Search Results - "Klein, Mara E."
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1
Homozygous Loss of BHD Causes Early Embryonic Lethality and Kidney Tumor Development with Activation of mTORC1 and mTORC2
Published in Proceedings of the National Academy of Sciences - PNAS (03-11-2009)“…Germline mutations in the BHD/FLCN tumor suppressor gene pre-dispose patients to develop renal tumors in the hamartoma syndrome, Birt-Hogg-Dubé (BHD). BHD…”
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2
Regulation of mitochondrial oxidative metabolism by tumor suppressor FLCN
Published in JNCI : Journal of the National Cancer Institute (21-11-2012)“…Birt-Hogg-Dubé (BHD) syndrome is a hereditary hamartoma syndrome that predisposes patients to develop hair follicle tumors, lung cysts, and kidney cancer…”
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3
The folliculin-FNIP1 pathway deleted in human Birt-Hogg-Dubé syndrome is required for murine B-cell development
Published in Blood (09-08-2012)“…Birt-Hogg-Dubé (BHD) syndrome is an autosomal dominant disorder characterized by cutaneous fibrofolliculomas, pulmonary cysts, and kidney malignancies…”
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4
Regulation of Mitochondria Oxidative Metabolism by Tumor Suppressor FLCN
Published in JNCI : Journal of the National Cancer Institute (21-11-2012)“…Birt-Hogg-Dube (BHD) syndrome is a hereditary hamartoma syndrome that predisposes patients to develop hair follicle tumors, lung cysts, and kidney cancer…”
Get full text
Journal Article -
5
Regulation of Mitochondrial Oxidative Metabolism byTumor Suppressor FLCN
Published in JNCI : Journal of the National Cancer Institute (2012)Get full text
Journal Article