(Q28585898)

31 January 2017

title

Apoptotic cell death in mouse models of GM2 gangliosidosis and observations on human Tay-Sachs and Sandhoff diseases (English)

1 reference

31 January 2017

Apoptotic Cell Death in Mouse Models of GM2 Gangliosidosis and Observations on Human Tay-Sachs and Sandhoff Diseases (English)

1 reference

https://api.crossref.org/works/10.1093/HMG/6.11.1879

16 November 2024

0 references

0 references

1 reference

GOA release 2020-03-11

author name string

J. Q. Huang

1

1 reference

31 January 2017

J. M. Trasler

2

1 reference

31 January 2017

S. Igdoura

3

1 reference

31 January 2017

J. Michaud

4

1 reference

31 January 2017

N. Hanal

5

1 reference

31 January 2017

R. A. Gravel

6

1 reference

31 January 2017

language of work or name

English

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=9302266

16 November 2024

publication date

1 October 1997

1 reference

31 January 2017

October 1997

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=9302266

16 November 2024

published in

Human Molecular Genetics

1 reference

31 January 2017

volume

6

1 reference

31 January 2017

issue

11

1 reference

31 January 2017

page(s)

1879–1885

1 reference

Occurrence of lysoganglioside lyso-GM2 (II3-Neu5Ac-gangliotriaosylsphingosine) in GM2 gangliosidosis brain.

31 January 2017

cites work

2

1 reference

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Neuroaxonal dystrophy in neuronal storage disorders: evidence for major GABAergic neuron involvement

16 November 2024

3

1 reference

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Targeted disruption of the Hexa gene results in mice with biochemical and pathologic features of Tay-Sachs disease

16 November 2024

4

1 reference

https://api.crossref.org/works/10.1093/HMG/6.11.1879

Neuropathology of mice with targeted disruption of Hexa gene, a model of Tay-Sachs disease

16 November 2024

5

1 reference

https://api.crossref.org/works/10.1093/HMG/6.11.1879

Mouse models of Tay-Sachs and Sandhoff diseases differ in neurologic phenotype and ganglioside metabolism

16 November 2024

6

1 reference

https://api.crossref.org/works/10.1093/HMG/6.11.1879

Disruption of murine Hexa gene leads to enzymatic deficiency and to neuronal lysosomal storage, similar to that observed in Tay-Sachs disease

16 November 2024

7

1 reference

https://api.crossref.org/works/10.1093/HMG/6.11.1879

Dramatically different phenotypes in mouse models of human Tay-Sachs and Sandhoff diseases

16 November 2024

8

1 reference

https://api.crossref.org/works/10.1093/HMG/6.11.1879

Cell death: the significance of apoptosis

16 November 2024

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1 reference

https://api.crossref.org/works/10.1093/HMG/6.11.1879

The molecular biology of apoptosis

16 November 2024

10

1 reference

https://api.crossref.org/works/10.1093/HMG/6.11.1879

Apoptosis in the pathogenesis and treatment of disease

16 November 2024

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1 reference

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Developmental cell death: morphological diversity and multiple mechanisms

16 November 2024

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Interstitial cells of the adult neocortical white matter are the remnant of the early generated subplate neuron population

16 November 2024

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Functional dichotomy of neutral and acidic sphingomyelinases in tumor necrosis factor signaling

16 November 2024

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1 reference

https://api.crossref.org/works/10.1093/HMG/6.11.1879

Induction of apoptotic DNA damage and cell death by activation of the sphingomyelin pathway

16 November 2024

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1 reference

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Functions of ceramide in coordinating cellular responses to stress

16 November 2024

17

1 reference

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Requirement for ceramide-initiated SAPK/JNK signalling in stress-induced apoptosis.

16 November 2024

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1 reference

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Ceramide synthase mediates daunorubicin-induced apoptosis: An alternative mechanism for generating death signals

16 November 2024

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1 reference

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Acid sphingomyelinase-deficient human lymphoblasts and mice are defective in radiation-induced apoptosis.

16 November 2024

21

1 reference

https://api.crossref.org/works/10.1093/HMG/6.11.1879

16 November 2024

Identifiers

0 references

1 reference