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Kirsi Alakurtti

Showing results (1-10 of 10) with videos related to

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The Journal of Biological Chemistry|May 2, 2012
Prevention of premature fusion of calvarial suture in GLI-Kruppel family member 3 (Gli3)-deficient mice by removing one allele of Runt-related transcription factor 2 (Runx2)Yukiho Tanimoto, Lotta Veistinen, Kirsi Alakurtti, et al.
Frontiers in Cell and Developmental Biology|March 13, 2023
RAB23 regulates musculoskeletal development and patterningMd Rakibul Hasan, Anna Koskenranta, Kirsi Alakurtti, et al.
Plos One|September 1, 2021
Next-generation sequencing in childhood-onset epilepsies: Diagnostic yield and impact on neuronal ceroid lipofuscinosis type 2 (CLN2) disease diagnosisKimberly Gall, Emanuela Izzo, Eija H Seppälä, et al.
European Journal of Human Genetics : EJHG|September 28, 2006
Cystatin B: mutation detection, alternative splicing and expression in progressive myclonus epilepsy of Unverricht-Lundborg type (EPM1) patientsTarja Joensuu, Mervi Kuronen, Kirsi Alakurtti, et al.
European Journal of Human Genetics : EJHG|October 16, 2004
Loss of lysosomal association of cystatin B proteins representing progressive myoclonus epilepsy, EPM1, mutationsKirsi Alakurtti, Ekkehard Weber, Riitta Rinne, et al.
Human Molecular Genetics|August 9, 2011
Noggin null allele mice exhibit a microform of holoprosencephalyEva Lana-Elola, Przemko Tylzanowski, Maarit Takatalo, et al.
Molecular Immunology|December 18, 2007
Functional interaction of AIRE with PIAS1 in transcriptional regulationTanja Ilmarinen, Hannele Kangas, Taina Kytömaa, et al.
Human Molecular Genetics|August 5, 2008
A high-density association screen of 155 ion transport genes for involvement with common migraineDale R Nyholt, K Steven LaForge, Mikko Kallela, et al.
Brain Communications|October 5, 2023
Lunapark deficiency leads to an autosomal recessive neurodevelopmental phenotype with a degenerative course, epilepsy and distinct brain anomaliesAndrea Accogli, Maha S Zaki, Mohammed Al-Owain, et al.
Nature Genetics|August 31, 2010
Genome-wide association study of migraine implicates a common susceptibility variant on 8q22.1Verneri Anttila, Hreinn Stefansson, Mikko Kallela, et al.
Pageof 1

Showing results (1-10 of 10) with videos related to

Sort By:
Pageof 1
The Journal of Biological Chemistry|May 2, 2012
Prevention of premature fusion of calvarial suture in GLI-Kruppel family member 3 (Gli3)-deficient mice by removing one allele of Runt-related transcription factor 2 (Runx2)Yukiho Tanimoto, Lotta Veistinen, Kirsi Alakurtti, et al.
Frontiers in Cell and Developmental Biology|March 13, 2023
RAB23 regulates musculoskeletal development and patterningMd Rakibul Hasan, Anna Koskenranta, Kirsi Alakurtti, et al.
Plos One|September 1, 2021
Next-generation sequencing in childhood-onset epilepsies: Diagnostic yield and impact on neuronal ceroid lipofuscinosis type 2 (CLN2) disease diagnosisKimberly Gall, Emanuela Izzo, Eija H Seppälä, et al.
European Journal of Human Genetics : EJHG|September 28, 2006
Cystatin B: mutation detection, alternative splicing and expression in progressive myclonus epilepsy of Unverricht-Lundborg type (EPM1) patientsTarja Joensuu, Mervi Kuronen, Kirsi Alakurtti, et al.
European Journal of Human Genetics : EJHG|October 16, 2004
Loss of lysosomal association of cystatin B proteins representing progressive myoclonus epilepsy, EPM1, mutationsKirsi Alakurtti, Ekkehard Weber, Riitta Rinne, et al.
Human Molecular Genetics|August 9, 2011
Noggin null allele mice exhibit a microform of holoprosencephalyEva Lana-Elola, Przemko Tylzanowski, Maarit Takatalo, et al.
Molecular Immunology|December 18, 2007
Functional interaction of AIRE with PIAS1 in transcriptional regulationTanja Ilmarinen, Hannele Kangas, Taina Kytömaa, et al.
Human Molecular Genetics|August 5, 2008
A high-density association screen of 155 ion transport genes for involvement with common migraineDale R Nyholt, K Steven LaForge, Mikko Kallela, et al.
Brain Communications|October 5, 2023
Lunapark deficiency leads to an autosomal recessive neurodevelopmental phenotype with a degenerative course, epilepsy and distinct brain anomaliesAndrea Accogli, Maha S Zaki, Mohammed Al-Owain, et al.
Nature Genetics|August 31, 2010
Genome-wide association study of migraine implicates a common susceptibility variant on 8q22.1Verneri Anttila, Hreinn Stefansson, Mikko Kallela, et al.
Pageof 1