Supplementary file including original confocal images, CellProfiler pipeline used to analyze them and output with segmented images used for measuring tubes and cells. Additional information can be found in the corresponding manuscript: Supplementary analysis of snRNAseq data in the manuscript: Novel ARPKD mouse model with near complete deletion of Polycystic Kidney and Hepatic Disease 1 (Pkhd1) genomic locus has multiple phenotypes but no renal cysts Authors: Yu Ishimoto1,5, Luis F Menezes1,5,6, Fang Zhou1, Teruhiko Yoshida1, Taishi Komori2, Jiahe Qiu1, Marian F Young2, Huiyan Lu3, Svetlana Potapova3, Patricia Outeda4, Terry Watnick4, Gregory G Germino1, 6. Affiliations: 1 Kidney Disease Branch; National Institute of Diabetes and Digesti...
Manuscript title: Mice with a Pax2 missense variant display impaired glomerular repairAuthors: Joann...
Manuscript title: Mice with a Pax2 missense variant display impaired glomerular repairAuthors: Joann...
Manuscript title: Mice with a Pax2 missense variant display impaired glomerular repairAuthors: Joann...
Supplementary analysis of snRNAseq data in the manuscript: Novel ARPKD mouse model with near c...
Cellranger output from the folder filtered_feature_bc_matrix for each sample in the following manusc...
Supplementary material for the manuscript: Novel ARPKD mouse model with near complete deletion o...
Additional file 1: Figure S1. Mural cells heterogeneity and responses to PS-MPs plus HFD Treatment. ...
Background: Nephronophthisis (NPH) is the most common genetic cause of end-stage renal disease (ESRD...
The entire thesis text is included in the research.pdf file; the official abstract appears in the sh...
Background: Nephronophthisis (NPH) is the most common genetic cause of end-stage renal disease (ESRD...
Background: Nephronophthisis (NPH) is the most common genetic cause of end-stage renal disease (ESRD...
Background: Nephronophthisis (NPH) is the most common genetic cause of end-stage renal disease (ESRD...
Data repository for the manuscript: Kuppe, Ibrahim et al. "Decoding myofibroblast origins in human k...
Background: Nephronophthisis (NPH) is the most common genetic cause of end-stage renal disease (ESRD...
Kidney Precision Medicine Project (KPMP) is building a spatially specified human kidney tissue atlas...
Manuscript title: Mice with a Pax2 missense variant display impaired glomerular repairAuthors: Joann...
Manuscript title: Mice with a Pax2 missense variant display impaired glomerular repairAuthors: Joann...
Manuscript title: Mice with a Pax2 missense variant display impaired glomerular repairAuthors: Joann...
Supplementary analysis of snRNAseq data in the manuscript: Novel ARPKD mouse model with near c...
Cellranger output from the folder filtered_feature_bc_matrix for each sample in the following manusc...
Supplementary material for the manuscript: Novel ARPKD mouse model with near complete deletion o...
Additional file 1: Figure S1. Mural cells heterogeneity and responses to PS-MPs plus HFD Treatment. ...
Background: Nephronophthisis (NPH) is the most common genetic cause of end-stage renal disease (ESRD...
The entire thesis text is included in the research.pdf file; the official abstract appears in the sh...
Background: Nephronophthisis (NPH) is the most common genetic cause of end-stage renal disease (ESRD...
Background: Nephronophthisis (NPH) is the most common genetic cause of end-stage renal disease (ESRD...
Background: Nephronophthisis (NPH) is the most common genetic cause of end-stage renal disease (ESRD...
Data repository for the manuscript: Kuppe, Ibrahim et al. "Decoding myofibroblast origins in human k...
Background: Nephronophthisis (NPH) is the most common genetic cause of end-stage renal disease (ESRD...
Kidney Precision Medicine Project (KPMP) is building a spatially specified human kidney tissue atlas...
Manuscript title: Mice with a Pax2 missense variant display impaired glomerular repairAuthors: Joann...
Manuscript title: Mice with a Pax2 missense variant display impaired glomerular repairAuthors: Joann...
Manuscript title: Mice with a Pax2 missense variant display impaired glomerular repairAuthors: Joann...