-
1
-
-
1542510700
-
Acquired and inherited lipodystrophies
-
CrossRef PubMed
-
Garg, A. (2004) Acquired and inherited lipodystrophies. N. Engl. J. Med. 350, 1220-1234 CrossRef PubMed
-
(2004)
N. Engl. J. Med.
, vol.350
, pp. 1220-1234
-
-
Garg, A.1
-
2
-
-
60649090586
-
Clinical and molecular aspects of Berardinelli-Seip Congenital Lipodystrophy (BSCL)
-
CrossRef PubMed
-
Gomes, K. B., Pardini, V. C. and Fernandes, A. P. (2009) Clinical and molecular aspects of Berardinelli-Seip Congenital Lipodystrophy (BSCL). Clin. Chim. Acta 402, 1-6 CrossRef PubMed
-
(2009)
Clin. Chim. Acta
, vol.402
, pp. 1-6
-
-
Gomes, K.B.1
Pardini, V.C.2
Fernandes, A.P.3
-
3
-
-
0036093225
-
Serum adiponectin and leptin levels in patients with lipodystrophies
-
CrossRef PubMed
-
Haque, W. A., Shimomura, I., Matsuzawa, Y. and Garg, A. (2002) Serum adiponectin and leptin levels in patients with lipodystrophies. J. Clin. Endocrinol. Metab. 87, 2395-2398 CrossRef PubMed
-
(2002)
J. Clin. Endocrinol. Metab.
, vol.87
, pp. 2395-2398
-
-
Haque, W.A.1
Shimomura, I.2
Matsuzawa, Y.3
Garg, A.4
-
4
-
-
0034941121
-
Identification of the gene altered in Berardinelli-Seip congenital lipodystrophy on chromosome 11q13
-
CrossRef PubMed
-
Magre, J., Delepine, M., Khallouf, E., Gedde-Dahl, Jr, T., Van Maldergem, L., Sobel, E., Papp, J., Meier, M., Megarbane, A., Bachy, A. et al. (2001) Identification of the gene altered in Berardinelli-Seip congenital lipodystrophy on chromosome 11q13. Nat. Genet. 28, 365-370 CrossRef PubMed
-
(2001)
Nat. Genet.
, vol.28
, pp. 365-370
-
-
Magre, J.1
Delepine, M.2
Khallouf, E.3
Gedde-Dahl, T.4
Van Maldergem, L.5
Sobel, E.6
Papp, J.7
Meier, M.8
Megarbane, A.9
Bachy, A.10
-
5
-
-
0001617185
-
An undiagnosed endocrinometabolic syndrome: Report of 2 cases
-
CrossRef PubMed
-
Berardinelli, W. (1954) An undiagnosed endocrinometabolic syndrome: report of 2 cases. J. Clin. Endocrinol. Metab. 14, 193-204 CrossRef PubMed
-
(1954)
J. Clin. Endocrinol. Metab.
, vol.14
, pp. 193-204
-
-
Berardinelli, W.1
-
6
-
-
84925556001
-
Lipodystrophy and gigantism with associated endocrine manifestation: A new diencephalic syndrome?
-
PubMed
-
Seip, M. (1959) Lipodystrophy and gigantism with associated endocrine manifestation: a new diencephalic syndrome? Acta Paediatr. 48, 555-574 PubMed
-
(1959)
Acta Paediatr.
, vol.48
, pp. 555-574
-
-
Seip, M.1
-
7
-
-
0344442411
-
Phenotypic heterogeneity in body fat distribution in patients with congenital generalized lipodystrophy caused by mutations in the AGPAT2 or seipin genes
-
CrossRef PubMed
-
Simha, V. (2003) Phenotypic heterogeneity in body fat distribution in patients with congenital generalized lipodystrophy caused by mutations in the AGPAT2 or seipin genes. J. Clin. Endocrinol. Metab. 88, 5433-5437 CrossRef PubMed
-
(2003)
J. Clin. Endocrinol. Metab.
, vol.88
, pp. 5433-5437
-
-
Simha, V.1
-
8
-
-
0026767508
-
Peculiar distribution of adipose tissue in patients with congenital generalized lipodystrophy
-
Garg, A., Fleckenstein, J. L., Peshock, R. M. and Grundy, S. M. (1992) Peculiar distribution of adipose tissue in patients with congenital generalized lipodystrophy. J. Clin. Endocrinol. Metabol. 75, 358-361
-
(1992)
J. Clin. Endocrinol. Metabol.
, vol.75
, pp. 358-361
-
-
Garg, A.1
Fleckenstein, J.L.2
Peshock, R.M.3
Grundy, S.M.4
-
9
-
-
18644371065
-
Genotype-phenotype relationships in Berardinelli-Seip congenital lipodystrophy
-
CrossRef PubMed
-
Maldergem, L. V., Magre, J., Khallouf, T. E., Gedde-Dahl, Jr, T., Delepine, M., Trygstad, O., Seemanova, E., STephenson, T., Albott, C. S., Bonnici, F. et al. (2002) Genotype-phenotype relationships in Berardinelli-Seip congenital lipodystrophy. J. Med. Genet. 39, 722-733 CrossRef PubMed
-
(2002)
J. Med. Genet.
, vol.39
, pp. 722-733
-
-
Maldergem, L.V.1
Magre, J.2
Khallouf, T.E.3
Gedde-Dahl, T.4
Delepine, M.5
Trygstad, O.6
Seemanova, E.7
Stephenson, T.8
Albott, C.S.9
Bonnici, F.10
-
10
-
-
0036578783
-
AGPAT2 is mutated in congenital generalized lipodystrophy linked to chromosome 9q34
-
CrossRef PubMed
-
Agarwal, A. K., Arioglu, E., De Almeida, S., Akkoc, N., Taylor, S. I., Bowcock, A. M., Barnes, R. I. and Garg, A. (2002) AGPAT2 is mutated in congenital generalized lipodystrophy linked to chromosome 9q34. Nat. Genet. 31, 21-23 CrossRef PubMed
-
(2002)
Nat. Genet.
, vol.31
, pp. 21-23
-
-
Agarwal, A.K.1
Arioglu, E.2
De Almeida, S.3
Akkoc, N.4
Taylor, S.I.5
Bowcock, A.M.6
Barnes, R.I.7
Garg, A.8
-
11
-
-
0033305362
-
A gene for congenital generalized lipodystrophy maps to human chrmosome 9q34
-
CrossRef PubMed
-
Garg, A., Wilson, R., Barnes, R. I., Arioglu, E., Zaidi, Z., Gurakan, F., Kocak, N., O'Rahilly, S., Taylor, S. I., Patel, S. B. and Bowcock, A. M. (1999) A gene for congenital generalized lipodystrophy maps to human chrmosome 9q34. J. Clin. Endocrinol. Metab. 84, 3390-3394 CrossRef PubMed
-
(1999)
J. Clin. Endocrinol. Metab.
, vol.84
, pp. 3390-3394
-
-
Garg, A.1
Wilson, R.2
Barnes, R.I.3
Arioglu, E.4
Zaidi, Z.5
Gurakan, F.6
Kocak, N.7
O'Rahilly, S.8
Taylor, S.I.9
Patel, S.B.10
Bowcock, A.M.11
-
12
-
-
0030789284
-
Human lysophosphatidic acid acyltransferase. cDNA cloning, expression, and localization to chromosome 9q34.3
-
CrossRef PubMed
-
Eberhardt, C., Gray, P. W. and Tjoelker, L. W. (1997) Human lysophosphatidic acid acyltransferase. cDNA cloning, expression, and localization to chromosome 9q34.3. J. Biol. Chem. 272, 20299-20305 CrossRef PubMed
-
(1997)
J. Biol. Chem.
, vol.272
, pp. 20299-20305
-
-
Eberhardt, C.1
Gray, P.W.2
Tjoelker, L.W.3
-
13
-
-
0010044876
-
The structure and functions of human lysophosphatidic acid acyltransferases
-
CrossRef PubMed
-
Leung, D. W. (2001) The structure and functions of human lysophosphatidic acid acyltransferases. Front. Biosci. 6, D944-D953 CrossRef PubMed
-
(2001)
Front. Biosci.
, vol.6
, pp. D944-D953
-
-
Leung, D.W.1
-
14
-
-
0033522379
-
Analysis of Amino Acid Motifs Diagnostic for the sn -Glycerol-3-phosphate Acyltransferase Reaction
-
CrossRef PubMed
-
Lewin, T. M., Wang, P. and Coleman, R. A. (1999) Analysis of Amino Acid Motifs Diagnostic for the sn -Glycerol-3-phosphate Acyltransferase Reaction. Biochemistry 38, 5764-5771 CrossRef PubMed
-
(1999)
Biochemistry
, vol.38
, pp. 5764-5771
-
-
Lewin, T.M.1
Wang, P.2
Coleman, R.A.3
-
15
-
-
0037982806
-
Prevalence of mutations in AGPAT2 among human lipodystrophies
-
CrossRef PubMed
-
Magre, J., Delepine, M., Maldergem, L. V., Robert, J.-J., Maassen, J. A., Meier, M., Panz, V. R., Kim, C. A., Tubiana-Rufi, N., Czernichow, P. et al. (2003) Prevalence of mutations in AGPAT2 among human lipodystrophies. Diabetes 52, 1573-1578 CrossRef PubMed
-
(2003)
Diabetes
, vol.52
, pp. 1573-1578
-
-
Magre, J.1
Delepine, M.2
Maldergem, L.V.3
Robert, J.-J.4
Maassen, J.A.5
Meier, M.6
Panz, V.R.7
Kim, C.A.8
Tubiana-Rufi, N.9
Czernichow, P.10
-
16
-
-
79955869569
-
-/- mice
-
CrossRef PubMed
-
-/- mice. Vet. Pathol. 48, 642-654 CrossRef PubMed
-
(2011)
Vet. Pathol.
, vol.48
, pp. 642-654
-
-
Vogel, P.1
Read, R.2
Hansen, G.3
Wingert, J.4
Dacosta, C.M.5
Buhring, L.M.6
Shadoan, M.7
-
17
-
-
80054911514
-
Forming functional fat: A growing understanding of adipocyte differentiation
-
CrossRef PubMed
-
Cristancho, A. G. and Lazar, M. A. (2011) Forming functional fat: a growing understanding of adipocyte differentiation. Nat. Rev. Mol. Cell Biol. 12, 722-734 CrossRef PubMed
-
(2011)
Nat. Rev. Mol. Cell Biol.
, vol.12
, pp. 722-734
-
-
Cristancho, A.G.1
Lazar, M.A.2
-
18
-
-
69949134811
-
Novel mutations of the BSCL2 and AGPAT2 genes in 10 families with Berardinelli-Seip congenital generalized lipodystrophy syndrome
-
CrossRef PubMed
-
Miranda, D. M., Wajchenberg, B. L., Calsolari, M. R., Aguiar, M. J., Silva, J. M., Ribeiro, M. G., Fonseca, C., Amaral, D., Boson, W. L., Resende, B. A. and De Marco, L. (2009) Novel mutations of the BSCL2 and AGPAT2 genes in 10 families with Berardinelli-Seip congenital generalized lipodystrophy syndrome. Clin. Endocrinol. (Oxf.) 71, 512-517 CrossRef PubMed
-
(2009)
Clin. Endocrinol. (Oxf.)
, vol.71
, pp. 512-517
-
-
Miranda, D.M.1
Wajchenberg, B.L.2
Calsolari, M.R.3
Aguiar, M.J.4
Silva, J.M.5
Ribeiro, M.G.6
Fonseca, C.7
Amaral, D.8
Boson, W.L.9
Resende, B.A.10
De Marco, L.11
-
19
-
-
2442507575
-
Gene and phenotype analysis of congenital generalized lipodystrophy in Japanese: A novel homozygous nonsense mutation in seipin gene
-
CrossRef PubMed
-
Ebihara, K. (2004) Gene and phenotype analysis of congenital generalized lipodystrophy in Japanese: a novel homozygous nonsense mutation in seipin gene. J. Clin. Endocrinol. Metab. 89, 2360-2364 CrossRef PubMed
-
(2004)
J. Clin. Endocrinol. Metab.
, vol.89
, pp. 2360-2364
-
-
Ebihara, K.1
-
20
-
-
0034969438
-
The Silver syndrome variant of hereditary spastic paraplegia maps to chromosome 11q12-q14, with evidence for genetic heterogeneity within this subtype
-
CrossRef PubMed
-
Patel, H., Hart, P. E., Warner, T. T., Houlston, R. S., Patton, M. A., Jeffery, S. and Crosby, A. H. (2001) The Silver syndrome variant of hereditary spastic paraplegia maps to chromosome 11q12-q14, with evidence for genetic heterogeneity within this subtype. Am. J. Hum. Genet. 69, 209-215 CrossRef PubMed
-
(2001)
Am. J. Hum. Genet.
, vol.69
, pp. 209-215
-
-
Patel, H.1
Hart, P.E.2
Warner, T.T.3
Houlston, R.S.4
Patton, M.A.5
Jeffery, S.6
Crosby, A.H.7
-
21
-
-
0842285550
-
Refinement of the Silver syndrome locus on chromosome 11q12-q14 in four families and exclusion of eight candidate genes
-
CrossRef PubMed
-
Windpassinger, C., Wagner, K., Petek, E., Fischer, R. and Auer-Grumbach, M. (2003) Refinement of the Silver syndrome locus on chromosome 11q12-q14 in four families and exclusion of eight candidate genes. Hum. Genet. 114, 99-109 CrossRef PubMed
-
(2003)
Hum. Genet.
, vol.114
, pp. 99-109
-
-
Windpassinger, C.1
Wagner, K.2
Petek, E.3
Fischer, R.4
Auer-Grumbach, M.5
-
22
-
-
10744229057
-
Heterozygous missense mutations in BSCL2 are associated with distal hereditary motor neuropathy and Silver syndrome
-
CrossRef PubMed
-
Windpassinger, C., Auer-Grumbach, M., Irobi, J., Patel, H., Petek, E., Horl, G., Malli, R., Reed, J. A., Dierick, I., Verpoorten, N. et al. (2004) Heterozygous missense mutations in BSCL2 are associated with distal hereditary motor neuropathy and Silver syndrome. Nat. Genet. 36, 271-276 CrossRef PubMed
-
(2004)
Nat. Genet.
, vol.36
, pp. 271-276
-
-
Windpassinger, C.1
Auer-Grumbach, M.2
Irobi, J.3
Patel, H.4
Petek, E.5
Horl, G.6
Malli, R.7
Reed, J.A.8
Dierick, I.9
Verpoorten, N.10
-
23
-
-
10744220431
-
Phenotypic and genetic heterogeneity in congenital generalized lipodystrophy
-
CrossRef PubMed
-
Agarwal, A. K. (2003) Phenotypic and genetic heterogeneity in congenital generalized lipodystrophy. J. Clin. Endocrinol. Metab. 88, 4840-4847 CrossRef PubMed
-
(2003)
J. Clin. Endocrinol. Metab.
, vol.88
, pp. 4840-4847
-
-
Agarwal, A.K.1
-
24
-
-
84898012607
-
Motor neuropathy-associated mutation impairs Seipin functions in neurotransmission
-
CrossRef PubMed
-
Wei, S., Soh, S. L., Xia, J., Ong, W. Y., Pang, Z. P. and Han, W. (2014) Motor neuropathy-associated mutation impairs Seipin functions in neurotransmission. J. Neurochem. 129, 328-338 CrossRef PubMed
-
(2014)
J. Neurochem.
, vol.129
, pp. 328-338
-
-
Wei, S.1
Soh, S.L.2
Xia, J.3
Ong, W.Y.4
Pang, Z.P.5
Han, W.6
-
25
-
-
84873321219
-
Seipin regulates excitatory synaptic transmission in cortical neurons
-
CrossRef PubMed
-
Wei, S., Soh, S. L., Qiu, W., Yang, W., Seah, C. J., Guo, J., Ong, W. Y., Pang, Z. P. and Han, W. (2013) Seipin regulates excitatory synaptic transmission in cortical neurons. J. Neurochem. 124, 478-489 CrossRef PubMed
-
(2013)
J. Neurochem.
, vol.124
, pp. 478-489
-
-
Wei, S.1
Soh, S.L.2
Qiu, W.3
Yang, W.4
Seah, C.J.5
Guo, J.6
Ong, W.Y.7
Pang, Z.P.8
Han, W.9
-
26
-
-
84878858814
-
A new seipin-associated neurodegenerative syndrome
-
CrossRef PubMed
-
Guillen-Navarro, E., Sanchez-Iglesias, S., Domingo-Jimenez, R., Victoria, B., Ruiz-Riquelme, A., Rabano, A., Loidi, L., Beiras, A., Gonzalez-Mendez, B., Ramos, A. et al. (2013) A new seipin-associated neurodegenerative syndrome. J. Med. Genet. 50, 401-409 CrossRef PubMed
-
(2013)
J. Med. Genet.
, vol.50
, pp. 401-409
-
-
Guillen-Navarro, E.1
Sanchez-Iglesias, S.2
Domingo-Jimenez, R.3
Victoria, B.4
Ruiz-Riquelme, A.5
Rabano, A.6
Loidi, L.7
Beiras, A.8
Gonzalez-Mendez, B.9
Ramos, A.10
-
27
-
-
41549146084
-
Association of a homozygous nonsense caveolin-1 mutation with Berardinelli-Seip congenital lipodystrophy
-
CrossRef PubMed
-
Kim, C. A., Delepine, M., Boutet, E., El Mourabit, H., Le Lay, S., Meier, M., Nemani, M., Bridel, E., Leite, C. C., Bertola, D. R. et al. (2008) Association of a homozygous nonsense caveolin-1 mutation with Berardinelli-Seip congenital lipodystrophy. J. Clin. Endocrinol. Metab. 93, 1129-1134 CrossRef PubMed
-
(2008)
J. Clin. Endocrinol. Metab.
, vol.93
, pp. 1129-1134
-
-
Kim, C.A.1
Delepine, M.2
Boutet, E.3
El Mourabit, H.4
Le Lay, S.5
Meier, M.6
Nemani, M.7
Bridel, E.8
Leite, C.C.9
Bertola, D.R.10
-
28
-
-
41549088813
-
Heterozygous CAV1 frameshift mutations (MIM 601047) in patients with atypical partial lipodystrophy and hypertriglyceridemia
-
CrossRef PubMed
-
Cao, H., Alston, L., Ruschman, J. and Hegele, R. A. (2008) Heterozygous CAV1 frameshift mutations (MIM 601047) in patients with atypical partial lipodystrophy and hypertriglyceridemia. Lipids Health Dis. 7, 3 CrossRef PubMed
-
(2008)
Lipids Health Dis.
, vol.7
, pp. 3
-
-
Cao, H.1
Alston, L.2
Ruschman, J.3
Hegele, R.A.4
-
29
-
-
33847181297
-
The multiple faces of caveolae
-
CrossRef PubMed
-
Parton, R. G. and Simons, K. (2007) The multiple faces of caveolae. Nat. Rev. Mol. Cell Biol. 8, 185-194 CrossRef PubMed
-
(2007)
Nat. Rev. Mol. Cell Biol.
, vol.8
, pp. 185-194
-
-
Parton, R.G.1
Simons, K.2
-
30
-
-
0033525003
-
Identification of caveolin-1 as a fatty acid binding protein
-
CrossRef PubMed
-
Trigatti, B. L., Anderson, R. G. W. and Gerber, G. E. (1999) Identification of caveolin-1 as a fatty acid binding protein. Biochem. Biophys. Res. Commun. 255, 34-39 CrossRef PubMed
-
(1999)
Biochem. Biophys. Res. Commun.
, vol.255
, pp. 34-39
-
-
Trigatti, B.L.1
Anderson, R.G.W.2
Gerber, G.E.3
-
31
-
-
15944365201
-
Caveolin, cholesterol, and lipid bodies
-
CrossRef PubMed
-
Martin, S. and Parton, R. G. (2005) Caveolin, cholesterol, and lipid bodies. Semin. Cell. Dev. Biol. 16, 163-174 CrossRef PubMed
-
(2005)
Semin. Cell. Dev. Biol.
, vol.16
, pp. 163-174
-
-
Martin, S.1
Parton, R.G.2
-
32
-
-
0346099345
-
Dynamic and regulated association of caveolin with lipid bodies: Modulation of lipid body motility and function by a dominant negative mutant
-
CrossRef PubMed
-
Pol, A., Martin, S., Fernandez, M. A., Ferguson, C., Carozzi, A., Luetterforst, R., Enrich, C. and Parton, R. G. (2004) Dynamic and regulated association of caveolin with lipid bodies: modulation of lipid body motility and function by a dominant negative mutant. Mol. Biol. Cell. 15, 99-110 CrossRef PubMed
-
(2004)
Mol. Biol. Cell.
, vol.15
, pp. 99-110
-
-
Pol, A.1
Martin, S.2
Fernandez, M.A.3
Ferguson, C.4
Carozzi, A.5
Luetterforst, R.6
Enrich, C.7
Parton, R.G.8
-
33
-
-
33644675358
-
Role of caveolin-1 and cholesterol in transmembrane fatty acid movement
-
CrossRef PubMed
-
Meshulam, T., Simard, J. R., Wharton, J., Hamilton, J. A. and Pilch, P. F. (2006) Role of caveolin-1 and cholesterol in transmembrane fatty acid movement. Biochemistry 45, 2882-2893 CrossRef PubMed
-
(2006)
Biochemistry
, vol.45
, pp. 2882-2893
-
-
Meshulam, T.1
Simard, J.R.2
Wharton, J.3
Hamilton, J.A.4
Pilch, P.F.5
-
34
-
-
0035964954
-
Loss of caveolae, vascular dysfunction, and pulmonary defects in caveolin-1 gene-disrupted mice
-
CrossRef PubMed
-
Drab, M., Verkade, P., Elger, M., Kasper, M., Lohn, M., Lauterbach, B., Menne, J., Lindschau, C., Mende, F., Luft, F. C. et al. (2001) Loss of caveolae, vascular dysfunction, and pulmonary defects in caveolin-1 gene-disrupted mice. Science 293, 2449-2452 CrossRef PubMed
-
(2001)
Science
, vol.293
, pp. 2449-2452
-
-
Drab, M.1
Verkade, P.2
Elger, M.3
Kasper, M.4
Lohn, M.5
Lauterbach, B.6
Menne, J.7
Lindschau, C.8
Mende, F.9
Luft, F.C.10
-
35
-
-
0035851197
-
Caveolin-1 null mice are viable but show evidence of hyperproliferative and vascular abnormalities
-
CrossRef PubMed
-
Razani, B., Engelman, J. A., Wang, X. B., Schubert, W., Zhang, X. L., Marks, C. B., Macaluso, F., Russell, R. G., Li, M., Pestell, R. G. et al. (2001) Caveolin-1 null mice are viable but show evidence of hyperproliferative and vascular abnormalities. J. Biol. Chem. 276, 38121-38138 CrossRef PubMed
-
(2001)
J. Biol. Chem.
, vol.276
, pp. 38121-38138
-
-
Razani, B.1
Engelman, J.A.2
Wang, X.B.3
Schubert, W.4
Zhang, X.L.5
Marks, C.B.6
Macaluso, F.7
Russell, R.G.8
Li, M.9
Pestell, R.G.10
-
36
-
-
13644266312
-
Caveolin-1 in oncogenic transformation, cancer, and metastasis
-
CrossRef PubMed
-
Williams, T. M. and Lisanti, M. P. (2005) Caveolin-1 in oncogenic transformation, cancer, and metastasis. Am. J. Physiol. Cell Physiol. 288, C494-C506 CrossRef PubMed
-
(2005)
Am. J. Physiol. Cell Physiol.
, vol.288
, pp. C494-C506
-
-
Williams, T.M.1
Lisanti, M.P.2
-
37
-
-
0037663884
-
Caveolin-1-deficient mice show insulin resistance and defective insulin receptor protein expression in adipose tissue
-
CrossRef PubMed
-
Cohen, A. W., Razani, B., Wang, X. B., Combs, T. P., Williams, T. M., Scherer, P. E. and Lisanti, M. P. (2003) Caveolin-1-deficient mice show insulin resistance and defective insulin receptor protein expression in adipose tissue. Am. J. Physiol. Cell Physiol. 285, C222-C235 CrossRef PubMed
-
(2003)
Am. J. Physiol. Cell Physiol.
, vol.285
, pp. C222-C235
-
-
Cohen, A.W.1
Razani, B.2
Wang, X.B.3
Combs, T.P.4
Williams, T.M.5
Scherer, P.E.6
Lisanti, M.P.7
-
38
-
-
0037040994
-
Caveolin-1-deficient mice are lean, resistant to diet-induced obesity, and show hypertriglyceridemia with adipocyte abnormalities
-
CrossRef PubMed
-
Razani, B., Combs, T. P., Wang, X. B., Frank, P. G., Park, D. S., Russell, R. G., Li, M., Tang, B., Jelicks, L. A., Scherer, P. E. and Lisanti, M. P. (2002) Caveolin-1-deficient mice are lean, resistant to diet-induced obesity, and show hypertriglyceridemia with adipocyte abnormalities. J. Biol. Chem. 277, 8635-8647 CrossRef PubMed
-
(2002)
J. Biol. Chem.
, vol.277
, pp. 8635-8647
-
-
Razani, B.1
Combs, T.P.2
Wang, X.B.3
Frank, P.G.4
Park, D.S.5
Russell, R.G.6
Li, M.7
Tang, B.8
Jelicks, L.A.9
Scherer, P.E.10
Lisanti, M.P.11
-
39
-
-
0036644298
-
Heterogeneity for congenital generalized lipodystrophy in seventeen patients from Oman
-
CrossRef PubMed
-
Rajab, A., Heathcote, K., Joshi, S., Jeffery, S. and Patton, M. (2002) Heterogeneity for congenital generalized lipodystrophy in seventeen patients from Oman. Am. J. Med. Genet. 110, 219-225 CrossRef PubMed
-
(2002)
Am. J. Med. Genet.
, vol.110
, pp. 219-225
-
-
Rajab, A.1
Heathcote, K.2
Joshi, S.3
Jeffery, S.4
Patton, M.5
-
40
-
-
0036224182
-
Molecular analysis of Berardinelli-Seip congenital lipodystrophy in Oman-evidence for multiple loci
-
CrossRef PubMed
-
Heathcote, K., Rajab, A., Magre, J., Syrris, P., Besti, M., Patton, M., Delepine, M., Lathrop, M., Capeau, J. and Jeffery, S. (2002) Molecular analysis of Berardinelli-Seip congenital lipodystrophy in Oman-evidence for multiple loci. Diabetes 51, 1291-1293 CrossRef PubMed
-
(2002)
Diabetes
, vol.51
, pp. 1291-1293
-
-
Heathcote, K.1
Rajab, A.2
Magre, J.3
Syrris, P.4
Besti, M.5
Patton, M.6
Delepine, M.7
Lathrop, M.8
Capeau, J.9
Jeffery, S.10
-
41
-
-
77950431859
-
Fatal cardiac arrhythmia and long-QT syndrome in a new form of congenital generalized lipodystrophy with muscle rippling (CGL4) due to PTRF-CAVIN mutations
-
CrossRef PubMed
-
Rajab, A., Straub, V., McCann, L. J., Seelow, D., Varon, R., Barresi, R., Schulze, A., Lucke, B., Lutzkendorf, S., Karbasiyan, M. et al. (2010) Fatal cardiac arrhythmia and long-QT syndrome in a new form of congenital generalized lipodystrophy with muscle rippling (CGL4) due to PTRF-CAVIN mutations. PLoS Genet. 6, e1000874 CrossRef PubMed
-
(2010)
PLoS Genet.
, vol.6
, pp. e1000874
-
-
Rajab, A.1
Straub, V.2
McCann, L.J.3
Seelow, D.4
Varon, R.5
Barresi, R.6
Schulze, A.7
Lucke, B.8
Lutzkendorf, S.9
Karbasiyan, M.10
-
42
-
-
70349195987
-
Human PTRF mutations cause secondary deficiency of caveolins resulting in muscular dystrophy with generalized lipodystrophy
-
CrossRef PubMed
-
Hayashi, Y. K., Matsuda, C., Ogawa, M., Goto, K., Tominaga, K., Mitsuhashi, S., Park, Y. E., Nonaka, I., Hino-Fukuyo, N., Haginoya, K. et al. (2009) Human PTRF mutations cause secondary deficiency of caveolins resulting in muscular dystrophy with generalized lipodystrophy. J. Clin. Invest. 119, 2623-2633 CrossRef PubMed
-
(2009)
J. Clin. Invest.
, vol.119
, pp. 2623-2633
-
-
Hayashi, Y.K.1
Matsuda, C.2
Ogawa, M.3
Goto, K.4
Tominaga, K.5
Mitsuhashi, S.6
Park, Y.E.7
Nonaka, I.8
Hino-Fukuyo, N.9
Haginoya, K.10
-
43
-
-
37649011760
-
PTRF-Cavin, a conserved cytoplasmic protein required for caveola formation and function
-
CrossRef PubMed
-
Hill, M. M., Bastiani, M., Luetterforst, R., Kirkham, M., Kirkham, A., Nixon, S. J., Walser, P., Abankwa, D., Oorschot, V. M., Martin, S. et al. (2008) PTRF-Cavin, a conserved cytoplasmic protein required for caveola formation and function. Cell 132, 113-124 CrossRef PubMed
-
(2008)
Cell
, vol.132
, pp. 113-124
-
-
Hill, M.M.1
Bastiani, M.2
Luetterforst, R.3
Kirkham, M.4
Kirkham, A.5
Nixon, S.J.6
Walser, P.7
Abankwa, D.8
Oorschot, V.M.9
Martin, S.10
-
44
-
-
42949174820
-
A critical role of cavin (polymerase I and transcript release factor) in caveolae formation and organization
-
CrossRef PubMed
-
Liu, L. and Pilch, P. F. (2008) A critical role of cavin (polymerase I and transcript release factor) in caveolae formation and organization. J. Biol. Chem. 283, 4314-4322 CrossRef PubMed
-
(2008)
J. Biol. Chem.
, vol.283
, pp. 4314-4322
-
-
Liu, L.1
Pilch, P.F.2
-
45
-
-
84861432786
-
Seipin: From human disease to molecular mechanism
-
CrossRef PubMed
-
Cartwright, B. R. and Goodman, J. M. (2012) Seipin: from human disease to molecular mechanism. J. Lipid Res. 53, 1042-1055 CrossRef PubMed
-
(2012)
J. Lipid Res.
, vol.53
, pp. 1042-1055
-
-
Cartwright, B.R.1
Goodman, J.M.2
-
46
-
-
4344641102
-
The phenotype of motor neuropathies associated with BSCL2 mutations is broader than Silver syndrome and distal HMN type V
-
CrossRef PubMed
-
Irobi, J., Van den Bergh, P., Merlini, L., Verellen, C., Van Maldergem, L., Dierick, I., Verpoorten, N., Jordanova, A., Windpassinger, C., De Vriendt, E. et al. (2004) The phenotype of motor neuropathies associated with BSCL2 mutations is broader than Silver syndrome and distal HMN type V. Brain 127, 2124-2130 CrossRef PubMed
-
(2004)
Brain
, vol.127
, pp. 2124-2130
-
-
Irobi, J.1
Van Den Bergh, P.2
Merlini, L.3
Verellen, C.4
Van Maldergem, L.5
Dierick, I.6
Verpoorten, N.7
Jordanova, A.8
Windpassinger, C.9
De Vriendt, E.10
-
47
-
-
33645966850
-
Membrane topology of the human seipin protein
-
CrossRef PubMed
-
Lundin, C., Nordstrom, R., Wagner, K., Windpassinger, C., Andersson, H., von Heijne, G. and Nilsson, I. (2006) Membrane topology of the human seipin protein. FEBS Lett. 580, 2281-2284 CrossRef PubMed
-
(2006)
FEBS Lett.
, vol.580
, pp. 2281-2284
-
-
Lundin, C.1
Nordstrom, R.2
Wagner, K.3
Windpassinger, C.4
Andersson, H.5
Von Heijne, G.6
Nilsson, I.7
-
48
-
-
84876899536
-
Seipin differentially regulates lipogenesis and adipogenesis through a conserved core sequence and an evolutionarily acquired C-terminus
-
PubMed
-
Yang, W., Thein, S., Guo, X., Xu, F., Venkatesh, B., Sugii, S., Radda, G. K. and Han, W. (2013) Seipin differentially regulates lipogenesis and adipogenesis through a conserved core sequence and an evolutionarily acquired C-terminus. Biochem. J. 452, 37-44 PubMed
-
(2013)
Biochem. J.
, vol.452
, pp. 37-44
-
-
Yang, W.1
Thein, S.2
Guo, X.3
Xu, F.4
Venkatesh, B.5
Sugii, S.6
Radda, G.K.7
Han, W.8
-
49
-
-
78649718251
-
A taiwanese boy with congenital generalized lipodystrophy caused by homozygous Ile262fs mutation in the BSCL2 gene
-
CrossRef
-
Huang, H.-H., Chen, T.-H., Hsiao, H.-P., Huang, C.-T., Wang, C.-C., Shiau, Y.-H. and Chao, M.-C. (2010) A taiwanese boy with congenital generalized lipodystrophy caused by homozygous Ile262fs mutation in the BSCL2 gene. The Kaohsiung J. Med. Sci. 26, 615-620 CrossRef
-
(2010)
The Kaohsiung J. Med. Sci.
, vol.26
, pp. 615-620
-
-
Huang, H.-H.1
Chen, T.-H.2
Hsiao, H.-P.3
Huang, C.-T.4
Wang, C.-C.5
Shiau, Y.-H.6
Chao, M.-C.7
-
50
-
-
73349134670
-
Two Japanese infants with congenital generalized lipodystrophy due to BSCL2 mutations
-
CrossRef PubMed
-
Nishiyama, A., Yagi, M., Awano, H., Okizuka, Y., Maeda, T., Yoshida, S., Takeshima, Y. and Matsuo, M. (2009) Two Japanese infants with congenital generalized lipodystrophy due to BSCL2 mutations. Pediatr. Int. 51, 775-779 CrossRef PubMed
-
(2009)
Pediatr. Int.
, vol.51
, pp. 775-779
-
-
Nishiyama, A.1
Yagi, M.2
Awano, H.3
Okizuka, Y.4
Maeda, T.5
Yoshida, S.6
Takeshima, Y.7
Matsuo, M.8
-
51
-
-
84885845981
-
Analysis of naturally occurring mutations in the human lipodystrophy protein seipin reveals multiple potential pathogenic mechanisms
-
CrossRef PubMed
-
Sim, M. F., Talukder, M. M., Dennis, R. J., O'Rahilly, S., Edwardson, J. M. and Rochford, J. J. (2013) Analysis of naturally occurring mutations in the human lipodystrophy protein seipin reveals multiple potential pathogenic mechanisms. Diabetologia 56, 2498-2506 CrossRef PubMed
-
(2013)
Diabetologia
, vol.56
, pp. 2498-2506
-
-
Sim, M.F.1
Talukder, M.M.2
Dennis, R.J.3
O'Rahilly, S.4
Edwardson, J.M.5
Rochford, J.J.6
-
52
-
-
78650388357
-
Seipin is a discrete homooligomer
-
CrossRef PubMed
-
Binns, D., Lee, S., Hilton, C. L., Jiang, Q. X. and Goodman, J. M. (2010) Seipin is a discrete homooligomer. Biochemistry 49, 10747-10755 CrossRef PubMed
-
(2010)
Biochemistry
, vol.49
, pp. 10747-10755
-
-
Binns, D.1
Lee, S.2
Hilton, C.L.3
Jiang, Q.X.4
Goodman, J.M.5
-
53
-
-
81855177041
-
Molecular characterization of seipin and its mutants: Implications for seipin in triacylglycerol synthesis
-
CrossRef PubMed
-
Fei, W., Li, H., Shui, G., Kapterian, T. S., Bielby, C., Du, X., Brown, A. J., Li, P., Wenk, M. R., Liu, P. and Yang, H. (2011) Molecular characterization of seipin and its mutants: implications for seipin in triacylglycerol synthesis. J. Lipid Res. 52, 2136-2147 CrossRef PubMed
-
(2011)
J. Lipid Res.
, vol.52
, pp. 2136-2147
-
-
Fei, W.1
Li, H.2
Shui, G.3
Kapterian, T.S.4
Bielby, C.5
Du, X.6
Brown, A.J.7
Li, P.8
Wenk, M.R.9
Liu, P.10
Yang, H.11
-
54
-
-
50949112676
-
The human lipodystrophy gene BSCL2/seipin may be essential for normal adipocyte differentiation
-
CrossRef PubMed
-
Payne, V. A., Grimsey, N., Tuthill, A., Virtue, S., Gray, S. L., Dalla Nora, E., Semple, R. K., O'Rahilly, S. and Rochford, J. J. (2008) The human lipodystrophy gene BSCL2/seipin may be essential for normal adipocyte differentiation. Diabetes 57, 2055-2060 CrossRef PubMed
-
(2008)
Diabetes
, vol.57
, pp. 2055-2060
-
-
Payne, V.A.1
Grimsey, N.2
Tuthill, A.3
Virtue, S.4
Gray, S.L.5
Dalla Nora, E.6
Semple, R.K.7
O'Rahilly, S.8
Rochford, J.J.9
-
55
-
-
70349323186
-
The human lipodystrophy gene product Berardinelli-Seip congenital lipodystrophy 2/seipin plays a key role in adipocyte differentiation
-
CrossRef PubMed
-
Chen, W., Yechoor, V. K., Chang, B. H., Li, M. V., March, K. L. and Chan, L. (2009) The human lipodystrophy gene product Berardinelli-Seip congenital lipodystrophy 2/seipin plays a key role in adipocyte differentiation. Endocrinology 150, 4552-4561 CrossRef PubMed
-
(2009)
Endocrinology
, vol.150
, pp. 4552-4561
-
-
Chen, W.1
Yechoor, V.K.2
Chang, B.H.3
Li, M.V.4
March, K.L.5
Chan, L.6
-
56
-
-
84863245021
-
Berardinelli-Seip congenital lipodystrophy 2/seipin is a cell-autonomous regulator of lipolysis essential for adipocyte differentiation
-
CrossRef PubMed
-
Chen, W., Chang, B., Saha, P., Hartig, S. M., Li, L., Reddy, V. T., Yang, Y., Yechoor, V., Mancini, M. A. and Chan, L. (2012) Berardinelli-Seip congenital lipodystrophy 2/seipin is a cell-autonomous regulator of lipolysis essential for adipocyte differentiation. Mol. Cell Biol. 32, 1099-1111 CrossRef PubMed
-
(2012)
Mol. Cell Biol.
, vol.32
, pp. 1099-1111
-
-
Chen, W.1
Chang, B.2
Saha, P.3
Hartig, S.M.4
Li, L.5
Reddy, V.T.6
Yang, Y.7
Yechoor, V.8
Mancini, M.A.9
Chan, L.10
-
57
-
-
84879955522
-
Thiazolidinediones partially reverse the metabolic disturbances observed in Bscl2/seipin-deficient mice
-
CrossRef PubMed
-
Prieur, X., Dollet, L., Takahashi, M., Nemani, M., Pillot, B., Le May, C., Mounier, C., Takigawa-Imamura, H., Zelenika, D., Matsuda, F. et al. (2013) Thiazolidinediones partially reverse the metabolic disturbances observed in Bscl2/seipin-deficient mice. Diabetologia 56, 1813-1825 CrossRef PubMed
-
(2013)
Diabetologia
, vol.56
, pp. 1813-1825
-
-
Prieur, X.1
Dollet, L.2
Takahashi, M.3
Nemani, M.4
Pillot, B.5
Le May, C.6
Mounier, C.7
Takigawa-Imamura, H.8
Zelenika, D.9
Matsuda, F.10
-
58
-
-
84874773907
-
Suppression of adipogenesis by pathogenic seipin mutant is associated with inflammatory response
-
CrossRef PubMed
-
Qiu, W., Wee, K., Takeda, K., Lim, X., Sugii, S., Radda, G. K. and Han, W. (2013) Suppression of adipogenesis by pathogenic seipin mutant is associated with inflammatory response. PLoS ONE 8, e57874 CrossRef PubMed
-
(2013)
PLoS ONE
, vol.8
, pp. e57874
-
-
Qiu, W.1
Wee, K.2
Takeda, K.3
Lim, X.4
Sugii, S.5
Radda, G.K.6
Han, W.7
-
59
-
-
84898017031
-
BSCL2/seipin regulates adipogenesis through actin cytoskeleton remodelling
-
CrossRef PubMed
-
Yang, W., Thein, S., Wang, X., Bi, X., Ericksen, R. E., Xu, F. and Han, W. (2014) BSCL2/seipin regulates adipogenesis through actin cytoskeleton remodelling. Hum. Mol. Genet. 23, 502-513 CrossRef PubMed
-
(2014)
Hum. Mol. Genet.
, vol.23
, pp. 502-513
-
-
Yang, W.1
Thein, S.2
Wang, X.3
Bi, X.4
Ericksen, R.E.5
Xu, F.6
Han, W.7
-
60
-
-
84890563376
-
Function of seipin: New insights from Bscl2/seipin knockout mouse models
-
CrossRef PubMed
-
Dollet, L., Magre, J., Cariou, B. and Prieur, X. (2014) Function of seipin: new insights from Bscl2/seipin knockout mouse models. Biochimie 96, 166-172 CrossRef PubMed
-
(2014)
Biochimie
, vol.96
, pp. 166-172
-
-
Dollet, L.1
Magre, J.2
Cariou, B.3
Prieur, X.4
-
61
-
-
34147092113
-
Molecular pathogenesis of seipin/BSCL2-related motor neuron diseases
-
CrossRef PubMed
-
Ito, D. and Suzuki, N. (2007) Molecular pathogenesis of seipin/BSCL2-related motor neuron diseases. Ann. Neurol. 61, 237-250 CrossRef PubMed
-
(2007)
Ann. Neurol.
, vol.61
, pp. 237-250
-
-
Ito, D.1
Suzuki, N.2
-
62
-
-
84875894905
-
Motor neuron degeneration in a mouse model of seipinopathy
-
CrossRef PubMed
-
Guo, J., Qiu, W., Soh, S. L., Wei, S., Radda, G. K., Ong, W. Y., Pang, Z. P. and Han, W. (2013) Motor neuron degeneration in a mouse model of seipinopathy. Cell Death Dis. 4, e535 CrossRef PubMed
-
(2013)
Cell Death Dis.
, vol.4
, pp. e535
-
-
Guo, J.1
Qiu, W.2
Soh, S.L.3
Wei, S.4
Radda, G.K.5
Ong, W.Y.6
Pang, Z.P.7
Han, W.8
-
63
-
-
39049151385
-
Fld1p, a functional homologue of human seipin, regulates the size of lipid droplets in yeast
-
CrossRef PubMed
-
Fei, W., Shui, G., Gaeta, B., Du, X., Kuerschner, L., Li, P., Brown, A. J., Wenk, M. R., Parton, R. G. and Yang, H. (2008) Fld1p, a functional homologue of human seipin, regulates the size of lipid droplets in yeast. J. Cell Biol. 180, 473-482 CrossRef PubMed
-
(2008)
J. Cell Biol.
, vol.180
, pp. 473-482
-
-
Fei, W.1
Shui, G.2
Gaeta, B.3
Du, X.4
Kuerschner, L.5
Li, P.6
Brown, A.J.7
Wenk, M.R.8
Parton, R.G.9
Yang, H.10
-
64
-
-
84856731141
-
A role for seipin in lipid droplet dynamics and inheritance in yeast
-
CrossRef PubMed
-
Wolinski, H., Kolb, D., Hermann, S., Koning, R. I. and Kohlwein, S. D. (2011) A role for seipin in lipid droplet dynamics and inheritance in yeast. J. Cell Sci. 124, 3894-3904 CrossRef PubMed
-
(2011)
J. Cell Sci.
, vol.124
, pp. 3894-3904
-
-
Wolinski, H.1
Kolb, D.2
Hermann, S.3
Koning, R.I.4
Kohlwein, S.D.5
-
65
-
-
84884172288
-
Role of seipin in lipid droplet morphology and hepatitis C virus life cycle
-
CrossRef PubMed
-
Clement, S., Fauvelle, C., Branche, E., Kaddai, V., Conzelmann, S., Boldanova, T., Bartosch, B., Minehira, K. and Negro, F. (2013) Role of seipin in lipid droplet morphology and hepatitis C virus life cycle. J. Gen. Virol. 94, 2208-2214 CrossRef PubMed
-
(2013)
J. Gen. Virol.
, vol.94
, pp. 2208-2214
-
-
Clement, S.1
Fauvelle, C.2
Branche, E.3
Kaddai, V.4
Conzelmann, S.5
Boldanova, T.6
Bartosch, B.7
Minehira, K.8
Negro, F.9
-
66
-
-
84885850160
-
The human lipodystrophy protein seipin is an ER membrane adaptor for the adipogenic PA phosphatase lipin 1
-
CrossRef PubMed
-
Sim, M. F., Dennis, R. J., Aubry, E. M., Ramanathan, N., Sembongi, H., Saudek, V., Ito, D., O'Rahilly, S., Siniossoglou, S. and Rochford, J. J. (2012) The human lipodystrophy protein seipin is an ER membrane adaptor for the adipogenic PA phosphatase lipin 1. Mol. Metab. 2, 38-46 CrossRef PubMed
-
(2012)
Mol. Metab.
, vol.2
, pp. 38-46
-
-
Sim, M.F.1
Dennis, R.J.2
Aubry, E.M.3
Ramanathan, N.4
Sembongi, H.5
Saudek, V.6
Ito, D.7
O'Rahilly, S.8
Siniossoglou, S.9
Rochford, J.J.10
-
67
-
-
58049218441
-
Lipin1 is a key factor for the maturation and maintenance of adipocytes in the regulatory network with CCAAT/enhancer-binding protein alpha and peroxisome proliferator-activated receptor gamma 2
-
CrossRef PubMed
-
Koh, Y. K., Lee, M. Y., Kim, J. W., Kim, M., Moon, J. S., Lee, Y. J., Ahn, Y. H. and Kim, K. S. (2008) Lipin1 is a key factor for the maturation and maintenance of adipocytes in the regulatory network with CCAAT/enhancer-binding protein alpha and peroxisome proliferator-activated receptor gamma 2. J. Biol. Chem. 283, 34896-34906 CrossRef PubMed
-
(2008)
J. Biol. Chem.
, vol.283
, pp. 34896-34906
-
-
Koh, Y.K.1
Lee, M.Y.2
Kim, J.W.3
Kim, M.4
Moon, J.S.5
Lee, Y.J.6
Ahn, Y.H.7
Kim, K.S.8
-
68
-
-
84863292690
-
Overexpression of a short human seipin/BSCL2 isoform in mouse adipose tissue results in mild lipodystrophy
-
CrossRef PubMed
-
Cui, X., Wang, Y., Meng, L., Fei, W., Deng, J., Xu, G., Peng, X., Ju, S., Zhang, L., Liu, G. et al. (2012) Overexpression of a short human seipin/BSCL2 isoform in mouse adipose tissue results in mild lipodystrophy. Am. J. Physiol. Endocrinol. Metab. 302, E705-E713 CrossRef PubMed
-
(2012)
Am. J. Physiol. Endocrinol. Metab.
, vol.302
, pp. E705-E713
-
-
Cui, X.1
Wang, Y.2
Meng, L.3
Fei, W.4
Deng, J.5
Xu, G.6
Peng, X.7
Ju, S.8
Zhang, L.9
Liu, G.10
-
69
-
-
84899942026
-
(2)(+)-ATPase SERCA
-
CrossRef PubMed
-
(2)(+)-ATPase SERCA. Cell Metab. 19, 861-871 CrossRef PubMed
-
(2014)
Cell Metab.
, vol.19
, pp. 861-871
-
-
Bi, J.1
Wang, W.2
Liu, Z.3
Huang, X.4
Jiang, Q.5
Liu, G.6
Wang, Y.7
-
70
-
-
0034492351
-
Association of severe insulin resistance with both loss of limb fat and elevated serum tumor necrosis factor receptor levels in HIV lipodystrophy
-
CrossRef PubMed
-
Mynarcik, D. C., McNurlan, M. A., Steigbigel, R. T., Fuhrer, J. and Gelato, M. C. (2000) Association of severe insulin resistance with both loss of limb fat and elevated serum tumor necrosis factor receptor levels in HIV lipodystrophy. J. Acquir. Immune Defic. Syndr. 25, 312-321 CrossRef PubMed
-
(2000)
J. Acquir. Immune Defic. Syndr.
, vol.25
, pp. 312-321
-
-
Mynarcik, D.C.1
McNurlan, M.A.2
Steigbigel, R.T.3
Fuhrer, J.4
Gelato, M.C.5
-
71
-
-
76249121423
-
Chronic atypical neutrophilic dermatosis with lipodystrophy and elevated temperature (CANDLE) syndrome
-
CrossRef PubMed
-
Torrelo, A., Patel, S., Colmenero, I., Gurbindo, D., Lendinez, F., Hernandez, A., Lopez-Robledillo, J. C., Dadban, A., Requena, L. and Paller, A. S. (2010) Chronic atypical neutrophilic dermatosis with lipodystrophy and elevated temperature (CANDLE) syndrome. J. Am. Acad. Dermatol. 62, 489-495 CrossRef PubMed
-
(2010)
J. Am. Acad. Dermatol.
, vol.62
, pp. 489-495
-
-
Torrelo, A.1
Patel, S.2
Colmenero, I.3
Gurbindo, D.4
Lendinez, F.5
Hernandez, A.6
Lopez-Robledillo, J.C.7
Dadban, A.8
Requena, L.9
Paller, A.S.10
-
72
-
-
76249097775
-
Inflammation and adipose tissue macrophages in lipodystrophic mice
-
CrossRef PubMed
-
Herrero, L., Shapiro, H., Nayer, A., Lee, J. and Shoelson, S. E. (2010) Inflammation and adipose tissue macrophages in lipodystrophic mice. Proc. Natl. Acad. Sci. U. S. A. 107, 240-245 CrossRef PubMed
-
(2010)
Proc. Natl. Acad. Sci. U. S. A.
, vol.107
, pp. 240-245
-
-
Herrero, L.1
Shapiro, H.2
Nayer, A.3
Lee, J.4
Shoelson, S.E.5
-
73
-
-
0036894360
-
Interleukin-6 induces cellular insulin resistance in hepatocytes
-
CrossRef PubMed
-
Senn, J. J., Klover, P. J., Nowak, I. A. and Mooney, R. A. (2002) Interleukin-6 induces cellular insulin resistance in hepatocytes. Diabetes 51, 3391-3399 CrossRef PubMed
-
(2002)
Diabetes
, vol.51
, pp. 3391-3399
-
-
Senn, J.J.1
Klover, P.J.2
Nowak, I.A.3
Mooney, R.A.4
-
74
-
-
0242580711
-
Interleukin-6 (IL-6) induces insulin resistance in 3T3-L1 adipocytes and is, like IL-8 and tumor necrosis factor-alpha, overexpressed in human fat cells from insulin-resistant subjects
-
CrossRef PubMed
-
Rotter, V., Nagaev, I. and Smith, U. (2003) Interleukin-6 (IL-6) induces insulin resistance in 3T3-L1 adipocytes and is, like IL-8 and tumor necrosis factor-alpha, overexpressed in human fat cells from insulin-resistant subjects. J. Biol. Chem. 278, 45777-45784 CrossRef PubMed
-
(2003)
J. Biol. Chem.
, vol.278
, pp. 45777-45784
-
-
Rotter, V.1
Nagaev, I.2
Smith, U.3
-
75
-
-
84869184022
-
Obesity-induced endoplasmic reticulum stress causes chronic inflammation in adipose tissue
-
CrossRef PubMed
-
Kawasaki, N., Asada, R., Saito, A., Kanemoto, S. and Imaizumi, K. (2012) Obesity-induced endoplasmic reticulum stress causes chronic inflammation in adipose tissue. Sci. Rep. 2, 799 CrossRef PubMed
-
(2012)
Sci. Rep.
, vol.2
, pp. 799
-
-
Kawasaki, N.1
Asada, R.2
Saito, A.3
Kanemoto, S.4
Imaizumi, K.5
-
76
-
-
77953400436
-
Lipin 1 represses NFATc4 transcriptional activity in adipocytes to inhibit secretion of inflammatory factors
-
CrossRef PubMed
-
Kim, H. B., Kumar, A., Wang, L., Liu, G. H., Keller, S. R., Lawrence, Jr, J. C., Finck, B. N. and Harris, T. E. (2010) Lipin 1 represses NFATc4 transcriptional activity in adipocytes to inhibit secretion of inflammatory factors. Mol. Cell Biol. 30, 3126-3139 CrossRef PubMed
-
(2010)
Mol. Cell Biol.
, vol.30
, pp. 3126-3139
-
-
Kim, H.B.1
Kumar, A.2
Wang, L.3
Liu, G.H.4
Keller, S.R.5
Lawrence, J.C.6
Finck, B.N.7
Harris, T.E.8
-
77
-
-
80755188929
-
Suppression of lipin-1 expression increases monocyte chemoattractant protein-1 expression in 3T3-L1 adipocytes
-
CrossRef PubMed
-
Takahashi, N., Yoshizaki, T., Hiranaka, N., Suzuki, T., Yui, T., Akanuma, M., Oka, K., Kanazawa, K., Yoshida, M., Naito, S. et al. (2011) Suppression of lipin-1 expression increases monocyte chemoattractant protein-1 expression in 3T3-L1 adipocytes. Biochem. Biophys. Res. Commun. 415, 200-205 CrossRef PubMed
-
(2011)
Biochem. Biophys. Res. Commun.
, vol.415
, pp. 200-205
-
-
Takahashi, N.1
Yoshizaki, T.2
Hiranaka, N.3
Suzuki, T.4
Yui, T.5
Akanuma, M.6
Oka, K.7
Kanazawa, K.8
Yoshida, M.9
Naito, S.10
|