M. Neishabury

发表

The modifying effect of Xmn1-HBG2 on thalassemic phenotype is associated with its linked elements in the beta globin locus control region, including the palindromic site at 5'HS4.

H. Najmabadi, S. S. Abedini, H. Darvish, 2012, Blood cells, molecules & diseases.

Spontaneous mutation, oxidative DNA damage, and the roles of base and nucleotide excision repair in the yeast Saccharomyces cerevisiae

R. Waters, S. Boiteux, S. Reed, 1999, Yeast.

The XmnI and BCL11A Single Nucleotide Polymorphisms May Help Predict Hydroxyurea Response in Iranian β-Thalassemia Patients

S. Farashi, H. Najmabadi, M. Banan, 2012, Hemoglobin.

Frequency of positive XmnIGgamma polymorphism and coinheritance of common alpha thalassemia mutations do not show statistically significant difference between thalassemia major and intermedia cases with homozygous IVSII-1 mutation.

H. Najmabadi, A. Azarkeivan, M. Neishabury, 2010, Blood cells, molecules & diseases.

Molecular mechanisms underlying thalassemia intermedia in Iran.

H. Najmabadi, C. Oberkanins, N. Amirizadeh, 2008, Genetic testing.

Novel variants in Iranian individuals suspected to have inherited red blood cell disorders, including bone marrow failure syndromes

H. Najmabadi, Z. Fattahi, A. Azarkeivan, 2020, Haematologica.

The Role of BCL11A and HBS1L-MYB Polymorphisms in Predicting Blood Transfusion Requirements of Thalassemia Patients with Homozygous 5’HS4-LCR/Xmn1-HBG2 Background

H. Najmabadi, S. S. Abedini, A. Azarkeivan, 2015 .

Novel mutations in mitochondrial carrier family gene SLC25A38, causing congenital sideroblastic anemia in Iranian families, identified by whole exome sequencing.

H. Najmabadi, A. Azarkeivan, M. Neishabury, 2018, Blood cells, molecules & diseases.

Analyzing 5'HS3 and 5'HS4 LCR core regions and NF-E2 in Iranian thalassemia intermedia patients with normal or carrier status for beta-globin mutations.

H. Najmabadi, S. S. Abedini, C. Oberkanins, 2011, Blood cells, molecules & diseases.

A REPORT OF 8 CASES WITH HEMOGLOBIN H DISEASE IN AN IRANIAN FAMILY

Najmabadi Hossein, V. Hadavi, M. Neishabury, 2010, Pediatric hematology and oncology.

The Iranian Human Mutation Gene Bank: A data and sample resource for worldwide collaborative genetics research

Mehrdad Mohammadi, K. Kahrizi, H. Najmabadi, 2003, Human mutation.

Electromobility Shift Assay Reveals Evidence in Favor of Allele-Specific Binding of RUNX1 to the 5′ Hypersensitive Site 4-Locus Control Region

M. Neishabury, Sepideh Ghobakhloo, Hossein Dehghani, 2016, Hemoglobin.

High Prevalence of the −α3.7 Deletion Among Thalassemia Patients in Iran

K. Kahrizi, H. Najmabadi, A. Pourfathollah, 2003 .

Rare and unexpected mutations among Iranian beta-thalassemia patients and prenatal samples discovered by reverse-hybridization and DNA sequencing.

H. Najmabadi, A. Pourfathollah, C. Oberkanins, 2002, Haematologica.

Genetic Diagnosis of Pyruvate Kinase Deficiency in Undiagnosed Iranian Patients with Severe Hemolytic Anemia, using Whole Exome Sequencing

H. Najmabadi, A. Azarkeivan, M. Neishabury, 2022, Archives of Iranian medicine.

The First Case of BENTA Disease (B Cell Expansion with NF-κB and T Cell Anergy) from Iran

H. Najmabadi, A. Azarkeivan, M. Neishabury, 2021, Journal of Clinical Immunology.

Mycorrhizal colonization improves onion (Allium cepa L.) yield and water use efficiency under water deficit condition

N. Chaparzadeh, S. Bolandnazar, M. Neishabury, 2007 .

Spontaneous mutation, oxidative DNA damage, and the roles of base and nucleotide excision repair in the yeast Saccharomyces cerevisiae

R. Waters, S. Boiteux, S. Reed, 1999, Yeast.

HFE and Non-HFE Hereditary Hemochromatosis Based on Screening of 854 Individuals: 12 Years of an Iranian Experience.

A. Azarkeivan, M. Neishabury, Mina Makvand, 2024, Genetic testing and molecular biomarkers.