Search Results - "A. Bolkov, Mikhail"

Health-related quality of life in patients with inborn errors of immunity: a bibliometric analysis by Xiao, Ningkun, Huang, Xinlin, Zang, Wanli, Kiselev, Sergey, Bolkov, Mikhail A, Tuzankina, Irina A, Chereshnev, Valery A

“…Inborn Errors of Immunity (IEI) are characterized by a heightened susceptibility to infections, allergies, and various other health complications…”
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A co-expression network for differentially expressed genes in bladder cancer and a risk score model for predicting survival by Chen, Zihao, Liu, Guojun, Hossain, Aslam, Danilova, Irina G, Bolkov, Mikhail A, Liu, Guoqing, Tuzankina, Irina A, Tan, Wanlong

“…Urothelial bladder cancer (BLCA) is one of the most common internal malignancies worldwide with poor prognosis. This study aims to explore effective prognostic…”
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Identification of miR-200c and miR141-Mediated lncRNA-mRNA Crosstalks in Muscle-Invasive Bladder Cancer Subtypes by Liu, Guojun, Chen, Zihao, Danilova, Irina G, Bolkov, Mikhail A, Tuzankina, Irina A, Liu, Guoqing

“…Basal and luminal subtypes of muscle-invasive bladder cancer (MIBC) have distinct molecular profiles and heterogeneous clinical behaviors. The interactions…”
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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 by Shinwari, Khyber, Bolkov, Mikhail A., Yasir Akbar, Muhammad, Guojun, Liu, Deryabina, Svetlana S., Tuzankina, Irina A., Chereshnev, Valery. A.

“…Single-nucleotide polymorphisms in the ELANE (Elastase, Neutrophil Expressed) gene are associated with severe congenital neutropenia, while the ELANE gene…”
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Defining muscle-invasive bladder cancer immunotypes by introducing tumor mutation burden, CD8+ T cells, and molecular subtypes by Chen, Zihao, Liu, Guojun, Liu, Guoqing, Bolkov, Mikhail A, Shinwari, Khyber, Tuzankina, Irina A, Chereshnev, Valery A, Wang, Zhifeng

“…Immunotherapy, especially anti-PD-1, is becoming a pillar of modern muscle-invasive bladder cancer (MIBC) treatment. However, the objective response rates…”
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Predicting the Most Deleterious Missense Nonsynonymous Single-Nucleotide Polymorphisms of Hennekam Syndrome-Causing CCBE1 Gene, In Silico Analysis by Shinwari, Khyber, Guojun, Liu, Deryabina, Svetlana S., Bolkov, Mikhail A., Tuzankina, Irina A., Chereshnev, Valery A.

“…Hennekam lymphangiectasia-lymphedema syndrome has been linked to single-nucleotide polymorphisms in the CCBE1 (collagen and calcium-binding EGF domains 1)…”
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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 by Shinwari, Khyber, Rehman, Hafiz Muzzammel, Liu, Guojun, Bolkov, Mikhail A, Tuzankina, Irina A, Chereshnev, Valery A

“…T Cell Immune Regulator 1, ATPase H + Transporting V0 Subunit A3 (TCIRG1 gene provides instructions for making one part, the a3 subunit, of a large protein…”
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Effectiveness of animal-assisted activities and therapies for autism spectrum disorder: a systematic review and meta-analysis by Xiao, Ningkun, Bagayi, Vaishnavi, Yang, Dandan, Huang, Xinlin, Zhong, Lei, Kiselev, Sergey, Bolkov, Mikhail A, Tuzankina, Irina A, Chereshnev, Valery A

“…Given the rising interest in complementary therapeutic strategies for autism spectrum disorder (ASD), this research aims to provide a comprehensive analysis of…”
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Identification of The Immune Subtype Among Muscle-invasive Bladder Cancer Patients by Multiple Datasets by Shinwari, Khyber, Chen, Zihao, Liu, Guojun, Chen, Lu, Bolkov, Mikhail A, Tuzankina, Irina A, Chereshnev, Valery A

“…Immunotherapies including PD-1/PD-L1 antibodies have been approved for the treatment of Muscle-invasive Bladder Cancer (MIBC) patients. However,…”
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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? by Shinwari, Khyber, Liu, Guojun, A. Bolkov, Mikhail, Ahmad, Izaz, Daud, Muhmmad, A. Tuzankina, Irina, ., Valery. A. Chereshnev

“…This article is a Letter to the Editor and does not include an Abstract…”
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Health-related quality of life in patients with inborn errors of immunity: A systematic review and meta-analysis by Xiao, Ningkun, Huang, Xinlin, Yang, Dandan, Zang, Wanli, Kiselev, Sergey, Bolkov, Mikhail A., Shinwari, Khyber, Tuzankina, Irina, Chereshnev, Valery

“…Inborn Errors of Immunity (IEI) significantly affect patients' health-related quality of life (HRQOL), presenting greater challenges than those faced by the…”
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Novel high-risk missense mutations identification in FAT4 gene causing Hennekam syndrome and Van Maldergem syndrome 2 through molecular dynamics simulation by Shinwari, Khyber, Rehman, Hafiz Muzzammel, Xiao, Ningkun, Guojun, Liu, Khan, Muhammad Ajmal, Bolkov, Mikhail A., Tuzankina, Irina A., Chereshnev, Valery A.

“…Hennekam syndrome (HS) is an autosomal recessive disease in the pathogenesis of which lymphangiectasia and lymphedema plays a key role. HS is associated with…”
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Identifying Main Genes and Pathways by Using Gene Expression Profiling in Primary Immunodeficiency HOIL-1/RBCK1 Disorder Patients by Shinwari, Khyber, Liu, Guojun, Bolkov, Mikhail, Ullah, Monib, Tuzankina, Irina

“…HOIL-1/RBCK1 deficiency is a new autosomal receiving disorder with dysfunctional cellular responses to pro-inflammatory cytokines, leading to…”
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Identification of Key Genes and Pathways in RBCK1 Deficient patients by Gene Expression Profiling by Khyber Shinwari, Mikhail A. Bolkov, Irina A. Tuzankina, Valery A. Chereshnev

“…HOIL-1/RBCK1 deficiency is a new autosomal receive disorder with unstable cellular responses to pro-inflammatory cytokines, resulting in auto-inflammation,…”
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Neonatal Screening for Severe Combined Immune Deficiency in Russia: Glorious Future or Tomorrow’s Reality? by Deryabina, S. S., Tuzankina, I. A., Vlasova, E. V., Bolkov, M. A., Shershnev, V. N.

“…Mass screening of newborns in Russia for five hereditary diseases does not meet the requirements of the world community for the neonatal screening program…”
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