friptură Comportament Biserica ifitm5 gene mentalitatea Excavare De Nord
Frontiers | IFITM Genes, Variants, and Their Roles in the Control and Pathogenesis of Viral Infections
IJMS | Free Full-Text | The Osteogenesis Imperfecta Type V Mutant BRIL/ IFITM5 Promotes Transcriptional Activation of MEF2, NFATc, and NR4A in Osteoblasts
IFITM5 pathogenic variant causes osteogenesis imperfecta V with various phenotype severity in Ukrainian and Vietnamese patients | Human Genomics | Full Text
IFITM5 Gene - GeneCards | IFM5 Protein | IFM5 Antibody
A Single Recurrent Mutation in the 5′-UTR of IFITM5 Causes Osteogenesis Imperfecta Type V - ScienceDirect
IFITM5 pathogenic variant causes osteogenesis imperfecta V with various phenotype severity in Ukrainian and Vietnamese patients | Human Genomics | Full Text
Bayesian tree of the vertebrate IFITM gene family.
IFITM5 Gene - GeneCards | IFM5 Protein | IFM5 Antibody
Role of S-Palmitoylation on IFITM5 for the Interaction with FKBP11 in Osteoblast Cells | PLOS ONE
Alterations of bone material properties in growing Ifitm5/ BRIL p.S42 knock-in mice, a new model for atypical type VI osteogenes
IFITM5 Gene - GeneCards | IFM5 Protein | IFM5 Antibody
IFITM5 Gene - GeneCards | IFM5 Protein | IFM5 Antibody
Localization of ifitm genes in different species (13). Human IFITM1,... | Download Scientific Diagram
IFITM5 pathogenic variant causes osteogenesis imperfecta V with various phenotype severity in Ukrainian and Vietnamese patients | Human Genomics | Full Text
Effect of immunosuppressants on a mouse model of osteogenesis imperfecta type V harboring a heterozygous Ifitm5 c.-14C > T mutation | Scientific Reports
IJMS | Free Full-Text | The Osteogenesis Imperfecta Type V Mutant BRIL/ IFITM5 Promotes Transcriptional Activation of MEF2, NFATc, and NR4A in Osteoblasts
A novel variant of the IFITM5 gene within the 5′‐UTR causes neonatal transverse clavicular fracture: Expanding the genetic spectrum - Wu - 2020 - Molecular Genetics & Genomic Medicine - Wiley Online Library
IFITM5 mutations and osteogenesis imperfecta | SpringerLink