Hasil Pencarian - Javad Mohammadi‐Asl

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  1. 1
    AHI1 gene mutation in a consanguineous Iranian family affected by Joubert syndrome: A case report

    AHI1 gene mutation in a consanguineous Iranian family affected by Joubert syndrome: A case report oleh Mostafa Neissi, Hadideh Mabudi, Javad Mohammadi‐Asl

    Diterbitkan 2021-10-01
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  2. 2
    The worldwide molecular spectrum and distribution of thalassaemia: a systematic review

    The worldwide molecular spectrum and distribution of thalassaemia: a systematic review oleh Mina Ebrahimi, Javad Mohammadi-Asl, Fakher Rahim

    Diterbitkan 2021-05-01
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  3. 3
    Comparison of the effects of olsalazine and decitabine on the expression of CDH1 and uPA genes and cytotoxicity in MDA-MB-231 breast cancer cells

    Comparison of the effects of olsalazine and decitabine on the expression of CDH1 and uPA genes and cytotoxicity in MDA-MB-231 breast cancer cells oleh Misagh Mohammadi Asl, Javad Mohammadi Asl, Mojgan Naghitorabi

    Diterbitkan 2021-01-01
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  4. 4
    Retinitis pigmentosa‐1 due to an RP1 mutation in a consanguineous Iranian family: Report of a novel mutation

    Retinitis pigmentosa‐1 due to an RP1 mutation in a consanguineous Iranian family: Report of a novel mutation oleh Mostafa Neissi, Motahareh Sheikh‐Hosseini, Javad Mohammadi‐Asl

    Diterbitkan 2024-03-01
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  5. 5
    A Novel Disease-Causing ASPA Gene Mutation (c.432+1 G>C) in an Iranian Patient with Canavan Disease: A Case Report

    A Novel Disease-Causing ASPA Gene Mutation (c.432+1 G>C) in an Iranian Patient with Canavan Disease: A Case Report oleh Mostafa Neissi, Motahareh Sheikh-Hosseini, Javad Mohammadi-Asl

    Diterbitkan 2021-12-01
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  6. 6
    A Novel Deleterious MYO15A Gene Mutation Causes Nonsyndromic Hearing Loss

    A Novel Deleterious MYO15A Gene Mutation Causes Nonsyndromic Hearing Loss oleh Mostafa Neissi, Adnan Al-Badran, Javad Mohammadi-Asl

    Diterbitkan 2024-01-01
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  7. 7
    Exome sequencing identifies a novel GUCY2D mutation in an Iranian family with Leber congenital amaurosis-1: a case report

    Exome sequencing identifies a novel GUCY2D mutation in an Iranian family with Leber congenital amaurosis-1: a case report oleh Mostafa Neissi, Adnan Issa Al-Badran, Javad Mohammadi-Asl

    Diterbitkan 2022-01-01
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  8. 8
    An intelligent prenatal screening system for the prediction of Trisomy-21

    An intelligent prenatal screening system for the prediction of Trisomy-21 oleh Amir Jamshidnezhad, Seyed Mohsen Hosseini, Javad Mohammadi-Asl, Mandana Mahmudi

    Diterbitkan 2021-01-01
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  9. 9
    Evaluation of the effect of oral taurine supplementation on fasting levels of fibroblast growth factors, β-Klotho co-receptor, some biochemical indices and body composition in obese women on a weight-loss diet: a study protocol for a double-blind, randomized controlled trial

    Evaluation of the effect of oral taurine supplementation on fasting levels of fibroblast growth factors, β-Klotho co-receptor, some biochemical indices and body composition in obes... oleh Fatemeh Haidari, Maryam Asadi, Javad mohammadi-asl, Kambiz Ahmadi-Angali

    Diterbitkan 2019-05-01
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  10. 10
    Folate gene polymorphisms CBS 844ins68 and RFC1 A80G and risk of Down syndrome offspring in young Iranian women: A cross-sectional study

    Folate gene polymorphisms CBS 844ins68 and RFC1 A80G and risk of Down syndrome offspring in young Iranian women: A cross-sectional study oleh Neda Farajnezhad, Pegah Ghandil, Maryam Tahmasebi-Birgani, Javad Mohammadi-Asl

    Diterbitkan 2024-03-01
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  11. 11
    Identification of a novel non-stop mutation in PDE6C gene in an Iranian family with Con-Rod Dystrophy

    Identification of a novel non-stop mutation in PDE6C gene in an Iranian family with Con-Rod Dystrophy oleh Shahram Nasiri, Farah Talebi, Javad Mohammadi Asl, Farideh Ghanbari Mardasi

    Diterbitkan 2020-08-01
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  12. 12
    Identification of a Novel Frameshift Mutation in the TECTA Gene in an Iranian Family With Autosomal Nonsyndromic Hearing Loss

    Identification of a Novel Frameshift Mutation in the TECTA Gene in an Iranian Family With Autosomal Nonsyndromic Hearing Loss oleh Javad Mohammadi-Asl, Nader Saki, Majid Karimi, Farideh Ghanbari Mardasi

    Diterbitkan 2021-03-01
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  13. 13
    Do NGS‐based techniques represent a first‐line testing in suspected Duchenne muscular dystrophy?

    Do NGS‐based techniques represent a first‐line testing in suspected Duchenne muscular dystrophy? oleh Seyed Mohammad Hosseini, Nosratollah Alizadeh, Abolfazl Amini, Javad Mohammadi‐Asl

    Diterbitkan 2022-06-01
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  14. 14
    Melatonin improves spermatogonial stem cells transplantation efficiency in azoospermic mice

    Melatonin improves spermatogonial stem cells transplantation efficiency in azoospermic mice oleh Mohammadreza Gholami, Ghasem Saki, Masoud Hemadi, Ali Khodadadi, Javad Mohammadi-asl

    Diterbitkan 2014-02-01
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  15. 15
    Up-regulation of SNHG5 Expression Level in Patients with Chronic Myeloid Leukemia Compared with Normal Individuals

    Up-regulation of SNHG5 Expression Level in Patients with Chronic Myeloid Leukemia Compared with Normal Individuals oleh Zahra Shahpouri-Arani, Mohamad Reza Hajari, Javad Mohammadi-Asl, Najmaldin Saki

    Diterbitkan 2022-03-01
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  16. 16
    Exome sequencing identified a novel Col6α1 mutation in an Iranian patient with Ullrich congenital muscular dystrophy: a case report

    Exome sequencing identified a novel Col6α1 mutation in an Iranian patient with Ullrich congenital muscular dystrophy: a case report oleh Elaheh Nekouei, Elmira Shokrolahi Yancheshmeh, Javad Mohammadi-Asl, Zafar Maasoumi Moghaddam

    Diterbitkan 2022-12-01
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  17. 17
    A novel heterozygous TPM2 gene mutation (c.456G>C; p.Lys152Asn) in an Iranian family affected by distal arthrogryposis type 1: a case report

    A novel heterozygous TPM2 gene mutation (c.456G>C; p.Lys152Asn) in an Iranian family affected by distal arthrogryposis type 1: a case report oleh Mostafa Neissi, Motahareh Sheikh-Hosseini, Javad Mohammadi-Asl, Adnan Issa Al-Badran

    Diterbitkan 2022-03-01
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  18. 18
    Identification of A Novel Missense Mutation in The Norrie Disease Gene: The First Molecular Genetic Analysis and Prenatal Diagnosis of Norrie Disease in An Iranian Family

    Identification of A Novel Missense Mutation in The Norrie Disease Gene: The First Molecular Genetic Analysis and Prenatal Diagnosis of Norrie Disease in An Iranian Family oleh Farah Talebi, Farideh Ghanbari Mardasi, Javad Mohammadi Asl, Ali Lashgari, Freidoon Farhadi

    Diterbitkan 2018-04-01
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  19. 19
    بررسی پلی‌مورفیسم ژن سوپراکسید دیسموتاز 1 و ارتباط آن با رتینوپاتی و نفروپاتی در بیماران مبتلا به دیابت نوع 2 در اهواز

    بررسی پلی‌مورفیسم ژن سوپراکسید دیسموتاز 1 و ارتباط آن با رتینوپاتی و نفروپاتی در بیماران مبتلا به دیابت نوع 2 در اهواز... oleh Javad Mohammadi-Asl, Arghavan Soleimanizadeh, Hajieh Bibi Shahbazian, Heshmatollah Shahbazian, Neda Golchin

    Diterbitkan 2014-06-01
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  20. 20
    Digenic Mutations in Junctional Epidermolysis Bullosa in An Iranian Family

    Digenic Mutations in Junctional Epidermolysis Bullosa in An Iranian Family oleh Kourosh Riahi, Farideh Ghanbari Mardasi, Farah Talebi, Farzad Jasemi, Javad Mohammadi Asl

    Diterbitkan 2021-10-01
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