Adrenal Cancer
What's New
Last Posted: Mar 15, 2023
- Elevated sphingosine-1-phosphate lyase leads to increased metabolism and reduced survival in adrenocortical carcinoma.
Williams Jack L, et al. European journal of endocrinology 2023 0 (1) - A transcriptional MAPK Pathway Activity Score (MPAS) is a clinically relevant biomarker in multiple cancer types.
Wagle Marie-Claire et al. NPJ precision oncology 2018 2(1) 7 - Molecular screening for a personalized treatment approach in advanced adrenocortical cancer.
De Martino Maria Cristina, et al. The Journal of clinical endocrinology and metabolism 2013 10 (10) 4080-8 - TMEM127 screening in a large cohort of patients with pheochromocytoma and/or paraganglioma.
Abermil Nassera, et al. The Journal of clinical endocrinology and metabolism 2012 5 (5) E805-9 - Pancreatic ductal and acinar cell neoplasms in Carney complex: a possible new association.
Gaujoux Sébastien, et al. The Journal of clinical endocrinology and metabolism 2011 11 (11) E1888-95 - Adrenal cancer
From NCATS Genetic and Rare Diseases Information Center - Isocitrate dehydrogenase mutations are rare in pheochromocytomas and paragangliomas.
Gaal José, et al. The Journal of clinical endocrinology and metabolism 2010 3 (3) 1274-8 - Prevalence of HLA-DRB1 genotype and altered Fas/Fas ligand expression in adrenocortical carcinoma.
Wolkersdörfer Gernot W, et al. The Journal of clinical endocrinology and metabolism 2005 3 (3) 1768-74
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Rare Disease PHGKB is an online, continuously updated, searchable database of published scientific literature, CDC and NIH resources, and other information that address the public health impact and translation of genomic and other precision health discoveries into improved health outcomes related to rare diseases...more
Content Summary
Selected Rare Diseases
- Alpha-1 Antitrypsin Deficiency
- Amyotrophic Lateral Sclerosis
- Brugada Syndrome
- Cerebral Palsy
- Cystic Fibrosis
- Duchenne Muscular Dystrophy
- Eclampsia
- Erythema Multiforme
- Familial Mediterranean Fever
- Fragile X Syndrome
- Gaucher Disease
- Glomerulonephritis
- Graves Disease
- Hemophilia
- Huntington Disease
- Microcephaly
- Myasthenia Gravis
- Phenylketonuria
- Retinitis Pigmentosa
- Severe Combined Immunodeficiency
Disclaimer: Articles listed in the Public Health Knowledge Base are selected by the CDC Office of Public Health Genomics to provide current awareness of the literature and news. Inclusion in the update does not necessarily represent the views of the Centers for Disease Control and Prevention nor does it imply endorsement of the article's methods or findings. CDC and DHHS assume no responsibility for the factual accuracy of the items presented. The selection, omission, or content of items does not imply any endorsement or other position taken by CDC or DHHS. Opinion, findings and conclusions expressed by the original authors of items included in the update, or persons quoted therein, are strictly their own and are in no way meant to represent the opinion or views of CDC or DHHS. References to publications, news sources, and non-CDC Websites are provided solely for informational purposes and do not imply endorsement by CDC or DHHS.
- Page last reviewed:Feb 1, 2023
- Page last updated:Mar 28, 2023
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