How does the kidney filter plasma?
暂无分享,去创建一个
[1] K. Tryggvason,et al. Unraveling the mechanisms of glomerular ultrafiltration: nephrin, a key component of the slit diaphragm. , 1999, Journal of the American Society of Nephrology : JASN.
[2] L Peltonen,et al. Positionally cloned gene for a novel glomerular protein--nephrin--is mutated in congenital nephrotic syndrome. , 1998, Molecular cell.
[3] T. B. Huber,et al. NEPH1 defines a novel family of podocin‐interacting proteins , 2003, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.
[4] S. Furuta,et al. Three-dimensional study of glomerular slit diaphragm by the quick-freezing and deep-etching replica method. , 1990, European journal of cell biology.
[5] H. Rennke,et al. Glomerular permeability: in vivo tracer studies with polyanionic and polycationic ferritins. , 1977, Kidney international.
[6] J. Sanes,et al. The renal glomerulus of mice lacking s-laminin/laminin beta 2: nephrosis despite molecular compensation by laminin beta 1. , 1995, Nature genetics.
[7] K. Tryggvason,et al. Nephrin is specifically located at the slit diaphragm of glomerular podocytes. , 1999, Proceedings of the National Academy of Sciences of the United States of America.
[8] S. Rennard,et al. Isolation of a heparan sulfate-containing proteoglycan from basement membrane. , 1980, Proceedings of the National Academy of Sciences of the United States of America.
[9] B. Haraldsson,et al. Why do we not all have proteinuria? An update of our current understanding of the glomerular barrier. , 2004, News in physiological sciences : an international journal of physiology produced jointly by the International Union of Physiological Sciences and the American Physiological Society.
[10] M. Karnovsky,et al. The structural basis of glomerular filtration. , 1972, Advances in nephrology from the Necker Hospital.
[11] T. Benzing,et al. Homodimerization and heterodimerization of the glomerular podocyte proteins nephrin and NEPH1. , 2003, Journal of the American Society of Nephrology : JASN.
[12] T. Oegema,et al. Heparan sulfate--rich anionic sites in the human glomerular basement membrane. Decreased concentration in congenital nephrotic syndrome. , 1983, The New England journal of medicine.
[13] M. Ruegg,et al. Agrin Is a Major Heparan Sulfate Proteoglycan in the Human Glomerular Basement Membrane , 1998, The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society.
[14] P. Yurchenco,et al. Basal lamina assembly. , 1994, Current opinion in cell biology.
[15] B. Haraldsson,et al. Glomerular charge selectivity for horseradish peroxidase and albumin at low and normal ionic strengths. , 1998, Acta physiologica Scandinavica.
[16] Tsutomu Inoue,et al. FAT is a component of glomerular slit diaphragms. , 2001, Kidney international.
[17] K. Tryggvason,et al. Alport's syndrome, Goodpasture's syndrome, and type IV collagen. , 2003, The New England journal of medicine.
[18] Eetu Mäkelä,et al. Nephrin strands contribute to a porous slit diaphragm scaffold as revealed by electron tomography. , 2004, The Journal of clinical investigation.
[19] Y. Kanwar,et al. Neph1 and nephrin interaction in the slit diaphragm is an important determinant of glomerular permeability. , 2003, The Journal of clinical investigation.
[20] O. Smithies. Why the kidney glomerulus does not clog: A gel permeation/diffusion hypothesis of renal function , 2003, Proceedings of the National Academy of Sciences of the United States of America.
[21] L. Chodosh,et al. Precocious Mammary Gland Development in P-Cadherin–deficient Mice , 1997, The Journal of cell biology.
[22] B. Duling,et al. Permeation of the luminal capillary glycocalyx is determined by hyaluronan. , 1999, American journal of physiology. Heart and circulatory physiology.
[23] K. Tryggvason,et al. The murine nephrin gene is specifically expressed in kidney, brain and pancreas: inactivation of the gene leads to massive proteinuria and neonatal death. , 2001, Human molecular genetics.
[24] N. Kashihara,et al. Current status of the structural and functional basis of glomerular filtration and proteinuria. , 1991, Seminars in nephrology.
[25] M. Saleem,et al. Podocin, a raft-associated component of the glomerular slit diaphragm, interacts with CD2AP and nephrin. , 2001, The Journal of clinical investigation.
[26] G. Remuzzi,et al. Abnormal protein traffic through the glomerular barrier induces proximal tubular cell dysfunction and causes renal injury. , 1995, Current opinion in nephrology and hypertension.
[27] P. Avasthi,et al. Glomerular endothelial glycocalyx. , 1988, Contributions to nephrology.
[28] M. Farquhar,et al. Anionic sites in the glomerular basement membrane. In vivo and in vitro localization to the laminae rarae by cationic probes , 1979, The Journal of cell biology.
[29] Michael Loran Dustin,et al. Congenital nephrotic syndrome in mice lacking CD2-associated protein. , 1999, Science.
[30] Karnovsky Mj,et al. The structural basis of glomerular filtration. , 1972 .
[31] K. Sigmundsson,et al. Nephrin promotes cell-cell adhesion through homophilic interactions. , 2003, The American journal of pathology.
[32] B. Schermer,et al. The Carboxyl Terminus of Neph Family Members Binds to the PDZ Domain Protein Zonula Occludens-1* , 2003, The Journal of Biological Chemistry.
[33] B. Olsen,et al. Heparan sulfate chains of perlecan are indispensable in the lens capsule but not in the kidney , 2003, The EMBO journal.
[34] M. Karnovsky,et al. POROUS SUBSTRUCTURE OF THE GLOMERULAR SLIT DIAPHRAGM IN THE RAT AND MOUSE , 1974, The Journal of cell biology.
[35] A. Groffen,et al. Recent insights into the structure and functions of heparan sulfate proteoglycans in the human glomerular basement membrane. , 1999, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.
[36] M. Farquhar,et al. Increased permeability of the glomerular basement membrane to ferritin after removal of glycosaminoglycans (heparan sulfate) by enzyme digestion , 1980, The Journal of cell biology.
[37] James M. Anderson,et al. The tight junction protein ZO-1 is concentrated along slit diaphragms of the glomerular epithelium , 1990, The Journal of cell biology.
[38] R. Ramirez-Solis,et al. Proteinuria and Perinatal Lethality in Mice Lacking NEPH1, a Novel Protein with Homology to NEPHRIN , 2001, Molecular and Cellular Biology.
[39] K. Tryggvason,et al. Type IV collagen: structure, gene organization, and role in human diseases. Molecular basis of Goodpasture and Alport syndromes and diffuse leiomyomatosis. , 1993, The Journal of biological chemistry.
[40] R. Cotran,et al. Role of molecular charge in glomerular permeability. Tracer studies with cationized ferritins , 1975, The Journal of cell biology.
[41] T. Benzing,et al. Interaction with Podocin Facilitates Nephrin Signaling* , 2001, The Journal of Biological Chemistry.
[42] J. Sanes,et al. The Laminin α Chains: Expression, Developmental Transitions, and Chromosomal Locations of α1-5, Identification of Heterotrimeric Laminins 8–11, and Cloning of a Novel α3 Isoform , 1997, The Journal of cell biology.
[43] M. Skolnick,et al. Identification of mutations in the COL4A5 collagen gene in Alport syndrome. , 1990, Science.
[44] Corinne Antignac,et al. NPHS2, encoding the glomerular protein podocin, is mutated in autosomal recessive steroid-resistant nephrotic syndrome , 2000, Nature Genetics.
[45] Sara Sandin,et al. Structure and flexibility of individual immunoglobulin G molecules in solution. , 2004, Structure.
[46] M. Kretzler,et al. The glomerular slit diaphragm is a modified adherens junction. , 2000, Journal of the American Society of Nephrology : JASN.
[47] C. ffrench-Constant,et al. Mice Lacking the Giant Protocadherin mFAT1 Exhibit Renal Slit Junction Abnormalities and a Partially Penetrant Cyclopia and Anophthalmia Phenotype , 2003, Molecular and Cellular Biology.
[48] R. Cotran,et al. Tracer Studies with Cationized Ferritins , 1975 .