Authors:
Mwale, F
Billinghurst, C
Wu, W
Alini, M
Webber, C
Reiner, MI
Poole, J
Poole, AR
Citation: F. Mwale et al., Selective assembly and remodeling of collagens II and IX associated with expression of the chondrocyte hypertrophic phenotype (vol 218, pg 648, 2000), DEV DYNAM, 220(2), 2001, pp. 187-187
Authors:
Lee, S
Russo, DCW
Reiner, AP
Lee, JH
Sy, MY
Telen, MJ
Judd, WJ
Simon, P
Rodrigues, MJ
Chabert, T
Poole, J
Jovanovic-Srzentic, S
Levene, C
Yahalom, V
Redman, CM
Citation: S. Lee et al., Molecular defects underlying the Kell null phenotype, J BIOL CHEM, 276(29), 2001, pp. 27281-27289
Authors:
Ericson, KG
Fadeel, B
Nilsson-Ardnor, S
Soderhall, C
Samuelsson, A
Janka, G
Schneider, M
Gurgey, A
Yalman, N
Revesz, T
Egeler, RM
Jahnukainen, K
Storm-Mathiesen, I
Haraldsson, A
Poole, J
de Saint Basile, G
Nordenskjold, M
Henter, JI
Citation: Kg. Ericson et al., Spectrum of perforin gene mutations in familial hemophagocytic lymphohistiocytosis, AM J HU GEN, 68(3), 2001, pp. 590-597
Authors:
Mwale, F
Billinghurst, C
Wu, W
Alini, M
Webber, C
Reiner, A
Ionescu, M
Poole, J
Poole, AR
Citation: F. Mwale et al., Selective assembly and remodelling of collagens II and IX associated with expression of the chondrocyte hypertrophic phenotype, DEV DYNAM, 218(4), 2000, pp. 648-662
Authors:
Storry, JR
Coghlan, G
Poole, J
Figueroa, D
Reid, ME
Citation: Jr. Storry et al., The MNS blood group antigens, Vr (MNS12) and mts (MNS14), each arise from an amino acid substitution on glycophorin A, VOX SANGUIN, 78(1), 2000, pp. 52-56
Citation: J. Poole, Spanish pottery 1248-1898 with a catalogue of the collection in the Victoria and Albert Museum, BURLINGTON, 142(1171), 2000, pp. 635-635
Authors:
Rios, M
Chaudhuri, A
Mallinson, G
Sausais, L
Gomensoro-Garcia, AE
Hannon, J
Rosenberger, S
Poole, J
Burgess, G
Pogo, O
Reid, M
Citation: M. Rios et al., New genotypes in Fy(a-b-) individuals: nonsense mutations (Trp to stop) inthe coding sequence of either FY A or FY B, BR J HAEM, 108(2), 2000, pp. 448-454
Authors:
Faivre, L
Guardiola, P
Lewis, C
Dokal, I
Ebell, W
Zatterale, Z
Altay, C
Poole, J
Stones, D
Kwee, ML
van Weel-Sipman, M
Havenga, C
Morgan, N
de Winter, J
Digweed, M
Savoia, A
Pronk, J
de Ravel, T
Jansen, S
Joenje, H
Gluckman, E
Mathew, CG
Citation: L. Faivre et al., Association of complementation group and mutation type with clinical outcome in Fanconi anemia, BLOOD, 96(13), 2000, pp. 4064-4070
Authors:
Poole, J
Herrell, R
Ashton, S
Goldberg, J
Buchwald, D
Citation: J. Poole et al., Results of isoproterenol tilt table testing in monozygotic twins discordant for chronic fatigue syndrome, ARCH IN MED, 160(22), 2000, pp. 3461-3468
Authors:
Poole, J
Banks, J
Bruce, LJ
Ring, SM
Levene, C
Stern, H
Overbeeke, MAM
Tanner, MJA
Citation: J. Poole et al., Glycophorin A mutation Ala65 -> Pro gives rise to a novel pair of MNS alleles ENEP (MNS39) and HAG (MNS41) and altered Wr(b) expression: direct evidence for GPA band 3 interaction necessary for normal Wr(b) expression, TRANSFUS M, 9(2), 1999, pp. 167-174
Citation: H. Zhang et al., Cobalt sputtering target and sputter deposition of Co thin films for cobalt silicide metallization, J VAC SCI A, 17(4), 1999, pp. 1904-1910
Authors:
Olsson, ML
Smythe, JS
Hansson, C
Poole, J
Mallinson, G
Jones, J
Avent, ND
Daniels, G
Citation: Ml. Olsson et al., The Fy(x) phenotype is associated with a missense mutation in the Fy(b) allele predicting Arg89Cys in the Duffy glycoprotein, BR J HAEM, 103(4), 1998, pp. 1184-1191