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Gene-Related Peptide, Calcitonin -- See Calcitonin Gene-Related Peptide


A 37-amino acid peptide derived from the calcitonin gene. It occurs as a result of alternative processing of mRNA from the calcitonin gene. The neuropeptide is widely distributed in the brain, gut, perivascular nerves, and other tissue. The peptide produces multiple biological effects and has both circulatory and neurotransmitter modes of action. In particular, it is a potent endogenous vasodilator
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Gene, Reporter -- See Genes, Reporter


Genes whose expression is easily detectable and therefore used to study promoter activity at many positions in a target genome. In recombinant DNA technology, these genes may be attached to a promoter region of interest
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Gene resources -- See Germplasm resources


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Gene, Selfish -- See Repetitive Sequences, Nucleic Acid


Sequences of DNA or RNA that occur in multiple copies. There are several types: INTERSPERSED REPETITIVE SEQUENCES are copies of transposable elements (DNA TRANSPOSABLE ELEMENTS or RETROELEMENTS) dispersed throughout the genome. TERMINAL REPEAT SEQUENCES flank both ends of another sequence, for example, the long terminal repeats (LTRs) on RETROVIRUSES. Variations may be direct repeats, those occurring in the same direction, or inverted repeats, those opposite to each other in direction. TANDEM REPEAT SEQUENCES are copies which lie adjacent to each other, direct or inverted (INVERTED REPEAT SEQUENCES)
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  Gene Silencing -- 3 Related Subjects   3
Gene Silencing   35
Gene Silencing -- drug effects : Synthetic nucleic acids as inhibitors of gene expression : mechanisms, applications, and therapeutics implications / edited by Levon Michael Khachigian  2005 1
Gene silencing -- Handbooks, manuals, etc.   2
Gene silencing -- Laboratory manuals   4
Gene silencing -- Periodicals : Journal of RNAi and gene silencing : an international journal of RNA and gene targeting research  2005 1
 

Gene Silencing, Post-Transcriptional -- See RNA Interference


A gene silencing phenomenon whereby specific dsRNAs (RNA, DOUBLE-STRANDED) trigger the degradation of homologous mRNA (RNA, MESSENGER). The specific dsRNAs are processed into SMALL INTERFERING RNA (siRNA) which serves as a guide for cleavage of the homologous mRNA in the RNA-INDUCED SILENCING COMPLEX. DNA METHYLATION may also be triggered during this process
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Gene Silencing, Posttranscriptional -- See RNA Interference


A gene silencing phenomenon whereby specific dsRNAs (RNA, DOUBLE-STRANDED) trigger the degradation of homologous mRNA (RNA, MESSENGER). The specific dsRNAs are processed into SMALL INTERFERING RNA (siRNA) which serves as a guide for cleavage of the homologous mRNA in the RNA-INDUCED SILENCING COMPLEX. DNA METHYLATION may also be triggered during this process
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Gene Silencings, Posttranscriptional -- See RNA Interference


A gene silencing phenomenon whereby specific dsRNAs (RNA, DOUBLE-STRANDED) trigger the degradation of homologous mRNA (RNA, MESSENGER). The specific dsRNAs are processed into SMALL INTERFERING RNA (siRNA) which serves as a guide for cleavage of the homologous mRNA in the RNA-INDUCED SILENCING COMPLEX. DNA METHYLATION may also be triggered during this process
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Gene splicing -- See Genetic engineering


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Gene, src -- See Genes, src


Retrovirus-associated DNA sequences (src) originally isolated from the Rous sarcoma virus (RSV). The proto-oncogene src (c-src) codes for a protein that is a member of the tyrosine kinase family and was the first proto-oncogene identified in the human genome. The human c-src gene is located at 20q12-13 on the long arm of chromosome 20
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Gene, Switch -- See Genes, Switch


Genes that cause the epigenotype (i.e., the interrelated developmental pathways through which the adult organism is realized) to switch to an alternate cell lineage-related pathway. Switch complexes control the expression of normal functional development as well as oncogenic transformation
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Gene, Synthetic -- See Genes, Synthetic


Biologically functional sequences of DNA chemically synthesized in vitro
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Gene, T-Cell Receptor -- See Genes, T-Cell Receptor


DNA sequences, in cells of the T-lymphocyte lineage, that code for T-cell receptors. The TcR genes are formed by somatic rearrangement (see GENE REARRANGEMENT, T-LYMPHOCYTE and its children) of germline gene segments, and resemble Ig genes in their mechanisms of diversity generation and expression
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Gene targeting.   24
Gene targeting -- Laboratory manuals.   5
Gene Targeting -- methods   8
 

Gene Targetings -- See Gene Targeting


The integration of exogenous DNA into the genome of an organism at sites where its expression can be suitably controlled. This integration occurs as a result of homologous recombination
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Gene, TcR -- See Genes, T-Cell Receptor


DNA sequences, in cells of the T-lymphocyte lineage, that code for T-cell receptors. The TcR genes are formed by somatic rearrangement (see GENE REARRANGEMENT, T-LYMPHOCYTE and its children) of germline gene segments, and resemble Ig genes in their mechanisms of diversity generation and expression
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Gene, TcR delta -- See Genes, T-Cell Receptor delta


DNA sequences encoding the delta chain of the T-cell receptor. The delta-chain locus is located entirely within the alpha-chain locus
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Gene, TcR gamma -- See Genes, T-Cell Receptor gamma


DNA sequences encoding the gamma chain of the T-cell receptor. The human gamma-chain locus is organized similarly to the TcR beta-chain locus
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Australia. Gene Technology Act 2000   4
Australia. Parliament. House of Representatives. Gene Technology Bill 2000 : A cautionary tale : fish don't lay tomatoes : a report on the Gene Technology Bill 2000 / Senate Community Affairs References Committee  2000 1
Australia. Parliament. Senate. Gene Technology Bill 2000 : A cautionary tale : fish don't lay tomatoes : a report on the Gene Technology Bill 2000 / Senate Community Affairs References Committee  2000 1
 

Gene Therapy -- See Genetic Therapy


Techniques and strategies which include the use of coding sequences and other conventional or radical means to transform or modify cells for the purpose of treating or reversing disease conditions
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Gene therapy.   148
AIDS (Disease) -- Gene therapy : Gene therapy for HIV : from inception to a possible cure / Gerhard Bauer, Joseph S. Anderson  2014 1
Gene therapy -- Australia. : Ethical aspects of research on human gene therapy : report to the NHMRC / by the Medical Research Ethics Committee of NHMRC  1987 1
Autoimmune diseases -- Gene therapy   3
Blood-vessels -- Diseases -- Gene therapy -- Laboratory manuals : Vascular disease : molecular biology and gene therapy protocols / edited by Andrew H. Baker  1999 1
Brain -- Cancer -- Gene therapy : Therapeutic ribonucleic acids in brain tumors / edited by Volker A. Erdmann, Guido Reifenberger, Jan Barciszewski  2009 1
Cancer -- Gene therapy.   29
Cancer -- Chemotherapy -- Complications -- Gene therapy : Marrow protection : transduction of hematopoietic cells with drug resistance genes / volume editor, Joseph R. Bertino  1999 1
Cancer -- Gene therapy -- Congresses : Cancer gene therapy / edited by David T. Curiel, Joanne T. Douglas  2005 1
Cancer in children -- Gene therapy : Molecularly targeted therapy for childhood cancer / Peter J. Houghton, Robert J. Arceci, editors  2010 1
Cancer -- Gene therapy -- Laboratory manuals   7
Cancer -- Gene therapy -- Periodicals   2
Cardiovascular system -- Diseases -- Gene therapy   4
Gene therapy -- Case studies. : Gene technology  2003 1
Central nervous system -- Diseases -- Gene therapy. : Viral vectors : gene therapy and neuroscience applications / edited by Michael G. Kaplitt, Arthur D. Loewy  1995 1
Cochlea -- Diseases -- Gene therapy : Gene therapy of cochlear deafness : present concepts and future aspects / volume editor, Allen F. Ryan  2009 1
Gene therapy -- Congresses.   6
Gene therapy -- England -- London : Great Ormond Street. Series 3, Episode 1, Fix my genes / filmed, produced & directed by Catey Sexton ; Films of Record, a Ten Alps Company  2015 1
Eye -- Diseases -- Gene therapy   2
Gene therapy -- Government policy : Regulatory aspects of gene therapy and cell therapy products : a global perspective / Maria Cristina Galli, editor  2023 1
Gene therapy -- Government policy -- Australia.   2
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