-
2
-
-
2042527868
-
Polymorphism screening of the human peroxisome proliferator activated receptor α gene in diabetic patients by AB1 sequencing and high density oligonucleotide array technology
-
abs997 (data on poster, noted by A.J. Brookes and entered into HGBASE).
-
(1998)
Am. J. Hum. Genet.
, vol.63
-
-
Au, K.G.1
Zhang, J.2
Purdy, G.D.3
Fraser, D.J.4
Lee, D.5
Noren, N.K.6
Cronin, M.T.7
Chen, J.8
-
4
-
-
0035116287
-
Melanocortin-1 receptor genotype is a risk factor for basal and squamous cell carcinoma
-
(2001)
J. Invest. Dermatol.
, vol.116
, pp. 224-229
-
-
Box, N.F.1
Duff, D.L.2
Irving, R.E.3
Russell, A.4
Chen, W.5
Griffyths, L.R.6
Parsons, P.G.7
Green, A.C.8
Sturm, R.A.9
-
5
-
-
17344391629
-
HGBASE: A database of SNPs and other variations in and around human genes
-
(2000)
Nucleic Acids Res.
, vol.28
, pp. 356-360
-
-
Brookes, A.J.1
Lehvaslaiho, H.2
Siegfried, M.3
Boehm, J.G.4
Yuan, Y.P.5
Sarkar, C.M.6
Bork, P.7
Ortigao, F.8
-
7
-
-
0032991552
-
Characterization of single-nucleotide polymorphisms in coding regions of human genes
-
(1999)
Nat. Genet.
, vol.22
, pp. 231-238
-
-
Cargill, M.1
Altshuler, D.2
Ireland, J.3
Sklar, P.4
Ardlie, K.5
Patil, N.6
Lane, C.R.7
Lim, E.P.8
Kalyanaraman, N.9
Nemesh, J.10
-
8
-
-
0035937259
-
Predicting the functional consequences of non-synonymous single nucleotide polymorphisms: Structure-based assessment of amino acid variation
-
(2001)
J. Mol. Biol.
, vol.307
, pp. 683-706
-
-
Chasman, D.1
Adams, R.M.2
-
10
-
-
0035399728
-
SNP association studies in Alzheimer's disease highlight problems for complex disease analysis
-
(2001)
Trends Genet.
, vol.17
, pp. 407-413
-
-
Emahazion, T.1
Feuk, L.2
Jobs, M.3
Sawyer, S.L.4
Fredman, D.5
St. Clair, D.6
Prince, J.A.7
Brookes, A.J.8
-
12
-
-
0034182779
-
Variation in the PPARα gene is associated with altered function in vitro and plasma lipid concentrations in Type II diabetic subjects
-
(2000)
Diabetologia
, vol.43
, pp. 673-680
-
-
Flavell, D.M.1
Pineda Torra, I.2
Jamshidi, Y.3
Evans, D.4
Diamon, J.R.5
Elkeles, R.S.6
Bujac, S.R.7
Miller, G.8
Talmud, P.J.9
Staels, B.10
-
13
-
-
0029049553
-
A candidate genetic risk factor for vascular disease: A common mutation in methylenetetrahydrofolate reductase
-
(1995)
Nat. Genet.
, vol.10
, pp. 111-113
-
-
Frosst, P.1
Blom, H.J.2
Milos, R.3
Goyette, P.4
Sheppard, C.A.5
Matthews, R.G.6
Boers, G.J.7
den Heijer, M.8
Kluijtmans, L.A.9
van den Heuvel, L.P.10
-
16
-
-
0032990407
-
Patterns of single-nucleotide polymorphisms in candidate genes for blood-pressure homeostasis
-
(1999)
Nat. Genet.
, vol.22
, pp. 239-247
-
-
Halushka, M.K.1
Fan, J.2
Bentley, K.3
Hsie, L.4
Shen, N.5
Weder, A.6
Cooper, R.7
Lipshutz, R.8
Chakravarti, A.9
-
18
-
-
0033927855
-
Evidence for variable selective pressures at MC1R
-
(2000)
Am. J. Hum. Genet.
, vol.66
, pp. 1351-1361
-
-
Harding, R.M.1
Healy, E.2
Ray, A.J.3
Ellis, N.S.4
Flanagan, N.5
Todd, C.6
Dixon, C.7
Sajantila, A.8
Jackson, I.J.9
Birch-Machin, M.A.10
-
23
-
-
0033625985
-
Mutation screening of the PPARα gene in type 2 diabetes associated with coronary heart disease
-
(2000)
Diabetes Metab.
, vol.26
, pp. 393-401
-
-
Lacquemant, C.1
Lepretre, F.2
Pineda Torra, I.3
Manraj, M.4
Charpentier, G.5
Ruiz, J.6
Staels, B.7
Froguel, P.H.8
-
25
-
-
0030615085
-
Methylenetetrahydrofolate reductase polymorphism, dietary interacations, and risk of colorectal cancer
-
(1997)
Cancer Res.
, vol.57
, pp. 1098-1102
-
-
Ma, J.1
Stampfer, M.J.2
Giovannucci, E.3
Artigas, C.4
Hunter, D.J.5
Fuchs, C.6
Willet, W.C.7
Selhub, J.8
Hennekens, C.H.9
Rozen, R.10
-
29
-
-
0033910271
-
Melanocortin-1 receptor polymorphisms and risk of melanoma: Is the association explained solely by pigmentation phenotype?
-
(2000)
Am. J. Hum. Genet.
, vol.66
, pp. 176-186
-
-
Palmer, J.S.1
Duffy, D.L.2
Box, N.F.3
Aitken, J.F.4
O'Gorman, L.E.5
Green, A.C.6
Hayward, N.K.7
Martin, N.G.8
Sturm, R.A.9
-
30
-
-
0035865322
-
A map of human genome sequence variation containing 1.42 million single nucleotide polymorphisms
-
(2001)
Nature
, vol.409
, pp. 928-933
-
-
Sachidanandam, R.1
Weissman, D.2
Schmidt, S.C.3
Kakol, J.M.4
Stein, L.D.5
Marth, G.6
Sherry, S.7
Mullikin, J.C.8
Mortimore, B.J.9
-
35
-
-
0033922356
-
Molecular scanning of the human PPARα gene: Association of the L162V mutation with hyperapobetalipoproteinemia
-
(2000)
J. Lipid Res.
, vol.41
, pp. 945-952
-
-
Vohl, M.1
Lepage, P.2
Gaudet, D.3
Brewer, C.G.4
Betard, C.5
Perron, P.6
Houde, G.7
Cellier, C.8
Faith, J.M.9
Despres, J.P.10
|