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Results: 1-18 |
Results: 18
Imprinting and evolution of two Kruppel-type zinc-finger genes, ZIM3 and ZNF264, located in the PEG3/USP29 imprinted domain
Authors: Kim, J Bergmann, A Wehri, E Lu, XC Stubbs, L
Citation: J. Kim et al., Imprinting and evolution of two Kruppel-type zinc-finger genes, ZIM3 and ZNF264, located in the PEG3/USP29 imprinted domain, GENOMICS, 77(1-2), 2001, pp. 91-98
Homology-driven assembly of a sequence-ready mouse BAC contig map spanningregions related to the 46-Mb gene-rich euchromatic segments of human chromosome 19
Authors: Kim, J Gordon, L Dehal, P Badri, H Christensen, M Groza, M Ha, C Hammond, S Vargas, M Wehri, E Wagner, M Olsen, A Stubbs, L
Citation: J. Kim et al., Homology-driven assembly of a sequence-ready mouse BAC contig map spanningregions related to the 46-Mb gene-rich euchromatic segments of human chromosome 19, GENOMICS, 74(2), 2001, pp. 129-141
Human chromosome 19 and related regions in mouse: Conservative and lineage-specific evolution
Authors: Dehal, P Predki, P Olsen, AS Kobayashi, A Folta, P Lucas, S Land, M Terry, A Zhou, CLE Rash, S Zhang, Q Gordon, L Kim, J Elkin, C Pollard, MJ Richardson, P Rokhsar, D Uberbacher, E Hawkins, T Branscomb, E Stubbs, L
Citation: P. Dehal et al., Human chromosome 19 and related regions in mouse: Conservative and lineage-specific evolution, SCIENCE, 293(5527), 2001, pp. 104-111
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
Discovery of a novel, paternally expressed ubiquitin-specific processing protease gene through comparative analysis of an imprinted region of mouse chromosome 7 and human chromosome 19q13.4
Authors: Kim, J Noskov, VN Li, XC Bergmann, A Ren, XJ Warth, T Richardson, P Kouprina, N Stubbs, L
Citation: J. Kim et al., Discovery of a novel, paternally expressed ubiquitin-specific processing protease gene through comparative analysis of an imprinted region of mouse chromosome 7 and human chromosome 19q13.4, GENOME RES, 10(8), 2000, pp. 1138-1147
Exon sharing of a novel human zinc-finger gene, ZIM2, and paternally expressed gene 3 (PEG3)
Authors: Kim, J Bergmann, A Stubbs, L
Citation: J. Kim et al., Exon sharing of a novel human zinc-finger gene, ZIM2, and paternally expressed gene 3 (PEG3), GENOMICS, 64(1), 2000, pp. 114-118
Neuroepithelial defects of the inner ear in a new allele of the mouse mutation Ames waltzer
Authors: Alagramam, KN Zahorsky-Reeves, J Wright, CG Pawlowski, KS Erway, LC Stubbs, L Woychik, RP
Citation: Kn. Alagramam et al., Neuroepithelial defects of the inner ear in a new allele of the mouse mutation Ames waltzer, HEARING RES, 148(1-2), 2000, pp. 181-191
DNA
Authors: Stubbs, L
Citation: L. Stubbs, DNA, COMMENTARY, 110(2), 2000, pp. 4-4
Zim1, a maternally expressed mouse Kruppel-type zinc-finger gene located in proximal chromosome 7
Authors: Kim, JY Lu, XC Stubbs, L
Citation: Jy. Kim et al., Zim1, a maternally expressed mouse Kruppel-type zinc-finger gene located in proximal chromosome 7, HUM MOL GEN, 8(5), 1999, pp. 847-854
The ancestral gene for transcribed, low-copy repeats in the Prader-Willi/Angelman region encodes a large protein implicated in protein trafficking, which is deficient in mice with neuromuscular and spermiogenic abnormalities
Authors: Ji, YG Walkowicz, MJ Buiting, K Johnson, DK Tarvin, RE Rinchik, EM Horsthemke, B Stubbs, L Nicholls, RD
Citation: Yg. Ji et al., The ancestral gene for transcribed, low-copy repeats in the Prader-Willi/Angelman region encodes a large protein implicated in protein trafficking, which is deficient in mice with neuromuscular and spermiogenic abnormalities, HUM MOL GEN, 8(3), 1999, pp. 533-542
Molecular characterization of radiation- and chemically induced mutations associated with neuromuscular tremors, runting, juvenile lethality, and sperm defects in jdf2 mice
Authors: Walkowicz, M Ji, YG Ren, XJ Horsthemke, B Russell, LB Johnson, D Rinchik, EM Nicholls, RD Stubbs, L
Citation: M. Walkowicz et al., Molecular characterization of radiation- and chemically induced mutations associated with neuromuscular tremors, runting, juvenile lethality, and sperm defects in jdf2 mice, MAMM GENOME, 10(9), 1999, pp. 870-878
Molecular characterization of Zfp54, a zinc-finger-containing gene that isdeleted in the embryonic lethal mutation t(w18)
Authors: Shannon, M Stubbs, L
Citation: M. Shannon et L. Stubbs, Molecular characterization of Zfp54, a zinc-finger-containing gene that isdeleted in the embryonic lethal mutation t(w18), MAMM GENOME, 10(7), 1999, pp. 739-743
Sequence and chromosomal localization of the mouse ortholog of the human olfactory receptor gene 912-93
Authors: Rouquier, S Stubbs, L Gaillard-Sanchez, I Giorgi, D
Citation: S. Rouquier et al., Sequence and chromosomal localization of the mouse ortholog of the human olfactory receptor gene 912-93, MAMM GENOME, 10(12), 1999, pp. 1172-1174
Physical mapping of EMR1 and CD97 in human Chromosome 19 and assignment ofCd97 to mouse Chromosome 8 suggest an ancient genomic duplication
Authors: Carver, EA Hamann, J Olsen, AS Stubbs, L
Citation: Ea. Carver et al., Physical mapping of EMR1 and CD97 in human Chromosome 19 and assignment ofCd97 to mouse Chromosome 8 suggest an ancient genomic duplication, MAMM GENOME, 10(10), 1999, pp. 1039-1040
Characterization of the mouse Xpf DNA repair gene and differential expression during spermatogenesis
Authors: Shannon, M Lamerdin, JE Richardson, L McCutchen-Maloney, SL Hwang, MH Handel, MA Stubbs, L Thelen, MP
Citation: M. Shannon et al., Characterization of the mouse Xpf DNA repair gene and differential expression during spermatogenesis, GENOMICS, 62(3), 1999, pp. 427-435
Expression specificity of the mouse exonuclease 1 (mExo1) gene
Authors: Lee, BI Shannon, M Stubbs, L Wilson, DM
Citation: Bi. Lee et al., Expression specificity of the mouse exonuclease 1 (mExo1) gene, NUCL ACID R, 27(20), 1999, pp. 4114-4120
A new mouse insertional mutation that causes sensorineural deafness and vestibular defects
Authors: Alagramam, KN Kwon, HY Cacheiro, NLA Stubbs, L Wright, CG Erway, LC Woychik, RP
Citation: Kn. Alagramam et al., A new mouse insertional mutation that causes sensorineural deafness and vestibular defects, GENETICS, 152(4), 1999, pp. 1691-1699
Tandem zinc-finger gene families in mammals: Insights and unanswered questions
Authors: Shannon, M Kim, J Ashworth, L Branscomb, E Stubbs, L
Citation: M. Shannon et al., Tandem zinc-finger gene families in mammals: Insights and unanswered questions, DNA SEQ, 8(5), 1998, pp. 303-315
Risultati: 1-18 |