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Results: 1-8 |
Results: 8
Characterisation of a cDNA encoding chick eukaryotic translation initiation factor-2 beta
Authors: Sneesby, KJ Crane, DI Murrell, WG
Citation: Kj. Sneesby et al., Characterisation of a cDNA encoding chick eukaryotic translation initiation factor-2 beta, DNA SEQ, 12(1), 2001, pp. 59-65
Isolation and characterisation of a chick cDNA encoding the RNA polymerasecommon subunit RPB6
Authors: Kaarbo, M Crane, DI Murrell, WG
Citation: M. Kaarbo et al., Isolation and characterisation of a chick cDNA encoding the RNA polymerasecommon subunit RPB6, DNA SEQ, 11(1-2), 2000, pp. 155-162
Placental growth hormone (GH), GH-binding protein, and insulin-like growthfactor axis in normal, growth-retarded, and diabetic pregnancies: Correlations with fetal growth
Authors: McIntyre, HD Serek, R Crane, DI Veveris-Lowe, T Parry, A Johnson, S Leung, KC Ho, KKY Bougoussa, M Hennen, G Igout, A Chan, FY Cowley, D Cotterill, A Barnard, R
Citation: Hd. Mcintyre et al., Placental growth hormone (GH), GH-binding protein, and insulin-like growthfactor axis in normal, growth-retarded, and diabetic pregnancies: Correlations with fetal growth, J CLIN END, 85(3), 2000, pp. 1143-1150
Interaction of Pex5p, the type 1 peroxisome targeting signal receptor, with the peroxisomal membrane proteins Pex14p and Pex13p
Authors: Urquhart, AJ Kennedy, D Gould, SJ Crane, DI
Citation: Aj. Urquhart et al., Interaction of Pex5p, the type 1 peroxisome targeting signal receptor, with the peroxisomal membrane proteins Pex14p and Pex13p, J BIOL CHEM, 275(6), 2000, pp. 4127-4136
A common PEX1 frameshift mutation in patients with disorders of peroxisomebiogenesis correlates with the severe Zellweger syndrome phenotype
Authors: Maxwell, MA Nelson, PV Chin, SJ Paton, BC Carey, WF Crane, DI
Citation: Ma. Maxwell et al., A common PEX1 frameshift mutation in patients with disorders of peroxisomebiogenesis correlates with the severe Zellweger syndrome phenotype, HUM GENET, 105(1-2), 1999, pp. 38-44
Localization of a portion of extranuclear ATM to peroxisomes
Authors: Watters, D Kedar, P Spring, K Bjorkmann, J Chen, P Gatei, M Birrell, G Garrone, B Srinivasa, P Crane, DI Lavin, MF
Citation: D. Watters et al., Localization of a portion of extranuclear ATM to peroxisomes, J BIOL CHEM, 274(48), 1999, pp. 34277-34282
PEX13 is mutated in complementation group 13 of the peroxisome-biogenesis disorders
Authors: Liu, YF Bjorkman, J Urquhart, A Wanders, RJA Crane, DI Gould, SJ
Citation: Yf. Liu et al., PEX13 is mutated in complementation group 13 of the peroxisome-biogenesis disorders, AM J HU GEN, 65(3), 1999, pp. 621-634
Genomic structure of PEX13, a candidate peroxisome biogenesis disorder gene
Authors: Bjorkman, J Stetten, G Moore, CS Gould, SJ Crane, DI
Citation: J. Bjorkman et al., Genomic structure of PEX13, a candidate peroxisome biogenesis disorder gene, GENOMICS, 54(3), 1998, pp. 521-528
Risultati: 1-8 |