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Regulation of expression of transgenes in developing fish
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1007/978-1-4615-3760-1_15openalex-snapshot
Transgenic Fish for Aquaculture
inferredcites →https://doi.org/10.1007/bf00004731openalex-snapshot
Molecular cloning and expression of salmon pituitary hormones
inferredcites →https://doi.org/10.1007/bf00004736openalex-snapshot
Transgenic fish: present status and future directions
inferredcites →https://doi.org/10.1007/bf00273596openalex-snapshot
Transient expression of foreign DNA during embryonic and larval development of the medaka fish (Oryzias latipes)
inferredcites →https://doi.org/10.1007/bf00652482openalex-snapshot
�ber die Aufzucht isolierter Teile des Amphibienkeimes
inferredcites →https://doi.org/10.1016/0003-2697(90)90595-zopenalex-snapshot
Molecular cloning: A laboratory manual
inferredcites →https://doi.org/10.1016/0168-9525(87)90164-8openalex-snapshot
Oncogenes and tumor suppressor genes in Xiphophorus
inferredcites →https://doi.org/10.1016/0168-9525(89)90103-0openalex-snapshot
Genetics and early development of zebrafish
inferredcites →https://doi.org/10.1016/0378-1119(89)90378-8openalex-snapshot
Identification of a site that mediates transcriptional response of the human β-actin gene to serum factors
inferredcites →https://doi.org/10.1016/0378-1119(91)90436-fopenalex-snapshot
Importance of the CArG box in regulation of β-actin-encoding genes
inferredcites →https://doi.org/10.1038/335683a0openalex-snapshot
How eukaryotic transcriptional activators work
inferredcites →https://doi.org/10.1038/340064a0openalex-snapshot
Negative regulation of serum-responsive enhancer elements
inferredcites →https://doi.org/10.1038/nbt0292-176openalex-snapshot
Growth Enhancement in Transgenic Atlantic Salmon by the Use of an “All Fish” Chimeric Growth Hormone Gene Construct
inferredcites →https://doi.org/10.1038/nbt1290-1268openalex-snapshot
Development of Expression Vectors for Transgenic Fish
inferredcites →https://doi.org/10.1073/pnas.81.10.2980openalex-snapshot
Expression and regulation of chicken actin genes introduced into mouse myogenic and nonmyogenic cells.
inferredcites →https://doi.org/10.1073/pnas.85.5.1389openalex-snapshot
A 40-base-pair sequence in the 3' end of the beta-actin gene regulates beta-actin mRNA transcription during myogenesis.
inferredcites →https://doi.org/10.1093/nar/17.2.601openalex-snapshot
Regulation of the human β-actin promoter by upstream and intron domains
inferredcites →https://doi.org/10.1093/nar/18.11.3299openalex-snapshot
Transient expression directed by homologus and heterologous prometer and enhancer sequences in fish cells
inferredcites →https://doi.org/10.1101/gad.1.3.268openalex-snapshot
An albumin enhancer located 10 kb upstream functions along with its promoter to direct efficient, liver-specific expression in transgenic mice.
inferredcites →https://doi.org/10.1101/gad.3.5.687openalex-snapshot
Differential requirements for cell-specific elastase I enhancer domains in transfected cells and transgenic mice.
inferredcites →https://doi.org/10.1101/gad.4.6.943openalex-snapshot
Assembly of alternative multiprotein complexes directs rRNA promoter selectivity.
inferredcites →https://doi.org/10.1101/gad.6.1.1openalex-snapshot
Of fin and fur: mutational analysis of vertebrate embryonic development.
inferredcites →https://doi.org/10.1101/gad.6.4.591openalex-snapshot
Specific activation of mammalian Hox promoters in mosaic transgenic zebrafish.
inferredcites →https://doi.org/10.1126/science.2667136openalex-snapshot
Transcriptional Regulation in Mammalian Cells by Sequence-Specific DNA Binding Proteins
inferredcites →https://doi.org/10.1128/mcb.10.2.528openalex-snapshot
A combination of closely associated positive and negative cis-acting promoter elements regulates transcription of the skeletal alpha-actin gene.
inferredcites →https://doi.org/10.1128/mcb.10.2.528-538.1990openalex-snapshot
A Combination of Closely Associated Positive and Negative cis -Acting Promoter Elements Regulates Transcription of the Skeletal α-Actin Gene
inferredcites →https://doi.org/10.1128/mcb.10.7.3432openalex-snapshot
Functional analysis of elements affecting expression of the beta-actin gene of carp.
inferredcites →https://doi.org/10.1128/mcb.10.7.3432-3440.1990openalex-snapshot
Functional Analysis of Elements Affecting Expression of the β-Actin Gene of Carpt
inferredcites →https://doi.org/10.1128/mcb.2.9.1044openalex-snapshot
Recombinant Genomes Which Express Chloramphenicol Acetyltransferase in Mammalian Cells
inferredcites →https://doi.org/10.1128/mcb.6.6.2125openalex-snapshot
Upstream Regions of the Human Cardiac Actin Gene That Modulate Its Transcription in Muscle Cells: Presence of an Evolutionarily Conserved Repeated Motif
inferredcites →https://doi.org/10.1128/mcb.8.1.267openalex-snapshot
Identification of the human beta-actin enhancer and its binding factor.
inferredcites →https://doi.org/10.1128/mcb.8.1.267-272.1988openalex-snapshot
Identification of the Human β-Actin Enhancer and Its Binding Factor
inferredcites →https://doi.org/10.1128/mcb.9.11.4759openalex-snapshot
The Rat Albumin Promoter: Cooperation with Upstream Elements Is Required when Binding of APF/HNF1 to the Proximal Element Is Partially Impaired by Mutation or Bacterial Methylation
inferredcites →https://doi.org/10.1128/mcb.9.2.515openalex-snapshot
The sarcomeric actin CArG-binding factor is indistinguishable from the c-fos serum response factor.
inferredcites →https://doi.org/10.1128/mcb.9.2.515-522.1989openalex-snapshot
The Sarcomeric Actin CArG-Binding Factor Is Indistinguishable from the c-fos Serum Response Factor
inferredcites →https://doi.org/10.1128/mcb.9.5.2191openalex-snapshot
Cross-Binding of Factors to Functionally Different Promoter Elements in c -fos and Skeletal Actin Genes
inferredcites →https://doi.org/10.1128/mcb.9.9.3785openalex-snapshot
The chicken skeletal muscle alpha-actin promoter is tissue specific in transgenic mice.
inferredcites →https://doi.org/10.1128/mcb.9.9.3785-3792.1989openalex-snapshot
The Chicken Skeletal Muscle α-Actin Promoter Is Tissue Specific in Transgenic Mice
inferredcites →https://doi.org/10.1142/9789814503600_0007openalex-snapshot
Expression of Heterologous Genes in Transgenic Fish
inferredcites →https://doi.org/10.1142/9789814503600_0010openalex-snapshot
Growth Hormone Gene Transfer in Atlantic Salmon: Use of Fish Antifreeze/Growth Hormone Chimeric Gene Construct
inferredcites →https://doi.org/10.3109/10425179009016040openalex-snapshot
Isolation and characterization of β-act in gene of carp ( Cyprinus carpio )
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.2139/ssrn.4791175openalex-extracted
Beta Actin Gene Promoter of Salmo (Trutta) Macrostigma: Isolation, Cloning, Molecular Characterization, and Functionality in Phylogeny Studies
inferred← citeshttps://doi.org/10.1002/(sici)1098-2795(199610)45:2<117::aid-mrd2>3.0.co;2-wopenalex-snapshot
Comparison of the activity of carp and rat β-actin gene regulatory sequences in tilapia and rainbow trout embryos
inferred← citeshttps://doi.org/10.1007/978-94-011-5234-1_26openalex-snapshot
The application of gene transfer techniques to marine resource management: recent advances, problems and future directions
inferred← citeshttps://doi.org/10.1007/bf01969704openalex-snapshot
Regulation and expression of transgenes in fish—a review
inferred← citeshttps://doi.org/10.1007/bf01974089openalex-snapshot
Liposome-mediated gene transfer in fish embryos
inferred← citeshttps://doi.org/10.1007/bf01980208openalex-snapshot
High transgene activity in the yolk syncytial layer affects quantitative transient expression assays in zebrafish (Danio rerio) embryos
inferred← citeshttps://doi.org/10.1007/s10126-002-0059-0openalex-snapshot
RecA-Mediated, Targeted Mutagenesis in Zebrafish
inferred← citeshttps://doi.org/10.1007/s10126-004-0068-2openalex-snapshot
Fishing for Answers with Transposons
inferred← citeshttps://doi.org/10.1007/s11248-012-9606-2openalex-snapshot
Isolation of yellow catfish β-actin promoter and generation of transgenic yellow catfish expressing enhanced yellow fluorescent protein
inferred← citeshttps://doi.org/10.1007/s40009-012-0023-0openalex-snapshot
Molecular Cloning and Characterization of Asian Seabass (Lates calcarifer) Beta-Actin Gene Promoter
inferred← citeshttps://doi.org/10.1016/0044-8486(95)01093-9openalex-snapshot
Inheritance of recombinant carp β-actin/GH cDNA gene in transgenic carp
inferred← citeshttps://doi.org/10.1016/b978-012340440-4/50059-3openalex-snapshot
Transgenic Animals in Rheumatoid Arthritis Research
inferred← citeshttps://doi.org/10.1016/j.aquaculture.2013.01.001openalex-snapshot
Somatic gene transfer in European sea bass (Dicentrarchus labrax): Optimal fish conditions and exogenous control of foreign genes
inferred← citeshttps://doi.org/10.1016/s0012-1606(02)00083-0openalex-snapshot
Windows into development: historic, current, and future perspectives on transgenic zebrafish
inferred← citeshttps://doi.org/10.1016/s0044-8486(98)00452-9openalex-snapshot
Growth performance studies in transgenic Cyprinus carpio
inferred← citeshttps://doi.org/10.1016/s0070-2153(08)60567-0openalex-snapshot
6 Transgenic Fish in Aquaculture and Developmental Biology
inferred← citeshttps://doi.org/10.1016/s0167-4781(02)00534-1openalex-snapshot
Isolation and characterisation of tilapia β-actin promoter and comparison of its activity with carp β-actin promoter
inferred← citeshttps://doi.org/10.1016/s0379-4172(06)60032-2openalex-snapshot
Cloning of Black Carp β-actin Gene and Primarily Detecting the Function of Its Promoter Region
inferred← citeshttps://doi.org/10.1017/s1479236208002283openalex-snapshot
Isolation and primary function detection of Nile tilapia (Oreochromis niloticus) β-actinpromoter
inferred← citeshttps://doi.org/10.1023/a:1003000127867openalex-snapshot
The application of gene transfer techniques to marine resource management: recent advances, problems and future directions
inferred← citeshttps://doi.org/10.1080/00212210.1994.10688765openalex-snapshot
DEVELOPMENTAL AND MOLECULAR GENETICS IN FISH
inferred← citeshttps://doi.org/10.1098/rstb.1995.0096openalex-snapshot
Predicting developmental processes from evolutionary patterns: a molecular phylogeny of the zebrafish ( Danio rerio ) and its relatives
inferred← citeshttps://doi.org/10.1111/j.1749-6632.2000.tb06875.xopenalex-snapshot
Transgenic Zebrafish as Sentinels for Aquatic Pollution
inferred← citeshttps://doi.org/10.1134/s1022795408070156openalex-snapshot
The effect of regulatory sequences of αSl-casein gene on the expression of the lacZ-gene in loach Misgurnus fossilis L. transgenic embryos
inferred← citeshttps://doi.org/10.1387/ijdb.072514jdopenalex-snapshot
Expression and comparative genomics of two serum response factor genes in zebrafish
inferred← citeshttps://doi.org/10.1515/cmble-2015-0010openalex-snapshot
The beta-actin gene promoter of rohu carp (Labeo rohita) drives reporter gene expressions in transgenic rohu and various cell lines, including spermatogonial stem cells
inferred← citeshttps://doi.org/10.15578/jra.4.1.2009.23-31openalex-snapshot
KLONING PROMOTER b-AKTIN DARI IKAN GURAMI (Osphronemus gouramy)
inferred← citeshttps://doi.org/10.1787/9789264079151-enopenalex-snapshot
Detailed Review Paper on Fish Screening Assays for the Detection of Endocrine Active Substances
inferred← citeshttps://doi.org/10.19027/jai.7.115-127openalex-snapshot
Characterization of β-Actin Promoter from Nile Tilapia (Oreochromis niloticus)
inferred← citeshttps://doi.org/10.2903/sp.efsa.2010.en-69openalex-snapshot
Defining environmental risk assessment criteria for genetically modified fishes to be placed on the EU market
inferred← citeshttps://doi.org/10.3389/fendo.2014.00182openalex-snapshot
A Novel Model for Development, Organization, and Function of Gonadotropes in Fish Pituitary
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