De-repressing LncRNA-Targeted Genes to Upregulate Gene Expression: Focus on Small Molecule Therapeutics

by Roya Pedram Fatemi, Dmitry Velmeshev, Mohammad Ali Faghihi
Published 2014-01-01

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
Published 2020-12-01

Cytokine Gene Expression Alterations In Human Macrophages Infected By Leishmania Major

by Khodaberdi Kalavi, Ogholniaz Jorjani, Mohammad Ali Faghihi, Seyed Javad Mowla
Published 2021-01-01

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
Published 2021-09-01

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
Published 2008-01-01

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
Published 2017-08-01

Antisense RNA Controls LRP1 Sense Transcript Expression through Interaction with a Chromatin-Associated Protein, HMGB2

by Yasunari Yamanaka, Mohammad Ali Faghihi, Marco Magistri, Oscar Alvarez-Garcia, Martin Lotz, Claes Wahlestedt
Published 2015-05-01

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
Published 2019-09-01

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
Published 2020-06-01

Generalized exfoliative skin rash as an early predictor of supratherapeutic voriconazole trough levels in a leukemic child: A case report

by Ali Amanati, Parisa Badiee, Mehrzad Lotfi, Ahmad Monabati, Mohammad Ali Faghihi, Majid Yavarian, Nazafarin Hatami-Mazinani
Published 2020-09-01

Knockdown of BACE1-AS Nonprotein-Coding Transcript Modulates Beta-Amyloid-Related Hippocampal Neurogenesis

by Farzaneh Modarresi, Mohammad Ali Faghihi, Nikunj S. Patel, Barbara G. Sahagan, Claes Wahlestedt, Miguel A. Lopez-Toledano
Published 2011-01-01

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
Published 2020-07-01

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
Published 2018-05-01

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
Published 2017-05-01

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
Published 2019-07-01

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
Published 2019-03-01

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
Published 2020-02-01

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
Published 2020-05-01

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
Published 2019-01-01

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
Published 2017-07-01