(Q45887234)

17 December 2017

title

Development and maturation of invariant NKT cells in the presence of lysosomal engulfment (English)

1 reference

17 December 2017

author

Maria Pia Cosma

6

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17 December 2017

Alessia Capotondo

Alessia Capotondo

3

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Luigi Naldini

Luigi Naldini

5

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Mario Buono

4

Mario Buono

1 reference

17 December 2017

Ilaria Visigalli

2

Ilaria Visigalli

1 reference

17 December 2017

author name string

Tiziana Plati

1

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17 December 2017

Alessandra Biffi

7

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17 December 2017

language of work or name

English

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publication date

1 October 2009

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17 December 2017

European Journal of Immunology

published in

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17 December 2017

volume

39

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17 December 2017

issue

10

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17 December 2017

page(s)

2748-2754

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17 December 2017

Multiple defects in antigen presentation and T cell development by mice expressing cytoplasmic tail-truncated CD1d

cites work

1 reference

https://api.crossref.org/works/10.1002%2FEJI.200939639

7 January 2021

Thymocyte expression of cathepsin L is essential for NKT cell development

1 reference

https://api.crossref.org/works/10.1002%2FEJI.200939639

7 January 2021

Lysosomal glycosphingolipid recognition by NKT cells

1 reference

https://api.crossref.org/works/10.1002%2FEJI.200939639

7 January 2021

Binding and antigen presentation of ceramide-containing glycolipids by soluble mouse and human CD1d molecules

1 reference

https://api.crossref.org/works/10.1002%2FEJI.200939639

7 January 2021

Defective presentation of the CD1d1-restricted natural Va14Ja18 NKT lymphocyte antigen caused by beta-D-glucosylceramide synthase deficiency

1 reference

https://api.crossref.org/works/10.1002%2FEJI.200939639

7 January 2021

Control points in NKT-cell development

1 reference

https://api.crossref.org/works/10.1002%2FEJI.200939639

7 January 2021

Normal development and function of invariant natural killer T cells in mice with isoglobotrihexosylceramide (iGb3) deficiency

1 reference

https://api.crossref.org/works/10.1002%2FEJI.200939639

7 January 2021

Implications for invariant natural killer T cell ligands due to the restricted presence of isoglobotrihexosylceramide in mammals

1 reference

https://api.crossref.org/works/10.1002%2FEJI.200939639

7 January 2021

Impaired selection of invariant natural killer T cells in diverse mouse models of glycosphingolipid lysosomal storage diseases

1 reference

https://api.crossref.org/works/10.1002%2FEJI.200939639

7 January 2021

Differential alteration of lipid antigen presentation to NKT cells due to imbalances in lipid metabolism

1 reference

https://api.crossref.org/works/10.1002%2FEJI.200939639

7 January 2021

Molecular Genetics of Metachromatic Leukodystrophy

1 reference

https://api.crossref.org/works/10.1002%2FEJI.200939639

7 January 2021

Phenotype of arylsulfatase A-deficient mice: relationship to human metachromatic leukodystrophy

1 reference

https://api.crossref.org/works/10.1002%2FEJI.200939639

7 January 2021

Globoid Cell Leukodystrophy (Krabbe's Disease): Update

1 reference

https://api.crossref.org/works/10.1002%2FEJI.200939639

7 January 2021

The twitcher mouse: a model for Krabbe disease and for experimental therapies

1 reference

https://api.crossref.org/works/10.1002%2FEJI.200939639

7 January 2021

Molecular genetics of mucopolysaccharidosis type I: diagnostic, clinical, and biological implications.

1 reference

https://api.crossref.org/works/10.1002%2FEJI.200939639

7 January 2021

The multiple sulfatase deficiency gene encodes an essential and limiting factor for the activity of sulfatases

1 reference

https://api.crossref.org/works/10.1002%2FEJI.200939639

7 January 2021

Multiple sulfatase deficiency is caused by mutations in the gene encoding the human C(alpha)-formylglycine generating enzyme

1 reference

https://api.crossref.org/works/10.1002%2FEJI.200939639

7 January 2021

Sulfatases and sulfatase modifying factors: an exclusive and promiscuous relationship

1 reference

https://api.crossref.org/works/10.1002%2FEJI.200939639

7 January 2021

Systemic inflammation and neurodegeneration in a mouse model of multiple sulfatase deficiency

1 reference

https://api.crossref.org/works/10.1002%2FEJI.200939639

7 January 2021

Autonomic denervation of lymphoid organs leads to epigenetic immune atrophy in a mouse model of Krabbe disease.

1 reference

https://api.crossref.org/works/10.1002%2FEJI.200939639

7 January 2021

Evidence for a link between sphingolipid metabolism and expression of CD1d and MHC-class II: monocytes from Gaucher disease patients as a model

1 reference

https://api.crossref.org/works/10.1002%2FEJI.200939639

7 January 2021

Identifiers

DOI

10.1002/EJI.200939639

1 reference

17 December 2017

1 reference

17 December 2017