Congenital focal segmental glomerulosclerosis associated with β4 integrin mutation and epidermolysis bullosa

Positionally Cloned Gene for a Novel Glomerular Protein—Nephrin—Is Mutated in Congenital Nephrotic Syndrome

Marjo Kestilä, Ulla Lenkkeri, Minna Männikkö et al. · Molecular Cell · 1998 · 1.9K citations · Full text

Medicine, Genetics, Molecular Genetics +12

Mutations in ACTN4, encoding α-actinin-4, cause familial focal segmental glomerulosclerosis

Joshua M. Kaplan, Sung Hyun Kim, Kathryn N. North et al. · Nature Genetics · 2000 · 1.2K citations

Medicine, Genetics, Molecular Genetics +12

Alpha 3 beta 1 integrin has a crucial role in kidney and lung organogenesis

Jordan A. Kreidberg, Michael J. Donovan, Stuart L. Goldstein et al. · Development · 1996 · 718 citations

Life Sciences, Developmental Biology, Genetics +17

α3β1 Integrin Is Required for Normal Development of the Epidermal Basement Membrane

C. Michael DiPersio, Kairbaan Hodivala‐Dilke, Rudolf Jaenisch et al. · The Journal of Cell Biology · 1997 · 409 citations · Full text

Life Sciences, Cell Biology, Developmental Biology +17

Structure of the Gene for Congenital Nephrotic Syndrome of the Finnish Type (NPHS1) and Characterization of Mutations

Ulla Lenkkeri, Minna Männikkö, Paula McCready et al. · The American Journal of Human Genetics · 1999 · 402 citations · Full text

Medicine, Genetics, Molecular Genetics +14