Browsing by Author Shinwari, K.
Showing results 1 to 9 of 9
| Issue Date | Title | Author(s) |
| 2022 | Additional Pathogenic Pathways in RBCK1 Deficiency | Demicheva, E. I.; Shinwari, K.; Ushenin, K. S.; Bolkov, M. A. |
| 2022 | Analysis of the TREC and KREC Levels in the Dried Blood Spots of Healthy Newborns with Different Gestational Ages and Weights | Cheremokhin, D. A.; Shinwari, K.; Deryabina, S. S.; Bolkov, M. A.; Tuzankina, I. A.; Kudlay, D. A. |
| 2020 | Bioinformatics and biotechnology – two sides of the same analysis | Shinwari, K. |
| 2021 | Defining muscle-invasive bladder cancer immunotypes by introducing tumor mutation burden, CD8+ T cells, and molecular subtypes | Chen, Z.; Liu, G.; Liu, G.; Bolkov, M. A.; Shinwari, K.; Tuzankina, I. A.; Chereshnev, V. A.; Wang, Z. |
| 2021 | Identifying Main Genes and Pathways by Using Gene Expression Profiling in Primary Immunodeficiency HOIL-1/RBCK1 Disorder Patients | Shinwari, K.; Liu, G.; Bolkov, M.; Ullah, M.; Tuzankina, I. |
| 2022 | In Silico Analysis Revealed Five Novel High-Risk Single-Nucleotide Polymorphisms (rs200384291, rs201163886, rs193141883, rs201139487, and rs201723157) in ELANE Gene Causing Autosomal Dominant Severe Congenital Neutropenia 1 and Cyclic Hematopoiesis | Shinwari, K.; Bolkov, M. A.; Yasir Akbar, M.; Guojun, L.; Deryabina, S. S.; Tuzankina, I. A.; Chereshnev, V. A. |
| 2020 | Is up-regulation gene expression of the certain genes during the viral respiratory tract infection would have any influence in pathogenesis of the SAR-CoV-2 infection? | Shinwari, K.; Liu, G.; Bolkov, M. A.; Ahmad, I.; Daud, M.; Tuzankina, I. A.; Chereshnev, V. A. |
| 2022 | Novel Disease-Associated Missense Single-Nucleotide Polymorphisms Variants Predication by Algorithms Tools and Molecular Dynamics Simulation of Human TCIRG1 Gene Causing Congenital Neutropenia and Osteopetrosis | Shinwari, K.; Rehman, H. M.; Liu, G.; Bolkov, M. A.; Tuzankina, I. A.; Chereshnev, V. A. |
| 2021 | Predicting the Most Deleterious Missense Nonsynonymous Single-Nucleotide Polymorphisms of Hennekam Syndrome-Causing CCBE1 Gene, in Silico Analysis | Shinwari, K.; Guojun, L.; Deryabina, S. S.; Bolkov, M. A.; Tuzankina, I. A.; Chereshnev, V. A. |
