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Results: 1-22 |
Results: 22
Epigenetic inactivation of RASSF14 in lung and breast cancers and malignant phenotype suppression
Authors: Burbee, DG Forgacs, E Zochbauer-Muller, S Shivakumar, L Fong, K Gao, BN Randle, D Kondo, M Virmani, A Bader, S Sekido, Y Latif, F Milchgrub, S Toyooka, S Gazdar, AF Lerman, MI Zabarovsky, E White, M Minna, JD
Citation: Dg. Burbee et al., Epigenetic inactivation of RASSF14 in lung and breast cancers and malignant phenotype suppression, J NAT CANC, 93(9), 2001, pp. 691-699
Chromosome 3p allele loss in early invasive breast cancer: detailed mapping and association with clinicopathological features
Authors: Martinez, A Walker, RA Shaw, JA Dearing, SJ Maher, ER Latif, F
Citation: A. Martinez et al., Chromosome 3p allele loss in early invasive breast cancer: detailed mapping and association with clinicopathological features, J CL PATH-M, 54(5), 2001, pp. 300-306
Microsatellite instability and mutational analysis of transforming growth factor beta receptor type II gene (TGFBR2) in sporadic ovarian cancer
Authors: Alvi, AJ Rader, JS Broggini, M Latif, F Maher, ER
Citation: Aj. Alvi et al., Microsatellite instability and mutational analysis of transforming growth factor beta receptor type II gene (TGFBR2) in sporadic ovarian cancer, J CL PATH-M, 54(4), 2001, pp. 240-243
Angiotensin II type 1 receptor blockade with 80 and 160 mg valsartan in healthy, normotensive subjects
Authors: Latif, F Tandon, S Obeleniene, R Hankins, SR Berlowitz, MS Ennezat, PV Le Jemtel, TH
Citation: F. Latif et al., Angiotensin II type 1 receptor blockade with 80 and 160 mg valsartan in healthy, normotensive subjects, J CARD FAIL, 7(3), 2001, pp. 265-268
WFS1/Wolframin mutations, Wolfram syndrome, and associated diseases
Authors: Khanim, F Kirk, J Latif, F Barrett, TG
Citation: F. Khanim et al., WFS1/Wolframin mutations, Wolfram syndrome, and associated diseases, HUM MUTAT, 17(5), 2001, pp. 357-367
Production of ethanol and xylitol from corn cobs by yeasts
Authors: Latif, F Rajoka, MI
Citation: F. Latif et Mi. Rajoka, Production of ethanol and xylitol from corn cobs by yeasts, BIORES TECH, 77(1), 2001, pp. 57-63
RASSF1A promoter region CpG island hypermethylation in phaeochromocytomas and neuroblastoma tumours
Authors: Astuti, D Agathanggelou, A Honorio, S Dallol, A Martinsson, T Kogner, P Cummins, C Neumann, HPH Voutilainen, R Dahia, P Eng, C Maher, ER Latif, F
Citation: D. Astuti et al., RASSF1A promoter region CpG island hypermethylation in phaeochromocytomas and neuroblastoma tumours, ONCOGENE, 20(51), 2001, pp. 7573-7577
Methylation associated inactivation of RASSF1A from region 3p21.3 in lung,breast and ovarian tumours
Authors: Agathanggelou, A Honorio, S Macartney, DP Martinez, A Dallol, A Radar, J Fullwood, P Chauhan, A Walker, R Shaw, JA Hosoe, S Lerman, MI Minna, JD Maher, ER Latif, F
Citation: A. Agathanggelou et al., Methylation associated inactivation of RASSF1A from region 3p21.3 in lung,breast and ovarian tumours, ONCOGENE, 20(12), 2001, pp. 1509-1518
Opposite association of two PPARG variants with cancer: overrepresentationof H449H in endometrial carcinoma cases and underrepresentation of P12A inrenal cell carcinoma cases
Authors: Smith, WM Zhou, XP Kurose, K Gao, X Latif, F Kroll, T Sugano, K Cannistra, SA Clinton, SK Maher, ER Prior, TW Eng, C
Citation: Wm. Smith et al., Opposite association of two PPARG variants with cancer: overrepresentationof H449H in endometrial carcinoma cases and underrepresentation of P12A inrenal cell carcinoma cases, HUM GENET, 109(2), 2001, pp. 146-151
Dose-dependent blockade of the angiotensin II type 1 receptor with losartan in normal volunteers
Authors: Berlowitz, MS Latif, F Hankins, SR Ennezat, PV Moskowitz, R Tandon, S Colombo, PC Le Jemtel, TH
Citation: Ms. Berlowitz et al., Dose-dependent blockade of the angiotensin II type 1 receptor with losartan in normal volunteers, J CARDIO PH, 37(6), 2001, pp. 692-696
Germline SDHD mutation in familial phaeochromocytoma
Authors: Astuti, D Douglas, F Lennard, TWJ Aligianis, IA Woodward, ER Evans, DGR Eng, C Latif, F Maher, ER
Citation: D. Astuti et al., Germline SDHD mutation in familial phaeochromocytoma, LANCET, 357(9263), 2001, pp. 1181-1182
Rett syndrome and the MECP2 gene
Authors: Webb, T Latif, F
Citation: T. Webb et F. Latif, Rett syndrome and the MECP2 gene, J MED GENET, 38(4), 2001, pp. 217-223
Epigenetic inactivation of the RASSF1A 3p21.3 tumor suppressor gene in both clear cell and papillary renal cell carcinoma
Authors: Morrissey, C Martinez, A Zatyka, M Agathanggelou, A Honorio, S Astuti, D Morgan, NV Moch, H Richards, FM Kishida, T Yao, M Schraml, P Latif, F Maher, ER
Citation: C. Morrissey et al., Epigenetic inactivation of the RASSF1A 3p21.3 tumor suppressor gene in both clear cell and papillary renal cell carcinoma, CANCER RES, 61(19), 2001, pp. 7277-7281
Gene mutations in the succinate dehydrogenase subunit SDHB cause susceptibility to familial pheochromocytoma and to familial paraganglioma
Authors: Astuti, D Latif, F Dallol, A Dahia, PLM Douglas, F George, E Skoldberg, F Husebye, ES Eng, C Maher, ER
Citation: D. Astuti et al., Gene mutations in the succinate dehydrogenase subunit SDHB cause susceptibility to familial pheochromocytoma and to familial paraganglioma, AM J HU GEN, 69(1), 2001, pp. 49-54
Role of chromosome 3p12-p21 tumour suppressor genes in clear cell renal cell carcinoma: analysis of VHL dependent and VHL independent pathways of tumorigenesis
Authors: Martinez, A Fullwood, P Kondo, K Kishida, T Yao, M Maher, ER Latif, F
Citation: A. Martinez et al., Role of chromosome 3p12-p21 tumour suppressor genes in clear cell renal cell carcinoma: analysis of VHL dependent and VHL independent pathways of tumorigenesis, J CL PATH-M, 53(3), 2000, pp. 137-144
Detailed mapping of a congenital heart disease gene in chromosome 3p25
Authors: Green, EK Priestley, MD Waters, J Maliszewska, C Latif, F Maher, ER
Citation: Ek. Green et al., Detailed mapping of a congenital heart disease gene in chromosome 3p25, J MED GENET, 37(8), 2000, pp. 581-587
Mutations in the MECP2 gene in a cohort of girls with Rett syndrome
Authors: Hampson, K Woods, CG Latif, F Webb, T
Citation: K. Hampson et al., Mutations in the MECP2 gene in a cohort of girls with Rett syndrome, J MED GENET, 37(8), 2000, pp. 610-612
Functional properties of a new voltage-dependent calcium channel alpha(2)delta auxiliary subunit gene (CACNA2D2)
Authors: Gao, BN Sekido, Y Maximov, A Saad, M Forgacs, E Latif, F Wei, MH Lerman, M Lee, JH Perez-Reyes, E Bezprozvanny, I Minna, JD
Citation: Bn. Gao et al., Functional properties of a new voltage-dependent calcium channel alpha(2)delta auxiliary subunit gene (CACNA2D2), J BIOL CHEM, 275(16), 2000, pp. 12237-12242
High resolution chromosome 3p allelotyping of human lung cancer and preneoplastic/preinvasive bronchial epithelium reveals multiple, discontinuous sites of 3p allele loss and three regions of frequent breakpoints
Authors: Wistuba, II Behrens, C Virmani, AK Mele, G Milchgrub, S Girard, L Fondon, JW Garner, HR McKay, B Latif, F Lerman, MI Lam, S Gazdar, AF Minna, JD
Citation: Ii. Wistuba et al., High resolution chromosome 3p allelotyping of human lung cancer and preneoplastic/preinvasive bronchial epithelium reveals multiple, discontinuous sites of 3p allele loss and three regions of frequent breakpoints, CANCER RES, 60(7), 2000, pp. 1949-1960
CALL gene is haploinsufficient in a 3p-syndrome patient
Authors: Angeloni, D Lindor, NM Pack, S Latif, F Wei, MH Lerman, MI
Citation: D. Angeloni et al., CALL gene is haploinsufficient in a 3p-syndrome patient, AM J MED G, 86(5), 1999, pp. 482-485
Detailed genetic and physical mapping of tumor suppressor loci on chromosome 3p in ovarian cancer
Authors: Fullwood, P Marchini, S Rader, JS Martinez, A Macartney, D Broggini, M Morelli, C Barbanti-Brodano, G Maher, ER Latif, F
Citation: P. Fullwood et al., Detailed genetic and physical mapping of tumor suppressor loci on chromosome 3p in ovarian cancer, CANCER RES, 59(18), 1999, pp. 4662-4667
Clinical and molecular genetic analysis of 19 Wolfram syndrome kindreds demonstrating a wide spectrum of mutations in WFS1
Authors: Hardy, C Khanim, F Torres, R Scott-Brown, M Seller, A Poulton, J Collier, D Kirk, J Polymeropoulos, M Latif, F Barrett, T
Citation: C. Hardy et al., Clinical and molecular genetic analysis of 19 Wolfram syndrome kindreds demonstrating a wide spectrum of mutations in WFS1, AM J HU GEN, 65(5), 1999, pp. 1279-1290
Risultati: 1-22 |