-
1
-
-
80051974356
-
Primary pigmented nodular adrenocortical disease and its associated conditions
-
Carney JA, Young WF: Primary pigmented nodular adrenocortical disease and its associated conditions. Endocrinologist 1992;2:6-21.
-
(1992)
Endocrinologist
, vol.2
, pp. 6-21
-
-
Carney, J.A.1
Young, W.F.2
-
2
-
-
0000164745
-
The familial lentiginosis syndromes are emerging from the obscurity imposed by rarity: New genes and genetic loci for multiple tumors and developmental defects
-
Stratakis CA: The familial lentiginosis syndromes are emerging from the obscurity imposed by rarity: New genes and genetic loci for multiple tumors and developmental defects. Horm Metabol Res 1998;30:285-290.
-
(1998)
Horm Metabol Res
, vol.30
, pp. 285-290
-
-
Stratakis, C.A.1
-
3
-
-
58149212170
-
Carney complex: The complex of myxomas, spotty pigmentation, endocrine overactivity and schwannomas
-
Carney JA: Carney complex: The complex of myxomas, spotty pigmentation, endocrine overactivity and schwannomas. Semin Dermatol 1995;14:90-98.
-
(1995)
Semin Dermatol
, vol.14
, pp. 90-98
-
-
Carney, J.A.1
-
4
-
-
0031732467
-
Carney complex: Diagnosis and management of the complex of spotty skin pigmentation, myxomas, endocrine overactivity and schwannomas
-
Stratakis CA, Kirschner LS, Carney JA: Carney complex: Diagnosis and management of the complex of spotty skin pigmentation, myxomas, endocrine overactivity and schwannomas. Am J Med Genet 1998;80:183-185.
-
(1998)
Am J Med Genet
, vol.80
, pp. 183-185
-
-
Stratakis, C.A.1
Kirschner, L.S.2
Carney, J.A.3
-
5
-
-
0022446058
-
Dominant inheritance of the complex of myxomas, spotty pigmentation and endocrine overactivity
-
Carney JA, Hruska LS, Beauchamp GD, Gordon H: Dominant inheritance of the complex of myxomas, spotty pigmentation and endocrine overactivity. Mayo Clin Proc 1986;61:165-172.
-
(1986)
Mayo Clin Proc
, vol.61
, pp. 165-172
-
-
Carney, J.A.1
Hruska, L.S.2
Beauchamp, G.D.3
Gordon, H.4
-
6
-
-
0030049026
-
Carney complex, a familial multiple neoplasia and lentiginosis syndrome: Analysis of 11 kindreds and linkage to the short arm of chromosome 2
-
Stratakis CA, Carney JA, Lin JP, Papanicolaou DA, Karl M, Kastner DL, et al: Carney complex, a familial multiple neoplasia and lentiginosis syndrome: Analysis of 11 kindreds and linkage to the short arm of chromosome 2. J Clin Invest 1996;97:699-705.
-
(1996)
J Clin Invest
, vol.97
, pp. 699-705
-
-
Stratakis, C.A.1
Carney, J.A.2
Lin, J.P.3
Papanicolaou, D.A.4
Karl, M.5
Kastner, D.L.6
-
7
-
-
0032497947
-
Identification of a novel genetic locus for familial cardiac myxomas and Carney complex
-
Casey M, Mah C, Merliss AD, Kirschner LS, Taymans SE, Denio AE, et al: Identification of a novel genetic locus for familial cardiac myxomas and Carney complex. Circulation 1998;98:2560-2566.
-
(1998)
Circulation
, vol.98
, pp. 2560-2566
-
-
Casey, M.1
Mah, C.2
Merliss, A.D.3
Kirschner, L.S.4
Taymans, S.E.5
Denio, A.E.6
-
8
-
-
4244180319
-
Genetic heterogeneity in Carney complex (OMIM 160980): Contributions of loci at chromosomes 2 and 17 in its genetics
-
Stratakis CA, Kirschner LS, Taymans SE, Carney JA, Basson CT: Genetic heterogeneity in Carney complex (OMIM 160980): Contributions of loci at chromosomes 2 and 17 in its genetics. Am J Hum Genet 1999;65(suppl):A447.
-
(1999)
Am J Hum Genet
, vol.65
-
-
Stratakis, C.A.1
Kirschner, L.S.2
Taymans, S.E.3
Carney, J.A.4
Basson, C.T.5
-
9
-
-
0002221562
-
Familial acromegaly beyond MEN-1: Genetic and clinical studies in non-GHRH dependent somatomammotroph hyperplasia in patients with Carney complex or an inherited chromosome 11 inversion
-
New Orleans, La, June
-
Stratakis CA, Kirschner LS, Papanicolaou DA, Sarlis NJ, Raff S, Veldhuis JD, et al: Familial acromegaly beyond MEN-1: Genetic and clinical studies in non-GHRH dependent somatomammotroph hyperplasia in patients with Carney complex or an inherited chromosome 11 inversion. 80th Annual Meeting of the Endocrine Society, New Orleans, La, June 1998, P3-552.
-
(1998)
80th Annual Meeting of the Endocrine Society
-
-
Stratakis, C.A.1
Kirschner, L.S.2
Papanicolaou, D.A.3
Sarlis, N.J.4
Raff, S.5
Veldhuis, J.D.6
-
10
-
-
0034087332
-
Prolactin abnormalities in patients with the syndrome of spotty skin pigmentation, myxomas, endocrine overactivity, and skin myxomas (Carney complex)
-
Raff SB, Carney JA, Krugman D, Doppman JL, Stratakis CA: Prolactin abnormalities in patients with the syndrome of spotty skin pigmentation, myxomas, endocrine overactivity, and skin myxomas (Carney complex). J Pediatr Endocrinol Metab 2000;13:373-379.
-
(2000)
J Pediatr Endocrinol Metab
, vol.13
, pp. 373-379
-
-
Raff, S.B.1
Carney, J.A.2
Krugman, D.3
Doppman, J.L.4
Stratakis, C.A.5
-
11
-
-
0034002207
-
The neurosurgical implications of Carney complex
-
Watson JC, Stratakis CA, Bryant-Greenwood PK, Koch CA, Kirschner LS, et al: The neurosurgical implications of Carney complex. J Neurosurg 2000;92:413-418.
-
(2000)
J Neurosurg
, vol.92
, pp. 413-418
-
-
Watson, J.C.1
Stratakis, C.A.2
Bryant-Greenwood, P.K.3
Koch, C.A.4
Kirschner, L.S.5
-
12
-
-
0031690215
-
Evidence for a second genetic locus in Carney complex
-
Irvine AD, Armstrong DK, Bingham EA, Hadden DR, Nevin NC, Hughes AE: Evidence for a second genetic locus in Carney complex. Br J Dermatol 1998;139:572-576.
-
(1998)
Br J Dermatol
, vol.139
, pp. 572-576
-
-
Irvine, A.D.1
Armstrong, D.K.2
Bingham, E.A.3
Hadden, D.R.4
Nevin, N.C.5
Hughes, A.E.6
-
13
-
-
0026003074
-
Activating mutations of the stimulatory G protein in the McCune-Albright syndrome
-
Weinstein LS, Shenker A, Gejman PV, Merino MJ, Friedman E, Spiegel AM: Activating mutations of the stimulatory G protein in the McCune-Albright syndrome. N Engl J Med 1991;325:1688-1695.
-
(1991)
N Engl J Med
, vol.325
, pp. 1688-1695
-
-
Weinstein, L.S.1
Shenker, A.2
Gejman, P.V.3
Merino, M.J.4
Friedman, E.5
Spiegel, A.M.6
-
14
-
-
0028096993
-
Growth hormoneprolactin-thyrotropin-secreting pituitary adenoma in atypical McCune-Albright syndrome with functionally normal Gs_ protein
-
Gessl A, Freissmuth M, Czech T, Matula C, Hainfellner JA, Buchfelder M, et al: Growth hormoneprolactin-thyrotropin-secreting pituitary adenoma in atypical McCune-Albright syndrome with functionally normal Gs_ protein. J Clin Endocrinol Metab 1994;79:1128-1134.
-
(1994)
J Clin Endocrinol Metab
, vol.79
, pp. 1128-1134
-
-
Gessl, A.1
Freissmuth, M.2
Czech, T.3
Matula, C.4
Hainfellner, J.A.5
Buchfelder, M.6
-
15
-
-
0028337114
-
Acromegaly and hyperprolactinemia in a patient with polyostotic fibrous dysplasia: Dynamic endocrine studies and treatment with the somatostatin analogue octreotide
-
Garcia MB, Koppeschaar HIP, Lips CJ, Thijsen JH, Krenning EP: Acromegaly and hyperprolactinemia in a patient with polyostotic fibrous dysplasia: Dynamic endocrine studies and treatment with the somatostatin analogue octreotide. J Endocrinol Invest 1994;17:59-65.
-
(1994)
J Endocrinol Invest
, vol.17
, pp. 59-65
-
-
Garcia, M.B.1
Koppeschaar, H.I.P.2
Lips, C.J.3
Thijsen, J.H.4
Krenning, E.P.5
-
16
-
-
0024389295
-
Hypersecretion of growth hormone and prolactin in McCune-Albright syndrome
-
Cuttler L, Jackson JA, Uz-Zafar S, Levitsky LL, Mellinger RC, Frohman LA: Hypersecretion of growth hormone and prolactin in McCune-Albright syndrome. J Clin Endocrinol Metab 1989;68:1148-1154.
-
(1989)
J Clin Endocrinol Metab
, vol.68
, pp. 1148-1154
-
-
Cuttler, L.1
Jackson, J.A.2
Uz-Zafar, S.3
Levitsky, L.L.4
Mellinger, R.C.5
Frohman, L.A.6
-
17
-
-
0029838757
-
Cytogenetic and microsatellite alterations in tumors from patients with the syndrome of myxomas, spotty skin pigmentation and endocrine overactivity (Carney complex)
-
Stratakis CA, Jenkins RB, Pras E, Mitsiadis CS, Raff SB, Stalboerger PG, et al: Cytogenetic and microsatellite alterations in tumors from patients with the syndrome of myxomas, spotty skin pigmentation and endocrine overactivity (Carney complex). J Clin Endocrinol Metab 1996;81:3607-3614.
-
(1996)
J Clin Endocrinol Metab
, vol.81
, pp. 3607-3614
-
-
Stratakis, C.A.1
Jenkins, R.B.2
Pras, E.3
Mitsiadis, C.S.4
Raff, S.B.5
Stalboerger, P.G.6
-
18
-
-
8944258927
-
Sporadic cardiac myxomas and tumors from patients with Carney complex are not associated with activating mutations of the Gs_ gene
-
DeMarco L, Stratakis CA, Boson WL, Yakbovitz O, Carson E, Adrade LM, et al: Sporadic cardiac myxomas and tumors from patients with Carney complex are not associated with activating mutations of the Gs_ gene. Hum Genet 1996;98:185-188.
-
(1996)
Hum Genet
, vol.98
, pp. 185-188
-
-
Demarco, L.1
Stratakis, C.A.2
Boson, W.L.3
Yakbovitz, O.4
Carson, E.5
Adrade, L.M.6
-
19
-
-
0033812849
-
Mutations of the gene encoding the protein kinase A type I-_ regulatory subunit in patients with the Carney complex
-
Kirschner LS, Carney JA, Pack SD, Taymans SE, Giatzakis C, Cho YS, Cho-Chung YS, Stratakis CA: Mutations of the gene encoding the protein kinase A type I-_ 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
Taymans, S.E.4
Giatzakis, C.5
Cho, Y.S.6
Cho-Chung, Y.S.7
Stratakis, C.A.8
-
20
-
-
0034642302
-
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
-
21
-
-
0034853288
-
Clinical and molecular features of the Carney complex: Diagnostic criteria and recommendations for patient evaluation
-
Stratakis CA, Kirschner LS, Carney JA: Clinical and molecular features of the Carney complex: Diagnostic criteria and recommendations for patient evaluation. J Clin Endocrinol Metab 2001;86:4041-4046.
-
(2001)
J Clin Endocrinol Metab
, vol.86
, pp. 4041-4046
-
-
Stratakis, C.A.1
Kirschner, L.S.2
Carney, J.A.3
-
22
-
-
0038538463
-
Human tumors associated with Carney complex and germline PRKAR1A mutations: A protein kinase A disease!
-
Stergiopoulos S, Stratakis CA: Human tumors associated with Carney complex and germline PRKAR1A mutations: A protein kinase A disease! FEBS Lett 2003;546:59-64.
-
(2003)
FEBS Lett
, vol.546
, pp. 59-64
-
-
Stergiopoulos, S.1
Stratakis, C.A.2
-
23
-
-
0036907704
-
Molecular analysis of the cyclic AMP-dependent protein kinase A (PKA) regulatory subunit 1A (PRKAR1A) gene in patients with Carney complex and primary pigmented nodular adrenocortical disease (PPNAD)reveals novel mutations and clues for pathophysiology: Augmented PKA signaling is associated with adrenal tumorigenesis in PPNAD
-
Groussin L, Kirschner LS, Vincent-Dejean C, Perlemoine K, Jullian E, Delemer B, Zacharieva S, Pignatelli D, Carney JA, Luton JP, Bertagna X, Stratakis CA, Bertherat J: Molecular analysis of the cyclic AMP-dependent protein kinase A (PKA) regulatory subunit 1A (PRKAR1A) gene in patients with Carney complex and primary pigmented nodular adrenocortical disease (PPNAD)reveals novel mutations and clues for pathophysiology: Augmented PKA signaling is associated with adrenal tumorigenesis in PPNAD. Am J Hum Genet 2002;71:1433-1442.
-
(2002)
Am J Hum Genet
, vol.71
, pp. 1433-1442
-
-
Groussin, L.1
Kirschner, L.S.2
Vincent-Dejean, C.3
Perlemoine, K.4
Jullian, E.5
Delemer, B.6
Zacharieva, S.7
Pignatelli, D.8
Carney, J.A.9
Luton, J.P.10
Bertagna, X.11
Stratakis, C.A.12
Bertherat, J.13
-
24
-
-
0038335335
-
CAMP signaling in cancer genesis and treatment
-
Cho-Chung Y: cAMP signaling in cancer genesis and treatment. Cancer Treat Res 2003;115:123-143.
-
(2003)
Cancer Treat Res
, vol.115
, pp. 123-143
-
-
Cho-Chung, Y.1
-
25
-
-
0033767048
-
Genetic and histologic studies of somatomammotropic pituitary tumors in patients with the 'complex of spotty skin pigmentation, myxomas, endocrine overactivity and schwannomas' (Carney complex)
-
Pack SD, Kirschner LS, Pak E, Zhuang Z, Carney JA, Stratakis CA: Genetic and histologic studies of somatomammotropic pituitary tumors in patients with the 'complex of spotty skin pigmentation, myxomas, endocrine overactivity and schwannomas' (Carney complex). J Clin Endocrinol Metab 2000;85:3860-3865.
-
(2000)
J Clin Endocrinol Metab
, vol.85
, pp. 3860-3865
-
-
Pack, S.D.1
Kirschner, L.S.2
Pak, E.3
Zhuang, Z.4
Carney, J.A.5
Stratakis, C.A.6
-
26
-
-
12244284607
-
Pituitary adenoma in Carney complex: An immunohistochemical, ultrastructural and immunoelectron microscopic study
-
Kurtkaya-Yapicier O, Scheithauer BW, Carney JA, Kovacs K, Horvath E, Stratakis CA, Vidal S, Vella A, Young WF Jr, Atkinson JL, Lloyd RV, Kontogeorgos G: Pituitary adenoma in Carney complex: An immunohistochemical, ultrastructural and immunoelectron microscopic study. Ultrastruct Pathol 2002;26:345-353.
-
(2002)
Ultrastruct Pathol
, vol.26
, pp. 345-353
-
-
Kurtkaya-Yapicier, O.1
Scheithauer, B.W.2
Carney, J.A.3
Kovacs, K.4
Horvath, E.5
Stratakis, C.A.6
Vidal, S.7
Vella, A.8
Young Jr., W.F.9
Atkinson, J.L.10
Lloyd, R.V.11
Kontogeorgos, G.12
-
27
-
-
0027320997
-
Acromegaly with hyperprolactinemia developed after bilateral adrenalectomy in a patient with Cushing's syndrome due to adrenocortical nodular hyperplasia
-
Ogo A, Haji M, Natori S, Kanzaki T, Kabayama Y, Osamura RY, et al: Acromegaly with hyperprolactinemia developed after bilateral adrenalectomy in a patient with Cushing's syndrome due to adrenocortical nodular hyperplasia. Endocr J 1993;40:17-25.
-
(1993)
Endocr J
, vol.40
, pp. 17-25
-
-
Ogo, A.1
Haji, M.2
Natori, S.3
Kanzaki, T.4
Kabayama, Y.5
Osamura, R.Y.6
-
28
-
-
0032246451
-
The cytogenesis and pathogenesis of pituitary adenomas
-
Asa SL, Ezzat S: The cytogenesis and pathogenesis of pituitary adenomas. Endocr Rev 1998;19:798-827.
-
(1998)
Endocr Rev
, vol.19
, pp. 798-827
-
-
Asa, S.L.1
Ezzat, S.2
-
29
-
-
0037937433
-
Epigenetic change in pituitary tumorigenesis
-
Farrell WE, Clayton RN: Epigenetic change in pituitary tumorigenesis. Endocr Relat Cancer 2003;10:323-330.
-
(2003)
Endocr Relat Cancer
, vol.10
, pp. 323-330
-
-
Farrell, W.E.1
Clayton, R.N.2
-
30
-
-
0029090355
-
Two different pituitary adenomas in a patient with multiple endocrine neoplasia type 1 associated with growth hormonereleasing hormone-producing pancreatic tumor: Clinical and genetic features
-
Shintani Y, Yoshimoto K, Horie H, Sano T, Kanesaki Y, Hosoi E, et al: Two different pituitary adenomas in a patient with multiple endocrine neoplasia type 1 associated with growth hormonereleasing hormone-producing pancreatic tumor: Clinical and genetic features. Endocr J 1995;42:331-340.
-
(1995)
Endocr J
, vol.42
, pp. 331-340
-
-
Shintani, Y.1
Yoshimoto, K.2
Horie, H.3
Sano, T.4
Kanesaki, Y.5
Hosoi, E.6
-
31
-
-
0030835716
-
Thyroid gland abnormalities in patients with the 'syndrome of spotty skin pigmentation, myxomas, and endocrine overactivity'
-
Stratakis CA, Courcoutsakis NA, Abati A, Filie A, Doppman JL, Carney JA, Shawker T: Thyroid gland abnormalities in patients with the 'syndrome of spotty skin pigmentation, myxomas, and endocrine overactivity'. J Clin Endocrinol Metab 1997;82:2037-2043.
-
(1997)
J Clin Endocrinol Metab
, vol.82
, pp. 2037-2043
-
-
Stratakis, C.A.1
Courcoutsakis, N.A.2
Abati, A.3
Filie, A.4
Doppman, J.L.5
Carney, J.A.6
Shawker, T.7
-
32
-
-
0032697639
-
Paradoxical response to dexamethasone in the diagnosis of primary pigmented nodular adrenocortical disease
-
Stratakis CA, Sarlis N, Kirschner LS, Carney JA, Doppman JL, Nieman LK, et al: Paradoxical response to dexamethasone in the diagnosis of primary pigmented nodular adrenocortical disease. Ann Intern Med 1999;131:585-591.
-
(1999)
Ann Intern Med
, vol.131
, pp. 585-591
-
-
Stratakis, C.A.1
Sarlis, N.2
Kirschner, L.S.3
Carney, J.A.4
Doppman, J.L.5
Nieman, L.K.6
-
33
-
-
0021272053
-
Mammosomatotroph hyperplasia associated with acromegaly and hyperprolactinemia in a patient with the McCune-Albright syndrome
-
Kovacs K, Horvath E, Thomer MO, Rogol AD: Mammosomatotroph hyperplasia associated with acromegaly and hyperprolactinemia in a patient with the McCune-Albright syndrome. Virchows Arch Pathol Anat 1984;403:77-86.
-
(1984)
Virchows Arch Pathol Anat
, vol.403
, pp. 77-86
-
-
Kovacs, K.1
Horvath, E.2
Thomer, M.O.3
Rogol, A.D.4
-
34
-
-
0028941260
-
Growth hormone hypersecretion in a girl with McCune-Albright syndrome: Comparison with controls and response to a dose of long-acting somatostatin analog
-
Feuillan PP, Jones J, Ross JL: Growth hormone hypersecretion in a girl with McCune-Albright syndrome: Comparison with controls and response to a dose of long-acting somatostatin analog. J Clin Endocrinol Metab 1995;80:1357-1360.
-
(1995)
J Clin Endocrinol Metab
, vol.80
, pp. 1357-1360
-
-
Feuillan, P.P.1
Jones, J.2
Ross, J.L.3
-
35
-
-
0024065111
-
Growth hormone-releasing hormone-producing tumors: Clinical, biochemical and morphological manifestations
-
Sano T, Asa SL, Kovacs K: Growth hormone-releasing hormone-producing tumors: Clinical, biochemical and morphological manifestations. Endocr Rev 1988;9:357-373.
-
(1988)
Endocr Rev
, vol.9
, pp. 357-373
-
-
Sano, T.1
Asa, S.L.2
Kovacs, K.3
-
36
-
-
0028196956
-
Somatotroph hyperplasia without pituitary adenoma associated with a long-standing growth hormone-releasing hormone-producing bronchial carcinoid
-
Ezzat S, Asa SL, Stefaneanu L, Whittom R, Smyth HS, Horvath E, et al: Somatotroph hyperplasia without pituitary adenoma associated with a long-standing growth hormone-releasing hormone-producing bronchial carcinoid. J Clin Endocrinol Metab 1994;78:555-560.
-
(1994)
J Clin Endocrinol Metab
, vol.78
, pp. 555-560
-
-
Ezzat, S.1
Asa, S.L.2
Stefaneanu, L.3
Whittom, R.4
Smyth, H.S.5
Horvath, E.6
-
37
-
-
0027161684
-
Association of somatotrophinomas with loss of alleles on chromosome 11 and with gsp mutations
-
Thakker RV, Pook MA, Wooding C, Boscaro M, Scanarini M, Clayton RN: Association of somatotrophinomas with loss of alleles on chromosome 11 and with gsp mutations. J Clin Invest 1993;91:2815-2821.
-
(1993)
J Clin Invest
, vol.91
, pp. 2815-2821
-
-
Thakker, R.V.1
Pook, M.A.2
Wooding, C.3
Boscaro, M.4
Scanarini, M.5
Clayton, R.N.6
-
38
-
-
0031867878
-
Comparative genomic hybridization studies in tumours from a patient with multiple endocrine neoplasia type 1
-
Kytola S, Makinen MJ, Kahkonen M, Teh BT, Leisti J, Salmela P: Comparative genomic hybridization studies in tumours from a patient with multiple endocrine neoplasia type 1. Eur J Endocrinol 1998;139:202-206.
-
(1998)
Eur J Endocrinol
, vol.139
, pp. 202-206
-
-
Kytola, S.1
Makinen, M.J.2
Kahkonen, M.3
Teh, B.T.4
Leisti, J.5
Salmela, P.6
-
39
-
-
0026648941
-
Genetic alterations in the adenoma-carcinoma sequence
-
Cho KR, Vogelstein B: Genetic alterations in the adenoma-carcinoma sequence. Cancer 1992;70:1727-1731.
-
(1992)
Cancer
, vol.70
, pp. 1727-1731
-
-
Cho, K.R.1
Vogelstein, B.2
-
41
-
-
0029919109
-
Hereditary cancer: Two hits revisited
-
Knudson AG: Hereditary cancer: Two hits revisited. J Cancer Res Clin Oncol 1996;122:135-140.
-
(1996)
J Cancer Res Clin Oncol
, vol.122
, pp. 135-140
-
-
Knudson, A.G.1
-
42
-
-
0036886062
-
PRKAR1A, one of the Carney complex genes, and its locus (17q22-24) are rarely altered in pituitary tumours outside the Carney complex
-
Sandrini F, Kirschner LS, Bei T, Farmakidis C, Yasufuku-Takano J, Takano K, Prezant TR, Marx SJ, Farrell WE, Clayton RN, Groussin L, Bertherat J, Stratakis CA: PRKAR1A, one of the Carney complex genes, and its locus (17q22-24) are rarely altered in pituitary tumours outside the Carney complex. J Med Genet 2002;39:e78.
-
(2002)
J Med Genet
, vol.39
-
-
Sandrini, F.1
Kirschner, L.S.2
Bei, T.3
Farmakidis, C.4
Yasufuku-Takano, J.5
Takano, K.6
Prezant, T.R.7
Marx, S.J.8
Farrell, W.E.9
Clayton, R.N.10
Groussin, L.11
Bertherat, J.12
Stratakis, C.A.13
-
43
-
-
18644370689
-
Sequence analysis of the PRKAR1A gene in sporadic somatotroph and other pituitary tumours
-
Kaltsas GA, Kola B, Borboli N, Morris DG, Gueorguiev M, Swords FM, Czirjak S, Kirschner LS, Stratakis CA, Korbonits M, Grossman AB: Sequence analysis of the PRKAR1A gene in sporadic somatotroph and other pituitary tumours. Clin Endocrinol (Oxf) 2002;57:443-448.
-
(2002)
Clin Endocrinol (Oxf)
, vol.57
, pp. 443-448
-
-
Kaltsas, G.A.1
Kola, B.2
Borboli, N.3
Morris, D.G.4
Gueorguiev, M.5
Swords, F.M.6
Czirjak, S.7
Kirschner, L.S.8
Stratakis, C.A.9
Korbonits, M.10
Grossman, A.B.11
-
44
-
-
0037380199
-
GH-secreting pituitary adenomas infrequently contain inactivating mutations of PRKAR1A and LOH of 17q23-24
-
Yamasaki H, Mizusawa N, Nagahiro S, Yamada S, Sano T, Itakura M, Yoshimoto K: GH-secreting pituitary adenomas infrequently contain inactivating mutations of PRKAR1A and LOH of 17q23-24. Clin Endocrinol (Oxf) 2003;58:464-470.
-
(2003)
Clin Endocrinol (Oxf)
, vol.58
, pp. 464-470
-
-
Yamasaki, H.1
Mizusawa, N.2
Nagahiro, S.3
Yamada, S.4
Sano, T.5
Itakura, M.6
Yoshimoto, K.7
-
45
-
-
0031797339
-
The MEN-1 gene is rarely down-regulated in pituitary adenomas
-
Asa SL, Somers K, Ezzat S: The MEN-1 gene is rarely down-regulated in pituitary adenomas. J Clin Endocrinol Metab 1998;83:3210-3212.
-
(1998)
J Clin Endocrinol Metab
, vol.83
, pp. 3210-3212
-
-
Asa, S.L.1
Somers, K.2
Ezzat, S.3
|