-
1
-
-
0031951973
-
Meta-analysis of linkage data under worst-case conditions. A demonstration using the human ob region
-
ALLISON, D. & HEO, M. (1998). Meta-analysis of linkage data under worst-case conditions. A demonstration using the human ob region. Genetics 148, 859-866.
-
(1998)
Genetics
, vol.148
, pp. 859-866
-
-
Allison, D.1
Heo, M.2
-
2
-
-
0030813619
-
Identification of a placental enhancer for the human leptin gene
-
BI, S., GAVRILOVA, O., GONG, D. W. et al. (1997). Identification of a placental enhancer for the human leptin gene. J. Biol. Chem. 272, 30583-8.
-
(1997)
J. Biol. Chem.
, vol.272
, pp. 30583-30588
-
-
Bi, S.1
Gavrilova, O.2
Gong, D.W.3
-
3
-
-
0030642286
-
Obese (ob) gene defects are rare in human obesity
-
CARLSSON, B., LINDELL, K., GABRIELSSON, B. et al. (1997). Obese (ob) gene defects are rare in human obesity. Obesity Research 5, 30-35.
-
(1997)
Obesity Research
, vol.5
, pp. 30-35
-
-
Carlsson, B.1
Lindell, K.2
Gabrielsson, B.3
-
4
-
-
0345335191
-
Indication for linkage of the human OB gene region with extreme obesity
-
CLEMENT, K., GARNER, C., HAGER, J. et al. (1996). Indication for linkage of the human OB gene region with extreme obesity. Diabetes 45, 687-690.
-
(1996)
Diabetes
, vol.45
, pp. 687-690
-
-
Clement, K.1
Garner, C.2
Hager, J.3
-
5
-
-
0029020677
-
Evidence against either a premature stop codon or the absence of obese gene mRNA in human obesity
-
CONSIDINE, R. V., CONSIDINE, E. L., WILLIAMS, C. J. et al. (1995). Evidence against either a premature stop codon or the absence of obese gene mRNA in human obesity. J. Clin. Invest. 95, 2986-2988.
-
(1995)
J. Clin. Invest.
, vol.95
, pp. 2986-2988
-
-
Considine, R.V.1
Considine, E.L.2
Williams, C.J.3
-
6
-
-
0029893230
-
Mutation screening and identification of a sequence variation in the human OB gene coding region
-
CONSIDINE, R. V., CONSIDINE, E. L., WILLIAMS, C. J. et al. (1996). Mutation screening and identification of a sequence variation in the human OB gene coding region. Biochem. Biophysical Res. Commun. 220, 735-739.
-
(1996)
Biochem. Biophysical Res. Commun.
, vol.220
, pp. 735-739
-
-
Considine, R.V.1
Considine, E.L.2
Williams, C.J.3
-
7
-
-
0030935153
-
Identification of two novel missense mutations in the human OB gene
-
ECHWALD, S., RASMUSSEN, S., SORENSON, T. et al. (1997). Identification of two novel missense mutations in the human OB gene. Int. J. Obesity 21, 321-326.
-
(1997)
Int. J. Obesity
, vol.21
, pp. 321-326
-
-
Echwald, S.1
Rasmussen, S.2
Sorenson, T.3
-
8
-
-
0032558725
-
Leptin and regulation of body weight in mammals
-
FRIEDMAN, J. M. & HALAAS, J. L. (1998). Leptin and regulation of body weight in mammals. Nature 395, 763-770.
-
(1998)
Nature
, vol.395
, pp. 763-770
-
-
Friedman, J.M.1
Halaas, J.L.2
-
9
-
-
0030032754
-
Genomic structure and promoter analysis of the human obese gene
-
GONG, D.-W., BI, S., PRATLEY, R. et al. (1996). Genomic structure and promoter analysis of the human obese gene. J. Biol. Chem. 271, 3971-3974.
-
(1996)
J. Biol. Chem.
, vol.271
, pp. 3971-3974
-
-
Gong, D.-W.1
Bi, S.2
Pratley, R.3
-
10
-
-
2342609965
-
A polymorphism in the 5′ untranslated region of the human ob gene is associated with low leptin levels
-
HAGER, J., CLEMENT, K., FRANCKE, S. et al. (1998). A polymorphism in the 5′ untranslated region of the human ob gene is associated with low leptin levels. Int. J. Obesity 22, 200-205.
-
(1998)
Int. J. Obesity
, vol.22
, pp. 200-205
-
-
Hager, J.1
Clement, K.2
Francke, S.3
-
12
-
-
0031860393
-
Databases on transcriptional regulation: TRANSFAC, TRRD and COMPEL
-
HEINEMEYER, T., WINGENDER, E., REUTER, I. et al. (1998). Databases on transcriptional regulation: TRANSFAC, TRRD and COMPEL. Nucleic Acids Res. 26, 362-367.
-
(1998)
Nucleic Acids Res.
, vol.26
, pp. 362-367
-
-
Heinemeyer, T.1
Wingender, E.2
Reuter, I.3
-
13
-
-
0031766048
-
No evidence for involvement of the leptin gene in anorexia nervosa, bulimia nervosa, underweight or early onset extreme obesity: Identification of two novel mutations in the coding sequence and a novel polymorphism in the leptin gene linked upstream region
-
HINNEY, A., BORNSCHEUER, A., DEPENBUSCH, M. et al. (1998). No evidence for involvement of the leptin gene in anorexia nervosa, bulimia nervosa, underweight or early onset extreme obesity: identification of two novel mutations in the coding sequence and a novel polymorphism in the leptin gene linked upstream region. Mol. Psychiatry 3, 539-543.
-
(1998)
Mol. Psychiatry
, vol.3
, pp. 539-543
-
-
Hinney, A.1
Bornscheuer, A.2
Depenbusch, M.3
-
14
-
-
0025783550
-
Medium reiteration frequency repetitive sequences in the human genome
-
KAPLAN, D. J., JURKA, J., SOLUS, J. F. et al. (1991). Medium reiteration frequency repetitive sequences in the human genome. Nucleic Acids Res. 19, 4731-4738.
-
(1991)
Nucleic Acids Res.
, vol.19
, pp. 4731-4738
-
-
Kaplan, D.J.1
Jurka, J.2
Solus, J.F.3
-
15
-
-
0031741688
-
Identification of new sequence variants in the leptin gene
-
KARVONEN, M. K., PESONEN, U., HEINONEN, P. et al. (1998). Identification of new sequence variants in the leptin gene. J. Clin. Endocrinol. Metab. 83, 3239-3242.
-
(1998)
J. Clin. Endocrinol. Metab.
, vol.83
, pp. 3239-3242
-
-
Karvonen, M.K.1
Pesonen, U.2
Heinonen, P.3
-
16
-
-
0026080111
-
A rapid nonenzymatic method for the precipitation of HMW DNA from blood for RFLP studies
-
LAHIRI, D. K., &, NURNBERGER, J. I. (1991). A rapid nonenzymatic method for the precipitation of HMW DNA from blood for RFLP studies. Nucleic. Acids Res. 19, 5444.
-
(1991)
Nucleic. Acids Res.
, vol.19
, pp. 5444
-
-
Lahiri, D.K.1
Nurnberger, J.I.2
-
17
-
-
15844373886
-
Absense of mutations in the human OB gene in obese/diabetic subjects
-
MAFFEI, M., STOFFEL, M., BARONE, M. et al. (1996). Absense of mutations in the human OB gene in obese/diabetic subjects. Diabetes 45, 679-682.
-
(1996)
Diabetes
, vol.45
, pp. 679-682
-
-
Maffei, M.1
Stoffel, M.2
Barone, M.3
-
18
-
-
0031892748
-
Novel polymorphisms in the 5′ region of the LEP gene. Association with leptin levels and response to lowcalorie diet in human obesity
-
MAMMES, O., BETOULLE, D., AUBERT, R. et al. (1998). Novel polymorphisms in the 5′ region of the LEP gene. Association with leptin levels and response to lowcalorie diet in human obesity. Diabetes 47, 487-489.
-
(1998)
Diabetes
, vol.47
, pp. 487-489
-
-
Mammes, O.1
Betoulle, D.2
Aubert, R.3
-
19
-
-
0030878110
-
Congenital leptin deficiency is associated with severe early-onset obesity in humans
-
MONTAGUE, C. T., FAROOQI, S., WHITEHEAD, J. P. et al. (1997). Congenital leptin deficiency is associated with severe early-onset obesity in humans. Nature 387, 903-908.
-
(1997)
Nature
, vol.387
, pp. 903-908
-
-
Montague, C.T.1
Farooqi, S.2
Whitehead, J.P.3
-
20
-
-
17344364213
-
DNA sequence diversity in a 9.7-kb region of the human lipoprotein lipase gene
-
NICKERSON, D. A., TAYLOR, S. L., WEISS, K. M. et al. (1998). DNA sequence diversity in a 9.7-kb region of the human lipoprotein lipase gene [see comments]. Nat Genet 19, 233-240.
-
(1998)
Nat Genet
, vol.19
, pp. 233-240
-
-
Nickerson, D.A.1
Taylor, S.L.2
Weiss, K.M.3
-
21
-
-
15844399534
-
Human obese gene: Molecular screening in Japanese and Asian Indian NIDDM patients associated with obesity
-
NIKI, T., MORI, H., TAMORI, Y. et al. (1996). Human obese gene: molecular screening in Japanese and Asian Indian NIDDM patients associated with obesity. Diabetes 45, 675-678.
-
(1996)
Diabetes
, vol.45
, pp. 675-678
-
-
Niki, T.1
Mori, H.2
Tamori, Y.3
-
22
-
-
0030994425
-
Novel polymorphism of the human ob gene promoter in lean and morbidly obese subjects
-
OKSANEN, L., KAINULAINEN, K., HEIMAN, M. et al. (1997). Novel polymorphism of the human ob gene promoter in lean and morbidly obese subjects. Int. J. Obesity 21, 489-494.
-
(1997)
Int. J. Obesity
, vol.21
, pp. 489-494
-
-
Oksanen, L.1
Kainulainen, K.2
Heiman, M.3
-
23
-
-
0031723523
-
Functional analysis of the C(-188) a polymorphism of the human leptin promoter
-
OKSANEN, L., PALVIMO, J. J., JANNE, O. A. et al. (1998). Functional analysis of the C(-188) A polymorphism of the human leptin promoter. Hum. Genet. 103, 527-528.
-
(1998)
Hum. Genet.
, vol.103
, pp. 527-528
-
-
Oksanen, L.1
Palvimo, J.J.2
Janne, O.A.3
-
24
-
-
0031945229
-
Obesity related phenotypes in families selected for extreme obesity and leanness
-
PRICE, R. A., REED, D. R. & LEE, J. H. (1998). Obesity related phenotypes in families selected for extreme obesity and leanness. Int. J. Obesity 22, 406-413.
-
(1998)
Int. J. Obesity
, vol.22
, pp. 406-413
-
-
Price, R.A.1
Reed, D.R.2
Lee, J.H.3
-
25
-
-
0029938057
-
Extreme obesity may be linked to markers flanking the human OB gene
-
REED, D. R., DING, Y., XU, W. et al. (1996). Extreme obesity may be linked to markers flanking the human OB gene. Diabetes 45, 691-694.
-
(1996)
Diabetes
, vol.45
, pp. 691-694
-
-
Reed, D.R.1
Ding, Y.2
Xu, W.3
-
26
-
-
0030705974
-
Molecular screening of both the promoter and the protein coding regions in the human ob gene in Japanese obese subjects with non-insulin-dependent diabetes mellitus
-
SHIGEMOTO, M., NISHI, S., OGAWA, Y. et al. (1997). Molecular screening of both the promoter and the protein coding regions in the human ob gene in Japanese obese subjects with non-insulin-dependent diabetes mellitus. Eur. J. Endocrinol. 137, 511-513.
-
(1997)
Eur. J. Endocrinol.
, vol.137
, pp. 511-513
-
-
Shigemoto, M.1
Nishi, S.2
Ogawa, Y.3
-
27
-
-
0032014836
-
A leptin missense mutation associated with hypogonadism and morbid obesity
-
STROBEL, A., ISSAD, T., CAMOIN, L. et al. (1998). A leptin missense mutation associated with hypogonadism and morbid obesity. Nat. Genet. 18, 213-214.
-
(1998)
Nat. Genet.
, vol.18
, pp. 213-214
-
-
Strobel, A.1
Issad, T.2
Camoin, L.3
|