Hasil Pencarian - Masoud Garshasbi

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  1. 1
    Whole-exome sequencing identifies R1279X of MYH6 gene to be associated with congenital heart disease

    Whole-exome sequencing identifies R1279X of MYH6 gene to be associated with congenital heart disease oleh Ehsan Razmara, Masoud Garshasbi

    Diterbitkan 2018-07-01
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  2. 2
    Molecular genetic analysis of polycystic kidney disease 1 and polycystic kidney disease 2 mutations in pedigrees with autosomal dominant polycystic kidney disease

    Molecular genetic analysis of polycystic kidney disease 1 and polycystic kidney disease 2 mutations in pedigrees with autosomal dominant polycystic kidney disease oleh Fatemeh Bitarafan, Masoud Garshasbi

    Diterbitkan 2019-01-01
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  3. 3
    Novel compound heterozygote mutations in the ATP7B gene in an Iranian family with Wilson disease: a case report

    Novel compound heterozygote mutations in the ATP7B gene in an Iranian family with Wilson disease: a case report oleh Omid Daneshjoo, Masoud Garshasbi

    Diterbitkan 2018-03-01
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  4. 4
    A novel ISCA2 variant responsible for an early-onset neurodegenerative mitochondrial disorder: a case report of multiple mitochondrial dysfunctions syndrome 4

    A novel ISCA2 variant responsible for an early-onset neurodegenerative mitochondrial disorder: a case report of multiple mitochondrial dysfunctions syndrome 4 oleh Milad Eidi, Masoud Garshasbi

    Diterbitkan 2019-07-01
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  5. 5
    Novel in-frame deletion in MFSD8 gene revealed by trio whole exome sequencing in an Iranian affected with neuronal ceroid lipofuscinosis type 7: a case report

    Novel in-frame deletion in MFSD8 gene revealed by trio whole exome sequencing in an Iranian affected with neuronal ceroid lipofuscinosis type 7: a case report oleh Ali Hosseini Bereshneh, Masoud Garshasbi

    Diterbitkan 2018-09-01
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  6. 6
    Investigation of Inherited Causes of Autosomal Recessive Non-syndromic Epilepsy in an Iranian Family Using Whole Exome Sequencing Method

    Investigation of Inherited Causes of Autosomal Recessive Non-syndromic Epilepsy in an Iranian Family Using Whole Exome Sequencing Method oleh Raziyeh Khalesi, Masoud Garshasbi, Mahmood Tavallaei

    Diterbitkan 2017-02-01
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  7. 7
    Improving Classification of Cancer and Mining Biomarkers from Gene Expression Profiles Using Hybrid Optimization Algorithms and Fuzzy Support Vector Machine

    Improving Classification of Cancer and Mining Biomarkers from Gene Expression Profiles Using Hybrid Optimization Algorithms and Fuzzy Support Vector Machine oleh Niloofar Yousefi Moteghaed, Keivan Maghooli, Masoud Garshasbi

    Diterbitkan 2018-01-01
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  8. 8
    miR-31 and miR-145 as potential non-invasive regulatory biomarkers in patients with endometriosis

    miR-31 and miR-145 as potential non-invasive regulatory biomarkers in patients with endometriosis oleh Oranous Bashti, Mehrdad Noruzinia, Masoud Garshasbi, Morteza Abtahi

    Diterbitkan 2018-01-01
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  9. 9
    miR-31 and miR-145 as Potential Non-Invasive Regulatory Biomarkers in Patients with Endometriosis

    miR-31 and miR-145 as Potential Non-Invasive Regulatory Biomarkers in Patients with Endometriosis oleh Oranous Bashti, Mehrdad Noruzinia, Masoud Garshasbi, Morteza Abtahi

    Diterbitkan 2018-04-01
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  10. 10
    Presenting a Text Mining Algorithm to Identify Emotion in Persian Corpus

    Presenting a Text Mining Algorithm to Identify Emotion in Persian Corpus oleh Masoud Garshasbi, Anahid Rais-Rohani, Mohammadreza Kabaranzadeh Ghadim

    Diterbitkan 2018-06-01
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  11. 11
    Biomarker discovery based on hybrid optimization algorithm and artificial neural networks on microarray data for cancer classification

    Biomarker discovery based on hybrid optimization algorithm and artificial neural networks on microarray data for cancer classification oleh Niloofar Yousefi Moteghaed, Keivan Maghooli, Shiva Pirhadi, Masoud Garshasbi

    Diterbitkan 2015-01-01
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  12. 12
    Novel compound heterozygous variants in XYLT1 gene caused Desbuquois dysplasia type 2 in an aborted fetus: a case report

    Novel compound heterozygous variants in XYLT1 gene caused Desbuquois dysplasia type 2 in an aborted fetus: a case report oleh Fatemeh Rajabi, Ali Hosseini Bereshneh, Mahboubeh Ramezanzadeh, Masoud Garshasbi

    Diterbitkan 2022-01-01
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  13. 13
    123VCF: an intuitive and efficient tool for filtering VCF files

    123VCF: an intuitive and efficient tool for filtering VCF files oleh Milad Eidi, Samaneh Abdolalizadeh, Soheila Moeini, Masoud Garshasbi, Javad Zahiri

    Diterbitkan 2024-02-01
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  14. 14
    Neurodevelopmental disorder with microcephaly, hypotonia, and variable brain anomalies in a consanguineous Iranian family is associated with a homozygous start loss variant in the PRUNE1 gene

    Neurodevelopmental disorder with microcephaly, hypotonia, and variable brain anomalies in a consanguineous Iranian family is associated with a homozygous start loss variant in the... oleh Mehdi Agha Gholizadeh, Mina Mohammadi-Sarband, Fatemeh Fardanesh, Masoud Garshasbi

    Diterbitkan 2022-04-01
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  15. 15
    Pharmacogenetics and Personalized Medicine in Pancreatic Cancer

    Pharmacogenetics and Personalized Medicine in Pancreatic Cancer oleh Ali Hosseini Bereshneh, Fatemeh Morshedi, Mahsa Hematyar, Arastoo Kaki, Masoud Garshasbi

    Diterbitkan 2017-03-01
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  16. 16
    Identification of a novel RUNX2 gene mutation and early diagnosis of CCD in a cleidocranial dysplasia suspected Iranian family

    Identification of a novel RUNX2 gene mutation and early diagnosis of CCD in a cleidocranial dysplasia suspected Iranian family oleh Omid Daneshjoo, Pirooz Ebrahimi, Leila B. Salehi, Antonio Pizzuti, Masoud Garshasbi

    Diterbitkan 2020-12-01
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  17. 17
    The first case of NSHL by direct impression on EYA1 gene and identification of one novel mutation in MYO7A in the Iranian families

    The first case of NSHL by direct impression on EYA1 gene and identification of one novel mutation in MYO7A in the Iranian families oleh Ehsan Razmara, Fatemeh Bitarafan, Elika Esmaeilzadeh-Gharehdaghi, Navid Almadani, Masoud Garshasbi

    Diterbitkan 2018-03-01
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  18. 18
    Biomarker discovery by imperialist competitive algorithm in mass spectrometry data for ovarian cancer prediction

    Biomarker discovery by imperialist competitive algorithm in mass spectrometry data for ovarian cancer prediction oleh Shiva Pirhadi, Keivan Maghooli, Niloofar Yousefi Moteghaed, Masoud Garshasbi, Seyed Jalaleddin Mousavirad

    Diterbitkan 2021-01-01
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  19. 19
    Novel homozygous frameshift variant in the ATCAY gene in an Iranian patient with Cayman cerebellar ataxia; expanding the neuroimaging and clinical features: a case report

    Novel homozygous frameshift variant in the ATCAY gene in an Iranian patient with Cayman cerebellar ataxia; expanding the neuroimaging and clinical features: a case report oleh Elham Salehi Siavashani, Mahmoud Reza Ashrafi, Homa Ghabeli, Morteza Heidari, Masoud Garshasbi

    Diterbitkan 2023-09-01
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  20. 20
    Identification of a novel HEXB Mutation in an Iranian Family with suspected patient to GM2‐gangliosidoses

    Identification of a novel HEXB Mutation in an Iranian Family with suspected patient to GM2‐gangliosidoses oleh Fatemeh Mansouri‐Movahed, Fatemeh Akhoundi, Parvaneh Nikpour, Masoud Garshasbi, Modjtaba Emadi‐Baygi

    Diterbitkan 2020-12-01
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