IFITM5 Gene - GeneCards | IFM5 Protein | IFM5 Antibody
Role of S-Palmitoylation on IFITM5 for the Interaction with FKBP11 in Osteoblast Cells | PLOS ONE
![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
DMP1 and IFITM5 Regulate Osteogenic Differentiation of MC3T3-E1 on PEO-Treated Ti-6Al-4V-Ca2+/Pi surface | ACS Biomaterials Science & Engineering
Role of S-Palmitoylation on IFITM5 for the Interaction with FKBP11 in Osteoblast Cells | PLOS ONE
The IFITM5 mutation c.-14C > T results in an elongated transcript expressed in human bone; and causes varying phenotypic severity of osteogenesis imperfecta type V – topic of research paper in Biological
Ifitm5 MGI Mouse Gene Detail - MGI:1934923 - interferon induced transmembrane protein 5
IFITM5 Gene - GeneCards | IFM5 Protein | IFM5 Antibody
Clinical utility gene card for: osteogenesis imperfecta | European Journal of Human Genetics
Genetic results in a family with a novel heterozygous IFITM5 missense... | Download Scientific Diagram
Frontiers | Functional Involvement of Interferon-Inducible Transmembrane Proteins in Antiviral Immunity
IFITM5 mutations and osteogenesis imperfecta | SpringerLink
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
IJMS | Free Full-Text | The Osteogenesis Imperfecta Type V Mutant BRIL/ IFITM5 Promotes Transcriptional Activation of MEF2, NFATc, and NR4A in Osteoblasts
IFITM5 Gene - GeneCards | IFM5 Protein | IFM5 Antibody
IFITM5 siRNA (m), shRNA and Lentiviral Particle Gene Silencers | SCBT - Santa Cruz Biotechnology
IFITM5 siRNA (m), shRNA and Lentiviral Particle Gene Silencers | SCBT - Santa Cruz Biotechnology
IFITM5 Gene - GeneCards | IFM5 Protein | IFM5 Antibody
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
Biochemical analyses for the S-palmitoylation on IFITM5. A) Molecular... | Download Scientific Diagram
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
Effects of the overexpression of IFITM5 and IFITM5 c.‑14C>T mutation on human osteosarcoma cells
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
