171 related articles for article (PubMed ID: 24856573)
1. Glomerular epithelial cell phenotype in diffuse mesangial sclerosis: a report of 2 cases with markedly increased urinary podocyte excretion.
Ikezumi Y; Suzuki T; Karasawa T; Kaneko U; Yamada T; Hasegawa H; Nagata M; Saitoh A
Hum Pathol; 2014 Aug; 45(8):1778-83. PubMed ID: 24856573
[TBL] [Abstract][Full Text] [Related]
2. Murine Denys-Drash syndrome: evidence of podocyte de-differentiation and systemic mediation of glomerulosclerosis.
Patek CE; Fleming S; Miles CG; Bellamy CO; Ladomery M; Spraggon L; Mullins J; Hastie ND; Hooper ML
Hum Mol Genet; 2003 Sep; 12(18):2379-94. PubMed ID: 12915483
[TBL] [Abstract][Full Text] [Related]
3. [Clinical and pathological features of Denys-Drash syndrome: report of 3 cases].
Wang HY; Sun LZ; Yue ZH; Yang J; Jiang XY; Mo Y
Zhonghua Er Ke Za Zhi; 2012 Nov; 50(11):855-8. PubMed ID: 23302619
[TBL] [Abstract][Full Text] [Related]
4. WT1 and PAX-2 podocyte expression in Denys-Drash syndrome and isolated diffuse mesangial sclerosis.
Yang Y; Jeanpierre C; Dressler GR; Lacoste M; Niaudet P; Gubler MC
Am J Pathol; 1999 Jan; 154(1):181-92. PubMed ID: 9916932
[TBL] [Abstract][Full Text] [Related]
5. Denys-Drash syndrome with neonatal renal failure in monozygotic twins due to c.1097G>A mutation in the WT1 gene.
Furtado LV; Pysher T; Opitz J; Lamb R; Comstock J; Batish S; Mauch T; Nelson R; Zhou H
Fetal Pediatr Pathol; 2011; 30(4):266-72. PubMed ID: 21434831
[TBL] [Abstract][Full Text] [Related]
6. The dysregulated glomerular cell growth in Denys-Drash syndrome.
Yang AH; Chen JY; Chen BF
Virchows Arch; 2004 Sep; 445(3):305-14. PubMed ID: 15232745
[TBL] [Abstract][Full Text] [Related]
7. Impaired glomerular maturation and lack of VEGF165b in Denys-Drash syndrome.
Schumacher VA; Jeruschke S; Eitner F; Becker JU; Pitschke G; Ince Y; Miner JH; Leuschner I; Engers R; Everding AS; Bulla M; Royer-Pokora B
J Am Soc Nephrol; 2007 Mar; 18(3):719-29. PubMed ID: 17267748
[TBL] [Abstract][Full Text] [Related]
8. A review of the phenotypic variation due to the Denys-Drash syndrome-associated germline WT1 mutation R362X.
Heathcott RW; Morison IM; Gubler MC; Corbett R; Reeve AE
Hum Mutat; 2002 Apr; 19(4):462. PubMed ID: 11933209
[TBL] [Abstract][Full Text] [Related]
9. WT1 and glomerular diseases.
Niaudet P; Gubler MC
Pediatr Nephrol; 2006 Nov; 21(11):1653-60. PubMed ID: 16927106
[TBL] [Abstract][Full Text] [Related]
10. AJKD Atlas of Renal Pathology: Diffuse Mesangial Sclerosis.
Fogo AB; Lusco MA; Najafian B; Alpers CE
Am J Kidney Dis; 2015 Oct; 66(4):e23-4. PubMed ID: 26408240
[No Abstract] [Full Text] [Related]
11. A murine model of Denys-Drash syndrome reveals novel transcriptional targets of WT1 in podocytes.
Ratelade J; Arrondel C; Hamard G; Garbay S; Harvey S; Biebuyck N; Schulz H; Hastie N; Pontoglio M; Gubler MC; Antignac C; Heidet L
Hum Mol Genet; 2010 Jan; 19(1):1-15. PubMed ID: 19797313
[TBL] [Abstract][Full Text] [Related]
12. [A case of Denys-Drash syndrome with prophylactic bilateral nephrectomy].
Yamamoto K; Santo Y; Satomura K
Nihon Jinzo Gakkai Shi; 2003; 45(1):42-6. PubMed ID: 12680320
[TBL] [Abstract][Full Text] [Related]
13. Clinical pictures and novel mutations of WT1-associated Denys-Drash syndrome in two Chinese children.
Yue Z; Pei Y; Sun L; Huang W; Huang H; Hu B; Yang J; Jiang X; Mo Y; Chen S; Lai KN; Wang Y
Ren Fail; 2011; 33(9):910-4. PubMed ID: 21851196
[TBL] [Abstract][Full Text] [Related]
14. New insights into the function of the Wilms tumor suppressor gene WT1 in podocytes.
Morrison AA; Viney RL; Saleem MA; Ladomery MR
Am J Physiol Renal Physiol; 2008 Jul; 295(1):F12-7. PubMed ID: 18385267
[TBL] [Abstract][Full Text] [Related]
15. Embryonal hyperplasia of Bowman's capsular epithelium in patients with WT1 mutations.
Fukuzawa R; Eccles MR; Ikeda M; Hata J
Pediatr Nephrol; 2003 Jan; 18(1):9-13. PubMed ID: 12488983
[TBL] [Abstract][Full Text] [Related]
16. Novel WT1 mutation (C388Y) in a female child with Denys-Drash syndrome.
Swiatecka-Urban A; Mokrzycki MH; Kaskel F; Da Silva F; Denamur E
Pediatr Nephrol; 2001 Aug; 16(8):627-30. PubMed ID: 11519891
[TBL] [Abstract][Full Text] [Related]
17. A mutant form of the Wilms' tumor suppressor gene WT1 observed in Denys-Drash syndrome interferes with glomerular capillary development.
Natoli TA; Liu J; Eremina V; Hodgens K; Li C; Hamano Y; Mundel P; Kalluri R; Miner JH; Quaggin SE; Kreidberg JA
J Am Soc Nephrol; 2002 Aug; 13(8):2058-67. PubMed ID: 12138137
[TBL] [Abstract][Full Text] [Related]
18. Focal Segmental Membranoproliferative Glomerulonephritis: A Histological Variant of Denys-Drash Syndrome.
Karmila AB; Yap YC; Appadurai M; Oh L; Fazarina M; Abd Ghani F; Ariffin H
Fetal Pediatr Pathol; 2021 Apr; 40(2):113-120. PubMed ID: 31707902
[No Abstract] [Full Text] [Related]
19. Refining the Diagnosis of Congenital Nephrotic Syndrome on Long-term Stored Tissue: c.1097G>A (p.(Arg366His)) WT1 Mutation Causing Denys Drash Syndrome.
Hillen LM; Kamsteeg EJ; Schoots J; Tiebosch AT; Speel EJ; Roemen GM; Peutz-Koostra CJ; Stumpel CT
Fetal Pediatr Pathol; 2016; 35(2):112-9. PubMed ID: 26882358
[TBL] [Abstract][Full Text] [Related]
20. Glomerular sclerosis in kidneys with congenital nephrotic syndrome (NPHS1).
Kuusniemi AM; Merenmies J; Lahdenkari AT; Holmberg C; Salmela K; Karikoski R; Rapola J; Jalanko H
Kidney Int; 2006 Oct; 70(8):1423-31. PubMed ID: 16941028
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]