Characterisation of lipofuscin-like lysosomal inclusion bodies from human placenta. (Q52575698)

3 May 2018

title

Characterisation of lipofuscin-like lysosomal inclusion bodies from human placenta. (English)

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3 May 2018

author name string

Bernd Schröder

1

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3 May 2018

Hans-Peter Elsässer

2

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Bernhard Schmidt

3

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3 May 2018

Andrej Hasilik

4

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3 May 2018

language of work or name

English

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publication date

12 December 2006

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3 May 2018

number of pages

7

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based on heuristic

inferred from page(s)

published in

FEBS Letters

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volume

581

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issue

1

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page(s)

102-108

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https://api.crossref.org/works/10.1016/J.FEBSLET.2006.12.005

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You say lipofuscin, we say ceroid: defining autofluorescent storage material

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The lysosomal-mitochondrial axis theory of postmitotic aging and cell death

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A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding

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Cleavage of Structural Proteins during the Assembly of the Head of Bacteriophage T4

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Improved staining of proteins in polyacrylamide gels including isoelectric focusing gels with clear background at nanogram sensitivity using Coomassie Brilliant Blue G-250 and R-250.

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Technical innovations for the automated identification of gel-separated proteins by MALDI-TOF mass spectrometry

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Proteome analysis of lipofuscin in human retinal pigment epithelial cells

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https://api.crossref.org/works/10.1016/J.FEBSLET.2006.12.005

Batten's disease: clues to neuronal protein catabolism in lysosomes

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1 reference

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Apoptotic changes occur in syncytiotrophoblast of human placental villi where fibrin type fibrinoid is deposited at discontinuities in the villous trophoblast

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1 reference

https://api.crossref.org/works/10.1016/J.FEBSLET.2006.12.005

Phagocytosis as a potential mechanism for microbial defense of mouse placental trophoblast cells

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The phagocytic activity of human first trimester extravillous trophoblast

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Biochemical characterization of a lysosomal protease deficient in classical late infantile neuronal ceroid lipofuscinosis (LINCL) and development of an enzyme-based assay for diagnosis and exclusion of LINCL in human specimens and animal models

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1 reference

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Purification and characterization of bovine brain lysosomal pepstatin-insensitive proteinase, the gene product deficient in the human late-infantile neuronal ceroid lipofuscinosis

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Rat tripeptidyl peptidase I: molecular cloning, functional expression, tissue localization and enzymatic characterization

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Purification and characterization of a tripeptidyl peptidase I from human osteoclastomas: evidence for its role in bone resorption

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1 reference

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Tripeptidyl-peptidase I in health and disease

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Neuronal ceroid lipofuscinoses are connected at molecular level: interaction of CLN5 protein with CLN2 and CLN3

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21 January 2018

Identifiers

DOI

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3 May 2018

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3 May 2018