Predicting the Most Deleterious Missense Nonsynonymous Single-Nucleotide Polymorphisms of Hennekam Syndrome-Causing CCBE1 Gene, In Silico Analysis

অনুরূপ উপাদানগুলি

• In-silico assessment of high-risk non-synonymous SNPs in ADAMTS3 gene associated with Hennekam syndrome and their impact on protein stability and function
  অনুযায়ী: Khyber Shinwari, অন্যান্য
  প্রকাশিত: (2023-06-01)
• Novel high-risk missense mutations identification in FAT4 gene causing Hennekam syndrome and Van Maldergem syndrome 2 through molecular dynamics simulation
  অনুযায়ী: Khyber Shinwari, অন্যান্য
  প্রকাশিত: (2023-01-01)
• 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
  অনুযায়ী: Khyber Shinwari, অন্যান্য
  প্রকাশিত: (2022-01-01)
• 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
  অনুযায়ী: Khyber Shinwari, অন্যান্য
  প্রকাশিত: (2022-04-01)
• Identification of Key Genes and Pathways in RBCK1 Deficient patients by Gene Expression Profiling
  অনুযায়ী: Khyber Shinwari, অন্যান্য
  প্রকাশিত: (2021-07-01)