{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,6,1]],"date-time":"2026-06-01T22:03:35Z","timestamp":1780351415589,"version":"3.54.1"},"reference-count":20,"publisher":"Springer Science and Business Media LLC","issue":"1","content-domain":{"domain":["link.springer.com"],"crossmark-restriction":false},"short-container-title":["Diagn Pathol"],"published-print":{"date-parts":[[2014,12]]},"DOI":"10.1186\/1746-1596-9-40","type":"journal-article","created":{"date-parts":[[2014,2,21]],"date-time":"2014-02-21T18:01:41Z","timestamp":1393005701000},"update-policy":"https:\/\/doi.org\/10.1007\/springer_crossmark_policy","source":"Crossref","is-referenced-by-count":5,"title":["Podocin and Beta Dystroglycan expression to study Podocyte-Podocyte and basement membrane matrix connections in adult protienuric states"],"prefix":"10.1186","volume":"9","author":[{"given":"Praveen B","family":"Shankar","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Ritambhra","family":"Nada","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Kusum","family":"Joshi","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Ashwani","family":"Kumar","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Charan Singh","family":"Rayat","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Vinay","family":"Sakhuja","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"297","published-online":{"date-parts":[[2014,2,21]]},"reference":[{"key":"1100_CR1","doi-asserted-by":"publisher","first-page":"3016","DOI":"10.1097\/01.ASN.0000039569.34360.5E","volume":"13","author":"MR Pollak","year":"2002","unstructured":"Pollak MR: Inherited Podocytopathies: FSGS and Nephrotic Syndrome from a Genetic Viewpoint. J Am Soc Nephrol. 2002, 13: 3016-3023. 10.1097\/01.ASN.0000039569.34360.5E.","journal-title":"J Am Soc Nephrol"},{"key":"1100_CR2","doi-asserted-by":"publisher","first-page":"445","DOI":"10.2215\/CJN.03531006","volume":"2","author":"M Waldman","year":"2007","unstructured":"Waldman M, Crew RJ, Valeri A, Busch J, Stokes B, Markowitz G, D'Agati V, Appel G: Adult Minimal-Change Disease: Clinical Characteristics, Treatment, and Outcomes. Clin J Am Soc Nephrol. 2007, 2: 445-453. 10.2215\/CJN.03531006.","journal-title":"Clin J Am Soc Nephrol"},{"key":"1100_CR3","doi-asserted-by":"publisher","first-page":"230","DOI":"10.1152\/ajprenal.90507.2008","volume":"296","author":"A Skoberne","year":"2008","unstructured":"Skoberne A, Konieczny A, Schiffer M: Glomerular epithelial cells in the urine: what has to be done to make them worthwhile?. Am J Physiol Renal Physiol. 2008, 296: 230-241. 10.1152\/ajprenal.90507.2008.","journal-title":"Am J Physiol Renal Physiol"},{"key":"1100_CR4","doi-asserted-by":"publisher","first-page":"175","DOI":"10.1159\/000013580","volume":"20","author":"T Nakamura","year":"2000","unstructured":"Nakamura T, Ushiyama C, Suzuki S, Hara M, Shimada N, Ebihara I, Koide H: The urinary pododcyte as a marker for the differential diagnosis of idiopathic focal segmental glomerulosclerosis and minimal change nephrotic syndrome. Am J Nephrol. 2000, 20: 175-179. 10.1159\/000013580.","journal-title":"Am J Nephrol"},{"key":"1100_CR5","doi-asserted-by":"crossref","first-page":"403","DOI":"10.1681\/ASN.V113403","volume":"11","author":"Hm FE Regele","year":"2000","unstructured":"Regele Hm FE, Langer B, Poczewki H, Kraxberger I, Bittner Re, Kerjaschki D: Glomerular Expression of Dystroglycans Is Reduced in Minimal Change Nephrosis But Not in Focal Segmental Glomerulosclerosis. J Am Soc Nephrol. 2000, 11: 403-412.","journal-title":"J Am Soc Nephrol"},{"key":"1100_CR6","doi-asserted-by":"publisher","first-page":"478","DOI":"10.1093\/ndt\/gfp465","volume":"25","author":"NP Vogtl\u00e4nder","year":"2010","unstructured":"Vogtl\u00e4nder NP, Van der Vlag J, Bakker MA, Dijkman HB, Wevers RA, Campbell KP, Wetzels JF, Berden JH: Expression of sialidase and dystroglycan in human glomerular diseases. Nephrol Dial Transplant. 2010, 25: 478-484. 10.1093\/ndt\/gfp465.","journal-title":"Nephrol Dial Transplant"},{"key":"1100_CR7","doi-asserted-by":"publisher","first-page":"1747","DOI":"10.2215\/CJN.01510209","volume":"4","author":"G Giannico","year":"2009","unstructured":"Giannico G, Yang H, Neilson EG, Fogo AB: Dystroglycan in the Diagnosis of FSGS. Cin J Am Soc Nephrol. 2009, 4: 1747-1753. 10.2215\/CJN.01510209.","journal-title":"Cin J Am Soc Nephrol"},{"key":"1100_CR8","doi-asserted-by":"publisher","first-page":"2958","DOI":"10.1097\/01.ASN.0000090745.85482.06","volume":"14","author":"H Schmid","year":"2003","unstructured":"Schmid H, Henger A, Cohen CD, Frach K, Gr\u00f6ne H-J, Schl\u00f6ndorff D, Kretzler M: Gene Expression Profiles of Podocyte-Associated Molecules as Diagnostic Markers in Acquired Proteinuric Diseases. J Am Soc Nephrol. 2003, 14: 2958-2966. 10.1097\/01.ASN.0000090745.85482.06.","journal-title":"J Am Soc Nephrol"},{"key":"1100_CR9","doi-asserted-by":"publisher","first-page":"2063","DOI":"10.1097\/01.ASN.0000078803.53165.C9","volume":"14","author":"K Koop","year":"2003","unstructured":"Koop K, Eikmans M, Baelde HJ, Kawachi H, de Heer E, Paul LC, Bruijn JA: Expression of Podocyte-Associated Molecules in Acquired Human Kidney Diseases. J Am Soc Nephrol. 2003, 14: 2063-2071. 10.1097\/01.ASN.0000078803.53165.C9.","journal-title":"J Am Soc Nephrol"},{"key":"1100_CR10","doi-asserted-by":"publisher","first-page":"2092","DOI":"10.1046\/j.1523-1755.2003.00303.x","volume":"64","author":"I Horinouchi","year":"2003","unstructured":"Horinouchi I, Nakazato H, Kawano T, Iyama K-i, Furuse A, Arizono K, Machida J, Sakamoto T, Endo F, Hattori S: In situ evaluation of podocin in normal and glomerular diseases. Kidney Int. 2003, 64: 2092-2099. 10.1046\/j.1523-1755.2003.00303.x.","journal-title":"Kidney Int"},{"key":"1100_CR11","doi-asserted-by":"publisher","first-page":"1666","DOI":"10.1007\/s00467-006-0218-z","volume":"16","author":"J Mao","year":"2006","unstructured":"Mao J, Zhang Y, Du L, Dai Y, Yang C, Liang L: Expression profile of nephrin, podocin, and CD2AP in Chinese children with MCNS and IgA nephropathy. Pediatr Nephrol. 2006, 16: 1666-1675.","journal-title":"Pediatr Nephrol"},{"key":"1100_CR12","doi-asserted-by":"publisher","first-page":"1122","DOI":"10.1007\/s00467-003-1240-z","volume":"18","author":"N Guan","year":"2003","unstructured":"Guan N, Ding J, Zhang J, Yang J: Expression of nephrin, podocin, alpha-actinin, and WT1 in children with nephrotic syndrome. Pediatr Nephrol. 2003, 18: 1122-1127. 10.1007\/s00467-003-1240-z.","journal-title":"Pediatr Nephrol"},{"key":"1100_CR13","doi-asserted-by":"publisher","first-page":"1209","DOI":"10.1681\/ASN.2009121309","volume":"21","author":"E Machuca","year":"2010","unstructured":"Machuca E, Benoit G, Nevo F, T\u00eate M-J, Gribouval O, Pawtowski A, Brandstr\u00f6m P, Loirat C, Niaudet P, Gubler M-C: Genotype-Phenotype Correlations in Non-Finnish Congenital Nephrotic Syndrome. J Am Soc Nephrol. 2010, 21: 1209-1217. 10.1681\/ASN.2009121309.","journal-title":"J Am Soc Nephrol"},{"key":"1100_CR14","doi-asserted-by":"publisher","first-page":"349","DOI":"10.1038\/74166","volume":"24","author":"N Boute","year":"2000","unstructured":"Boute N, Gribouval O, Roselli S, Benessy F, Lee H, Fuchshuber A, Dahan K, Gubler M-C, Niaudet P, Antignac C: NPHS2, encoding the glomerular protein podocin, is mutated in autosomal recessive steroid-resistant nephrotic syndrome. Nat Genet. 2000, 24: 349-354. 10.1038\/74166.","journal-title":"Nat Genet"},{"key":"1100_CR15","doi-asserted-by":"publisher","first-page":"722","DOI":"10.1097\/01.ASN.0000113552.59155.72","volume":"15","author":"RG Ruf","year":"2004","unstructured":"Ruf RG, Lichtenberger A, Karle SM, Haas JP, Anacleto FE, Schultheiss M, Zalewski I, Imm A, Ruf E-M, Mucha B: Patients with Mutations in NPHS2 (Podocin) Do Not Respond to Standard Steroid Treatment of Nephrotic Syndrome. J Am Soc Nephrol. 2004, 15: 722-732. 10.1097\/01.ASN.0000113552.59155.72.","journal-title":"J Am Soc Nephrol"},{"key":"1100_CR16","doi-asserted-by":"publisher","first-page":"571","DOI":"10.1111\/j.1523-1755.2004.00776.x","volume":"66","author":"S Weber","year":"2004","unstructured":"Weber S, Gribouval O, Esquivel EL, Moriniere V, Tete M-J, Legendre C, Niaudet P, Antignac C: NPSH2 mutation analysis show genetic heterogeneity of steroid resistant nephrotic syndrome and low post transplant recurrence. Kidney Int. 2004, 66: 571-579. 10.1111\/j.1523-1755.2004.00776.x.","journal-title":"Kidney Int"},{"key":"1100_CR17","doi-asserted-by":"publisher","first-page":"31","DOI":"10.2215\/CJN.02690806","volume":"2","author":"N He","year":"2007","unstructured":"He N, Zahirieh A, Mei Y, Lee B, Senthilnathan S, Wong B, Mucha B, Hildebrandt F, Cole DE, Cattran D: Recessive NPHS2 (Podocin) mutations are rare in adult-onset idiopathic focal segmental glomerulosclerosis. Clin J Am Soc Nephrol. 2007, 2: 31-37.","journal-title":"Clin J Am Soc Nephrol"},{"key":"1100_CR18","doi-asserted-by":"publisher","first-page":"365","DOI":"10.1046\/j.1523-1755.2003.00084.x","volume":"64","author":"G Caridi","year":"2003","unstructured":"Caridi G, Bertelli R, Scolari F, Sanna- Cherchi S, Di Duca M, Ghiggeri GM: Podocin mutations in sporadic focal segmental glomerulosclerosis occurring in adulthood. Kidney Int. 2003, 64: 365-","journal-title":"Kidney Int"},{"key":"1100_CR19","doi-asserted-by":"publisher","first-page":"1659","DOI":"10.1172\/JCI0216242","volume":"110","author":"H Tsukaguchi","year":"2002","unstructured":"Tsukaguchi H, Sudhakar A, Le TC, Nguyen T, Yao J, Schwimmer JA, Schachter AD, Poch E, Abreu PF, Appel GB: NPHS2 mutations in late onset focal segmental glomerulosclerosis; R229Q is a common disease associated allele. J Clin Invest. 2002, 110: 1659-1666. 10.1172\/JCI0216242.","journal-title":"J Clin Invest"},{"key":"1100_CR20","doi-asserted-by":"publisher","first-page":"33A","DOI":"10.1097\/01.ASN.0000102476.50041.44","volume":"15","author":"TB Huber","year":"2004","unstructured":"Huber TB, Reinhardt C, Simons M, Petraschka D: Direct binding of cholesterol and targeting to nephrin to lipid rafts are disrupted in disease causing podocin mutation. J Am Soc Nephrol. 2004, 15: 33A-10.1097\/01.ASN.0000102476.50041.44.","journal-title":"J Am Soc Nephrol"}],"container-title":["Diagnostic Pathology"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/link.springer.com\/content\/pdf\/10.1186\/1746-1596-9-40.pdf","content-type":"application\/pdf","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2021,9,2]],"date-time":"2021-09-02T11:52:49Z","timestamp":1630583569000},"score":1,"resource":{"primary":{"URL":"https:\/\/diagnosticpathology.biomedcentral.com\/articles\/10.1186\/1746-1596-9-40"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2014,2,21]]},"references-count":20,"journal-issue":{"issue":"1","published-print":{"date-parts":[[2014,12]]}},"alternative-id":["1100"],"URL":"https:\/\/doi.org\/10.1186\/1746-1596-9-40","relation":{},"ISSN":["1746-1596"],"issn-type":[{"value":"1746-1596","type":"electronic"}],"subject":[],"published":{"date-parts":[[2014,2,21]]},"assertion":[{"value":"14 October 2013","order":1,"name":"received","label":"Received","group":{"name":"ArticleHistory","label":"Article History"}},{"value":"19 January 2014","order":2,"name":"accepted","label":"Accepted","group":{"name":"ArticleHistory","label":"Article History"}},{"value":"21 February 2014","order":3,"name":"first_online","label":"First Online","group":{"name":"ArticleHistory","label":"Article History"}}],"article-number":"40"}}