V. Ruotsalainen

发表

Loss-of-function mutations in TYROBP (DAP12) result in a presenile dementia with bone cysts

Leena Peltonen, Tuomo Timonen, Tom Böhling, 2000, Nature Genetics.

Positionally cloned gene for a novel glomerular protein--nephrin--is mutated in congenital nephrotic syndrome.

L Peltonen, L. Peltonen, J. Lamerdin, 1998, Molecular cell.

Nephrin is specifically located at the slit diaphragm of glomerular podocytes.

K. Tryggvason, H. Jalanko, M. Kestilä, 1999, Proceedings of the National Academy of Sciences of the United States of America.

CD2AP is expressed with nephrin in developing podocytes and is found widely in mature kidney and elsewhere.

A. Shaw, K. Tryggvason, J. Miner, 2000, American journal of physiology. Renal physiology.

Nephrin redistribution on podocytes is a potential mechanism for proteinuria in patients with primary acquired nephrotic syndrome.

G. Camussi, S. Doublier, K. Tryggvason, 2001, The American journal of pathology.

Co-localization of nephrin, podocin, and the actin cytoskeleton: evidence for a role in podocyte foot process formation.

M. Saleem, P. Mathieson, K. Tryggvason, 2002, The American journal of pathology.

Expression of nephrin in acquired human glomerular disease.

Mi-kyung Kim, K. Tryggvason, W. Huh, 2002, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

Discovery of the congenital nephrotic syndrome gene discloses the structure of the mysterious molecular sieve of the kidney.

K. Tryggvason, V. Ruotsalainen, J. Wartiovaara, 1999, The International journal of developmental biology.

Congenital nephrotic syndrome (NPHS1): features resulting from different mutations in Finnish patients.

K. Tryggvason, P. Tissari, M. Männikkö, 2000, Kidney international.

The effect of dexamethasone on defective nephrin transport caused by ER stress: a potential mechanism for the therapeutic action of glucocorticoids in the acquired glomerular diseases.

F. Bessho, A. Kudo, K. Tryggvason, 2006, Kidney international.

N-linked glycosylation is critical for the plasma membrane localization of nephrin.

K. Yan, K. Tryggvason, V. Ruotsalainen, 2002, Journal of the American Society of Nephrology : JASN.

Monoclonal antibodies to human nephrin.

K. Tryggvason, V. Ruotsalainen, P. Kilpeläinen, 2004, Hybridoma and hybridomics.

Expression of nephrin in pediatric kidney diseases.

K. Tryggvason, M. Heikinheimo, H. Jalanko, 2001, Journal of the American Society of Nephrology : JASN.

Recurrence of proteinuria following renal transplantation in congenital nephrotic syndrome of the Finnish type

T. Srivastava, K. Tryggvason, V. Savin, 2006, Pediatric Nephrology.

Recurrence of nephrotic syndrome in kidney grafts of patients with congenital nephrotic syndrome of the Finnish type: role of nephrin.

K. Tryggvason, H. Jalanko, V. Ruotsalainen, 2002, Transplantation.

rapid communication CD 2 AP is expressed with nephrin in developing podocytes and is found widely in mature kidney and elsewhere

A. Shaw, K. Tryggvason, J. Miner, 2000 .

Proteinuria and prenatal diagnosis of congenital nephrosis in fetal carriers of nephrin gene mutations

R. Salonen, K. Tryggvason, M. Männikkö, 2002, The Lancet.

Nephrin : role in the renal ultrafilter and involvement in proteinuria

V. Ruotsalainen, Vesa Ruotsalainen, 2004 .

Tissue Expression of Nephrin in Human and Pig

R. Salonen, K. Tryggvason, H. Jalanko, 2004, Pediatric Research.

Role of nephrin in cell junction formation in human nephrogenesis.

R. Salonen, K. Tryggvason, P. Tissari, 2000, The American journal of pathology.

Altered ultrastructural distribution of nephrin in minimal change nephrotic syndrome.

U. Berg, K. Tryggvason, K. Hultenby, 2003, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

Nephrin strands contribute to a porous slit diaphragm scaffold as revealed by electron tomography.

Eetu Mäkelä, Sara Sandin, K. Tryggvason, 2004, The Journal of clinical investigation.

Disease-causing missense mutations in NPHS2 gene alter normal nephrin trafficking to the plasma membrane.

Eiji Higashihara, F. Bessho, E. Higashihara, 2004, Kidney international.

Clustering-induced tyrosine phosphorylation of nephrin by Src family kinases.

K. Tryggvason, J. Lahdenperä, X. Liu, 2003, Kidney international.

Nephrin expression is reduced in human diabetic nephropathy: evidence for a distinct role for glycated albumin and angiotensin II.

G. Camussi, G. Deferrari, S. Doublier, 2003, Diabetes.

Podocyte proteins in Galloway-Mowat syndrome

T. Srivastava, K. Tryggvason, U. Alon, 2001, Pediatric Nephrology.

Difference between total and intact assays for N-terminal propeptide of type I procollagen reflects degradation of pN-collagen rather than denaturation of intact propeptide

J. Risteli, R. Ikäheimo, Kari E Savolainen, 2010, Annals of clinical biochemistry.