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Frontiers | IFITM Genes, Variants, and Their Roles in the Control and  Pathogenesis of Viral Infections
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
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 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
IFITM5 Gene - GeneCards | IFM5 Protein | IFM5 Antibody

A Single Recurrent Mutation in the 5′-UTR of IFITM5 Causes Osteogenesis  Imperfecta Type V - ScienceDirect
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
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.
Bayesian tree of the vertebrate IFITM gene family.

IFITM5 Gene - GeneCards | IFM5 Protein | IFM5 Antibody
IFITM5 Gene - GeneCards | IFM5 Protein | IFM5 Antibody

Role of S-Palmitoylation on IFITM5 for the Interaction with FKBP11 in  Osteoblast Cells | PLOS ONE
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
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

IFITM5 Gene - GeneCards | IFM5 Protein | IFM5 Antibody
IFITM5 Gene - GeneCards | IFM5 Protein | IFM5 Antibody

Ifitm5 MGI Mouse Gene Detail - MGI:1934923 - interferon induced  transmembrane protein 5
Ifitm5 MGI Mouse Gene Detail - MGI:1934923 - interferon induced transmembrane protein 5

Osteogenesis Imperfecta Type V - ScienceDirect
Osteogenesis Imperfecta Type V - ScienceDirect

Localization of ifitm genes in different species (13). Human IFITM1,... |  Download Scientific Diagram
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
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
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
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
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
IFITM5 mutations and osteogenesis imperfecta | SpringerLink