Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Hashem, Imanian"'
Autor:
Parvin, Rostami, Kazem, Zendehdel, Reza, Shirkoohi, Elmira, Ebrahimi, Mitra, Ataei, Hashem, Imanian, Hossein, Najmabadi, Mohammad Reza, Akbari, Mohammad Hossein, Sanati
Publikováno v:
Archives of Iranian medicine. 23(3)
Breast cancer (BC) is a highly complex, heterogeneous and multifactorial disease and is the most commonly diagnosed cancer and the leading cause of cancer-related mortality in women worldwide. Family history and genetic mutations are important risk f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::b1d9cf6a980274bf761afbf9eb91c7f7
https://pubmed.ncbi.nlm.nih.gov/32126783
https://pubmed.ncbi.nlm.nih.gov/32126783
Autor:
Mehri Ashki, Hashem Imanian, Azita Azarkeivan, Samaneh Farashi, Shadi Vakili, Hossein Najmabadi, Negin Faramarzi Garous
Publikováno v:
Hemoglobin. 39:398-402
In the present study, a total of 11 individuals with hypochromic microcytic anemia who did not reveal the most common α-thalassemia (α-thal) deletions or mutations, were subjected to more investigations by DNA sequencing of the α-globin genes. Sev
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f4915862d128634cc68682356dd811f2
https://doi.org/10.3109/03630269.2015.1075890
https://doi.org/10.3109/03630269.2015.1075890
Autor:
Azita Azarkeivan, Shadi Vakili, Samaneh Farashi, Hashem Imanian, Hossein Najmabadi, Mehri Ashki, Negin Faramarzi Garous
Publikováno v:
Expert Review of Hematology. 8:693-698
Copy number variations in α-globin genes are results of unequal crossover between homologous segments in the α-globin gene cluster that misalign during the meiosis phase of the gametogenesis process. Reduction or augmentation of α-globin genes lea
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::14dbe55a6f6a4a2bc5ee8b93b640b169
https://doi.org/10.1586/17474086.2015.1075385
https://doi.org/10.1586/17474086.2015.1075385
Autor:
Samaneh Farashi, Shadi Vakili, Mehri Ashki, Hashem Imanian, Hossein Najmabadi, Azita Azarkeivan, Negin Faramarzi Garous
Publikováno v:
Hemoglobin. 40:53-55
Hemoglobin (Hb) variants are abnormalities resulting from point mutations in either of the two α-globin genes (HBA2 or HBA1) or the β-globin gene (HBB). Various reports of Hb variants have been described in Iran and other countries around the world
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e42f0cd76cfe7a2851dd002e0d7a5745
https://doi.org/10.3109/03630269.2015.1091357
https://doi.org/10.3109/03630269.2015.1091357
Autor:
Sana D Jalal, Nasir A. S. Al-Allawi, Najeeb S. Rasheed, Hashem Imanian, Hossein Najmabadi, Azad H. Faraj, Nooshin Bayat
Publikováno v:
Hemoglobin. 37:56-64
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 adults with unexplained hypochromia and/or microcytosis were enrolled. α-Thalasssemia mutatio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d95e7122ecfa530e448790ee2246f0dd
https://doi.org/10.3109/03630269.2012.749490
https://doi.org/10.3109/03630269.2012.749490
Autor:
Fariba Rad, Hashem Imanian, Hossein Najmabadi, Samaneh Farashi, Bahram Shahmohammadi, Azita Azarkeivan
Publikováno v:
Hemoglobin. 40(2)
A distinct set of mutations on the β-globin gene leads to dominantly inherited β-thalassemia (β-thal) that is associated with a disease phenotype in a single mutant copy. We described molecular and hematological characteristics of a novel elongate
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5802e97f6cd4c7b37228772d7fb797bb
https://pubmed.ncbi.nlm.nih.gov/26850598
https://pubmed.ncbi.nlm.nih.gov/26850598
Autor:
Azita Azarkeivan, Nooshin Bayat, Valeh Hadavi, Hashem Imanian, Christian Oberkanins, Sayeh Jalil-Nejad, Zahra Golkar, Mahdieh Houry-Parvin, Shima Zand, Hossein Najmabadi, Saedieh Ebrahimkhani
Publikováno v:
Hemoglobin. 35:40-46
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 blood transfusions. In this study, 40 patients were analyzed for the molecular basis and the g
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3152e48e68660a746665e6a7d3ca91b5
https://doi.org/10.3109/03630269.2010.546314
https://doi.org/10.3109/03630269.2010.546314
Screening of Iranian Thalassemic Families for the Most Common Deletions of the β-Globin Gene Cluster
Autor:
Azita Azarkeivan, Farzin Pourfarzad, Hossein Najmabadi, Fatemehsadat Esteghamat, Navid Almadani, Hashem Imanian
Publikováno v:
Hemoglobin. 31:463-469
Deltabeta-thalassemia (thal) is a disorder, characterized by increased levels of fetal hemoglobin (Hb F) in adult life. A considerable number of deletions of variable size and position in the beta-globin gene cluster are associated with the clinical
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::59e90c2c3883c0ae596d526f0b6888aa
https://doi.org/10.1080/03630260701641286
https://doi.org/10.1080/03630260701641286
Autor:
Nooshin Bayat, Samaneh Farashi, Shadi Vakili, Negin Faramarzi Garous, Mehri Ashki, Azita Azarkeivan, Hashem Imanian, Hossein Najmabadi
Publikováno v:
Expert review of hematology. 9(1)
Background: 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 function due to completely deletions or different kind of mutations.Objectiv
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::19efa840bb81161b21cd8ab97269bb63
https://pubmed.ncbi.nlm.nih.gov/26523940
https://pubmed.ncbi.nlm.nih.gov/26523940
Autor:
Samaneh, Farashi, Negin F, Garous, Mehri, Ashki, Shadi, Vakili, Fatemeh, Zeinali, Hashem, Imanian, Azita, Azarkeivan, Piero C, Giordano, Hossein, Najmabadi
Publikováno v:
Hemoglobin. 39(5)
We describe a case of Hb H disease associated with homozygosity for a two nucleotide deletion in the polyadenylation signal of the α2-globin gene (HBA2: c.*93_*94delAA). The patient, a 27-year-old son of a consanguineous couple, needs regular blood
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::22b3d452e237ee3239e019ea460b3920
https://pubmed.ncbi.nlm.nih.gov/26193977
https://pubmed.ncbi.nlm.nih.gov/26193977