Nieminen P - Search Results

1

Regulation of hair follicle development by the TNF signal ectodysplasin and its receptor Edar.

Laurikkala J, Pispa J, Jung HS, Nieminen P, Mikkola M, Wang X, Saarialho-Kere U, Galceran J, Grosschedl R, Thesleff I. Laurikkala J, et al. Among authors: nieminen p. Development. 2002 May;129(10):2541-53. doi: 10.1242/dev.129.10.2541. Development. 2002. PMID: 11973284

2

Ectodysplasin, a protein required for epithelial morphogenesis, is a novel TNF homologue and promotes cell-matrix adhesion.

Mikkola ML, Pispa J, Pekkanen M, Paulin L, Nieminen P, Kere J, Thesleff I. Mikkola ML, et al. Among authors: nieminen p. Mech Dev. 1999 Nov;88(2):133-46. doi: 10.1016/s0925-4773(99)00180-x. Mech Dev. 1999. PMID: 10534613 Free article.

3

TNF signaling via the ligand-receptor pair ectodysplasin and edar controls the function of epithelial signaling centers and is regulated by Wnt and activin during tooth organogenesis.

Laurikkala J, Mikkola M, Mustonen T, Aberg T, Koppinen P, Pispa J, Nieminen P, Galceran J, Grosschedl R, Thesleff I. Laurikkala J, et al. Among authors: nieminen p. Dev Biol. 2001 Jan 15;229(2):443-55. doi: 10.1006/dbio.2000.9955. Dev Biol. 2001. PMID: 11203701 Free article.

4

Tooth morphogenesis and cell differentiation.

Thesleff I, Nieminen P. Thesleff I, et al. Among authors: nieminen p. Curr Opin Cell Biol. 1996 Dec;8(6):844-50. doi: 10.1016/s0955-0674(96)80086-x. Curr Opin Cell Biol. 1996. PMID: 8939666 Review.

5

Mutations in AXIN2 cause familial tooth agenesis and predispose to colorectal cancer.

Lammi L, Arte S, Somer M, Jarvinen H, Lahermo P, Thesleff I, Pirinen S, Nieminen P. Lammi L, et al. Among authors: nieminen p. Am J Hum Genet. 2004 May;74(5):1043-50. doi: 10.1086/386293. Epub 2004 Mar 23. Am J Hum Genet. 2004. PMID: 15042511 Free PMC article.

6

A missense mutation in PAX9 in a family with distinct phenotype of oligodontia.

Lammi L, Halonen K, Pirinen S, Thesleff I, Arte S, Nieminen P. Lammi L, et al. Among authors: nieminen p. Eur J Hum Genet. 2003 Nov;11(11):866-71. doi: 10.1038/sj.ejhg.5201060. Eur J Hum Genet. 2003. PMID: 14571272

7

Inactivation of IL11 signaling causes craniosynostosis, delayed tooth eruption, and supernumerary teeth.

Nieminen P, Morgan NV, Fenwick AL, Parmanen S, Veistinen L, Mikkola ML, van der Spek PJ, Giraud A, Judd L, Arte S, Brueton LA, Wall SA, Mathijssen IM, Maher ER, Wilkie AO, Kreiborg S, Thesleff I. Nieminen P, et al. Am J Hum Genet. 2011 Jul 15;89(1):67-81. doi: 10.1016/j.ajhg.2011.05.024. Am J Hum Genet. 2011. PMID: 21741611 Free PMC article.

8

Gene defect in hypodontia: exclusion of MSX1 and MSX2 as candidate genes.

Nieminen P, Arte S, Pirinen S, Peltonen L, Thesleff I. Nieminen P, et al. Hum Genet. 1995 Sep;96(3):305-8. doi: 10.1007/BF00210412. Hum Genet. 1995. PMID: 7649547

9

A graphical WWW-database on gene expression in tooth.

Nieminen P, Pekkanen M, Aberg T, Thesleff I. Nieminen P, et al. Eur J Oral Sci. 1998 Jan;106 Suppl 1:7-11. doi: 10.1111/j.1600-0722.1998.tb02146.x. Eur J Oral Sci. 1998. PMID: 9541196

10

Identification of a nonsense mutation in the PAX9 gene in molar oligodontia.

Nieminen P, Arte S, Tanner D, Paulin L, Alaluusua S, Thesleff I, Pirinen S. Nieminen P, et al. Eur J Hum Genet. 2001 Oct;9(10):743-6. doi: 10.1038/sj.ejhg.5200715. Eur J Hum Genet. 2001. PMID: 11781684

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