Genetic results in a family with a novel heterozygous IFITM5 missense... | Download Scientific Diagram
IFITM5 pathogenic variant causes osteogenesis imperfecta V with various phenotype severity in Ukrainian and Vietnamese patients | Human Genomics | Full Text
Ifitm5 MGI Mouse Gene Detail - MGI:1934923 - interferon induced transmembrane protein 5
Frontiers | IFITM Genes, Variants, and Their Roles in the Control and Pathogenesis of Viral Infections
IFITM5 Gene - GeneCards | IFM5 Protein | IFM5 Antibody
Role of S-Palmitoylation on IFITM5 for the Interaction with FKBP11 in Osteoblast Cells | PLOS ONE
Clinical utility gene card for: osteogenesis imperfecta | European Journal of Human Genetics
IFITM5 Gene - GeneCards | IFM5 Protein | IFM5 Antibody
Effects of the overexpression of IFITM5 and IFITM5 c.‑14C>T mutation on human osteosarcoma cells
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
Role of S-Palmitoylation on IFITM5 for the Interaction with FKBP11 in Osteoblast Cells | PLOS ONE
New genes in bone development: what's new in osteogenesis imperfecta. - Abstract - Europe PMC
IFITM5 siRNA (m), shRNA and Lentiviral Particle Gene Silencers | SCBT - Santa Cruz Biotechnology
IFITM5 Gene - GeneCards | IFM5 Protein | IFM5 Antibody
![PDF] Role of S-Palmitoylation on IFITM5 for the Interaction with FKBP11 in Osteoblast Cells | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/80e67644e16a38aefd253237cde870f533f4f1c1/11-Figure6-1.png "PDF] Role of S-Palmitoylation on IFITM5 for the Interaction with FKBP11 in Osteoblast Cells | Semantic Scholar")
PDF] Role of S-Palmitoylation on IFITM5 for the Interaction with FKBP11 in Osteoblast Cells | Semantic Scholar
IFITM5 pathogenic variant causes osteogenesis imperfecta V with various phenotype severity in Ukrainian and Vietnamese patients | Human Genomics | Full Text
Figure 2 from A mutation in the 5'-UTR of IFITM5 creates an in-frame start codon and causes autosomal-dominant osteogenesis imperfecta type V with hyperplastic callus. | Semantic Scholar
IFITM5 siRNA (m), shRNA and Lentiviral Particle Gene Silencers | SCBT - Santa Cruz Biotechnology
Osteogenesis Imperfecta Type V - ScienceDirect
IJMS | Free Full-Text | The Osteogenesis Imperfecta Type V Mutant BRIL/ IFITM5 Promotes Transcriptional Activation of MEF2, NFATc, and NR4A in Osteoblasts
