Search Results - "Koulivand, Leila"

Telomere Structure and Its Role in DNA Damage and Genetic Disorders by Majid Kheirollahi, Leila Koulivand

“…Telomeres are special structures at the ends of chromosomes, especially in eukaryotes, that include repetitive sequences of deoxyribonucleic acid (DNA) and…”
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Detection of Mutation in Exons 3 and 8 of SLC3A1 and Exons 4 and 10 of SLC7A9 Genes in Patients with Cystinuria in Iran by Leila Koulivand, Mehrdad Mohammadi, Rasoul Salehi, Behrouz Ezatpour, Majid Kheirollahi

“…Background: Cystinuria, one of the first diagnosed inborn errors of metabolism, recognized by hyperexcretion of cystine, lysine, ornithine and arginine into…”
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Expression of prostaglandin I2 (prostacyclin) receptor in blood of migraine patients: A potential biomarker by Kheirollahi, Majid, Kazemi, Mohammad, Amini, Gilda, Khorvash, Fariborz, Ahangari, Fatemeh, Kolahdouz, Mahsa, Koulivand, Leila

“…Migraine is the most common chronic neurological disorders that may be associated with vasodilatation. According to the role of prostaglandin I2 (prostacyclin)…”
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In silico analysis of SLC3A1 and SLC7A9 mutations in Iranian patients with Cystinuria by Mahdavi, Manijeh, Koulivand, Leila, Khorrami, Mehdi, Mirsafaie, Maryam, Kheirollahi, Majid

“…Cystinuria is an autosomal recessive defect in reabsorptive transport of cystine and the dibasic amino acids ornithine, arginine, and lysine from renal tubule…”
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Mutation analysis of SLC3A1 and SLC7A9 genes in patients with cystinuria by Koulivand, Leila, Mohammadi, Mehrdad, Ezatpour, Behrouz, Salehi, Rasoul, Markazi, Samane, Dashti, Sepideh, Kheirollahi, Majid

“…Cystinuria is an autosomal inherited disorder of renal reabsorption of cystine, arginine, lysine, and ornithine. Increased urinary excretion of cystine results…”
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Cystinuria in a patient with a novel mutation in SLC7A9 gene by Koulivand, Leila, Mohammadi, Mehrdad, Ezatpour, Behrouz, Kheirollahi, Majid

“…Cystinuria, one of the first inborn errors of metabolism, is characterized by hyperexcretion of cystine, arginine, lysine, and ornithine into urine. Cystinuria…”
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A Novel Mutation in SLC3A1 Gene in Patients With Cystinuria by Markazi, Samaneh, Kheirollahi, Majid, Doosti, Abbas, Mohammadi, Mehrdad, Koulivand, Leila

“…Cystinuria is an inherited disease characterized by the formation of cystine calculi in the kidneys, ureters,  and bladder. Cystinuria is associated with…”
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The Role of Telomere in Cell; Telomere Dysfunction and Tumorigenesis by Majid Kheirollahi, Mahsa Kolahdouz, Fatemeh Ahangari, Leila Koulivand, Fariborz Khorvash

“…Telomeres consist of repetitive DNA sequences and a variety of non-nucleosomal proteins which are essential to survive chromosome. Telomeres protect the ends…”
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Expression of prostaglandin I2 by Kheirollahi, Majid, Kazemi, Mohammad, Amini, Gilda, Khorvash, Fariborz, Ahangari, Fatemeh, Kolahdouz, Mahsa, Koulivand, Leila

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