-
1
-
-
0017643827
-
Effects of diabetes mellitus on cholesterol metabolism in man
-
Bennion, L.J., Grundy, S.M., Effects of diabetes mellitus on cholesterol metabolism in man. N. Engl. J. Med. 296 (1977), 1365–1371.
-
(1977)
N. Engl. J. Med.
, vol.296
, pp. 1365-1371
-
-
Bennion, L.J.1
Grundy, S.M.2
-
2
-
-
57349098220
-
Fibroblast growth factor 21 corrects obesity in mice
-
Coskun, T., Bina, H.A., Schneider, M.A., Dunbar, J.D., Hu, C.C., Chen, Y., Moller, D.E., Kharitonenkov, A., Fibroblast growth factor 21 corrects obesity in mice. Endocrinology 149 (2008), 6018–6027.
-
(2008)
Endocrinology
, vol.149
, pp. 6018-6027
-
-
Coskun, T.1
Bina, H.A.2
Schneider, M.A.3
Dunbar, J.D.4
Hu, C.C.5
Chen, Y.6
Moller, D.E.7
Kharitonenkov, A.8
-
3
-
-
84865741904
-
betaKlotho is required for fibroblast growth factor 21 effects on growth and metabolism
-
Ding, X., Boney-Montoya, J., Owen, B.M., Bookout, A.L., Coate, K.C., Mangelsdorf, D.J., Kliewer, S.A., betaKlotho is required for fibroblast growth factor 21 effects on growth and metabolism. Cell Metab. 16 (2012), 387–393.
-
(2012)
Cell Metab.
, vol.16
, pp. 387-393
-
-
Ding, X.1
Boney-Montoya, J.2
Owen, B.M.3
Bookout, A.L.4
Coate, K.C.5
Mangelsdorf, D.J.6
Kliewer, S.A.7
-
4
-
-
2542505481
-
Fibroblast growth factor 19 increases metabolic rate and reverses dietary and leptin-deficient diabetes
-
Fu, L., John, L.M., Adams, S.H., Yu, X.X., Tomlinson, E., Renz, M., Williams, P.M., Soriano, R., Corpuz, R., Moffat, B., et al. Fibroblast growth factor 19 increases metabolic rate and reverses dietary and leptin-deficient diabetes. Endocrinology 145 (2004), 2594–2603.
-
(2004)
Endocrinology
, vol.145
, pp. 2594-2603
-
-
Fu, L.1
John, L.M.2
Adams, S.H.3
Yu, X.X.4
Tomlinson, E.5
Renz, M.6
Williams, P.M.7
Soriano, R.8
Corpuz, R.9
Moffat, B.10
-
5
-
-
84867068010
-
Aberrantly elevated microRNA-34a in obesity attenuates hepatic responses to FGF19 by targeting a membrane coreceptor beta-Klotho
-
Fu, T., Choi, S.E., Kim, D.H., Seok, S., Suino-Powell, K.M., Xu, H.E., Kemper, J.K., Aberrantly elevated microRNA-34a in obesity attenuates hepatic responses to FGF19 by targeting a membrane coreceptor beta-Klotho. Proc. Natl. Acad. Sci. U. S. A. 109 (2012), 16137–16142.
-
(2012)
Proc. Natl. Acad. Sci. U. S. A.
, vol.109
, pp. 16137-16142
-
-
Fu, T.1
Choi, S.E.2
Kim, D.H.3
Seok, S.4
Suino-Powell, K.M.5
Xu, H.E.6
Kemper, J.K.7
-
6
-
-
84920702690
-
Opposite alterations in FGF21 and FGF19 levels and disturbed expression of the receptor machinery for endocrine FGFs in obese patients
-
Gallego-Escuredo, J.M., Gomez-Ambrosi, J., Catalan, V., Domingo, P., Giralt, M., Fruhbeck, G., Villarroya, F., Opposite alterations in FGF21 and FGF19 levels and disturbed expression of the receptor machinery for endocrine FGFs in obese patients. Int. J. Obes. 39 (2015), 121–129.
-
(2015)
Int. J. Obes.
, vol.39
, pp. 121-129
-
-
Gallego-Escuredo, J.M.1
Gomez-Ambrosi, J.2
Catalan, V.3
Domingo, P.4
Giralt, M.5
Fruhbeck, G.6
Villarroya, F.7
-
7
-
-
84863379532
-
Characterization of a FGF19 variant with altered receptor specificity revealed a central role for FGFR1c in the regulation of glucose metabolism
-
Ge, H., Baribault, H., Vonderfecht, S., Lemon, B., Weiszmann, J., Gardner, J., Lee, K.J., Gupte, J., Mookherjee, P., Wang, M., et al. Characterization of a FGF19 variant with altered receptor specificity revealed a central role for FGFR1c in the regulation of glucose metabolism. PLoS One, 7, 2012, e33603.
-
(2012)
PLoS One
, vol.7
-
-
Ge, H.1
Baribault, H.2
Vonderfecht, S.3
Lemon, B.4
Weiszmann, J.5
Gardner, J.6
Lee, K.J.7
Gupte, J.8
Mookherjee, P.9
Wang, M.10
-
8
-
-
84910077652
-
Fibroblast growth factor receptor 4 (FGFR4) deficiency improves insulin resistance and glucose metabolism under diet-induced obesity conditions
-
Ge, H., Zhang, J., Gong, Y., Gupte, J., Ye, J., Weiszmann, J., Samayoa, K., Coberly, S., Gardner, J., Wang, H., et al. Fibroblast growth factor receptor 4 (FGFR4) deficiency improves insulin resistance and glucose metabolism under diet-induced obesity conditions. J. Biol. Chem. 289 (2014), 30470–30480.
-
(2014)
J. Biol. Chem.
, vol.289
, pp. 30470-30480
-
-
Ge, H.1
Zhang, J.2
Gong, Y.3
Gupte, J.4
Ye, J.5
Weiszmann, J.6
Samayoa, K.7
Coberly, S.8
Gardner, J.9
Wang, H.10
-
9
-
-
84861355961
-
Klotho coreceptors inhibit signaling by paracrine fibroblast growth factor 8 subfamily ligands
-
Goetz, R., Ohnishi, M., Ding, X., Kurosu, H., Wang, L., Akiyoshi, J., Ma, J., Gai, W., Sidis, Y., Pitteloud, N., et al. Klotho coreceptors inhibit signaling by paracrine fibroblast growth factor 8 subfamily ligands. Mol. Cell. Biol. 32 (2012), 1944–1954.
-
(2012)
Mol. Cell. Biol.
, vol.32
, pp. 1944-1954
-
-
Goetz, R.1
Ohnishi, M.2
Ding, X.3
Kurosu, H.4
Wang, L.5
Akiyoshi, J.6
Ma, J.7
Gai, W.8
Sidis, Y.9
Pitteloud, N.10
-
10
-
-
84881349710
-
Serum levels of fibroblast growth factor 19 are inversely associated with coronary artery disease in Chinese individuals
-
Hao, Y., Zhou, J., Zhou, M., Ma, X., Lu, Z., Gao, M., Pan, X., Tang, J., Bao, Y., Jia, W., Serum levels of fibroblast growth factor 19 are inversely associated with coronary artery disease in Chinese individuals. PLoS One, 8, 2013, e72345.
-
(2013)
PLoS One
, vol.8
-
-
Hao, Y.1
Zhou, J.2
Zhou, M.3
Ma, X.4
Lu, Z.5
Gao, M.6
Pan, X.7
Tang, J.8
Bao, Y.9
Jia, W.10
-
11
-
-
0037663483
-
Definition of a novel growth factor-dependent signal cascade for the suppression of bile acid biosynthesis
-
Holt, J.A., Luo, G., Billin, A.N., Bisi, J., McNeill, Y.Y., Kozarsky, K.F., Donahee, M., Wang, D.Y., Mansfield, T.A., Kliewer, S.A., et al. Definition of a novel growth factor-dependent signal cascade for the suppression of bile acid biosynthesis. Genes Dev. 17 (2003), 1581–1591.
-
(2003)
Genes Dev.
, vol.17
, pp. 1581-1591
-
-
Holt, J.A.1
Luo, G.2
Billin, A.N.3
Bisi, J.4
McNeill, Y.Y.5
Kozarsky, K.F.6
Donahee, M.7
Wang, D.Y.8
Mansfield, T.A.9
Kliewer, S.A.10
-
12
-
-
70349324370
-
Fibroblast growth factor 21 regulates lipolysis in white adipose tissue but is not required for ketogenesis and triglyceride clearance in liver
-
Hotta, Y., Nakamura, H., Konishi, M., Murata, Y., Takagi, H., Matsumura, S., Inoue, K., Fushiki, T., Itoh, N., Fibroblast growth factor 21 regulates lipolysis in white adipose tissue but is not required for ketogenesis and triglyceride clearance in liver. Endocrinology 150 (2009), 4625–4633.
-
(2009)
Endocrinology
, vol.150
, pp. 4625-4633
-
-
Hotta, Y.1
Nakamura, H.2
Konishi, M.3
Murata, Y.4
Takagi, H.5
Matsumura, S.6
Inoue, K.7
Fushiki, T.8
Itoh, N.9
-
13
-
-
27844546989
-
Fibroblast growth factor 15 functions as an enterohepatic signal to regulate bile acid homeostasis
-
Inagaki, T., Choi, M., Moschetta, A., Peng, L., Cummins, C.L., McDonald, J.G., Luo, G., Jones, S.A., Goodwin, B., Richardson, J.A., et al. Fibroblast growth factor 15 functions as an enterohepatic signal to regulate bile acid homeostasis. Cell Metab. 2 (2005), 217–225.
-
(2005)
Cell Metab.
, vol.2
, pp. 217-225
-
-
Inagaki, T.1
Choi, M.2
Moschetta, A.3
Peng, L.4
Cummins, C.L.5
McDonald, J.G.6
Luo, G.7
Jones, S.A.8
Goodwin, B.9
Richardson, J.A.10
-
14
-
-
23644437321
-
Impaired negative feedback suppression of bile acid synthesis in mice lacking betaKlotho
-
Ito, S., Fujimori, T., Furuya, A., Satoh, J., Nabeshima, Y., Nabeshima, Y., Impaired negative feedback suppression of bile acid synthesis in mice lacking betaKlotho. J. Clin. Invest. 115 (2005), 2202–2208.
-
(2005)
J. Clin. Invest.
, vol.115
, pp. 2202-2208
-
-
Ito, S.1
Fujimori, T.2
Furuya, A.3
Satoh, J.4
Nabeshima, Y.5
Nabeshima, Y.6
-
15
-
-
84930584701
-
Detection of FGF15 in plasma by stable isotope standards and capture by anti-peptide antibodies and targeted mass spectrometry
-
Katafuchi, T., Esterhazy, D., Lemoff, A., Ding, X., Sondhi, V., Kliewer, S.A., Mirzaei, H., Mangelsdorf, D.J., Detection of FGF15 in plasma by stable isotope standards and capture by anti-peptide antibodies and targeted mass spectrometry. Cell Metab. 21 (2015), 898–904.
-
(2015)
Cell Metab.
, vol.21
, pp. 898-904
-
-
Katafuchi, T.1
Esterhazy, D.2
Lemoff, A.3
Ding, X.4
Sondhi, V.5
Kliewer, S.A.6
Mirzaei, H.7
Mangelsdorf, D.J.8
-
16
-
-
20444435873
-
FGF-21 as a novel metabolic regulator
-
Kharitonenkov, A., Shiyanova, T.L., Koester, A., Ford, A.M., Micanovic, R., Galbreath, E.J., Sandusky, G.E., Hammond, L.J., Moyers, J.S., Owens, R.A., et al. FGF-21 as a novel metabolic regulator. J. Clin. Invest. 115 (2005), 1627–1635.
-
(2005)
J. Clin. Invest.
, vol.115
, pp. 1627-1635
-
-
Kharitonenkov, A.1
Shiyanova, T.L.2
Koester, A.3
Ford, A.M.4
Micanovic, R.5
Galbreath, E.J.6
Sandusky, G.E.7
Hammond, L.J.8
Moyers, J.S.9
Owens, R.A.10
-
17
-
-
33846418834
-
The metabolic state of diabetic monkeys is regulated by fibroblast growth factor-21
-
Kharitonenkov, A., Wroblewski, V.J., Koester, A., Chen, Y.F., Clutinger, C.K., Tigno, X.T., Hansen, B.C., Shanafelt, A.B., Etgen, G.J., The metabolic state of diabetic monkeys is regulated by fibroblast growth factor-21. Endocrinology 148 (2007), 774–781.
-
(2007)
Endocrinology
, vol.148
, pp. 774-781
-
-
Kharitonenkov, A.1
Wroblewski, V.J.2
Koester, A.3
Chen, Y.F.4
Clutinger, C.K.5
Tigno, X.T.6
Hansen, B.C.7
Shanafelt, A.B.8
Etgen, G.J.9
-
18
-
-
84865540426
-
Mechanism of tissue-specific farnesoid X receptor in suppressing the expression of genes in bile-acid synthesis in mice
-
Kong, B., Wang, L., Chiang, J.Y., Zhang, Y., Klaassen, C.D., Guo, G.L., Mechanism of tissue-specific farnesoid X receptor in suppressing the expression of genes in bile-acid synthesis in mice. Hepatology 56 (2012), 1034–1043.
-
(2012)
Hepatology
, vol.56
, pp. 1034-1043
-
-
Kong, B.1
Wang, L.2
Chiang, J.Y.3
Zhang, Y.4
Klaassen, C.D.5
Guo, G.L.6
-
19
-
-
34848869695
-
Tissue-specific expression of betaKlotho and fibroblast growth factor (FGF) receptor isoforms determines metabolic activity of FGF19 and FGF21
-
Kurosu, H., Choi, M., Ogawa, Y., Dickson, A.S., Goetz, R., Eliseenkova, A.V., Mohammadi, M., Rosenblatt, K.P., Kliewer, S.A., Kuro-o, M., Tissue-specific expression of betaKlotho and fibroblast growth factor (FGF) receptor isoforms determines metabolic activity of FGF19 and FGF21. J. Biol. Chem. 282 (2007), 26687–26695.
-
(2007)
J. Biol. Chem.
, vol.282
, pp. 26687-26695
-
-
Kurosu, H.1
Choi, M.2
Ogawa, Y.3
Dickson, A.S.4
Goetz, R.5
Eliseenkova, A.V.6
Mohammadi, M.7
Rosenblatt, K.P.8
Kliewer, S.A.9
Kuro-o, M.10
-
20
-
-
77955667250
-
Transgenic expression of cholesterol 7alpha-hydroxylase in the liver prevents high-fat diet-induced obesity and insulin resistance in mice
-
Li, T., Owsley, E., Matozel, M., Hsu, P., Novak, C.M., Chiang, J.Y., Transgenic expression of cholesterol 7alpha-hydroxylase in the liver prevents high-fat diet-induced obesity and insulin resistance in mice. Hepatology 52 (2010), 678–690.
-
(2010)
Hepatology
, vol.52
, pp. 678-690
-
-
Li, T.1
Owsley, E.2
Matozel, M.3
Hsu, P.4
Novak, C.M.5
Chiang, J.Y.6
-
21
-
-
79952218554
-
Overexpression of cholesterol 7alpha-hydroxylase promotes hepatic bile acid synthesis and secretion and maintains cholesterol homeostasis
-
Li, T., Matozel, M., Boehme, S., Kong, B., Nilsson, L.M., Guo, G., Ellis, E., Chiang, J.Y., Overexpression of cholesterol 7alpha-hydroxylase promotes hepatic bile acid synthesis and secretion and maintains cholesterol homeostasis. Hepatology 53 (2011), 996–1006.
-
(2011)
Hepatology
, vol.53
, pp. 996-1006
-
-
Li, T.1
Matozel, M.2
Boehme, S.3
Kong, B.4
Nilsson, L.M.5
Guo, G.6
Ellis, E.7
Chiang, J.Y.8
-
22
-
-
79960564639
-
Serum FGF21 levels are increased in newly diagnosed type 2 diabetes with nonalcoholic fatty liver disease and associated with hsCRP levels independently
-
Li, X., Fan, X., Ren, F., Zhang, Y., Shen, C., Ren, G., Sun, J., Zhang, N., Wang, W., Ning, G., et al. Serum FGF21 levels are increased in newly diagnosed type 2 diabetes with nonalcoholic fatty liver disease and associated with hsCRP levels independently. Diabetes Res. Clin. Pract. 93 (2011), 10–16.
-
(2011)
Diabetes Res. Clin. Pract.
, vol.93
, pp. 10-16
-
-
Li, X.1
Fan, X.2
Ren, F.3
Zhang, Y.4
Shen, C.5
Ren, G.6
Sun, J.7
Zhang, N.8
Wang, W.9
Ning, G.10
-
23
-
-
84862909056
-
Glucose and insulin induction of bile acid synthesis: mechanisms and implication in diabetes and obesity
-
Li, T., Francl, J.M., Boehme, S., Ochoa, A., Zhang, Y., Klaassen, C.D., Erickson, S.K., Chiang, J.Y., Glucose and insulin induction of bile acid synthesis: mechanisms and implication in diabetes and obesity. J. Biol. Chem. 287 (2012), 1861–1873.
-
(2012)
J. Biol. Chem.
, vol.287
, pp. 1861-1873
-
-
Li, T.1
Francl, J.M.2
Boehme, S.3
Ochoa, A.4
Zhang, Y.5
Klaassen, C.D.6
Erickson, S.K.7
Chiang, J.Y.8
-
24
-
-
34848866633
-
Liver-specific activities of FGF19 require Klotho beta
-
Lin, B.C., Wang, M., Blackmore, C., Desnoyers, L.R., Liver-specific activities of FGF19 require Klotho beta. J. Biol. Chem. 282 (2007), 27277–27284.
-
(2007)
J. Biol. Chem.
, vol.282
, pp. 27277-27284
-
-
Lin, B.C.1
Wang, M.2
Blackmore, C.3
Desnoyers, L.R.4
-
25
-
-
33751115468
-
Circulating intestinal fibroblast growth factor 19 has a pronounced diurnal variation and modulates hepatic bile acid synthesis in man
-
Lundasen, T., Galman, C., Angelin, B., Rudling, M., Circulating intestinal fibroblast growth factor 19 has a pronounced diurnal variation and modulates hepatic bile acid synthesis in man. J. Intern. Med. 260 (2006), 530–536.
-
(2006)
J. Intern. Med.
, vol.260
, pp. 530-536
-
-
Lundasen, T.1
Galman, C.2
Angelin, B.3
Rudling, M.4
-
26
-
-
0017600531
-
Cholesterol 7 alpha-hydroxylase
-
Myant, N.B., Mitropoulos, K.A., Cholesterol 7 alpha-hydroxylase. J. Lipid Res. 18 (1977), 135–153.
-
(1977)
J. Lipid Res.
, vol.18
, pp. 135-153
-
-
Myant, N.B.1
Mitropoulos, K.A.2
-
27
-
-
34249697012
-
BetaKlotho is required for metabolic activity of fibroblast growth factor 21
-
Ogawa, Y., Kurosu, H., Yamamoto, M., Nandi, A., Rosenblatt, K.P., Goetz, R., Eliseenkova, A.V., Mohammadi, M., Kuro-o, M., BetaKlotho is required for metabolic activity of fibroblast growth factor 21. Proc. Natl. Acad. Sci. U. S. A. 104 (2007), 7432–7437.
-
(2007)
Proc. Natl. Acad. Sci. U. S. A.
, vol.104
, pp. 7432-7437
-
-
Ogawa, Y.1
Kurosu, H.2
Yamamoto, M.3
Nandi, A.4
Rosenblatt, K.P.5
Goetz, R.6
Eliseenkova, A.V.7
Mohammadi, M.8
Kuro-o, M.9
-
29
-
-
84960923970
-
A long-acting FGF21 molecule, PF-05231023, decreases body weight and improves lipid profile in non-human primates and type 2 diabetic subjects
-
Talukdar, S., Zhou, Y., Li, D., Rossulek, M., Dong, J., Somayaji, V., Weng, Y., Clark, R., Lanba, A., Owen, B.M., et al. A long-acting FGF21 molecule, PF-05231023, decreases body weight and improves lipid profile in non-human primates and type 2 diabetic subjects. Cell Metab. 23 (2016), 427–440.
-
(2016)
Cell Metab.
, vol.23
, pp. 427-440
-
-
Talukdar, S.1
Zhou, Y.2
Li, D.3
Rossulek, M.4
Dong, J.5
Somayaji, V.6
Weng, Y.7
Clark, R.8
Lanba, A.9
Owen, B.M.10
-
30
-
-
48749113401
-
Targeting bile-acid signalling for metabolic diseases
-
Thomas, C., Pellicciari, R., Pruzanski, M., Auwerx, J., Schoonjans, K., Targeting bile-acid signalling for metabolic diseases. Nat. Rev. Drug Discov. 7 (2008), 678–693.
-
(2008)
Nat. Rev. Drug Discov.
, vol.7
, pp. 678-693
-
-
Thomas, C.1
Pellicciari, R.2
Pruzanski, M.3
Auwerx, J.4
Schoonjans, K.5
-
31
-
-
18344394556
-
Transgenic mice expressing human fibroblast growth factor-19 display increased metabolic rate and decreased adiposity
-
Tomlinson, E., Fu, L., John, L., Hultgren, B., Huang, X., Renz, M., Stephan, J.P., Tsai, S.P., Powell-Braxton, L., French, D., et al. Transgenic mice expressing human fibroblast growth factor-19 display increased metabolic rate and decreased adiposity. Endocrinology 143 (2002), 1741–1747.
-
(2002)
Endocrinology
, vol.143
, pp. 1741-1747
-
-
Tomlinson, E.1
Fu, L.2
John, L.3
Hultgren, B.4
Huang, X.5
Renz, M.6
Stephan, J.P.7
Tsai, S.P.8
Powell-Braxton, L.9
French, D.10
-
32
-
-
84903814274
-
Bile acid diarrhoea and FGF19: new views on diagnosis, pathogenesis and therapy
-
Walters, J.R., Bile acid diarrhoea and FGF19: new views on diagnosis, pathogenesis and therapy. Nat. Rev. Gastroenterol. Hepatol. 11 (2014), 426–434.
-
(2014)
Nat. Rev. Gastroenterol. Hepatol.
, vol.11
, pp. 426-434
-
-
Walters, J.R.1
-
33
-
-
80054696665
-
Therapeutic utilities of fibroblast growth factor 19
-
Wu, X., Li, Y., Therapeutic utilities of fibroblast growth factor 19. Expert Opin. Ther. Targets 15 (2011), 1307–1316.
-
(2011)
Expert Opin. Ther. Targets
, vol.15
, pp. 1307-1316
-
-
Wu, X.1
Li, Y.2
-
34
-
-
35748973876
-
Co-receptor requirements for fibroblast growth factor-19 signaling
-
Wu, X., Ge, H., Gupte, J., Weiszmann, J., Shimamoto, G., Stevens, J., Hawkins, N., Lemon, B., Shen, W., Xu, J., et al. Co-receptor requirements for fibroblast growth factor-19 signaling. J. Biol. Chem. 282 (2007), 29069–29072.
-
(2007)
J. Biol. Chem.
, vol.282
, pp. 29069-29072
-
-
Wu, X.1
Ge, H.2
Gupte, J.3
Weiszmann, J.4
Shimamoto, G.5
Stevens, J.6
Hawkins, N.7
Lemon, B.8
Shen, W.9
Xu, J.10
-
35
-
-
57749105436
-
C-terminal tail of FGF19 determines its specificity toward Klotho co-receptors
-
Wu, X., Lemon, B., Li, X., Gupte, J., Weiszmann, J., Stevens, J., Hawkins, N., Shen, W., Lindberg, R., Chen, J.L., et al. C-terminal tail of FGF19 determines its specificity toward Klotho co-receptors. J. Biol. Chem. 283 (2008), 33304–33309.
-
(2008)
J. Biol. Chem.
, vol.283
, pp. 33304-33309
-
-
Wu, X.1
Lemon, B.2
Li, X.3
Gupte, J.4
Weiszmann, J.5
Stevens, J.6
Hawkins, N.7
Shen, W.8
Lindberg, R.9
Chen, J.L.10
-
36
-
-
70149120326
-
Selective activation of FGFR4 by an FGF19 variant does not improve glucose metabolism in Ob/Ob mice
-
Wu, X., Ge, H., Lemon, B., Weiszmann, J., Gupte, J., Hawkins, N., Li, X., Tang, J., Lindberg, R., Li, Y., Selective activation of FGFR4 by an FGF19 variant does not improve glucose metabolism in Ob/Ob mice. Proc. Natl. Acad. Sci. U. S. A. 106 (2009), 14379–14384.
-
(2009)
Proc. Natl. Acad. Sci. U. S. A.
, vol.106
, pp. 14379-14384
-
-
Wu, X.1
Ge, H.2
Lemon, B.3
Weiszmann, J.4
Gupte, J.5
Hawkins, N.6
Li, X.7
Tang, J.8
Lindberg, R.9
Li, Y.10
-
37
-
-
77949328590
-
FGF19-induced hepatocyte proliferation is mediated through FGFR4 activation
-
Wu, X., Ge, H., Lemon, B., Vonderfecht, S., Weiszmann, J., Hecht, R., Gupte, J., Hager, T., Wang, Z., Lindberg, R., et al. FGF19-induced hepatocyte proliferation is mediated through FGFR4 activation. J. Biol. Chem. 285 (2010), 5165–5170.
-
(2010)
J. Biol. Chem.
, vol.285
, pp. 5165-5170
-
-
Wu, X.1
Ge, H.2
Lemon, B.3
Vonderfecht, S.4
Weiszmann, J.5
Hecht, R.6
Gupte, J.7
Hager, T.8
Wang, Z.9
Lindberg, R.10
-
38
-
-
79952803104
-
FGF19 regulates cell proliferation, glucose and bile acid metabolism via FGFR4-dependent and independent pathways
-
Wu, A.L., Coulter, S., Liddle, C., Wong, A., Eastham-Anderson, J., French, D.M., Peterson, A.S., Sonoda, J., FGF19 regulates cell proliferation, glucose and bile acid metabolism via FGFR4-dependent and independent pathways. PLoS One, 6, 2011, e17868.
-
(2011)
PLoS One
, vol.6
-
-
Wu, A.L.1
Coulter, S.2
Liddle, C.3
Wong, A.4
Eastham-Anderson, J.5
French, D.M.6
Peterson, A.S.7
Sonoda, J.8
-
39
-
-
61649127208
-
Fibroblast growth factor 21 reverses hepatic steatosis, increases energy expenditure, and improves insulin sensitivity in diet-induced obese mice
-
Xu, J., Lloyd, D.J., Hale, C., Stanislaus, S., Chen, M., Sivits, G., Vonderfecht, S., Hecht, R., Li, Y.S., Lindberg, R.A., et al. Fibroblast growth factor 21 reverses hepatic steatosis, increases energy expenditure, and improves insulin sensitivity in diet-induced obese mice. Diabetes 58 (2009), 250–259.
-
(2009)
Diabetes
, vol.58
, pp. 250-259
-
-
Xu, J.1
Lloyd, D.J.2
Hale, C.3
Stanislaus, S.4
Chen, M.5
Sivits, G.6
Vonderfecht, S.7
Hecht, R.8
Li, Y.S.9
Lindberg, R.A.10
-
40
-
-
70350455732
-
Acute glucose-lowering and insulin-sensitizing action of FGF21 in insulin-resistant mouse models–association with liver and adipose tissue effects
-
Xu, J., Stanislaus, S., Chinookoswong, N., Lau, Y.Y., Hager, T., Patel, J., Ge, H., Weiszmann, J., Lu, S.C., Graham, M., et al. Acute glucose-lowering and insulin-sensitizing action of FGF21 in insulin-resistant mouse models–association with liver and adipose tissue effects. Am. J. Physiol. Endocrinol. Metab. 297 (2009), E1105–E1114.
-
(2009)
Am. J. Physiol. Endocrinol. Metab.
, vol.297
, pp. E1105-E1114
-
-
Xu, J.1
Stanislaus, S.2
Chinookoswong, N.3
Lau, Y.Y.4
Hager, T.5
Patel, J.6
Ge, H.7
Weiszmann, J.8
Lu, S.C.9
Graham, M.10
-
41
-
-
84863338708
-
Differential specificity of endocrine FGF19 and FGF21 to FGFR1 and FGFR4 in complex with KLB
-
Yang, C., Jin, C., Li, X., Wang, F., McKeehan, W.L., Luo, Y., Differential specificity of endocrine FGF19 and FGF21 to FGFR1 and FGFR4 in complex with KLB. PLoS One, 7, 2012, e33870.
-
(2012)
PLoS One
, vol.7
-
-
Yang, C.1
Jin, C.2
Li, X.3
Wang, F.4
McKeehan, W.L.5
Luo, Y.6
-
42
-
-
0034685916
-
Elevated cholesterol metabolism and bile acid synthesis in mice lacking membrane tyrosine kinase receptor FGFR4
-
Yu, C., Wang, F., Kan, M., Jin, C., Jones, R.B., Weinstein, M., Deng, C.X., McKeehan, W.L., Elevated cholesterol metabolism and bile acid synthesis in mice lacking membrane tyrosine kinase receptor FGFR4. J. Biol. Chem. 275 (2000), 15482–15489.
-
(2000)
J. Biol. Chem.
, vol.275
, pp. 15482-15489
-
-
Yu, C.1
Wang, F.2
Kan, M.3
Jin, C.4
Jones, R.B.5
Weinstein, M.6
Deng, C.X.7
McKeehan, W.L.8
-
43
-
-
79956113302
-
Circadian rhythm of circulating fibroblast growth factor 21 is related to diurnal changes in fatty acids in humans
-
Yu, H., Xia, F., Lam, K.S., Wang, Y., Bao, Y., Zhang, J., Gu, Y., Zhou, P., Lu, J., Jia, W., et al. Circadian rhythm of circulating fibroblast growth factor 21 is related to diurnal changes in fatty acids in humans. Clin. Chem. 57 (2011), 691–700.
-
(2011)
Clin. Chem.
, vol.57
, pp. 691-700
-
-
Yu, H.1
Xia, F.2
Lam, K.S.3
Wang, Y.4
Bao, Y.5
Zhang, J.6
Gu, Y.7
Zhou, P.8
Lu, J.9
Jia, W.10
-
44
-
-
84901496215
-
Fibroblast growth factor 21, the endocrine FGF pathway and novel treatments for metabolic syndrome
-
Zhang, J., Li, Y., Fibroblast growth factor 21, the endocrine FGF pathway and novel treatments for metabolic syndrome. Drug Discov. Today 19 (2014), 579–589.
-
(2014)
Drug Discov. Today
, vol.19
, pp. 579-589
-
-
Zhang, J.1
Li, Y.2
-
45
-
-
48349146527
-
Serum FGF21 levels are increased in obesity and are independently associated with the metabolic syndrome in humans
-
Zhang, X., Yeung, D.C., Karpisek, M., Stejskal, D., Zhou, Z.G., Liu, F., Wong, R.L., Chow, W.S., Tso, A.W., Lam, K.S., et al. Serum FGF21 levels are increased in obesity and are independently associated with the metabolic syndrome in humans. Diabetes 57 (2008), 1246–1253.
-
(2008)
Diabetes
, vol.57
, pp. 1246-1253
-
-
Zhang, X.1
Yeung, D.C.2
Karpisek, M.3
Stejskal, D.4
Zhou, Z.G.5
Liu, F.6
Wong, R.L.7
Chow, W.S.8
Tso, A.W.9
Lam, K.S.10
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