Rezultati - 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) od Irma Järvelä

    Izdano 1999
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    Artigo
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  2. 2
    Molecular genetics of human lactase deficiencies

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

    Izdano 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 od Jaana Oikkonen, Päivi Onkamo, Irma Järvelä, Chakravarthi Kanduri

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

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

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

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

    Izdano 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 od Irma Järvelä, Nabil Enattah, Jorma Kokkonen, Teppo Varilo, Erkki Savilahti, Leena Peltonen

    Izdano 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 od Chakravarthi Kanduri, Tuire Kuusi, Minna Ahvenainen, Anju K. Philips, Harri Lähdesmäki, Irma Järvelä

    Izdano 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 od Kristiina Pulli, Kai Karma, Reijo Norio, P. Sistonen, H H H Goring, Irma Järvelä

    Izdano 2008
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    Carta
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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 od Irma Järvelä, Markku Sainio, Tomi Rantamäki, Vesa M. Olkkonen, Olli Carpén, L. Peltonen, Anu Jalanko

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

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

    Izdano 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 od Chakravarthi Kanduri, Pirre Raijas, Minna Ahvenainen, Anju K. Philips, Liisa Ukkola‐Vuoti, Harri Lähdesmäki, Irma Järvelä

    Izdano 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 od Jaana Oikkonen, Yungui Huang, Päivi Onkamo, Liisa Ukkola‐Vuoti, Pirre Raijas, Kai Karma, Veronica J. Vieland, Irma Järvelä

    Izdano 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 od Mikko Kuokkanen, Jorma Kokkonen, Nabil Enattah, Tero Ylisaukko‐oja, Hanna Komu, Teppo Varilo, Leena Peltonen, Erkki Savilahti, Irma Järvelä

    Izdano 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 od Liisa Ukkola‐Vuoti, Chakravarthi Kanduri, Jaana Oikkonen, Gemma Buck, Christine Blancher, Pirre Raijas, Kai Karma, Harri Lähdesmäki, Irma Järvelä

    Izdano 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 od Elise Renkonen, Pekka Nieminen, Wael M. Abdel‐Rahman, Anu‐Liisa Moisio, Irma Järvelä, Sirpa Arte, Heikki Järvinen, Païvi Peltomäki

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

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

    Izdano 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 od Faiqa Imtiaz, Erkki Savilahti, Annikki Sarnesto, Daniah Trabzuni, Khalid Al-Kahtani, Ingvar Kagevi, M. S. Rashed, Brian F. Meyer, Irma Järvelä

    Izdano 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 od Mari Auranen, Raija Vanhala, Teppo Varilo, Kristin L. Ayers, Elli Kempas, Tero Ylisaukko‐oja, Janet S. Sinsheimer, Leena Peltonen, Irma Järvelä

    Izdano 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 od A. Inkeri Lokki, Irma Järvelä, Elisabeth Israelsson, Bakary Maiga, Marita Troye‐Blomberg, Amagana Dolo, Ogobara K. Doumbo, Seppo Meri, Ville Holmberg

    Izdano 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 od Susanna Lemmelä, Eva Forsman, Päivi Onkamo, Hanna Nurmi, Hannele Laivuori, Tero Kivelä, Päivi Puska, Martin Heger, Aldur W. Eriksson, Henrik Forsius, Irma Järvelä

    Izdano 2009
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