The Wayback Machine - https://web.archive.org/web/20200618081132/https://academic.oup.com/jes
Skip to Main Content

Latest Published Articles

Primary Adrenal Leiomyosarcoma: Clinical, Radiological, and Histopathological Characteristics
Fatema Jabarkhel et al.
Abstract Primary adrenal leiomyosarcoma (PAL) is a rare, high-grade proliferating mesenchymal tumor with a considerable risk of metastasis, deriving from the smooth muscle wall of a central adrenal vein, or its tributaries. Roughly 40 patients with PAL have been reported in the literature. Herein, we present 3 patients ...
The Importance of Natriuretic Peptides in Cardiometabolic Diseases
Shravya Vinnakota, Horng H Chen
Abstract The natriuretic peptide (NP) system is composed of 3 distinct peptides (atrial natriuretic peptide or ANP, B-type natriuretic peptide or BNP, and C-type natriuretic peptide or CNP) and 3 receptors (natriuretic peptide receptor-A or NPR-A or particulate guanynyl cyclase-A natriuretic peptide receptor-B or NPR-B or ...
Dissection of Clinical and Gene Expression Signatures of Familial versus Multifactorial Chylomicronemia
Karine Tremblay et al.
Abstract Familial chylomicronemia syndrome (FCS) is a rare disorder associated with chylomicronemia (CM) and an increased risk of pancreatitis. Most individuals with CM do not have FCS but exhibit multifactorial CM (MCM), which differs from FCS in terms of risk and disease management. This study aimed to investigate ...
Risk of Islet and Celiac Autoimmunity in Cotwins of Probands With Type 1 Diabetes
Taylor M Triolo et al.
Abstract Context Concordance for persistent islet autoimmunity (IA) and type 1 diabetes in monozygotic twins after probands are diagnosed is variable (30%-70%). Risk for development of IA in dizygotic twins is thought to be similar to nontwin siblings. Little is known in regard to the development of celiac autoimmunity ...
SUN-284 Rare Case of Adipsic Diabetes Insipidus Post Astrocytoma Resection: Case Report
Alanoud Alanazi, MD, MBBS et al.
Abstract Background: Adipsic diabetes insipidus (ADI) is a rare disorder triggered by injury to the hypothalamus impairing thirst osmoreceptors and the antidiuretic hormone syntheses leading to absence of thirst. We are reporting a rare case of ADI Post astrocytoma resection who presented with a severe hypernatremia ...
SUN-198 Metastatic Progression of Adrenocortical Carcinoma: Phenotypic Transformation to ACTH-Independent Cushing’s Syndrome
Javier Ocampo, MD et al.
Abstract Background : Adrenocortical carcinoma (ACC) is a rare malignancy. Around 60% of adrenal carcinomas are functioning tumors and may present with distinctive phenotypes (1). Very rarely, as the disease progresses, changes in secretory patterns may be observed. Clinical Case : A 39-year-old female presented to the ...
SUN-LB52 The Protective Effects of Hepatocyte GH Receptor (GHR) Signaling Against Steatosis and Liver Injury Is Sexually Dimorphic and Autonomous of IGF1
Andre Sarmento-Cabral, PhD et al.
Abstract GH dysregulation contributes to the development of non-alcoholic fatty liver disease (NAFLD), however debate remains as to the relative contribution of the direct vs indirect effects of GH, via IGF1. Mouse models with congenital, liver-specific knockout of the GHR, JAK2 or STAT5, as adults exhibit steatosis, ...
MON-LB84 Validation of TI-RADS (Thyroid Imaging, Reporting and Data System) Follow-Up Recommendations
Sindhura Ravindra, MD et al.
Abstract Background: Thyroid nodules are exceedingly common, leading to costly interventions for many lesions that ultimately prove benign. Therefore, a reliable, noninvasive method to identify which nodules warrant fine needle aspiration and/or follow-up on the basis of a reasonable likelihood of malignancy is highly ...
SAT-718 Inhibition of Androgen Receptor Activity by DDE Is Affected by Mutations in the BF3 Site
Andrea Lozano, BS et al.
Abstract The androgen receptor (AR) plays an important role in the development of the male phenotype and traits. Some diphenyl compounds inhibit AR activity by binding to a hydrophobic surface binding site, BF3. A similar diphenyl structure is found in 4,4’ DDT and its breakdown product 4,4’ DDE. Previous results showed ...
SAT-173 SAMD9 (Sterile Alpha Motif Domain-Containing 9) Expression in Adrenocortical Tumors
Ana C Bueno, PhD et al.
Abstract Introduction : SAMD9 variants are associated with colon, breast and lung tumors. SAMD9 mutations result in adrenal hypoplasia, suggesting its importance in adrenal development. We investigated the contribution of abnormal expression of SAMD9 and its homologous, SAMD9L , to the pathogenesis of pediatric ...

JES now featured in ESCI

Journal of the Endocrine Society (JES) is included in the Emerging Sources Citation Index (ESCI), part of the Core Collection of the Clarivate Web of Science. JES’s inclusion enhances its visibility and discoverability.

JES articles in PMC

Journal of the Endocrine Society (JES) is now available as full text from PubMed Central, the Library's archive of open access articles. All JES articles are deposited immediately upon publication in their final form. Subsequently they will also be listed in PubMed and receive PMIDs.

Why publish in JES?

J. Larry Jameson, MD, PhD, Editor-in-Chief, discusses the benefits of publishing open access in Journal of the Endocrine Society (JES). JES invites submissions in all areas of basic, translational, and clinical endocrinology. Article types include original research, methods & tools, databases, and images. Submit your paper or preprint today.

ORCiD

All submitting authors are required to provide an ORCiD (Open Researcher and Contributor ID) when uploading a manuscript. An author identification registry, ORCiD allows you to be uniquely identified with your work by eliminating name ambiguity. Register for free today!

Alerts in the Inbox

Sign up for Alerts

Register to receive email alerts as soon as new Journal of the Endocrine Society articles are published online.

Committee on Publication Ethics

JES is a member of and subscribes to the principles of the Committee on Publication Ethics (COPE).

Benefits of Open Access

Read about OUP's expertise in both gold and green Open Access models. Journal of the Endocrine Society is listed in the Directory of Open Access Journals, a curated online directory of high quality, open access, peer-reviewed journals.

Close
This Feature Is Available To Subscribers Only

Sign In or Create an Account

Close

This PDF is available to Subscribers Only

View Article Abstract & Purchase Options

For full access to this pdf, sign in to an existing account, or purchase an annual subscription.

Close