메뉴 건너뛰기




Volumn 99, Issue 10, 2014, Pages 3629-3633

Erratum: E pluribus unum? The main protein kinase a catalytic subunit (PRKACA), a likely oncogene, and cortisol-producing tumors (Journal of Clinical Endocrinology and Metabolism (2014) 99:10 (3629-3633) DOI: 10.1210/jc.2014-3295);E pluribus unum? The main protein kinase a catalytic subunit (PRKACA), a likely oncogene, and cortisol-producing tumors

Author keywords

[No Author keywords available]

Indexed keywords

CYCLIC AMP; CYCLIC AMP DEPENDENT PROTEIN KINASE; G PROTEIN COUPLED RECEPTOR; HYDROCORTISONE; PROTEIN KINASE; CYCLIC AMP DEPENDENT PROTEIN KINASE CATALYTIC SUBUNIT; PRKACA PROTEIN, HUMAN;

EID: 84907637520     PISSN: 0021972X     EISSN: 19457197     Source Type: Journal    
DOI: 10.1210/jc.2014-4426     Document Type: Erratum
Times cited : (24)

References (52)
  • 1
    • 0031748315 scopus 로고    scopus 로고
    • Clinical and genetic analysis of primary bilateral adrenal diseases (micro- and macronodular disease) leading to Cushing syndrome
    • Stratakis CA, Kirschner LS. Clinical and genetic analysis of primary bilateral adrenal diseases (micro- and macronodular disease) leading to Cushing syndrome. Horm Metab Res. 1998;30:456-463.
    • (1998) Horm Metab Res. , vol.30 , pp. 456-463
    • Stratakis, C.A.1    Kirschner, L.S.2
  • 2
    • 84876083813 scopus 로고    scopus 로고
    • Camp/PKA signaling defects in tumors: Genetics and tissue-specific pluripotential cell-derived lesions in human and mouse
    • Stratakis CA. cAMP/PKA signaling defects in tumors: genetics and tissue-specific pluripotential cell-derived lesions in human and mouse. Mol Cell Endocrinol. 2013;371:208-220.
    • (2013) Mol Cell Endocrinol. , vol.371 , pp. 208-220
    • Stratakis, C.A.1
  • 3
    • 81155161059 scopus 로고    scopus 로고
    • Primary bimorphic adrenocortical disease: Cause of hypercortisolism in McCune-Albright syndrome
    • Carney JA, Young WF, Stratakis CA. Primary bimorphic adrenocortical disease: cause of hypercortisolism in McCune-Albright syndrome. Am J Surg Pathol. 2011;35:1311-1326.
    • (2011) Am J Surg Pathol. , vol.35 , pp. 1311-1326
    • Carney, J.A.1    Young, W.F.2    Stratakis, C.A.3
  • 4
    • 84888346827 scopus 로고    scopus 로고
    • Heredity and cortisol regulation in bilateral macronodular adrenal hyperplasia
    • Lacroix A. Heredity and cortisol regulation in bilateral macronodular adrenal hyperplasia. N Engl J Med. 2013;369:2147-2149.
    • (2013) N Engl J Med. , vol.369 , pp. 2147-2149
    • Lacroix, A.1
  • 6
    • 68549109424 scopus 로고    scopus 로고
    • Clinical and genetic heterogeneity, overlap with other tumor syndromes, and atypical glucocorticoid hormone secretion in adrenocorticotropin-independent macronodular adrenal hyperplasia compared with other adrenocortical tumors
    • Hsiao HP, Kirschner LS, Bourdeau I, et al. Clinical and genetic heterogeneity, overlap with other tumor syndromes, and atypical glucocorticoid hormone secretion in adrenocorticotropin-independent macronodular adrenal hyperplasia compared with other adrenocortical tumors. J Clin Endocrinol Metab. 2009;94:2930-2937.
    • (2009) J Clin Endocrinol Metab. , vol.94 , pp. 2930-2937
    • Hsiao, H.P.1    Kirschner, L.S.2    Bourdeau, I.3
  • 7
    • 0033812849 scopus 로고    scopus 로고
    • Mutations of the gene encoding the protein kinase A type I-a regulatory subunit in patients with the Carney complex
    • Kirschner LS, Carney JA, Pack SD, et al. Mutations of the gene encoding the protein kinase A type I-a regulatory subunit in patients with the Carney complex. Nat Genet. 2000;26:89-92.
    • (2000) Nat Genet. , vol.26 , pp. 89-92
    • Kirschner, L.S.1    Carney, J.A.2    Pack, S.D.3
  • 8
    • 0034642302 scopus 로고    scopus 로고
    • Genetic heterogeneity and spectrum of mutations of the PRKAR1A gene in patients with the Carney complex
    • Kirschner LS, Sandrini F, Monbo J, Lin JP, Carney JA, Stratakis CA. Genetic heterogeneity and spectrum of mutations of the PRKAR1A gene in patients with the Carney complex. Hum Mol Genet. 2000;9:3037-3046.
    • (2000) Hum Mol Genet. , vol.9 , pp. 3037-3046
    • Kirschner, L.S.1    Sandrini, F.2    Monbo, J.3    Lin, J.P.4    Carney, J.A.5    Stratakis, C.A.6
  • 9
    • 33748748991 scopus 로고    scopus 로고
    • 17q22-24 chromosomal losses and alterations of protein kinase A subunit expression and activity in adrenocorticotropin-independent macronodular adrenal hyperplasia
    • Bourdeau I, Matyakhina L, Stergiopoulos SG, Sandrini F, Boikos S, Stratakis CA. 17q22-24 chromosomal losses and alterations of protein kinase A subunit expression and activity in adrenocorticotropin-independent macronodular adrenal hyperplasia. J Clin Endocrinol Metab. 2006;91:3626-3632.
    • (2006) J Clin Endocrinol Metab. , vol.91 , pp. 3626-3632
    • Bourdeau, I.1    Matyakhina, L.2    Stergiopoulos, S.G.3    Sandrini, F.4    Boikos, S.5    Stratakis, C.A.6
  • 10
    • 0038721027 scopus 로고    scopus 로고
    • Molecular and functional analysis of PRKAR1A and its locus (17q22-24) in sporadic adrenocortical tumors: 17q losses, somatic mutations, and protein kinase A expression and activity
    • Bertherat J, Groussin L, Sandrini F, et al. Molecular and functional analysis of PRKAR1A and its locus (17q22-24) in sporadic adrenocortical tumors: 17q losses, somatic mutations, and protein kinase A expression and activity. Cancer Res. 2003;63:5308-5319.
    • (2003) Cancer Res. , vol.63 , pp. 5308-5319
    • Bertherat, J.1    Groussin, L.2    Sandrini, F.3
  • 11
    • 67650767017 scopus 로고    scopus 로고
    • Abnormalities of cAMP signaling are present in adrenocortical lesions associated with ACTH-independent Cushing syndrome despite the absence of mutations in known genes
    • Bimpaki EI, Nesterova M, Stratakis CA. Abnormalities of cAMP signaling are present in adrenocortical lesions associated with ACTH-independent Cushing syndrome despite the absence of mutations in known genes. Eur J Endocrinol. 2009;161:153-161.
    • (2009) Eur J Endocrinol. , vol.161 , pp. 153-161
    • Bimpaki, E.I.1    Nesterova, M.2    Stratakis, C.A.3
  • 12
    • 33745548423 scopus 로고    scopus 로고
    • A genome-wide scan identifies mutations in the gene encoding phosphodiesterase 11A4 (PDE11A) in individuals with adrenocortical hyperplasia
    • Horvath A, Boikos S, Giatzakis C, et al. A genome-wide scan identifies mutations in the gene encoding phosphodiesterase 11A4 (PDE11A) in individuals with adrenocortical hyperplasia. Nat Genet. 2006;38:794-800.
    • (2006) Nat Genet. , vol.38 , pp. 794-800
    • Horvath, A.1    Boikos, S.2    Giatzakis, C.3
  • 13
    • 45549099523 scopus 로고    scopus 로고
    • Phosphodiesterase 11A expression in the adrenal cortex, primary pigmented nodular adrenocortical disease, and other corticotropin-independent lesions
    • Boikos SA, Horvath A, Heyerdahl S, et al. Phosphodiesterase 11A expression in the adrenal cortex, primary pigmented nodular adrenocortical disease, and other corticotropin-independent lesions. Horm Metab Res. 2008;40:347-353.
    • (2008) Horm Metab Res. , vol.40 , pp. 347-353
    • Boikos, S.A.1    Horvath, A.2    Heyerdahl, S.3
  • 14
    • 39049101528 scopus 로고    scopus 로고
    • Mutation in PDE8B, a cyclic AMP-specific phosphodiesterase in adrenal hyperplasia
    • Horvath A, Mericq V, Stratakis CA. Mutation in PDE8B, a cyclic AMP-specific phosphodiesterase in adrenal hyperplasia. N Engl J Med. 2008;358:750-752.
    • (2008) N Engl J Med. , vol.358 , pp. 750-752
    • Horvath, A.1    Mericq, V.2    Stratakis, C.A.3
  • 15
    • 53249142160 scopus 로고    scopus 로고
    • A cAMP-specific phosphodiesterase (PDE8B) that is mutated in adrenal hyperplasia is expressed widely in human and mouse tissues: A novel PDE8B isoform in human adrenal cortex
    • Horvath A, Giatzakis C, Tsang K, et al. A cAMP-specific phosphodiesterase (PDE8B) that is mutated in adrenal hyperplasia is expressed widely in human and mouse tissues: a novel PDE8B isoform in human adrenal cortex. Eur J Hum Genet. 2008;16:1245-1253.
    • (2008) Eur J Hum Genet. , vol.16 , pp. 1245-1253
    • Horvath, A.1    Giatzakis, C.2    Tsang, K.3
  • 16
    • 84897425079 scopus 로고    scopus 로고
    • Clinical and molecular genetics of the phosphodiesterases (PDEs)
    • Azevedo MF, Faucz FR, Bimpaki E, et al. Clinical and molecular genetics of the phosphodiesterases (PDEs). Endocr Rev. 2014;35:195-233.
    • (2014) Endocr Rev. , vol.35 , pp. 195-233
    • Azevedo, M.F.1    Faucz, F.R.2    Bimpaki, E.3
  • 17
    • 52449114622 scopus 로고    scopus 로고
    • Phosphodiesterase 11A (PDE11A) and genetic predisposition to adrenocortical tumors
    • Libé R, Fratticci A, Coste J, et al. Phosphodiesterase 11A (PDE11A) and genetic predisposition to adrenocortical tumors. Clin Cancer Res. 2008;14:4016-4024.
    • (2008) Clin Cancer Res. , vol.14 , pp. 4016-4024
    • Libé, R.1    Fratticci, A.2    Coste, J.3
  • 18
    • 84868611190 scopus 로고    scopus 로고
    • Phosphodiesterase 11A (PDE11A) gene defects in patients with ACTH-independent macronodular adrenal hyperplasia (AIMAH): Functional variants may contributetogenetic susceptibility of bilateral adrenal tumors
    • Vezzosi D, Libé R, Baudry C, et al. Phosphodiesterase 11A (PDE11A) gene defects in patients with ACTH-independent macronodular adrenal hyperplasia (AIMAH): functional variants may contributetogenetic susceptibility of bilateral adrenal tumors. J Clin Endocrinol Metab. 2012;97:E2063-E2069.
    • (2012) J Clin Endocrinol Metab. , vol.97 , pp. E2063-E2069
    • Vezzosi, D.1    Libé, R.2    Baudry, C.3
  • 19
    • 84863664769 scopus 로고    scopus 로고
    • Identification of novel genetic variants in phosphodiesterase 8B (PDE8B), a cAMP-specific phosphodiesterase highly expressed in the adrenal cortex, in a cohort of patients with adrenal tumours
    • Rothenbuhler A, Horvath A, Libé R, et al. Identification of novel genetic variants in phosphodiesterase 8B (PDE8B), a cAMP-specific phosphodiesterase highly expressed in the adrenal cortex, in a cohort of patients with adrenal tumours. Clin Endocrinol (Oxf). 2012;77:195-199.
    • (2012) Clin Endocrinol (Oxf). , vol.77 , pp. 195-199
    • Rothenbuhler, A.1    Horvath, A.2    Libé, R.3
  • 20
    • 78650898282 scopus 로고    scopus 로고
    • Frequent phosphodiesterase 11 Agene (PDE11A) defectsinpatients with Carney complex (CNC) caused by PRKAR1A mutations: PDE11A may contribute to adrenal and testicular tumors in CNC as a modifier of the phenotype
    • Libé R, Horvath A, Vezzosi D, et al. Frequent phosphodiesterase 11 Agene (PDE11A) defectsinpatients with Carney complex (CNC) caused by PRKAR1A mutations: PDE11A may contribute to adrenal and testicular tumors in CNC as a modifier of the phenotype. J Clin Endocrinol Metab. 2011;96:E208-E214.
    • (2011) J Clin Endocrinol Metab. , vol.96 , pp. E208-E214
    • Libé, R.1    Horvath, A.2    Vezzosi, D.3
  • 21
    • 84896745936 scopus 로고    scopus 로고
    • Constitutive activation of PKA catalytic subunit in a drenal Cushing's syndrome
    • Beuschlein F, Fassnacht M, Assié G, et al. Constitutive activation of PKA catalytic subunit in a drenal Cushing's syndrome. N Engl J Med. 2014;370:1019-1028.
    • (2014) N Engl J Med. , vol.370 , pp. 1019-1028
    • Beuschlein, F.1    Fassnacht, M.2    Assié, G.3
  • 22
    • 84901283149 scopus 로고    scopus 로고
    • Activating hotspot L205R mutation in PRKACA and adrenal Cushing's syndrome
    • Cao Y, He M, Gao Z, et al. Activating hotspot L205R mutation in PRKACA and adrenal Cushing's syndrome. Science. 2014;344:913-917.
    • (2014) Science , vol.344 , pp. 913-917
    • Cao, Y.1    He, M.2    Gao, Z.3
  • 23
    • 84901217805 scopus 로고    scopus 로고
    • Recurrent somatic mutations underlie corticotropin-independent Cushing's syndrome
    • Sato Y, Maekawa S, Ishii R, et al. Recurrent somatic mutations underlie corticotropin-independent Cushing's syndrome. Science. 2014;344:917-920.
    • (2014) Science , vol.344 , pp. 917-920
    • Sato, Y.1    Maekawa, S.2    Ishii, R.3
  • 24
    • 84901670628 scopus 로고    scopus 로고
    • Recurrent activating mutation in PRKACA in cortisol-producing adrenal tumors
    • Goh G, Scholl UI, Healy JM, et al. Recurrent activating mutation in PRKACA in cortisol-producing adrenal tumors. Nat Genet. 2014;46:613-617.
    • (2014) Nat Genet. , vol.46 , pp. 613-617
    • Goh, G.1    Scholl, U.I.2    Healy, J.M.3
  • 25
    • 84901218218 scopus 로고    scopus 로고
    • 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.
    • (2014) Science , vol.344 , pp. 804-805
    • Kirschner, L.S.1
  • 26
    • 84901296893 scopus 로고    scopus 로고
    • Neuroendocrine cancer. An activating hotspot mutation in PRKACA provides clues for adrenal Cushing syndrome therapeutics
    • Sargent J. Neuroendocrine cancer. An activating hotspot mutation in PRKACA provides clues for adrenal Cushing syndrome therapeutics. Nat Rev Endocrinol. 2014;10:311.
    • (2014) Nat Rev Endocrinol. , vol.10 , pp. 311
    • Sargent, J.1
  • 27
    • 84904728652 scopus 로고    scopus 로고
    • Genetics: Pinpointing a hotspot in adrenal Cushing syndrome
    • Giordano TJ. Genetics: pinpointing a hotspot in adrenal Cushing syndrome. Nat Rev Endocrinol. 2014;10:447-448.
    • (2014) Nat Rev Endocrinol. , vol.10 , pp. 447-448
    • Giordano, T.J.1
  • 28
    • 84907610884 scopus 로고    scopus 로고
    • 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, 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. J Clin Endocrinol Metab. 2014:99: E2093-E2100.
    • (2014) J Clin Endocrinol Metab. , vol.99 , pp. E2093-E2100
    • Di Dalmazi, G.1    Kisker, C.2    Calebiro, D.3
  • 29
    • 9444247656 scopus 로고    scopus 로고
    • Minireview: PRKAR1A: Normal and abnormal functions
    • Bossis I, Stratakis CA. Minireview: PRKAR1A: normal and abnormal functions. Endocrinology. 2004;145:5452-5458.
    • (2004) Endocrinology , vol.145 , pp. 5452-5458
    • Bossis, I.1    Stratakis, C.A.2
  • 30
    • 44849132922 scopus 로고    scopus 로고
    • Protein kinase A effects of an expressed PRKAR1A mutation associated with aggressive tumors
    • Meoli E, Bossis I, Cazabat L, et al. Protein kinase A effects of an expressed PRKAR1A mutation associated with aggressive tumors. Cancer Res. 2008;68:3133-3141.
    • (2008) Cancer Res. , vol.68 , pp. 3133-3141
    • Meoli, E.1    Bossis, I.2    Cazabat, L.3
  • 31
    • 84870758157 scopus 로고    scopus 로고
    • One single signaling pathway for so many different biological functions: Lessons from the cyclic adenosine monophosphate/protein kinase A pathway-related diseases
    • Assié G. One single signaling pathway for so many different biological functions: lessons from the cyclic adenosine monophosphate/protein kinase A pathway-related diseases. J Clin Endocrinol Metab. 2012;97:4355-4357.
    • (2012) J Clin Endocrinol Metab. , vol.97 , pp. 4355-4357
    • Assié, G.1
  • 32
    • 79958182720 scopus 로고    scopus 로고
    • Recurrent PRKAR1A mutation in acrodysostosis with hormone resistance
    • Linglart A, Menguy C, Couvineau A, et al. Recurrent PRKAR1A mutation in acrodysostosis with hormone resistance. N Engl J Med. 2011;364:2218-2226.
    • (2011) N Engl J Med. , vol.364 , pp. 2218-2226
    • Linglart, A.1    Menguy, C.2    Couvineau, A.3
  • 33
    • 84870743491 scopus 로고    scopus 로고
    • PRKAR1A and PDE4D mutations cause acrodysostosis but two distinct syndromes with or without GPCR-signaling hormone resistance
    • Linglart A, Fryssira H, Hiort O, et al. PRKAR1A and PDE4D mutations cause acrodysostosis but two distinct syndromes with or without GPCR-signaling hormone resistance. J Clin Endocrinol Metab. 2012;97:E2328-E2338.
    • (2012) J Clin Endocrinol Metab. , vol.97 , pp. E2328-E2338
    • Linglart, A.1    Fryssira, H.2    Hiort, O.3
  • 34
    • 84866170771 scopus 로고    scopus 로고
    • PRKAR1A mutation affecting cAMP-mediated G protein-coupled receptor signaling in a patient with acrodysostosis and hormone resistance
    • Nagasaki K, Iida T, Sato H, et al. PRKAR1A mutation affecting cAMP-mediated G protein-coupled receptor signaling in a patient with acrodysostosis and hormone resistance. J Clin Endocrinol Metab. 2012;97:E1808-E1813.
    • (2012) J Clin Endocrinol Metab. , vol.97 , pp. E1808-E1813
    • Nagasaki, K.1    Iida, T.2    Sato, H.3
  • 35
    • 0026590175 scopus 로고
    • Mutations in the catalytic subunit of cAMP-dependent protein kinase result in unregulated biological activity
    • Orellana SA, McKnight GS. Mutations in the catalytic subunit of cAMP-dependent protein kinase result in unregulated biological activity. Proc Natl Acad Sci USA. 1992;89:4726-4730.
    • (1992) Proc Natl Acad Sci USA. , vol.89 , pp. 4726-4730
    • Orellana, S.A.1    McKnight, G.S.2
  • 36
    • 0027409422 scopus 로고
    • Mutations in the catalytic subunit of the cAMP-dependent protein kinase interfere with holoenzyme formation without disrupting inhibition by protein kinase inhibitor
    • Orellana SA, Amieux PS, Zhao X, McKnight GS. Mutations in the catalytic subunit of the cAMP-dependent protein kinase interfere with holoenzyme formation without disrupting inhibition by protein kinase inhibitor. J Biol Chem. 1993;268:6843-6846.
    • (1993) J Biol Chem. , vol.268 , pp. 6843-6846
    • Orellana, S.A.1    Amieux, P.S.2    Zhao, X.3    McKnight, G.S.4
  • 37
    • 62749134006 scopus 로고    scopus 로고
    • Identifying critical non-catalytic residues that modulate protein kinase A activity
    • Kennedy EJ, Yang J, Pillus L, Taylor SS, Ghosh G. Identifying critical non-catalytic residues that modulate protein kinase A activity. PLoS One. 2009;4:e4746.
    • (2009) PLoS One , vol.4 , pp. e4746
    • Kennedy, E.J.1    Yang, J.2    Pillus, L.3    Taylor, S.S.4    Ghosh, G.5
  • 38
    • 84859728157 scopus 로고    scopus 로고
    • Identification and characterization of novel mutations in the human gene encoding the catalytic subunit Ca of protein kinase A (PKA)
    • Søberg K, Larsen AC, Diskar M, et al. Identification and characterization of novel mutations in the human gene encoding the catalytic subunit Ca of protein kinase A (PKA). PLoS One. 2012;7:e34838.
    • (2012) PLoS One , vol.7 , pp. e34838
    • Søberg, K.1    Larsen, A.C.2    Diskar, M.3
  • 39
    • 0032723515 scopus 로고    scopus 로고
    • Mutation analysis of protein kinase A catalytic subunit in thyroid adenomas and pituitary tumours
    • Esapa CT, Harris PE. Mutation analysis of protein kinase A catalytic subunit in thyroid adenomas and pituitary tumours. Eur J Endocrinol. 1999;141:409-412.
    • (1999) Eur J Endocrinol. , vol.141 , pp. 409-412
    • Esapa, C.T.1    Harris, P.E.2
  • 40
    • 84896695230 scopus 로고    scopus 로고
    • Carney complex and McCune Albright syndrome: An overview of clinical manifestations and human molecular genetics
    • Salpea P, Stratakis CA. Carney complex and McCune Albright syndrome: an overview of clinical manifestations and human molecular genetics. Mol Cell Endocrinol. 2014;386:85-91.
    • (2014) Mol Cell Endocrinol. , vol.386 , pp. 85-91
    • Salpea, P.1    Stratakis, C.A.2
  • 41
    • 84896732099 scopus 로고    scopus 로고
    • Detection of a recurrent DNAJB1-PRKACA chimeric transcript in fibrolamellar hepatocellular carcinoma
    • Honeyman JN, Simon EP, Robine N, et al. Detection of a recurrent DNAJB1-PRKACA chimeric transcript in fibrolamellar hepatocellular carcinoma. Science. 2014;343:1010-1014.
    • (2014) Science , vol.343 , pp. 1010-1014
    • Honeyman, J.N.1    Simon, E.P.2    Robine, N.3
  • 42
    • 10844257526 scopus 로고    scopus 로고
    • Down-regulation of regulatory subunit type 1A of protein kinase A leads to endocrine and other tumors
    • Griffin KJ, Kirschner LS, Matyakhina L, et al. Down-regulation of regulatory subunit type 1A of protein kinase A leads to endocrine and other tumors. Cancer Res. 2004;64:8811-8815.
    • (2004) Cancer Res. , vol.64 , pp. 8811-8815
    • Griffin, K.J.1    Kirschner, L.S.2    Matyakhina, L.3
  • 43
    • 4644277913 scopus 로고    scopus 로고
    • Comparative PRKAR1A genotype-phenotype analyses in humans with Carney complex and prkar1a haploinsufficient mice
    • Veugelers M, Wilkes D, Burton K, et al. Comparative PRKAR1A genotype-phenotype analyses in humans with Carney complex and prkar1a haploinsufficient mice. Proc Natl Acad Sci USA. 2004;101:14222-14227.
    • (2004) Proc Natl Acad Sci USA. , vol.101 , pp. 14222-14227
    • Veugelers, M.1    Wilkes, D.2    Burton, K.3
  • 44
    • 54049112731 scopus 로고    scopus 로고
    • A novel PRKAR1A mutation associated with hepatocellular carcinoma in a young patient and a variable Carney complex phenotype in affected subjects in older generations
    • Gennari M, Stratakis CA, Hovarth A, Pirazzoli P, Cicognani A. A novel PRKAR1A mutation associated with hepatocellular carcinoma in a young patient and a variable Carney complex phenotype in affected subjects in older generations. Clin Endocrinol (Oxf). 2008;69:751-755.
    • (2008) Clin Endocrinol (Oxf). , vol.69 , pp. 751-755
    • Gennari, M.1    Stratakis, C.A.2    Hovarth, A.3    Pirazzoli, P.4    Cicognani, A.5
  • 45
    • 84939885519 scopus 로고    scopus 로고
    • PRKACA mediates resistance to HER2-targeted therapy in breast cancer cells and restores antiapoptotic signaling [published online June 9, 2014]
    • Moody SE, Schinzel AC, Singh S, et al. PRKACA mediates resistance to HER2-targeted therapy in breast cancer cells and restores antiapoptotic signaling [published online June 9, 2014]. Oncogene. doi: 10/1038/onc.2014.153.
    • Oncogene
    • Moody, S.E.1    Schinzel, A.C.2    Singh, S.3
  • 46
    • 19644364776 scopus 로고    scopus 로고
    • A mouse model for the Carney complex tumor syndrome develops neoplasia in cyclic AMP-responsive tissues
    • Kirschner LS, Kusewitt DF, Matyakhina L, et al. A mouse model for the Carney complex tumor syndrome develops neoplasia in cyclic AMP-responsive tissues. Cancer Res. 2005;65:4506-4514.
    • (2005) Cancer Res. , vol.65 , pp. 4506-4514
    • Kirschner, L.S.1    Kusewitt, D.F.2    Matyakhina, L.3
  • 47
    • 77952692816 scopus 로고    scopus 로고
    • Alternate protein kinase A activity identifies a unique population of stromal cells in adult bone
    • Tsang KM, Starost MF, Nesterova M, et al. Alternate protein kinase A activity identifies a unique population of stromal cells in adult bone. Proc Natl Acad Sci USA. 2010;107:8683-8688.
    • (2010) Proc Natl Acad Sci USA. , vol.107 , pp. 8683-8688
    • Tsang, K.M.1    Starost, M.F.2    Nesterova, M.3
  • 50
    • 80053450655 scopus 로고    scopus 로고
    • Differential role of PKA catalytic subunits in mediating phenotypes caused by knockout of the Carney complex gene Prkar1a
    • Yin Z, Pringle DR, Jones GN, Kelly KM, Kirschner LS. Differential role of PKA catalytic subunits in mediating phenotypes caused by knockout of the Carney complex gene Prkar1a. Mol Endocrinol. 2011;25:1786-1793.
    • (2011) Mol Endocrinol. , vol.25 , pp. 1786-1793
    • Yin, Z.1    Pringle, D.R.2    Jones, G.N.3    Kelly, K.M.4    Kirschner, L.S.5
  • 51
    • 0034682564 scopus 로고    scopus 로고
    • Serine-53 at the tip of the glycinerich loop of cAMP-dependent protein kinase: Role in catalysis, P-site specificity, and interaction with inhibitors
    • Aimes RT, Hemmer W, Taylor SS. Serine-53 at the tip of the glycinerich loop of cAMP-dependent protein kinase: role in catalysis, P-site specificity, and interaction with inhibitors. Biochemistry. 2000;39:8325-8332.
    • (2000) Biochemistry. , vol.39 , pp. 8325-8332
    • Aimes, R.T.1    Hemmer, W.2    Taylor, S.S.3
  • 52
    • 0037047423 scopus 로고    scopus 로고
    • Protein engineering of protein kinase A catalytic subunits results in the acquisition of novel inhibitor sensitivity
    • Niswender CM, Ishihara RW, Judge LM, Zhang C, Shokat KM, McKnight GS. Protein engineering of protein kinase A catalytic subunits results in the acquisition of novel inhibitor sensitivity. J Biol Chem. 2002;277:28916-28922.
    • (2002) J Biol Chem. , vol.277 , pp. 28916-28922
    • Niswender, C.M.1    Ishihara, R.W.2    Judge, L.M.3    Zhang, C.4    Shokat, K.M.5    McKnight, G.S.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.