1 - 25 of 34 results for author:"Zbar B." in Literature citations
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| Improved identification of von Hippel-Lindau gene alterations in clear cell renal tumors. Nickerson M.L., Jaeger E., Shi Y., Durocher J.A., Mahurkar S., Zaridze D., Matveev V., Janout V., Kollarova H., Bencko V. et al. Clin. Cancer Res. 14:4726-4734(2008) · Mapped (3) |
| Kidney-targeted Birt-Hogg-Dube gene inactivation in a mouse model: Erk1/2 and Akt-mTOR activation, cell hyperproliferation, and polycystic kidneys. Baba M., Furihata M., Hong S.B., Tessarollo L., Haines D.C., Southon E., Patel V., Igarashi P., Alvord W.G., Leighty R. et al. J. Natl. Cancer Inst. 100:140-154(2008) · Mapped (2) |
| Folliculin encoded by the BHD gene interacts with a binding protein, FNIP1, and AMPK, and is involved in AMPK and mTOR signaling. Baba M., Hong S.-B., Sharma N., Warren M.B., Nickerson M.L., Iwamatsu A., Esposito D., Gillette W.K., Hopkins R.F. III, Hartley J.L. et al. Proc. Natl. Acad. Sci. U.S.A. 103:15552-15557(2006) · UniProtKB (6) · Mapped (11) |
| Vascular defects and liver damage by the acute inactivation of the VHL gene during mouse embryogenesis. Hong S.B., Furihata M., Baba M., Zbar B., Schmidt L.S. Lab. Invest. 86:664-675(2006) · Mapped (2) |
| The Drosophila homolog of the human tumor suppressor gene BHD interacts with the JAK-STAT and Dpp signaling pathways in regulating male germline stem cell maintenance. Singh S.R., Zhen W., Zheng Z., Wang H., Oh S.W., Liu W., Zbar B., Schmidt L.S., Hou S.X. Oncogene 25:5933-5941(2006) · Mapped (33) |
| Fumarate hydratase enzyme activity in lymphoblastoid cells and fibroblasts of individuals in families with hereditary leiomyomatosis and renal cell cancer. Pithukpakorn M., Wei M.H., Toure O., Steinbach P.J., Glenn G.M., Zbar B., Linehan W.M., Toro J.R. J. Med. Genet. 43:755-762(2006) · Mapped (2) |
| HIF overexpression correlates with biallelic loss of fumarate hydratase in renal cancer: novel role of fumarate in regulation of HIF stability. Isaacs J.S., Jung Y.J., Mole D.R., Lee S., Torres-Cabala C., Chung Y.L., Merino M., Trepel J., Zbar B., Toro J. et al. Cancer Cell 8:143-153(2005) · Mapped (2) |
| High frequency of somatic frameshift BHD gene mutations in Birt-Hogg-Dube-associated renal tumors. Vocke C.D., Yang Y., Pavlovich C.P., Schmidt L.S., Nickerson M.L., Torres-Cabala C.A., Merino M.J., Walther M.M., Zbar B., Linehan W.M. J. Natl. Cancer Inst. 97:931-935(2005) · Mapped (2) |
| Novel mutations in FH and expansion of the spectrum of phenotypes expressed in families with hereditary leiomyomatosis and renal cell cancer. Wei M.H., Toure O., Glenn G.M., Pithukpakorn M., Neckers L., Stolle C., Choyke P., Grubb R., Middelton L., Turner M.L. et al. |
| Germline BHD-mutation spectrum and phenotype analysis of a large cohort of families with Birt-Hogg-Dube syndrome. Schmidt L.S., Nickerson M.L., Warren M.B., Glenn G.M., Toro J.R., Merino M.J., Turner M.L., Choyke P.L., Sharma N., Peterson J. et al. Am. J. Hum. Genet. 76:1023-1033(2005) · UniProtKB (1) · Mapped (1) |
| A germ-line insertion in the Birt-Hogg-Dube (BHD) gene gives rise to the Nihon rat model of inherited renal cancer. Okimoto K., Sakurai J., Kobayashi T., Mitani H., Hirayama Y., Nickerson M.L., Warren M.B., Zbar B., Schmidt L.S., Hino O. Proc. Natl. Acad. Sci. U.S.A. 101:2023-2027(2004) · UniProtKB (1) |
| A mutation in the canine BHD gene is associated with hereditary multifocal renal cystadenocarcinoma and nodular dermatofibrosis in the German Shepherd dog. Lingaas F., Comstock K.E., Kirkness E.F., Sorensen A., Aarskaug T., Hitte C., Nickerson M.L., Moe L., Schmidt L.S., Thomas R. et al. Hum. Mol. Genet. 12:3043-3053(2003) · UniProtKB (1) |
| Hepatic vascular tumors, angiectasis in multiple organs, and impaired spermatogenesis in mice with conditional inactivation of the VHL gene. Ma W., Tessarollo L., Hong S.B., Baba M., Southon E., Back T.C., Spence S., Lobe C.G., Sharma N., Maher G.W. et al. Cancer Res. 63:5320-5328(2003) · Mapped (2) |
| Mutations in a novel gene lead to kidney tumors, lung wall defects, and benign tumors of the hair follicle in patients with the Birt-Hogg-Dube syndrome. Nickerson M.L., Warren M.B., Toro J.R., Matrosova V., Glenn G., Turner M.L., Duray P., Merino M., Choyke P.L., Pavlovich C.P. et al. |
| Disruption of a novel MFS transporter gene, DIRC2, by a familial renal cell carcinoma-associated t(2;3)(q35;q21). Bodmer D., Eleveld M., Kater-Baats E., Janssen I., Janssen B., Weterman M., Schoenmakers E., Nickerson M., Linehan M., Zbar B. et al. Hum. Mol. Genet. 11:641-649(2002) · UniProtKB (1) · Mapped (2) |
| A novel germ line juxtamembrane Met mutation in human gastric cancer. Lee J.-H., Han S.-U., Cho H., Jennings B., Gerrard B., Dean M., Schmidt L., Zbar B., Vande Woude G.F.V. Oncogene 19:4947-4953(2000) · UniProtKB (1) |
| Hereditary and sporadic papillary renal carcinomas with c-met mutations share a distinct morphological phenotype. Lubensky I.A., Schmidt L., Zhuang Z., Weirich G., Pack S., Zambrano N., Walther M.M., Choyke P., Linehan W.M., Zbar B. Am. J. Pathol. 155:517-526(1999) · UniProtKB (1) |
| Novel mutations of the MET proto-oncogene in papillary renal carcinomas. Schmidt L., Junker K., Nakaigawa N., Kinjerski T., Weirich G., Miller M., Lubensky I., Neumann H.P.H., Brauch H., Decker J. et al. Oncogene 18:2343-2350(1999) · UniProtKB (1) |
| Somatic mutations in the kinase domain of the Met/hepatocyte growth factor receptor gene in childhood hepatocellular carcinomas. Park W.S., Dong S.M., Kim S.Y., Na E.Y., Shin M.S., Pi J.H., Kim B.J., Bae J.H., Hong Y.K., Lee K.S. et al. |
| Improved detection of germline mutations in the von Hippel-Lindau disease tumor suppressor gene. Stolle C., Glenn G., Zbar B., Humphrey J.S., Choyke P., Walther M., Pack S., Hurley K., Andrey C., Klausner R. et al. Hum. Mutat. 12:417-423(1998) · UniProtKB (1) |
| Two North American families with hereditary papillary renal carcinoma and identical novel mutations in the MET proto-oncogene. Schmidt L., Junker K., Weirich G., Glenn G., Choyke P., Lubensky I., Zhuang Z., Jeffers M., Vande Woude G., Neumann H. et al. Cancer Res. 58:1719-1722(1998) · UniProtKB (1) |
| Germline and somatic mutations in the tyrosine kinase domain of the MET proto-oncogene in papillary renal carcinomas. Schmidt L., Duh F.-M., Chen F., Kishida T., Glenn G., Choyke P., Scherer S.W., Zhuang Z., Lubensky I., Dean M. et al. |
| The human homolog of the rodent immediate early response genes, PC4 and TIS7, resides in the lung cancer tumor suppressor gene region on chromosome 3p21. Latif F., Duh F.-M., Bader S., Sekido Y., Li H., Geil L., Zbar B., Minna J.D., Lerman M.I. Hum. Genet. 99:334-341(1997) · UniProtKB (1) |
| Germline mutations in the von Hippel-Lindau disease (VHL) gene in families from North America, Europe, and Japan. Zbar B., Kishida T., Chen F., Schmidt L., Maher E.R., Richards F.M., Crossey P.A., Webster A.R., Affara N.A., Ferguson-Smith M.A. et al. Hum. Mutat. 8:348-357(1996) · UniProtKB (1) |
| Genotype-phenotype correlation in von Hippel-Lindau disease: identification of a mutation associated with VHL type 2A. Chen F., Slife L., Kishida T., Mulvihill J., Tisherman S.E., Zbar B. J. Med. Genet. 33:716-717(1996) · Mapped (3) |

