Resultats de la cerca - Irma Järvelä

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  1. 1
    Defective intracellular transport of CLN3 is the molecular basis of Batten disease (JNCL)

    Defective intracellular transport of CLN3 is the molecular basis of Batten disease (JNCL) per Irma Järvelä

    Publicat 1999
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  2. 2
    Molecular genetics of human lactase deficiencies

    Molecular genetics of human lactase deficiencies per Irma Järvelä, Suvi Torniainen, Kaija‐Leena Kolho

    Publicat 2009
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  3. 3
    Convergent evidence for the molecular basis of musical traits

    Convergent evidence for the molecular basis of musical traits per Jaana Oikkonen, Päivi Onkamo, Irma Järvelä, Chakravarthi Kanduri

    Publicat 2016
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  4. 4
    Musical Aptitude Is Associated with AVPR1A-Haplotypes

    Musical Aptitude Is Associated with AVPR1A-Haplotypes per Liisa T. Ukkola, Päivi Onkamo, Pirre Raijas, Kai Karma, Irma Järvelä

    Publicat 2009
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  5. 5
    Elevated lysosomal pH in neuronal ceroid lipofuscinoses (NCLs)

    Elevated lysosomal pH in neuronal ceroid lipofuscinoses (NCLs) per Juha M. Holopainen, Juhani Saarikoski, Paavo K.J. Kinnunen, Irma Järvelä

    Publicat 2001
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  6. 6
    Assignment of the Locus for Congenital Lactase Deficiency to 2q21, in the Vicinity of but Separate from the Lactase-Phlorizin Hydrolase Gene

    Assignment of the Locus for Congenital Lactase Deficiency to 2q21, in the Vicinity of but Separate from the Lactase-Phlorizin Hydrolase Gene per Irma Järvelä, Nabil Enattah, Jorma Kokkonen, Teppo Varilo, Erkki Savilahti, Leena Peltonen

    Publicat 1998
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  7. 7
    The effect of music performance on the transcriptome of professional musicians

    The effect of music performance on the transcriptome of professional musicians per Chakravarthi Kanduri, Tuire Kuusi, Minna Ahvenainen, Anju K. Philips, Harri Lähdesmäki, Irma Järvelä

    Publicat 2015
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  8. 8
    Genome-wide linkage scan for loci of musical aptitude in Finnish families: evidence for a major locus at 4q22

    Genome-wide linkage scan for loci of musical aptitude in Finnish families: evidence for a major locus at 4q22 per Kristiina Pulli, Kai Karma, Reijo Norio, P. Sistonen, H H H Goring, Irma Järvelä

    Publicat 2008
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  9. 9
    Biosynthesis and Intracellular Targeting of the CLN3 Protein Defective in Batten Disease

    Biosynthesis and Intracellular Targeting of the CLN3 Protein Defective in Batten Disease per Irma Järvelä, Markku Sainio, Tomi Rantamäki, Vesa M. Olkkonen, Olli Carpén, L. Peltonen, Anu Jalanko

    Publicat 1998
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  10. 10
    Music-listening regulates human microRNA expression

    Music-listening regulates human microRNA expression per Preethy Sasidharan Nair, Pirre Raijas, Minna Ahvenainen, Anju K. Philips, Liisa Ukkola‐Vuoti, Irma Järvelä

    Publicat 2020
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  11. 11
    The effect of listening to music on human transcriptome

    The effect of listening to music on human transcriptome per Chakravarthi Kanduri, Pirre Raijas, Minna Ahvenainen, Anju K. Philips, Liisa Ukkola‐Vuoti, Harri Lähdesmäki, Irma Järvelä

    Publicat 2015
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  12. 12
    A genome-wide linkage and association study of musical aptitude identifies loci containing genes related to inner ear development and neurocognitive functions

    A genome-wide linkage and association study of musical aptitude identifies loci containing genes related to inner ear development and neurocognitive functions per Jaana Oikkonen, Yungui Huang, Päivi Onkamo, Liisa Ukkola‐Vuoti, Pirre Raijas, Kai Karma, Veronica J. Vieland, Irma Järvelä

    Publicat 2014
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  13. 13
    Mutations in the Translated Region of the Lactase Gene (LCT) Underlie Congenital Lactase Deficiency

    Mutations in the Translated Region of the Lactase Gene (LCT) Underlie Congenital Lactase Deficiency per Mikko Kuokkanen, Jorma Kokkonen, Nabil Enattah, Tero Ylisaukko‐oja, Hanna Komu, Teppo Varilo, Leena Peltonen, Erkki Savilahti, Irma Järvelä

    Publicat 2006
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  14. 14
    Genome-Wide Copy Number Variation Analysis in Extended Families and Unrelated Individuals Characterized for Musical Aptitude and Creativity in Music

    Genome-Wide Copy Number Variation Analysis in Extended Families and Unrelated Individuals Characterized for Musical Aptitude and Creativity in Music per Liisa Ukkola‐Vuoti, Chakravarthi Kanduri, Jaana Oikkonen, Gemma Buck, Christine Blancher, Pirre Raijas, Kai Karma, Harri Lähdesmäki, Irma Järvelä

    Publicat 2013
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  15. 15
    Adenomatous Polyposis Families That Screen <i>APC</i> Mutation–Negative by Conventional Methods Are Genetically Heterogeneous

    Adenomatous Polyposis Families That Screen <i>APC</i> Mutation–Negative by Conventional Methods Are Genetically Heterogeneous per Elise Renkonen, Pekka Nieminen, Wael M. Abdel‐Rahman, Anu‐Liisa Moisio, Irma Järvelä, Sirpa Arte, Heikki Järvinen, Païvi Peltomäki

    Publicat 2005
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  16. 16
    Genome-wide scan for loci of Asperger syndrome

    Genome-wide scan for loci of Asperger syndrome per Tero Ylisaukko‐oja, Taina Nieminen‐von Wendt, Elli Kempas, Susan Sarenius, Teppo Varilo, L. von Wendt, Leena Peltonen, Irma Järvelä

    Publicat 2004
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  17. 17
    The T/G 13915 variant upstream of the lactase gene (LCT) is the founder allele of lactase persistence in an urban Saudi population

    The T/G 13915 variant upstream of the lactase gene (LCT) is the founder allele of lactase persistence in an urban Saudi population per Faiqa Imtiaz, Erkki Savilahti, Annikki Sarnesto, Daniah Trabzuni, Khalid Al-Kahtani, Ingvar Kagevi, M. S. Rashed, Brian F. Meyer, Irma Järvelä

    Publicat 2007
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  18. 18
    A Genomewide Screen for Autism-Spectrum Disorders: Evidence for a Major Susceptibility Locus on Chromosome 3q25-27

    A Genomewide Screen for Autism-Spectrum Disorders: Evidence for a Major Susceptibility Locus on Chromosome 3q25-27 per Mari Auranen, Raija Vanhala, Teppo Varilo, Kristin L. Ayers, Elli Kempas, Tero Ylisaukko‐oja, Janet S. Sinsheimer, Leena Peltonen, Irma Järvelä

    Publicat 2002
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  19. 19
    Lactase persistence genotypes and malaria susceptibility in Fulani of Mali

    Lactase persistence genotypes and malaria susceptibility in Fulani of Mali per A. Inkeri Lokki, Irma Järvelä, Elisabeth Israelsson, Bakary Maiga, Marita Troye‐Blomberg, Amagana Dolo, Ogobara K. Doumbo, Seppo Meri, Ville Holmberg

    Publicat 2011
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  20. 20
    Association of LOXL1 gene with Finnish exfoliation syndrome patients

    Association of LOXL1 gene with Finnish exfoliation syndrome patients per Susanna Lemmelä, Eva Forsman, Päivi Onkamo, Hanna Nurmi, Hannele Laivuori, Tero Kivelä, Päivi Puska, Martin Heger, Aldur W. Eriksson, Henrik Forsius, Irma Järvelä

    Publicat 2009
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