Found: 28
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Bone-targeting agents in prostate cancer.
- Published in:
- Cancer & Metastasis Reviews, 2014, v. 33, n. 2/3, p. 619, doi. 10.1007/s10555-013-9480-2
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- Publication type:
- Article
A genome-wide scan identifies mutations in the gene encoding phosphodiesterase 11A4 (PDE11A) in individuals with adrenocortical hyperplasia.
- Published in:
- Nature Genetics, 2006, v. 38, n. 7, p. 794, doi. 10.1038/ng1809
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- Publication type:
- Article
Association of the M1V PRKAR1A mutation with primary pigmented nodular adrenocortical disease in two large families.
- Published in:
- 2010
- By:
- Publication type:
- journal article
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.
- Published in:
- 2009
- By:
- Publication type:
- journal article
Mutations in regulatory subunit type 1A of cyclic adenosine 5'-monophosphate-dependent protein kinase (PRKAR1A): phenotype analysis in 353 patients and 80 different genotypes.
- Published in:
- 2009
- By:
- Publication type:
- journal article
Multiple Gastrointestinal Stromal and Other Tumors Caused by Platelet-Derived Growth Factor Receptor α Gene Mutations: A Case Associated with a Germline V561D Defect.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2007, v. 92, n. 9, p. 3728, doi. 10.1210/jc.2007-0894
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- Publication type:
- Article
Genetics of Carney Triad: Recurrent Losses at Chromosome 1 but Lack of Germline Mutations in Genes Associated with Paragangliomas and Gastrointestinal Stromal Tumors.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2007, v. 92, n. 8, p. 2938, doi. 10.1210/jc.2007-0797
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- Publication type:
- Article
17q22–24 Chromosomal Losses and Alterations of Protein Kinase A Subunit Expression and Activity in Adrenocorticotropin-Independent Macronodular Adrenal Hyperplasia.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2006, v. 91, n. 9, p. 3626, doi. 10.1210/jc.2005-2608
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- Publication type:
- Article
PRKAR1A Mutations and Protein Kinase A Interactions with Other Signaling Pathways in the Adrenal Cortex.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2006, v. 91, n. 6, p. 2380, doi. 10.1210/jc.2006-0188
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- Publication type:
- Article
A PRKAR1A Mutation Associated with Primary Pigmented Nodular Adrenocortical Disease in 12 Kindreds.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2006, v. 91, n. 5, p. 1943, doi. 10.1210/jc.2005-2708
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- Publication type:
- Article
Pituitary pathology in patients with Carney Complex: growth-hormone producing hyperplasia or tumors and their association with other abnormalities.
- Published in:
- Pituitary, 2006, v. 9, n. 3, p. 203, doi. 10.1007/s11102-006-0265-2
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- Publication type:
- Article
Unmasking BCL-2 Addiction in Synovial Sarcoma by Overcoming Low NOXA.
- Published in:
- Cancers, 2021, v. 13, n. 10, p. 2310, doi. 10.3390/cancers13102310
- By:
- Publication type:
- Article
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.
- Published in:
- European Journal of Human Genetics, 2008, v. 16, n. 10, p. 1245, doi. 10.1038/ejhg.2008.85
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- Publication type:
- Article
Clinical and molecular genetics of patients with the Carney–Stratakis syndrome and germline mutations of the genes coding for the succinate dehydrogenase subunits SDHB, SDHC, and SDHD.
- Published in:
- European Journal of Human Genetics, 2008, v. 16, n. 1, p. 79, doi. 10.1038/sj.ejhg.5201904
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- Publication type:
- Article
Known VDR polymorphisms are not associated with bone mineral density measures in pediatric Cushing disease.
- Published in:
- Journal of Pediatric Endocrinology & Metabolism, 2012, v. 25, n. 1/2, p. 221, doi. 10.1515/jpem-2011-0364
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- Publication type:
- Article
A Reappraisal of Superficial Pleomorphic Liposarcoma.
- Published in:
- 2020
- By:
- Publication type:
- journal article
Recurrent epimutation of SDHC in gastrointestinal stromal tumors.
- Published in:
- Science Translational Medicine, 2014, v. 6, n. 268, p. 1, doi. 10.1126/scitranslmed.3009961
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- Publication type:
- Article
Advances and Challenges on Management of Gastrointestinal Stromal Tumors.
- Published in:
- Frontiers in Oncology, 2018, p. 1, doi. 10.3389/fonc.2018.00135
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- Publication type:
- Article
Immunotherapy for Prostate Cancer Enters Its Golden Age.
- Published in:
- Clinical Medicine Insights: Oncology, 2012, n. 6, p. 263, doi. 10.4137/CMO.S7475
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- Publication type:
- Article
Immunotherapy for Prostate Cancer Enters Its Golden Age.
- Published in:
- Clinical Medicine Insights: Oncology, 2012, n. 6, p. 263, doi. 10.4137/CMO.S7475
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- Publication type:
- Article
The genetic landscape of gastrointestinal stromal tumor lacking KIT and PDGFRA mutations.
- Published in:
- Endocrine (1355008X), 2014, v. 47, n. 2, p. 401, doi. 10.1007/s12020-014-0346-3
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- Publication type:
- Article
Molecular and immunohistochemical investigation of protein kinase a regulatory subunit type 1A (PRKAR1A) in odontogenic myxomasThis article is a US Government work and, as such, is in the public domain in the United States of America.
- Published in:
- Genes, Chromosomes & Cancer, 2005, v. 44, n. 2, p. 204
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- Publication type:
- Article
Carney Complex: Pathology and Molecular Genetics.
- Published in:
- Neuroendocrinology, 2006, v. 83, n. 3/4, p. 189, doi. 10.1159/000095527
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- Publication type:
- Article
Mouse Prkar1a haploinsufficiency leads to an increase in tumors in the Trp53+/− or Rb1+/− backgrounds and chemically induced skin papillomas by dysregulation of the cell cycle and Wnt signaling.
- Published in:
- Human Molecular Genetics, 2010, v. 19, n. 8, p. 1387, doi. 10.1093/hmg/ddq014
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- Publication type:
- Article
Molecular genetics of the cAMP-dependent protein kinase pathway and of sporadic pituitary tumorigenesis.
- Published in:
- Human Molecular Genetics, 2007, v. 16, n. R1, p. R80, doi. 10.1093/hmg/ddm019
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- Publication type:
- Article
The cytologic features of primary pseudomyogenic hemangioendothelioma of bone.
- Published in:
- Diagnostic Cytopathology, 2021, v. 49, n. 12, p. 1261, doi. 10.1002/dc.24887
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- Publication type:
- Article
Novel polymorphisms and lack of mutations in the ACD gene in patients with ACTH resistance syndromes.
- Published in:
- Clinical Endocrinology, 2007, v. 67, n. 2, p. 168, doi. 10.1111/j.1365-2265.2007.02855.x
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- Publication type:
- Article
Differences in cortisol levels and body mass index between East Asians and Caucasians with Cushing's syndrome: an ‘East Asian’ phenotype for Cushing syndrome.
- Published in:
- 2007
- By:
- Publication type:
- Letter