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Nephrotic syndrome in the first year of life: two thirds of cases are caused by mutations in 4 genes (NPHS1, NPHS2, WT1, and LAMB2).

Hinkes BG, Mucha B, Vlangos CN, Gbadegesin R, Liu J, Hasselbacher K, Hangan D, Ozaltin F, Zenker M, Hildebrandt F; Arbeitsgemeinschaft für Paediatrische Nephrologie Study Group.

Pediatrics. 2007 Apr;119(4):e907-19. Epub 2007 Mar 19.


Recessive missense mutations in LAMB2 expand the clinical spectrum of LAMB2-associated disorders.

Hasselbacher K, Wiggins RC, Matejas V, Hinkes BG, Mucha B, Hoskins BE, Ozaltin F, Nürnberg G, Becker C, Hangan D, Pohl M, Kuwertz-Bröking E, Griebel M, Schumacher V, Royer-Pokora B, Bakkaloglu A, Nürnberg P, Zenker M, Hildebrandt F.

Kidney Int. 2006 Sep;70(6):1008-12. Epub 2006 Aug 16.


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. 2006 Feb;59(2):325-31.


Modulation of in vivo migratory function of alpha 2 beta 1 integrin in mouse liver.

Ho WC, Heinemann C, Hangan D, Uniyal S, Morris VL, Chan BM.

Mol Biol Cell. 1997 Oct;8(10):1863-75.


An epitope on VLA-6 (alpha6beta1) integrin involved in migration but not adhesion is required for extravasation of murine melanoma B16F1 cells in liver.

Hangan D, Morris VL, Boeters L, von Ballestrem C, Uniyal S, Chan BM.

Cancer Res. 1997 Sep 1;57(17):3812-7.


Integrin VLA-2 (alpha2beta1) function in postextravasation movement of human rhabdomyosarcoma RD cells in the liver.

Hangan D, Uniyal S, Morris VL, MacDonald IC, von Ballestrem C, Chau T, Schmidt EE, Chambers AF, Groom AC, Chan BM.

Cancer Res. 1996 Jul 1;56(13):3142-9.

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