Pascal and Francis Bibliographic Databases

Help

Search results

Your search

au.\*:("SCHMIDT, Laura S")

Publication Year[py]

A-Z Z-A Frequency ↓ Frequency ↑
Export in CSV

Discipline (document) [di]

A-Z Z-A Frequency ↓ Frequency ↑
Export in CSV

Author Country

A-Z Z-A Frequency ↓ Frequency ↑
Export in CSV

Results 1 to 21 of 21

  • Page / 1
Export

Selection :

  • and

The folliculin-FNIP1 pathway deleted in human Birt-Hogg-Dubé syndrome is required for murine B-cell developmentBABA, Masaya; KELLER, Jonathan R; HUGHES, Robert M et al.Blood. 2012, Vol 120, Num 6, pp 1254-1261, issn 0006-4971, 8 p.Article

Vascular defects and liver damage by the acute inactivation of the VHL gene during mouse embryogenesisHONG, Seung-Beom; FURIHATA, Mutsuo; BABA, Masaya et al.Laboratory investigation. 2006, Vol 86, Num 7, pp 664-675, issn 0023-6837, 12 p.Article

Germline BHD-mutation spectrum and phenotype analysis of a large cohort of families with birt-hogg-dubé syndromeSCHMIDT, Laura S; NICKERSON, Michael L; MORRISON, Patrick et al.American journal of human genetics. 2005, Vol 76, Num 6, pp 1023-1033, issn 0002-9297, 11 p.Article

Kidney-Targeted Birt-Hogg-Dubé Gene Inactivation in a Mouse Model : Erk1/2 and Akt-mTOR Activation, Cell Hyperproliferation, and Polycystic KidneysBABA, Masaya; FURIHATA, Mutsuo; YAO, Masahiro et al.Journal of the National Cancer Institute. 2008, Vol 100, Num 2, pp 140-154, issn 0027-8874, 15 p.Article

Acute Inactivation of the VHL Gene Contributes to Protective Effects of Ischemic Preconditioning in the Mouse KidneyIGUCHI, Mitsuko; KAKINUMA, Yoshihiko; KURABAYASHI, Atsushi et al.The Nephron journals. 2008, Vol 110, Num 3, issn 1660-8151, e82-e90Article

A mutation in the canine BHD gene is associated with hereditary multifocal renal cystadenocarcinoma and nodular dermatofibrosis in the German Shepherd dogLINGAAS, Frode; COMSTOCK, Kenine E; BREEN, Matthew et al.Human molecular genetics (Print). 2003, Vol 12, Num 23, pp 3043-3053, issn 0964-6906, 11 p.Article

Regulation of Mitochondrial Oxidative Metabolism byTumor Suppressor FLCNHASUMI, Hisashi; BABA, Masaya; MARSTON LINEHAN, W et al.Journal of the National Cancer Institute. 2012, Vol 104, Num 22, pp 1750-1764, issn 0027-8874, 15 p.Article

Serum Vascular Endothelial Growth Factor-D Prospectively Distinguishes Lymphangioleiomyomatosis From Other DiseasesYOUNG, Lisa R; VANDYKE, Rhonda; BISSLER, John J et al.Chest (American College of Chest Physicians). 2010, Vol 138, Num 3, pp 674-681, issn 0012-3692, 8 p.Article

Lung cysts, spontaneous pneumothorax, and genetic associations in 89 families with birt-hogg-dubé syndromeTORO, Jorge R; PAUTLER, Stephen E; CHOYKE, Peter et al.American journal of respiratory and critical care medicine. 2007, Vol 175, Num 10, pp 1044-1053, issn 1073-449X, 10 p.Article

Mutations in the fumarate hydratase gene cause hereditary leiomyomatosis and renal cell cancer in families in North AmericaTORO, Jorge R; NICKERSON, Michael L; CHOYKE, Peter et al.American journal of human genetics. 2003, Vol 73, Num 1, pp 95-106, issn 0002-9297, 12 p.Article

Improved Identification of von Hippel-Lindau Gene Alterations in Clear Cell Renal TumorsNICKERSON, Michael L; JAEGER, Erich; NAVRATILOVA, Marie et al.Clinical cancer research (Print). 2008, Vol 14, Num 15, pp 4726-4734, issn 1078-0432, 9 p.Article

Familial renal carcinoma: Clinical evaluation, clinical subtypes and risk of renal carcinoma development. CommentaryZBAR, Berton; GLENN, Gladys; LINEHAN, W. Marston et al.The Journal of urology. 2007, Vol 177, Num 2, pp 461-465, issn 0022-5347, 5 p.Article

The Met kinase inhibitor SU11274 exhibits a selective inhibition pattern toward different receptor mutated variantsBERTHOU, Sylvie; AEBERSOLD, Daniel M; CANDINAS, Daniel et al.Oncogene (Basingstoke). 2004, Vol 23, Num 31, pp 5387-5393, issn 0950-9232, 7 p.Article

Hepatic vascular tumors, angiectasis in multiple organs, and impaired spermatogenesis in mice with conditional inactivation of the VHL geneWENBIN MA; TESSAROLLO, Lino; PACK, Svetlana et al.Cancer research (Baltimore). 2003, Vol 63, Num 17, pp 5320-5328, issn 0008-5472, 9 p.Article

Birt-Hogg-Dubé syndrome, a genodermatosis associated with spontaneous pneumothorax and kidney neoplasia, maps to chromosome 17p11.2SCHMIDT, Laura S; WARREN, Michelle B; PAVLOVICH, Christian P et al.American journal of human genetics. 2001, Vol 69, Num 4, pp 876-882, issn 0002-9297Article

Succinate Dehydrogenase Kidney Cancer: An Aggressive Example of the Warburg Effect in CancerRICKETTS, Christopher J; SHUCH, Brian; STOLLE, Catherine A et al.The Journal of urology. 2012, Vol 188, Num 6, pp 2063-2071, issn 0022-5347, 9 p., 1Article

Proteomic Analysis of Ethene-Enriched Groundwater Microcosms from a Vinyl Chloride-Contaminated SiteCHUANG, Adina S; YANG OH JIN; SCHMIDT, Laura S et al.Environmental science & technology. 2010, Vol 44, Num 5, pp 1594-1601, issn 0013-936X, 8 p.Article

Hereditary Kidney Cancer: Unique Opportunity for Disease-based TherapyMARSTON LINEHAN, W; PINTO, Peter A; SRINIVASAN, Ramaprasad et al.Cancer. 2009, Vol 115, Num 10, pp 2252-2261, issn 0008-543X, 10 p., SUPConference Paper

High frequency of somatic frameshift BHD gene mutations in Birt-Hogg-Dubé-Associated renal tumorsVOCKE, Cathy D; YOUFENG YANG; PAVLOVICH, Christian P et al.Journal of the National Cancer Institute. 2005, Vol 97, Num 12, pp 931-935, issn 0027-8874, 5 p.Article

The Ter mutation in the dead end gene causes germ cell loss and testicular germ cell tumoursYOUNGREN, Kirsten K; COVENEY, Douglas; RUBIN, Edward M et al.Nature (London). 2005, Vol 435, Num 7040, pp 360-364, issn 0028-0836, 5 p.Article

Early onset hereditary papillary renal carcinoma: Germline missense mutations in the tyrosine kinase domain of the MET proto-oncogeneSCHMIDT, Laura S; NICKERSON, Michael L; BRUNET, Joan et al.The Journal of urology. 2004, Vol 172, Num 4, pp 1256-1261, issn 0022-5347, 6 p., 1Article

  • Page / 1