Raamatud Shahin Asadi
Effects of Synergistic Blend-of Three Plant Extracts of Yarrow Wormwoo
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Twenty-two New Mutations in Mitochondrial tRNA Genes in Patients with Alzheimers disease
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Effectiveness miR-93, miR-20a, miR-20b, RORC, STAT3, CD4+, SMAD6, SMAD7, MTO
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Factor 5 Leiden of genetic polymorphisms as Cardiovascular disease: Factor 5 Leiden genetic study of cardiovascular disease in young and middle-aged people of Tabriz in Iran
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Genomic analysis of one allele of a gene HER2 / NEU, ERBB1, BRCA1, BRC: New genetic mutations in breast cancer in women under 28 years Iran
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Genetic evaluation msx1 gene to induce ovulation disruption: Msx1 gene mutation in womens reproductive delay
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The role of satellite DNA in human colon cancer: DNA study in patients with colorectal cancer satellite city of Tabriz in Iran in 2016
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JAK2-V617F Mutation In Polycythemia Vera Of Iran: Evaluation of patients with myeloproliferative disorders Genetic mutation JAK2-V617F in polycythemia vera in the TABRIZ
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The God Gene of Adam and Eve: The God Gene of VMAT2 in Worship 2000 Humans Faith in Tabriz city Iran
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Genetic mutations in beta-thalassemia disease: Assessment of beta-globin gene mutations in patients with beta-thalassemia created in the chain, the population Tabriz
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The Role of HIV Genetic Pathway in Apoptosis: HIV physiological role in cell death and survival of cells in the human immune system
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EuGenics Gene: Clash of the Genes in choice Eugenics Gene
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The Molecular Clock of Human Embryonic Heart: Human Embryonic Heart Development by the four main Genes
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Genetic Mutations in juvenile Rheumatoid Arthritis: The presence of HLA-DRB1 alleles in children with juvenile rheumatoid arthritis in Tabriz city of IRAN by 2016
Zahra Gholizadeh, Shahin Asadi
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Gene Space: Genetic Mutations in Spinal Muscular Atrophy
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The Last Revelation: Assessment of EPM2A Gene Mutation Genetics in patients with Epilepsy seizure disorder
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Gene for Gene: Assessment of high frequency 35delG Mutation in GJB2-related deafness syndrome in a population without,Tabriz,city,IRAN
Zahra Gholizadeh, Shahin Asadi
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The Battle Genes for Survival: PGC-1a Gene RS2970847 Assess the Relationship between polymorphisms and susceptibility to type 2 diabetes
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The Genetics Damage: Assessment of Large deletions in Gene VLGR1 causes Ascher syndrome type IIC in male and female patients in Family TABRIZ
Zahra Gholizadeh, Mahsa Mir Sadat Jamali, Shahin Asadi
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The Last Of Us: Assessment of HEXA Gene Mutation induced Tay-Sachs disease of Tabriz Population in year 2016 IRAN
Mahsa Sadat Mir Jamali, Zahra Gholizadeh, Shahin Asadi
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The blood memory: Assessment of the chronic myeloproliferative disorders in patients with CML mutations Philadelphia chromosome BCR/ABL1
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The Dream Gene: Assessment of Genes Mutations HLA-DQB1,HLA-DR2,HLA-DR14, In patients with sleep disorders and insomnia Family
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Clash of the Genes: Assessment of Genetic Mutations in Genes DSM-IV, DRD4, SERT, HTR1B, SNAP25, GRIN2A, ADRA2A, TPH2, BDNF, induced ADHD
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The Shake Gene: Assessment of Genetic Mutations in Parkinsons disease (PD)
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The Love Gene: Genetic Evaluation Mutations in the Genes 5-HTTLPR and SLC6A4 and SCC6A4 in the Loyalty to Love or Betrayal of Love
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The Last Destiny: Assessment of Mutation Genetics in HTT (High Repetition-CAG), Gene for induced Huntingtons disease
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The Beyond Gene: Assessment of Genetics Mutation Gene HPRT1 in induce Lesch-Nyhan Disease
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The Migraine Gene: Assessment of Genetics Mutation NOTCH3 Gene in Patients with Migraine Disease
Elham Alizadeh Milani, Shahin Asadi
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The Amulet Gene: Assessment of Genetics Mutations in RNF213, ACTA2, GUCY1A3 Genes induction Moyamoya disease
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The Last Gene: Assessment of Genetics Mutations,PEX1,PEX2, PEX3,PEX5,PEX6,PEX10,PEX12,PEX13,PEX14,PEX16, PEX19,PEX26 Zellweger syndrome
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