Birt-Hogg-Dubé renal tumors are genetically distinct from other renal neoplasias and are associated...
Birt-Hogg-Dubé renal tumors are genetically distinct from other renal neoplasias and are associated with up-regulation of mitochondrial gene expression
About this item
Full title
Author / Creator
Klomp, Jeff A , Petillo, David , Niemi, Natalie M , Dykema, Karl J , Chen, Jindong , Yang, Ximing J , Sääf, Annika , Zickert, Peter , Aly, Markus , Bergerheim, Ulf , Nordenskjöld, Magnus , Gad, Sophie , Giraud, Sophie , Denoux, Yves , Yonneau, Laurent , Méjean, Arnaud , Vasiliu, Viorel , Richard, Stéphane , MacKeigan, Jeffrey P , Teh, Bin T and Furge, Kyle A
Publisher
England: BioMed Central Ltd
Journal title
Language
English
Formats
Publication information
Publisher
England: BioMed Central Ltd
Subjects
More information
Scope and Contents
Contents
Germline mutations in the folliculin (FLCN) gene are associated with the development of Birt-Hogg-Dubé syndrome (BHDS), a disease characterized by papular skin lesions, a high occurrence of spontaneous pneumothorax, and the development of renal neoplasias. The majority of renal tumors that arise in BHDS-affected individuals are histologically simil...
Alternative Titles
Full title
Birt-Hogg-Dubé renal tumors are genetically distinct from other renal neoplasias and are associated with up-regulation of mitochondrial gene expression
Authors, Artists and Contributors
Author / Creator
Petillo, David
Niemi, Natalie M
Dykema, Karl J
Chen, Jindong
Yang, Ximing J
Sääf, Annika
Zickert, Peter
Aly, Markus
Bergerheim, Ulf
Nordenskjöld, Magnus
Gad, Sophie
Giraud, Sophie
Denoux, Yves
Yonneau, Laurent
Méjean, Arnaud
Vasiliu, Viorel
Richard, Stéphane
MacKeigan, Jeffrey P
Teh, Bin T
Furge, Kyle A
Identifiers
Primary Identifiers
Record Identifier
TN_cdi_doaj_primary_oai_doaj_org_article_219aa39d0f174213b0b236a620037294
Permalink
https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_219aa39d0f174213b0b236a620037294
Other Identifiers
ISSN
1755-8794
E-ISSN
1755-8794
DOI
10.1186/1755-8794-3-59
