-
1
-
-
44649127452
-
Cytoprotective activity of Glycyrrhizae radix extract against arsenite-induced cytotoxicity
-
DOI 10.1093/ecam/nem014
-
Kim S. C., Park S. J., Lee J. R., Seo J. C., Yang C. H., Byun S. H., Cytoprotective activity of Glycyrrhizae radix extract against arsenite-induced cytotoxicity Evidence-Based Complementary and Alternative Medicine 2008 5 2 165 171 (Pubitemid 351786662)
-
(2008)
Evidence-based Complementary and Alternative Medicine
, vol.5
, Issue.2
, pp. 165-171
-
-
Kim, S.C.1
Park, S.J.2
Lee, J.R.3
Seo, J.C.4
Yang, C.H.5
Byun, S.H.6
-
2
-
-
70349484666
-
Hepatoprotective activity of licorice water extract against Cadmium-induced toxicity in rats
-
Lee J. R., Park S. J., Lee H.-S., Jee S. Y., Seo J., Kwon Y. K., Kwon T. K., Kim S. C., Hepatoprotective activity of licorice water extract against Cadmium-induced toxicity in rats Evidence-Based Complementary and Alternative Medicine 2009 6 2 195 201
-
(2009)
Evidence-Based Complementary and Alternative Medicine
, vol.6
, Issue.2
, pp. 195-201
-
-
Lee, J.R.1
Park, S.J.2
Lee, H.-S.3
Jee, S.Y.4
Seo, J.5
Kwon, Y.K.6
Kwon, T.K.7
Kim, S.C.8
-
3
-
-
0031046241
-
11β-Hydroxysteroid dehydrogenase and the syndrome of apparent mineralocorticoid excess
-
DOI 10.1210/er.18.1.135
-
White P. C., Mune T., Agarwal A. K., 11 -Hydroxysteroid dehydrogenase and the syndrome of apparent mineralocorticoid excess Endocrine Reviews 1997 18 135 156 (Pubitemid 27076458)
-
(1997)
Endocrine Reviews
, vol.18
, Issue.1
, pp. 135-156
-
-
White, P.C.1
Mune, T.2
Agarwal, A.K.3
-
4
-
-
0023242981
-
Mineralocorticoid activity of liquorice: 11-beta-hydroxysteroid dehydrogenase deficiency comes of age
-
Stewart P. M., Valentino R., Wallace A. M., Burt D., Shackleton C. H. L., Edwards C. R. W., Mineralocorticoid activity of liquorice: 11-beta- hydroxysteroid dehydrogenase deficiency comes of age The Lancet 1987 2 8563 821 824
-
(1987)
The Lancet
, vol.2
, Issue.8563
, pp. 821-824
-
-
Stewart, P.M.1
Valentino, R.2
Wallace, A.M.3
Burt, D.4
Shackleton, C.H.L.5
Edwards, C.R.W.6
-
5
-
-
0025372364
-
The influence of glycyrrhetinic acid on plasma cortisol and cortisone in healthy young volunteers
-
MacKenzie M. A., Hoefnagels W. H., Jansen R. W., Benraad T. J., Kloppenborg P. W., The influence of glycyrrhetinic acid on plasma cortisol and cortisone in healthy young volunteers Journal of Clinical Endocrinology Metabolism 1990 70 1637 1643
-
(1990)
Journal of Clinical Endocrinology Metabolism
, vol.70
, pp. 1637-1643
-
-
MacKenzie, M.A.1
Hoefnagels, W.H.2
Jansen, R.W.3
Benraad, T.J.4
Kloppenborg, P.W.5
-
7
-
-
0023760499
-
Syndrome of apparent mineralocorticoid excess. A defect in the cortisol-cortisone shuttle
-
Stewart P. M., Corrie J. E. T., Shackleton C. H. L., Edwards C. R. W., Syndrome of apparent mineralocorticoid excess. A defect in the cortisol-cortisone shuttle The Journal of Clinical Investigation 1988 82 1 340 349 (Pubitemid 18262536)
-
(1988)
Journal of Clinical Investigation
, vol.82
, Issue.1
, pp. 340-349
-
-
Stewart, P.M.1
Corrie, J.E.T.2
Shackleton, C.H.L.3
Edwards, C.R.W.4
-
8
-
-
0032051655
-
The role of 11β-hydroxysteroid dehydrogenase in the pathogenesis of hypertension
-
DOI 10.1016/S0008-6363(97)00299-X
-
Van Uum S. H. M., Hermus A. R. M. M., Smits P., Thien T., Lenders J. W. M., The role of 11 -hydroxysteroid dehydrogenase in the pathogenesis of hypertension Cardiovascular Research 1998 38 1 16 24 (Pubitemid 28275613)
-
(1998)
Cardiovascular Research
, vol.38
, Issue.1
, pp. 16-24
-
-
Van Uum, S.H.M.1
Hermus, A.R.M.M.2
Smits, P.3
Thien, T.4
Lenders, J.W.M.5
-
9
-
-
0029160972
-
Human hypertension caused by mutations in the kidney isozyme of 11 - Hydroxysteroid dehydrogenase
-
Mune T., Rogerson F. M., Nikkila H., Agarwal A. K., White P. C., Human hypertension caused by mutations in the kidney isozyme of 11 -hydroxysteroid dehydrogenase Nature Genetics 1995 10 4 394 399
-
(1995)
Nature Genetics
, vol.10
, Issue.4
, pp. 394-399
-
-
Mune, T.1
Rogerson, F.M.2
Nikkila, H.3
Agarwal, A.K.4
White, P.C.5
-
10
-
-
0042767044
-
Late-onset apparent mineralocorticoid excess caused by novel compound heterozygous mutations in the HSD11B2 gene
-
DOI 10.1161/01.HYP.0000083340.57063.35
-
Lavery G. G., Ronconi V., Draper N., Rabbitt E. H., Lyons V., Chapman K. E., Walker E. A., McTernan C. L., Giacchetti G., Mantero F., Seckl J. R., Edwards C. R. W., Connell J. M. C., Hewison M., Stewart P. M., Late-onset apparent mineralocorticoid excess caused by novel compound heterozygous mutations in the HSD11B2 gene Hypertension 2003 42 2 123 129 (Pubitemid 36944584)
-
(2003)
Hypertension
, vol.42
, Issue.2
, pp. 123-129
-
-
Lavery, G.G.1
Ronconi, V.2
Draper, N.3
Rabbitt, E.H.4
Lyons, V.5
Chapman, K.E.6
Walker, E.A.7
McTernan, C.L.8
Giacchetti, G.9
Mantero, F.10
Seckl, J.R.11
Edwards, C.R.W.12
Connell, J.M.C.13
Hewison, M.14
Stewart, P.M.15
-
11
-
-
0028785017
-
Several homozygous mutations in the gene for 11 beta-hydroxysteroid dehydrogenase type 2 in patients with apparent mineralocorticoid excess
-
Wilson R. C., Harbison M. D., Krozowski Z. S., Several homozygous mutations in the gene for 11 beta-hydroxysteroid dehydrogenase type 2 in patients with apparent mineralocorticoid excess Journal of Clinical Endocrinology Metabolism 1995 80 3145 3150
-
(1995)
Journal of Clinical Endocrinology Metabolism
, vol.80
, pp. 3145-3150
-
-
Wilson, R.C.1
Harbison, M.D.2
Krozowski, Z.S.3
-
12
-
-
13144265720
-
A genetic defect resulting in mild low-renin hypertension
-
DOI 10.1073/pnas.95.17.10200
-
Wilson R. C., Dave-Sharma S., Wei J.-Q., Obeyesekere V. R., Li K., Ferrari P., Krozowski Z. S., Shackleton C. H. L., Bradlow L., Wiens T., New M. I., A genetic defect resulting in mild low-renin hypertension Proceedings of the National Academy of Sciences of the United States of America 1998 95 17 10200 10205 (Pubitemid 28415318)
-
(1998)
Proceedings of the National Academy of Sciences of the United States of America
, vol.95
, Issue.17
, pp. 10200-10205
-
-
Wilson, R.C.1
Dave-Sharma, S.2
Wei, J.-Q.3
Obeyesekere, V.R.4
Li, K.5
Ferrari, P.6
Krozowski, Z.S.7
Shackleton, C.H.L.8
Bradlow, L.9
Wiens, T.10
New, M.I.11
-
13
-
-
7844240856
-
Examination of genotype and phenotype relationships in 14 patients with apparent mineralocorticoid excess
-
DOI 10.1210/jc.83.7.2244
-
Dave-Sharma S., Wilson R. C., Harbison M. D., Newfield R., Azar M. R., Krozowski Z. S., Funder J. W., Shackleton C. H. L., Bradlow H. L., Wei J. I.-Q., Hertecant J., Moran A., Neiberger R. E., Balfe J. W., Fattah A., Daneman D., Akkurt H. I., De Santis C., New M. I., Examination of genotype and phenotype relationships in 14 patients with apparent mineralocorticoid excess Journal of Clinical Endocrinology Metabolism 1998 83 7 2244 2254 (Pubitemid 28503009)
-
(1998)
Journal of Clinical Endocrinology and Metabolism
, vol.83
, Issue.7
, pp. 2244-2254
-
-
Dave-Sharma, S.1
Wilson, R.C.2
Harbison, M.D.3
Newfield, R.4
Azar, M.R.5
Krozowski, Z.S.6
Funder, J.W.7
Shackleton, C.H.L.8
Bradlow, H.L.9
Wei, J.I.-Q.10
Hertecant, J.11
Moran, A.12
Neiberger, R.E.13
Balfe, J.W.14
Fattah, A.15
Daneman, D.16
Akkurt, H.I.17
De Santis, C.18
New, M.I.19
-
14
-
-
17744397530
-
A mutation in the cofactor-binding domain of 11β-hydroxysteroid dehydrogenase type 2 associated with mineralocorticoid hypertension
-
DOI 10.1210/jc.86.3.1247
-
Odermatt A., Dick B., Arnold P., A mutation in the cofactor-binding domain of 11beta-hydroxysteroid dehydrogenase type 2 associated with mineralocorticoid hypertension Journal of Clinical Endocrinology Metabolism 2001 86 1247 1252 (Pubitemid 32323012)
-
(2001)
Journal of Clinical Endocrinology and Metabolism
, vol.86
, Issue.3
, pp. 1247-1252
-
-
Odermatt, A.1
Dick, B.2
Arnold, P.3
Zaehner, T.4
Plueschke, V.5
Deregibus, M.N.6
Repetto, H.7
Frey, B.M.8
Frey, F.J.9
Ferrari, P.10
-
15
-
-
0030049329
-
Hypertension in the syndrome of apparent mineralocorticoid excess due to mutation of the 11β-hydroxysteroid dehydrogenase type 2 gene
-
DOI 10.1016/S0140-6736(96)90211-1
-
Stewart P. M., Krozowski Z. S., Gupta A., Milford D. V., Howie A. J., Sheppard M. C., Whorwood C. B., Hypertension in the syndrome of apparent mineralocorticoid excess due to mutation of the 11 -hydroxysteroid dehydrogenase type 2 gene The Lancet 1996 347 8994 88 91 (Pubitemid 26017854)
-
(1996)
Lancet
, vol.347
, Issue.8994
, pp. 88-91
-
-
Stewart, P.M.1
Krozowski, Z.S.2
Gupta, A.3
Milford, D.V.4
Howie, A.J.5
Sheppard, M.C.6
Whorwood, C.B.7
-
16
-
-
33744948083
-
Genetic variations of HSD11B2 in hypertensive patients and in the general population, six rare missense/frameshift mutations
-
DOI 10.1291/hypres.29.243
-
Kamide K., Kokubo Y., Hanada H., Nagura J., Yang J., Takiuchi S., Tanaka C., Banno M., Miwa Y., Yoshii M., Matayoshi T., Yasuda H., Horio T., Okayama A., Tomoike H., Kawano Y., Miyata T., Genetic variations of HSD11B2 in hypertensive patients and in the general population, six rare missense/frameshift mutations Hypertension Research 2006 29 4 243 252 (Pubitemid 43853270)
-
(2006)
Hypertension Research
, vol.29
, Issue.4
, pp. 243-252
-
-
Kamide, K.1
Kokubo, Y.2
Hanada, H.3
Nagura, J.4
Yang, J.5
Takiuchi, S.6
Tanaka, C.7
Banno, M.8
Miwa, Y.9
Yoshii, M.10
Matayoshi, T.11
Yasuda, H.12
Horio, T.13
Okayama, A.14
Tomoike, H.15
Kawano, Y.16
Miyata, T.17
-
17
-
-
65349115394
-
Two novel mutations in the ED1 gene in Japanese families with X-linked hypohidrotic ectodermal dysplasia
-
Gunadi, Miura K., Ohta M., Two novel mutations in the ED1 gene in Japanese families with X-linked hypohidrotic ectodermal dysplasia Pediatric Research 2009 65 4 453 457
-
(2009)
Pediatric Research
, vol.65
, Issue.4
, pp. 453-457
-
-
Gunadi1
Miura, K.2
Ohta, M.3
-
18
-
-
34249710193
-
Severe hypokalemia, rhabdomyolysis, muscle paralysis, and respiratory impairment in a hypertensive patient taking herbal medicines containing licorice
-
DOI 10.2169/internalmedicine.46.6316
-
Yasue H., Itoh T., Mizuno Y., Harada E., Severe hypokalemia, rhabdomyolysis, muscle paralysis, and respiratory impairment in a hypertensive patient taking herbal medicines containing licorice Internal Medicine 2007 46 9 575 578 (Pubitemid 46845849)
-
(2007)
Internal Medicine
, vol.46
, Issue.9
, pp. 575-578
-
-
Yasue, H.1
Itoh, T.2
Mizuno, Y.3
Harada, E.4
-
19
-
-
62849083645
-
An unusual cause of ventricular fibrillation
-
Gerritsen K. G., Meulenbelt J., Spiering W., Kema I. P., Demir A., van Driel V. J., An unusual cause of ventricular fibrillation The Lancet 2009 373 9669 1144
-
(2009)
The Lancet
, vol.373
, Issue.9669
, pp. 1144
-
-
Gerritsen, K.G.1
Meulenbelt, J.2
Spiering, W.3
Kema, I.P.4
Demir, A.5
Van Driel, V.J.6
-
20
-
-
0027226069
-
Mitochondrial ribosomal RNA mutation associated with both antibiotic- induced and non-syndromic deafness
-
DOI 10.1038/ng0793-289
-
Prezant T. R., Agapian J. V., Bohlman M. C., Bu X., Oztas S., Qiu W.-Q., Arnos K. S., Cortopassi G. A., Jaber L., Rotter J. I., Shohat M., Fischel-Ghodsian N., Mitochondrial ribosomal RNA mutation associated with both antibiotic- induced and non-syndromic deafness Nature Genetics 1993 4 3 289 294 (Pubitemid 23205179)
-
(1993)
Nature Genetics
, vol.4
, Issue.3
, pp. 289-294
-
-
Prezant, T.R.1
Agapian, J.V.2
Bohlman, M.C.3
Bu, X.4
Oztas, S.5
Qiu, W.-Q.6
Arnos, K.S.7
Cortopassi, G.A.8
Jaber, L.9
Rotter, J.I.10
Shohat, M.11
Fischel-Ghodsian, N.12
-
21
-
-
0032833546
-
Rapid mass screening method and counseling for the 1555A→G mitochondrial mutation
-
DOI 10.1007/s100380050165
-
Usami S.-I., Abe S., Shinkawa H., Inoue Y., Yamaguchi T., Rapid mass screening method and counseling for the 1555A→G mitochondrial mutation Journal of Human Genetics 1999 44 5 304 307 (Pubitemid 29436697)
-
(1999)
Journal of Human Genetics
, vol.44
, Issue.5
, pp. 304-307
-
-
Usami, S.-I.1
Abe, S.2
Shinkawa, H.3
Inoue, Y.4
Yamaguchi, T.5
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