The research on prolonged stimulation of growth hormone (GH) and insulin-like growth factor I (IGF-I) secretion by CJC-1295 is supported by a dedicated user account that provides access to the full dataset, analytical tools, and collaborative features. Researchers can log in, review raw hormone levels, and share anonymized results with peers while maintaining compliance with data protection regulations.
**Save citation to file**
A standardized citation format (e.g., APA, Vancouver) is automatically generated for each study. Users can download a .bib or .ris file containing the bibliographic details—author list, title, journal, volume, issue, pages, DOI—and attach it directly to reference managers such as Zotero, EndNote, or Mendeley.
**Email citation**
The platform offers an “Email Citation” button that composes a pre-formatted email with the full reference and optional note. This feature facilitates quick sharing of findings with collaborators, reviewers, or institutional repositories without manual copy-paste errors.
**Add to Collections**
Researchers can curate personalized collections within the database. By clicking “Add to Collections,” they store studies under thematic folders (e.g., “Peptide Hormones”, “GH Analogues”) for future retrieval and meta-analysis. Collections support tagging and sorting by relevance, date, or citation count.
**Add to My Bibliography**
The system automatically aggregates all entries added by a user into a personal bibliography. Each record links to the full text, supplementary materials, and citation metrics. Users can export this bibliography in multiple formats for grant proposals or systematic reviews.
**Your saved search**
Custom searches—such as “CJC-1295 AND GH secretion” or “long-acting analogs”—are saved with filters (date range, study design). The platform notifies users when new publications match the criteria, ensuring that investigators remain up to date on emerging evidence without re-running queries.
**Create a file for external citation management software**
Beyond native export options, users can generate files compatible with external reference managers. A “Create File” button produces a structured data package (JSON or XML) containing all metadata, abstracts, and links, allowing seamless integration into third-party tools for advanced bibliometric analysis.
**Your RSS Feed**
An RSS feed is available for each search or collection. Subscribers receive instant updates in their preferred reader whenever new articles are indexed, ensuring continuous surveillance of the literature landscape surrounding GH analogues.
**Full text links**
For every entry, direct hyperlinks lead to full-text PDFs hosted by publishers, institutional repositories, or preprint servers. Where access is restricted, the system provides a DOI link and offers options for interlibrary loan requests.
**Actions**
The “Actions” menu presents context-specific operations: download PDF, open in new tab, request full text, annotate, add to collection, export citation, share on social media, or request a copy via research gate. These streamlined workflows reduce administrative overhead for researchers.
**Page navigation**
Pagination controls enable efficient traversal through large result sets. Users can jump to specific pages, adjust results per page (25, 50, 100), and view summaries of key metrics such as citation counts and impact factors on each landing page.
**Affiliation**
The affiliation field lists the institutional home of each author or collaborating group. This information facilitates networking, identification of potential co-authors, and assessment of research output by organization or country.
**Authors**
A comprehensive list of contributing scientists appears for every study, including first authors, senior investigators, and corresponding contacts. Links to ORCID IDs allow verification of identity and retrieval of full author profiles.
**Abstract**
The abstract provides a concise synopsis of the study’s objectives, methods, results, and conclusions. For the CJC-1295 investigation, it highlights that chronic administration in healthy adults led to sustained elevations in GH and IGF-I levels compared with placebo, supporting its therapeutic potential for anabolic disorders.
**Similar articles**
The platform recommends related publications based on citation overlap, shared keywords, or co-authorship networks. This feature helps researchers discover complementary studies on GH analogues, peptide therapeutics, or endocrine modulation.
**Cited by**
A dynamic counter displays how many subsequent works reference the article, with a list of those citing papers. Researchers can examine downstream impacts and identify emerging trends in GH research.
**Publication types**
The publication type filter distinguishes peer-reviewed journal articles, conference proceedings, review articles, clinical trials, or meta-analyses, enabling precise literature searches tailored to study design preferences.
**MeSH terms**
Medical Subject Headings (MeSH) tags provide standardized indexing of key concepts such as “Growth Hormone”, “Insulin-like Growth Factor 1”, “Peptide Hormones”, and “Long-acting Analogues”. These controlled vocabularies enhance search precision across databases.
**Substances**
The substance field catalogs the pharmacological agents studied—CJC-1295, GHRH analogues, GH itself—and their chemical identifiers (CAS numbers, PubChem IDs). This information supports cross-database queries and drug–drug interaction checks.
**Related information**
Links to regulatory status, clinical trial registries, patent filings, or safety profiles appear under this heading. For CJC-1295, users can review its phase II trial data, FDA submissions, and ongoing studies.
**LinkOut – more resources**
The LinkOut feature aggregates external links to repositories (e.g., PubMed Central), institutional archives, clinical guidelines, and relevant conference abstracts, providing a one-stop hub for supplementary material.
**Full Text Sources**
A curated list of publishers, open-access journals, or institutional servers that host the full text is presented. Users can select their preferred source based on access rights or licensing agreements.
**Account**
The research on prolonged stimulation of growth hormone (GH) and insulin-like growth factor I (IGF-I) secretion by CJC-1295 is supported by a dedicated user account that provides access to the full dataset, analytical tools, and collaborative features. Researchers can log in, review raw hormone levels, and share anonymized results with peers while maintaining compliance with data protection regulations.
**Save citation to file**
A standardized citation format (e.g., APA, Vancouver) is automatically generated for each study. Users can download a .bib or .ris file containing the bibliographic details—author list, title, journal, volume, issue, pages, DOI—and attach it directly to reference managers such as Zotero, EndNote, or Mendeley.
**Email citation**
The platform offers an “Email Citation” button that composes a pre-formatted email with the full reference and optional note. This feature facilitates quick sharing of findings with collaborators, reviewers, or institutional repositories without manual copy-paste errors.
**Add to Collections**
Researchers can curate personalized collections within the database. By clicking “Add to Collections,” they store studies under thematic folders (e.g., “Peptide Hormones”, “GH Analogues”) for future retrieval and meta-analysis. Collections support tagging and sorting by relevance, date, or citation count.
**Add to My Bibliography**
The system automatically aggregates all entries added by a user into a personal bibliography. Each record links to the full text, supplementary materials, and citation metrics. Users can export this bibliography in multiple formats for grant proposals or systematic reviews.
**Your saved search**
Custom searches—such as “CJC-1295 AND GH secretion” or “long-acting analogs”—are saved with filters (date range, study design). The platform notifies users when new publications match the criteria, ensuring that investigators remain up to date on emerging evidence without re-running queries.
**Create a file for external citation management software**
Beyond native export options, users can generate files compatible with external reference managers. A “Create File” button produces a structured data package (JSON or XML) containing all metadata, abstracts, and links, allowing seamless integration into third-party tools for advanced bibliometric analysis.
**Your RSS Feed**
An RSS feed is available for each search or collection. Subscribers receive instant updates in their preferred reader whenever new articles are indexed, ensuring continuous surveillance of the literature landscape surrounding GH analogues.
**Full text links**
For every entry, direct hyperlinks lead to full-text PDFs hosted by publishers, institutional repositories, or preprint servers. Where access is restricted, the system provides a DOI link and offers options for interlibrary loan requests.
**Actions**
The “Actions” menu presents context-specific operations: download PDF, open in new tab, request full text, annotate, add to collection, export citation, share on social media, or request a copy via research gate. These streamlined workflows reduce administrative overhead for researchers.
**Page navigation**
Pagination controls enable efficient traversal through large result sets. Users can jump to specific pages, adjust results per page (25, 50, 100), and view summaries of key metrics such as citation counts and impact factors on each landing page.
**Affiliation**
The affiliation field lists the institutional home of each author or collaborating group. This information facilitates networking, identification of potential co-authors, and assessment of research output by organization or country.
**Authors**
A comprehensive list of contributing scientists appears for every study, including first authors, senior investigators, and corresponding contacts. Links to ORCID IDs allow verification of identity and retrieval of full author profiles.
**Abstract**
The abstract provides a concise synopsis of the study’s objectives, methods, results, and conclusions. For the CJC-1295 investigation, it highlights that chronic administration in healthy adults led to sustained elevations in GH and IGF-I levels compared with placebo, supporting its therapeutic potential for anabolic disorders.
**Similar articles**
The platform recommends related publications based on citation overlap, shared keywords, or co-authorship networks. This feature helps researchers discover complementary studies on GH analogues, peptide therapeutics, or endocrine modulation.
**Cited by**
A dynamic counter displays how many subsequent works reference the article, with a list of those citing papers. Researchers can examine downstream impacts and identify emerging trends in GH research.
**Publication types**
The publication type filter distinguishes peer-reviewed journal articles, conference proceedings, review articles, clinical trials, or meta-analyses, enabling precise literature searches tailored to study design preferences.
**MeSH terms**
Medical Subject Headings (MeSH) tags provide standardized indexing of key concepts such as “Growth Hormone”, “Insulin-like Growth Factor 1”, “Peptide Hormones”, and “Long-acting Analogues”. These controlled vocabularies enhance search precision across databases.
**Substances**
The substance field catalogs the pharmacological agents studied—CJC-1295, GHRH analogues, GH itself—and their chemical identifiers (CAS numbers, PubChem IDs). This information supports cross-database queries and drug–drug interaction checks.
**Related information**
Links to regulatory status, clinical trial registries, patent filings, or safety profiles appear under this heading. For CJC-1295, users can review its phase II trial data, FDA submissions, and ongoing studies.
**LinkOut – more resources**
The LinkOut feature aggregates external links to repositories (e.g., PubMed Central), institutional archives, clinical guidelines, and relevant conference abstracts, providing a one-stop hub for supplementary material.
**Full Text Sources**
A curated list of publishers, open-access journals, or institutional servers that host the full text is presented. Users can select their preferred source based on access rights or licensing agreements.