Zobrazeno 1 - 10
of 19
pro vyhledávání: '"Marziye Mohammadi‐Anaei"'
Autor:
Mohammad Hamid, Bijan keikhaei, Hamid Galehdari, Alihossein Saberi, Alireza Sedaghat, Gholamreza Shariati, Marziye Mohammadi-Anaei
Publikováno v:
Scientific Reports, Vol 12, Iss 1, Pp 1-7 (2022)
Abstract We studied the alpha-globin gene genotypes, hematologic values, and transfusion-dependence of patients with Hb H disease. Molecular characterization of alpha-thalassemia was performed. We identified 120 patients with Hb H disease. Of these p
Externí odkaz:
https://doaj.org/article/705c41e1ec984ca0873e9ba140e7c232
Autor:
Mohammad Hamid, Bijan keikhaei, Hamid Galehdari, Alihossein Saberi, Alireza Sedaghat, Gholamreza Shariati, Marziye Mohammadi‐Anaei
Publikováno v:
eJHaem, Vol 2, Iss 3, Pp 366-374 (2021)
Abstract The genotype and phenotype correlation between coinheritance of heterozygous beta‐thalassemia with the alpha‐globin triplication is unclear. In this study we have investigated and reviewed alpha triplication frequency in beta‐thalassem
Externí odkaz:
https://doaj.org/article/d6c6b109f1b7465fb91a3bb7d6af75af
Autor:
Marziye Mohammadi-Anaei, Alireza Sedaghat, Gholamreza Shariati, Hamid Galehdari, Mohammad Hamid, Alihossein Saberi, Bijan Keikhaei
Publikováno v:
eJHaem. 2:366-374
The genotype and phenotype correlation between coinheritance of heterozygous beta-thalassemia with the alpha-globin triplication is unclear. In this study we have investigated and reviewed alpha triplication frequency in beta-thalassemia carriers, si
Autor:
Mohammad Hamid, Zahra Shahbazi, Bijan Keikhaei, Hamid Galehdari, Alihossein Saberi, Alireza Sedaghat, Gholamreza Shariati, Marziye Mohammadi-Anaei
Publikováno v:
Archives of Iranian medicine. 25(5)
In this study, we describe a new missense variant on the β-globin gene in a heterozygous form in a female individual. Standard methods were used to determine red blood cell indices and perform hemoglobin analyses. Molecular studies were performed on
Autor:
Marziye Mohammadi-Anaei, Alireza Sedaghat, Gholamreza Shariati, Hamid Galehdari, Ebtesam Zargan Nezhad, Mohammad Hamid, Alihossein Saberi, Bijan Keikhaei
Publikováno v:
Hemoglobin. 44(4)
β-Thalassemia (β-thal) is one of the most frequent genetic disorder in Iran with great mutational diversity. In this study, we describe two novel and five rare mutations in the non coding regions of the β-globin gene; these mutations were identifi
Autor:
Alihossein Saberi, Mohammad Hamid, Ladan Dawoody Nejad, Marziye Mohammadi-Anaei, Hamid Galehdari, Gholamreza Shariati
Publikováno v:
Iranian Biomedical Journal
Background: β-thalassemia is one of the most widespread diseases in the world, including Iran. In this study, we reported, for the first time, a 290-bp β-globin gene deletion in the south of Iran. Methods: Four individuals from three unrelated fami
Hb AHVAZ [α83(F4)Leu→Arg, CTG>CGG (α2);HBA2: c.251T>G],A New Hemoglobin Variant of theα2-Globin Gene
Autor:
Alihossein Saberi, Mohammad Hamid, Marziye Mohammadi-Anaei, Bijan Kaikhaei, Gholamreza Shariati, Hamid Galehdari
Publikováno v:
Hemoglobin. 37:477-480
We report a novel mutation on the α2-globin gene, codon 83 (TG), which was detected in two members of two unrelated families from Khuzestan Province, South Iran, that we named Hb Ahvaz. This mutation was detected by cellulose acetate electrophoresis
Autor:
Mohammad, Hamid, Hanieh, Bokharaei Merci, Hamid, Galehdari, Ali Hossein, Saberi, Bijan, Kaikhaei, Marziye, Mohammadi-Anaei, Ahmad, Ahmadzadeh, Gholamreza, Shariati
Publikováno v:
Archives of Iranian medicine. 17(7)
In this study, a new alpha globin gene mutation on the α2-globin gene is reported. This mutation resulted in a Lysstop codon substitution at position 127 which was detected in four individuals (three males and one female). DNA sequencing revealed th
Autor:
Mohammad, Hamid, Gholamreza, Shariati, Alihossein, Saberi, Bijan, Kaikhaei, Hamid, Galehdari, Marziye, Mohammadi-Anaei
Publikováno v:
Archives of Iranian medicine. 16(9)
We described the first report of IVS-I (-1), codon 30 (GC) or Hb Monroe in five individuals from four unrelated families in Khuzestan Province. Polymerase chain reaction (PCR) followed by sequencing of the beta-globin gene confirmed the presence of H
Autor:
Hamid, Mohammad1 hamid143@yahoo.com, Shahbazi, Zahra1, Keikhaei, Bijan2, Galehdari, Hamid3, Saberi, Alihossein4, Sedaghat, Alireza5, Shariati, Gholamreza4,6 Shariatig@yahoo.com, Mohammadi-Anaei, Marziye6
Publikováno v:
Archives of Iranian Medicine (AIM). May2022, Vol. 25 Issue 5, p339-342. 4p.