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Results: 1-13 |
Results: 13
The LZTFL1 gene is a part of a transcriptional map covering 250 kb within the common eliminated region 1 (C3CER1) in 3p21.3
Authors: Kiss, H Kedra, D Kiss, C Kost-Alimova, M Yang, Y Klein, G Imreh, S Dumanski, JP
Citation: H. Kiss et al., The LZTFL1 gene is a part of a transcriptional map covering 250 kb within the common eliminated region 1 (C3CER1) in 3p21.3, GENOMICS, 73(1), 2001, pp. 10-19
Association of a novel constitutional translocation t(1q;3q) with familialrenal cell carcinoma
Authors: Kanayama, H Lui, WO Takahashi, M Naroda, T Kedra, D Wong, FI Kuroki, Y Nakahori, Y Larsson, C Kagawa, S Teh, BT
Citation: H. Kanayama et al., Association of a novel constitutional translocation t(1q;3q) with familialrenal cell carcinoma, J MED GENET, 38(3), 2001, pp. 165-170
Correspondence re: P. P. Claudio et al., mutations in the retinoblastoma-related gene RB2/p130 in primary nasopharyngeal carcinoma. Cancer Res., 60 :8-12, 2000.
Authors: Gray, SG Guo, X Kedra, D Teh, BT Guo, X Min, HQ
Citation: Sg. Gray et al., Correspondence re: P. P. Claudio et al., mutations in the retinoblastoma-related gene RB2/p130 in primary nasopharyngeal carcinoma. Cancer Res., 60 :8-12, 2000., CANCER RES, 61(15), 2001, pp. 5950-5951
Mutations in short stature homeobox containing gene (SHOX) in dyschondrosteosis but not in hypochondroplasia
Authors: Grigelioniene, G Eklof, O Ivarsson, SA Westphal, O Neumeyer, L Kedra, D Dumanski, J Hagenas, L
Citation: G. Grigelioniene et al., Mutations in short stature homeobox containing gene (SHOX) in dyschondrosteosis but not in hypochondroplasia, HUM GENET, 107(2), 2000, pp. 145-149
Fine mapping of the constitutional translocation t(11;22)(q23;q11)
Authors: Tapia-Paez, I O'Brien, KP Kost-Alimova, M Sahlen, S Kedra, D Bruder, CEG Andersson, B Roe, BA Hu, P Imreh, S Blennow, E Dumanski, JP
Citation: I. Tapia-paez et al., Fine mapping of the constitutional translocation t(11;22)(q23;q11), HUM GENET, 106(5), 2000, pp. 506-516
Characterization of five novel human genes in the 11q13-q22 region
Authors: O'Brien, KP Tapia-Paez, I Stahle-Backdahl, M Kedra, D Dumanski, JP
Citation: Kp. O'Brien et al., Characterization of five novel human genes in the 11q13-q22 region, BIOC BIOP R, 273(1), 2000, pp. 90-94
Duplications on human chromosome 22 reveal a novel ret finger protein-likegene family with sense and endogenous antisense transcripts
Authors: Seroussi, E Kedra, D Pan, HQ Peyrard, M Schwartz, C Scambler, P Donnai, D Roe, BA Dumanski, JP
Citation: E. Seroussi et al., Duplications on human chromosome 22 reveal a novel ret finger protein-likegene family with sense and endogenous antisense transcripts, GENOME RES, 9(9), 1999, pp. 803-814
A 1-Mb PAC contig spanning the common eliminated region 1 (CER1) in microcell hybrid-derived SCID tumors
Authors: Yang, Y Kiss, H Kost-Alimova, M Kedra, D Fransson, I Seroussi, E Li, JF Szeles, A Kholodnyuk, I Imreh, MP Fodor, K Hadlaczky, G Klein, G Dumanski, JP Imreh, S
Citation: Y. Yang et al., A 1-Mb PAC contig spanning the common eliminated region 1 (CER1) in microcell hybrid-derived SCID tumors, GENOMICS, 62(2), 1999, pp. 147-155
TOM1 genes map to human chromosome 22q13.1 and mouse chromosome 8C1 and encode proteins similar to the endosomal proteins HGS and STAM
Authors: Seroussi, E Kedra, D Kost-Alimova, M Sandberg-Nordqvist, AC Fransson, I Jacobs, JFM Fu, Y Pan, HQ Roe, BA Imreh, S Dumanski, JP
Citation: E. Seroussi et al., TOM1 genes map to human chromosome 22q13.1 and mouse chromosome 8C1 and encode proteins similar to the endosomal proteins HGS and STAM, GENOMICS, 57(3), 1999, pp. 380-388
A novel gene containing LIM domains (LIMD1) is located within the common eliminated region 1 (C3CER1) in 3p21.3
Authors: Kiss, H Kedra, D Yang, Y Kost-Alimova, M Kiss, C O'Brien, KP Fransson, I Klein, G Imreh, S Dumanski, JP
Citation: H. Kiss et al., A novel gene containing LIM domains (LIMD1) is located within the common eliminated region 1 (C3CER1) in 3p21.3, HUM GENET, 105(6), 1999, pp. 552-559
The DNA sequence of human chromosome 22
Authors: Dunham, I Shimizu, N Roe, BA Chissoe, S Dunham, I Hunt, AR Collins, JE Bruskiewich, R Beare, DM Clamp, M Smink, LJ Ainscough, R Almeida, JP Babbage, A Bagguley, C Balley, J Barlow, K Bates, KN Beasley, O Bird, CP Blakey, S Bridgeman, AM Buck, D Burgess, J Burrill, WD Burton, J Carder, C Carter, NP Chen, Y Clark, G Clegg, SM Cobley, V Cole, CG Collier, RE Connor, RE Conroy, D Corby, N Coville, GJ Cox, AV Davis, J Dawson, E Dhami, PD Dockree, C Dodsworth, SJ Durbin, RM Ellington, A Evans, KL Fey, JM Fleming, K French, L Garner, AA Gilbert, JGR Goward, ME Grafham, D Griffiths, MN Hall, C Hall, R Hall-Tamlyn, G Heathcott, RW Ho, S Holmes, S Hunt, SE Jones, MC Kershaw, J Kimberley, A King, A Laird, GK Langford, CF Leversha, MA Lloyd, C Lloyd, DM Martyn, ID Mashreghi-Mohammadi, M Matthews, L McCann, OT McClay, J McLaren, S McMurray, AA Milne, SA Mortimore, BJ Odell, CN Pavitt, R Pearce, AV Pearson, D Phillimore, BJ Phillips, SH Plumb, RW Ramsay, H Ramsey, Y Rogers, L Ross, MT Scott, CE Sehra, HK Skuce, CD Smalley, S Smith, ML Soderlund, C Spragon, L Steward, CA Sulston, JE Swann, RM Vaudin, M Wall, M Wallis, JM Whiteley, MN Willey, D Williams, L Williams, S Williamson, H Wilmer, TE Wilming, L Wright, CL Hubbard, T Bentley, DR Beck, S Rogers, J Shimizu, N Minoshima, S Kawasaki, K Sasaki, T Asakawa, S Kudoh, J Shintani, A Shibuya, K Yoshizaki, Y Aoki, N Mitsuyama, S Roe, BA Chen, F Chu, L Crabtree, J Deschamps, S Do, A Do, T Dorman, A Fang, F Fu, Y Hu, P Hua, A Kenton, S Lai, H Lao, HI Lewis, J Lewis, S Lin, SP Loh, P Malaj, E Nguyen, T Pan, H Phan, S Qi, S Qian, Y Ray, L Ren, Q Shaull, S Sloan, D Song, L Wang, Q Wang, Y Wang, Z White, J Willingham, D Wu, H Yao, Z Zhan, M Zhang, G Chissoe, S Murray, J Miller, N Minx, P Fulton, R Johnson, D Bemis, G Bentley, D Bradshaw, H Bourne, S Cordes, M Du, Z Fulton, L Goela, D Graves, T Hawkins, J Hinds, K Kemp, K Latreille, P Layman, D Ozersky, P Rohlfing, T Scheet, P Walker, C Wamsley, A Wohldmann, P Pepin, K Nelson, J Korf, I Bedell, JA Hillier, L Mardis, E Waterston, R Wilson, R Emanuel, BS Shaikh, T Kurahashi, H Saitta, S Budarf, ML McDermid, HE Johnson, A Wong, ACC Morrow, BE Edelman, L Kim, UJ Shizuya, H Simon, MI Dumanski, JP Peyrard, M Kedra, D Seroussi, E Fransson, I Tapia, I Bruder, CE O'Brien, KP
Citation: I. Dunham et al., The DNA sequence of human chromosome 22, NATURE, 402(6761), 1999, pp. 489-495
The mouse ortholog of the human SMARCB1 gene encodes two splice forms
Authors: Bruder, CEG Dumanski, JP Kedra, D
Citation: Ceg. Bruder et al., The mouse ortholog of the human SMARCB1 gene encodes two splice forms, BIOC BIOP R, 257(3), 1999, pp. 886-890
Genomic structure, 5 ' flanking sequences, and precise localization in 1P31.1 of the human prostaglandin F receptor gene
Authors: Betz, R Lagercrantz, J Kedra, D Dumanski, JP Nordenskjold, A
Citation: R. Betz et al., Genomic structure, 5 ' flanking sequences, and precise localization in 1P31.1 of the human prostaglandin F receptor gene, BIOC BIOP R, 254(2), 1999, pp. 413-416
Risultati: 1-13 |