Work

om92, a glp-1 enhancer mutation, is an allele of ekl-1

Year: 2022

Type: article

Abstract: is a 244 bp deletion predicted to generate a frameshift and premature termination codon, yielding a severely truncated protein, suggesting it is a null allele.

Source: PubMed Central

DOI: 10.17912/micropub.biology.000698

Authors: Samantha A. Stein, Olivia F. Zucaro, Harold E. Smith, Kevin F. O'Connell, Jill M. Spoerke, Eleanor M. Maine, James L. Lissemore

Institutions: John Carroll University, National Institutes of Health, National Institute of Diabetes and Digestive and Kidney Diseases, Syracuse University

Language: English

Topic: Developmental Biology and Gene Regulation

Subfield: Molecular Biology

Field: Biochemistry, Genetics and Molecular Biology

Domain: Life Sciences

SDG: Good health and well-being

Open Access status: green

OpenAlex ID: W4312067085

FWCI:

Cites: 12

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Related to: 10