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Scientific Reports
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June 12, 2019
Pleomorphic Adenoma Gene 1 Is Needed For Timely Zygotic Genome Activation and Early Embryo Development
Elo Madissoon, Anastasios Damdimopoulos, Shintaro Katayama, et al.
Environment International
|
August 21, 2023
Ambient black carbon particles in human ovarian tissue and follicular fluid
Eva Bongaerts, Katariina Mamia, Ilmatar Rooda, et al.
Elife
|
December 13, 2021
Rapid genome editing by CRISPR-Cas9-POLD3 fusion
Ganna 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 signaling
Pu 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 responses
Meri 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 Immunity
Katariina 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 dysfunction
Meri Kaustio, Naemeh Nayebzadeh, Reetta Hinttala, et al.
Page
of 1
Search research articles
Search
Showing results (1-10 of 7) with videos related to
Sort By:
Page
of 1
Scientific Reports
|
June 12, 2019
Pleomorphic Adenoma Gene 1 Is Needed For Timely Zygotic Genome Activation and Early Embryo Development
Elo Madissoon, Anastasios Damdimopoulos, Shintaro Katayama, et al.
Environment International
|
August 21, 2023
Ambient black carbon particles in human ovarian tissue and follicular fluid
Eva Bongaerts, Katariina Mamia, Ilmatar Rooda, et al.
Elife
|
December 13, 2021
Rapid genome editing by CRISPR-Cas9-POLD3 fusion
Ganna 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 signaling
Pu 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 responses
Meri 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 Immunity
Katariina 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 dysfunction
Meri Kaustio, Naemeh Nayebzadeh, Reetta Hinttala, et al.
Page
of 1