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Advances in Enzyme Regulation (AER)

Publisher :

Elsevier Ltd.

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Peer reviewed only
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Open Access
  • Biochemistry
  • Molecular Biology
e-ISSN :

2212-4934

Issue Frequency :

Monthly

p-ISSN :

2212-4926

Est. Year :

2025

Mobile :

31204853911

Country :

Netherlands The

Language :

English

APC :

YES

Impact Factor Assignee :

Google Scholar

Email :

y.schemm@elsevier.com

Journal Descriptions

Advances in Biological Regulation (formerly Advances in Enzyme Regulation) reports cutting edge scientific progress on regulation at the molecular level, covering: The molecular biology of control of gene expression by hormones, drugs and growth factors in cancer cells and in clinical situations of metabolic diseases, inborn errors of metabolism and neoplasia. Stem cell biology and regenerative medicine issues Regulatory networks, mainly in cellular signalling, differentiation, cell cycle & growth control, structure-function relationships, cell fate and lineage commitment or assembly mechanisms in cells Viruses, or supramolecular constructs, and signaling mechanisms mediating transcription Genomic, proteomic, bioinformatics and systems biology approaches to identify and characterize steps of biological control in cells. Complex cellular, pathogenic, clinical, or animal model systems studied by biochemical, molecular, genetic, epigenetic or quantitative ultrastructural approaches


Advances in Enzyme Regulation (AER) is :

International, Peer-Reviewed, Open Access, Refereed, Biochemistry, Molecular Biology , Online or Print, Monthly Journal

UGC Approved, ISSN Approved: P-ISSN - 2212-4926, E-ISSN - 2212-4934, Established in - 2025, Impact Factor

Not Provide Crossref DOI

Indexed in Scopus

Not indexed in WoS, DOAJ, PubMed, UGC CARE

Indexing

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Scopus
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Elsevier
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Science Direct

+1 More

Publications of AER

  • dott image January, 1964

The role of phosphofructokinase in metabolic regulation

The kinetics of phosphofructokinase have been investigated with especial reference to possible physiological controls. ATP, citrate and Mg were found to be inhibitors for liver and brain PFK...

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