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a<sub>2</sub>-Heremans-Schmid glycoprotein gene polymorphisms are associated with adipocyte insulin action.
Published in:
Diabetologia, 2004, v. 47, n. 11, p. 1974, doi. 10.1007/s00125-004-1556-7
By:
- Dahlman, I.;
- Eriksson, P.;
- Kaaman, M.;
- Jiao, H.;
- Lindgren, C.M.;
- Kere, J.;
- Arner, P.
Publication type:
Article
Evidence of streptococcal origin of acute non-necrotising cellulitis: a serological study.
Published in:
European Journal of Clinical Microbiology & Infectious Diseases, 2015, v. 34, n. 4, p. 669, doi. 10.1007/s10096-014-2274-9
By:
- Karppelin, M.;
- Siljander, T.;
- Haapala, A.-M.;
- Aittoniemi, J.;
- Huttunen, R.;
- Kere, J.;
- Vuopio, J.;
- Syrjänen, J.
Publication type:
Article
Recurrent cellulitis with benzathine penicillin prophylaxis is associated with diabetes and psoriasis.
Published in:
European Journal of Clinical Microbiology & Infectious Diseases, 2013, v. 32, n. 3, p. 369, doi. 10.1007/s10096-012-1751-2
By:
- Karppelin, M.;
- Siljander, T.;
- Huhtala, H.;
- Aromaa, A.;
- Vuopio, J.;
- Hannula-Jouppi, K.;
- Kere, J.;
- Syrjänen, J.
Publication type:
Article
Study of Estrogen Receptor-[alpha] and Receptor-[beta] Gene Polymorphisms on Alzheimer's Disease.
Published in:
2011
By:
- Goumidi L;
- Dahlman-Wright K;
- Tapia-Paez I;
- Matsson H;
- Pasquier F;
- Amouyel P;
- Kere J;
- Lambert JC;
- Meirhaeghe A
Publication type:
Journal Article
Mechanisms of inactivation of MLH1 in hereditary nonpolyposis colorectal carcinoma: a novel approach.
Published in:
Oncogene, 2007, v. 26, n. 31, p. 4541, doi. 10.1038/sj.onc.1210236
By:
- Ollikainen, M.;
- Hannelius, U.;
- Lindgren, C. M.;
- Abdel-Rahman, W. M.;
- Kere, J.;
- Peltomäki, P.
Publication type:
Article
ROCK2 allelic variants are not associated with pre-eclampsia susceptibility in the Finnish population.
Published in:
Molecular Human Reproduction, 2009, v. 15, n. 7, p. 443, doi. 10.1093/molehr/gap032
By:
- Peterson, H.;
- Laivuori, H.;
- Kerkelä, E.;
- Jiao, H.;
- Hiltunen, L.;
- Heino, S.;
- Tiala, I.;
- Knuutila, S.;
- Rasi, V.;
- Kere, J.;
- Kivinen, K.
Publication type:
Article
Expression of SLC26A3, CFTR and NHE3 in the human male reproductive tract: role in male subfertility caused by congenital chloride diarrhoea.
Published in:
Molecular Human Reproduction, 2006, v. 12, n. 2, p. 107, doi. 10.1093/molehr/gal009
By:
- Hihnala, S.;
- Kujala, M.;
- Toppari, J.;
- Kere, J.;
- Holmberg, C.;
- Höglund, P.
Publication type:
Article
Mutational analysis of the human SLC26A8 gene: exclusion as a candidate for male infertility due to primary spermatogenic failure.
Published in:
Molecular Human Reproduction, 2005, v. 11, n. 2, p. 129
By:
- Mäkelä, S.;
- Eklund, R.;
- Lähdetie, J.;
- Mikkola, M.;
- Hovatta, O.;
- Kere, J.
Publication type:
Article
The role of inflammatory bowel disease susceptibility loci in multiple sclerosis and systemic lupus erythematosus.
Published in:
Genes & Immunity, 2006, v. 7, n. 4, p. 327, doi. 10.1038/sj.gene.6364303
By:
- De Jager, P. L.;
- Graham, R.;
- Farwell, L.;
- Sawcer, S.;
- Richardson, A.;
- Behrens, T. W.;
- Compston, A.;
- Hafler, D. A.;
- Kere, J.;
- Vyse, T. J.;
- Rioux, J. D.
Publication type:
Article
Expression of the anhidrotic ectodermal dysplasia gene is reduced in skin cancer coinciding with reduced E-cadherin.
Published in:
Experimental Dermatology, 1998, v. 7, n. 4, p. 168, doi. 10.1111/j.1600-0625.1998.tb00319.x
By:
- Montonen, O.;
- Ezer, S.;
- Laurikkala, J.;
- Karjalainen-Lindsberg, M.-L.;
- Thesleff, I.;
- Kere, J.;
- Saarialho-Kere, U.
Publication type:
Article
Evidence for two molecular steps in the pathogenesis of myeloid disorders associated with deletion of chromosome 7 long arm.
Published in:
1997
By:
- Kiuru-Kuhlefelt, S;
- Kristo, P;
- Ruutu, T;
- Knuutila, S;
- Kere, J
Publication type:
journal article
Association and Mutation Analyses of the IRF6 Gene in Families With Nonsyndromic and Syndromic Cleft Lip and/or Cleft Palate.
Published in:
Cleft Palate Craniofacial Journal, 2014, v. 51, n. 1, p. 49, doi. 10.1597/11-220
By:
- Pegelow, M.;
- Koillinen, H.;
- Magnusson, M.;
- Fransson, I.;
- Unneberg, P.;
- Kere, J.;
- Karsten, A.;
- Peyrard-Janvid, M.
Publication type:
Article
EVALUATION OF CELIAC DISEASE RISK MARKERS IN A FOUNDER POPULATION.
Published in:
Journal of Pediatric Gastroenterology & Nutrition, 1999, v. 28, n. 5, p. 557
By:
- Holopainen, P.;
- Ollikainen, V.;
- Klinger, N.;
- Mustalahti, K.;
- Mäki, M.;
- Kere, J.;
- Partanen, J.
Publication type:
Article
Single-cell transcriptome analysis of endometrial tissue.
Published in:
2016
By:
- Krjutškov, K.;
- Katayama, S.;
- Saare, M.;
- Vera-Rodriguez, M.;
- Lubenets, D.;
- Samuel, K.;
- Laisk-Podar, T.;
- Teder, H.;
- Einarsdottir, E.;
- Salumets, A.;
- Kere, J.
Publication type:
journal article
Molecular genetic and epigenetic analysis of NCX2/ SLC8A2 at 19q13.3 in human gliomas.
Published in:
Neuropathology & Applied Neurobiology, 2010, v. 36, n. 3, p. 198, doi. 10.1111/j.1365-2990.2010.01070.x
By:
- Qu, M.;
- Jiao, H.;
- Zhao, J.;
- Ren, Z.-P.;
- Smits, A.;
- Kere, J.;
- Nistér, M.
Publication type:
Article
Concomitant DNA copy number amplification at 17q and 22q in dermatofibrosarcoma protuberans.
Published in:
Cytogenetics & Cell Genetics, 2001, v. 92, n. 3/4, p. 192, doi. 10.1159/000056901
By:
- Kiuru-Kuhlefelt, S.;
- El-Rifai, W.;
- Fanburg-Smith, J.;
- Kere, J.;
- Miettinen, M.;
- Knuutila, S.
Publication type:
Article
Population Structure in Contemporary Sweden—A Y-Chromosomal and Mitochondrial DNA Analysis.
Published in:
Annals of Human Genetics, 2009, v. 73, n. 1, p. 61, doi. 10.1111/j.1469-1809.2008.00487.x
By:
- Lappalainen, T.;
- Hannelius, U.;
- Salmela, E.;
- von Döbeln, U.;
- Lindgren, C. M.;
- Huoponen, K.;
- Savontaus, M.-L.;
- Kere, J.;
- Lahermo, P.
Publication type:
Article
Founder effects facilitate the use of a genotyping‐based approach to molecular diagnosis in Swedish patients with familial hypercholesterolaemia.
Published in:
Journal of Internal Medicine, 2021, v. 290, n. 2, p. 404, doi. 10.1111/joim.13287
By:
- Benedek, P.;
- Jiao, H.;
- Duvefelt, K.;
- Skoog, T.;
- Linde, M.;
- Kiviluoma, P.;
- Kere, J.;
- Eriksson, M.;
- Angelin, B.
Publication type:
Article
Reactive oxygen species of neutrophils from patients with monosomy 7 in the bone marrow: Contradictory chemiluminescence activity by whole blood or by purified cells.
Published in:
European Journal of Haematology, 1994, v. 52, n. 1, p. 28, doi. 10.1111/j.1600-0609.1994.tb01281.x
By:
- Ristola, M.;
- Kere, J.;
- Ruutu, T.;
- Repo, H.
Publication type:
Article
Enrichment of rare copy number variation in children with developmental language disorder.
Published in:
Clinical Genetics, 2018, v. 94, n. 3/4, p. 313, doi. 10.1111/cge.13389
By:
- Kalnak, N.;
- Stamouli, S.;
- Peyrard‐Janvid, M.;
- Rabkina, I.;
- Becker, M.;
- Klingberg, T.;
- Kere, J.;
- Forssberg, H.;
- Tammimies, K.
Publication type:
Article
NPSR1 polymorphisms influence recurrent abdominal pain in children: a population-based study.
Published in:
Neurogastroenterology & Motility, 2014, v. 26, n. 10, p. 1417, doi. 10.1111/nmo.12401
By:
- Henström, M.;
- Zucchelli, M.;
- Söderhäll, C.;
- Bergström, A.;
- Kere, J.;
- Melén, E.;
- Olén, O.;
- D'Amato, M.
Publication type:
Article
Neuropeptide S receptor 1 expression in the intestine and skin – putative role in peptide hormone secretion.
Published in:
Neurogastroenterology & Motility, 2010, v. 22, n. 1, p. 79, doi. 10.1111/j.1365-2982.2009.01366.x
By:
- SUNDMAN, L.;
- SAARIALHO-KERE, U.;
- VENDELIN, J.;
- LINDFORS, K.;
- ASSADI, G.;
- KAUKINEN, K.;
- WESTERHOLM-ORMIO, M.;
- SAVILAHTI, E.;
- MÄKI, M.;
- ALENIUS, H.;
- D'AMATO, M.;
- PULKKINEN, V.;
- KERE, J.;
- SAAVALAINEN, P.
Publication type:
Article
Azacitidine induces profound genome-wide hypomethylation in primary myelodysplastic bone marrow cultures but may also reduce histone acetylation.
Published in:
Leukemia (08876924), 2014, v. 28, n. 2, p. 411, doi. 10.1038/leu.2013.265
By:
- Grövdal, M;
- Karimi, M;
- Tobiasson, M;
- Reinius, L;
- Jansson, M;
- Ekwall, K;
- Ungerstedt, J;
- Kere, J;
- Greco, D;
- Hellström-Lindberg, E
Publication type:
Article
A novel SERPINA12 variant and first European patients with diffuse palmoplantar keratoderma.
Published in:
Journal of the European Academy of Dermatology & Venereology, 2024, v. 38, n. 2, p. 413, doi. 10.1111/jdv.19498
By:
- Brandt, E.;
- Harjama, L.;
- Elomaa, O.;
- Saarela, J.;
- Donner, K.;
- Lappalainen, K.;
- Kivirikko, S.;
- Ranki, A.;
- Kere, J.;
- Kettunen, K.;
- Hannula‐Jouppi, K.
Publication type:
Article
A novel desmoplakin mutation causes dilated cardiomyopathy with palmoplantar keratoderma as an early clinical sign.
Published in:
Journal of the European Academy of Dermatology & Venereology, 2022, v. 36, n. 8, p. 1349, doi. 10.1111/jdv.18164
By:
- Karvonen, V.;
- Harjama, L.;
- Heliö, K.;
- Kettunen, K.;
- Elomaa, O.;
- Koskenvuo, J.W.;
- Kere, J.;
- Weckström, S.;
- Holmström, M.;
- Saarela, J.;
- Ranki, A.;
- Heliö, T.;
- Hannula‐Jouppi, K.
Publication type:
Article
Hereditary palmoplantar keratoderma – phenotypes and mutations in 64 patients.
Published in:
Journal of the European Academy of Dermatology & Venereology, 2021, v. 35, n. 9, p. 1874, doi. 10.1111/jdv.17314
By:
- Harjama, L.;
- Karvonen, V.;
- Kettunen, K.;
- Elomaa, O.;
- Einarsdottir, E.;
- Heikkilä, H.;
- Kivirikko, S.;
- Ellonen, P.;
- Saarela, J.;
- Ranki, A.;
- Kere, J.;
- Hannula‐Jouppi, K.
Publication type:
Article
Neuropeptide S receptor 1 (NPSR1) activates cancer-related pathways and is widely expressed in neuroendocrine tumors.
Published in:
Virchows Archiv: European Journal of Pathology, 2014, v. 465, n. 2, p. 173, doi. 10.1007/s00428-014-1602-x
By:
- Pulkkinen, V.;
- Ezer, S.;
- Sundman, L.;
- Hagström, J.;
- Remes, S.;
- Söderhäll, C.;
- Dario, G.;
- Haglund, C.;
- Kere, J.;
- Arola, J.
Publication type:
Article
Erratum to: 'Neuropeptide S receptor 1 (NPSR1) activates cancer-related pathways and is widely expressed in neuroendocrine tumors.
Published in:
2014
By:
- Pulkkinen, V.;
- Ezer, S.;
- Sundman, L.;
- Hagström, J.;
- Remes, S.;
- Söderhäll, C.;
- Greco, D.;
- Haglund, C.;
- Kere, J.;
- Arola, J.
Publication type:
Erratum
Patterns of matrix metalloproteinase and TIMP-1 expression in chronic and normally healing human cutaneous wounds.
Published in:
British Journal of Dermatology, 1996, v. 135, n. 1, p. 52, doi. 10.1111/j.1365-2133.1996.tb03607.x
By:
- Vaalamo, M.;
- Weckroth, M.;
- Puolakkainen, P.;
- Kere, J.;
- Saarinen, P.;
- Lauharanta, J.;
- Saarialho-Kere, U. K.
Publication type:
Article
Interaction between early maternal smoking and variants in TNF and GSTP1 in childhood wheezing.
Published in:
Clinical & Experimental Allergy, 2010, v. 40, n. 3, p. 458, doi. 10.1111/j.1365-2222.2010.03452.x
By:
- Panasevich, S.;
- Lindgren, C.;
- Kere, J.;
- Wickman, M.;
- Pershagen, G.;
- Nyberg, F.;
- Melén, E.
Publication type:
Article
Introduction of complementary foods in infancy and atopic sensitization at the age of 5 years: timing and food diversity in a Finnish birth cohort.
Published in:
Allergy, 2013, v. 68, n. 4, p. 507, doi. 10.1111/all.12118
By:
- Nwaru, B. I.;
- Takkinen, H.‐M.;
- Niemelä, O.;
- Kaila, M.;
- Erkkola, M.;
- Ahonen, S.;
- Tuomi, H.;
- Haapala, A.‐M.;
- Kenward, M. G.;
- Pekkanen, J.;
- Lahesmaa, R.;
- Kere, J.;
- Simell, O.;
- Veijola, R.;
- Ilonen, J.;
- Hyöty, H.;
- Knip, M.;
- Virtanen, S. M.
Publication type:
Article
Chromosome 7p linkage and GPR154 gene association in Italian families with allergic asthma.
Published in:
Clinical & Experimental Allergy, 2007, v. 37, n. 1, p. 83, doi. 10.1111/j.1365-2222.2006.02615.x
By:
- Malerba, G.;
- Lindgren, C. M.;
- Xumerle, L.;
- Kiviluoma, P.;
- Trabetti, E.;
- Laitinen, T.;
- Galavotti, R.;
- Pescollderungg, L.;
- Boner, A. L.;
- Kere, J.;
- Pignatti, P. F.
Publication type:
Article
Interaction between variants in the interleukin-4 receptor α and interleukin-9 receptor genes in childhood wheezing: evidence from a birth cohort study.
Published in:
Clinical & Experimental Allergy, 2006, v. 36, n. 11, p. 1391, doi. 10.1111/j.1365-2222.2006.02577.x
By:
- Melén, E.;
- Umerkajeff, S.;
- Nyberg, F.;
- Zucchelli, M.;
- Lindstedt, A.;
- Gullstén, H.;
- Wickman, M.;
- Pershagen, G.;
- Kere, J.
Publication type:
Article
Association study of 15 novel single-nucleotide polymorphisms of the T-bet locus among Finnish asthma families.
Published in:
Clinical & Experimental Allergy, 2004, v. 34, n. 7, p. 1049, doi. 10.1111/j.1365-2222.2004.01995.x
By:
- Ylikoski, E.;
- Kinos, R.;
- Sirkkanen, N.;
- Pykäläinen, M.;
- Savolainen, J.;
- Laitinen, L. A.;
- Kere, J.;
- Laitinen, T.;
- Lahesmaa, R.
Publication type:
Article
Influence of male sex and parental allergic disease on childhood wheezing: role of interactions.
Published in:
Clinical & Experimental Allergy, 2004, v. 34, n. 6, p. 839, doi. 10.1111/j.1365-2222.2004.01957.x
By:
- Melén, E.;
- Kere, J.;
- Pershagen, G.;
- Svartengren, M.;
- Wickman, M.
Publication type:
Article
Phenotyping asthma patients for a gene mapping study in Finland.
Published in:
Clinical & Experimental Allergy, 1998, v. 28, p. 40, doi. 10.1046/j.1365-2222.1998.0280s1040.x
By:
- Kauppi, P.;
- Laitinen, L.A.;
- Laitinen, H.;
- Kere, J.;
- Laitinen, T.
Publication type:
Article
Genome scan on Swedish Alzheimer's disease families.
Published in:
Molecular Psychiatry, 2006, v. 11, n. 2, p. 182, doi. 10.1038/sj.mp.4001772
By:
- Sillén, A.;
- Forsell, C.;
- Lilius, L.;
- Axelman, K.;
- Björk, B. F.;
- Onkamo, P.;
- Kere, J.;
- Winblad, B.;
- Graff, C.
Publication type:
Article
Deletions at 14q in malignant mesothelioma detected by microsatellite marker analysis.
Published in:
British Journal of Cancer, 1999, v. 81, n. 7, p. 1111
By:
- Björkqvist, A-M;
- Wolf, M;
- Nordling, S;
- Tammilehto, L;
- Knuuttila, A;
- Kere, J;
- Mattson, K;
- Knuutila, S
Publication type:
Article
A variation in the gene coding for aldosterone synthase affects urinary sodium excretion and dopaminergic response in healthy males during high and low salt intake.
Published in:
European Journal of Heart Failure, 2000, v. 2, n. S1, p. 92, doi. 10.1016/S1388-9842(00)80325-6
By:
- Reissell, E.;
- Mäkynen, H.;
- Kere, J.;
- Hautanen, A.;
- Kupari, M.
Publication type:
Article
Gene Mapping in Isolated Populations: New Roles for Old Friends?
Published in:
Human Heredity, 2000, v. 50, n. 1, p. 57, doi. 10.1159/000022891
By:
- Jorde, L.B.;
- Watkins, W.S.;
- Kere, J.;
- Nyman, D.;
- Eriksson, A.W.
Publication type:
Article
Ultrastructural features resembling those of harlequin ichthyosis in patients with severe congenital ichthyosiform erythroderma.
Published in:
British Journal of Dermatology, 2001, v. 145, n. 3, p. 480, doi. 10.1046/j.1365-2133.2001.04401.x
By:
- Virolainen, E.;
- Niemi, K-M.;
- Gånemo, A.;
- Kere, J.;
- Vahlquist, A.;
- Saarialho-Kere, U.
Publication type:
Article
Association analysis of positional obesity candidate genes based on integrated data from transcriptomics and linkage analysis.
Published in:
International Journal of Obesity, 2008, v. 32, n. 5, p. 816, doi. 10.1038/sj.ijo.0803789
By:
- Jiao, H.;
- Kaaman, M.;
- Dungner, E.;
- Kere, J.;
- Arner, P.;
- Dahlman, I.
Publication type:
Article
Familial non-syndromic cleft lip and palate--analysis of the IRF6 gene and clinical phenotypes.
Published in:
European Journal of Orthodontics, 2008, v. 30, n. 2, p. 169, doi. 10.1093/ejo/cjm097
By:
- Pegelow, M.;
- Peyrard-Janvid, M.;
- Zucchelli, M.;
- Fransson, I.;
- Larson, O.;
- Kere, J.;
- Larsson, C.;
- Karsten, A.
Publication type:
Article
Characterization of neoplasia-associated chromosome abnormalities by Southern blot analysis.
Published in:
Clinical Genetics, 1986, v. 29, n. 5, p. 462, doi. 10.1111/j.1399-0004.1986.tb00528.x
By:
- Kere, J.;
- Ruutu, T.;
- Chapelle, A. de la
Publication type:
Article

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