FKBP

FKBP

FKBP

Connective tissue alterations in Fkbp10 −/− mice

Electrostatic effects on the folding stability of FKBP12

Cytosolic HSP90 Cochaperones HOP and FKBP Interact with Freshly Synthesized Chloroplast Preproteins of Arabidopsis

Long-range activation of FKBP51 transcription by the androgen receptor via distal intronic enhancers

Schizophrenia in the Spectrum of Gene–Stress Interactions: The FKBP5 Example

DNA sequence variants of the FKBP5 gene are associated with unipolar depression

The RET51/FKBP52 complex and its involvement in Parkinson disease

HSP47 and FKBP65 cooperate in the synthesis of type I procollagen

Interaction of presenilins with FKBP38 promotes apoptosis by reducing mitochondrial Bcl-2

Relationship between the Subcellular Localization and Structures of Catalytic Domains of FKBP-Type PPIases

An evaluation tool for FKBP12-dependent and -independent mTOR inhibitors using a combination of FKBP-mTOR fusion protein, DSC and NMR

Mutations in the chromosome pairing gene FKBP6 are not a common cause of non-obstructive azoospermia

Altered interaction of FKBP12.6 with ryanodine receptor as a cause of abnormal Ca2+ release in heart failure

The inotropic adaptation during late preconditioning against myocardial stunning is associated with an increase in FKBP12.6

Inhibition of SR Ca2+ uptake: A novel action of the RyR2–FKBP12.6 antagonist K201

A mechanism of ryanodine receptor modulation by FKBP12/12.6, protein kinase A, and K201

Mutations in FKBP10, which result in Bruck syndrome and recessive forms of osteogenesis imperfecta, inhibit the hydroxylation of telopeptide lysines in bone collagen