-
1
-
-
0027227288
-
Molecular cloning, expression, and gene localization of a fourth melanocortin receptor
-
Gantz I., Miwa H., Konda Y., Shimoto Y., Tashiro T., Watson S.J., DelValle J., and Yamada T. Molecular cloning, expression, and gene localization of a fourth melanocortin receptor. J. Biol. Chem. 268 (1993) 15174-15179
-
(1993)
J. Biol. Chem.
, vol.268
, pp. 15174-15179
-
-
Gantz, I.1
Miwa, H.2
Konda, Y.3
Shimoto, Y.4
Tashiro, T.5
Watson, S.J.6
DelValle, J.7
Yamada, T.8
-
2
-
-
0027456619
-
Molecular cloning of a novel melanocortin receptor
-
Gantz I., Konda Y., Tashiro T., Shimoto Y., Miwa H., Munzert G., Watson S.J., DelValle J., and Yamada T. Molecular cloning of a novel melanocortin receptor. J. Biol. Chem. 268 (1993) 8246-8250
-
(1993)
J. Biol. Chem.
, vol.268
, pp. 8246-8250
-
-
Gantz, I.1
Konda, Y.2
Tashiro, T.3
Shimoto, Y.4
Miwa, H.5
Munzert, G.6
Watson, S.J.7
DelValle, J.8
Yamada, T.9
-
3
-
-
0027436690
-
Identification of a receptor for γ melanotropin and other proopiomelanocortin peptides in the hypothalamus and limbic system
-
Roselli-Rehfuss L., Mountjoy K.G., Robbins L.S., Mortrud M.T., Low M.J., Tatro J.B., Entwistle M.L., Simerly R.B., and Cone R.D. Identification of a receptor for γ melanotropin and other proopiomelanocortin peptides in the hypothalamus and limbic system. Proc. Natl. Acad. Sci. U. S. A. 90 (1993) 8856-8860
-
(1993)
Proc. Natl. Acad. Sci. U. S. A.
, vol.90
, pp. 8856-8860
-
-
Roselli-Rehfuss, L.1
Mountjoy, K.G.2
Robbins, L.S.3
Mortrud, M.T.4
Low, M.J.5
Tatro, J.B.6
Entwistle, M.L.7
Simerly, R.B.8
Cone, R.D.9
-
4
-
-
0030889192
-
Targeted disruption of the melanocortin-4 receptor results in obesity in mice
-
Huszar D., Lynch C.A., Fairchild-Huntress V., Dunmore J.H., Fang Q., Berkemeier L.R., Gu W., Kesterson R.A., Boston B.A., Cone R.D., Smith F.J., Campfield L.A., Burn P., and Lee F. Targeted disruption of the melanocortin-4 receptor results in obesity in mice. Cell 88 (1997) 131-141
-
(1997)
Cell
, vol.88
, pp. 131-141
-
-
Huszar, D.1
Lynch, C.A.2
Fairchild-Huntress, V.3
Dunmore, J.H.4
Fang, Q.5
Berkemeier, L.R.6
Gu, W.7
Kesterson, R.A.8
Boston, B.A.9
Cone, R.D.10
Smith, F.J.11
Campfield, L.A.12
Burn, P.13
Lee, F.14
-
5
-
-
0033818103
-
Inactivation of the mouse melanocortin-3 receptor results in increased fat mass and reduced lean body mass
-
Chen A.S., Marsh D.J., Trumbauer M.E., Frazier E.G., Guan X.M., Yu H., Rosenblum C.I., Vongs A., Feng Y., Cao L., Metzger J.M., Strack A.M., Camacho R.E., Mellin T.N., Nunes C.N., Min W., Fisher J., Gopal-Truter S., MacIntyre D.E., Chen H.Y., and Van der Ploeg L.H. Inactivation of the mouse melanocortin-3 receptor results in increased fat mass and reduced lean body mass. Nat. Genet. 26 (2000) 97-102
-
(2000)
Nat. Genet.
, vol.26
, pp. 97-102
-
-
Chen, A.S.1
Marsh, D.J.2
Trumbauer, M.E.3
Frazier, E.G.4
Guan, X.M.5
Yu, H.6
Rosenblum, C.I.7
Vongs, A.8
Feng, Y.9
Cao, L.10
Metzger, J.M.11
Strack, A.M.12
Camacho, R.E.13
Mellin, T.N.14
Nunes, C.N.15
Min, W.16
Fisher, J.17
Gopal-Truter, S.18
MacIntyre, D.E.19
Chen, H.Y.20
Van der Ploeg, L.H.21
more..
-
6
-
-
0034456398
-
A unique metabolic syndrome causes obesity in the melanocortin-3 receptor-deficient mouse
-
Butler A.A., Kesterson R.A., Khong K., Cullen M.J., Pelleymounter M.A., Dekoning J., Baetscher M., and Cone R.D. A unique metabolic syndrome causes obesity in the melanocortin-3 receptor-deficient mouse. Endocrinology 141 (2000) 3518-3521
-
(2000)
Endocrinology
, vol.141
, pp. 3518-3521
-
-
Butler, A.A.1
Kesterson, R.A.2
Khong, K.3
Cullen, M.J.4
Pelleymounter, M.A.5
Dekoning, J.6
Baetscher, M.7
Cone, R.D.8
-
7
-
-
24644451507
-
Targeted deletion of melanocortin receptor subtypes 3 and 4, but not CART, alters nutrient partitioning and compromises behavioral and metabolic responses to leptin
-
Zhang Y., Kilroy G.E., Henagan T.M., Prpic-Uhing V., Richards W.G., Bannon A.W., Mynatt R.L., and Gettys T.W. Targeted deletion of melanocortin receptor subtypes 3 and 4, but not CART, alters nutrient partitioning and compromises behavioral and metabolic responses to leptin. FASEB J. 19 (2005) 1482-1491
-
(2005)
FASEB J.
, vol.19
, pp. 1482-1491
-
-
Zhang, Y.1
Kilroy, G.E.2
Henagan, T.M.3
Prpic-Uhing, V.4
Richards, W.G.5
Bannon, A.W.6
Mynatt, R.L.7
Gettys, T.W.8
-
8
-
-
0033977437
-
Melanocortin 3 receptor (MC3R) gene variants in extremely obese women
-
Li W.D., Joo E.J., Furlong E.B., Galvin M., Abel K., Bell C.J., and Price R.A. Melanocortin 3 receptor (MC3R) gene variants in extremely obese women. Int. J. Obe. Relat. Metab. Disord. 24 (2000) 206-210
-
(2000)
Int. J. Obe. Relat. Metab. Disord.
, vol.24
, pp. 206-210
-
-
Li, W.D.1
Joo, E.J.2
Furlong, E.B.3
Galvin, M.4
Abel, K.5
Bell, C.J.6
Price, R.A.7
-
9
-
-
0035380668
-
Naturally occurring mutations in the melanocortin receptor 3 gene are not associated with type 2 diabetes mellitus in French Caucasians
-
Hani E.H., Dupont S., Durand E., Dina C., Gallina S., Gantz I., and Froguel P. Naturally occurring mutations in the melanocortin receptor 3 gene are not associated with type 2 diabetes mellitus in French Caucasians. J. Clin. Endocrinol. Metab. 86 (2001) 2895-2898
-
(2001)
J. Clin. Endocrinol. Metab.
, vol.86
, pp. 2895-2898
-
-
Hani, E.H.1
Dupont, S.2
Durand, E.3
Dina, C.4
Gallina, S.5
Gantz, I.6
Froguel, P.7
-
10
-
-
0036021083
-
Melanocortin-3 receptor gene variants in a Maori kindred with obesity and early onset type 2 diabetes
-
Wong J., Love D.R., Kyle C., Daniels A., White M., Stewart A.W., Schnell A.H., Elston R.C., Holdaway I.M., and Mountjoy K.G. Melanocortin-3 receptor gene variants in a Maori kindred with obesity and early onset type 2 diabetes. Diabetes Res. Clin. Pract. 58 (2002) 61-71
-
(2002)
Diabetes Res. Clin. Pract.
, vol.58
, pp. 61-71
-
-
Wong, J.1
Love, D.R.2
Kyle, C.3
Daniels, A.4
White, M.5
Stewart, A.W.6
Schnell, A.H.7
Elston, R.C.8
Holdaway, I.M.9
Mountjoy, K.G.10
-
11
-
-
0037255271
-
Melanocortin-3-receptor gene variants in morbid obesity
-
Schalin-Jantti C., Valli-Jaakola K., Oksanen L., Martelin E., Laitinen K., Krusius T., Mustajoki P., Heikinheimo M., and Kontula K. Melanocortin-3-receptor gene variants in morbid obesity. Int. J. Obes. Relat. Metab. Disord. 27 (2003) 70-74
-
(2003)
Int. J. Obes. Relat. Metab. Disord.
, vol.27
, pp. 70-74
-
-
Schalin-Jantti, C.1
Valli-Jaakola, K.2
Oksanen, L.3
Martelin, E.4
Laitinen, K.5
Krusius, T.6
Mustajoki, P.7
Heikinheimo, M.8
Kontula, K.9
-
12
-
-
1842292786
-
Identification of an obesity quantitative trait locus on mouse chromosome 2 and evidence of linkage to body fat and insulin on the human homologous region 20q
-
Lembertas A.V., Perusse L., Chagnon Y.C., Fisler J.S., Warden C.H., Purcell-Huynh D.A., Dionne F.T., Gagnon J., Nadeau A., Lusis A.J., and Bouchard C. Identification of an obesity quantitative trait locus on mouse chromosome 2 and evidence of linkage to body fat and insulin on the human homologous region 20q. J. Clin. Invest. 100 (1997) 1240-1247
-
(1997)
J. Clin. Invest.
, vol.100
, pp. 1240-1247
-
-
Lembertas, A.V.1
Perusse, L.2
Chagnon, Y.C.3
Fisler, J.S.4
Warden, C.H.5
Purcell-Huynh, D.A.6
Dionne, F.T.7
Gagnon, J.8
Nadeau, A.9
Lusis, A.J.10
Bouchard, C.11
-
13
-
-
0030766446
-
A susceptibility locus for early-onset non-insulin dependent (type 2) diabetes mellitus maps to chromosome 20q, proximal to the phosphoenolpyruvate carboxykinase gene
-
Zouali H., Hani E.H., Philippi A., Vionnet N., Beckmann J.S., Demenais F., and Froguel P. A susceptibility locus for early-onset non-insulin dependent (type 2) diabetes mellitus maps to chromosome 20q, proximal to the phosphoenolpyruvate carboxykinase gene. Hum. Mol. Genet. 6 (1997) 1401-1408
-
(1997)
Hum. Mol. Genet.
, vol.6
, pp. 1401-1408
-
-
Zouali, H.1
Hani, E.H.2
Philippi, A.3
Vionnet, N.4
Beckmann, J.S.5
Demenais, F.6
Froguel, P.7
-
14
-
-
0030907295
-
New susceptibility locus for NIDDM is localized to human chromosome 20q
-
Ji L., Malecki M., Warram J.H., Yang Y., Rich S.S., and Krolewski A.S. New susceptibility locus for NIDDM is localized to human chromosome 20q. Diabetes 46 (1997) 876-881
-
(1997)
Diabetes
, vol.46
, pp. 876-881
-
-
Ji, L.1
Malecki, M.2
Warram, J.H.3
Yang, Y.4
Rich, S.S.5
Krolewski, A.S.6
-
15
-
-
0030897631
-
Linkage of genetic markers on human chromosomes 20 and 12 to NIDDM in Caucasian sib pairs with a history of diabetic nephropathy
-
Bowden D.W., Sale M., Howard T.D., Qadri A., Spray B.J., Rothschild C.B., Akots G., Rich S.S., and Freedman B.I. Linkage of genetic markers on human chromosomes 20 and 12 to NIDDM in Caucasian sib pairs with a history of diabetic nephropathy. Diabetes 46 (1997) 882-886
-
(1997)
Diabetes
, vol.46
, pp. 882-886
-
-
Bowden, D.W.1
Sale, M.2
Howard, T.D.3
Qadri, A.4
Spray, B.J.5
Rothschild, C.B.6
Akots, G.7
Rich, S.S.8
Freedman, B.I.9
-
16
-
-
13044277561
-
Type 2 diabetes: evidence for linkage on chromosome 20 in 716 Finnish affected sib pairs
-
Ghosh S., Watanabe R.M., Hauser E.R., Valle T., Magnuson V.L., Erdos M.R., Langefeld C.D., Balow Jr. J., Ally D.S., Kohtamaki K., Chines P., Birznieks G., Kaleta H.S., Musick A., Te C., Tannenbaum J., Eldridge W., Shapiro S., Martin C., Witt A., So A., Chang J., Shurtleff B., Porter R., Kudelko K., Unni A., Segal L., Sharaf R., Blaschak-Harvan J., Eriksson J., Tenkula T., Vidgren G., Ehnholm C., Tuomilehto-Wolf E., Hagopian W., Buchanan T.A., Tuomilehto J., Bergman R.N., Collins F.S., and Boehnke M. Type 2 diabetes: evidence for linkage on chromosome 20 in 716 Finnish affected sib pairs. Proc. Natl. Acad. Sci. U. S. A. 96 (1999) 2198-2203
-
(1999)
Proc. Natl. Acad. Sci. U. S. A.
, vol.96
, pp. 2198-2203
-
-
Ghosh, S.1
Watanabe, R.M.2
Hauser, E.R.3
Valle, T.4
Magnuson, V.L.5
Erdos, M.R.6
Langefeld, C.D.7
Balow Jr., J.8
Ally, D.S.9
Kohtamaki, K.10
Chines, P.11
Birznieks, G.12
Kaleta, H.S.13
Musick, A.14
Te, C.15
Tannenbaum, J.16
Eldridge, W.17
Shapiro, S.18
Martin, C.19
Witt, A.20
So, A.21
Chang, J.22
Shurtleff, B.23
Porter, R.24
Kudelko, K.25
Unni, A.26
Segal, L.27
Sharaf, R.28
Blaschak-Harvan, J.29
Eriksson, J.30
Tenkula, T.31
Vidgren, G.32
Ehnholm, C.33
Tuomilehto-Wolf, E.34
Hagopian, W.35
Buchanan, T.A.36
Tuomilehto, J.37
Bergman, R.N.38
Collins, F.S.39
Boehnke, M.40
more..
-
17
-
-
0036963510
-
A novel melanocortin 3 receptor gene (MC3R) mutation associated with severe obesity
-
Lee Y.S., Poh L.K., and Loke K.Y. A novel melanocortin 3 receptor gene (MC3R) mutation associated with severe obesity. J. Clin. Endocrinol. Metab. 87 (2002) 1423-1426
-
(2002)
J. Clin. Endocrinol. Metab.
, vol.87
, pp. 1423-1426
-
-
Lee, Y.S.1
Poh, L.K.2
Loke, K.Y.3
-
18
-
-
4043093705
-
Functional characterization of melanocortin-3 receptor variants identify a loss-of-function mutation involving an amino acid critical for G protein-coupled receptor activation
-
Tao Y.X., and Segaloff D.L. Functional characterization of melanocortin-3 receptor variants identify a loss-of-function mutation involving an amino acid critical for G protein-coupled receptor activation. J. Clin. Endocrinol. Metab. 89 (2004) 3936-3942
-
(2004)
J. Clin. Endocrinol. Metab.
, vol.89
, pp. 3936-3942
-
-
Tao, Y.X.1
Segaloff, D.L.2
-
19
-
-
3242795783
-
Inactivation and intracellular retention of the human I183N mutated melanocortin 3 receptor associated with obesity
-
Rached M., Buronfosse A., Begeot M., and Penhoat A. Inactivation and intracellular retention of the human I183N mutated melanocortin 3 receptor associated with obesity. Biochim. Biophys. Acta 1689 (2004) 229-234
-
(2004)
Biochim. Biophys. Acta
, vol.1689
, pp. 229-234
-
-
Rached, M.1
Buronfosse, A.2
Begeot, M.3
Penhoat, A.4
-
20
-
-
84991847410
-
The role of melanocortin 3 receptor gene in childhood obesity
-
Lee Y.S., Poh L.K., Kek B.L., and Loke K.Y. The role of melanocortin 3 receptor gene in childhood obesity. Diabetes 56 (2007) 2622-2630
-
(2007)
Diabetes
, vol.56
, pp. 2622-2630
-
-
Lee, Y.S.1
Poh, L.K.2
Kek, B.L.3
Loke, K.Y.4
-
21
-
-
33746538324
-
-
Mencarelli M., Maestrini S., Tagliaferri M., Brunani A., Petroni M.L., Liuzzi A., and DiBlasio A.M. The Endocrine Society's 86th Annual Meeting (2004) 140
-
(2004)
The Endocrine Society's 86th Annual Meeting
, pp. 140
-
-
Mencarelli, M.1
Maestrini, S.2
Tagliaferri, M.3
Brunani, A.4
Petroni, M.L.5
Liuzzi, A.6
DiBlasio, A.M.7
-
22
-
-
0141450537
-
Functional characterization of melanocortin-4 receptor mutations associated with childhood obesity
-
Tao Y.X., and Segaloff D.L. Functional characterization of melanocortin-4 receptor mutations associated with childhood obesity. Endocrinology 144 (2003) 4544-4551
-
(2003)
Endocrinology
, vol.144
, pp. 4544-4551
-
-
Tao, Y.X.1
Segaloff, D.L.2
-
23
-
-
0023392945
-
High-efficiency transformation of mammalian cells by plasmid DNA
-
Chen C., and Okayama H. High-efficiency transformation of mammalian cells by plasmid DNA. Mol. Cell. Biol. 7 (1987) 2745-2752
-
(1987)
Mol. Cell. Biol.
, vol.7
, pp. 2745-2752
-
-
Chen, C.1
Okayama, H.2
-
24
-
-
0000448866
-
4-Norleucine, 7-d-phenylalanine-α-melanocyte-stimulating hormone: a highly potent α-melanotropin with ultralong biological activity
-
Sawyer T.K., Sanfilippo P.J., Hruby V.J., Engel M.H., Heward C.B., Burnett J.B., and Hadley M.E. 4-Norleucine, 7-d-phenylalanine-α-melanocyte-stimulating hormone: a highly potent α-melanotropin with ultralong biological activity. Proc. Natl. Acad. Sci. U. S. A. 77 (1980) 5754-5758
-
(1980)
Proc. Natl. Acad. Sci. U. S. A.
, vol.77
, pp. 5754-5758
-
-
Sawyer, T.K.1
Sanfilippo, P.J.2
Hruby, V.J.3
Engel, M.H.4
Heward, C.B.5
Burnett, J.B.6
Hadley, M.E.7
-
25
-
-
20544469112
-
Molecular mechanisms of the neural melanocortin receptor dysfunction in severe early onset obesity
-
Tao Y.X. Molecular mechanisms of the neural melanocortin receptor dysfunction in severe early onset obesity. Mol. Cell. Endocrinol. 239 (2005) 1-14
-
(2005)
Mol. Cell. Endocrinol.
, vol.239
, pp. 1-14
-
-
Tao, Y.X.1
-
26
-
-
33746527488
-
Inactivating mutations of G protein-coupled receptors and diseases: structure-function insights and therapeutic implications
-
Tao Y.X. Inactivating mutations of G protein-coupled receptors and diseases: structure-function insights and therapeutic implications. Pharmacol. Ther. 111 (2006) 949-973
-
(2006)
Pharmacol. Ther.
, vol.111
, pp. 949-973
-
-
Tao, Y.X.1
-
27
-
-
0037439274
-
Intracellular retention is a common characteristic of childhood obesity-associated MC4R mutations
-
Lubrano-Berthelier C., Durand E., Dubern B., Shapiro A., Dazin P., Weill J., Ferron C., Froguel P., and Vaisse C. Intracellular retention is a common characteristic of childhood obesity-associated MC4R mutations. Hum. Mol. Genet. 12 (2003) 145-153
-
(2003)
Hum. Mol. Genet.
, vol.12
, pp. 145-153
-
-
Lubrano-Berthelier, C.1
Durand, E.2
Dubern, B.3
Shapiro, A.4
Dazin, P.5
Weill, J.6
Ferron, C.7
Froguel, P.8
Vaisse, C.9
-
28
-
-
0037341511
-
Mutations in the human melanocortin-4 receptor gene associated with severe familial obesity disrupts receptor function through multiple molecular mechanisms
-
Yeo G.S., Lank E.J., Farooqi I.S., Keogh J., Challis B.G., and O'Rahilly S. Mutations in the human melanocortin-4 receptor gene associated with severe familial obesity disrupts receptor function through multiple molecular mechanisms. Hum. Mol. Genet. 12 (2003) 561-574
-
(2003)
Hum. Mol. Genet.
, vol.12
, pp. 561-574
-
-
Yeo, G.S.1
Lank, E.J.2
Farooqi, I.S.3
Keogh, J.4
Challis, B.G.5
O'Rahilly, S.6
-
29
-
-
0037927578
-
Poor cell surface expression of human melanocortin-4 receptor mutations associated with obesity
-
Nijenhuis W.A., Garner K.M., VanRozen R.J., and Adan R.A. Poor cell surface expression of human melanocortin-4 receptor mutations associated with obesity. J. Biol. Chem. 278 (2003) 22939-22945
-
(2003)
J. Biol. Chem.
, vol.278
, pp. 22939-22945
-
-
Nijenhuis, W.A.1
Garner, K.M.2
VanRozen, R.J.3
Adan, R.A.4
-
30
-
-
26444449038
-
Altered cell surface expression of human MC1R variant receptor alleles associated with red hair and skin cancer risk
-
Beaumont K.A., Newton R.A., Smit D.J., Leonard J.H., Stow J.L., and Sturm R.A. Altered cell surface expression of human MC1R variant receptor alleles associated with red hair and skin cancer risk. Hum. Mol. Genet. 14 (2005) 2145-2154
-
(2005)
Hum. Mol. Genet.
, vol.14
, pp. 2145-2154
-
-
Beaumont, K.A.1
Newton, R.A.2
Smit, D.J.3
Leonard, J.H.4
Stow, J.L.5
Sturm, R.A.6
-
31
-
-
24144443764
-
Co-occurrence of two partially inactivating polymorphisms of MC3R is associated with pediatric-onset obesity
-
Feng N., Young S.F., Aguilera G., Puricelli E., Adler-Wailes D.C., Sebring N.G., and Yanovski J.A. Co-occurrence of two partially inactivating polymorphisms of MC3R is associated with pediatric-onset obesity. Diabetes 54 (2005) 2663-2667
-
(2005)
Diabetes
, vol.54
, pp. 2663-2667
-
-
Feng, N.1
Young, S.F.2
Aguilera, G.3
Puricelli, E.4
Adler-Wailes, D.C.5
Sebring, N.G.6
Yanovski, J.A.7
-
32
-
-
0033928278
-
Haploinsufficiency of the melanocortin-4 receptor: part of a thrifty genotype?
-
Cone R.D. Haploinsufficiency of the melanocortin-4 receptor: part of a thrifty genotype?. J. Clin. Invest. 106 (2000) 185-187
-
(2000)
J. Clin. Invest.
, vol.106
, pp. 185-187
-
-
Cone, R.D.1
-
33
-
-
26244440175
-
Functional analyses of melanocortin-4 receptor mutations identified from patients with binge eating disorder and nonobese or obese subjects
-
Tao Y.X., and Segaloff D.L. Functional analyses of melanocortin-4 receptor mutations identified from patients with binge eating disorder and nonobese or obese subjects. J. Clin. Endocrinol. Metab. 90 (2005) 5632-5638
-
(2005)
J. Clin. Endocrinol. Metab.
, vol.90
, pp. 5632-5638
-
-
Tao, Y.X.1
Segaloff, D.L.2
-
34
-
-
33746040561
-
Identification and functional characterization of three novel human melanocortin-4 receptor gene variants in an obese Chinese population
-
Rong R., Tao Y.X., Cheung B.M., Xu A., Cheung G.C., and Lam K.S. Identification and functional characterization of three novel human melanocortin-4 receptor gene variants in an obese Chinese population. Clin. Endocrinol. 65 (2006) 198-205
-
(2006)
Clin. Endocrinol.
, vol.65
, pp. 198-205
-
-
Rong, R.1
Tao, Y.X.2
Cheung, B.M.3
Xu, A.4
Cheung, G.C.5
Lam, K.S.6
-
35
-
-
33646423288
-
Prevalence, spectrum, and functional characterization of melanocortin-4 receptor gene mutations in a representative population-based sample and obese adults from Germany
-
Hinney A., Bettecken T., Tarnow P., Brumm H., Reichwald K., Lichtner P., Scherag A., Nguyen T.T., Schlumberger P., Rief W., Vollmert C., Illig T., Wichmann H.E., Schafer H., Platzer M., Biebermann H., Meitinger T., and Hebebrand J. Prevalence, spectrum, and functional characterization of melanocortin-4 receptor gene mutations in a representative population-based sample and obese adults from Germany. J. Clin. Endocrinol. Metab. 91 (2006) 1761-1769
-
(2006)
J. Clin. Endocrinol. Metab.
, vol.91
, pp. 1761-1769
-
-
Hinney, A.1
Bettecken, T.2
Tarnow, P.3
Brumm, H.4
Reichwald, K.5
Lichtner, P.6
Scherag, A.7
Nguyen, T.T.8
Schlumberger, P.9
Rief, W.10
Vollmert, C.11
Illig, T.12
Wichmann, H.E.13
Schafer, H.14
Platzer, M.15
Biebermann, H.16
Meitinger, T.17
Hebebrand, J.18
-
36
-
-
0034625358
-
Mutation of Asn-391 within the conserved NPXXY motif of the cholecystokinin B receptor abolishes Gq protein activation without affecting its association with the receptor
-
Gales C., Kowalski-Chauvel A., Dufour M.N., Seva C., Moroder L., Pradayrol L., Vaysse N., Fourmy D., and Silvente-Poirot S. Mutation of Asn-391 within the conserved NPXXY motif of the cholecystokinin B receptor abolishes Gq protein activation without affecting its association with the receptor. J. Biol. Chem. 275 (2000) 17321-17327
-
(2000)
J. Biol. Chem.
, vol.275
, pp. 17321-17327
-
-
Gales, C.1
Kowalski-Chauvel, A.2
Dufour, M.N.3
Seva, C.4
Moroder, L.5
Pradayrol, L.6
Vaysse, N.7
Fourmy, D.8
Silvente-Poirot, S.9
-
37
-
-
0344406765
-
5,6F motif in the rhodopsin ground state and during activation
-
5,6F motif in the rhodopsin ground state and during activation. Proc. Natl. Acad. Sci. U. S. A. 100 (2003) 2290-2295
-
(2003)
Proc. Natl. Acad. Sci. U. S. A.
, vol.100
, pp. 2290-2295
-
-
Fritze, O.1
Filipek, S.2
Kuksa, V.3
Palczewski, K.4
Hofmann, K.P.5
Ernst, O.P.6
-
38
-
-
3843130785
-
Mutation of tyrosine in the conserved NPXXY sequence leads to constitutive phosphorylation and internalization, but not signaling, of the human B2 bradykinin receptor
-
Kalatskaya I., Schussler S., Blaukat A., Muller-Esterl W., Jochum M., Proud D., and Faussner A. Mutation of tyrosine in the conserved NPXXY sequence leads to constitutive phosphorylation and internalization, but not signaling, of the human B2 bradykinin receptor. J. Biol. Chem. 279 (2004) 31268-31276
-
(2004)
J. Biol. Chem.
, vol.279
, pp. 31268-31276
-
-
Kalatskaya, I.1
Schussler, S.2
Blaukat, A.3
Muller-Esterl, W.4
Jochum, M.5
Proud, D.6
Faussner, A.7
-
39
-
-
0032617816
-
Severe autosomal dominant retinitis pigmentosa caused by a novel rhodopsin mutation (Ter349Glu). Mutations in brief no. 208. Online
-
Bessant D.A., Khaliq S., Hameed A., Anwar K., Payne A.M., Mehdi S.Q., and Bhattacharya S.S. Severe autosomal dominant retinitis pigmentosa caused by a novel rhodopsin mutation (Ter349Glu). Mutations in brief no. 208. Online. Hum. Mutat. 13 (1999) 83
-
(1999)
Hum. Mutat.
, vol.13
, pp. 83
-
-
Bessant, D.A.1
Khaliq, S.2
Hameed, A.3
Anwar, K.4
Payne, A.M.5
Mehdi, S.Q.6
Bhattacharya, S.S.7
-
40
-
-
0142091653
-
The GPR54 gene as a regulator of puberty
-
Seminara S.B., Messager S., Chatzidaki E.E., Thresher R.R., Acierno Jr. J.S., Shagoury J.K., Bo-Abbas Y., Kuohung W., Schwinof K.M., Hendrick A.G., Zahn D., Dixon J., Kaiser U.B., Slaugenhaupt S.A., Gusella J.F., O'Rahilly S., Carlton M.B., Crowley Jr. W.F., Aparicio S.A., and Colledge W.H. The GPR54 gene as a regulator of puberty. N. Engl. J. Med. 349 (2003) 1614-1627
-
(2003)
N. Engl. J. Med.
, vol.349
, pp. 1614-1627
-
-
Seminara, S.B.1
Messager, S.2
Chatzidaki, E.E.3
Thresher, R.R.4
Acierno Jr., J.S.5
Shagoury, J.K.6
Bo-Abbas, Y.7
Kuohung, W.8
Schwinof, K.M.9
Hendrick, A.G.10
Zahn, D.11
Dixon, J.12
Kaiser, U.B.13
Slaugenhaupt, S.A.14
Gusella, J.F.15
O'Rahilly, S.16
Carlton, M.B.17
Crowley Jr., W.F.18
Aparicio, S.A.19
Colledge, W.H.20
more..
|