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Evaluation of Hsp90 and mTOR inhibitors as potential drugs for the treatment of TSC1/TSC2 deficient...

Evaluation of Hsp90 and mTOR inhibitors as potential drugs for the treatment of TSC1/TSC2 deficient...

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_plos_journals_2517338878

Evaluation of Hsp90 and mTOR inhibitors as potential drugs for the treatment of TSC1/TSC2 deficient cancer

About this item

Full title

Evaluation of Hsp90 and mTOR inhibitors as potential drugs for the treatment of TSC1/TSC2 deficient cancer

Publisher

United States: Public Library of Science

Journal title

PloS one, 2021-04, Vol.16 (4), p.e0248380-e0248380

Language

English

Formats

Publication information

Publisher

United States: Public Library of Science

More information

Scope and Contents

Contents

Inactivating mutations in either
TSC1
or
TSC2
cause Tuberous Sclerosis Complex, an autosomal dominant disorder, characterized by multi-system tumor and hamartoma development. Mutation and loss of function of
TSC1
and/or
TSC2
also occur in a variety of sporadic cancers, and rapamycin and related drugs show highly variable tre...

Alternative Titles

Full title

Evaluation of Hsp90 and mTOR inhibitors as potential drugs for the treatment of TSC1/TSC2 deficient cancer

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_plos_journals_2517338878

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_plos_journals_2517338878

Other Identifiers

ISSN

1932-6203

E-ISSN

1932-6203

DOI

10.1371/journal.pone.0248380

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