183 results on '"Saberi, Alihossein"'
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2. Genetic features of patients with MPS type IIIB: Description of five pathogenic gene variations
3. Integrative bioinformatics analysis of miRNA and mRNA expression profiles identified some potential biomarkers for breast cancer
4. Quantitative Investigation of MicroRNA-32 in the Urine of Prostate Cancer Patients and Its Relationship With Clinicopathological Characteristics
5. Identification of a new mutation in the ACTL9 gene in men with unexplained infertility
6. KCNQ1 rs2237895 polymorphism is associated with the therapeutic response to sulfonylureas in Iranian type 2 diabetes mellitus patients
7. Breast cancer prediction with transcriptome profiling using feature selection and machine learning methods
8. Genotype–phenotype correlation in patients with deletional and nondeletional mutations of Hb H disease in Southwest of Iran
9. LncRNAs as putative biomarkers and therapeutic targets for Parkinson’s disease
10. Genotypic variants of the tetrahydrobiopterin (BH4) biosynthesis genes in patients with hyperphenylalaninemia from different regions of Iran
11. Identification of new variants in patients with mucopolysaccharidosis in consanguineous Iranian families.
12. Genotypic variants of the tetrahydrobiopterin (BH4) biosynthesis genes in patients with hyperphenylalaninemia from different regions of Iran.
13. Biallelic MED27 variants lead to variable ponto-cerebello-lental degeneration with movement disorders
14. Molecular and in Silico Analysis of MEFV Variants in Familial Mediterranean Fever Patients in Southwest Iran
15. Organ-specific metastasis of breast cancer: molecular and cellular mechanisms underlying lung metastasis
16. Supplementary Data from Multiple Repair Pathways Mediate Tolerance to Chemotherapeutic Cross-linking Agents in Vertebrate Cells
17. Association of rs1570360 and rs2010963 in VEGF and rs2279744 in MDM2 gene with Recurrent Implantation Failure in Iranian Women
18. Whole exome sequencing reveals several novel variants in congenital disorders of glycosylation and glycogen storage diseases in seven patients from Iran
19. Copy number analysis in a large-scale study of spinal muscular atrophy patients between two continuous generations in Iran
20. Integrative bioinformatics analysis of miRNA and mRNA expression profiles identified some potential biomarkers for breast cancer
21. Hb Narges Lab, a Novel Hemoglobin Variant of the β-Globin Gene
22. Whole exome sequencing reveals several novel variants in congenital disorders of glycosylation and glycogen storage diseases in seven patients from Iran.
23. Abnormal angiogenesis associated with HIF-1α/VEGF signaling pathway in recurrent miscarriage along with therapeutic goals
24. An Essential Role for Cdk1 in S Phase Control Is Revealed via Chemical Genetics in Vertebrate Cells
25. Alpha‐globin gene triplication and its effect in beta‐thalassemia carrier, sickle cell trait, and healthy individual
26. Niemann-Pick Diseases: The Largest Iranian Cohort with Genetic Analysis
27. Whole-Exome Sequencing Application for Genetic Diagnosis of Kidney Diseases: A Study from Southwest of Iran
28. Identification of the PRM1 gene mutations in oligoasthenoteratozoospermic men
29. Identification of Cytochrome b‐245, beta‐chain gene mutations, and clinical presentations in Iranian patients with X‐linked chronic granulomatous disease
30. Differential usage of non-homologous end-joining and homologous recombination in double strand break repair
31. Two Novel and Five Rare Mutations in the Non Coding Regions of the β-Globin Gene in the Iranian Population
32. The Effect of CYP2C9 Genotype Variants in Type 2 Diabetes on the Pharmacological Effectiveness of Sulfonylureas, Diabetic Retinopathy, and Nephropathy
33. Deletion and duplication mutations spectrum in Duchenne muscular dystrophy in the southwest of Iran
34. Association of vascular endothelial growth factor A polymorphisms and aberrant expression of connexin 43 and VEGFA with idiopathic recurrent spontaneous miscarriage
35. Identification of three novel mutations in the FANCA, FANCC, and ,ITGA2B genes by whole exome sequencing
36. Adipose tissue miRNA level variation through conjugated linoleic acid supplementation in diet-induced obese rats
37. Identification of Cytochrome b‐245, beta‐chain gene mutations, and clinical presentations in Iranian patients with X‐linked chronic granulomatous disease.
38. Identification of Three Novel Mutations in the FANCA, FANCC, and ITGA2B Genes by Whole Exome Sequencing.
39. Genotype–phenotype correlation and the size of microdeletion or microduplication of 7q11.23 region in patients with Williams‐Beuren syndrome
40. Prenatal diagnosis of a rare de novo 1q22-q25.1 chromosomal deletion syndrome using oligo array CGH
41. Frequent novel mutations are causative for maple syrup urine disease from Southwest Iran
42. Mutation Screening of the Krüppel-like Factor 1 Gene in Individuals With Increased Fetal Hemoglobin Referred for Hemoglobinopathy Investigation in South of Iran
43. Validity of chromosomal aneuploidies testing during pregnancy: A comparison of karyotype, interphase-FISH and QF-PCR techniques
44. MiR-328 May be Considered as an Oncogene in Human Invasive Breast Carcinoma
45. Gold nanoparticles in combination with megavoltage radiation energy increased radiosensitization and apoptosis in colon cancer HT-29 cells
46. Effect of Temporal Pattern of Radiation in Intensity Modulated Radiotherapy on Cell Cycle Progression and Apoptosis of ACHN Renal Cell Carcinoma Cell Line
47. Dose–Response Curves of the FDXR and RAD51 Genes with 6 and 18 MV Beam Energies in Human Peripheral Blood Lymphocytes
48. Influence of L-carnitine on the Expression Level of Adipose Tissue miRNAs Related to Weight Changes in Obese Rats
49. Gene Expression Biodosimetry: Quantitative Assessment of Radiation Dose with Total Body Exposure of Rats
50. Culturing in serum-free culture medium on collagen type-I-coated plate increases expression of CD133 and retains original phenotype of HT-29 cancer stem cell
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