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Methods in Molecular Biology (Clifton, N.J.)
|
September 2, 2016
High Throughput siRNA Screening Using Reverse Transfection
Carina von Schantz, Jani Saarela
Human Mutation
|
September 15, 2004
A novel aspartylglucosaminuria mutation affects translocation of aspartylglucosaminidase
Jani Saarela, Carina von Schantz, Leena Peltonen, et al.
Combinatorial Chemistry & High Throughput Screening
|
March 26, 2014
The high throughput biomedicine unit at the institute for molecular medicine Finland: high throughput screening meets precision medicine
Vilja Pietiainen, Jani Saarela, Carina von Schantz, et al.
International Journal of Molecular Sciences
|
May 5, 2017
Induced Pluripotent Stem Cells Derived from a CLN5 Patient Manifest Phenotypic Characteristics of Neuronal Ceroid Lipofuscinoses
Kristiina Uusi-Rauva, Tea Blom, Carina von Schantz-Fant, et al.
BMC Cell Biology
|
November 28, 2009
Novel interactions of CLN5 support molecular networking between Neuronal Ceroid Lipofuscinosis proteins
Annina Lyly, Carina von Schantz, Claudia Heine, et al.
BMC Cell Biology
|
June 15, 2007
Glycosylation, transport, and complex formation of palmitoyl protein thioesterase 1 (PPT1)--distinct characteristics in neurons
Annina Lyly, Carina von Schantz, Tarja Salonen, et al.
NPJ Biofilms and Microbiomes
|
June 29, 2022
Genome-wide siRNA screening reveals several host receptors for the binding of human gut commensal Bifidobacterium bifidum
Veera Kainulainen, Carina von Schantz-Fant, Ruusu-Maria Kovanen, et al.
BMC Genomics
|
March 29, 2008
Brain gene expression profiles of Cln1 and Cln5 deficient mice unravels common molecular pathways underlying neuronal degeneration in NCL diseases
Carina von Schantz, Juha Saharinen, Outi Kopra, et al.
Neurobiology of Disease
|
April 23, 2009
Progressive thalamocortical neuron loss in Cln5 deficient mice: Distinct effects in Finnish variant late infantile NCL
Carina von Schantz, Catherine Kielar, Stine N Hansen, et al.
Neurobiology of Disease
|
January 15, 2005
Mice with Ppt1Deltaex4 mutation replicate the INCL phenotype and show an inflammation-associated loss of interneurons
Anu Jalanko, Jouni Vesa, Tuula Manninen, et al.
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Search research articles
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Showing results (1-10 of 15) with videos related to
Sort By:
Page
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Methods in Molecular Biology (Clifton, N.J.)
|
September 2, 2016
High Throughput siRNA Screening Using Reverse Transfection
Carina von Schantz, Jani Saarela
Human Mutation
|
September 15, 2004
A novel aspartylglucosaminuria mutation affects translocation of aspartylglucosaminidase
Jani Saarela, Carina von Schantz, Leena Peltonen, et al.
Combinatorial Chemistry & High Throughput Screening
|
March 26, 2014
The high throughput biomedicine unit at the institute for molecular medicine Finland: high throughput screening meets precision medicine
Vilja Pietiainen, Jani Saarela, Carina von Schantz, et al.
International Journal of Molecular Sciences
|
May 5, 2017
Induced Pluripotent Stem Cells Derived from a CLN5 Patient Manifest Phenotypic Characteristics of Neuronal Ceroid Lipofuscinoses
Kristiina Uusi-Rauva, Tea Blom, Carina von Schantz-Fant, et al.
BMC Cell Biology
|
November 28, 2009
Novel interactions of CLN5 support molecular networking between Neuronal Ceroid Lipofuscinosis proteins
Annina Lyly, Carina von Schantz, Claudia Heine, et al.
BMC Cell Biology
|
June 15, 2007
Glycosylation, transport, and complex formation of palmitoyl protein thioesterase 1 (PPT1)--distinct characteristics in neurons
Annina Lyly, Carina von Schantz, Tarja Salonen, et al.
NPJ Biofilms and Microbiomes
|
June 29, 2022
Genome-wide siRNA screening reveals several host receptors for the binding of human gut commensal Bifidobacterium bifidum
Veera Kainulainen, Carina von Schantz-Fant, Ruusu-Maria Kovanen, et al.
BMC Genomics
|
March 29, 2008
Brain gene expression profiles of Cln1 and Cln5 deficient mice unravels common molecular pathways underlying neuronal degeneration in NCL diseases
Carina von Schantz, Juha Saharinen, Outi Kopra, et al.
Neurobiology of Disease
|
April 23, 2009
Progressive thalamocortical neuron loss in Cln5 deficient mice: Distinct effects in Finnish variant late infantile NCL
Carina von Schantz, Catherine Kielar, Stine N Hansen, et al.
Neurobiology of Disease
|
January 15, 2005
Mice with Ppt1Deltaex4 mutation replicate the INCL phenotype and show an inflammation-associated loss of interneurons
Anu Jalanko, Jouni Vesa, Tuula Manninen, et al.
Page
of 2