Hans J. Baelde - Publications

Clinicopathological and Molecular Characteristics of Plasma Cell-Rich Rejection in Renal Transplant Biopsies.

Journal: Transplantation

Published: July 30, 2026

A study on the distribution of BK and JC polyomavirus in discarded donor kidneys.

Journal: Frontiers in transplantation

Published: October 17, 2025

Rapid liquid biopsy assessment through gene profiling from the kidney biopsy transport medium: A technical validation and a proof-of-concept pilot study.

Journal: American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons

Published: September 24, 2025

Author Correction: Identification of stable housekeeping genes for induced pluripotent stem cells and -derived endothelial cells for drug testing.

Journal: Scientific reports

Published: June 16, 2025

Cell Type-Specific Expression of Long Noncoding RNAs in Human Diabetic Kidneys Identifies TARID as a Key Regulator of Podocyte Function.

Journal: Diabetes

Published: March 20, 2025

The VEGF decoy receptor soluble Fms-like tyrosine kinase 1 binds to macrophages.

Journal: Angiogenesis

Published: January 09, 2025

Spatial Transcriptomics Reveals Injured Cells, Signature Genes, and Communication Patterns in the Cyst Microenvironment of Polycystic Kidney Disease.

Journal: Journal of the American Society of Nephrology : JASN

Published: October 24, 2024

Identification of transcription factors that regulate placental sFLT1 expression.

Journal: Molecular human reproduction

Published: July 23, 2024

Recurrent CLTC::SYK fusions and CSF1R mutations in juvenile xanthogranuloma of soft tissue.

Journal: Blood

Published: May 14, 2024

Near-infrared microscopy reveals diabetic nephropathy in ob/ob mice.

Journal: Talanta

Published: May 06, 2024

Antisense oligonucleotide-mediated terminal intron retention of endoglin: A potential strategy to inhibit renal interstitial fibrosis.

Journal: Biochimica et biophysica acta. Molecular basis of disease

Published: January 04, 2024

Bi-allelic NIT1 variants cause a brain small vessel disease characterized by movement disorders, massively dilated perivascular spaces, and intracerebral hemorrhage.

Journal: Genetics in medicine : official journal of the American College of Medical Genetics

Published: October 18, 2023