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Results: 1-16 |
Results: 16
Molecular genetic diagnosis of inherited cancer predisposition
Authors: Petty, EM Yashar, BM
Citation: Em. Petty et Bm. Yashar, Molecular genetic diagnosis of inherited cancer predisposition, MOLECULAR BASIS OF HUMAN CANCER, 2002, pp. 497-520
Overexpressed genes/ESTs and characterization of distinct amplicons on 17q23 in breast cancer cells
Authors: Erson, AE Niell, BL DeMers, SK Rouillard, JM Hanash, SM Petty, EM
Citation: Ae. Erson et al., Overexpressed genes/ESTs and characterization of distinct amplicons on 17q23 in breast cancer cells, NEOPLASIA, 3(6), 2001, pp. 521-526
Virtual genome scan: A tool for restriction landmark-based scanning of thehuman genome
Authors: Rouillard, JM Erson, AE Kuick, R Asakawa, J Wimmer, K Muleris, M Petty, EM Hanash, S
Citation: Jm. Rouillard et al., Virtual genome scan: A tool for restriction landmark-based scanning of thehuman genome, GENOME RES, 11(8), 2001, pp. 1453-1459
Genomic characterization of human SEC14L1 splice variants within a 17q25 candidate tumor suppressor gene region and identification of an unrelated embedded expressed sequence tag
Authors: Kalikin, LM Bugeaud, EM Palmbos, PL Lyons, RH Petty, EM
Citation: Lm. Kalikin et al., Genomic characterization of human SEC14L1 splice variants within a 17q25 candidate tumor suppressor gene region and identification of an unrelated embedded expressed sequence tag, MAMM GENOME, 12(12), 2001, pp. 925-929
Systemic lupus erythematosus in a man with Noonan syndrome
Authors: Martin, DM Gencyuz, CF Petty, EM
Citation: Dm. Martin et al., Systemic lupus erythematosus in a man with Noonan syndrome, AM J MED G, 102(1), 2001, pp. 59-62
Fusion of a novel gene, RCC17, to the TFE3 gene in t(X;17)(p11.2;q25,3)-bearing papillary renal cell carcinomas
Authors: Heimann, P El Housni, H Ogur, G Weterman, MAJ Petty, EM Vassart, G
Citation: P. Heimann et al., Fusion of a novel gene, RCC17, to the TFE3 gene in t(X;17)(p11.2;q25,3)-bearing papillary renal cell carcinomas, CANCER RES, 61(10), 2001, pp. 4130-4135
Expression and mutational analyses of the human MAD2LI gene in breast cancer
Authors: Percy, MJ Myrie, EA Neeley, CK Azim, JN Ethier, SP Petty, EM
Citation: Mj. Percy et al., Expression and mutational analyses of the human MAD2LI gene in breast cancer, GENE CHROM, 29(4), 2000, pp. 356-362
Genomic and expression analyses of alternatively spliced transcripts of the MLL septin-like fusion gene (MSF) that map to a 17q25 region of loss in breast and ovarian tumors
Authors: Kalikin, LM Sims, HL Petty, EM
Citation: Lm. Kalikin et al., Genomic and expression analyses of alternatively spliced transcripts of the MLL septin-like fusion gene (MSF) that map to a 17q25 region of loss in breast and ovarian tumors, GENOMICS, 63(2), 2000, pp. 165-172
Mutation and expression analysis of human BUB1 and BUB1B in aneuploid breast cancer cell lines
Authors: Myrie, KA Percy, MJ Azim, JN Neeley, CK Petty, EM
Citation: Ka. Myrie et al., Mutation and expression analysis of human BUB1 and BUB1B in aneuploid breast cancer cell lines, CANCER LETT, 152(2), 2000, pp. 193-199
Successful bone marrow transplantation in a patient with Schimke immuno-osseous dysplasia
Authors: Petty, EM Yanik, GA Hutchinson, RJ Alter, BP Schmalstieg, FC Levine, JE Ginsburg, D Robillard, JE Castle, VP
Citation: Em. Petty et al., Successful bone marrow transplantation in a patient with Schimke immuno-osseous dysplasia, J PEDIAT, 137(6), 2000, pp. 882-886
Characterisation and genetic mapping of a new X linked deafness syndrome
Authors: Martin, DM Probst, FJ Camper, SA Petty, EM
Citation: Dm. Martin et al., Characterisation and genetic mapping of a new X linked deafness syndrome, J MED GENET, 37(11), 2000, pp. 836-841
Isolation and mapping of a human septin gene to a region on chromosome 17q, commonly deleted in sporadic epithelial ovarian tumors
Authors: Russell, SEH McIlhatton, MA Burrows, JF Donaghy, PG Chanduloy, S Petty, EM Kalikin, LM Church, SW McIlroy, S Harkin, DP Keilty, GW Cranston, AN Weissenbach, J Hickey, I Johnston, PG
Citation: Seh. Russell et al., Isolation and mapping of a human septin gene to a region on chromosome 17q, commonly deleted in sporadic epithelial ovarian tumors, CANCER RES, 60(17), 2000, pp. 4729-4734
Direct molecular diagnosis of multiple endocrine neoplasia type 1
Authors: Petty, EM Glynn, M Bale, AE
Citation: Em. Petty et al., Direct molecular diagnosis of multiple endocrine neoplasia type 1, METH MOL M, 49, 2000, pp. 227-242
Absence of PTEN germ-line mutations in men with a potential inherited predisposition to prostate cancer
Authors: Cooney, KA Tsou, HC Petty, EM Miesfeldt, S Ping, XL Gruener, AC Peacocke, M
Citation: Ka. Cooney et al., Absence of PTEN germ-line mutations in men with a potential inherited predisposition to prostate cancer, CLIN CANC R, 5(6), 1999, pp. 1387-1391
An integrated physical and gene map of human distal chromosome 17q24-proximal 17q25 encompassing multiple disease loci
Authors: Kalikin, LM George, RAV Keller, MP Bort, S Bowler, NS Law, DJ Chance, PF Petty, EM
Citation: Lm. Kalikin et al., An integrated physical and gene map of human distal chromosome 17q24-proximal 17q25 encompassing multiple disease loci, GENOMICS, 57(1), 1999, pp. 36-42
Is happiness heritable or hard won? Reflections on Kevin Sharpe's The 'Sense of Happiness, Biological Explanations and Ultimate Reality and Meaning'
Authors: Petty, EM
Citation: Em. Petty, Is happiness heritable or hard won? Reflections on Kevin Sharpe's The 'Sense of Happiness, Biological Explanations and Ultimate Reality and Meaning', ULTIMATE R, 21(4), 1998, pp. 326-332
Risultati: 1-16 |