Nissinen M - Search Results

1

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: nissinen m. Mol Cell. 1998 Mar;1(4):575-82. doi: 10.1016/s1097-2765(00)80057-x. Mol Cell. 1998. PMID: 9660941 Free article.

2

Human laminin M chain (merosin): complete primary structure, chromosomal assignment, and expression of the M and A chain in human fetal tissues.

Vuolteenaho R, Nissinen M, Sainio K, Byers M, Eddy R, Hirvonen H, Shows TB, Sariola H, Engvall E, Tryggvason K. Vuolteenaho R, et al. Among authors: nissinen m. J Cell Biol. 1994 Feb;124(3):381-94. doi: 10.1083/jcb.124.3.381. J Cell Biol. 1994. PMID: 8294519 Free PMC article.

3

Primary structure of the human laminin A chain. Limited expression in human tissues.

Nissinen M, Vuolteenaho R, Boot-Handford R, Kallunki P, Tryggvason K. Nissinen M, et al. Biochem J. 1991 Jun 1;276 ( Pt 2)(Pt 2):369-79. doi: 10.1042/bj2760369. Biochem J. 1991. PMID: 2049067 Free PMC article.

4

Substitution of a conserved cysteine-996 in a cysteine-rich motif of the laminin alpha2-chain in congenital muscular dystrophy with partial deficiency of the protein.

Nissinen M, Helbling-Leclerc A, Zhang X, Evangelista T, Topaloglu H, Cruaud C, Weissenbach J, Fardeau M, Tomé FM, Schwartz K, Tryggvason K, Guicheney P. Nissinen M, et al. Am J Hum Genet. 1996 Jun;58(6):1177-84. Am J Hum Genet. 1996. PMID: 8651294 Free PMC article.

5

Genetics of laminin alpha 2 chain (or merosin) deficient congenital muscular dystrophy: from identification of mutations to prenatal diagnosis.

Guicheney P, Vignier N, Helbling-Leclerc A, Nissinen M, Zhang X, Cruaud C, Lambert JC, Richelme C, Topaloglu H, Merlini L, Barois A, Schwartz K, Tomé FM, Tryggvason K, Fardeau M. Guicheney P, et al. Among authors: nissinen m. Neuromuscul Disord. 1997 May;7(3):180-6. doi: 10.1016/s0960-8966(97)00460-4. Neuromuscul Disord. 1997. PMID: 9185182

6

Distribution of histamine in the rat kidney during pregnancy and development.

Nissinen MJ, Castrèn E, Holthöfer H, Panula P. Nissinen MJ, et al. Cell Tissue Res. 1992 Feb;267(2):233-9. doi: 10.1007/BF00302960. Cell Tissue Res. 1992. PMID: 1600560

7

Congenital pseudarthrosis of neurofibromatosis type 1: impaired osteoblast differentiation and function and altered NF1 gene expression.

Leskelä HV, Kuorilehto T, Risteli J, Koivunen J, Nissinen M, Peltonen S, Kinnunen P, Messiaen L, Lehenkari P, Peltonen J. Leskelä HV, et al. Among authors: nissinen m. Bone. 2009 Feb;44(2):243-50. doi: 10.1016/j.bone.2008.10.050. Epub 2008 Nov 12. Bone. 2009. PMID: 19061981

8

Neurofibromatosis type 1 tumour suppressor gene expression is deficient in psoriatic skin in vivo and in vitro: a potential link to increased Ras activity.

Karvonen SL, Koivunen J, Nissinen M, Ylä-Outinen H, Björkstrand AS, Peltonen J. Karvonen SL, et al. Among authors: nissinen m. Br J Dermatol. 2004 Feb;150(2):211-9. doi: 10.1111/j.1365-2133.2004.05767.x. Br J Dermatol. 2004. PMID: 14996090

9

Influenza virus infection in multinucleated skeletal myofibers.

Nevalainen M, Nissinen M, Kaakinen M, Metsikkö K. Nevalainen M, et al. Among authors: nissinen m. Exp Cell Res. 2010 Jul 1;316(11):1784-94. doi: 10.1016/j.yexcr.2010.03.020. Epub 2010 Apr 1. Exp Cell Res. 2010. PMID: 20362571

10

NF1 tumor suppressor protein and mRNA in skeletal tissues of developing and adult normal mouse and NF1-deficient embryos.

Kuorilehto T, Nissinen M, Koivunen J, Benson MD, Peltonen J. Kuorilehto T, et al. Among authors: nissinen m. J Bone Miner Res. 2004 Jun;19(6):983-9. doi: 10.1359/JBMR.040130. Epub 2004 Jan 27. J Bone Miner Res. 2004. PMID: 15125795 Free article.

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