characterization of a patient with mitochondrial Neurogastrointestinal Encephalomyopathy by Parham Habibzadeh, Mohammad Silawi, Hassan Dastsooz, Shima Bahramjahan, Shahrokh Ezzatzadegan Jahromi, Vahid Reza Ostovan, Majid Yavarian, Mohammad Mofatteh, Mohammad Ali Faghihi

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A Novel Mutation in ERCC8 Gene Causing Cockayne Syndrome by Maryam Taghdiri, Maryam Taghdiri, Hassan Dastsooz, Majid Fardaei, Majid Fardaei, Majid Fardaei, Sanaz Mohammadi, Mohammad Ali Farazi Fard, Mohammad Ali Faghihi

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