-
1
-
-
0022397926
-
The complex of myxomas, spotty pigmentation and endocrine overactivity
-
Carney J.A., Gordon H., Carpenter P.C., Shenoy B.V., and Go V.L. The complex of myxomas, spotty pigmentation and endocrine overactivity. Medicine 64 (1985) 270-283
-
(1985)
Medicine
, vol.64
, pp. 270-283
-
-
Carney, J.A.1
Gordon, H.2
Carpenter, P.C.3
Shenoy, B.V.4
Go, V.L.5
-
2
-
-
0030049026
-
Carney Complex, a familial multiple neoplasia and lentiginosis syndrome. Analysis of 11 kindreds and linkage to the short arm of chromosome 2
-
Stratakis C.A., Carney J.A., Lin J.P., Papanicolaou D.A., Karl M., Kastner D.L., 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 97 (1996) 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
-
3
-
-
0033812849
-
Mutations of the gene encoding the protein kinase A type I-α regulatory subunit in patients with the Carney complex
-
Kirschner L.S., Carney J.A., Pack S.D., Taymans S.E., Giatzakis C., Cho Y.S., et al. Mutations of the gene encoding the protein kinase A type I-α regulatory subunit in patients with the Carney complex. Nat Genet 26 (2000) 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
-
4
-
-
9444247656
-
Minireview: PRKAR1A: normal and abnormal functions
-
Bossis I., and Stratakis C.A. Minireview: PRKAR1A: normal and abnormal functions. Endocrinology 145 (2004) 5452-5458
-
(2004)
Endocrinology
, vol.145
, pp. 5452-5458
-
-
Bossis, I.1
Stratakis, C.A.2
-
5
-
-
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 signalling is associated with adrenal tumorigenesis in PPNAD
-
Groussin L., Kirschner L.S., Vincent-Dejean C., Perlemoine K., Jullian E., Delemer B., et al. 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 signalling is associated with adrenal tumorigenesis in PPNAD. Am J Hum Genet 71 (2002) 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
-
6
-
-
0034853288
-
Genetics of endocrine disease. Clinical and molecular features of the Carney complex: diagnostic criteria and recommendations for patient evaluation
-
Stratakis C.A., Kirschner L.S., and Carney J.A. Genetics of endocrine disease. Clinical and molecular features of the Carney complex: diagnostic criteria and recommendations for patient evaluation. J Clin Endocrinol Metab 86 (2001) 4041-4046
-
(2001)
J Clin Endocrinol Metab
, vol.86
, pp. 4041-4046
-
-
Stratakis, C.A.1
Kirschner, L.S.2
Carney, J.A.3
-
8
-
-
0023882897
-
The validity and practicality of sun reaction skin types I through VI
-
Fitzpatrick T.B. The validity and practicality of sun reaction skin types I through VI. Arch Dermatol 124 (1988) 869-871
-
(1988)
Arch Dermatol
, vol.124
, pp. 869-871
-
-
Fitzpatrick, T.B.1
-
9
-
-
0030049959
-
The epithelioid blue nevus. a multicentric, familial tumour with important associations, including cardiac myxoma and psammomatous melanotic schwannoma
-
Carney J.A., and Ferreiro J.A. The epithelioid blue nevus. a multicentric, familial tumour with important associations, including cardiac myxoma and psammomatous melanotic schwannoma. Am J Surg Pathol 20 (1996) 259-272
-
(1996)
Am J Surg Pathol
, vol.20
, pp. 259-272
-
-
Carney, J.A.1
Ferreiro, J.A.2
-
10
-
-
0024853439
-
Familial Cushing's syndrome due to primary pigmented nodular adrenocortical disease: reinvestigation 50 years later
-
Young W.F., Carney J.A., Musa B.U., Wulffraat N.M., Lens J.W., and Drexhage H.M. Familial Cushing's syndrome due to primary pigmented nodular adrenocortical disease: reinvestigation 50 years later. N Engl J Med 321 (1989) 1659-1664
-
(1989)
N Engl J Med
, vol.321
, pp. 1659-1664
-
-
Young, W.F.1
Carney, J.A.2
Musa, B.U.3
Wulffraat, N.M.4
Lens, J.W.5
Drexhage, H.M.6
-
11
-
-
0347419011
-
Pigmented epithelioid melanocytoma, a low grade melanocytic tumor with metastatic potential indistinguishable from animal-type melanoma and epithelioid blue nevus
-
Zembowicz A., Carney J.A., and Mihm M.C. Pigmented epithelioid melanocytoma, a low grade melanocytic tumor with metastatic potential indistinguishable from animal-type melanoma and epithelioid blue nevus. Am J Surg Pathol 28 (2004) 31-40
-
(2004)
Am J Surg Pathol
, vol.28
, pp. 31-40
-
-
Zembowicz, A.1
Carney, J.A.2
Mihm, M.C.3
-
12
-
-
0034642302
-
Genetic heterogeneity and spectrum of mutations of the PRKAR1A gene in patients with the Carney complex
-
Kirschner L.S., Sandrini F., Monbo J., Lin J.P., Carney J.A., and Stratakis C.A. Genetic heterogeneity and spectrum of mutations of the PRKAR1A gene in patients with the Carney complex. Hum Mol Genet 9 (2000) 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
-
13
-
-
33646427720
-
A PRKAR1A mutation associated with primary pigmented nodular adrenocortical disease in 12 kindreds
-
Groussin L., Horvath A., Jullian E., Boikos S., Rene-Corail F., Lefebvre H., et al. A PRKAR1A mutation associated with primary pigmented nodular adrenocortical disease in 12 kindreds. J Clin Endocrinol Metab 91 (2006) 1943-1949
-
(2006)
J Clin Endocrinol Metab
, vol.91
, pp. 1943-1949
-
-
Groussin, L.1
Horvath, A.2
Jullian, E.3
Boikos, S.4
Rene-Corail, F.5
Lefebvre, H.6
-
14
-
-
15444365234
-
Role of G protein-coupled receptor kinases in the homologous desensitization of the human and mouse melanocortin 1 receptors
-
Sanchez-Mas J., Guillo L.A., Zanna P., Jimenez-Cervantes C., and Garcia-Borron J.C. Role of G protein-coupled receptor kinases in the homologous desensitization of the human and mouse melanocortin 1 receptors. Mol Endocrinol 19 (2005) 1035-1048
-
(2005)
Mol Endocrinol
, vol.19
, pp. 1035-1048
-
-
Sanchez-Mas, J.1
Guillo, L.A.2
Zanna, P.3
Jimenez-Cervantes, C.4
Garcia-Borron, J.C.5
-
15
-
-
0034127724
-
Cyclic AMP a key messenger in the regulation of skin pigmentation
-
Busca R., and Ballotti R. Cyclic AMP a key messenger in the regulation of skin pigmentation. Pigment Cell Res 13 (2000) 60-69
-
(2000)
Pigment Cell Res
, vol.13
, pp. 60-69
-
-
Busca, R.1
Ballotti, R.2
-
16
-
-
0038105075
-
Protein kinase-A activity in PRKAR1A-mutant cells, and regulation of mitogen-activated protein kinases ERK1/2
-
Robinson-White A., Hundley T.R., Shiferaw M., Bertherat J., Sandrini F., and Stratakis C.A. Protein kinase-A activity in PRKAR1A-mutant cells, and regulation of mitogen-activated protein kinases ERK1/2. Hum Mol Genet 12 (2003) 1475-1484
-
(2003)
Hum Mol Genet
, vol.12
, pp. 1475-1484
-
-
Robinson-White, A.1
Hundley, T.R.2
Shiferaw, M.3
Bertherat, J.4
Sandrini, F.5
Stratakis, C.A.6
-
17
-
-
0037331680
-
Clinical and molecular genetics of Carney complex
-
Sandrini F., and Stratakis C. Clinical and molecular genetics of Carney complex. Mol Gen Metabol 78 (2003) 83-92
-
(2003)
Mol Gen Metabol
, vol.78
, pp. 83-92
-
-
Sandrini, F.1
Stratakis, C.2
-
18
-
-
0037389713
-
Chromosome 2 (2p16) abnormalities in Carney Complex tumours
-
Matyakhina L., Pack S., Kirschner L.S., Pak E., Mannan P., Jaikumar J., et al. Chromosome 2 (2p16) abnormalities in Carney Complex tumours. J Med Genet 40 (2003) 268-277
-
(2003)
J Med Genet
, vol.40
, pp. 268-277
-
-
Matyakhina, L.1
Pack, S.2
Kirschner, L.S.3
Pak, E.4
Mannan, P.5
Jaikumar, J.6
-
19
-
-
23044468132
-
The Carney complex: unusual skin findings and recurrent cardiac myxoma
-
Bennett K.R., Heath B.J., Creswell L.L., Veugelers M.A., McDermott D.A., Barksdale S., et al. The Carney complex: unusual skin findings and recurrent cardiac myxoma. Arch Dermatol 141 (2005) 916-918
-
(2005)
Arch Dermatol
, vol.141
, pp. 916-918
-
-
Bennett, K.R.1
Heath, B.J.2
Creswell, L.L.3
Veugelers, M.A.4
McDermott, D.A.5
Barksdale, S.6
-
20
-
-
27744531210
-
The lentiginoses: cutaneous markers of systemic disease and a window to new aspects of tumourigenesis
-
Bauer A.J., and Stratakis C.A. The lentiginoses: cutaneous markers of systemic disease and a window to new aspects of tumourigenesis. J Med Genet 42 (2005) 801-810
-
(2005)
J Med Genet
, vol.42
, pp. 801-810
-
-
Bauer, A.J.1
Stratakis, C.A.2
-
21
-
-
33749000851
-
Depletion of the type IA regulatory subunit (RIalpha) of protein kinase A (PKA) in mammalian cells and tissues activates mTOR and causes autophagic deficiency
-
Mavrakis K., Lippincott-Schwartz J., Stratakis C.A., and Bossis I. Depletion of the type IA regulatory subunit (RIalpha) of protein kinase A (PKA) in mammalian cells and tissues activates mTOR and causes autophagic deficiency. Hum Mol Genet 15 (2006) 2962-2971
-
(2006)
Hum Mol Genet
, vol.15
, pp. 2962-2971
-
-
Mavrakis, K.1
Lippincott-Schwartz, J.2
Stratakis, C.A.3
Bossis, I.4
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