Search
Search Results
-
Lung perfusion scintigraphy to detect chronic lung allograft dysfunction after living-donor lobar lung transplantation
Because chronic lung allograft dysfunction (CLAD) develops predominantly on one side after bilateral living-donor lobar lung transplantation (LDLLT),...
-
Donor-derived cell-free DNA is associated with acute rejection and decreased oxygenation in primary graft dysfunction after living donor-lobar lung transplantation
Donor-derived cell-free DNA (dd-cf-DNA) has been shown to be an informative biomarker of rejection after lung transplantation (LT) from deceased...
-
Identification of genetic loci associated with renal dysfunction after lung transplantation using an ethnic-specific single-nucleotide polymorphism array
Renal dysfunction is a long-term complication associated with an increased mortality after lung transplantation (LT). We investigated the association...
-
Tau protein binds to the P53 E3 ubiquitin ligase MDM2
Tau gene mutations cause a progressive dementia and neurotoxic Tau forms deposited in neurofibrillary tangles are hallmarks of neurodegenerative...
-
Local and systemic responses to SARS-CoV-2 infection in children and adults
It is not fully understood why COVID-19 is typically milder in children
1 –3 . Here, to examine the differences between children and adults in their... -
Regeneration of severely damaged lungs using an interventional cross-circulation platform
The number of available donor organs limits lung transplantation, the only lifesaving therapy for the increasing population of patients with...
-
Pulmonary rehabilitation improves survival in patients with idiopathic pulmonary fibrosis undergoing lung transplantation
This study was conducted to evaluate whether a pulmonary rehabilitation program (PRP) is independently associated with survival in patients with...
-
Mutant Huntingtin stalls ribosomes and represses protein synthesis in a cellular model of Huntington disease
The polyglutamine expansion of huntingtin (mHTT) causes Huntington disease (HD) and neurodegeneration, but the mechanisms remain unclear. Here, we...
-
Novel GRN Mutations in Patients with Corticobasal Syndrome
Loss-of-function GRN mutations lead to GRN haploinsufficiency and consequently neurodegeneration with significant heterogeneity in clinical...
-