Männikkö M - Search Results

1

Congenital nephrotic syndrome of the Finnish type maps to the long arm of chromosome 19.

Kestilä M, Männikkö M, Holmberg C, Gyapay G, Weissenbach J, Savolainen ER, Peltonen L, Tryggvason K. Kestilä M, et al. Among authors: mannikko m. Am J Hum Genet. 1994 May;54(5):757-64. Am J Hum Genet. 1994. PMID: 8178817 Free PMC article.

2

The collagen V homotrimer [alpha1(V)](3) production is unexpectedly favored over the heterotrimer [alpha1(V)](2)alpha2(V) in recombinant expression systems.

Roulet M, Välkkilä M, Chanut-Delalande H, Hämäläinen ER, Kessler E, Ala-Kokko L, Männikkö M, Bonod-Bidaud C, Ruggiero F. Roulet M, et al. Among authors: mannikko m. J Biomed Biotechnol. 2010;2010:376927. doi: 10.1155/2010/376927. Epub 2010 Jun 27. J Biomed Biotechnol. 2010. PMID: 20625483 Free PMC article.

3

Exclusion of eight genes as mutated loci in congenital nephrotic syndrome of the Finnish type.

Kestilä M, Männikkö M, Holmberg C, Korpela K, Savolainen ER, Peltonen L, Tryggvason K. Kestilä M, et al. Among authors: mannikko m. Kidney Int. 1994 Apr;45(4):986-90. doi: 10.1038/ki.1994.133. Kidney Int. 1994. PMID: 8007602 Free article.

4

Congenital nephrotic syndrome of the Finnish type is not associated with the Pax-2 gene despite the promising transgenic animal model.

Kestilä M, Männikkö M, Holmberg C, Tryggvason K, Peltonen L. Kestilä M, et al. Among authors: mannikko m. Genomics. 1994 Feb;19(3):570-2. doi: 10.1006/geno.1994.1109. Genomics. 1994. PMID: 8188301

5

Fine mapping and haplotype analysis of the locus for congenital nephrotic syndrome on chromosome 19q13.1.

Männikkö M, Kestailä M, Holmberg C, Norio R, Ryynänen M, Olsen A, Peltonen L, Tryggvason K. Männikkö M, et al. Am J Hum Genet. 1995 Dec;57(6):1377-83. Am J Hum Genet. 1995. PMID: 8533767 Free PMC article.

6

Haplotype analysis of congenital nephrotic syndrome of the Finnish type in non-Finnish families.

Männikkö M, Lenkkeri U, Kashtan CE, Kestilä M, Holmberg C, Tryggvason K. Männikkö M, et al. J Am Soc Nephrol. 1996 Dec;7(12):2700-3. doi: 10.1681/ASN.V7122700. J Am Soc Nephrol. 1996. PMID: 8989752

7

Improved prenatal diagnosis of the congenital nephrotic syndrome of the Finnish type based on DNA analysis.

Männikkö M, Kestilä M, Lenkkeri U, Alakurtti H, Holmberg C, Leisti J, Salonen R, Aula P, Mustonen A, Peltonen L, Tryggvason K. Männikkö M, et al. Kidney Int. 1997 Mar;51(3):868-72. doi: 10.1038/ki.1997.122. Kidney Int. 1997. PMID: 9067923 Free article.

8

Positionally cloned gene for a novel glomerular protein--nephrin--is mutated in congenital nephrotic syndrome.

Kestilä M, Lenkkeri U, Männikkö M, Lamerdin J, McCready P, Putaala H, Ruotsalainen V, Morita T, Nissinen M, Herva R, Kashtan CE, Peltonen L, Holmberg C, Olsen A, Tryggvason K. Kestilä M, et al. Among authors: mannikko m. Mol Cell. 1998 Mar;1(4):575-82. doi: 10.1016/s1097-2765(00)80057-x. Mol Cell. 1998. PMID: 9660941 Free article.

9

Structure of the gene for congenital nephrotic syndrome of the finnish type (NPHS1) and characterization of mutations.

Lenkkeri U, Männikkö M, McCready P, Lamerdin J, Gribouval O, Niaudet PM, Antignac C K, Kashtan CE, Homberg C, Olsen A, Kestilä M, Tryggvason K. Lenkkeri U, et al. Among authors: mannikko m. Am J Hum Genet. 1999 Jan;64(1):51-61. doi: 10.1086/302182. Am J Hum Genet. 1999. PMID: 9915943 Free PMC article.

10

Congenital nephrotic syndrome (NPHS1): features resulting from different mutations in Finnish patients.

Patrakka J, Kestilä M, Wartiovaara J, Ruotsalainen V, Tissari P, Lenkkeri U, Männikkö M, Visapää I, Holmberg C, Rapola J, Tryggvason K, Jalanko H. Patrakka J, et al. Among authors: mannikko m. Kidney Int. 2000 Sep;58(3):972-80. doi: 10.1046/j.1523-1755.2000.00254.x. Kidney Int. 2000. PMID: 10972661 Free article.

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