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Results: 1-18 |
Results: 18
Genetics of endocrine disease - Clinical and molecular features of the Carney complex: Diagnostic criteria and recommendations for patient evaluation
Authors: Stratakis, CA Kirschner, LS Carney, JA
Citation: Ca. Stratakis et al., Genetics of endocrine disease - Clinical and molecular features of the Carney complex: Diagnostic criteria and recommendations for patient evaluation, J CLIN END, 86(9), 2001, pp. 4041-4046
Spectrum of mutations of the AAAS gene in Allgrove syndrome: Lack of mutations in six kindreds with isolated resistance to corticotropin
Authors: Sandrini, F Farmakidis, C Kirschner, LS Wu, SM Tullio-Pelet, A Lyonnet, S Metzger, DL Bourdony, CJ Tiosano, D Chan, WY Stratakis, CA
Citation: F. Sandrini et al., Spectrum of mutations of the AAAS gene in Allgrove syndrome: Lack of mutations in six kindreds with isolated resistance to corticotropin, J CLIN END, 86(11), 2001, pp. 5433-5437
Mutations of the gene encoding the protein kinase A type I-alpha regulatory subunit in patients with the Carney complex
Authors: Kirschner, LS Carney, JA Pack, SD Taymans, SE Giatzakis, C Cho, YS Cho-Chung, YS Stratakis, CA
Citation: Ls. Kirschner et al., Mutations of the gene encoding the protein kinase A type I-alpha regulatory subunit in patients with the Carney complex, NAT GENET, 26(1), 2000, pp. 89-92
Genetic heterogeneity and spectrum of mutations of the PRKAR1A gene in patients with the Carney complex
Authors: Kirschner, LS Sandrini, F Monbo, J Lin, JP Carney, JA Stratakis, CA
Citation: Ls. Kirschner et al., Genetic heterogeneity and spectrum of mutations of the PRKAR1A gene in patients with the Carney complex, HUM MOL GEN, 9(20), 2000, pp. 3037-3046
Neurosurgical implications of Carney complex
Authors: Watson, JC Stritakis, CA Bryant-Greenwood, PK Koch, CA Kirschner, LS Nguyen, T Carney, JA Oldfield, EH
Citation: Jc. Watson et al., Neurosurgical implications of Carney complex, J NEUROSURG, 92(3), 2000, pp. 413-418
Isolated familial somatotropinomas: Does the disease map to 11q13 or to 2p16?
Authors: Stratakis, CA Kirschner, LS
Citation: Ca. Stratakis et Ls. Kirschner, Isolated familial somatotropinomas: Does the disease map to 11q13 or to 2p16?, J CLIN END, 85(12), 2000, pp. 4920-4920
Ovarian lesions in Carney complex: Clinical genetics and possible predisposition to malignancy
Authors: Stratakis, CA Papageorgiou, T Premkumar, A Pack, S Kirschner, LS Taymans, SE Zhuang, ZP Oelkers, WH Carney, JA
Citation: Ca. Stratakis et al., Ovarian lesions in Carney complex: Clinical genetics and possible predisposition to malignancy, J CLIN END, 85(11), 2000, pp. 4359-4366
Genetic and histologic studies of somatomammotropic pituitary tumors in patients with the "complex of spotty skin pigmentation, myxomas, endocrine overactivity and schwannomas" (Carney complex)
Authors: Pack, SD Kirschner, LS Pak, E Zhuang, ZP Carney, JA Stratakis, CA
Citation: Sd. Pack et al., 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 END, 85(10), 2000, pp. 3860-3865
Structure of the human ubiquitin fusion gene Uba80 (RPS27a) and one of itspseudogenes
Authors: Kirschner, LS Stratakis, CA
Citation: Ls. Kirschner et Ca. Stratakis, Structure of the human ubiquitin fusion gene Uba80 (RPS27a) and one of itspseudogenes, BIOC BIOP R, 270(3), 2000, pp. 1106-1110
Adipose S14 mRNA is abnormally regulated in obese subjects
Authors: Kirschner, LS Mariash, CN
Citation: Ls. Kirschner et Cn. Mariash, Adipose S14 mRNA is abnormally regulated in obese subjects, THYROID, 9(2), 1999, pp. 143-148
Genomic mapping of chromosomal region 2p15-p21 (D2S378-D2S391): Integration of Genemap'98 within a framework of yeast and bacterial artificial chromosomes
Authors: Kirschner, LS Taymans, SE Pack, S Pak, E Pike, BL Chandrasekharappa, SC Zhuang, ZP Stratakis, CA
Citation: Ls. Kirschner et al., Genomic mapping of chromosomal region 2p15-p21 (D2S378-D2S391): Integration of Genemap'98 within a framework of yeast and bacterial artificial chromosomes, GENOMICS, 62(1), 1999, pp. 21-33
Radiation hybrid mapping of chromosomal region 2p15-p16: Integration of expressed and polymorphic sequences maps at the Carney complex (CNC) and Doyne honeycomb retinal dystrophy (DHRD) loci
Authors: Taymans, SE Kirschner, LS Giatzakis, C Stratakis, CA
Citation: Se. Taymans et al., Radiation hybrid mapping of chromosomal region 2p15-p16: Integration of expressed and polymorphic sequences maps at the Carney complex (CNC) and Doyne honeycomb retinal dystrophy (DHRD) loci, GENOMICS, 56(3), 1999, pp. 344-349
Large-scale preparation of sequence-ready bacterial artificial chromosome DNA using QIAGEN (R) columns
Authors: Kirschner, LS Stratakis, CA
Citation: Ls. Kirschner et Ca. Stratakis, Large-scale preparation of sequence-ready bacterial artificial chromosome DNA using QIAGEN (R) columns, BIOTECHNIQU, 27(1), 1999, pp. 72
Synaptophysin immunoreactivity in primary pigmented nodular adrenocorticaldisease: Neuroendocrine properties of tumors associated with Carney complex
Authors: Stratakis, CA Carney, JA Kirschner, LS Willenberg, HS Brauer, S Ehrhart-Bornstein, M Bornstein, SR
Citation: Ca. Stratakis et al., Synaptophysin immunoreactivity in primary pigmented nodular adrenocorticaldisease: Neuroendocrine properties of tumors associated with Carney complex, J CLIN END, 84(3), 1999, pp. 1122-1128
Cloning and characterization of a novel orphan G-protein-coupled receptor localized to human chromosome 2p16
Authors: Tarttelin, EE Kirschner, LS Bellingham, J Baffi, J Taymans, SE Gregory-Evans, K Csaky, K Stratakis, CA Gregory-Evans, CY
Citation: Ee. Tarttelin et al., Cloning and characterization of a novel orphan G-protein-coupled receptor localized to human chromosome 2p16, BIOC BIOP R, 260(1), 1999, pp. 174-180
Paradoxical response to dexamethasone in the diagnosis of primary pigmented nodular adrenocortical disease
Authors: Stratakis, CA Sarlis, N Kirschner, LS Carney, JA Doppman, JL Nieman, LK Chrousos, GP Papanicolaou, DA
Citation: Ca. Stratakis et al., Paradoxical response to dexamethasone in the diagnosis of primary pigmented nodular adrenocortical disease, ANN INT MED, 131(8), 1999, pp. 585
Characterization of the adrenal gland pathology of Carney complex, and molecular genetics of the disease.
Authors: Kirschner, LS Taymans, SE Stratakis, CA
Citation: Ls. Kirschner et al., Characterization of the adrenal gland pathology of Carney complex, and molecular genetics of the disease., ENDOCRINE R, 24(3-4), 1998, pp. 863-864
Identification of a novel genetic locus for familial cardiac myxomas and Carney complex
Authors: Casey, M Mah, C Merliss, AD Kirschner, LS Taymans, SE Denio, AE Korf, B Irvine, AD Hughes, A Carney, JA Stratakis, CA Basson, CT
Citation: M. Casey et al., Identification of a novel genetic locus for familial cardiac myxomas and Carney complex, CIRCULATION, 98(23), 1998, pp. 2560-2566
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