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Results:
1-12
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Results: 12
Authors:
Vulliamy, TJ
Knight, SW
Mason, PJ
Dokal, I
Citation: Tj. Vulliamy et al., Very short telomeres in the peripheral blood of patients with X-linked andautosomal dyskeratosis congenita, BL CELL M D, 27(2), 2001, pp. 353-357
Authors:
Vulliamy, TJ
Knight, SW
Mason, PJ
Dokal, I
Citation: Tj. Vulliamy et al., Very short telomeres in the peripheral blood of patients with X-linked andautosomal dyskeratosis congenita, BL CELL M D, 27(2), 2001, pp. 353-357
Authors:
Knight, SW
Vulliamy, TJ
Morgan, B
Devriendt, K
Mason, PJ
Dokal, I
Citation: Sw. Knight et al., Identification of novel DKC1 mutations in patients with dyskeratosis congenita: implications for pathophysiology and diagnosis, HUM GENET, 108(4), 2001, pp. 299-303
Authors:
Knight, SW
Bass, BL
Citation: Sw. Knight et Bl. Bass, A role for the RNase III enzyme DCR-1 in RNA interference and germ line development in Caenorhabditis elegans, SCIENCE, 293(5538), 2001, pp. 2269-2271
Authors:
Domeier, ME
Morse, DP
Knight, SW
Portereiko, M
Bass, BL
Mango, SE
Citation: Me. Domeier et al., A link between RNA interference and nonsense-mediated decay in Caenorhabditis elegans, SCIENCE, 289(5486), 2000, pp. 1928-1930
Authors:
Knight, SW
Kimmel, BJ
Eggers, CH
Samuels, DS
Citation: Sw. Knight et al., Disruption of the Borrelia burgdorferi gac gene, encoding the naturally synthesized GyrA C-terminal domain, J BACT, 182(7), 2000, pp. 2048-2051
Authors:
Mason, PJ
Stevens, D
Diez, A
Knight, SW
Scopes, DA
Vulliamy, TJ
Citation: Pj. Mason et al., Human hexose-6-phosphate dehydrogenase (Glucose 1-dehydrogenase) encoded at 1p36: Coding sequence and expression, BL CELL M D, 25(2), 1999, pp. 30-37
Authors:
Knight, SW
Samuels, DS
Citation: Sw. Knight et Ds. Samuels, Natural synthesis of a DNA-binding protein from the C-terminal domain of DNA gyrase A in Borrelia burgdorferi, EMBO J, 18(17), 1999, pp. 4875-4881
Authors:
Heiss, NS
Poustka, A
Knight, SW
Aradhya, S
Nelson, DL
Lewis, RA
Esposito, T
Ciccodicola, A
D'Urso, M
Smahi, A
Heuertz, S
Munnich, A
Vabres, P
Woffendin, H
Kenwrick, S
Citation: Ns. Heiss et al., Mutation analysis of the DKC1 gene in incontinentia pigmenti, J MED GENET, 36(11), 1999, pp. 860-862
Authors:
Knight, SW
Heiss, NS
Vulliamy, TJ
Aalfs, CM
McMahon, C
Richmond, P
Jones, A
Hennekam, RCM
Poustka, A
Mason, PJ
Dokal, I
Citation: Sw. Knight et al., Unexplained aplastic anaemia, immunodeficiency, and cerebellar hypoplasia (Hoyeraal-Hreidarsson syndrome) due to mutations in the dyskeratosis congenita gene, DKC1, BR J HAEM, 107(2), 1999, pp. 335-339
Authors:
Vulliamy, TJ
Knight, SW
Heiss, NS
Smith, OP
Poustka, A
Dokal, I
Mason, PJ
Citation: Tj. Vulliamy et al., Dyskeratosis congenita caused by a 3 ' deletion: Germline and somatic mosaicism in a female carrier, BLOOD, 94(4), 1999, pp. 1254-1260
Authors:
Knight, SW
Heiss, NS
Vulliamy, TJ
Greschner, S
Stavrides, G
Pai, GS
Lestringant, G
Varma, N
Mason, PJ
Dokal, I
Poustka, A
Citation: Sw. Knight et al., X-linked dyskeratosis congenita is predominantly caused by missense mutations in the DKC1 gene, AM J HU GEN, 65(1), 1999, pp. 50-58
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