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- Nephrin Preserves Podocyte Viability and Glomerular Structure and Function in Adult Kidneys
- TBC1D8B Mutations Implicate RAB11-Dependent Vesicular Trafficking in the Pathogenesis of Nephrotic Syndrome
- Notch Signaling, Wt1 and Foxc2 Are Key Regulators of the Podocyte Gene Regulatory Network in Xenopus Jeffrey T
- Nephrin, a Key Component of the Slit Diaphragm
- Tissue Expression of Nephrin in Human and Pig
- Nephrin Is Involved in Podocyte Maturation but Not Survival During Glomerular Development
- Kruppel-Like Factor 4 (Klf4) Is a Regulator Of
- CIN85: Implications for the Development of Proteinuria in Diabetic Nephropathy
- KIRREL3 Antibody Cat
- The Beneficial Effects of Allicin in Chronic Kidney Disease Are
- Focal Segmental Glomerulosclerosis: Molecular Genetics and Targeted Therapies Ying Maggie Chen1* and Helen Liapis2,3
- Kirrel3-Mediated Synapse Formation Is Attenuated by Disease-Associated Missense Variants
- Adhesion Molecule Kirrel3/Neph2 Is Required for the Elongated Shape Of
- Focal Segmental Glomerulosclerosis: Towards a Better Understanding for the Practicing Nephrologist
- The Role of Kirrel Family Members During Circuit Formation of the Accessory Olfactory System
- Nephrin Is Expressed on the Surface of Insulin Vesicles and Facilitates
- FSGS and Nephrotic Syndrome
- Congenital Nephrotic Syndrome (NPHS1): Features Resulting from Different Mutations in Finnish Patients
- Association Between NPHS1 and NPHS2 Gene Variants Nephrotic Syndrome in Children
- Cell Junction-Associated Proteins IQGAP1, MAGI-2, CASK, Spectrins, and -Actinin Are Components of the Nephrin Multiprotein Compl
- 629.Full-Text.Pdf
- Slit Diaphragms Contain Tight Junction Proteins
- NPHS1 Gene NPHS1, Nephrin
- Supplemental Material.Pdf
- Rat KIRREL3 / NEPH2 Protein (His Tag)
- The Number of Podocyte Slit Diaphragms Is Decreased in Minimal Change Nephrotic Syndrome
- Structural Basis of Highly Specific Interaction Between Nephrin And
- Primary Focal Segmental Glomerulosclerosis, an Important Component of Childhood Nephrotic Syndrome: Therapeutic Options and Genetic Basis James C.M
- NPHS2 Gene, Nephrotic Syndrome and Focal Segmental Glomerulosclerosis: a Huge Review Nora Franceschini, MD, MPH1, Kari E
- Nephrin – Mutations in Congenital Nephrotic Syndrome of the Finnish Type and Cell Lineage Specific Gene Regulation
- Podocyte-Associated Talin1 Is Critical for Glomerular Filtration Barrier Maintenance Xuefei Tian,1 Jin Ju Kim,2 Susan M
- Primary Structure of Mouse and Rat Nephrin Cdna and Structure and Expression of the Mouse Gene
- Nephrin-Associated Molecule in Human Glomerular Diseases
- Nephrin. Role in the Renal Ultrafilter and Involvement in Proteinuria