(Q44756774)

6 December 2017

The analytical approach to the nature of lipofuscin (age pigment). (English)

1 reference

6 December 2017

Robert D Jolly

1

1 reference

PubMed ID

14764324

6 December 2017

David N Palmer

series ordinal

2

1 reference

PubMed ID

14764324

6 December 2017

Rosalind R Dalefield

series ordinal

3

1 reference

6 December 2017

1 May 2002

1 reference

Archives of Gerontology and Geriatrics

6 December 2017

1 reference

6 December 2017

34

1 reference

6 December 2017

3

1 reference

6 December 2017

205-217

1 reference

Corpora-amylacea and the family of polyglucosan diseases

6 December 2017

1 reference

https://api.crossref.org/works/10.1016%2FS0167-4943%2801%2900219-9

7 January 2021

Peroxidation of subcellular organelles: formation of lipofuscinlike fluorescent pigments

1 reference

https://api.crossref.org/works/10.1016%2FS0167-4943%2801%2900219-9

7 January 2021

When lysosomes get old.

1 reference

https://api.crossref.org/works/10.1016%2FS0167-4943%2801%2900219-9

7 January 2021

Lipofuscin and abnormalities in colloid in the equine thyroid gland in relation to age

1 reference

https://api.crossref.org/works/10.1016%2FS0167-4943%2801%2900219-9

7 January 2021

Lipofuscin fluorophore inhibits lysosomal protein degradation and may cause early stages of macular degeneration

1 reference

https://api.crossref.org/works/10.1016%2FS0167-4943%2801%2900219-9

7 January 2021

The lipid peroxidation theory of lipofuscinogenesis cannot yet be confirmed

1 reference

https://api.crossref.org/works/10.1016%2FS0167-4943%2801%2900219-9

7 January 2021

Tissue culture loading test with storage granules from animal models of neuronal ceroid-lipofuscinosis (Batten disease): testing their lysosomal degradability by normal and Batten cells.

1 reference

https://api.crossref.org/works/10.1016%2FS0167-4943%2801%2900219-9

7 January 2021

The sequence of the major protein stored in ovine ceroid lipofuscinosis is identical with that of the dicyclohexylcarbodiimide-reactive proteolipid of mitochondrial ATP synthase

1 reference

https://api.crossref.org/works/10.1016%2FS0167-4943%2801%2900219-9

7 January 2021

Expression studies of CLN3 protein (battenin) in fusion with the green fluorescent protein in mammalian cells in vitro

1 reference

https://api.crossref.org/works/10.1016%2FS0167-4943%2801%2900219-9

7 January 2021

Aging: a theory based on free radical and radiation chemistry

1 reference

https://api.crossref.org/works/10.1016%2FS0167-4943%2801%2900219-9

7 January 2021

The properties of isolated human cardiac age pigment. I. Preparation and physical properties

1 reference

https://api.crossref.org/works/10.1016%2FS0167-4943%2801%2900219-9

7 January 2021

THE PROPERTIES OF ISOLATED HUMAN CARDIAC AGE PIGMENT. II. CHEMICAL AND ENZYMATIC PROPERTIES

1 reference

https://api.crossref.org/works/10.1016%2FS0167-4943%2801%2900219-9

7 January 2021

Palmitoyl-protein thioesterase and the molecular pathogenesis of infantile neuronal ceroid lipofuscinosis

1 reference

https://api.crossref.org/works/10.1016%2FS0167-4943%2801%2900219-9

7 January 2021

Genotype-phenotype correlations in neuronal ceroid lipofuscinosis due to palmitoyl-protein thioesterase deficiency

1 reference

https://api.crossref.org/works/10.1016%2FS0167-4943%2801%2900219-9

7 January 2021

Immunohistochemical localization of advanced glycation end products, pentosidine, and carboxymethyllysine in lipofuscin pigments of Alzheimer's disease and aged neurons.

1 reference

https://api.crossref.org/works/10.1016%2FS0167-4943%2801%2900219-9

7 January 2021

S100 proteins in Corpora amylacea from normal human brain.

1 reference

https://api.crossref.org/works/10.1016%2FS0167-4943%2801%2900219-9

7 January 2021

Biosynthesis and intracellular targeting of the CLN3 protein defective in Batten disease

1 reference

https://api.crossref.org/works/10.1016%2FS0167-4943%2801%2900219-9

7 January 2021

The ovine model of neuronal ceroid lipofuscinosis (NCL): its contribution to understanding the pathogenesis of Batten disease

1 reference

https://api.crossref.org/works/10.1016%2FS0167-4943%2801%2900219-9

7 January 2021

Lipofuscin in bovine muscle and brain: a model for studying age pigment

1 reference

https://api.crossref.org/works/10.1016%2FS0167-4943%2801%2900219-9

7 January 2021

Inhibitors of lysosomal enzymes: accumulation of lipofuscin-like dense bodies in the brain

1 reference

https://api.crossref.org/works/10.1016%2FS0167-4943%2801%2900219-9

7 January 2021

Advanced glycosylation end-products and heat shock proteins accumulate in the basophilic degeneration of the myocardium and the corpora amylacea of the glia

1 reference

https://api.crossref.org/works/10.1016%2FS0167-4943%2801%2900219-9

7 January 2021

Mitochondrial DNA mutations as an important contributor to ageing and degenerative diseases

1 reference

https://api.crossref.org/works/10.1016%2FS0167-4943%2801%2900219-9

7 January 2021

Turkish variant late infantile neuronal ceroid lipofuscinosis (CLN7) may be allelic to CLN8.

1 reference

https://api.crossref.org/works/10.1016%2FS0167-4943%2801%2900219-9

7 January 2021

Batten's disease: eight genes and still counting?

1 reference

https://api.crossref.org/works/10.1016%2FS0167-4943%2801%2900219-9

7 January 2021

Formation of flourescent pigment in vitamin E deficiency

1 reference

https://api.crossref.org/works/10.1016%2FS0167-4943%2801%2900219-9

7 January 2021

Mitochondrial ATP synthase subunit c storage in the ceroid-lipofuscinoses (Batten disease)

1 reference

https://api.crossref.org/works/10.1016%2FS0167-4943%2801%2900219-9

7 January 2021

Storage bodies in the ceroid-lipofuscinoses (Batten disease): low-molecular-weight components, unusual amino acids and reconstitution of fluorescent bodies from non-fluorescent components

1 reference

https://api.crossref.org/works/10.1016%2FS0167-4943%2801%2900219-9

7 January 2021

The lipopigments in human brain tissue necroses. I. Ceroid.

1 reference

https://api.crossref.org/works/10.1016%2FS0167-4943%2801%2900219-9

7 January 2021

The lipopigments in human brain tissue necroses. II. Hemoceroid.

1 reference

https://api.crossref.org/works/10.1016%2FS0167-4943%2801%2900219-9

7 January 2021

[Isolation and properties of lipofuscin from human heart tissue]

1 reference

https://api.crossref.org/works/10.1016%2FS0167-4943%2801%2900219-9

7 January 2021

Association of mutations in a lysosomal protein with classical late-infantile neuronal ceroid lipofuscinosis

1 reference

https://api.crossref.org/works/10.1016%2FS0167-4943%2801%2900219-9

7 January 2021

Studies on chemical nature of lipofuscin (age pigment) isolated from normal human brain

1 reference

https://api.crossref.org/works/10.1016%2FS0167-4943%2801%2900219-9

7 January 2021

A mutation in the ovine cathepsin D gene causes a congenital lysosomal storage disease with profound neurodegeneration

1 reference

https://api.crossref.org/works/10.1016%2FS0167-4943%2801%2900219-9

7 January 2021

Classical late infantile neuronal ceroid lipofuscinosis fibroblasts are deficient in lysosomal tripeptidyl peptidase I

1 reference

https://api.crossref.org/works/10.1016%2FS0167-4943%2801%2900219-9

7 January 2021

Mitochondrial DNA mutations in human degenerative diseases and aging

1 reference

https://api.crossref.org/works/10.1016%2FS0167-4943%2801%2900219-9

7 January 2021

Presidential address: Studies in the neuronal ceroid-lipofuscinoses.

1 reference

https://api.crossref.org/works/10.1016%2FS0167-4943%2801%2900219-9

7 January 2021

10.1016/S0167-4943(01)00219-9

Identifiers

DOI

1 reference

6 December 2017

1 reference

PubMed ID

14764324