Citations for
1NCK1, NPHS1, WTIP
Nephrin Suppresses Hippo Signaling through the Adaptor Proteins Nck and WTIP.
Keyvani Chahi A, Martin CE, Jones N.
J Biol Chem 291(24):12799-808. doi: 10.1074/jbc.M116.724245. Epub 2016 Mar 31. 2016
2KIRREL2, NPHS1
Functions of the podocyte proteins nephrin and Neph3 and the transcriptional regulation of their genes.
Ristola M, Lehtonen S.
Clin Sci (Lond) 126(5):315-28. doi: 10.1042/CS20130258. 2014
3FYN, NCK1, NPHS1
Direct regulation of nephrin tyrosine phosphorylation by Nck adaptor proteins.
New LA, Keyvani Chahi A, Jones N.
J Biol Chem 288(3):1500-10. doi: 10.1074/jbc.M112.439463. Epub 2012 Nov 27. 2013
4CD2AP, NPHS1, SEPTIN7
Septin 7 forms a complex with CD2AP and nephrin and regulates glucose transporter trafficking.
Wasik AA, Polianskyte-Prause Z, Dong MQ, Shaw AS, Yates JR 3rd, Farquhar MG, Lehtonen S.
Mol Biol Cell 23(17):3370-9. doi: 10.1091/mbc.E11-12-1010. Epub 2012 Jul 18. 2012
5NPHS1
Mutations in NPHS1 in a Chinese child with congenital nephrotic syndrome.
Yu ZH, Wang DJ, Meng DC, Huang J, Nie XJ.
Genet Mol Res 11(2):1460-4. doi: 10.4238/2012.May.18.6. 2012
6NPHS1, ROBO2
Inhibitory effects of Robo2 on nephrin: a crosstalk between positive and negative signals regulating podocyte structure.
Fan X, Li Q, Pisarek-Horowitz A, Rasouly HM, Wang X, Bonegio RG, Wang H, McLaughlin M, Mangos S, Kalluri R, Holzman LB, Drummond IA, Brown D, Salant DJ, Lu W.
Cell Rep 2(1):52-61. doi: 10.1016/j.celrep.2012.06.002. Epub 2012 Jul 12. 2012
7NPHS1, SIRPA
SIRPα interacts with nephrin at the podocyte slit diaphragm.
Kajiho Y, Harita Y, Kurihara H, Horita S, Matsunaga A, Tsurumi H, Kanda S, Sugawara N, Miura K, Sekine T, Hattori S, Hattori M, Igarashi T.
FEBS J 279(17):3010-21. doi: 10.1111/j.1742-4658.2012.08682.x. Epub 2012 Jul 23. 2012
8NPHS1, NPHS2, SRN1
A spectrum of novel NPHS1 and NPHS2 gene mutations in pediatric nephrotic syndrome patients from Pakistan.
Abid A, Khaliq S, Shahid S, Lanewala A, Mubarak M, Hashmi S, Kazi J, Masood T, Hafeez F, Naqvi SA, Rizvi SA, Mehdi SQ.
Gene Jul 10;502(2):133-7. doi: 10.1016/j.gene.2012.04.063. Epub 2012 Apr 28. 2012
9KIRREL, KIRREL2, NPHS1
Trans-interaction of nephrin and Neph1/Neph3 induces cell adhesion that associates with decreased tyrosine phosphorylation of nephrin.
Heikkilä E, Ristola M, Havana M, Jones N, Holthöfer H, Lehtonen S.
Biochem J 435(3):619-28. 2011
10KIRREL, MYO1C, NPHS1
Motor protein Myo1c is a podocyte protein that facilitates the transport of slit diaphragm protein Neph1 to the podocyte membrane.
Arif E, Wagner MC, Johnstone DB, Wong HN, George B, Pruthi PA, Lazzara MJ, Nihalani D.
Mol Cell Biol 31(10):2134-50. Epub 2011 Mar 14. 2011
11NGFR, NPHS1
The podocyte protein nephrin is required for cardiac vessel formation.
Wagner N, Morrison H, Pagnotta S, Michiels JF, Schwab Y, Tryggvason K, Schedl A, Wagner KD.
Hum Mol Genet 20(11):2182-94. Epub 2011 Mar 14. 2011
12NPHS1, PICK1, PRKCA
PKC alpha mediates beta-arrestin2-dependent nephrin endocytosis in hyperglycemia.
Quack I, Woznowski M, Potthoff SA, Palmer R, Königshausen E, Sivritas S, Schiffer M, Stegbauer J, Vonend O, Rump LC, Sellin L.
J Biol Chem 286(15):12959-70. doi: 10.1074/jbc.M110.204024. Epub 2011 Feb 14. 2011
13FLNA, INPPL1, NPHS, NPHS1, RAPH1
Nephrin regulates lamellipodia formation by assembling a protein complex that includes Ship2, filamin and lamellipodin.
Venkatareddy M, Cook L, Abuarquob K, Verma R, Garg P.
PLoS One 6(12):e28710. doi: 10.1371/journal.pone.0028710. Epub 2011 Dec 14. 2011
14KIRREL, KIRREL2, KIRREL3, NPHS1, XPR1
A model organism approach: defining the role of Neph proteins as regulators of neuron and kidney morphogenesis.
Neumann-Haefelin E, Kramer-Zucker A, Slanchev K, Hartleben B, Noutsou F, Martin K, Wanner N, Ritter A, Gödel M, Pagel P, Fu X, Müller A, Baumeister R, Walz G, Huber TB.
Hum Mol Genet 19(12):2347-59. Epub 2010 Mar 16.PMID: 20233749 2010
15KIRREL2, NPHS1
Ptf1a directly controls expression of immunoglobulin superfamily molecules Nephrin and Neph3 in the developing central nervous system.
Nishida K, Hoshino M, Kawaguchi Y, Murakami F.
J Biol Chem 285(1):373-80. Epub 2009 Nov 2.PMID: 19887377 2010
16CD2AP, NPHS1, SH3KBP1
CIN85/RukL is a novel binding partner of nephrin and podocin and mediates slit diaphragm turnover in podocytes.
Tossidou I, Teng B, Drobot L, Meyer-Schwesinger C, Worthmann K, Haller H, Schiffer M.
J Biol Chem 285(33):25285-95. Epub 2010 May 10. 2010
17KIRREL2, NPHS1, PTF1A
Ptf1a directly controls expression of immunoglobulin superfamily molecules Nephrin and Neph3 in the developing central nervous system.
Nishida K, Hoshino M, Kawaguchi Y, Murakami F.
J Biol Chem 285(1):373-80. doi: 10.1074/jbc.M109.060657. Epub 2009 Nov 2. 2010
18NPHS1
Analysis of polymorphism in renin angiotensin system and other related genes in South Indian chronic kidney disease patients.
Anbazhagan K, Sampathkumar K, Ramakrishnan M, Gomathi P, Gomathi S, Selvam GS.
Clin Chim Acta 406(1-2):108-12. Epub 2009 Jun 9. 2009
19NPHS1, NPHS2, SRN1
Clinical features and long-term outcome of nephrotic syndrome associated with heterozygous NPHS1 and NPHS2 mutations.
Caridi G, Gigante M, Ravani P, Trivelli A, Barbano G, Scolari F, Dagnino M, Murer L, Murtas C, Edefonti A, Allegri L, Amore A, Coppo R, Emma F, De Palo T, Penza R, Gesualdo L, Ghiggeri GM.
Clin J Am Soc Nephrol 4(6):1065-72. Epub 2009 Apr 30. 2009
20NPHS1
A role for nephrin, a renal protein, in vertebrate skeletal muscle cell fusion.
Sohn RL, Huang P, Kawahara G, Mitchell M, Guyon J, Kalluri R, Kunkel LM, Gussoni E.
Proc Natl Acad Sci U S A 106(23):9274-9. Epub 2009 May 22. 2009
21NPHS1, NPHS2
Predisposition to relapsing nephrotic syndrome by a nephrin mutation that interferes with assembly of functioning microdomains.
Shono A, Tsukaguchi H, Kitamura A, Hiramoto R, Qin XS, Doi T, Iijima K.
Hum Mol Genet 18(16):2943-56. Epub 2009 May 14.PMID: 19443487 2009
22KIRREL, NPHP1, NPHS1, PAED6B, PARD3, PARD6A
Neph-Nephrin proteins bind the Par3-Par6-atypical protein kinase C (aPKC) complex to regulate podocyte cell polarity.
Hartleben B, Schweizer H, Lübben P, Bartram MP, Möller CC, Herr R, Wei C, Neumann-Haefelin E, Schermer B, Zentgraf H, Kerjaschki D, Reiser J, Walz G, Benzing T, Huber TB.
J Biol Chem 283(34):23033-8. Epub 2008 Jun 18. 2008
23NPHS1
Thirteen novel NPHS1 mutations in a large cohort of children with congenital nephrotic syndrome.
Heeringa SF, Vlangos CN, Chernin G, Hinkes B, Gbadegesin R, Liu J, Hoskins BE, Ozaltin F, Hildebrandt F; Members of the APN Study Group.
Nephrol Dial Transplant 23(11):3527-33. Epub 2008 May 23. 2008
24KCNMA1, NPHS1
Nephrin binds to the COOH terminus of a large-conductance Ca2+-activated K+ channel isoform and regulates its expression on the cell surface.
Kim EY, Choi KJ, Dryer SE.
Am J Physiol Renal Physiol 295(1):F235-46. Epub 2008 May 14. 2008
25NPHS1
Transcriptional suppression of nephrin in podocytes by macrophages: roles of inflammatory cytokines and involvement of the PI3K/Akt pathway.
Takano Y, Yamauchi K, Hayakawa K, Hiramatsu N, Kasai A, Okamura M, Yokouchi M, Shitamura A, Yao J, Kitamura M.
FEBS Lett 581(3):421-6. Epub 2007 Jan 12. 2007
26NPHS1
Nephrin--a unique structural and signaling protein of the kidney filter.
Patrakka J, Tryggvason K.
Trends Mol Med 13(9):396-403. Epub 2007 Sep 4. Review. 2007
27NPHS1
Nephrin is critical for the action of insulin on human glomerular podocytes.
Coward RJ, Welsh GI, Koziell A, Hussain S, Lennon R, Ni L, Tavaré JM, Mathieson PW, Saleem MA.
Diabetes 56(4):1127-35. 2007
28KIRREL, NPHS1
Neph1 cooperates with nephrin to transduce a signal that induces actin polymerization.
Garg P, Verma R, Nihalani D, Johnstone DB, Holzman LB.
Mol Cell Biol 27(24):8698-712. Epub 2007 Oct 8.PMID: 17923684 2007
29NPHS1
beta-Arrestin2 mediates nephrin endocytosis and impairs slit diaphragm integrity.
Quack I, Rump LC, Gerke P, Walther I, Vinke T, Vonend O, Grunwald T, Sellin L.
Proc Natl Acad Sci U S A 103(38):14110-5. Epub 2006 Sep 12. 2006
30ACTN4, CD2AP, NPHS1, NPHS2, SRN1, SRN4, WT1
Mutations in the Wilms' tumor 1 gene cause isolated steroid resistant nephrotic syndrome and occur in exons 8 and 9.
Mucha B, Ozaltin F, Hinkes BG, Hasselbacher K, Ruf RG, Schultheiss M, Hangan D, Hoskins BE, Everding AS, Bogdanovic R, Seeman T, Hoppe B, Hildebrandt F; Members of the APN Study Group.
Pediatr Res 59(2):325-31. 2006
31ACTN4, NPHS1, NPHS2, CD2AP
The relationship among nephrin, podocin, CD2AP, and alpha-actinin might not be a true 'interaction' in podocyte.
Fan Q, Xing Y, Ding J, Guan N, Zhang J.
Kidney Int 69(7):1207-15. 2006
32NPHS1, IQGAP1
Characterization of the interactions of the nephrin intracellular domain.
Liu XL, Kilpelainen P, Hellman U, Sun Y, Wartiovaara J, Morgunova E, Pikkarainen T, Yan K, Jonsson AP, Tryggvason K.
FEBS J 272(1):228-43. 2005
33KIRREL3, KIRREL, NPHS1
NEPH2 is located at the glomerular slit diaphragm, interacts with nephrin and is cleaved from podocytes by metalloproteinases.
Gerke P, Sellin L, Kretz O, Petraschka D, Zentgraf H, Benzing T, Walz G.
J Am Soc Nephrol 16(6):1693-702. Epub 2005 Apr 20. 2005
34NPHS1, PPARA
PPARalpha activation upregulates nephrin expression in human embryonic kidney epithelial cells and podocytes by a dual mechanism.
Ren S, Xin C, Beck KF, Saleem MA, Mathieson P, Pavenstadt H, Pfeilschifter J, Huwiler A.
Biochem Biophys Res Commun 338(4):1818-24. Epub 2005 Nov 2. 2005
35NPHS1
Nephrin gene (NPHS1) in patients with minimal change nephrotic syndrome (MCNS).
Lahdenkari AT, Kestila M, Holmberg C, Koskimies O, Jalanko H.
Kidney Int 65(5):1856-63. 2004
36KIRREL, NPHS1
Neph1 and nephrin interaction in the slit diaphragm is an important determinant of glomerular permeability.
Liu G, Kaw B, Kurfis J, Rahmanuddin S, Kanwar YS, Chugh SS.
J Clin Invest 112(2):209-21. 2003
37KIRREL, NPHS1
Homodimerization and heterodimerization of the glomerular podocyte proteins nephrin and NEPH1.
Gerke P, Huber TB, Sellin L, Benzing T, Walz G.
J Am Soc Nephrol 14(4):918-26. 2003
38NPHS1, NPHS2
Genotype/phenotype correlations of NPHS1 and NPHS2 mutations in nephrotic syndrome advocate a functional inter-relationship in glomerular filtration.
Koziell A, Grech V, Hussain S, Lee G, Lenkkeri U, Tryggvason K, Scambler P.
Hum Mol Genet 11(4):379-88. 2002
39NPHS1
Mutation spectrum in the nephrin gene (NPHS1) in congenital nephrotic syndrome.
Beltcheva O, Martin P, Lenkkeri U, Tryggvason K.
Hum Mutat 17(5):368-73. 2001
40NPHS1
Defective nephrin trafficking caused by missense mutations in the NPHS1 gene: insight into the mechanisms of congenital nephrotic syndrome.
Liu L, Done SC, Khoshnoodi J, Bertorello A, Wartiovaara J, Berggren PO, Tryggvason K.
Hum Mol Genet 10(23):2637-44. 2001
41NPHS1
Novel mutation in the nephrin gene of a Japanese patient with congenital nephrotic syndrome of the Finnish type.
Aya K, Tanaka H, Seino Y.
Kidney Int 57(2):401-4. 2000
42NPHS1
Structure of the gene for congenital nephrotic syndrome of the Finnish type (NPHS1) and characterization of mutations.
Lenkkeri U, et al.
Am J Hum Genet 64 : 51-61. 1999
43NPHS1
Altered gene expression and functions of mitochondria in human nephrotic syndrome.
Holthofer H, et al.
FASEB J 13(3):523-32. 1999
44CD2AP, NPHS1
Congenital Nephrotic Syndrome in Mice Lacking CD2-Associated Protein.
Shih, N.-Y.; Li, J.; Karpitskii, V.; Nguyen, A.; Dustin, M. L.; Kanagawa, O.; Miner, J. H.; Shaw, A. S.
Science 286(5438):312-315 1999
45NPHS1
Nephrin is specifically located at the slit diaphragm of glomerular podocytes.
Ruotsalainen V, et al.
Proc Natl Acad Sci U S A 96(14):7962-7 1999
46NPHS1
Discovery of the congenital nephrotic syndrome gene discloses the structure of the mysterious molecular sieve of the kidney.
Tryggvason K, Ruotsalainen V, Wartiovaara J.
Int J Dev Biol 43(5 Spec No):445-51. Review 1999
47NPHS1
Elevated frequency and allelic heterogeneity of congenital nephrotic syndrome, Finnish type, in the old order Mennonites.
Bolk S, Puffenberger EG, Hudson J, Morton DH, Chakravarti A.
Am J Hum Genet 65(6):1785-90. No abstract available 1999
48NPHS1
Positionally cloned gene for a novel glomerular protein-nephrin-is mutated in congenital nephrotic syndrome.
KestilŠ M, et al.
Mol Cell 1 : 575-582. 1998
49NPHS1
Assembly of a 1-Mb restriction-mapped cosmid contig spanning the candidate region for Finnish congenital nephrosis (NPHS1) in 19q13.1.
Olsen AS, et al.
Genomics 34 : 223-225. 1996
50NPHS1
Fine mapping and haplotype analysis of the locus for congenital nephrotic syndrome on chromosome 19q13.1.
MŠnnikkš M, et al.
Am J Hum Genet 57 : 1377-1383. 1995
51NPHS1
Congenital nephrotic syndrome of the finnish type maps to the long arm of chromosome 19.
KestilŠ M, et al.
Am J Hum Genet 54 : 757-764. 1994