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Deletion of cathepsin H perturbs angiogenic switching, vascularization and growth of tumors in a mouse model of pancreatic islet cell cancer
scientific journal article
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scholarly article
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PubMed
PubMed ID
20731543
retrieved
24 January 2017
title
Deletion of cathepsin H perturbs angiogenic switching, vascularization and growth of tumors in a mouse model of pancreatic islet cell cancer
(English)
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PubMed
PubMed ID
20731543
retrieved
24 January 2017
main subject
Cathepsin H
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GOA release 2020-03-11
author name string
Vasilena Gocheva
series ordinal
1
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PubMed
PubMed ID
20731543
retrieved
24 January 2017
Xiaoping Chen
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2
1 reference
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PubMed
PubMed ID
20731543
retrieved
24 January 2017
Christoph Peters
series ordinal
3
1 reference
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PubMed
PubMed ID
20731543
retrieved
24 January 2017
Thomas Reinheckel
series ordinal
4
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PubMed
PubMed ID
20731543
retrieved
24 January 2017
Johanna A. Joyce
series ordinal
5
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PubMed
PubMed ID
20731543
retrieved
24 January 2017
language of work or name
English
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publication date
1 August 2010
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PubMed ID
20731543
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24 January 2017
published in
Biological Chemistry
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PubMed
PubMed ID
20731543
retrieved
24 January 2017
volume
391
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PubMed
PubMed ID
20731543
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24 January 2017
issue
8
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PubMed
PubMed ID
20731543
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24 January 2017
page(s)
937–945
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PubMed
PubMed ID
20731543
retrieved
24 January 2017
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Cathepsin L is required for endothelial progenitor cell-induced neovascularization
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Cathepsin cysteine proteases are effectors of invasive growth and angiogenesis during multistage tumorigenesis
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Selective disruption of lysosomes in HeLa cells triggers apoptosis mediated by cleavage of Bid by multiple papain-like lysosomal cathepsins
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Recombinant human cathepsin H lacking the mini chain is an endopeptidase
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Elevated levels of IGF-1 receptor convey invasive and metastatic capability in a mouse model of pancreatic islet tumorigenesis
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Biosyntheses and processing of lysosomal cysteine proteinases in rat macrophages
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PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/20731543
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based on heuristic
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The potential role of human kidney cortex cysteine proteinases in glomerular basement membrane degradation
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PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/20731543
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12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Cathepsins B, H and L in human breast carcinoma
1 reference
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PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/20731543
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Lysosomal proteases cathepsins D, B, H, L and their inhibitors stefins A and B in head and neck cancer
1 reference
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PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/20731543
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Prognostic value of cathepsins B, H, L, D and their endogenous inhibitors stefins A and B in head and neck carcinoma
1 reference
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PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/20731543
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Activity, expression, and transcription rate of the cathepsins B, D, H, and L in cutaneous malignant melanoma
1 reference
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PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/20731543
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Identifiers
DOI
10.1515/BC.2010.080
1 reference
stated in
PubMed
PubMed ID
20731543
retrieved
24 January 2017
PMCID
3126667
0 references
PubMed ID
20731543
1 reference
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PubMed
PubMed ID
20731543
retrieved
24 January 2017
ResearchGate publication ID
45819682
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