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Genes
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March 28, 2024
Understanding the Variability of 22q11.2 Deletion Syndrome: The Role of Epigenetic Factors
Francesca Cillo, Emma Coppola, Federico Habetswallner, et al.
Frontiers in Immunology
|
April 18, 2024
Case report: EBV-related eye orbits and sinuses lymphohistiocytic infiltration responsive to rituximab in a patient with X lymphoproliferative syndrome type 1
Giuliana Giardino, Vittoria Lanni, Massimo Mascolo, et al.
Immunology
|
August 31, 2022
Epigenetics: An opportunity to shape innate and adaptive immune responses
Antonietta Liotti, Anne Lise Ferrara, Stefania Loffredo, et al.
Clinical Immunology (Orlando, Fla.)
|
March 26, 2023
Immune tolerance breakdown in inborn errors of immunity: Paving the way to novel therapeutic approaches
Giuliana Giardino, Roberta Romano, Vassilios Lougaris, et al.
Frontiers in Immunology
|
February 7, 2025
Characterization of a <i>WAS</i> splice-site variant in a patient with Wiskott-Aldrich syndrome
Elisabetta Toriello, Rosa Maritato, Antonio De Rosa, et al.
Cells
|
April 25, 2020
Charcot-Marie-Tooth Type 2B: A New Phenotype Associated with a Novel <i>RAB7A</i> Mutation and Inhibited EGFR Degradation
Paola Saveri, Maria De Luca, Veronica Nisi, et al.
The New England Journal of Medicine
|
August 16, 2023
Gene Therapy in Patients with the Crigler-Najjar Syndrome
Lorenzo D'Antiga, Ulrich Beuers, Giuseppe Ronzitti, et al.
Med (New York, N.Y.)
|
November 15, 2024
Multi-year enzyme expression in patients with mucopolysaccharidosis type VI after liver-directed gene therapy
Alessandro Rossi, Roberta Romano, Simona Fecarotta, et al.
Cellular and Molecular Life Sciences : CMLS
|
March 31, 2023
Functional effects of disease-associated variants reveal that the S1-M1 linker of the NMDA receptor critically controls channel opening
Lingling Xie, Miranda J McDaniel, Riley E Perszyk, et al.
Journal of Clinical Immunology
|
November 3, 2023
Correction to: Antibody Deficiency in Patients with Biallelic KARS1 Mutations
Francesco Saettini, Fabiola Guerra, Grazia Fazio, et al.
Page
of 8
Search research articles
Search
Showing results (61-70 of 78) with videos related to
Sort By:
Page
of 8
Genes
|
March 28, 2024
Understanding the Variability of 22q11.2 Deletion Syndrome: The Role of Epigenetic Factors
Francesca Cillo, Emma Coppola, Federico Habetswallner, et al.
Frontiers in Immunology
|
April 18, 2024
Case report: EBV-related eye orbits and sinuses lymphohistiocytic infiltration responsive to rituximab in a patient with X lymphoproliferative syndrome type 1
Giuliana Giardino, Vittoria Lanni, Massimo Mascolo, et al.
Immunology
|
August 31, 2022
Epigenetics: An opportunity to shape innate and adaptive immune responses
Antonietta Liotti, Anne Lise Ferrara, Stefania Loffredo, et al.
Clinical Immunology (Orlando, Fla.)
|
March 26, 2023
Immune tolerance breakdown in inborn errors of immunity: Paving the way to novel therapeutic approaches
Giuliana Giardino, Roberta Romano, Vassilios Lougaris, et al.
Frontiers in Immunology
|
February 7, 2025
Characterization of a <i>WAS</i> splice-site variant in a patient with Wiskott-Aldrich syndrome
Elisabetta Toriello, Rosa Maritato, Antonio De Rosa, et al.
Cells
|
April 25, 2020
Charcot-Marie-Tooth Type 2B: A New Phenotype Associated with a Novel <i>RAB7A</i> Mutation and Inhibited EGFR Degradation
Paola Saveri, Maria De Luca, Veronica Nisi, et al.
The New England Journal of Medicine
|
August 16, 2023
Gene Therapy in Patients with the Crigler-Najjar Syndrome
Lorenzo D'Antiga, Ulrich Beuers, Giuseppe Ronzitti, et al.
Med (New York, N.Y.)
|
November 15, 2024
Multi-year enzyme expression in patients with mucopolysaccharidosis type VI after liver-directed gene therapy
Alessandro Rossi, Roberta Romano, Simona Fecarotta, et al.
Cellular and Molecular Life Sciences : CMLS
|
March 31, 2023
Functional effects of disease-associated variants reveal that the S1-M1 linker of the NMDA receptor critically controls channel opening
Lingling Xie, Miranda J McDaniel, Riley E Perszyk, et al.
Journal of Clinical Immunology
|
November 3, 2023
Correction to: Antibody Deficiency in Patients with Biallelic KARS1 Mutations
Francesco Saettini, Fabiola Guerra, Grazia Fazio, et al.
Page
of 8