关注
Samaneh Farashi
Samaneh Farashi
University of Melbourne
在 wehi.edu.au 的电子邮件经过验证
标题
引用次数
引用次数
年份
Molecular basis of α-thalassemia
S Farashi, CL Harteveld
Blood Cells, Molecules, and Diseases 70, 43-53, 2018
2482018
Post-GWAS in prostate cancer: from genetic association to biological contribution
S Farashi, T Kryza, J Clements, J Batra
Nature Reviews Cancer 19 (1), 46-59, 2019
982019
The XmnI and BCL11A Single Nucleotide Polymorphisms May Help Predict Hydroxyurea Response in Iranian β-Thalassemia Patients
M Banan, H Bayat, A Azarkeivan, S Mohammadparast, K Kamali, ...
Hemoglobin 36 (4), 371-380, 2012
472012
Interaction of an α-Globin Gene Triplication with β-Globin Gene Mutations in Iranian Patients with β-Thalassemia Intermedia
S Farashi, N Bayat, N Faramarzi Garous, M Ashki, M Montajabi Niat, ...
Hemoglobin 39 (3), 201-206, 2015
352015
Skewed mutational spectrum of RET proto-oncogene Exon10 in Iranian patients with medullary thyroid carcinoma
M Zarif Yeganeh, S Sheikholeslami, G Dehbashi Behbahani, S Farashi, ...
Tumor Biology 36, 5225-5231, 2015
342015
Identification of genetic factors influencing metabolic dysregulation and retinal support for MacTel, a retinal disorder
R Bonelli, VE Jackson, A Prasad, JE Munro, S Farashi, TFC Heeren, ...
Communications biology 4 (1), 274, 2021
282021
Core promoter STRs: novel mechanism for inter-individual variation in gene expression in humans
A Heidari, ZNS Fam, E Esmaeilzadeh-Gharehdaghi, M Banan, ...
Gene 492 (1), 195-198, 2012
242012
Diagnostic pitfalls of less well recognized HbH disease
S Farashi, H Najmabadi
Blood Cells, Molecules, and Diseases 55 (4), 387-395, 2015
182015
Novel mutations responsible for α-thalassemia in Iranian families
N Bayat, S Farashi, N Hafezi-Nejad, N Faramarzi, M Ashki, S Vakili, ...
Hemoglobin 37 (2), 148-159, 2013
182013
Support for down-tuning of the calreticulin gene in the process of human evolution
E Esmaeilzadeh-Gharehdaghi, M Banan, S Farashi, A Mirabzadeh, ...
Progress in Neuro-Psychopharmacology and Biological Psychiatry 35 (7), 1770-1773, 2011
172011
Point mutations which should not be overlooked in Hb H disease
S Farashi, N Bayat, S Vakili, N Faramarzi Garous, M Ashki, H Imanian, ...
Expert review of hematology 9 (1), 107-113, 2016
122016
Copy number variations of six and seven α-globin genes in a family with intermedia and major thalassemia phenotypes
S Farashi, S Vakili, N Faramarzi Garous, M Ashki, H Imanian, ...
Expert Review of Hematology 8 (5), 693-698, 2015
122015
c AMP response element‐binding protein 1 is required for hydroxyurea‐mediated induction of γ‐globin expression in K 562 cells
M Banan, E Esmaeilzadeh‐Gharehdaghi, M Nezami, Z Deilami, S Farashi, ...
Clinical and Experimental Pharmacology and Physiology 39 (6), 510-517, 2012
102012
Homozygosity for the AATAAA > AATA– – Polyadenylation Site Mutation on the α2-Globin Gene Causing Transfusion-Dependent Hb H Disease in an Iranian …
S Farashi, NF Garous, M Ashki, S Vakili, F Zeinali, H Imanian, ...
Hemoglobin 39 (5), 355-358, 2015
82015
Frequency of α-globin gene triplications and coinheritance with β-globin gene mutations in the Iranian population
SS Abedini, F Forouzesh Pour, K Karimi, Z Ghaderi, S Farashi, ...
Hemoglobin 42 (4), 252-256, 2018
72018
Point mutations in ret proto-oncogene exon 10 in Patients with medullary thyroid carcinoma
M Zarif-Yeganeh, S Sheikholeslami, G Dehbashi-Behbahani, S Farashi, ...
Journal of Kerman University of Medical Sciences 22 (3), 249-260, 2015
72015
Pathway analysis of genes identified through post-GWAS to underpin prostate cancer aetiology
S Farashi, T Kryza, J Batra
Genes 11 (5), 526, 2020
62020
Hb Dartmouth (HBA2: c.200T>C): An α2-Globin Gene Associated with Hb H Disease in One Homozygous Patient
S Farashi, N Faramarzi Garous, M Ashki, S Vakili, F Zeinali, H Imanian, ...
Hemoglobin 39 (3), 152-155, 2015
62015
First report of a dominantly inherited β-thalassemia caused by a novel elongated β-globin chain
S Farashi, F Rad, B Shahmohammadi, H Imanian, A Azarkeivan, ...
Hemoglobin 40 (2), 102-107, 2016
42016
iPSC–derived retinal pigmented epithelial cells from patients with macular telangiectasia show decreased mitochondrial function
KT Eade, BRE Ansell, S Giles, R Fallon, S Harkins-Perry, T Nagasaki, ...
The Journal of Clinical Investigation 133 (9), 2023
32023
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