Autosomal Recessive Polycystic Kidney Disease Latest Advances

The fibrocystin C-terminal domain inhibits Src/STAT3 signal induced cystogenesis of kidney epithelial cells.

Journal: American journal of physiology. Cell physiology

Published: August 28, 2026

Structural and diagnostic implications of exonic splice-disrupting variants in PKHD1-related Caroli disease.

Journal: Gene

Published: August 11, 2026

Variants and variability - a cohort of Omani children sheds more light on autosomal recessive polycystic kidney disease.

Journal: Pediatric nephrology (Berlin, Germany)

Published: June 09, 2026

Enhancer collapse dictates PKHD1 silencing and centrosome-mediated chromosomal instability and metastasis in clear cell renal cell carcinoma.

Journal: Experimental cell research

Published: May 21, 2026

Modeling Complex Developmental Disease: The Case of Polycystic Kidney Disease.

Journal: Journal of developmental biology

Published: May 15, 2026

A novel PKHD1 missense variant disrupting splicing in a fetus with Caroli disease.

Journal: Gene

Published: April 27, 2026

Combined Liver-Kidney Transplantation in Pediatric Patients From Colombia: A Case Series.

Journal: Pediatric transplantation

Published: April 13, 2026

Advanced MRI methods for children and young adults with autosomal recessive polycystic kidney disease (ARPKD) to support future multi-center clinical trials.

Journal: Pediatric radiology

Published: March 31, 2026

Studies of mice with a large deletion of the ARPKD-associated Pkhd1 locus likely explain its GWAS association with glaucoma in humans.

Journal: bioRxiv : the preprint server for biology

Published: February 27, 2026

Scoping Review on Polycystic Liver Disease in PKD1/PKD2 Gene Carriers: Genetic Aspects, Pathophysiology, and Therapeutic Approaches.

Journal: Journal of clinical and experimental hepatology

Published: February 07, 2026

Identification of Pathogenic PKHD1 Variants in Infants with Autosomal Recessive Polycystic Kidney Disease from the Dhofar Region, Oman.

Journal: F1000Research

Published: February 02, 2026

Comparison of genetic profile and kidney outcomes between very early-onset and non-very-early-onset autosomal dominant polycystic kidney disease in children: a systematic review and meta-analysis.

Journal: BMC nephrology

Published: January 19, 2026

Autosomal Recessive Polycystic Kidney Disease Latest Advances

Find the Latest Research About Autosomal Recessive Polycystic Kidney Disease

The fibrocystin C-terminal domain inhibits Src/STAT3 signal induced cystogenesis of kidney epithelial cells.

The fibrocystin C-terminal domain inhibits Src/STAT3 signal induced cystogenesis of kidney epithelial cells.

Structural and diagnostic implications of exonic splice-disrupting variants in PKHD1-related Caroli disease.

Structural and diagnostic implications of exonic splice-disrupting variants in PKHD1-related Caroli disease.

Variants and variability - a cohort of Omani children sheds more light on autosomal recessive polycystic kidney disease.

Variants and variability - a cohort of Omani children sheds more light on autosomal recessive polycystic kidney disease.

Enhancer collapse dictates PKHD1 silencing and centrosome-mediated chromosomal instability and metastasis in clear cell renal cell carcinoma.

Enhancer collapse dictates PKHD1 silencing and centrosome-mediated chromosomal instability and metastasis in clear cell renal cell carcinoma.

Modeling Complex Developmental Disease: The Case of Polycystic Kidney Disease.

Modeling Complex Developmental Disease: The Case of Polycystic Kidney Disease.

A novel PKHD1 missense variant disrupting splicing in a fetus with Caroli disease.

A novel PKHD1 missense variant disrupting splicing in a fetus with Caroli disease.

Combined Liver-Kidney Transplantation in Pediatric Patients From Colombia: A Case Series.

Combined Liver-Kidney Transplantation in Pediatric Patients From Colombia: A Case Series.

Advanced MRI methods for children and young adults with autosomal recessive polycystic kidney disease (ARPKD) to support future multi-center clinical trials.

Advanced MRI methods for children and young adults with autosomal recessive polycystic kidney disease (ARPKD) to support future multi-center clinical trials.

Studies of mice with a large deletion of the ARPKD-associated Pkhd1 locus likely explain its GWAS association with glaucoma in humans.

Studies of mice with a large deletion of the ARPKD-associated Pkhd1 locus likely explain its GWAS association with glaucoma in humans.

Scoping Review on Polycystic Liver Disease in PKD1/PKD2 Gene Carriers: Genetic Aspects, Pathophysiology, and Therapeutic Approaches.

Scoping Review on Polycystic Liver Disease in PKD1/PKD2 Gene Carriers: Genetic Aspects, Pathophysiology, and Therapeutic Approaches.

Identification of Pathogenic PKHD1 Variants in Infants with Autosomal Recessive Polycystic Kidney Disease from the Dhofar Region, Oman.

Identification of Pathogenic PKHD1 Variants in Infants with Autosomal Recessive Polycystic Kidney Disease from the Dhofar Region, Oman.

Comparison of genetic profile and kidney outcomes between very early-onset and non-very-early-onset autosomal dominant polycystic kidney disease in children: a systematic review and meta-analysis.

Comparison of genetic profile and kidney outcomes between very early-onset and non-very-early-onset autosomal dominant polycystic kidney disease in children: a systematic review and meta-analysis.