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Results: 1-17 |
Results: 17
Down syndrome congenital heart disease: A narrowed region and a candidate gene
Authors: Barlow, GM Chen, XN Shi, ZY Lyons, GE Kurnit, DM Celle, L Spinner, NB Zackai, E Pettenati, MJ Van Riper, AJ Vekemans, MJ Mjaatvedt, CH Korenberg, JR
Citation: Gm. Barlow et al., Down syndrome congenital heart disease: A narrowed region and a candidate gene, GENET MED, 3(2), 2001, pp. 91-101
Partial trisomy 7p defined by analysis of a complex chromosome rearrangement using a BAC clone panel
Authors: Tuck-Muller, CM Goodman, BK Li, SB Martinez, JE Chen, XN Wertelecki, W Korenberg, JR Stetten, G
Citation: Cm. Tuck-muller et al., Partial trisomy 7p defined by analysis of a complex chromosome rearrangement using a BAC clone panel, GENET MED, 3(2), 2001, pp. 126-131
A triple color FISH technique for mouse chromosome identification
Authors: Henegariu, O Dunai, J Chen, XN Korenberg, JR Ward, DC Greally, JM
Citation: O. Henegariu et al., A triple color FISH technique for mouse chromosome identification, MAMM GENOME, 12(6), 2001, pp. 462-465
Towards a full karyotype screening of interphase cells: 'FISH and chip' technology
Authors: Weier, HUG Munne, S Lersch, RA Hsieh, HB Smida, J Chen, XN Korenberg, JR Pedersen, RA Fung, J
Citation: Hug. Weier et al., Towards a full karyotype screening of interphase cells: 'FISH and chip' technology, MOL C ENDOC, 183, 2001, pp. S41-S45
Integration of cytogenetic landmarks into the draft sequence of the human genome
Authors: Cheung, VG Nowak, N Jang, W Kirsch, IR Zhao, S Chen, XN Furey, TS Kim, UJ Kuo, WL Olivier, M Conroy, J Kasprzyk, A Massa, H Yonescu, R Sait, S Thoreen, C Snijders, A Lemyre, E Bailey, JA Bruzel, A Burrill, WD Clegg, SM Collins, S Dhami, P Friedman, C Han, CS Herrick, S Lee, J Ligon, AH Lowry, S Morley, M Narasimhan, S Osoegawa, K Peng, Z Plajzer-Frick, I Quade, BJ Scott, D Sirotkin, K Thorpe, AA Gray, JW Hudson, J Pinkel, D Ried, T Rowen, L Shen-Ong, GL Strausberg, RL Birney, E Callen, DF Cheng, JF Cox, DR Doggett, NA Carter, NP Eichler, EE Haussler, D Korenberg, JR Morton, CC Albertson, D Schuler, G de Jong, PJ Trask, BJ
Citation: Vg. Cheung et al., Integration of cytogenetic landmarks into the draft sequence of the human genome, NATURE, 409(6822), 2001, pp. 953-958
Cryptic translocation identification in human and mouse using several telomeric multiplex FISH (TM-FISH) strategies
Authors: Henegariu, O Artan, S Greally, JM Chen, XN Korenberg, JR Vance, GH Stubbs, L Bray-Ward, P Ward, DC
Citation: O. Henegariu et al., Cryptic translocation identification in human and mouse using several telomeric multiplex FISH (TM-FISH) strategies, LAB INV, 81(4), 2001, pp. 483-491
Genome structure and cognitive map of Williams syndrome
Authors: Korenberg, JR Chen, XN Hirota, H Lai, Z Bellugi, U Burian, D Roe, B Matsuoka, R
Citation: Jr. Korenberg et al., Genome structure and cognitive map of Williams syndrome, J COGN NEUR, 12, 2000, pp. 89-107
Delayed membranous ossification of the cranium associated with familial translocation (2;3)(p15;q12)
Authors: Cargile, CB McIntosh, I Clough, MV Rutberg, J Yaghmai, R Goodman, BK Chen, XN Korenberg, JR Thomas, GH Geraghty, MT
Citation: Cb. Cargile et al., Delayed membranous ossification of the cranium associated with familial translocation (2;3)(p15;q12), AM J MED G, 92(5), 2000, pp. 328-335
The human synaptotagmin IV gene defines an evolutionary break point between syntenic mouse and human chromosome regions but retains ligand inducibility and tissue specificity
Authors: Ferguson, GD Chen, XN Korenberg, JR Herschman, HR
Citation: Gd. Ferguson et al., The human synaptotagmin IV gene defines an evolutionary break point between syntenic mouse and human chromosome regions but retains ligand inducibility and tissue specificity, J BIOL CHEM, 275(47), 2000, pp. 36920-36926
Deletion of a 5-cM region at chromosome 8p23 is associated with a spectrumof congenital heart defects
Authors: Giglio, S Graw, SL Gimelli, G Pirola, B Varone, P Voullaire, L Lerzo, F Rossi, E Dellavecchia, C Bonaglia, MC Digilio, MC Giannotti, A Marino, B Carrozzo, R Korenberg, JR Danesino, C Sujansky, E Dallapiccola, B Zuffardi, O
Citation: S. Giglio et al., Deletion of a 5-cM region at chromosome 8p23 is associated with a spectrumof congenital heart defects, CIRCULATION, 102(4), 2000, pp. 432-437
Mouse molecular cytogenetic resource: 157 BACs link the chromosomal and genetic maps
Authors: Korenberg, JR Chen, XN Devon, KL Noya, D Oster-Granite, ML Birren, BW
Citation: Jr. Korenberg et al., Mouse molecular cytogenetic resource: 157 BACs link the chromosomal and genetic maps, GENOME RES, 9(5), 1999, pp. 514-523
Human genome anatomy: BACs integrating the genetic and cytogenetic maps for bridging genome and biomedicine
Authors: Korenberg, JR Chen, XN Sun, ZG Shi, ZY Ma, SW Vataru, E Yimlamai, D Weissenbach, JS Shizuya, H Simon, MI Gerety, SS Nguyen, H Zemsteva, IS Hui, L Silva, J Wu, XY Birren, BW Hudson, TJ
Citation: Jr. Korenberg et al., Human genome anatomy: BACs integrating the genetic and cytogenetic maps for bridging genome and biomedicine, GENOME RES, 9(10), 1999, pp. 994-1001
Localization of a human nucleoporin 155 gene (NUP155) to the 5p13 region and cloning of its cDNA
Authors: Zhang, XQ Yang, HM Corydon, MJ Zhang, XX Pedersen, S Korenberg, JR Chen, XN Laporte, J Gregersen, N Niebuhr, E Liu, GY Bolund, L
Citation: Xq. Zhang et al., Localization of a human nucleoporin 155 gene (NUP155) to the 5p13 region and cloning of its cDNA, GENOMICS, 57(1), 1999, pp. 144-151
Bridging cognition, the brain and molecular genetics: evidence from Williams syndrome
Authors: Bellugi, U Lichtenberger, L Mills, D Galaburda, A Korenberg, JR
Citation: U. Bellugi et al., Bridging cognition, the brain and molecular genetics: evidence from Williams syndrome, TRENDS NEUR, 22(5), 1999, pp. 197-207
Involvement of protein kinase C epsilon (PKC epsilon) in thyroid cell death - A truncated chimeric PKC epsilon cloned from a thyroid cancer cell lineprotects thyroid cells from apoptosis
Authors: Knauf, JA Elisei, R Mochly-Rosen, D Liron, T Chen, XN Gonsky, R Korenberg, JR Fagin, JA
Citation: Ja. Knauf et al., Involvement of protein kinase C epsilon (PKC epsilon) in thyroid cell death - A truncated chimeric PKC epsilon cloned from a thyroid cancer cell lineprotects thyroid cells from apoptosis, J BIOL CHEM, 274(33), 1999, pp. 23414-23425
A novel human gene encoding an F-box/WD40 containing protein maps in the SHFM3 critical region on 10q24
Authors: Ianakiev, P Kilpatrick, MW Dealy, C Kosher, R Korenberg, JR Chen, XN Tsipouras, P
Citation: P. Ianakiev et al., A novel human gene encoding an F-box/WD40 containing protein maps in the SHFM3 critical region on 10q24, BIOC BIOP R, 261(1), 1999, pp. 64-70
Assignment of the GOV (Glioblastoma Overexpressed) gene to human chromosome band 19p13.2 by fluorescence in situ hybridization
Authors: Chen, XN Shi, ZY Korenberg, JR Sehgal, A
Citation: Xn. Chen et al., Assignment of the GOV (Glioblastoma Overexpressed) gene to human chromosome band 19p13.2 by fluorescence in situ hybridization, CYTOG C GEN, 83(3-4), 1998, pp. 230-231
Risultati: 1-17 |