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Results: 1-25 |
Results: 25
Random mutagenesis-PCR to introduce alterations into defined DNA sequencesfor validation of SNP and mutation detection methods
Authors: Nickerson, ML Warren, MB Zbar, B Schmidt, LS
Citation: Ml. Nickerson et al., Random mutagenesis-PCR to introduce alterations into defined DNA sequencesfor validation of SNP and mutation detection methods, HUM MUTAT, 17(3), 2001, pp. 210-219
Structural basis of oncogenic activation caused by point mutations in the kinase domain of the MET proto-oncogene: Modeling studies
Authors: Miller, M Ginalski, K Lesyng, B Nakaigawa, N Schmidt, L Zbar, B
Citation: M. Miller et al., Structural basis of oncogenic activation caused by point mutations in the kinase domain of the MET proto-oncogene: Modeling studies, PROTEINS, 44(1), 2001, pp. 32-43
Oncogenic mutants of RON and MET receptor tyrosine kinases cause activation of the beta-catenin pathway
Authors: Danilkovitch-Miagkova, A Miagkov, A Skeel, A Nakaigawa, N Zbar, B Leonard, EJ
Citation: A. Danilkovitch-miagkova et al., Oncogenic mutants of RON and MET receptor tyrosine kinases cause activation of the beta-catenin pathway, MOL CELL B, 21(17), 2001, pp. 5857-5868
The candidate tumor suppressor gene, RASSF1A, from human chromosome 3p21.3is involved in kidney tumorigenesis
Authors: Dreijerink, K Braga, E Kuzmin, I Geil, L Duh, FM Angeloni, D Zbar, B Lerman, MI Stanbridge, EJ Minna, JD Protopopov, A Li, JF Kashuba, V Klein, G Zabarovsky, ER
Citation: K. Dreijerink et al., The candidate tumor suppressor gene, RASSF1A, from human chromosome 3p21.3is involved in kidney tumorigenesis, P NAS US, 98(13), 2001, pp. 7504-7509
Birt-Hogg-Dube syndrome, a genodermatosis associated with spontaneous pneumothorax and kidney neoplasia, maps to chromosome 17p11.2
Authors: Schmidt, LS Warren, MB Nickerson, ML Weirich, G Matrosova, V Toro, JR Turner, ML Duray, P Merino, M Hewitt, S Pavlovich, CP Glenn, G Greenberg, CR Linehan, WM Zbar, B
Citation: Ls. Schmidt et al., Birt-Hogg-Dube syndrome, a genodermatosis associated with spontaneous pneumothorax and kidney neoplasia, maps to chromosome 17p11.2, AM J HU GEN, 69(4), 2001, pp. 876-882
Signature-based analysis of MET proto-oncogene mutations using DHPLC
Authors: Nickerson, ML Weirich, G Zbar, B Schmidt, LS
Citation: Ml. Nickerson et al., Signature-based analysis of MET proto-oncogene mutations using DHPLC, HUM MUTAT, 16(1), 2000, pp. 68-76
Inherited epithelial tumors of the kidney: old and new diseases
Authors: Zbar, B
Citation: B. Zbar, Inherited epithelial tumors of the kidney: old and new diseases, SEM CANC B, 10(4), 2000, pp. 313-318
A novel germ line juxtamembrane Met mutation in human gastric cancer
Authors: Lee, JH Han, SU Cho, H Jennings, B Gerrard, B Dean, M Schmidt, L Zbar, B Vande Woude, GF
Citation: Jh. Lee et al., A novel germ line juxtamembrane Met mutation in human gastric cancer, ONCOGENE, 19(43), 2000, pp. 4947-4953
Tumorigenesis mediated by MET mutant M1268T is inhibited by dominant-negative Src
Authors: Nakaigawa, N Weirich, G Schmidt, L Zbar, B
Citation: N. Nakaigawa et al., Tumorigenesis mediated by MET mutant M1268T is inhibited by dominant-negative Src, ONCOGENE, 19(26), 2000, pp. 2996-3002
Clinical and genetic analysis of patients with pancreatic neuroendocrine tumors associated with von Hippel-Lindau disease
Authors: Libutti, SK Choyke, PL Alexander, HR Glenn, G Bartlett, DL Zbar, B Lubensky, I McKee, SA Maher, ER Linehan, WM Walther, MM
Citation: Sk. Libutti et al., Clinical and genetic analysis of patients with pancreatic neuroendocrine tumors associated with von Hippel-Lindau disease, SURGERY, 128(6), 2000, pp. 1022-1027
Prevalence of microscopic tumors in normal appearing renal parenchyma of patients with hereditary papillary renal cancer
Authors: Ornstein, DK Lubensky, IA Venzon, D Zbar, B Linehan, WM Walther, MM
Citation: Dk. Ornstein et al., Prevalence of microscopic tumors in normal appearing renal parenchyma of patients with hereditary papillary renal cancer, J UROL, 163(2), 2000, pp. 431-433
Histopathology and molecular genetics of multiple cysts and microcystic (serous) adenomas of the pancreas in von Hippel-Lindau patients
Authors: Mohr, VH Vortmeyer, AO Zhuang, ZP Libutti, SK Walther, MM Choyke, PL Zbar, B Linehan, WM Lubensky, IA
Citation: Vh. Mohr et al., Histopathology and molecular genetics of multiple cysts and microcystic (serous) adenomas of the pancreas in von Hippel-Lindau patients, AM J PATH, 157(5), 2000, pp. 1615-1621
Mosaicism in von Hippel-Lindau disease: Lessons from kindreds with germline mutations identified in offspring with mosaic parents
Authors: Sgambati, MT Stolle, C Choyke, PL Walther, MM Zbar, B Linehan, WM Glenn, GM
Citation: Mt. Sgambati et al., Mosaicism in von Hippel-Lindau disease: Lessons from kindreds with germline mutations identified in offspring with mosaic parents, AM J HU GEN, 66(1), 2000, pp. 84-91
Molecular genetics of renal cell carcinoma
Authors: Enquist, E Zambrano, N Zbar, B Linehan, WM Walther, MM
Citation: E. Enquist et al., Molecular genetics of renal cell carcinoma, CUR CLIN ON, 4, 2000, pp. 79-92
Novel mutations of the MET proto-oncogene in papillary renal carcinomas
Authors: Schmidt, L Junker, K Nakaigawa, N Kinjerski, T Weirich, G Miller, M Lubensky, I Neumann, HPH Brauch, H Decker, J Vocke, C Brown, JA Jenkins, R Richard, S Bergerheim, U Gerrard, B Dean, M Linehan, WM Zbar, B
Citation: L. Schmidt et al., Novel mutations of the MET proto-oncogene in papillary renal carcinomas, ONCOGENE, 18(14), 1999, pp. 2343-2350
Protective function of von Hippel-Lindau protein against impaired protein processing in renal carcinoma cells
Authors: Gorospe, M Egan, JM Zbar, B Lerman, M Geil, L Kuzmin, I Holbrook, NJ
Citation: M. Gorospe et al., Protective function of von Hippel-Lindau protein against impaired protein processing in renal carcinoma cells, MOL CELL B, 19(2), 1999, pp. 1289-1300
Clinical and genetic characterization of pheochromocytoma in von Hippel-Lindau families: Comparison with sporadic pheochromocytoma gives insight intonatural history of pheochromocytoma
Authors: Walther, MM Reiter, R Keiser, HR Choyke, PL Venzon, D Hurley, K Gnarra, JR Reynolds, JC Glenn, GM Zbar, B Linehan, WM
Citation: Mm. Walther et al., Clinical and genetic characterization of pheochromocytoma in von Hippel-Lindau families: Comparison with sporadic pheochromocytoma gives insight intonatural history of pheochromocytoma, J UROL, 162(3), 1999, pp. 659-664
Synthetic peptides define critical contacts between elongin C, elongin B, and the von Hippel-Lindau protein
Authors: Ohh, M Takagi, Y Aso, T Stebbins, CE Pavletich, NP Zbar, B Conaway, RC Conaway, JW Kaelin, WG
Citation: M. Ohh et al., Synthetic peptides define critical contacts between elongin C, elongin B, and the von Hippel-Lindau protein, J CLIN INV, 104(11), 1999, pp. 1583-1591
Expression of von Hippel-Lindau protein in normal and pathological human tissues
Authors: Sakashita, N Takeya, M Kishida, T Stackhouse, TM Zbar, B Takahashi, K
Citation: N. Sakashita et al., Expression of von Hippel-Lindau protein in normal and pathological human tissues, HISTOCHEM J, 31(2), 1999, pp. 133-144
Constitutional von Hippel-Lindau (VHL) gene deletions detected in VHL families by fluorescence in situ hybridization
Authors: Pack, SD Zbar, B Pak, E Ault, DO Humphrey, JS Pham, T Hurley, K Weil, RJ Park, WS Kuzmin, I Stolle, C Glenn, G Liotta, LA Lerman, MI Klausner, RD Linehan, WM Zhuang, ZP
Citation: Sd. Pack et al., Constitutional von Hippel-Lindau (VHL) gene deletions detected in VHL families by fluorescence in situ hybridization, CANCER RES, 59(21), 1999, pp. 5560-5564
Somatic mutations in the kinase domain of the MET/hepatocyte growth factorreceptor gene in childhood hepatocellular carcinomas
Authors: Park, WS Dong, SM Kim, SY Na, EY Shin, MS Pi, JH Kim, BJ Bae, JH Hong, YK Lee, KS Lee, SH Yoo, NJ Jang, JJ Pack, S Zhuang, ZP Schmidt, L Zbar, B Lee, JY
Citation: Ws. Park et al., Somatic mutations in the kinase domain of the MET/hepatocyte growth factorreceptor gene in childhood hepatocellular carcinomas, CANCER RES, 59(2), 1999, pp. 307-310
An important von Hippel-Lindau tumor suppressor domain mediates Sp1-binding and self-association
Authors: Cohen, HT Zhou, M Welsh, AM Zarghamee, S Scholz, H Mukhopadhyay, D Kishida, T Zbar, B Knebelmann, B Sukhatme, VP
Citation: Ht. Cohen et al., An important von Hippel-Lindau tumor suppressor domain mediates Sp1-binding and self-association, BIOC BIOP R, 266(1), 1999, pp. 43-50
Birt-Hogg-Dube syndrome - A novel marker of kidney neoplasia
Authors: Toro, JR Glenn, G Duray, P Darling, T Weirich, G Zbar, B Linehan, M Turner, ML
Citation: Jr. Toro et al., Birt-Hogg-Dube syndrome - A novel marker of kidney neoplasia, ARCH DERMAT, 135(10), 1999, pp. 1195-1202
Hereditary and sporadic papillary renal carcinomas with c-met mutations share a distinct morphological phenotype
Authors: Lubensky, IA Schmidt, L Zhuang, ZP Weirich, G Pack, S Zambrano, N Walther, MM Choyke, P Linehan, WM Zbar, B
Citation: Ia. Lubensky et al., Hereditary and sporadic papillary renal carcinomas with c-met mutations share a distinct morphological phenotype, AM J PATH, 155(2), 1999, pp. 517-526
Inherited carcinomas of the kidney
Authors: Zbar, B Lerman, M
Citation: B. Zbar et M. Lerman, Inherited carcinomas of the kidney, ADV CANC R, 75, 1998, pp. 163-201
Risultati: 1-25 |