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Curative Cell and Gene Therapy for Osteogenesis Imperfecta - Schindeler - 2022 - Journal of Bone and Mineral Research - Wiley Online Library
Curative Cell and Gene Therapy for Osteogenesis Imperfecta - Schindeler - 2022 - Journal of Bone and Mineral Research - Wiley Online Library

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

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
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

DMP1 and IFITM5 Regulate Osteogenic Differentiation of MC3T3-E1 on PEO-Treated Ti-6Al-4V-Ca2+/Pi surface | ACS Biomaterials Science & Engineering
DMP1 and IFITM5 Regulate Osteogenic Differentiation of MC3T3-E1 on PEO-Treated Ti-6Al-4V-Ca2+/Pi surface | ACS Biomaterials Science & Engineering

IFITM5 mutations and osteogenesis imperfecta | SpringerLink
IFITM5 mutations and osteogenesis imperfecta | SpringerLink

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

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

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

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

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

Clinical utility gene card for: osteogenesis imperfecta | European Journal of Human Genetics
Clinical utility gene card for: osteogenesis imperfecta | European Journal of Human Genetics

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

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 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

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

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

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

Sanger sequencing showing c.–14C>T mutation in the IFITM5 gene. | Download Scientific Diagram
Sanger sequencing showing c.–14C>T mutation in the IFITM5 gene. | 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

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