Journal of Endocrinology And Hormones

Journal of Endocrinology And Hormones

Journal of Endocrinology And Hormones – Aim And Scope

Open Access & Peer-Reviewed

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Aims & Scope

Journal of Endocrinology and Hormones (JEH) publishes mechanistic research elucidating the molecular and cellular pathways underlying endocrine disorders and hormonal dysregulation. We focus on pathophysiological mechanisms, biomarker discovery, and disease models-not clinical management or therapeutic protocols.

Hormone Signaling Pathways Endocrine Pathophysiology Molecular Mechanisms Disease Biomarkers Cellular Models

Core Research Domains

Hormone Signaling Mechanisms Tier 1

  • Receptor-ligand interactions and downstream signaling cascades
  • Post-translational modifications in hormone signaling
  • Cross-talk between endocrine and metabolic pathways
  • Molecular mechanisms of hormone resistance
  • Epigenetic regulation of hormone receptor expression
  • Cellular models of hormone action and feedback loops
Typical Fit Example: "Molecular characterization of insulin receptor substrate phosphorylation patterns in adipocyte insulin resistance models" or "CRISPR-based dissection of thyroid hormone receptor beta signaling in hepatocytes"

Metabolic Endocrine Pathophysiology Tier 1

  • Molecular pathogenesis of diabetes mellitus (Type 1 and Type 2)
  • Beta-cell dysfunction mechanisms and biomarkers
  • Insulin resistance at molecular and cellular levels
  • Glucagon signaling dysregulation in metabolic disease
  • Adipokine signaling in metabolic syndrome pathogenesis
  • Molecular mechanisms linking obesity to endocrine dysfunction
Typical Fit Example: "Proteomic analysis of pancreatic beta-cell stress responses in hyperglycemic conditions" or "Mechanistic role of ER stress in adipocyte insulin signaling impairment"

Thyroid & Adrenal Pathophysiology Tier 1

  • Molecular mechanisms of thyroid hormone synthesis and secretion
  • Autoimmune thyroid disease pathogenesis (Graves', Hashimoto's)
  • Thyroid hormone transporter dysfunction
  • HPA axis dysregulation mechanisms
  • Adrenal steroidogenesis pathway alterations
  • Molecular biomarkers for thyroid and adrenal disorders
Typical Fit Example: "Single-cell RNA sequencing reveals thyrocyte heterogeneity in autoimmune thyroiditis" or "Molecular dissection of cortisol feedback mechanisms in chronic stress models"

Reproductive Endocrine Mechanisms Tier 1

  • Gonadal hormone synthesis and regulation pathways
  • Molecular pathogenesis of polycystic ovary syndrome (PCOS)
  • Hypothalamic-pituitary-gonadal axis dysfunction
  • Steroid hormone receptor signaling in reproductive tissues
  • Molecular mechanisms of ovarian and testicular dysfunction
  • Biomarkers for reproductive endocrine disorders
Typical Fit Example: "Transcriptomic profiling of granulosa cells in PCOS reveals altered androgen biosynthesis pathways" or "Molecular mechanisms of LH receptor desensitization in ovarian follicles"

Secondary Focus Areas

Neuroendocrine Pathophysiology

Molecular mechanisms of hypothalamic-pituitary axis dysfunction, pituitary adenoma pathogenesis, growth hormone signaling defects, prolactin pathway dysregulation, and neuropeptide signaling in endocrine disease. Focus on mechanistic understanding, not clinical pituitary disorders management.

Endocrine Neoplasia Mechanisms

Molecular pathogenesis of hormone-producing tumors, oncogenic signaling in endocrine tissues, tumor suppressor mechanisms in endocrine glands, biomarkers for endocrine malignancies. Emphasis on cancer biology mechanisms, not oncological treatment protocols.

Bone & Mineral Metabolism

Molecular mechanisms of parathyroid hormone action, vitamin D signaling pathways, calcium homeostasis dysregulation, osteoblast-osteoclast signaling in metabolic bone disease. Focus on pathophysiology of osteoporosis and mineral disorders at molecular level.

Endocrine Toxicology & Disruptors

Molecular mechanisms of endocrine-disrupting chemicals (EDCs), receptor-mediated toxicity pathways, environmental hormone mimics and antagonists, cellular stress responses to endocrine toxins. Mechanistic toxicology, not environmental health policy.

Emerging Research Areas

AI-Driven Endocrine Research

Machine learning models for biomarker discovery, AI-based prediction of hormone signaling outcomes, computational modeling of endocrine pathways, deep learning for disease mechanism elucidation. Must include experimental validation of computational predictions.

Single-Cell Endocrine Biology

Single-cell transcriptomics and proteomics of endocrine tissues, cellular heterogeneity in hormone-producing organs, lineage tracing in endocrine development and disease, spatial transcriptomics of endocrine glands.

Organoid & 3D Culture Models

Endocrine organoid development and characterization, 3D culture systems for hormone signaling studies, patient-derived models for mechanistic research, microfluidic endocrine tissue models.

Circadian & Chronobiology

Molecular mechanisms of circadian hormone regulation, clock gene dysfunction in endocrine disease, temporal dynamics of hormone signaling pathways, chronopathophysiology of metabolic disorders.

Note: Emerging area submissions undergo additional editorial review to ensure mechanistic depth and alignment with pathophysiology focus. Purely descriptive or correlative studies are not suitable.
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Article Types & Priorities

Priority 1

Fast-Track Review (10-14 days to first decision)

Priority 2

Standard Review (21-28 days to first decision)

Rarely Considered

Requires Strong Mechanistic Justification

Editorial Standards & Requirements

Reporting Guidelines

  • ARRIVE 2.0 for animal studies
  • MIQE for qPCR experiments
  • PRISMA for systematic reviews
  • STROBE for observational studies (if mechanistic)
  • CONSORT for interventional studies (if mechanistic)

Data Transparency

  • Raw data deposition in public repositories required
  • Omics data: GEO, ArrayExpress, or ProteomeXchange
  • Structural data: PDB or EMDB
  • Code availability for computational analyses
  • Materials availability statements required

Ethics & Integrity

  • IRB/IACUC approval required for human/animal studies
  • Informed consent documentation
  • Competing interests disclosure mandatory
  • Funding source transparency
  • COPE guidelines adherence

Preprint Policy

  • Preprints welcomed (bioRxiv, medRxiv)
  • No impact on novelty assessment
  • Must disclose preprint DOI at submission
  • Preprint servers must be non-commercial
  • Version control required

Editorial Decision Metrics

14 days
First Decision
28%
Acceptance Rate
45 days
To Publication
Open
Access Model