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Results: 1-25/34
Authors:
Wickham, CL
Sarsfield, P
Joyner, MV
Jones, DB
Ellard, S
Wilkins, B
Citation: Cl. Wickham et al., Formic acid decalcification of bone marrow trephines degrades DNA: alternative use of EDTA allows the amplification and sequencing of relatively longPCR products (vol 53, pg 336, 2000), J CL PATH-M, 54(2), 2001, pp. 120-120
Authors:
Kolatsi-Joannou, M
Bingham, C
Ellard, S
Bulman, MP
Allen, LIS
Hattersley, AT
Woolf, AS
Citation: M. Kolatsi-joannou et al., Hepatocyte nuclear factor-1 beta: A new kindred with renal cysts and diabetes and gene expression in normal human development, J AM S NEPH, 12(10), 2001, pp. 2175-2180
Authors:
Thomas, H
Jaschkowitz, K
Bulman, M
Frayling, TM
Mitchell, SMS
Roosen, S
Lingott-Frieg, A
Tack, CJ
Ellard, S
Ryffel, GU
Hattersley, AT
Citation: H. Thomas et al., A distant upstream promoter of the HNF-4 alpha gene connects the transcription factors involved in maturity-onset diabetes of the young, HUM MOL GEN, 10(19), 2001, pp. 2089-2097
Authors:
Kousta, E
Ellard, S
Allen, LIS
Saker, PJ
Huxtable, SJ
Hattersley, AT
McCarthy, MI
Citation: E. Kousta et al., Glucokinase mutations in a phenotypically selected multiethnic group of women with a history of gestational diabetes, DIABET MED, 18(8), 2001, pp. 683-684
Authors:
Shepherd, M
Ellis, I
Ahmad, AM
Todd, PJ
Bowen-Jones, D
Mannion, G
Ellard, S
Sparkes, AC
Hattersley, AT
Citation: M. Shepherd et al., Predictive genetic testing in maturity-onset diabetes of the young (MODY), DIABET MED, 18(5), 2001, pp. 417-421
Authors:
Kong, C
Ellard, S
Johnston, C
Farid, NR
Citation: C. Kong et al., Multiple endocrine neoplasia type 1(Burin) from Mauritius: A novel MEN 1 mutation, J ENDOC INV, 24(10), 2001, pp. 806-810
Authors:
Fava, S
Ellard, S
Azzopardi, J
Hattersley, AT
Citation: S. Fava et al., ACE gene polymorphism as a prognostic indicator in patients with type 2 diabetes and established renal disease, DIABET CARE, 24(12), 2001, pp. 2115-2120
Authors:
Shield, J
Owen, K
Robinson, DO
Mackay, D
Ellard, S
Hattersley, A
Temple, IK
Citation: J. Shield et al., Maturity onset diabetes of the young (MOBY) and early onset Type II diabetes are not caused by loss of imprinting at the transient neonatal diabetes (TNDM) locus, DIABETOLOG, 44(7), 2001, pp. 924-924
Authors:
Bingham, C
Ellard, S
Nicholls, AJ
Pennock, CA
Allen, J
James, AJ
Satchell, SC
Salzmann, MB
Hattersley, AT
Citation: C. Bingham et al., The generalized aminoaciduria seen in patients with hepatocyte nuclear factor-1 alpha mutations is a feature of all patients with diabetes and is associated with glucosuria, DIABETES, 50(9), 2001, pp. 2047-2052
Authors:
Frayling, TM
Evans, JC
Bulman, MP
Pearson, E
Allen, L
Owen, K
Bingham, C
Hannemann, M
Shepherd, M
Ellard, S
Hattersley, AT
Citation: Tm. Frayling et al., beta-cell genes and diabetes - Molecular and clinical characterization of mutations in transcription factors, DIABETES, 50, 2001, pp. S94-S100
Authors:
Pearson, ER
Velho, G
Clark, P
Stride, A
Shepherd, M
Frayling, TM
Bulman, MP
Ellard, S
Froguel, P
Hattersley, AT
Citation: Er. Pearson et al., beta-cell genes and diabetes: Quantitative and qualitative differences in the pathophysiology of hepatic nuclear factor-1 alpha and glucokinase mutations, DIABETES, 50, 2001, pp. S101-S107
Authors:
Evans, JC
Frayling, TM
Cassell, PG
Saker, PJ
Hitman, GA
Walker, M
Levy, JC
O'Rahilly, S
Rao, PVS
Bennett, AJ
Jones, EC
Menzel, S
Prestwich, P
Simecek, N
Wishart, M
Dhillon, R
Fletcher, C
Millward, A
Demaine, A
Wilkin, T
Horikawa, Y
Cox, NJ
Bell, GI
Ellard, S
McCarthy, MI
Hattersley, AT
Citation: Jc. Evans et al., Studies of association between the gene for calpain-10 and type 2 diabetesmellitus in the United Kingdom, AM J HU GEN, 69(3), 2001, pp. 544-552
Authors:
Bingham, C
Bulman, MP
Ellard, S
Allen, LIS
Lipkin, GW
van't Hoff, WG
Woolf, AS
Rizzoni, G
Novelli, G
Nicholls, AJ
Hattersley, AT
Citation: C. Bingham et al., Mutations in the hepatocyte nuclear factor-1 beta gene are associated withfamilial hypoplastic glomerulocystic kidney disease, AM J HU GEN, 68(1), 2001, pp. 219-224
Authors:
Sarsfield, P
Wickham, CL
Joyner, MV
Ellard, S
Jones, DB
Wilkins, BS
Citation: P. Sarsfield et al., Formic acid decalcification of bone marrow trephines degrades DNA: alternative use of EDTA allows the amplification and sequencing of relatively longPCR products, J CL PATH-M, 53(6), 2000, pp. 336-336
Authors:
Wickham, CL
Lynas, C
Ellard, S
Citation: Cl. Wickham et al., Detection of clonal T cell populations by high resolution PCR using fluorescently labelled nucleotides; evaluation using conventional LIS-SSCP, J CL PATH-M, 53(3), 2000, pp. 150-154
Authors:
Wickham, CL
Boyce, M
Joyner, MV
Sarsfield, P
Wilkins, BS
Jones, DB
Ellard, S
Citation: Cl. Wickham et al., Amplification of PCR products in excess of 600 base pairs using DNA extracted from decalcified, paraffin wax embedded bone marrow trephine biopsies, J CL PATH-M, 53(1), 2000, pp. 19-23
Authors:
de Bono, JS
Dalgleish, AG
Carmichael, J
Diffley, J
Lofts, FJ
Fyffe, D
Ellard, S
Gordon, RJ
Brindley, CJ
Evans, TRJ
Citation: Js. De Bono et al., Phase I study of ONO-4007, a synthetic analogue of the lipid a moiety of bacterial lipopolysaccharide, CLIN CANC R, 6(2), 2000, pp. 397-405
Authors:
Bulman, MP
Kusumi, K
Frayling, TM
McKeown, C
Garrett, C
Lander, ES
Krumlauf, R
Hattersley, AT
Ellard, S
Turnpenny, PD
Citation: Mp. Bulman et al., Mutations in the human Delta homologue, DLL3, cause axial skeletal defectsin spondylocostal dysostosis, NAT GENET, 24(4), 2000, pp. 438-441
Authors:
Ellard, S
Citation: S. Ellard, Hepatocyte nuclear factor 1 alpha (HNF-1 alpha) mutations in maturity-onset diabetes of the young, HUM MUTAT, 16(5), 2000, pp. 377-385
Authors:
Wickham, CL
Joyner, MV
Lynas, C
Ellard, S
Citation: Cl. Wickham et al., Detection of clonal B-cell populations using fluorescently labeled nucleotides, BIOTECHNIQU, 29(2), 2000, pp. 215
Authors:
Evans, JC
Frayling, TM
Ellard, S
Gutowski, NH
Citation: Jc. Evans et al., Confirmation of linkage of Duane's syndrome and refinement of the disease locus to an 8.8-cM interval on chromosome 2q31, HUM GENET, 106(6), 2000, pp. 636-638
Authors:
Tack, CJJ
Ellard, S
Hattersley, AT
Citation: Cjj. Tack et al., A severe clinical phenotype results from the co-inheritance of type 2 susceptibility genes and a hepatocyte nuclear factor-1 alpha mutation, DIABET CARE, 23(3), 2000, pp. 424-425
Authors:
Spyer, G
Ellard, S
Hattersley, A
Citation: G. Spyer et al., Growth-hormone treatment and risk of diabetes, LANCET, 355(9218), 2000, pp. 1913-1913
Authors:
Bingham, C
Ellard, S
Allen, L
Bulman, M
Shepherd, M
Frayling, T
Berry, PJ
Clark, PM
Lindner, T
Bell, GI
Ryffel, GU
Nicholls, AJ
Hattersley, AT
Citation: C. Bingham et al., Abnormal nephron development associated with a frameshift mutation in the transcription factor hepatocyte nuclear factor-1 beta, KIDNEY INT, 57(3), 2000, pp. 898-907
Authors:
Wild, W
von Strandmann, EP
Nastos, A
Senkel, S
Lingott-Frieg, A
Bulman, M
Bingham, C
Ellard, S
Hattersley, AT
Ryffel, GU
Citation: W. Wild et al., The mutated human gene encoding hepatocyte nuclear factor 1 beta inhibits kidney formation in developing Xenopus embryos, P NAS US, 97(9), 2000, pp. 4695-4700