Hasil Pencarian - Mohammad Ali Faghihi

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  1. 1
    De-repressing LncRNA-Targeted Genes to Upregulate Gene Expression: Focus on Small Molecule Therapeutics

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

    Diterbitkan 2014-01-01
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  2. 2
    Transcriptome Analysis May Be Beneficial for Identification of Specific Pathways in Host Cell-Leishmania major Interactions(letter to editor)

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

    Diterbitkan 2022-09-01
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  3. 3
    Case Report: Expanding the Genetic and Phenotypic Spectrum of Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay

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

    Diterbitkan 2020-12-01
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  4. 4
    Cytokine Gene Expression Alterations In Human Macrophages Infected By Leishmania Major

    Cytokine Gene Expression Alterations In Human Macrophages Infected By Leishmania Major oleh Khodaberdi Kalavi, Ogholniaz Jorjani, Mohammad Ali Faghihi, Seyed Javad Mowla

    Diterbitkan 2021-01-01
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  5. 5
    Genetic Testing in Various Neurodevelopmental Disorders Which Manifest as Cerebral Palsy: A Case Study From Iran

    Genetic Testing in Various Neurodevelopmental Disorders Which Manifest as Cerebral Palsy: A Case Study From Iran oleh 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

    Diterbitkan 2021-09-01
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  6. 6
    Novel mutations in PANK2 and PLA2G6 genes in patients with neurodegenerative disorders: two case reports

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

    Diterbitkan 2017-08-01
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  7. 7
    A novel RNA transcript with antiapoptotic function is silenced in fragile X syndrome.

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

    Diterbitkan 2008-01-01
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  8. 8
    Antisense RNA Controls LRP1 Sense Transcript Expression through Interaction with a Chromatin-Associated Protein, HMGB2

    Antisense RNA Controls LRP1 Sense Transcript Expression through Interaction with a Chromatin-Associated Protein, HMGB2 oleh Yasunari Yamanaka, Mohammad Ali Faghihi, Marco Magistri, Oscar Alvarez-Garcia, Martin Lotz, Claes Wahlestedt

    Diterbitkan 2015-05-01
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  9. 9
    A Novel TTC19 Mutation in a Patient With Neurological, Psychological, and Gastrointestinal Impairment

    A Novel TTC19 Mutation in a Patient With Neurological, Psychological, and Gastrointestinal Impairment oleh 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

    Diterbitkan 2019-09-01
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  10. 10
    A novel stop-gain mutation in DPYS gene causing Dihidropyrimidinase deficiency, a case report

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

    Diterbitkan 2020-06-01
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  11. 11
    Generalized exfoliative skin rash as an early predictor of supratherapeutic voriconazole trough levels in a leukemic child: A case report

    Generalized exfoliative skin rash as an early predictor of supratherapeutic voriconazole trough levels in a leukemic child: A case report oleh Ali Amanati, Parisa Badiee, Mehrzad Lotfi, Ahmad Monabati, Mohammad Ali Faghihi, Majid Yavarian, Nazafarin Hatami-Mazinani

    Diterbitkan 2020-09-01
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  12. 12
    Knockdown of BACE1-AS Nonprotein-Coding Transcript Modulates Beta-Amyloid-Related Hippocampal Neurogenesis

    Knockdown of BACE1-AS Nonprotein-Coding Transcript Modulates Beta-Amyloid-Related Hippocampal Neurogenesis oleh Farzaneh Modarresi, Mohammad Ali Faghihi, Nikunj S. Patel, Barbara G. Sahagan, Claes Wahlestedt, Miguel A. Lopez-Toledano

    Diterbitkan 2011-01-01
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  13. 13
    A case report of novel mutation in PRF1 gene, which causes familial autosomal recessive hemophagocytic lymphohistiocytosis

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

    Diterbitkan 2017-05-01
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  14. 14
    Molecular mechanisms of long non-coding RNAs in anaplastic thyroid cancer: a systematic review

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

    Diterbitkan 2020-07-01
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  15. 15
    Splicing defect in FKBP10 gene causes autosomal recessive osteogenesis imperfecta disease: a case report

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

    Diterbitkan 2018-05-01
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  16. 16
    Pre-Implantation Genetic Testing for Monogenic Disorders (PGT-M) in A Family with A Novel Mutation in DPAGT1 Gene

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

    Diterbitkan 2021-10-01
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  17. 17
    An immunocompetent patient with a nonsense mutation in NHEJ1 gene

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

    Diterbitkan 2019-03-01
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  18. 18
    A novel frame-shift deletion in FANCF gene causing autosomal recessive Fanconi anemia: a case report

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

    Diterbitkan 2019-07-01
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  19. 19
    AICAR and nicotinamide treatment synergistically augment the proliferation and attenuate senescence-associated changes in mesenchymal stromal cells

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

    Diterbitkan 2020-02-01
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  20. 20
    Case reports of juvenile GM1 gangliosidosisis type II caused by mutation in GLB1 gene

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

    Diterbitkan 2017-07-01
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