Log in to save to my catalogue

Napsin A, a new marker for lung adenocarcinoma, is complementary and more sensitive and specific tha...

Napsin A, a new marker for lung adenocarcinoma, is complementary and more sensitive and specific tha...

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_miscellaneous_919226034

Napsin A, a new marker for lung adenocarcinoma, is complementary and more sensitive and specific than thyroid transcription factor 1 in the differential diagnosis of primary pulmonary carcinoma: evaluation of 1674 cases by tissue microarray

About this item

Full title

Napsin A, a new marker for lung adenocarcinoma, is complementary and more sensitive and specific than thyroid transcription factor 1 in the differential diagnosis of primary pulmonary carcinoma: evaluation of 1674 cases by tissue microarray

Publisher

United States: College of American Pathologists

Journal title

Archives of pathology & laboratory medicine (1976), 2012-02, Vol.136 (2), p.163-171

Language

English

Formats

Publication information

Publisher

United States: College of American Pathologists

More information

Scope and Contents

Contents

Differentiation of non-small cell carcinoma into histologic types is important because of new, successful therapies that target lung adenocarcinoma (ACA). TTF-1 is a favored marker for lung ACA but has limited sensitivity and specificity. Napsin A (Nap-A) is a functional aspartic proteinase that may be an alternative marker for primary lung ACA.

Alternative Titles

Full title

Napsin A, a new marker for lung adenocarcinoma, is complementary and more sensitive and specific than thyroid transcription factor 1 in the differential diagnosis of primary pulmonary carcinoma: evaluation of 1674 cases by tissue microarray

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_proquest_miscellaneous_919226034

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_miscellaneous_919226034

Other Identifiers

ISSN

0003-9985,1543-2165

E-ISSN

1543-2165

DOI

10.5858/arpa.2011-0320-OA

How to access this item