Search Results - "Bayat, Nooshin"

Protoparvovirus Cell Entry by Ros, Carlos, Bayat, Nooshin, Wolfisberg, Raphael, Almendral, José M

“…The (PtPV) genus of the family of viruses includes important animal pathogens and reference molecular models for the entire family. Some virus members of the…”
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Hemoglobin Q-Iran detected in family members from Northern Iran: a case report by Khorshidi, Mohammad, Roshan, Payam, Bayat, Nooshin, Mahdavi, Mohammad Reza, Najmabadi, Hossein

“…Hemoglobin Q-Iran (α75Asp→His) is an important member of the hemoglobin Q family, molecularly characterized by the replacement of aspartic acid by histidine…”
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Characterization and comparative sequence analyzes of GABA receptor gene in Asian main malaria mosquito, Anopheles stephensi by Gholizadeh, Saber, Karimi, Ameneh, Bayat, Nooshin, Djadid, Navid Dinparast, Zakeri, Sedigheh

“…Background The mutations occurring in receptor genes of Gama Amino Butyric Acid (GABA) play important roles in resistance to cychlodien insecticides in…”
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Interaction of an α-Globin Gene Triplication with β-Globin Gene Mutations in Iranian Patients with β-Thalassemia Intermedia by Farashi, Samaneh, Bayat, Nooshin, Faramarzi Garous, Negin, Ashki, Mehri, Montajabi Niat, Mona, Vakili, Shadi, Imanian, Hashem, Zeinali, Sirous, Najmabadi, Hossein, Azarkeivan, Azita

“…Abstract The 3.7 kb triplicated α-globin gene (αααanti 3.7) mutation has been found in most populations. It results from an unequal crossover between…”
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Point mutations which should not be overlooked in Hb H disease by Farashi, Samaneh, Bayat, Nooshin, Vakili, Shadi, Faramarzi Garous, Negin, Ashki, Mehri, Imanian, Hashem, Najmabadi, Hossein, Azarkeivan, Azita

“…Hb H disease is an alpha-thalassemia (α-thal) syndrome characterized by chronic hemolytic anemia that occurs when three of total four α-globin genes lost their…”
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The XmnI and BCL11A Single Nucleotide Polymorphisms May Help Predict Hydroxyurea Response in Iranian β-Thalassemia Patients by Banan, Mehdi, Bayat, Hadi, Azarkeivan, Azita, Mohammadparast, Saeid, Kamali, Koorosh, Farashi, Samaneh, Bayat, Nooshin, Khani, Masumeh Hadavand, Neishabury, Maryam, Najmabadi, Hossein

“…Hydroxyurea (HU), a drug which can reactivate fetal hemoglobin (Hb F) production, is frequently prescribed to β-thalassemia (β-thal) patients. However,…”
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Characterizing a Cohort of α-Thalassemia Couples Collected During Screening for Hemoglobinopathies: 14 Years of an Iranian Experience by Hafezi-Nejad, Nima, Khosravi, Mohsen, Bayat, Nooshin, Kariminejad, Ariana, Hadavi, Valeh, Oberkanins, Christian, Azarkeivan, Azita, Najmabadi, Hossein

“…Abstract Our study aimed to determine the number of couples with normal hemoglobin (Hb) electrophoresis and low-borderline hematological values, which may come…”
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Synthesis of white pearlescent pigments using the surface response method of statistical analysis by Bayat, Nooshin, Baghshahi, Saeid, Alizadeh, Parvin

“…White pearlescent pigments were synthesized by coating mica flakes with a thin layer of TiO 2. To this aim a chemical bath deposition method was used…”
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Report of haemoglobin J-Toronto and alpha thalassemia in a family from North of Iran by Mahdavi, Mohammad Reza, Bayat, Nooshin, Hadavi, Valeh, Karami, Hosein, Roshan, Payam, Najmabadi, Hossein, Rohanizadeh, Hamed

“…We report of an Iranian family with history of a rare haemoglobin variant, Haemoglobin J associated with alpha thalassemia, discovered while performing…”
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Novel Mutations Responsible for α-Thalassemia in Iranian Families by Bayat, Nooshin, Farashi, Samaneh, Hafezi-Nejad, Nima, Faramarzi, Negin, Ashki, Mehri, Vakili, Shadi, Imanian, Hashem, Khosravi, Mohsen, and, Azita Azar-Keivan,2, Najmabadi, Hossein

“…α-Thalassemia (α-thal) is usually caused by deletions on the α-globin gene cluster and the role of point mutations is less well investigated. In the present…”
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β-Thalassemia Mutations in the Kurdish Population of Northeastern Iraq by Jalal, Sana D., Al-Allawi, Nasir A.S., Bayat, Nooshin, Imanian, Hasham, Najmabadi, Hossein, Faraj, Azad

“…A random 123 carriers of β-thalassemia (β-thal), identified by the Sulaimaniyah Provincial Premarital Screening Program in northeastern Iraq, were screened for…”
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The Spectrum of α-Thalassemia Mutations in the Kurdish Population of Northeastern Iraq by Al-Allawi, Nasir A.S., Jalal, Sana D., Rasheed, Najeeb S., Bayat, Nooshin, Imanian, Hashem, Najmabadi, Hossein, Faraj, Azad

“…In an attempt to determine the spectrum of α-thalassemia (α-thal) mutations in the Kurdish population of Northeastern (NE) Iraq, a total of 101 unrelated…”
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Genotype-Phenotype Correlation In Iranian Patients With Hb H Disease by Ebrahimkhani, Saedieh, Azarkeivan, Azita, Bayat, Nooshin, Houry-Parvin, Mahdieh, Jalil-Nejad, Sayeh, Zand, Shima, Golkar, Zahra, Hadavi, Valeh, Imanian, Hashem, Oberkanins, Christian, Najmabadi, Hossein

“…Thalassemia is the most common genetic disorder in Iran. Some α-globin genotypes leading to Hb H disease may cause severe anemia and dependence on regular…”
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Acute pancreatitis: an initial presentation of systemic lupus erythematosus by Ghamarchehreh, Mohammad Ebrahim, Alishiri, Gholamhossein, Bayat, Nooshin, Khajehpoor, Hadi, Nooranipour, Mehrdad

“…Acute pancreatitis is a rare, but fatal, manifestation of systemic lupus erythematosus. Only 10 systemic lupus erythematosus-associated pancreatitis cases were…”
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The X mn I and BCL11A Single Nucleotide Polymorphisms May Help Predict Hydroxyurea Response in Iranian β-Thalassemia Patients by Banan, Mehdi, Bayat, Hadi, Azarkeivan, Azita, Mohammadparast, Saeid, Kamali, Koorosh, Farashi, Samaneh, Bayat, Nooshin, Khani, Masumeh Hadavand, Neishabury, Maryam, Najmabadi, Hossein

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