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Katariina Mamia

Showing results (1-10 of 7) with videos related to

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Scientific Reports|June 12, 2019
Pleomorphic Adenoma Gene 1 Is Needed For Timely Zygotic Genome Activation and Early Embryo DevelopmentElo Madissoon, Anastasios Damdimopoulos, Shintaro Katayama, et al.
Environment International|August 21, 2023
Ambient black carbon particles in human ovarian tissue and follicular fluidEva Bongaerts, Katariina Mamia, Ilmatar Rooda, et al.
Elife|December 13, 2021
Rapid genome editing by CRISPR-Cas9-POLD3 fusionGanna Reint, Zhuokun Li, Kornel Labun, et al.
The Journal of Allergy and Clinical Immunology|May 13, 2026
Homozygous loss-of-function mutation in SIT1 leads to combined immunodeficiency due to dysregulated T cell receptor signalingPu Chen, Kim My Le, Weiwei Li, et al.
The Journal of Allergy and Clinical Immunology|July 27, 2025
Heterozygous loss of MAP4K1 causes immune dysregulation by amplifying T-cell responsesMeri Kaustio, Monika Szymanska, Weiwei Li, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|August 14, 2025
Precision T cell correction platform for Inborn Errors of ImmunityKatariina Mamia, Solrun Kolbeinsdottir, Kornel Labun, et al.
The Journal of Allergy and Clinical Immunology|March 4, 2021
Loss of DIAPH1 causes SCBMS, combined immunodeficiency, and mitochondrial dysfunctionMeri Kaustio, Naemeh Nayebzadeh, Reetta Hinttala, et al.
Pageof 1

Showing results (1-10 of 7) with videos related to

Sort By:
Pageof 1
Scientific Reports|June 12, 2019
Pleomorphic Adenoma Gene 1 Is Needed For Timely Zygotic Genome Activation and Early Embryo DevelopmentElo Madissoon, Anastasios Damdimopoulos, Shintaro Katayama, et al.
Environment International|August 21, 2023
Ambient black carbon particles in human ovarian tissue and follicular fluidEva Bongaerts, Katariina Mamia, Ilmatar Rooda, et al.
Elife|December 13, 2021
Rapid genome editing by CRISPR-Cas9-POLD3 fusionGanna Reint, Zhuokun Li, Kornel Labun, et al.
The Journal of Allergy and Clinical Immunology|May 13, 2026
Homozygous loss-of-function mutation in SIT1 leads to combined immunodeficiency due to dysregulated T cell receptor signalingPu Chen, Kim My Le, Weiwei Li, et al.
The Journal of Allergy and Clinical Immunology|July 27, 2025
Heterozygous loss of MAP4K1 causes immune dysregulation by amplifying T-cell responsesMeri Kaustio, Monika Szymanska, Weiwei Li, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|August 14, 2025
Precision T cell correction platform for Inborn Errors of ImmunityKatariina Mamia, Solrun Kolbeinsdottir, Kornel Labun, et al.
The Journal of Allergy and Clinical Immunology|March 4, 2021
Loss of DIAPH1 causes SCBMS, combined immunodeficiency, and mitochondrial dysfunctionMeri Kaustio, Naemeh Nayebzadeh, Reetta Hinttala, et al.
Pageof 1