Kere J - Search Results

1

Assessment of the neuropeptide S system in anxiety disorders.

Donner J, Haapakoski R, Ezer S, Melén E, Pirkola S, Gratacòs M, Zucchelli M, Anedda F, Johansson LE, Söderhäll C, Orsmark-Pietras C, Suvisaari J, Martín-Santos R, Torrens M, Silander K, Terwilliger JD, Wickman M, Pershagen G, Lönnqvist J, Peltonen L, Estivill X, D'Amato M, Kere J, Alenius H, Hovatta I. Donner J, et al. Among authors: kere j. Biol Psychiatry. 2010 Sep 1;68(5):474-83. doi: 10.1016/j.biopsych.2010.05.039. Biol Psychiatry. 2010. PMID: 20705147

2

Cystic fibrosis mutation delta F508 in Finland: other mutations predominate.

Kere J, Savilahti E, Norio R, Estivill X, de la Chapelle A. Kere J, et al. Hum Genet. 1990 Sep;85(4):413-5. doi: 10.1007/BF02428286. Hum Genet. 1990. PMID: 2210753

3

Cystic fibrosis in Finland: a molecular and genealogical study.

Kere J, Norio R, Savilahti E, Estivill X, de la Chapelle A. Kere J, et al. Hum Genet. 1989 Aug;83(1):20-5. doi: 10.1007/BF00274141. Hum Genet. 1989. PMID: 2570015

4

Anhidrotic ectodermal dysplasia (EDA) protein expressed in MCF-7 cells associates with cell membrane and induces rounding.

Ezer S, Schlessinger D, Srivastava A, Kere J. Ezer S, et al. Among authors: kere j. Hum Mol Genet. 1997 Sep;6(9):1581-7. doi: 10.1093/hmg/6.9.1581. Hum Mol Genet. 1997. PMID: 9285797

5

The anhidrotic ectodermal dysplasia gene (EDA) undergoes alternative splicing and encodes ectodysplasin-A with deletion mutations in collagenous repeats.

Bayés M, Hartung AJ, Ezer S, Pispa J, Thesleff I, Srivastava AK, Kere J. Bayés M, et al. Among authors: kere j. Hum Mol Genet. 1998 Oct;7(11):1661-9. doi: 10.1093/hmg/7.11.1661. Hum Mol Genet. 1998. PMID: 9736768

6

Expression of the anhidrotic ectodermal dysplasia gene is reduced in skin cancer coinciding with reduced E-cadherin.

Montonen O, Ezer S, Laurikkala J, Karjalainen-Lindsberg ML, Thesleff I, Kere J, Saarialho-Kere U. Montonen O, et al. Among authors: kere j. Exp Dermatol. 1998 Aug;7(4):168-74. doi: 10.1111/j.1600-0625.1998.tb00319.x. Exp Dermatol. 1998. PMID: 9758413

7

Assignment of a novel locus for autosomal recessive congenital ichthyosis to chromosome 19p13.1-p13.2.

Virolainen E, Wessman M, Hovatta I, Niemi KM, Ignatius J, Kere J, Peltonen L, Palotie A. Virolainen E, et al. Among authors: kere j. Am J Hum Genet. 2000 Mar;66(3):1132-7. doi: 10.1086/302813. Am J Hum Genet. 2000. PMID: 10712223 Free PMC article.

8

Association study of the chromosomal region containing the FCER2 gene suggests it has a regulatory role in atopic disorders.

Laitinen T, Ollikainen V, Lázaro C, Kauppi P, de Cid R, Antó JM, Estivill X, Lokki H, Mannila H, Laitinen LA, Kere J. Laitinen T, et al. Among authors: kere j. Am J Respir Crit Care Med. 2000 Mar;161(3 Pt 1):700-6. doi: 10.1164/ajrccm.161.3.9810056. Am J Respir Crit Care Med. 2000. PMID: 10712310

9

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. Among authors: kere j. Hum Mol Genet. 2002 Mar 1;11(5):589-97. doi: 10.1093/hmg/11.5.589. Hum Mol Genet. 2002. PMID: 11875053

10

Characterization of a common susceptibility locus for asthma-related traits.

Laitinen T, Polvi A, Rydman P, Vendelin J, Pulkkinen V, Salmikangas P, Mäkelä S, Rehn M, Pirskanen A, Rautanen A, Zucchelli M, Gullstén H, Leino M, Alenius H, Petäys T, Haahtela T, Laitinen A, Laprise C, Hudson TJ, Laitinen LA, Kere J. Laitinen T, et al. Among authors: kere j. Science. 2004 Apr 9;304(5668):300-4. doi: 10.1126/science.1090010. Science. 2004. PMID: 15073379

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