Search Results - "Fardi Golyan, Fatemeh"

Novel DNA variation of GPR54 gene in familial central precocious puberty by Ghaemi, Nosrat, Ghahraman, Martha, Noroozi Asl, Samaneh, Vakili, Rahim, Fardi Golyan, Fatemeh, Moghbeli, Meysam, Abbaszadegan, Mohammad Reza

“…Puberty can be considered the end point of a maturation process which is defined by the dynamic interactions of genes and environmental factors during prenatal…”
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TWIST1, MMP‐21, and HLAG‐1 co‐overexpression is associated with ESCC aggressiveness by Golyan, Fatemeh Fardi, Abbaszadegan, Mohammad Reza, Forghanifard, Mohammad Mahdi

“…Esophageal squamous cell carcinoma (ESCC) is one of the most aggressive types of cancer, requiring reliable biomarkers for prognosis and therapeutic…”
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A new gene panel as a marker for ESCC poor prognosis; INPP5A, TWIST1, MMP2, and EGFR by Fardi Golyan, Fatemeh, Forghanifard, Mohammad Mahdi

“…Esophageal squamous cell carcinoma (ESCC) is categorized among ten common aggressive malignancies, with a higher incidence and mortality rates in the…”
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The therapeutic potential value of Cancer-testis antigens in immunotherapy of gastric cancer by Alsadat Mahmoudian, Reihaneh, Amirhosein, Maharati, Mahmoudian, Parvaneh, Fardi Golyan, Fatemeh, Mokhlessi, Leila, Maftooh, Mina, Khazaei, Majid, Nassiri, Mohammadreza, Mahdi Hassanian, Seyed, Ghayour-Mobarhan, Majid, Ferns, Gordon A, Shahidsales, Soodabeh, Avan, Amir

“…•Cancer-testis antigens (CTAs) have been identified as a potential biomarker and target for immunotherapy.•The CTAs-restricted expression pattern in tumor…”
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Novel mutation in AIRE gene with autoimmune polyendocrine syndrome type 1 by Fardi Golyan, Fatemeh, Ghaemi, Nosrat, Abbaszadegan, Mohammad Reza, Dehghan Manshadi, Seyed Hossein, Vakili, Rahim, Druley, Todd E., Rahimi, Hamid Reza, Ghahraman, Martha

“…Autoimmune polyendocrine type 1 (APS-1) is a complex inherited autosomal recessive disorder. Classically, it appears within the first decade of life followed…”
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Identification of four novel mutations of the WFS1 gene in Iranian Wolfram syndrome pedigrees by Ghahraman, Martha, Abbaszadegan, Mohammad Reza, Vakili, Rahim, Hosseini, Sousan, Fardi Golyan, Fatemeh, Ghaemi, Nosrat, Forghanifard, Mohammad Mahdi

“…Aims Wolfram syndrome is a rare neurodegenerative disorder with an autosomal recessive pattern of inheritance characterized by various clinical manifestations…”
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Preclinical tumor mouse models for studying esophageal cancer by Mahmoudian, Reihaneh Alsadat, Farshchian, Moein, Golyan, Fatemeh Fardi, Mahmoudian, Parvaneh, Alasti, Ali, Moghimi, Vahid, Maftooh, Mina, Khazaei, Majid, Hassanian, Seyed Mahdi, Ferns, Gordon A., Mahaki, Hanie, Shahidsales, Soodabeh, Avan, Amir

“…Preclinical models are extensively employed in cancer research because they can be manipulated in terms of their environment, genome, molecular biology, organ…”
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Whole Exome Sequencing Reveals a Novel Damaging Mutation in Human Fibroblast Activation Protein in a Family with Esophageal Squamous Cell Carcinoma by Golyan, Fatemeh Fardi, Moghaddassian, Morteza, Forghanifard, Mohammad Mahdi, Talebi, Samaneh, Farshchian, Moein, Mahmoudian, Reihaneh Alsadat, Abbaszadegan, Mohammad Reza

“…Purpose Esophageal squamous cancer cell (ESCC), with late diagnosis and poor rate of survival, is a significant cause of mortality in the developing countries…”
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Novel mutations and their genotype-phenotype correlations in patients with Noonan syndrome, using next-generation sequencing by Tafazoli, Alireza, Eshraghi, Peyman, Pantaleoni, Francesca, Vakili, Rahim, Moghaddassian, Morteza, Ghahraman, Martha, Muto, Valentina, Paolacci, Stefano, Golyan, Fatemeh Fardi, Abbaszadegan, Mohammad Reza

“…Noonan Syndrome (NS) is an autosomal dominant disorder with many variable and heterogeneous conditions. The genetic basis for 20–30% of cases is still unknown…”
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