Oliver Semler

Human Genome Sequencing in Health and Disease

Bone Morphogenetic Protein (BMP) signaling in development and human diseases

The Ensembl Variant Effect Predictor

Wnt/β-catenin signalling: function, biological mechanisms, and therapeutic opportunities

The promise and challenge of therapeutic genome editing

Fracture healing: mechanisms and interventions

Osteoporosis

WNT1 Mutations in Families Affected by Moderately Severe and Progressive Recessive Osteogenesis Imperfecta

Wnt signaling in cancer

The role of magnesium ions in bone regeneration involves the canonical Wnt signaling pathway

Antiviral resistance of stem cells

WNT signaling in bone homeostasis and disease: from human mutations to treatments

Identification of a mutation causing deficient BMP1/mTLD proteolytic activity in autosomal recessive osteogenesis imperfecta

IFITMs Restrict the Replication of Multiple Pathogenic Viruses

Intrinsic Immunity Shapes Viral Resistance of Stem Cells

A Comprehensive Overview of Skeletal Phenotypes Associated with Alterations in Wnt/β-catenin Signaling in Humans and Mice

The AAV-mediated and RNA-guided CRISPR/Cas9 system for gene therapy of DMD and BMD

IFITM3 directly engages and shuttles incoming virus particles to lysosomes

Wnt/β-Catenin Signaling, Disease, and Emerging Therapeutic Modalities

Guidelines for the Treatment of Hypothyroidism: Prepared by the American Thyroid Association Task Force on Thyroid Hormone Replacement

MECHANISMS IN ENDOCRINOLOGY: Genetics of human bone formation

IFITM-Family Proteins: The Cell's First Line of Antiviral Defense

New Genes in Bone Development: What's New in Osteogenesis Imperfecta

Genetics of Osteoporosis

Regulation of the Trafficking and Antiviral Activity of IFITM3 by Post-Translational Modifications

Novel mutations affecting LRP5 splicing in patients with osteoporosis-pseudoglioma syndrome (OPPG)

Whole-body vibration training in children with Duchenne muscular dystrophy and spinal muscular atrophy

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

Exome Sequencing Identifies Truncating Mutations in Human SERPINF1 in Autosomal-Recessive Osteogenesis Imperfecta