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Gene · 1589

Papers3,802

Newest first. Swiss-Prot's references are curated; PubTator's text mining finds papers that name the gene, not always ones about it.

TitleJournalYearPMIDFound bySource
The Expression of Placental 17β-Hydroxysteroid Dehydrogenase Genes Is Associated with the Elevation of Active Androgens and Estrogens in Pregnant Women, but Does Not Affect 11-Oxygenated C19 Steroids.Int J Mol Sci202642196271PubTator, text miningPubMed
A Cross-Tissue Transcriptome-Wide Association Study Identifies Novel Susceptibility Genes for Glomerular Diseases.Biomedicines202642193397PubTator, text miningPubMed
Unraveling novel therapeutic targets for diffuse large B-cell lymphoma: a plasma multi-omics study.Front Pharmacol202642147334PubTator, text miningPubMed
From genetic diagnosis to healthy live births: implementing an integrated PGT-M pathway for 21-hydroxylase deficiency.J Endocrinol Invest202642096172PubTator, text miningPubMed
A 56-Year-Old Male Patient With 21-Hydroxylase Deficiency Presenting With Fatigue: A Case Report.Br J Hosp Med (Lond)202642053005PubTator, text miningPubMed
Diagnostic Criteria and Genetic Basis of Polycystic Ovary Syndrome: A Narrative Review.Metabolites202642042922PubTator, text miningPubMed
[Clinical and genetic characteristics of 165 children with salt-wasting 21-hydroxylase deficiency in Henan Province].Zhongguo Dang Dai Er Ke Za Zhi202642015704PubTator, text miningPubMed
Evolution of molecular diagnostic strategies for 21-hydroxylase deficiency: from classical methods to advanced genomic techniques.Front Endocrinol (Lausanne)202642006261PubTator, text miningPubMed
Genetic insights into pulmonary nodules and lung cancer: similarities and differences revealed by GWAS studies.Hum Mol Genet202641989865PubTator, text miningPubMed
Case Report: Compound heterozygous mutation comprising p.Pro31Leu and exons 1-3 ins/del variants in CYP21A2 causes non-classical congenital adrenal hyperplasia in a Chinese girl.Front Pediatr202641988147PubTator, text miningPubMed
Post-ACTH peak cortisol response is associated with genotype in children with nonclassic congenital adrenal hyperplasia.Front Endocrinol (Lausanne)202641938119PubTator, text miningPubMed
Long-Read Sequencing of CAH and ADPKD Provides Novel Insights Into the Genetic Diagnosis of Male Infertility.Reprod Med Biol202641937974PubTator, text miningPubMed
[Two cases of Non-classic adrenal hyperplasia: Diagnostic strategies and genetic variant analysis].Zhonghua Yi Xue Yi Chuan Xue Za Zhi202641918383PubTator, text miningPubMed
A preliminary study developing a scoring model incorporating fibrinogen-like protein 2 for predicting glucocorticoid resistance in thyroid eye disease.Thyroid Res202641917995PubTator, text miningPubMed
Reduced cortical thickness in individuals with congenital adrenal hyperplasia (CAH).Sci Rep202641876695PubTator, text miningPubMed
Integrating genetic counseling in endocrine practice: Prevention, reproductive care, and prenatal diagnosis.Ann Endocrinol (Paris)202641864331PubTator, text miningPubMed
Efficacy of Liquid-chromatography and Radioimmunoassay in False-positives' Drop-off in CAH Newborn Screening.J Clin Endocrinol Metab202641811754PubTator, text miningPubMed
Live Births Following IVF-FET in Two Adult Sisters with Nonclassic P450 Oxidoreductase Deficiency: A Case Report Identifying a Novel POR Variant.Int J Womens Health202641809679PubTator, text miningPubMed
Unveiling Salt-Wasting Congenital Adrenal Hyperplasia in an Infant: A Diagnostic Challenge.Cureus202641809282PubTator, text miningPubMed
Congenital adrenal hyperplasia in Saudi Arabia: Epidemiology, genetic mutations, and evolving management strategies.J Natl Med Assoc202641807209PubTator, text miningPubMed

gene-search-2026-11-11-0.2.0

Sources 12

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ChEMBL, through Open TargetsCC BY-SA 3.0
  • ClinicalTrials.govNo license stated
  • EMBL-EBI's patent proteinsNo added restrictions. Attribution expected
  • GenBank's patent filesNo restrictions from NCBI. Submitters may hold rights
  • HGNCCC0
  • NCBI GenePublic domain (US government)
  • NIH's project files and grant-paper linksPublic domain
  • Open TargetsCC0 1.0
  • PubMedNLM's terms
  • PubTator 3Public domain
  • UniProtCC BY 4.0
Each source's terms
  • ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
  • ChEMBL, through Open TargetsCC BY-SA 3.0, for the parts from ChEMBL. Read on 8 Nov 2026 at https://platform-docs.opentargets.org/licence
  • ClinicalTrials.govnone stated
  • EMBL-EBI's patent proteinsEMBL-EBI's patent protein files from the EPO, JPO, KIPO and USPTO. EMBL-EBI: "EMBL-EBI itself places no additional restrictions on the use or redistribution of the data available via its Data Resources and Tools other than those provided by the original data owners" and "EMBL-EBI expects attribution (e.g. in publications, services or products) for the use of any of its Data Resources and Tools." Read on 11 Nov 2026 at https://www.ebi.ac.uk/about/terms-of-use
  • GenBank's patent filesGenBank's patent files. NCBI: "NCBI places no restrictions on the use or distribution of the GenBank data. However, some submitters may claim patent, copyright, or other intellectual property rights in all or a portion of the data they have submitted." Read on 11 Nov 2026 at https://www.ncbi.nlm.nih.gov/genbank/about/
  • HGNCCC0: https://www.genenames.org/about/license/
  • NCBI GeneNone named for the file. NCBI says information created by or for the US government on its site is in the public domain, and asks that NLM be acknowledged: https://www.ncbi.nlm.nih.gov/home/about/policies/
  • NIH's project files and grant-paper linksPublic domain (NIH RePORTER)
  • Open TargetsCC0 1.0. Open Targets asks that users cite its latest paper: Buniello et al. 2025, Open Targets Platform: facilitating therapeutic hypotheses building in drug discovery, Nucleic Acids Research 53(D1):D1467, PMID 39657122. Read on 8 Nov 2026 at https://platform-docs.opentargets.org/licence
  • PubMedNLM's terms
  • PubTator 3Public domain
  • UniProtCC BY 4.0. UniProt's licence file: "All databases and documents in the UniProt FTP directory may be copied and redistributed freely, without advance permission, provided that this copyright statement is reproduced with each copy." UniProt asks that users cite its latest paper: The UniProt Consortium, UniProt: the Universal Protein Knowledgebase in 2025, Nucleic Acids Research 53:D609-D617, https://doi.org/10.1093/nar/gkae1010. Read on 9 Nov 2026 at https://www.uniprot.org/help/license

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

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