حذف

حذف

تاریخ | ارائه دهنده | مقطع | دوره | مقاله | |
---|---|---|---|---|---|
1 | 26/11/95 | خانم زهرا گلچهره | PhD | 14 | Resolution of Disease Phenotypes Resulting from Multilocus Genomic Variation |
2 | 10/12/95 | خانم طاهره نظری | PhD | 12 | Whole exome sequencing in recurrent early pregnancy loss |
3 | 12/2/96 | آقای دکتر مجید حسین زاده | PhD | 12 | Clinical Performance of an Ultrahigh Resolution Chromosomal Microarray Optimized for Neurodevelopmental Disorders |
4 | 26/2/96 | خانم پریسا آب | PhD | 14 | Mapping autosomal recessive intellectual disability: combined microarray and exome sequencing identifies 26 novel candidate genes in 192 consanguineous families |
5 | 9/3/96 | خانم زینب ایمانی صابر | PhD | 14 | Improving genetic diagnosis in Mendelian disease with transcriptome sequencing |
6 | 30/3/96 | خانم مريم پيرهوشياران | PhD | 13 | CRISPR-Cpf1 correction of muscular dystrophy mutations in human cardiomyocytes and mice |
7 | 13/4/96 | خانم شمسي صفري | PhD | 13 | Detection of Imprinted Genes by Single-Cell Allele-Specific Gene Expression |
8 | 27/4/96 | آقاي حمزه سلماني | PhD | 13 | Circulating Tumor DNA Mutation Profiling by Targeted Next Generation Sequencing Provides Guidance for Personalized Treatments in Multiple Cancer Types |
9 | 1/6/96 | خانم زهرا رضایی | PhD | 12 | comprehensive genetic testing in the clinical evaluation of 1119 patients with hearing loss |
10 | 14/6/96 | خانم فاطمه عرب | PhD | 11 | A method to convert mRNA into a gRNA library for CRISPR/Cas9 editing of any organism |
11 | 28/6/96 | آقاي رسول عبداله زاده | PhD | 14 | Development, Applications, Benefits, Challenges and Limitations of the New Genome Engineering Technique. An Update Study |
12 | 11/7/96 | خانم نسرین سهرابی | PhD | 14 | Preimplantation genetic diagnosis of hemophilia A |
13 | 25/7/96 | خانم نگین صفارزاده | PhD | 14 | Unexpected role of interferon-γ in regulating neuronal connectivity and social behaviou |
14 | 9/8/96 | آقای حسین پاشایی | PhD | 14 | Genomic Classification and Prognosis in Acute Myeloid Leukemia |
15 | 23/8/96 | خانم يگانه اسحاق خاني | PhD | 12 | Mutations in DZIP1L, which encodes a ciliary-transitionzone protein, cause autosomal recessive polycystic kidney disease |
16 | 14/9/96 | خانم الهه ولي پور | PhD | Biallelic mutations in the 3′ exonuclease TOE1 cause pontocerebellar hypoplasia and uncover a role in snRNA processing | |
17 | 28/9/96 | خانم مريم اقبالي | PhD | 12 | Removing The Maximum Assigned Value of the Genotype Quality Score Allows Specific Detection Of De Novo Mutations In Next generation Sequencing Data |
18 | 12/10/96 | خانم فاطمه وند رجب پور | PhD | 12 | Phase I trials using Sleeping Beauty to generate CD19-specific CAR T cells |
19 | 26/10/96 | آقاي محمدرضا احمدی فرد | PhD | 12 | Endogenous Reprogramming of Alpha Cells into Beta Cells, Induced by Viral Gene Therapy, Reverses Autoimmune Diabetes |
20 | 10/11/96 | آقاي اسعد آذرنژاد | PhD | 10 | In vivo CRISPR screening identifies Ptpn2 as a cancer immunotherapy target |
21 | 24/11/96 | خانم سپیده شاه کرمی | PhD | 10 | Predictive value of minimal residual disease in Philadelphia-chromosome-positive acute lymphoblastic leukemia treated with imatinib in the European intergroup study of post-induction treatment of Philadelphia-chromosome-positive acute lymphoblastic leukemia, based on immunoglobulin/T-cell receptor and BCR/ABL1 methodologies |
22 | 15/12/96 | خانم فاطمه علیزاده | PhD | 10 | CGG repeat length and AGG interruptions as indicators of fragile X–associated diminished ovarian reserve |