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The relationship between common mutations in CFTR, AR genes, Y chromosome microdeletions and karyoty** abnormalities with very severe oligozoospermia in Iranian men

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  1. Article

    Open Access

    Identification of novel mutations among Iranian NPC1 patients: a bioinformatics approach to predict pathogenic mutations

    Niemann-Pick disease type C (NPC) is a rare lysosomal neurovisceral storage disease caused by mutations in the NPC 1 (95%) or NPC2 (5%) genes. The products of NPC1 and NPC2 genes play considerable roles in glycol...

    Rezvan Abtahi, Parvaneh Karimzadeh, Omid Aryani, Diba Akbarzadeh in Hereditas (2022)

  2. Article

    Open Access

    Origin and spread of human mitochondrial DNA haplogroup U7

    Human mitochondrial DNA haplogroup U is among the initial maternal founders in Southwest Asia and Europe and one that best indicates matrilineal genetic continuity between late Pleistocene hunter-gatherer grou...

    Hovhannes Sahakyan, Baharak Hooshiar Kashani, Rakesh Tamang in Scientific Reports (2017)

  3. Article

    Open Access

    Mitochondrial A12308G alteration in tRNALeu(CUN) in colorectal cancer samples

    Colorectal cancer is the third most common type of cancer in men and women and the second leading cause of cancer-related deaths in the United States and UK. Colorectal cancer is strongly related to age, with ...

    Fawziah MA Mohammed, Ali Reza Rezaee khorasany, Elaheh Mosaieby in Diagnostic Pathology (2015)

  4. Article

    Open Access

    The mitochondrial ATPase6 gene is more susceptible to mutation than the ATPase8 gene in breast cancer patients

    Breast cancer is the most common malignancy in women throughout the world. Mitochondria play important roles in cellular energy production, free radical generation and apoptosis. Identification of mitochondria...

    Massoud Ghaffarpour, Reza Mahdian, Forouzandeh Fereidooni in Cancer Cell International (2014)

  5. Article

    Open Access

    The mitochondrial C16069T polymorphism, not mitochondrial D310 (D-loop) mononucleotide sequence variations, is associated with bladder cancer

    Bladder cancer is a relatively common and potentially life-threatening neoplasm that ranks ninth in terms of worldwide cancer incidence. The aim of this study was to determine deletions and sequence variations...

    Nasser Shakhssalim, Massoud Houshmand, Behnam Kamalidehghan in Cancer Cell International (2013)

  6. Article

    Open Access

    Association of fibroblast growth factor (FGF-21) as a biomarker with primary mitochondrial disorders, but not with secondary mitochondrial disorders (Friedreich Ataxia)

    Mitochondrial respiratory chain deficiencies are a group of more than 100 disorders of adults and children, with highly variable phenotypes. The high prevalence of mitochondrial disorders (MIDs) urges the cli...

    Mohammad Hossein Salehi, Behnam Kamalidehghan in Molecular Biology Reports (2013)

  7. Article

    Open Access

    Establishment and characterization of two human breast carcinoma cell lines by spontaneous immortalization: Discordance between Estrogen, Progesterone and HER2/neu receptors of breast carcinoma tissues with derived cell lines

    Breast cancer is one of the most common cancers among women throughout the world. Therefore, established cell lines are widely used as in vitro experimental models in cancer research.

    Behnam Kamalidehghan, Massoud Houshmand in Cancer Cell International (2012)

  8. Article

    Open Access

    Specific-mutational patterns of p53 gene in bladder transitional cell carcinoma among a group of Iraqi patients exposed to war environmental hazards

    To unfold specific-mutational patterns in TP53 gene due to exposures to war environmental hazards and to detect the association of TP53 gene alteration with the depth of bladder cancer.

    Thekra A Al-Kashwan, Massoud Houshmand, Asaad Al-Janabi in BMC Research Notes (2012)