Hasil Pencarian - Hassan Dastsooz

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  1. 1
    LncRNA–miRNA–mRNA Networks of Gastrointestinal Cancers Representing Common and Specific LncRNAs and mRNAs

    LncRNA–miRNA–mRNA Networks of Gastrointestinal Cancers Representing Common and Specific LncRNAs and mRNAs oleh Hassan Dastsooz, Hassan Dastsooz, Hassan Dastsooz, Ahad Alizadeh, Parham Habibzadeh, Ali Nariman, Asieh Hosseini, Yaser Mansoori, Yaser Mansoori, Hamed Haghi-Aminjan

    Diterbitkan 2022-01-01
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  2. 2
    DNA Sequence Fragment Containing C to A Mutation as a Convenient Mutation Standard for DHPLC Analysis

    DNA Sequence Fragment Containing C to A Mutation as a Convenient Mutation Standard for DHPLC Analysis oleh Hassan Dastsooz, Nazanin Vahedi, Majid Fardaei

    Diterbitkan 2013-08-01
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  3. 3
    A Comprehensive Bioinformatics Analysis of <i>UBE2C</i> in Cancers

    A Comprehensive Bioinformatics Analysis of <i>UBE2C</i> in Cancers oleh Hassan Dastsooz, Matteo Cereda, Daniela Donna, Salvatore Oliviero

    Diterbitkan 2019-05-01
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  4. 4
    Involvement of N4BP2L1, PLEKHA4, and BEGAIN genes in breast cancer and muscle cell development

    Involvement of N4BP2L1, PLEKHA4, and BEGAIN genes in breast cancer and muscle cell development oleh Hassan Dastsooz, Hassan Dastsooz, Hassan Dastsooz, Francesca Anselmi, Andrea Lauria, Chiara Cicconetti, Valentina Proserpio, Elham Mohammadisoleimani, Zahra Firoozi, Yaser Mansoori, Yaser Mansoori, Hamed Haghi-Aminjan, Livia Caizzi, Salvatore Oliviero, Salvatore Oliviero, Salvatore Oliviero

    Diterbitkan 2024-05-01
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  5. 5
    VSX1 and SOD1 mutation screening in patients with keratoconus in the South of Iran

    VSX1 and SOD1 mutation screening in patients with keratoconus in the South of Iran oleh Mahmood Nejabat, Payam Naghash, Hassan Dastsooz, Sanaz Mohammadi, Mohsen Alipour, Majid Fardaei

    Diterbitkan 2017-01-01
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  6. 6
    Author's reply

    Author's reply oleh Mahmood Nejabat, Payam Naghash, Hassan Dastsooz, Sanaz Mohammadi, Mohsen Alipour, Majid Fardaei

    Diterbitkan 2018-01-01
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  7. 7
    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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  8. 8
    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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  9. 9
    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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  10. 10
    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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  11. 11
    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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  12. 12
    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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  13. 13
    Clinical and molecular characterization of a patient with mitochondrial Neurogastrointestinal Encephalomyopathy

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

    Diterbitkan 2020-05-01
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  14. 14
    A Novel Mutation in ERCC8 Gene Causing Cockayne Syndrome

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

    Diterbitkan 2017-08-01
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  15. 15
    Clinical and molecular characterization of three patients with Hepatocerebral form of mitochondrial DNA depletion syndrome: a case series

    Clinical and molecular characterization of three patients with Hepatocerebral form of mitochondrial DNA depletion syndrome: a case series oleh Ghazale Mahjoub, Parham Habibzadeh, Hassan Dastsooz, Malihe Mirzaei, Arghavan Kavosi, Laila Jamali, Haniyeh Javanmardi, Pegah Katibeh, Mohammad Ali Faghihi, Seyed Alireza Dastgheib

    Diterbitkan 2019-10-01
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  16. 16
    A novel mutation in SEPN1 causing rigid spine muscular dystrophy 1: a Case report

    A novel mutation in SEPN1 causing rigid spine muscular dystrophy 1: a Case report oleh Fateme Ziyaee, Eslam Shorafa, Hassan Dastsooz, Parham Habibzadeh, Hamid Nemati, Amir Saeed, Mohammad Silawi, Mohammad Ali Farazi Fard, Mohammad Ali Faghihi, Seyed Alireza Dastgheib

    Diterbitkan 2019-01-01
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  17. 17
    A novel splice site mutation in WAS gene in patient with Wiskott-Aldrich syndrome and chronic colitis: a case report

    A novel splice site mutation in WAS gene in patient with Wiskott-Aldrich syndrome and chronic colitis: a case report oleh Hossein Esmaeilzadeh, Mohammad Reza Bordbar, Hassan Dastsooz, Mohammad Silawi, Mohammad Ali Farazi Fard, Ali Adib, Ali Kafashan, Zahra Tabatabaei, Forough Sadeghipour, Mohammad Ali Faghihi

    Diterbitkan 2018-07-01
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