Cargando…

Zebrafish Model of Severe Combined Immunodeficiency (SCID) Due to JAK3 Mutation

JAK3 is principally activated by members of the interleukin-2 receptor family and plays an essential role in lymphoid development, with inactivating JAK3 mutations causing autosomal-recessive severe combined immunodeficiency (SCID). This study aimed to generate an equivalent zebrafish model of SCID...

Descripción completa

Detalles Bibliográficos
Autores principales:	Basheer, Faiza, Lee, Effie, Liongue, Clifford, Ward, Alister C.
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	MDPI 2022
Materias:	Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9599616/ https://www.ncbi.nlm.nih.gov/pubmed/36291730 http://dx.doi.org/10.3390/biom12101521

Ejemplares similares

In vivo impact of JAK3 A573V mutation revealed using zebrafish
por: Basheer, Faiza, et al.
Publicado: (2022)

Zebrafish: A Relevant Genetic Model for Human Primary Immunodeficiency (PID) Disorders?
por: Basheer, Faiza, et al.
Publicado: (2023)

Generation and Characterization of a Zebrafish IL-2Rγc SCID Model
por: Sertori, Robert, et al.
Publicado: (2022)

Zebrafish as a model for leukemia and other hematopoietic disorders
por: Rasighaemi, Parisa, et al.
Publicado: (2015)

Evolution of the JAK-STAT pathway
por: Liongue, Clifford, et al.
Publicado: (2013)

Phylogenetic and Expression Analysis of Fos Transcription Factors in Zebrafish
por: Kubra, Khadizatul, et al.
Publicado: (2022)

Leukemia-associated truncation of granulocyte colony-stimulating factor receptor impacts granulopoiesis throughout the life-course
por: Bulleeraz, Vilasha, et al.
Publicado: (2023)

Cytokine Receptor-Like Factor 3 (CRLF3) Contributes to Early Zebrafish Hematopoiesis
por: Taznin, Tarannum, et al.
Publicado: (2022)

Granulocyte Colony-Stimulating Factor Receptor Mutations in Myeloid Malignancy
por: Liongue, Clifford, et al.
Publicado: (2014)

Functional Analysis of Zebrafish socs4a: Impacts on the Notochord and Sensory Function
por: Trengove, Monique, et al.
Publicado: (2022)

Evolution of JAK-STAT Pathway Components: Mechanisms and Role in Immune System Development
por: Liongue, Clifford, et al.
Publicado: (2012)

Universal Newborn Screening for Severe Combined Immunodeficiency (SCID)
por: van der Burg, Mirjam, et al.
Publicado: (2019)

Socs3b regulates the development and function of innate immune cells in zebrafish
por: Sobah, Mohamed L., et al.
Publicado: (2023)

Thymic epithelial cells of severe combined immunodeficiency (SCID) mice.
por: Lee, I., et al.
Publicado: (1994)

Hematopoietic Stem Cell Transplantation for Severe Combined Immunodeficiency (SCID)
por: Haddad, Elie, et al.
Publicado: (2019)

Severe Combined Immunodeficiency (SCID) and Its New Treatment Modalities
por: Wadbudhe, Akshad M, et al.
Publicado: (2023)

A high-quality severe combined immunodeficiency (SCID) rat bioresource
por: Miyasaka, Yoshiki, et al.
Publicado: (2022)

B cell lymphoma 6A regulates immune development and function in zebrafish
por: Almohaisen, Farooq L. J., et al.
Publicado: (2022)

Evolution of Class I cytokine receptors
por: Liongue, Clifford, et al.
Publicado: (2007)

A severe combined immunodeficient (SCID) mouse model for infection with Entamoeba histolytica
Publicado: (1992)

Transfer of human systemic lupus erythematosus in severe combined immunodeficient (SCID) mice
Publicado: (1990)

Human Ovarian Cancer Tumor Formation in Severe Combined Immunodeficient (SCID) Pigs
por: Boettcher, Adeline N., et al.
Publicado: (2019)

Severe Combined Immunodeficiency (SCID) in Canadian Children: A National Surveillance Study
por: Rozmus, Jacob, et al.
Publicado: (2013)

Review of Treatment for Adenosine Deaminase Deficiency (ADA) Severe Combined Immunodeficiency (SCID)
por: Secord, Elizabeth, et al.
Publicado: (2022)

A zebrafish model of growth hormone insensitivity syndrome with immune dysregulation 1 (GHISID1)
por: Heidary, Somayyeh, et al.
Publicado: (2023)

Severe combined immunodeficiency (SCID) in man: B cell-negative (B-) SCID patients exhibit an irregular recombination pattern at the JH locus
Publicado: (1991)

Rapid Growth and Spontaneous Metastasis of Human Germinal Tumors Ectopically Transplanted into Scid (Severe Combined Immunodeficiency) and Scid‐nude(streaker) Mice
por: Nomura, Taisei, et al.
Publicado: (1991)

Persistent Infection with Rotavirus Vaccine Strain in Severe Combined Immunodeficiency (SCID) Child: Is Rotavirus Vaccination in SCID Children a Janus Face?
por: De Francesco, Maria Antonia, et al.
Publicado: (2019)

Pegademase bovine (PEG-ADA) for the treatment of infants and children with severe combined immunodeficiency (SCID)
por: Booth, Claire, et al.
Publicado: (2009)

Facial vein injection of human cells in severe combined immunodeficiency (SCID) neonatal mice
por: Pavathuparambil Abdul Manaph, Nimshitha, et al.
Publicado: (2018)

Introducing Newborn Screening for Severe Combined Immunodeficiency (SCID) in the Dutch Neonatal Screening Program
por: Blom, Maartje, et al.
Publicado: (2018)

STAT proteins: a kaleidoscope of canonical and non-canonical functions in immunity and cancer
por: Awasthi, Nagendra, et al.
Publicado: (2021)

The ADAMTS5 Metzincin Regulates Zebrafish Somite Differentiation
por: Dancevic, Carolyn M., et al.
Publicado: (2018)

SOCS Proteins in Immunity, Inflammatory Diseases, and Immune-Related Cancer
por: Sobah, Mohamed Luban, et al.
Publicado: (2021)

Generation of biliary lesions after transfer of human lymphocytes into severe combined immunodeficient (SCID) mice
Publicado: (1989)

The severe combined immunodeficiency (scid) mouse. A laboratory model for the analysis of Lyme arthritis and carditis
Publicado: (1989)

Clinical, Immunological, and Molecular Findings in 57 Patients With Severe Combined Immunodeficiency (SCID) From India
por: Aluri, Jahnavi, et al.
Publicado: (2019)

A Novel Homozygous JAK3 Mutation Leading to T-B+NK– SCID in Two Brazilian Patients
por: Barreiros, Lucila A., et al.
Publicado: (2018)

Corrigendum: A Novel Homozygous JAK3 Mutation Leading to T-B+NK- SCID in Two Brazilian Patients
por: Barreiros, Lucila A., et al.
Publicado: (2018)

JAK3 mutations in Italian patients affected by SCID: New molecular aspects of a long‐known gene
por: Di Matteo, Gigliola, et al.
Publicado: (2018)

Cannot write session to /tmp/vufind_sessions/sess_73k6vem58mk262kak3fjmlgo35