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Results:
1-15
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Results: 15
Authors:
Hunt, DM
Rickman, L
Whittock, NV
Eady, RA
Simrak, D
Dopping-Hepenstal, PJC
Stevens, HP
Armstrong, DKB
Hennies, HC
Kuster, W
Hughes, AE
Arnemann, J
Leigh, IM
McGrath, JA
Kelsell, DP
Buxton, RS
Citation: Dm. Hunt et al., Spectrum of dominant mutations in the desmosomal cadherin desmoglein 1, causing the skin disease striate palmoplantar keratoderma, EUR J HUM G, 9(3), 2001, pp. 197-203
Authors:
Juffs, L
Hughes, AE
Paterson, PJK
Citation: L. Juffs et al., The use of macroscopic modelling of intermetallic phases in aluminium alloys in the study of ferricyanide accelerated chromate conversion coatings, MICRON, 32(8), 2001, pp. 777-787
Authors:
Lichanska, AM
McGibbon, D
Silvestri, G
Hughes, AE
Citation: Am. Lichanska et al., A physical and expression map of the D17S1810-D17S1353 region spanning thecentral areolar choroidal dystrophy locus, CYTOG C GEN, 93(1-2), 2001, pp. 43-47
Authors:
Nelson, KJH
Hughes, AE
Taylor, RJ
Hinton, BRW
Wilson, L
Henderson, M
Citation: Kjh. Nelson et al., Characterisation of aluminium alloys after HNO3/HF-NaOH-HNO3/HF pretreatment, MATER SCI T, 17(10), 2001, pp. 1211-1221
Authors:
McConnell, RS
Rubinsztein, DC
Fannin, TF
McKinstry, CS
Kelly, B
Bailey, IC
Hughes, AE
Citation: Rs. Mcconnell et al., Autosomal dominant polycystic kidney disease unlinked to the PKD1 and PKD2loci presenting as familial cerebral aneurysm, J MED GENET, 38(4), 2001, pp. 238-239
Authors:
Irvine, AD
Rugg, EL
Lane, EB
Hoare, S
Peret, C
Hughes, AE
Heagerty, AH
Citation: Ad. Irvine et al., Molecular confirmation of the unique phenotype of epidermolysis bullosa simplex with mottled pigmentation, BR J DERM, 144(1), 2001, pp. 40-45
Authors:
Hughes, AE
Ralston, SH
Marken, J
Bell, C
MacPherson, H
Wallace, RGH
van Hul, W
Whyte, MP
Nakatsuka, K
Hovy, L
Anderson, DM
Citation: Ae. Hughes et al., Mutations in TNFRSF11A, affecting the signal peptide of RANK, cause familial expansile osteolysis, NAT GENET, 24(1), 2000, pp. 45-48
Authors:
Smyth, AE
Hughes, AE
Bruce, IN
Bell, AL
Citation: Ae. Smyth et al., A case-control study of candidate vasoactive mediator genes in primary Raynaud's phenomenon, RHEUMATOLOG, 38(11), 1999, pp. 1094-1098
Authors:
Armstrong, DKB
McKenna, KE
Purkis, PE
Green, KJ
Eady, RAJ
Leigh, IM
Hughes, AE
Citation: Dkb. Armstrong et al., Haploinsufficiency of desmoplakin causes a striate subtype of palmoplantarkeratoderma (vol 8, pg 143, 1999), HUM MOL GEN, 8(5), 1999, pp. 943-943
Authors:
Keith, D
Armstrong, B
McKenna, KE
Purkis, PE
Green, KJ
Eady, RAJ
Leigh, IM
Hughes, AE
Citation: D. Keith et al., Haploinsufficiency of desmoplakin causes a striate subtype of palmoplantarkeratoderma, HUM MOL GEN, 8(1), 1999, pp. 143-148
Authors:
Warpeha, KM
Ah-Fat, F
Harding, S
Patterson, CC
Xu, W
Hart, PM
Chakravarthy, U
Hughes, AE
Citation: Km. Warpeha et al., Dinucleotide repeat polymorphisms in EDN1 and NOS3 are not associated withsevere diabetic retinopathy in type 1 or type 2 diabetes, EYE, 13, 1999, pp. 174-178
Authors:
Warpeha, KM
Xu, W
Liu, L
Charles, IG
Patterson, CC
Ah-Fat, F
Harding, S
Hart, PM
Chakravarthy, U
Hughes, AE
Citation: Km. Warpeha et al., Genotyping and functional analysis of a polymorphic (CCTTT)(n) repeat of NOS2A in diabetic retinopathy, FASEB J, 13(13), 1999, pp. 1825-1832
Authors:
Hughes, AE
Nelson, KJH
Miller, PR
Citation: Ae. Hughes et al., Desmutting of aluminium alloy 2024-T3 using rare earth electrolyte, MATER SCI T, 15(10), 1999, pp. 1124-1132
Authors:
Jiang, SP
Love, JG
Zhang, JP
Hoang, M
Ramprakash, Y
Hughes, AE
Badwal, SPS
Citation: Sp. Jiang et al., The electrochemical performance of LSM/zirconia-yttria interface as a function of a-site non-stoichiometry and cathodic current treatment, SOL ST ION, 121(1-4), 1999, pp. 1-10
Authors:
Savage, JM
Jefferson, JA
Maxwell, AP
Hughes, AE
Shanks, JH
Gill, D
Citation: Jm. Savage et al., Improved prognosis for congenital nephrotic syndrome of the Finnish type in Irish families, ARCH DIS CH, 80(5), 1999, pp. 466-469
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