-
1
-
-
84901218218
-
Medicine. A unified cause for adrenal Cushing's syndrome
-
Kirschner LS. Medicine. A unified cause for adrenal Cushing's syndrome. Science 2014 344 804-805. (doi:10.1126/science.1254901).
-
(2014)
Science
, vol.344
, pp. 804-805
-
-
Kirschner, L.S.1
-
2
-
-
0029650769
-
Cushing's syndrome
-
Orth DN. Cushing's syndrome. New England Journal of Medicine 1995 332 791-803. (doi:10.1056/NEJM199503233321207).
-
(1995)
New England Journal of Medicine
, vol.332
, pp. 791-803
-
-
Orth, D.N.1
-
3
-
-
84896745936
-
Constitutive activation of PKA catalytic subunit in adrenal Cushing's syndrome
-
Beuschlein F, FassnachtM, Assie G, Calebiro D, Stratakis CA, Osswald A, Ronchi CL, Wieland T, Sbiera S, Faucz FR et al. Constitutive activation of PKA catalytic subunit in adrenal Cushing's syndrome. New England Journal of Medicine 2014 370 1019-1028. (doi:10.1056/NEJMoa1310359).
-
(2014)
New England Journal of Medicine
, vol.370
, pp. 1019-1028
-
-
Beuschlein, F.1
Fassnacht, M.2
Assie, G.3
Calebiro, D.4
Stratakis, C.A.5
Osswald, A.6
Ronchi, C.L.7
Wieland, T.8
Sbiera, S.9
Faucz, F.R.10
-
4
-
-
84901283149
-
Activating hotspot L205R mutation in PRKACA and adrenal Cushing's syndrome
-
Cao Y, He M, Gao Z, Peng Y, Li Y, Li L, Zhou W, Li X, Zhong X, Lei Y et al. Activating hotspot L205R mutation in PRKACA and adrenal Cushing's syndrome. Science 2014 344 913-917. (doi:10.1126/science.1249480).
-
(2014)
Science
, vol.344
, pp. 913-917
-
-
Cao, Y.1
He, M.2
Gao, Z.3
Peng, Y.4
Li, Y.5
Li, L.6
Zhou, W.7
Li, X.8
Zhong, X.9
Lei, Y.10
-
5
-
-
84901217805
-
Recurrent somatic mutations underlie corticotropin-independent Cushing's syndrome
-
Sato Y, Maekawa S, Ishii R, Sanada M, Morikawa T, Shiraishi Y, Yoshida K, Nagata Y, Sato-Otsubo A, Yoshizato T et al. Recurrent somatic mutations underlie corticotropin-independent Cushing's syndrome. Science 2014 344 917-920. (doi:10.1126/science.1252328).
-
(2014)
Science
, vol.344
, pp. 917-920
-
-
Sato, Y.1
Maekawa, S.2
Ishii, R.3
Sanada, M.4
Morikawa, T.5
Shiraishi, Y.6
Yoshida, K.7
Nagata, Y.8
Sato-Otsubo, A.9
Yoshizato, T.10
-
6
-
-
84901670628
-
Recurrent activating mutation in PRKACA in cortisol-producing adrenal tumors
-
Goh G, Scholl UI, Healy JM, Choi M, Prasad ML, Nelson-Williams C, Kunstman JW, Korah R, Suttorp AC, Dietrich D et al. Recurrent activating mutation in PRKACA in cortisol-producing adrenal tumors. Nature Genetics 2014 46 613-617. (doi:10.1038/ng.2956).
-
(2014)
Nature Genetics
, vol.46
, pp. 613-617
-
-
Goh, G.1
Scholl, U.I.2
Healy, J.M.3
Choi, M.4
Prasad, M.L.5
Nelson-Williams, C.6
Kunstman, J.W.7
Korah, R.8
Suttorp, A.C.9
Dietrich, D.10
-
7
-
-
84906827864
-
Somatic mutations of the catalytic subunit of cyclic AMP-dependent protein kinase (PRKACA) gene in Japanese patients with several adrenal adenomas secreting cortisol [Rapid Communication]
-
Nakajima Y, Okamura T, Gohko T, Satoh T, Hashimoto K, Shibusawa N, Ozawa A, Ishii S, Tomaru T, Horiguchi K et al. Somatic mutations of the catalytic subunit of cyclic AMP-dependent protein kinase (PRKACA) gene in Japanese patients with several adrenal adenomas secreting cortisol [Rapid Communication]. Endocrine Journal 2014 61 825-832. (doi:10.1507/endocrj.EJ14-0282).
-
(2014)
Endocrine Journal
, vol.61
, pp. 825-832
-
-
Nakajima, Y.1
Okamura, T.2
Gohko, T.3
Satoh, T.4
Hashimoto, K.5
Shibusawa, N.6
Ozawa, A.7
Ishii, S.8
Tomaru, T.9
Horiguchi, K.10
-
8
-
-
84907610884
-
Novel somatic mutations in the catalytic subunit of the protein kinase A as a cause of adrenal Cushing's Syndrome: A European multicentric study
-
Di Dalmazi G, Kisker C, Calebiro D, Mannelli M, Canu L, Arnaldi G, Quinkler M, Rayes N, Tabarin A, Laure Jullie M et al. Novel somatic mutations in the catalytic subunit of the protein kinase A as a cause of adrenal Cushing's Syndrome: A European multicentric study. Journal of Clinical Endocrinology and Metabolism 2014 99 E2093-E2100. (doi:10.1210/jc.2014-2152).
-
(2014)
Journal of Clinical Endocrinology and Metabolism
, vol.99
, pp. E2093-E2100
-
-
Di Dalmazi, G.1
Kisker, C.2
Calebiro, D.3
Mannelli, M.4
Canu, L.5
Arnaldi, G.6
Quinkler, M.7
Rayes, N.8
Tabarin, A.9
Laure, J.M.10
-
10
-
-
38049130282
-
Frequent mutations of b-catenin gene in sporadic secreting adrenocortical adenomas
-
Tadjine M, Lampron A, Ouadi L & Bourdeau I. Frequent mutations of b-catenin gene in sporadic secreting adrenocortical adenomas. Clinical Endocrinology 2008 68 264-270. (doi:10.1111/j.1365-2265.2007.03033.x).
-
(2008)
Clinical Endocrinology
, vol.68
, pp. 264-270
-
-
Tadjine, M.1
Lampron, A.2
Ouadi, L.3
Bourdeau, I.4
-
11
-
-
77952300541
-
Constitutive b-catenin activation induces adrenal hyperplasia and promotes adrenal cancer development
-
Berthon A, Sahut-Barnola I, Lambert-Langlais S, de Joussineau C, Damon-Soubeyrand C, Louiset E, Taketo MM, Tissier F, Bertherat J, Lefrancois-Martinez AM et al. Constitutive b-catenin activation induces adrenal hyperplasia and promotes adrenal cancer development. Human Molecular Genetics 2010 19 1561-1576. (doi:10.1093/hmg/ddq029).
-
(2010)
Human Molecular Genetics
, vol.19
, pp. 1561-1576
-
-
Berthon, A.1
Sahut-Barnola, I.2
Lambert-Langlais, S.3
De Joussineau, C.4
Damon-Soubeyrand, C.5
Louiset, E.6
Taketo, M.M.7
Tissier, F.8
Bertherat, J.9
Lefrancois-Martinez, A.M.10
-
12
-
-
0038030796
-
Cushing's syndrome secondary to adrenocorticotropin-independent macronodular adrenocortical hyperplasia due to activating mutations of GNAS1 gene
-
Fragoso MC, Domenice S, Latronico AC, Martin RM, Pereira MA, Zerbini MC, Lucon AM & Mendonca BB. Cushing's syndrome secondary to adrenocorticotropin-independent macronodular adrenocortical hyperplasia due to activating mutations of GNAS1 gene. Journal of Clinical Endocrinology and Metabolism 2003 88 2147-2151. (doi:10.1210/jc.2002-021362).
-
(2003)
Journal of Clinical Endocrinology and Metabolism
, vol.88
, pp. 2147-2151
-
-
Fragoso, M.C.1
Domenice, S.2
Latronico, A.C.3
Martin, R.M.4
Pereira, M.A.5
Zerbini, M.C.6
Lucon, A.M.7
Mendonca, B.B.8
-
14
-
-
77956517756
-
Hypertension in Cushing's syndrome: From pathogenesis to treatment
-
Cicala MV & Mantero F. Hypertension in Cushing's syndrome: from pathogenesis to treatment. Neuroendocrinology 2010 92 (Suppl 1) 44-49. (doi:10.1159/000314315).
-
(2010)
Neuroendocrinology
, vol.92
, pp. 44-49
-
-
Cicala, M.V.1
Mantero, F.2
-
15
-
-
77951971879
-
Sporadic solitary aldosterone- And cortisol-co-secreting adenomas: Endocrine, histological and genetic findings in a subtype of primary aldosteronism
-
Willenberg HS, Spath M, Maser-Gluth C, Engers R, Anlauf M, Dekomien G, Schott M, Schinner S, Cupisti K & Scherbaum WA. Sporadic solitary aldosterone- And cortisol-co-secreting adenomas: endocrine, histological and genetic findings in a subtype of primary aldosteronism. Hypertension Research 2010 33 467-472. (doi:10.1038/hr.2010.18).
-
(2010)
Hypertension Research
, vol.33
, pp. 467-472
-
-
Willenberg, H.S.1
Spath, M.2
Maser-Gluth, C.3
Engers, R.4
Anlauf, M.5
Dekomien, G.6
Schott, M.7
Schinner, S.8
Cupisti, K.9
Scherbaum, W.A.10
-
16
-
-
84867917709
-
KCNJ5 mutations in aldosterone- And cortisol-co-secreting adrenal adenomas [Rapid Communication]
-
Yamada M, Nakajima Y, Taguchi R, Okamura T, Ishii S, Tomaru T, Ozawa A, Shibusawa N, Yoshino S, Toki A et al. KCNJ5 mutations in aldosterone- And cortisol-co-secreting adrenal adenomas [Rapid Communication]. Endocrine Journal 2012 59 735-741. (doi:10.1507/endocrj.EJ12-0247).
-
(2012)
Endocrine Journal
, vol.59
, pp. 735-741
-
-
Yamada, M.1
Nakajima, Y.2
Taguchi, R.3
Okamura, T.4
Ishii, S.5
Tomaru, T.6
Ozawa, A.7
Shibusawa, N.8
Yoshino, S.9
Toki, A.10
-
17
-
-
79953228533
-
Aldosteroneand cortisol-co-secreting adrenal tumors: The lost subtype of primary aldosteronism
-
SpathM, Korovkin S, Antke C, Anlauf M & Willenberg HS. Aldosteroneand cortisol-co-secreting adrenal tumors: The lost subtype of primary aldosteronism. European Journal of Endocrinology 2011 164 447-455. (doi:10.1530/EJE-10-1070).
-
(2011)
European Journal of Endocrinology
, vol.164
, pp. 447-455
-
-
Spath, M.1
Korovkin, S.2
Antke, C.3
Anlauf, M.4
Willenberg, H.S.5
-
19
-
-
79951506090
-
KC channel mutations in adrenal aldosterone-producing adenomas and hereditary hypertension
-
Choi M, Scholl UI, Yue P, Bjorklund P, Zhao B, Nelson-Williams C, Ji W, Cho Y, Patel A, Men CJ et al. KC channel mutations in adrenal aldosterone-producing adenomas and hereditary hypertension. Science 2011 331 768-772. (doi:10.1126/science.1198785).
-
(2011)
Science
, vol.331
, pp. 768-772
-
-
Choi, M.1
Scholl, U.I.2
Yue, P.3
Bjorklund, P.4
Zhao, B.5
Nelson-Williams, C.6
Ji, W.7
Cho, Y.8
Patel, A.9
Men, C.J.10
-
20
-
-
84875737352
-
Somatic mutations in ATP1A1 and ATP2B3 lead to aldosterone-producing adenomas and secondary hypertension
-
Beuschlein F, Boulkroun S, Osswald A, Wieland T, Nielsen HN, Lichtenauer UD, Penton D, Schack VR, Amar L, Fischer E et al. Somatic mutations in ATP1A1 and ATP2B3 lead to aldosterone-producing adenomas and secondary hypertension. Nature Genetics 2013 45 440-444. (doi:10.1038/ng.2550).
-
(2013)
Nature Genetics
, vol.45
, pp. 440-444
-
-
Beuschlein, F.1
Boulkroun, S.2
Osswald, A.3
Wieland, T.4
Nielsen, H.N.5
Lichtenauer, U.D.6
Penton, D.7
Schack, V.R.8
Amar, L.9
Fischer, E.10
-
21
-
-
84883452469
-
Somatic mutations in ATP1A1 and CACNA1D underlie a common subtype of adrenal hypertension
-
Azizan EA, Poulsen H, Tuluc P, Zhou J, Clausen MV, Lieb A, Maniero C, Garg S, Bochukova EG, Zhao Wet al. Somatic mutations in ATP1A1 and CACNA1D underlie a common subtype of adrenal hypertension. Nature Genetics 2013 45 1055-1060. (doi:10.1038/ng.2716).
-
(2013)
Nature Genetics
, vol.45
, pp. 1055-1060
-
-
Azizan, E.A.1
Poulsen, H.2
Tuluc, P.3
Zhou, J.4
Clausen, M.V.5
Lieb, A.6
Maniero, C.7
Garg, S.8
Bochukova, E.G.9
Zhao, W.A.10
-
22
-
-
84883464824
-
Somatic and germline CACNA1D calcium channel mutations in aldosteroneproducing adenomas and primary aldosteronism
-
Scholl UI, Goh G, Stolting G, de Oliveira RC, Choi M, Overton JD, Fonseca AL, Korah R, Starker LF, Kunstman JW et al. Somatic and germline CACNA1D calcium channel mutations in aldosteroneproducing adenomas and primary aldosteronism. Nature Genetics 2013 45 1050-1054. (doi:10.1038/ng.2695).
-
(2013)
Nature Genetics
, vol.45
, pp. 1050-1054
-
-
Scholl, U.I.1
Goh, G.2
Stolting, G.3
De Oliveira, R.C.4
Choi, M.5
Overton, J.D.6
Fonseca, A.L.7
Korah, R.8
Starker, L.F.9
Kunstman, J.W.10
-
23
-
-
84874106972
-
Control of CYP11B2/CYP11B1 expression ratio and consequences for the zonation of the adrenal cortex
-
Dringenberg T, Schwitalla M, Haase M, Scherbaum WA & Willenberg HS. Control of CYP11B2/CYP11B1 expression ratio and consequences for the zonation of the adrenal cortex. Hormone and Metabolic Research 2013 45 81-85. (doi:10.1055/s-0032-1331210).
-
(2013)
Hormone and Metabolic Research
, vol.45
, pp. 81-85
-
-
Dringenberg, T.1
Schwitalla, M.2
Haase, M.3
Scherbaum, W.A.4
Willenberg, H.S.5
-
24
-
-
84859410866
-
Potassium channel mutant KCNJ5 T158A expression in HAC-15 cells increases aldosterone synthesis
-
Oki K, Plonczynski MW, Luis Lam M, Gomez-Sanchez EP & Gomez- Sanchez CE. Potassium channel mutant KCNJ5 T158A expression in HAC-15 cells increases aldosterone synthesis. Endocrinology 2012 153 1774-1782. (doi:10.1210/en.2011-1733).
-
(2012)
Endocrinology
, vol.153
, pp. 1774-1782
-
-
Oki, K.1
Plonczynski, M.W.2
Luis, L.M.3
Gomez-Sanchez, E.P.4
Gomez-Sanchez, C.E.5
-
25
-
-
84864612057
-
Comprehensive re-sequencing of adrenal aldosterone producing lesions reveal three somatic mutations near the KCNJ5 potassium channel selectivity filter
-
Akerstrom T, Crona J, Delgado Verdugo A, Starker LF, Cupisti K, Willenberg HS, Knoefel WT, Saeger W, Feller A, Ip J et al. Comprehensive re-sequencing of adrenal aldosterone producing lesions reveal three somatic mutations near the KCNJ5 potassium channel selectivity filter. PLoS ONE 2012 7 e41926. (doi:10.1371/journal.pone.0041926).
-
(2012)
PLoS ONE
, vol.7
, pp. e41926
-
-
Akerstrom, T.1
Crona, J.2
Delgado, V.A.3
Starker, L.F.4
Cupisti, K.5
Willenberg, H.S.6
Knoefel, W.T.7
Saeger, W.8
Feller, A.9
Ip, J.10
-
26
-
-
0035118494
-
Adrenocorticotropin-independent unilateral adrenocortical hyperplasia with Cushing's syndrome: Immunohistochemical studies of steroidogenic enzymes, ultrastructural examination and a review of the literature
-
Takamura T, Nagai Y, Taniguchi M, Yamashita H, Nakamura S, Ikeda T, Kobayashi K, Suzuki T & Sasano H. Adrenocorticotropin-independent unilateral adrenocortical hyperplasia with Cushing's syndrome: Immunohistochemical studies of steroidogenic enzymes, ultrastructural examination and a review of the literature. Pathology International 2001 51 118-122. (doi:10.1046/j.1440-1827.2001.01169.x).
-
(2001)
Pathology International
, vol.51
, pp. 118-122
-
-
Takamura, T.1
Nagai, Y.2
Taniguchi, M.3
Yamashita, H.4
Nakamura, S.5
Ikeda, T.6
Kobayashi, K.7
Suzuki, T.8
Sasano, H.9
-
27
-
-
38649120030
-
Acthindependent Cushing's syndrome: Bilateral cortisol-producing adrenal adenomas
-
Dinneen SF, Carney JA, Carpenter PC, Grant CS & Young WF Jr. Acthindependent Cushing's syndrome: bilateral cortisol-producing adrenal adenomas. Endocrine Practice 1995 1 77-81. (doi:10.4158/EP.1.2.77).
-
(1995)
Endocrine Practice
, vol.1
, pp. 77-81
-
-
Dinneen, S.F.1
Carney, J.A.2
Carpenter, P.C.3
Grant, C.S.4
Young, W.F.5
|