| scholarly article | Q13442814 |
| P50 | author | Zeyang Ji | Q58888935 |
| Yuan Shang | Q82428027 | ||
| P2093 | author name string | Fei Ye | |
| Lin Lin | |||
| Rongguang Zhang | |||
| Jinwei Zhu | |||
| Zhuangfeng Weng | |||
| P2860 | cites work | A role for the PDZ-binding domain of the coxsackie B virus and adenovirus receptor (CAR) in cell adhesion and growth | Q24301014 |
| Positionally cloned gene for a novel glomerular protein--nephrin--is mutated in congenital nephrotic syndrome | Q24314612 | ||
| PHENIX: a comprehensive Python-based system for macromolecular structure solution | Q24654617 | ||
| Processing of X-ray diffraction data collected in oscillation mode | Q26778468 | ||
| Cell biology and pathology of podocytes | Q26853664 | ||
| Structural basis of the myosin X PH1N-PH2-PH1C tandem as a specific and acute cellular PI(3,4,5)P3 sensor | Q27674679 | ||
| Coot: model-building tools for molecular graphics | Q27860505 | ||
| Phasercrystallographic software | Q27860930 | ||
| The membrane-associated guanylate kinase protein MAGI-1 binds megalin and is present in glomerular podocytes | Q28207315 | ||
| Cell junction-associated proteins IQGAP1, MAGI-2, CASK, spectrins, and alpha-actinin are components of the nephrin multiprotein complex | Q28570208 | ||
| Slit diaphragms contain tight junction proteins | Q28573180 | ||
| The murine nephrin gene is specifically expressed in kidney, brain and pancreas: inactivation of the gene leads to massive proteinuria and neonatal death | Q28588477 | ||
| The long journey through renal filtration: new pieces in the puzzle of slit diaphragm architecture | Q33364815 | ||
| Nineteen novel NPHS1 mutations in a worldwide cohort of patients with congenital nephrotic syndrome (CNS) | Q34169609 | ||
| Role of the polarity protein Scribble for podocyte differentiation and maintenance | Q34269189 | ||
| Organization of signaling complexes by PDZ-domain scaffold proteins | Q35177318 | ||
| Nephrin mutations can cause childhood-onset steroid-resistant nephrotic syndrome | Q36906056 | ||
| MAGI-1 Interacts with Nephrin to Maintain Slit Diaphragm Structure through Enhanced Rap1 Activation in Podocytes | Q37421404 | ||
| The podocyte slit diaphragm--from a thin grey line to a complex signalling hub. | Q38133715 | ||
| Podocyte-actin dynamics in health and disease | Q38940494 | ||
| MAGI2 Mutations Cause Congenital Nephrotic Syndrome | Q39118036 | ||
| New Insights into Podocyte Biology in Glomerular Health and Disease | Q39238888 | ||
| Phosphatidylinositol-3,4,5-trisphosphate regulates the formation of the basolateral plasma membrane in epithelial cells | Q40241493 | ||
| Bigenic mouse models of focal segmental glomerulosclerosis involving pairwise interaction of CD2AP, Fyn, and synaptopodin | Q40289564 | ||
| Endothelial adhesion molecule ESAM binds directly to the multidomain adaptor MAGI-1 and recruits it to cell contacts | Q40512855 | ||
| Neph-Nephrin proteins bind the Par3-Par6-atypical protein kinase C (aPKC) complex to regulate podocyte cell polarity | Q42009574 | ||
| Bigenic heterozygosity and the development of steroid-resistant focal segmental glomerulosclerosis | Q45746724 | ||
| MAGI-1 is a component of the glomerular slit diaphragm that is tightly associated with nephrin | Q46697366 | ||
| MAGI-2 is critical for the formation and maintenance of the glomerular filtration barrier in mouse kidney. | Q53028656 | ||
| P4510 | describes a project that uses | ImageJ | Q1659584 |
| P433 | issue | 9 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | nephrology | Q177635 |
| P304 | page(s) | 2362-2371 | |
| P577 | publication date | 2018-07-13 | |
| P1433 | published in | Journal of the American Society of Nephrology | Q17123893 |
| P1476 | title | Structural Basis of Highly Specific Interaction between Nephrin and MAGI1 in Slit Diaphragm Assembly and Signaling | |
| P478 | volume | 29 |
Search more.