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  1. Ocimum herb species: a potential treatment strategy for diabetic kidney disease
    Indira Pandiri; Akhi Moni
    J Adv Biotechnol Exp Ther. 2018; 1(3): 88-91
    » Abstract » Full-text PDF » doi: 10.5455/jabet.2018.d16

  2. Molecular characterization and phylogenetic analysis of two minnows, Puntius sarana and Barbodes gonionotus
    Shirin Sultana; Mohammad Shahdat Hossain; Mohammad Nazrul Islam; Md. Shahidul Islam Bhuiyan; Md. Salimullah; Jahangir Alam
    J Adv Biotechnol Exp Ther. 2018; 1(3): 83-87
    » Abstract » Full-text PDF » doi: 10.5455/jabet.2018.d15

  3. Resveratrol attenuates inflammation through tristetraprolin expression in human hepatocytes
    Akhi Moni; Asif Iqbal; Md Jamal Uddin
    J Adv Biotechnol Exp Ther. 2018; 1(3): 78-82
    » Abstract » Full-text PDF » doi: 10.5455/jabet.2018.d14

  4. Analysis of telomere length in the coronary artery to determine the pathogenesis of coronary artery disease
    Mahaboob V Shaik; Subrahmanyam G
    J Adv Biotechnol Exp Ther. 2018; 1(3): 72-77
    » Abstract » Full-text PDF » doi: 10.5455/jabet.2018.d13

  5. Prophylactic effects of vitamin E and selenium on di(n-butyl) phthalate-induced testicular damage in prepubertal rats
    Mohammad Shah Alam; Md Nazmul Hoque
    J Adv Biotechnol Exp Ther. 2018; 1(3): 65-71
    » Abstract » Full-text PDF » doi: 10.5455/jabet.2018.d12

  6. ISCA2 Related Mitochondrial Disorder: A distinct cause of Infantile Leukodystrophy
    Sadia Tabassum, Ali Dhohyan Al Otaibi, Rowim Fahad Al Mutairi, Mohammed Al Mannai
    JBCGenetics. 2018; 1(2): 98-101
    » Abstract » Full-text PDF » doi: 10.24911/JBCGenetics/183-1530603908

  7. A new case of de novo chromosome 19p13.12 deletion in an Omani girl with multiple congenital anomalies: a first case report from Oman
    Musallam Said Al-Araimi, Aliya Mahmood Al-Hosni, Ali Ahmed Al-Yahmadi, Salma Mohammed Al-Harasi
    JBCGenetics. 2018; 1(2): 93-97
    » Abstract » Full-text PDF » doi: 10.24911/JBCGenetics/183-1532358706

  8. Mitchell-Riley Syndrome Report of Novel Mutation and Review of the Literature
    Nourah Alruqaie, Majid Alfadhel
    JBCGenetics. 2018; 1(2): 87-92
    » Abstract » Full-text PDF » doi: 10.24911/JBCGenetics/183-1529491124

  9. Denys-Drash Syndrome: a case report
    Ahmed AbuAlreesh, Zuhair A Rahbeeni, Rayah Asiri
    JBCGenetics. 2018; 1(2): 84-86
    » Abstract » Full-text PDF » doi: 10.24911/JBCGenetics/183-1542382146

  10. A case of Bethlem Myopathy with autosomal recessive inheritance with a novel mutation in the COL6A2 gene
    Muhsin Elmas, Basak Gogus,
    JBCGenetics. 2018; 1(2): 81-83
    » Abstract » Full-text PDF » doi: 10.24911/JBCGenetics/183-1541166651

  11. Dilated cardiomyopathy in a child with truncating mutation in NRAP gene
    Hind Abdelrahman Ahmed, Saleh Al-ghamdi, Fuad Al Mutairi
    JBCGenetics. 2018; 1(2): 77-80
    » Abstract » Full-text PDF » doi: 10.24911/JBCGenetics/183-1542267981

  12. Frontonasal dysplasia: a review
    Muhammad Umair, Farooq Ahmad, Muhammad Bilal, Muhammad Arshad
    JBCGenetics. 2018; 1(2): 66-76
    » Abstract » Full-text PDF » doi: 10.24911/JBCGenetics/183-1530765389

  13. Role of auxin and nitric oxide on growth and development of lateral root of plants: possible involvement of exogenously induced Phot1
    Akhi Moni, Mohammad Nazrul Islam, Md Jamal Uddin
    J Adv Biotechnol Exp Ther. 2018; 1(2): 61-64
    » Abstract » Full-text PDF » doi: 10.5455/jabet.2018.d11


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