Le informazioni sugli articoli di fonte ISI sono coperte da copyright

Per ulteriori informazioni selezionare i riferimenti di interesse.

1. Rippin, JD; Patel, A; Bain, SC
   Genetics of diabetic nephropathy
   BEST PRACTICE & RESEARCH CLINICAL ENDOCRINOLOGY & METABOLISM
   
   J.D. Rippin et al., "Genetics of diabetic nephropathy", BEST PRAC R, 15(3), 2001, pp. 345-358
2. Dunger, DB; Bain, SC
   Genetics of diabetes - Preface
   BEST PRACTICE & RESEARCH CLINICAL ENDOCRINOLOGY & METABOLISM
   
   D.B. Dunger e S.C. Bain, "Genetics of diabetes - Preface", BEST PRAC R, 15(3), 2001, pp. VII-VII
3. Cucca, F; Lampis, R; Congia, M; Angius, E; Nutland, S; Bain, SC; Barnett, AH; Todd, JA
   A correlation between the relative predisposition of MHC class II alleles to type 1 diabetes and the structure of their proteins
   HUMAN MOLECULAR GENETICS
   
   F. Cucca et al., "A correlation between the relative predisposition of MHC class II alleles to type 1 diabetes and the structure of their proteins", HUM MOL GEN, 10(19), 2001, pp. 2025-2037
4. Cucca, F; Dudbridge, F; Loddo, M; Mulargia, AP; Lampis, R; Angius, E; De Virgiliis, S; Koeleman, BPC; Bain, SC; Barnett, AH; Gilchrist, F; Cordell, H; Welsh, K; Todd, JA
   The HLA-DPB1-associated component of the IDDM1 and its relationship to themajor loci HLA-DQB1,-DQA1, and-DRB1
   DIABETES
   
   F. Cucca et al., "The HLA-DPB1-associated component of the IDDM1 and its relationship to themajor loci HLA-DQB1,-DQA1, and-DRB1", DIABETES, 50(5), 2001, pp. 1200-1205
5. Merriman, TR; Cordell, HJ; Eaves, IA; Danoy, PA; Coraddu, F; Barber, R; Cucca, F; Broadley, S; Sawcer, S; Comptson, A; Wordsworth, P; Shatford, J; Laval, S; Jirholt, J; Holmdahl, R; Theofilopoulos, AN; Kono, DH; Tuomilehto, J; Tuomilehto-Wolf, E; Buzzetti, R; Marrosu, MG; Undlien, DE; Ronningen, KS; Ionesco-Tirgoviste, C; Shield, JP; Pociot, F; Nerup, J; Jacob, CO; Polychronakos, C; Bain, SC; Todd, JA
   Suggestive evidence for association of human chromosome 18q12-q21 and its orthologue on rat and mouse chromosome 18 with several autoimmune diseases
   DIABETES
   
   T.R. Merriman et al., "Suggestive evidence for association of human chromosome 18q12-q21 and its orthologue on rat and mouse chromosome 18 with several autoimmune diseases", DIABETES, 50(1), 2001, pp. 184-194
6. Herr, M; Dudbridge, F; Zavattari, P; Cucca, F; Guja, C; March, R; Campbell, RD; Barnett, AH; Bain, SC; Todd, JA; Koeleman, BPC
   Evaluation of fine mapping strategies for a multifactorial disease locus: systematic linkage and association analysis of IDDM1 in the HLA region on chromosome 6p21
   HUMAN MOLECULAR GENETICS
   
   M. Herr et al., "Evaluation of fine mapping strategies for a multifactorial disease locus: systematic linkage and association analysis of IDDM1 in the HLA region on chromosome 6p21", HUM MOL GEN, 9(9), 2000, pp. 1291-1301
7. Bain, SC; Chowdhury, TA
   Genetics sf diabetic nephropathy and microalbuminuria
   JOURNAL OF THE ROYAL SOCIETY OF MEDICINE
   
   S.C. Bain e T.A. Chowdhury, "Genetics sf diabetic nephropathy and microalbuminuria", J ROY S MED, 93(2), 2000, pp. 62-66
8. Koeleman, BPC; Herr, MH; Zavattari, P; Dudbridge, F; March, R; Campbell, D; Barnett, AH; Bain, SC; Mulargia, AP; Loddo, M; Amos, W; Cucca, F; Todd, JA
   Conditional ETDT analysis of the Human Leukocyte Antigen region in type 1 diabetes
   ANNALS OF HUMAN GENETICS
   
   B.P.C. Koeleman et al., "Conditional ETDT analysis of the Human Leukocyte Antigen region in type 1 diabetes", ANN HUM GEN, 64, 2000, pp. 215-221
9. Dyer, PH; Chowdhury, TA; Bain, SC
   Genetics of diabetic nephropathy
   DIABETES ANNUAL/13
   
   P.H. Dyer et al., "Genetics of diabetic nephropathy", DIABETES ANNUAL/13, 2000, pp. 201-218
10. Smith, PR; Bain, SC; Good, PA; Hattersley, AT; Barnett, AH; Gibson, JM; Dodson, PM
    Pigmentary retinal dystrophy and the syndrome of maternally inherited diabetes and deafness caused by the mitochondrial DNA 3243 tRNA(Leu) A to G mutation
    OPHTHALMOLOGY
    
    P.R. Smith et al., "Pigmentary retinal dystrophy and the syndrome of maternally inherited diabetes and deafness caused by the mitochondrial DNA 3243 tRNA(Leu) A to G mutation", OPHTHALMOL, 106(6), 1999, pp. 1101-1108
11. Chowdhury, TA; Dyer, PH; Kumar, S; Barnett, AH; Bain, SC
    Genetic determinants of diabetic nephropathy
    CLINICAL SCIENCE
    
    T.A. Chowdhury et al., "Genetic determinants of diabetic nephropathy", CLIN SCI, 96(3), 1999, pp. 221-230
12. Chowdhury, TA; Dyer, PH; Mijovic, CH; Dunger, DB; Barnett, AH; Bain, SC
    Human leucocyte antigen and insulin gene regions and nephropathy in Type Idiabetes
    DIABETOLOGIA
    
    T.A. Chowdhury et al., "Human leucocyte antigen and insulin gene regions and nephropathy in Type Idiabetes", DIABETOLOG, 42(8), 1999, pp. 1017-1020
13. Dyer, PH; Chowdhury, TA; Dronsfield, MJ; Dunger, D; Barnett, AH; Bain, SC
    The 5 '-end polymorphism of the aldose reductase gene is not associated with diabetic nephropathy in Caucasian Type I diabetic patients
    DIABETOLOGIA
    
    P.H. Dyer et al., "The 5 '-end polymorphism of the aldose reductase gene is not associated with diabetic nephropathy in Caucasian Type I diabetic patients", DIABETOLOG, 42(8), 1999, pp. 1030-1031
14. MEIN CA; ESPOSITO L; DUNN MG; JOHNSON GCL; TIMMS AE; GOY JV; SMITH AN; SEBAGMONTEFIORE L; MERRIMAN ME; WILSON AJ; PRITCHARD LE; CUCCA F; BARNETT AH; BAIN SC; TODD JA
    A SEARCH FOR TYPE-1 DIABETES SUSCEPTIBILITY GENES IN FAMILIES FROM THE UNITED-KINGDOM
    Nature genetics
    
    C.A. Mein et al., "A SEARCH FOR TYPE-1 DIABETES SUSCEPTIBILITY GENES IN FAMILIES FROM THE UNITED-KINGDOM", Nature genetics, 19(3), 1998, pp. 297-300
15. CUCCA F; GOY JV; KAWAGUCHI Y; ESPOSITO L; MERRIMAN ME; WILSON AT; CORDELL HJ; BAIN SC; TODD JA
    A MALE-FEMALE BIAS IN TYPE-1 DIABETES AND LINKAGE TO CHROMOSOME XP INMHC HLA-DR3-POSITIVE PATIENTS
    Nature genetics
    
    F. Cucca et al., "A MALE-FEMALE BIAS IN TYPE-1 DIABETES AND LINKAGE TO CHROMOSOME XP INMHC HLA-DR3-POSITIVE PATIENTS", Nature genetics, 19(3), 1998, pp. 301-302
16. MERRIMAN TR; EAVES IA; TWELLS RCJ; MERRIMAN ME; DANOY PAC; MUXWORTHY CE; HUNTER KMD; COX RD; CUCCA F; MCKINNEY PA; SHIELD JPH; BAUM JD; TUOMILEHTO J; TUOMILEHTOWOLF E; IONESCOTIRGOVISTE C; JONER G; THORSBY E; UNDLIEN DE; POCIOT F; NERUP J; RONNINGEN KS; BAIN SC; TODD JA
    TRANSMISSION OF HAPLOTYPES OF MICROSATELLITE MARKERS RATHER THAN SINGLE MARKER ALLELES IN THE MAPPING OF A PUTATIVE TYPE-1 DIABETES SUSCEPTIBILITY GENE (IDDM6)
    Human molecular genetics
    
    T.R. Merriman et al., "TRANSMISSION OF HAPLOTYPES OF MICROSATELLITE MARKERS RATHER THAN SINGLE MARKER ALLELES IN THE MAPPING OF A PUTATIVE TYPE-1 DIABETES SUSCEPTIBILITY GENE (IDDM6)", Human molecular genetics, 7(3), 1998, pp. 517-524
17. DYER PH; LLOYD CE; LANCASHIRE RJ; BAIN SC; BARNETT AH
    FACTORS ASSOCIATED WITH CLINIC NONATTENDANCE IN ADULTS WITH TYPE-1 DIABETES-MELLITUS
    Diabetic medicine
    
    P.H. Dyer et al., "FACTORS ASSOCIATED WITH CLINIC NONATTENDANCE IN ADULTS WITH TYPE-1 DIABETES-MELLITUS", Diabetic medicine, 15(4), 1998, pp. 339-343
18. CHOWDHURY TA; DYER PH; BARNETT AH; BAIN SC
    HLA AND INSULIN (INS) GENES IN CAUCASIANS WITH TYPE-1 DIABETES AND NEPHROPATHY
    Diabetologia
    
    T.A. Chowdhury et al., "HLA AND INSULIN (INS) GENES IN CAUCASIANS WITH TYPE-1 DIABETES AND NEPHROPATHY", Diabetologia, 41, 1998, pp. 1144-1144
19. CUCCA F; ESPOSITO L; GOY JV; MERRIMAN ME; WILSON AJ; REED PW; BAIN SC; TODD JA
    INVESTIGATION OF LINKAGE OF CHROMOSOME-8 TO TYPE-1 DIABETES - MULTIPOINT ANALYSIS AND EXCLUSION MAPPING OF HUMAN-CHROMOSOME-8 IN 593 AFFECTED SIB-PAIR FAMILIES FROM THE UK AND US
    Diabetes
    
    F. Cucca et al., "INVESTIGATION OF LINKAGE OF CHROMOSOME-8 TO TYPE-1 DIABETES - MULTIPOINT ANALYSIS AND EXCLUSION MAPPING OF HUMAN-CHROMOSOME-8 IN 593 AFFECTED SIB-PAIR FAMILIES FROM THE UK AND US", Diabetes, 47(9), 1998, pp. 1525-1527
20. CHOWDHURY TA; DYER PH; KUMAR S; GIBSON SP; ROWE BR; DAVIES SJ; MARSHALL SM; MORRIS PJ; GILL GV; FEENEY S; MAXWELL P; SAVAGE D; BOULTON AJM; TODD JA; DUNGER D; BARNETT AH; BAIN SC
    ASSOCIATION OF APOLIPOPROTEIN EPSILON-2 ALLELE WITH DIABETIC NEPHROPATHY IN CAUCASIAN SUBJECTS WITH IDDM
    Diabetes
    
    T.A. Chowdhury et al., "ASSOCIATION OF APOLIPOPROTEIN EPSILON-2 ALLELE WITH DIABETIC NEPHROPATHY IN CAUCASIAN SUBJECTS WITH IDDM", Diabetes, 47(2), 1998, pp. 278-280
21. ESPOSITO L; HILL NJ; PRITCHARD LE; CUCCA F; MUXWORTHY C; MERRIMAN ME; WILSON A; JULIER C; DELEPINE M; TUOMILEHTO J; TUOMILEHTOWOLF E; IONESCOTIRGOVISTE C; NISTICO L; BUZZETTI R; POZZILLI P; FERRARI M; BOSI E; POCIOT F; NERUP J; BAIN SC; TODD JA
    GENETIC-ANALYSIS OF CHROMOSOME-2 IN TYPE-1 DIABETES - ANALYSIS OF PUTATIVE LOCI IDDM7, IDDM12, AND IDDM13 AND CANDIDATE GENES NRAMP1 AND IA-2 AND THE INTERLEUKIN-1 GENE-CLUSTER
    Diabetes
    
    L. Esposito et al., "GENETIC-ANALYSIS OF CHROMOSOME-2 IN TYPE-1 DIABETES - ANALYSIS OF PUTATIVE LOCI IDDM7, IDDM12, AND IDDM13 AND CANDIDATE GENES NRAMP1 AND IA-2 AND THE INTERLEUKIN-1 GENE-CLUSTER", Diabetes, 47(11), 1998, pp. 1797-1799
22. Chowdhury, TA; Dyer, PH; Bartlett, WA; Legge, ES; Durbin, SM; Barnett, AH; Bain, SC
    Glomerular filtration rate determination in diabetic patients using iohexol clearance - comparison of single and multiple plasma sampling methods
    CLINICA CHIMICA ACTA
    
    T.A. Chowdhury et al., "Glomerular filtration rate determination in diabetic patients using iohexol clearance - comparison of single and multiple plasma sampling methods", CLIN CHIM A, 277(2), 1998, pp. 153-158
23. NAKAGAWA Y; KAWAGUCHI Y; TWELLS RCJ; MUXWORTHY C; HUNTER KMD; WILSON A; MERRIMAN ME; COX RD; MERRIMAN T; CUCCA F; MCKINNEY PA; SHIELD JPH; TUOMILEHTO J; TUOMILEHTOWOLF E; NISTICO L; BUZZETTI R; POZZILLI P; JONER G; THORSBY E; UNDLIEN DE; POCIOT F; NERUP J; RONNINGEN KS; BAIN SC; TODD JA
    FINE MAPPING OF THE DIABETES-SUSCEPTIBILITY LOCUS, IDDM4, ON CHROMOSOME 11Q13
    American journal of human genetics
    
    Y. Nakagawa et al., "FINE MAPPING OF THE DIABETES-SUSCEPTIBILITY LOCUS, IDDM4, ON CHROMOSOME 11Q13", American journal of human genetics, 63(2), 1998, pp. 547-556
24. BENNETT ST; WILSON AJ; ESPOSITO L; BOUZEKRI N; UNDLIEN DE; CUCCA F; NISTICO L; BUZZETTI R; BOSI E; POCIOT F; NERUP J; CAMBONTHOMSEN A; PUGLIESE A; SHIELD JPH; MCKINNEY PA; BAIN SC; POLYCHRONAKOS C; TODD JA; POZZILLI P; VISALLI N; BARONI M; FIORITI E; MESTURINO C; SIGNORE A; CAVALLO M; LUCENTINI L; MATTEOLI M; CRINO A; TEODONIO C; AMORETTI R; TOMBESI A; RUGGERI M; PISANO L; SURACI C; PENNAFINA M; BOSCHERINI B; STODUTO S; FONTE M; MANCABITTI M; MULTARI G; SUPPA M; DEMATTIA G; FALDETTA MC; LAURENTI O; MARIETTI G; PITOCCO D; FERRAZZOLI F; BIZZARRI C; GHIRLANDA G
    INSULIN VNTR ALLELE-SPECIFIC EFFECT IN TYPE-1 DIABETES DEPENDS ON IDENTITY OF UNTRANSMITTED PATERNAL ALLELE
    Nature genetics
    
    S.T. Bennett et al., "INSULIN VNTR ALLELE-SPECIFIC EFFECT IN TYPE-1 DIABETES DEPENDS ON IDENTITY OF UNTRANSMITTED PATERNAL ALLELE", Nature genetics, 17(3), 1997, pp. 350-352
25. PRASHER VP; CHOWDHURY TA; ROWE BR; BAIN SC
    APOE GENOTYPE AND ALZHEIMERS-DISEASE IN ADULTS WITH DOWN-SYNDROME - METAANALYSIS
    American journal of mental retardation
    
    V.P. Prasher et al., "APOE GENOTYPE AND ALZHEIMERS-DISEASE IN ADULTS WITH DOWN-SYNDROME - METAANALYSIS", American journal of mental retardation, 102(2), 1997, pp. 103-110
26. SMITH PR; DRONSFIELD MJ; MIJOVIC CH; HATTERSLEY AT; YEUNG VTF; COCKRAM C; CHAN JCN; BARNETT AH; BAIN SC
    THE MITOCHONDRIAL TRNA(LEU(UUR))A TO G-3243 MUTATION IS ASSOCIATED WITH INSULIN-DEPENDENT AND NON-INSULIN-DEPENDENT DIABETES IN A CHINESE POPULATION
    Diabetic medicine
    
    P.R. Smith et al., "THE MITOCHONDRIAL TRNA(LEU(UUR))A TO G-3243 MUTATION IS ASSOCIATED WITH INSULIN-DEPENDENT AND NON-INSULIN-DEPENDENT DIABETES IN A CHINESE POPULATION", Diabetic medicine, 14(12), 1997, pp. 1026-1031
27. CHOWDHURY TA; DYER PH; KUMAR S; GOUGH SCL; GIBSON SP; ROWE BR; SMITH PR; DRONSFIELD MJ; MARSHALL SM; MACKIN P; DEAN JD; MORRIS PJ; DAVIES S; DUNGER DB; BOULTON AJM; BARNETT AH; BAIN SC
    LACK OF ASSOCIATION OF ANGIOTENSIN-II TYPE-1 RECEPTOR GENE POLYMORPHISM WITH DIABETIC NEPHROPATHY IN INSULIN-DEPENDENT DIABETES-MELLITUS
    Diabetic medicine
    
    T.A. Chowdhury et al., "LACK OF ASSOCIATION OF ANGIOTENSIN-II TYPE-1 RECEPTOR GENE POLYMORPHISM WITH DIABETIC NEPHROPATHY IN INSULIN-DEPENDENT DIABETES-MELLITUS", Diabetic medicine, 14(10), 1997, pp. 837-840
28. BULMAN MP; DRONSFIELD MJ; FRAYLING T; APPLETON M; BAIN SC; ELLARD S; HATTERSLEY AT
    A MISSENSE MUTATION IN THE HEPATOCYTE NUCLEAR FACTOR-4 ALPHA-GENE IN A UK PEDIGREE WITH MATURITY-ONSET DIABETES OF THE YOUNG
    Diabetologia
    
    M.P. Bulman et al., "A MISSENSE MUTATION IN THE HEPATOCYTE NUCLEAR FACTOR-4 ALPHA-GENE IN A UK PEDIGREE WITH MATURITY-ONSET DIABETES OF THE YOUNG", Diabetologia, 40(7), 1997, pp. 859-862
29. FRAYLING T; BULMAN M; ELLARD S; APPLETON M; DRONSFIELD MJ; BAIN SC; BELL GI; HATTERSLEY AT
    A MUTATIONAL HOTSPOT IN THE POLY-C TRACT OF EXON-4 OF THE HEPATIC NUCLEAR FACTOR 1ALPHA GENE - SCREENING IN MATURITY-ONSET DIABETES OF THE YOUNG
    Diabetologia
    
    T. Frayling et al., "A MUTATIONAL HOTSPOT IN THE POLY-C TRACT OF EXON-4 OF THE HEPATIC NUCLEAR FACTOR 1ALPHA GENE - SCREENING IN MATURITY-ONSET DIABETES OF THE YOUNG", Diabetologia, 40, 1997, pp. 18-18
30. BULMAN MP; FRAYLING T; ELLARD S; APPLETON M; DRONSFIELD MJ; BELL GI; BAIN SC; HATTERSLEY AT
    MUTATIONS IN THE HEPATIC NUCLEAR FACTOR-1-ALPHA IN MATURITY-ONSET DIABETES OF THE YOUNG
    Diabetologia
    
    M.P. Bulman et al., "MUTATIONS IN THE HEPATIC NUCLEAR FACTOR-1-ALPHA IN MATURITY-ONSET DIABETES OF THE YOUNG", Diabetologia, 40, 1997, pp. 618-618
31. FRAYLING TM; BULMAN MP; ELLARD S; APPLETON M; DRONSFIELD MJ; MACKLE ADR; BAIRD JD; KAISAKI PJ; YAMAGATA K; BELL GI; BAIN SC; HATTERSLEY AT
    MUTATIONS IN THE HEPATOCYTE NUCLEAR FACTOR-1-ALPHA GENE ARE A COMMON-CAUSE OF MATURITY-ONSET DIABETES OF THE YOUNG IN THE UK
    Diabetes
    
    T.M. Frayling et al., "MUTATIONS IN THE HEPATOCYTE NUCLEAR FACTOR-1-ALPHA GENE ARE A COMMON-CAUSE OF MATURITY-ONSET DIABETES OF THE YOUNG IN THE UK", Diabetes, 46(4), 1997, pp. 720-725
32. HANSEN PM; CHOWDHURY T; DECKERT T; HELLGREN A; BAIN SC; POCIOT F
    GENETIC-VARIATION OF THE HEPARAN-SULFATE PROTEOGLYCAN GENE (PERLECAN GENE) - ASSOCIATION WITH URINARY ALBUMIN EXCRETION IN IDDM PATIENTS
    Diabetes
    
    P.M. Hansen et al., "GENETIC-VARIATION OF THE HEPARAN-SULFATE PROTEOGLYCAN GENE (PERLECAN GENE) - ASSOCIATION WITH URINARY ALBUMIN EXCRETION IN IDDM PATIENTS", Diabetes, 46(10), 1997, pp. 1658-1659
33. CHOWDHURY TA; BARNETT AH; BAIN SC
    PATHOGENESIS OF DIABETIC NEPHROPATHY
    Trends in endocrinology and metabolism
    
    T.A. Chowdhury et al., "PATHOGENESIS OF DIABETIC NEPHROPATHY", Trends in endocrinology and metabolism, 7(9), 1996, pp. 320-323
34. DAVIES JL; CUCCA F; GOY JV; ATTA ZAA; MERRIMAN ME; WILSON A; BARNETT AH; BAIN SC; TODD JA
    LINKAGE OF CHROMOSOME-6 AND TYPE-1 DIABETES
    DNA sequence
    
    J.L. Davies et al., "LINKAGE OF CHROMOSOME-6 AND TYPE-1 DIABETES", DNA sequence, 7(1), 1996, pp. 25-26
35. DAVIES JL; CUCCA F; GOY JV; ATTA ZAA; MERRIMAN ME; WILSON A; BARNETT AH; BAIN SC; TODD JA
    SATURATION MULTIPOINT LINKAGE MAPPING OF CHROMOSOME 6Q IN TYPE-1 DIABETES
    Human molecular genetics
    
    J.L. Davies et al., "SATURATION MULTIPOINT LINKAGE MAPPING OF CHROMOSOME 6Q IN TYPE-1 DIABETES", Human molecular genetics, 5(7), 1996, pp. 1071-1074
36. NISTICO L; BUZZETTI R; PRITCHARD LE; VANDERAUWERA B; GIOVANNINI C; BOSI E; LARRAD MTM; RIOS MS; CHOW CC; COCKRAM CS; JACOBS K; MIJOVIC C; BAIN SC; BARNETT AH; VANDEWALLE CL; SCHUIT F; GORUS FK; TOSI R; POZZILLI P; TODD JA
    THE CTLA-4 GENE REGION OF CHROMOSOME 2Q33 IS LINKED TO, AND ASSOCIATED WITH, TYPE-1 DIABETES
    Human molecular genetics
    
    L. Nistico et al., "THE CTLA-4 GENE REGION OF CHROMOSOME 2Q33 IS LINKED TO, AND ASSOCIATED WITH, TYPE-1 DIABETES", Human molecular genetics, 5(7), 1996, pp. 1075-1080
37. BENNETT ST; WILSON AJ; CUCCA F; NERUP J; POCIOT F; MCKINNEY PA; BARNETT AH; BAIN SC; TODD JA
    IDDM2-VNTR-ENCODED SUSCEPTIBILITY TO TYPE-1 DIABETES - DOMINANT PROTECTION AND PARENTAL TRANSMISSION OF ALLELES OF THE INSULIN GENE-LINKED MINISATELLITE LOCUS
    Journal of autoimmunity
    
    S.T. Bennett et al., "IDDM2-VNTR-ENCODED SUSCEPTIBILITY TO TYPE-1 DIABETES - DOMINANT PROTECTION AND PARENTAL TRANSMISSION OF ALLELES OF THE INSULIN GENE-LINKED MINISATELLITE LOCUS", Journal of autoimmunity, 9(3), 1996, pp. 415-421
38. WATKISS E; WEBB M; BAIN SC; SHEPPARD MC; HEWISON M
    EXPRESSION OF VITAMIN-D-RECEPTOR POLYMORPHISMS IN TYPE-I DIABETICS
    Journal of bone and mineral research
    
    E. Watkiss et al., "EXPRESSION OF VITAMIN-D-RECEPTOR POLYMORPHISMS IN TYPE-I DIABETICS", Journal of bone and mineral research, 11(11), 1996, pp. 34-34
39. CHOWDHURY TA; DRONSFIELD MJ; KUMAR S; GOUGH S; BARNETT AH; BAIN SC
    THE ROLE OF GENETIC POLYMORPHISMS WITHIN THE RENIN-ANGIOTENSIN SYSTEMIN SUSCEPTIBILITY TO DIABETIC NEPHROPATHY IN IDDM SUBJECTS (VOL 13, PG 92 1996)
    Diabetic medicine
    
    T.A. Chowdhury et al., "THE ROLE OF GENETIC POLYMORPHISMS WITHIN THE RENIN-ANGIOTENSIN SYSTEMIN SUSCEPTIBILITY TO DIABETIC NEPHROPATHY IN IDDM SUBJECTS (VOL 13, PG 92 1996)", Diabetic medicine, 13(6), 1996, pp. 600-600
40. CHOWDHURY TA; DRONSFIELD MJ; KUMAR S; GOUGH SLC; GIBSON SP; KHATOON A; MACDONALD F; ROWE BR; DUNGER DB; DEAN JD; DAVIES SJ; WEBBER J; SMITH PR; MACKIN P; MARSHALL SM; ADU D; MORRIS PJM; TODD JA; BARNETT AH; BOULTON AJM; BAIN SC
    EXAMINATION OF 2 GENETIC POLYMORPHISMS WITHIN THE RENIN-ANGIOTENSIN SYSTEM - NO EVIDENCE FOR AN ASSOCIATION WITH NEPHROPATHY IN IDDM
    Diabetologia
    
    T.A. Chowdhury et al., "EXAMINATION OF 2 GENETIC POLYMORPHISMS WITHIN THE RENIN-ANGIOTENSIN SYSTEM - NO EVIDENCE FOR AN ASSOCIATION WITH NEPHROPATHY IN IDDM", Diabetologia, 39(9), 1996, pp. 1108-1114
41. OSHEA SJ; LLOYD AC; KEECH ML; ROWE BR; BAIN SC; BARNETT AH
    COSTS OF HYPOGLYCEMIA IN TYPE-II DIABETICS TREATED WITH ORAL HYPOGLYCEMIC AGENTS
    Diabetologia
    
    S.J. Oshea et al., "COSTS OF HYPOGLYCEMIA IN TYPE-II DIABETICS TREATED WITH ORAL HYPOGLYCEMIC AGENTS", Diabetologia, 39, 1996, pp. 871-871
42. CHOWDHURY TA; KUMAR S; GOUGH SCL; BARNETT AH; BAIN SC
    APOLIPOPROTEIN GENES IN DIABETIC NEPHROPATHY
    Diabetologia
    
    T.A. Chowdhury et al., "APOLIPOPROTEIN GENES IN DIABETIC NEPHROPATHY", Diabetologia, 39, 1996, pp. 1142-1142
43. BYRNE MM; STURIS J; MENZEL S; YAMAGATA K; FAJANS SS; DRONSFIELD MJ; BAIN SC; HATTERSLEY AT; VELHO G; FROGUEL P; BELL GI; POLONSKY KS
    ALTERED INSULIN SECRETORY RESPONSES TO GLUCOSE IN DIABETIC AND NONDIABETIC SUBJECTS WITH MUTATIONS IN THE DIABETES SUSCEPTIBILITY GENE MODY3 ON CHROMOSOME-12
    Diabetes
    
    M.M. Byrne et al., "ALTERED INSULIN SECRETORY RESPONSES TO GLUCOSE IN DIABETIC AND NONDIABETIC SUBJECTS WITH MUTATIONS IN THE DIABETES SUSCEPTIBILITY GENE MODY3 ON CHROMOSOME-12", Diabetes, 45(11), 1996, pp. 1503-1510
44. BENNETT ST; LUCASSEN AM; GOUGH SCL; POWELL EE; UNDLIEN DE; PRITCHARD LE; MERRIMAN ME; KAWAGUCHI Y; DRONSFIELD MJ; POCIOT F; NERUP J; BOUZEKRI N; CAMBONTHOMSEN A; RONNINGEN KS; BARNETT AH; BAIN SC; TODD JA
    SUSCEPTIBILITY TO HUMAN TYPE-1 DIABETES AT IDDM2 IS DETERMINED BY TANDEM REPEAT VARIATION AT THE INSULIN GENE MINISATELLITE LOCUS
    Nature genetics
    
    S.T. Bennett et al., "SUSCEPTIBILITY TO HUMAN TYPE-1 DIABETES AT IDDM2 IS DETERMINED BY TANDEM REPEAT VARIATION AT THE INSULIN GENE MINISATELLITE LOCUS", Nature genetics, 9(3), 1995, pp. 284-292
45. COPEMAN JB; CUCCA F; HEARNE CM; CORNALL RJ; REED PW; RONNINGEN KS; UNDLIEN DE; NISTICO L; BUZZETTI R; TOSI R; POCIOT F; NERUP J; CORNELIS F; BARNETT AH; BAIN SC; TODD JA
    LINKAGE DISEQUILIBRIUM MAPPING OF A TYPE-1 DIABETES SUSCEPTIBILITY GENE (IDDM7) TO CHROMOSOME 2Q31-Q33
    Nature genetics
    
    J.B. Copeman et al., "LINKAGE DISEQUILIBRIUM MAPPING OF A TYPE-1 DIABETES SUSCEPTIBILITY GENE (IDDM7) TO CHROMOSOME 2Q31-Q33", Nature genetics, 9(1), 1995, pp. 80-85
46. BENNETT ST; LUCASSEN AM; GOUGH SCL; POWELL EE; PRITCHARD LE; MERRIMAN ME; KAWAGUCHI Y; TODD JA; UNDLIEN DE; RONNINGEN KS; POCIOT F; NERUP J; BOUZEKRI N; CAMBONTHOMSEN A; DRONSFIELD MJ; BARNETT AH; BAIN SC
    INSULIN EXPRESSION - IS VNTR ALLELE-698 REALLY ANOMALOUS - REPLY
    Nature genetics
    
    S.T. Bennett et al., "INSULIN EXPRESSION - IS VNTR ALLELE-698 REALLY ANOMALOUS - REPLY", Nature genetics, 10(4), 1995, pp. 379-380
47. GOUGH SCL; SAKER PJ; PRITCHARD LE; MERRIMAN TR; MERRIMAN ME; ROWE BR; KUMAR S; AITMAN T; BARNETT AH; TURNER RC; BAIN SC; TODD JA
    MUTATION OF THE GLUCAGON RECEPTOR GENE AND DIABETES-MELLITUS IN THE UK - ASSOCIATION OR FOUNDER EFFECT
    Human molecular genetics
    
    S.C.L. Gough et al., "MUTATION OF THE GLUCAGON RECEPTOR GENE AND DIABETES-MELLITUS IN THE UK - ASSOCIATION OR FOUNDER EFFECT", Human molecular genetics, 4(9), 1995, pp. 1609-1612
48. PRITCHARD LE; KAWAGUCHI Y; REED PW; COPEMAN JB; DAVIES JL; BARNETT AH; BAIN SC; TODD JA
    ANALYSIS OF THE CD3 GENE REGION AND TYPE-1 DIABETES - APPLICATION OF FLUORESCENCE-BASED TECHNOLOGY TO LINKAGE DISEQUILIBRIUM MAPPING
    Human molecular genetics
    
    L.E. Pritchard et al., "ANALYSIS OF THE CD3 GENE REGION AND TYPE-1 DIABETES - APPLICATION OF FLUORESCENCE-BASED TECHNOLOGY TO LINKAGE DISEQUILIBRIUM MAPPING", Human molecular genetics, 4(2), 1995, pp. 197-202
49. CHOWDHURY TA; KUMAR S; BARNETT AH; BAIN SC
    NEPHROPATHY IN TYPE-1 DIABETES - THE ROLE OF GENETIC-FACTORS
    Diabetic medicine
    
    T.A. Chowdhury et al., "NEPHROPATHY IN TYPE-1 DIABETES - THE ROLE OF GENETIC-FACTORS", Diabetic medicine, 12(12), 1995, pp. 1059-1067
50. DRONSFIELD MJ; TACK CJJ; BAIN SC; HATTERSLEY
    LINKAGE OF THE GENE FOR MATURITY-ONSET DIABETES OF THE YOUNG (MODY) WITH MARKERS ON THE LONG ARM OF CHROMOSOME-12
    Diabetologia
    
    M.J. Dronsfield et al., "LINKAGE OF THE GENE FOR MATURITY-ONSET DIABETES OF THE YOUNG (MODY) WITH MARKERS ON THE LONG ARM OF CHROMOSOME-12", Diabetologia, 38, 1995, pp. 60-60
51. DAVIES JL; COPEMAN JB; CORDELL HJ; CUCCA F; GOUGH SCL; GOY JV; JENKINS SC; KAWAGUCHI Y; MERRIMAN ME; MERRIMAN TR; PRITCHARD LE; WILSON A; BARNETT AH; BAIN SC; TODD JA
    LINKAGE MAPPING OF TYPE-1 DIABETES
    American journal of human genetics
    
    J.L. Davies et al., "LINKAGE MAPPING OF TYPE-1 DIABETES", American journal of human genetics, 57(4), 1995, pp. 1-1
52. BAIN SC; BARNETT AH
    NATIONAL REPOSITORIES OF FAMILY MATERIAL - IMPORTANT RESEARCH RESOURCE
    British journal of rheumatology
    
    S.C. Bain e A.H. Barnett, "NATIONAL REPOSITORIES OF FAMILY MATERIAL - IMPORTANT RESEARCH RESOURCE", British journal of rheumatology, 33(10), 1994, pp. 899-900
53. CHOWDHURY TA; DRONSFIELD MJ; JONES AF; BAIN SC
    ANGIOTENSIN-II RECEPTOR GENE POLYMORPHISMS AND RISK OF MYOCARDIAL-INFARCTION
    Lancet
    
    T.A. Chowdhury et al., "ANGIOTENSIN-II RECEPTOR GENE POLYMORPHISMS AND RISK OF MYOCARDIAL-INFARCTION", Lancet, 344(8935), 1994, pp. 1502-1503
54. DAVIES JL; KAWAGUCHI Y; BENNETT ST; COPEMAN JB; CORDELL HJ; PRITCHARD LE; REED PW; GOUGH SCL; JENKINS SC; PALMER SM; BALFOUR KM; ROWE BR; FARRALL M; BARNETT AH; BAIN SC; TODD JA
    A GENOME-WIDE SEARCH FOR HUMAN TYPE-1 DIABETES SUSCEPTIBILITY GENES
    Nature
    
    J.L. Davies et al., "A GENOME-WIDE SEARCH FOR HUMAN TYPE-1 DIABETES SUSCEPTIBILITY GENES", Nature, 371(6493), 1994, pp. 130-136
55. PENNY MA; MIJOVIC CH; JACOBS KH; JENKINS D; LUCASSEN AM; BAIN SC; BARNETT AH
    TRANSRACIAL ANALYSIS FINE MAPS A COMPONENT OF GENETIC SUSCEPTIBILITY TO TYPE-1 DIABETES 3' OF THE INSULIN GENE
    Diabetologia
    
    M.A. Penny et al., "TRANSRACIAL ANALYSIS FINE MAPS A COMPONENT OF GENETIC SUSCEPTIBILITY TO TYPE-1 DIABETES 3' OF THE INSULIN GENE", Diabetologia, 37, 1994, pp. 10000005-10000005
56. BAIN SC; ROWE BR; BARNETT AH; TODD JA
    PARENTAL ORIGIN OF DIABETES-ASSOCIATED HLA TYPES IN SIBLING PAIRS WITH TYPE-I DIABETES
    Diabetes
    
    S.C. Bain et al., "PARENTAL ORIGIN OF DIABETES-ASSOCIATED HLA TYPES IN SIBLING PAIRS WITH TYPE-I DIABETES", Diabetes, 43(12), 1994, pp. 1462-1468
57. BARNETT AH; BAIN SC
    MICROALBUMINURIA AND INSULIN-RESISTANCE IN DIABETES-MELLITUS
    Lancet
    
    A.H. Barnett e S.C. Bain, "MICROALBUMINURIA AND INSULIN-RESISTANCE IN DIABETES-MELLITUS", Lancet, 342(8876), 1993, pp. 880-881