Saarialho-Kere U - Search Results

1

Transglutaminase 1 mutations in autosomal recessive congenital ichthyosis: private and recurrent mutations in an isolated population.

Laiho E, Ignatius J, Mikkola H, Yee VC, Teller DC, Niemi KM, Saarialho-Kere U, Kere J, Palotie A. Laiho E, et al. Am J Hum Genet. 1997 Sep;61(3):529-38. doi: 10.1086/515498. Am J Hum Genet. 1997. PMID: 9326318 Free PMC article.

2

Clinical and morphological correlations for transglutaminase 1 gene mutations in autosomal recessive congenital ichthyosis.

Laiho E, Niemi KM, Ignatius J, Kere J, Palotie A, Saarialho-Kere U. Laiho E, et al. Eur J Hum Genet. 1999 Sep;7(6):625-32. doi: 10.1038/sj.ejhg.5200353. Eur J Hum Genet. 1999. PMID: 10482949

3

Ultrastructural features resembling those of harlequin ichthyosis in patients with severe congenital ichthyosiform erythroderma.

Virolainen E, Niemi KM, Gånemo A, Kere J, Vahlquist A, Saarialho-Kere U. Virolainen E, et al. Br J Dermatol. 2001 Sep;145(3):480-3. doi: 10.1046/j.1365-2133.2001.04401.x. Br J Dermatol. 2001. PMID: 11531841

4

Mutations of the Down-regulated in adenoma (DRA) gene cause congenital chloride diarrhoea.

Höglund P, Haila S, Socha J, Tomaszewski L, Saarialho-Kere U, Karjalainen-Lindsberg ML, Airola K, Holmberg C, de la Chapelle A, Kere J. Höglund P, et al. Nat Genet. 1996 Nov;14(3):316-9. doi: 10.1038/ng1196-316. Nat Genet. 1996. PMID: 8896562

5

A candidate gene for psoriasis near HLA-C, HCR (Pg8), is highly polymorphic with a disease-associated susceptibility allele.

Asumalahti K, Laitinen T, Itkonen-Vatjus R, Lokki ML, Suomela S, Snellman E, Saarialho-Kere U, Kere J. Asumalahti K, et al. Hum Mol Genet. 2000 Jun 12;9(10):1533-42. doi: 10.1093/hmg/9.10.1533. Hum Mol Genet. 2000. PMID: 10888604

6

Ectodysplasin is released by proteolytic shedding and binds to the EDAR protein.

Elomaa O, Pulkkinen K, Hannelius U, Mikkola M, Saarialho-Kere U, Kere J. Elomaa O, et al. Hum Mol Genet. 2001 Apr 15;10(9):953-62. doi: 10.1093/hmg/10.9.953. Hum Mol Genet. 2001. PMID: 11309369

7

Coding haplotype analysis supports HCR as the putative susceptibility gene for psoriasis at the MHC PSORS1 locus.

Asumalahti K, Veal C, Laitinen T, Suomela S, Allen M, Elomaa O, Moser M, de Cid R, Ripatti S, Vorechovsky I, Marcusson JA, Nakagawa H, Lazaro C, Estivill X, Capon F, Novelli G, Saarialho-Kere U, Barker J, Trembath R, Kere J; Psoriasis Consortium. Asumalahti K, et al. Hum Mol Genet. 2002 Mar 1;11(5):589-97. doi: 10.1093/hmg/11.5.589. Hum Mol Genet. 2002. PMID: 11875053

8

Transgenic mouse models support HCR as an effector gene in the PSORS1 locus.

Elomaa O, Majuri I, Suomela S, Asumalahti K, Jiao H, Mirzaei Z, Rozell B, Dahlman-Wright K, Pispa J, Kere J, Saarialho-Kere U. Elomaa O, et al. Hum Mol Genet. 2004 Aug 1;13(15):1551-61. doi: 10.1093/hmg/ddh178. Epub 2004 Jun 9. Hum Mol Genet. 2004. PMID: 15190014

9

Interstitial collagenase is expressed by keratinocytes that are actively involved in reepithelialization in blistering skin disease.

Saarialho-Kere UK, Vaalamo M, Airola K, Niemi KM, Oikarinen AI, Parks WC. Saarialho-Kere UK, et al. J Invest Dermatol. 1995 Jun;104(6):982-8. doi: 10.1111/1523-1747.ep12606231. J Invest Dermatol. 1995. PMID: 7539470 Free article.

10

Downstream target genes of the neuropeptide S-NPSR1 pathway.

Vendelin J, Bruce S, Holopainen P, Pulkkinen V, Rytilä P, Pirskanen A, Rehn M, Laitinen T, Laitinen LA, Haahtela T, Saarialho-Kere U, Laitinen A, Kere J. Vendelin J, et al. Hum Mol Genet. 2006 Oct 1;15(19):2923-35. doi: 10.1093/hmg/ddl234. Epub 2006 Aug 22. Hum Mol Genet. 2006. PMID: 16926187

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