Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Matias Kinnunen

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

Pageof 1
Sort By:
Cancers|September 9, 2023
The Impact of ETV6-NTRK3 Oncogenic Gene Fusions on Molecular and Signaling Pathway AlterationsMatias Kinnunen, Xiaonan Liu, Elina Niemelä, et al.
Nature Communications|February 10, 2022
Human transcription factor protein interaction networksHelka Göös, Matias Kinnunen, Kari Salokas, et al.
Stem Cell Research & Therapy|March 19, 2021
GATA-targeted compounds modulate cardiac subtype cell differentiation in dual reporter stem cell lineMika J Välimäki, Robert S Leigh, Sini M Kinnunen, et al.
Human Mutation|January 6, 2017
Somatic MED12 Nonsense Mutation Escapes mRNA Decay and Reveals a Motif Required for Nuclear EntryTuomas Heikkinen, Kati Kämpjärvi, Salla Keskitalo, et al.
Cell Reports|April 14, 2017
An Activating STAT3 Mutation Causes Neonatal Diabetes through Premature Induction of Pancreatic DifferentiationJonna Saarimäki-Vire, Diego Balboa, Mark A Russell, et al.
Frontiers in Immunology|October 7, 2022
Common variable immunodeficiency in two kindreds with heterogeneous phenotypes caused by novel heterozygous <i>NFKB1</i> mutationsFrederik Staels, Kerstin De Keukeleere, Matias Kinnunen, et al.
Science Immunology|November 26, 2021
Loss-of-function mutation in <i>IKZF2</i> leads to immunodeficiency with dysregulated germinal center reactions and reduction of MAIT cellsIivo Hetemäki, Meri Kaustio, Matias Kinnunen, et al.
Frontiers in Immunology|September 15, 2022
Detrimental <i>NFKB1</i> missense variants affecting the Rel-homology domain of p105/p50Manfred Fliegauf, Matias Kinnunen, Sara Posadas-Cantera, et al.
Cell Reports. Medicine|April 9, 2024
Truncating NFKB1 variants cause combined NLRP3 inflammasome activation and type I interferon signaling and predispose to necrotizing fasciitisKatariina Nurmi, Kristiina Silventoinen, Salla Keskitalo, et al.
The Journal of Allergy and Clinical Immunology|April 13, 2020
Characterization of the clinical and immunologic phenotype and management of 157 individuals with 56 distinct heterozygous NFKB1 mutationsTiziana Lorenzini, Manfred Fliegauf, Nils Klammer, et al.
Pageof 1

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

Sort By:
Pageof 1
Cancers|September 9, 2023
The Impact of ETV6-NTRK3 Oncogenic Gene Fusions on Molecular and Signaling Pathway AlterationsMatias Kinnunen, Xiaonan Liu, Elina Niemelä, et al.
Nature Communications|February 10, 2022
Human transcription factor protein interaction networksHelka Göös, Matias Kinnunen, Kari Salokas, et al.
Stem Cell Research & Therapy|March 19, 2021
GATA-targeted compounds modulate cardiac subtype cell differentiation in dual reporter stem cell lineMika J Välimäki, Robert S Leigh, Sini M Kinnunen, et al.
Human Mutation|January 6, 2017
Somatic MED12 Nonsense Mutation Escapes mRNA Decay and Reveals a Motif Required for Nuclear EntryTuomas Heikkinen, Kati Kämpjärvi, Salla Keskitalo, et al.
Cell Reports|April 14, 2017
An Activating STAT3 Mutation Causes Neonatal Diabetes through Premature Induction of Pancreatic DifferentiationJonna Saarimäki-Vire, Diego Balboa, Mark A Russell, et al.
Frontiers in Immunology|October 7, 2022
Common variable immunodeficiency in two kindreds with heterogeneous phenotypes caused by novel heterozygous <i>NFKB1</i> mutationsFrederik Staels, Kerstin De Keukeleere, Matias Kinnunen, et al.
Science Immunology|November 26, 2021
Loss-of-function mutation in <i>IKZF2</i> leads to immunodeficiency with dysregulated germinal center reactions and reduction of MAIT cellsIivo Hetemäki, Meri Kaustio, Matias Kinnunen, et al.
Frontiers in Immunology|September 15, 2022
Detrimental <i>NFKB1</i> missense variants affecting the Rel-homology domain of p105/p50Manfred Fliegauf, Matias Kinnunen, Sara Posadas-Cantera, et al.
Cell Reports. Medicine|April 9, 2024
Truncating NFKB1 variants cause combined NLRP3 inflammasome activation and type I interferon signaling and predispose to necrotizing fasciitisKatariina Nurmi, Kristiina Silventoinen, Salla Keskitalo, et al.
The Journal of Allergy and Clinical Immunology|April 13, 2020
Characterization of the clinical and immunologic phenotype and management of 157 individuals with 56 distinct heterozygous NFKB1 mutationsTiziana Lorenzini, Manfred Fliegauf, Nils Klammer, et al.
Pageof 1