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A high-quality severe combined immunodeficiency (SCID) rat bioresource

open access: yesA high-quality severe combined immunodeficiency (SCID) rat bioresource
openaire  

Severe Combined Immunodeficiency (SCID)—the Irish Experience

Journal of Clinical Immunology, 2021
H. Burns   +7 more
semanticscholar   +3 more sources

Gene therapy of human severe combined immunodeficiency (SCID)-X1 disease.

Science, 2000
Severe combined immunodeficiency–X1 (SCID-X1) is an X-linked inherited disorder characterized by an early block in T and natural killer (NK) lymphocyte differentiation. This block is caused by mutations of the gene encoding the γc cytokine receptor subunit of interleukin-2, -4, -7, -9, and -15 receptors, which participates in the delivery ...
M. Cavazzana‐Calvo   +12 more
semanticscholar   +3 more sources

The Case for Mandatory Newborn Screening for Severe Combined Immunodeficiency (SCID)

Journal of Clinical Immunology, 2014
Severe combined immunodeficiency (SCID) is the most severe form of inherited primary immunodeficiency and is a paediatric emergency. Delay in recognising and detecting SCID can have fatal consequences and also reduces the chances of a successful haematopoietic stem cell transplant (HSCT).
H. Gaspar   +6 more
semanticscholar   +3 more sources

Human Taenia in Severe Combined Immunodeficiency (SCID) Mice

Parasitology Today, 1999
A rodent model for the development of the larval stages of human taeniid tapeworms would help advance immunodiagnosis in human and domestic animals and vaccine development for cysticercosis cellulosae or bovis in domestic animals. Here, Akira Ito and Mamoru Ito review recent results demonstrating the potential of the severe combined immunodeficiency ...
A, Ito, M, Ito
openaire   +2 more sources

Bacille Calmette-Guerin (BCG) complications in children with severe combined immunodeficiency (SCID)

Infectious Diseases, 2019
Background: Bacille Calmette-Guerin (BCG) is included in the routine vaccination program in Gaza and the West Bank. Although safe, complications can occur and include local, extra-regional and disseminated BCG infection.
G. Barkai   +4 more
semanticscholar   +1 more source

Cellular radiosensitivity in human severe-combined-immunodeficiency (SCID) syndromes

Radiotherapy and Oncology, 1997
The aim of the work was to establish to what extent a variety of human severe-combined-immunodeficiency (SCID) disorders are associated with in vitro cellular hypersensitivity to ionizing radiation.A study was made of fibroblast strains established from individuals with adenosine deaminase deficiency, T(-)B(-) SCID, Omenn's syndrome and a SCID ...
A R, Sproston, C M, West, J H, Hendry
openaire   +2 more sources

Lymphopenia and Severe Combined Immunodeficiency (SCID) - Think Before You Ink

The Indian Journal of Pediatrics, 2019
Severe combined immunodeficiency (SCID) represents one of the most severe forms of Primary immunodeficiency (PID) disorders, characterized by T cell lymphopenia (TCL) and lack of cellular and humoral immune responses. However, not all patients with low T cell lymphocyte counts may have an abnormal T cell immunity and the observed TCL may be a temporary
Jahnavi, Aluri   +7 more
openaire   +2 more sources

LPS-inducible responses in severe combined immunodeficiency (SCID) mice

Journal of Endotoxin Research, 1995
Lipopolysaccharide (LPS) is a potent bacterial product that has been shown to act on many different cell types both in vivo and in vitro. Injection of immunologically competent mice with LPS results in increased serum cytokine levels, followed by an array of pathophysiologic alterations that can ultimately lead to death. In this study, we examined the
L.A. Falk   +4 more
openaire   +1 more source

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