| Tech ID |
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| 23011 |
A Genetically Engineered Biosensor to Visualize Osmotic Stress in Plants
To optimize plant growth it is necessary to ensure proper nutrient uptake as well as monitor osmotic stress such as drought, temperature stress, and salinity. Current methods of detecting plant osmotic stress include visual assessment, sample testing, aerial imagery and radiometry. While visual assessment lacks the accuracy and resolution afforded by other methods, aerial imagery may be costlier; sample testing offers better accuracy and resolution but can be more labor- and cost-intensive. Radiometry strikes a better balance between volume and resolution, but its readings are sensitive to sunlight intensity, sun angle, cloud cover and interaction of sun angle with plant geometry; it needs to correct for these variations by taking the intensity of incoming light as well as the light reflected from the crop into account. Therefore there is a need for a different method that can improve the accuracy of the measurement of osmotic stress
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| 21512 |
A Humanized Mouse Model Of Severe Asthma
Asthma, a chronic inflammatory disease of the lung, affects an increasingly larger population every year and presents a major public health problem in terms of morbidity and cost. The cause and mechanisms of asthma and allergic diseases are not yet understood. As the spontaneous development of asthma in a non-human animal is next to impossible, the ability to engineer mouse models of the disease remains critical to the understanding and treatment of the disease.
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| 21218 |
REGULATION OF GENE EXPRESSION IN PLANTS USING ALTERNATIVE SPLICING
Plant growth and development depends on the coordination of gene expression in a tissue-, temporal-, or signal-dependent manner. Often, the complex expression pattern observed for a given gene derives from regulation at both the transcriptional and post-transcriptional levels. This multi-layered approach to gene control is part of what makes plants robust, adaptable, and efficient as living photosynthetic systems. Complex gene regulation requires a multi-level approach. Current technology for transgene regulation in plants is based almost exclusively on transcriptional activation. For example, tissue-specific and stress-responsive promoters are extensively employed for inducible gene regulation, though many of these conditional promoters are species-specific. Alternative splicing of mRNA is an important mechanism of gene regulation in plants. The two possible consequences of alternative splicing of an mRNA are: (i) to change the protein coding sequence, by inserting or deleting sequences, or by shifting the reading frame, or (ii) to change the fate of the mRNA, by inserting or deleting sequences that target the RNA for degradation, localization, or other processes. This research has identified how to use RNA elements that regulate alternative splicing of mRNAs for inducible control of gene expression.
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| 21021 |
Regulated Overexpression of NH3 Driven by its own Promoter enhances Disease Resistance in Plants
NPR1 (non-expresser of pathogenesis related genes 1) is the master regulator of salicyclic acid-mediated systemic acquired resistance. Over-expression of Arabidopsis NPR1 and rice NH1 (NPR1 homolog1)/OsNPR1 in rice results in enhanced resistance. Researchers at UC Davis investigated a rice NPR1 paralog for similar activity. Regulated overexpression of NH3, when driven by its own promoter (nNT-NH3), resulted in clear, enhanced resistance when challenged with Xanthomonas oryzae pv. oryzae.
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| 20973 |
Suppression of Flowering in Transgenic Plants Directed by Promoters of MADS-Box Floral Organ Genes AGL2, AGL4, and AGL9
The flowering process consumes 25 to 35 percent of the energy of a typical plant. Thus, for trees used for lumber or pulp production, for example, it can be advantageous to suppress flowering in order increase the yield of wood. Suppression of flowering also can be a desirable trait to eliminate the production of allergic pollen, or to prevent pollen dissemination.
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| 20963 |
Rice Genes that Regulate the Rice Stress Response
Three genes in rice have demonstrated a significant role in plant innate immunity. Two genes confer improved pathogen resistance when silenced (demonstrated by challenge experiments using Xanthomonas oryzae pv oryzae.) One gene confers improved pathogen resistance when overexpressed (demonstrated by challenge experiments with Xanthomonas oryzae pv oryzae). Further, researchers identified ten additional novel regulators of stress tolerance in rice, including three from protein classes not previously known to function in stress responses. Several lines of evidence suggest cross-talk between biotic and abiotic stress responses.
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| 20874 |
Crop Improvement And Production Of Value-Added Compound Using The Rice Beta-Glucanase Genes, Gns2-Gns9
Patent rights to a group of novel rice beta-glucanase genes and the corresponding beta-glucanase enzymes are available for non-exclusive licensing. The genes, and the gene promoters, are useful in a variety of transgenic monocot plants for achieving increased plant resistance to fungal infection, improved growth characteristics, biomass conversion and high levels of expression of heterologous protein in various tissues obtained from the plants.
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| 20827 |
T7 Transcription Enhancing Sequence (TEnBOX), Which Overexpresses Gene Products
UC San Diego researchers have discovered an enhancer function of an approximately 30 bp DNA fragment that had been reported to function as a protein transduction domain in microbial cells.
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| 19949 |
Nitrate-Responsive Synthetic Promoter Produces Nitrate-Regulated Gene Expression in Plants
Inorganic nitrogen is a vital nutrient for plants. Soil nitrate provides as much as 90 percent of the nitrogen taken up by most plants and leads to a dramatic change in gene expression, which is critical to direct the productivity and survival of the plant. Consequently, nitrate is commonly provided by way of fertilizer to improve crop yield. However, many crop plants are inefficient in their ability to utilize the nitrogen. For example, corn and wheat typically only utilize 50 percent of the nitrogen applied to the soil and paddy rice may recoup as little as 30 percent. Nitrogen not used by crops may contribute to severe environmental problems, including pollution of ground water, run-off into nearby bodies of water, and release of greenhouse gases into the atmosphere. Plants take up and assimilate nitrate in response to its availability in the soil and the demands of the plant, but with varying efficiency among species. Understanding and improving the ability of particular plant species to respond to and utilize nitrogen could therefore lead to increased crop productivity and decreased water and air pollution.
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| 19877 |
Haploid Plants through Seeds
Researchers at the University of California Davis have developed a novel method to produce haploid plants through seeds. This method induces genome elimination (from one parent in a cross) with a precise mutation, rather than by culturing haploid cells or by crossing distantly related plants.
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| 19817 |
DNA Demethylases and uses thereof
Normal 0 0 1 137 783 UC Berkeley 6 1 961 11.1282 0 0 0 Imprinting regulates a number of genes essential for normal development in mammals and angiosperms. In mammals such imprinted genes contribute to the control of fetal growth and development. Human diseases may also be linked to mutations in imprinted genes or aberrant regulation of their expression.. Differential DNA methylation can be established during oogenesis or spermatogenesis by de novo methyltransferases and maintained somatically by methyltransferases. The conversion of cytosine to 5'-methylcytosine in promoter associated CpG islands has been linked to changes in chromatin structure and often results in transcriptional silencing of the associated gene. Transcriptional silencing by DNA methylation has been linked to mammalian development, imprinting and X-Chromosome inactivation, suppression of parasitic DNA and numerous cancer types. This invention provides for demethylase polypeptides that excise methylated cytosines in DNA.
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| 19814 |
Maize plants with reduced gene silencing
Normal 0 0 1 95 543 UC Berkeley 4 1 666 11.1282 0 0 0 This invention relates to genes and methods to control eukaryotic mechanisms responsible for both the genesis and maintenance of heritable phenotypic variation. Paramutations represent specific types of epigenetic alterations that can be stably inherited without altering the DNA sequence. Several genes are known to be involved in regulating the paramutant state in maize plants. It is currently thought that these allelic interactions cause structural alterations to the chromatin. This invention relates to the use of the rmr1 gene for reducing or mitigating gene silencing in a transgenic maize plant and also to reduce or mitigate inbreeding depression
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| 19672 |
DNA:GST-AtNOS1 Plasmid
UC San Diego inventors have identified and cloned a nitric oxide (NO) synthase gene from plants, AtNOS1, which has been shown to play a role in plant growth, stomatal movement, hormonal signaling and fertility. The protein was expressed in bacteria as a fusion protein with glutathione-S-transferase (GST-AtNOS1), purified and assayed. The inventors were able to show that extracts from bacteria expressing the fusion protein had higher levels of NOS activity. It is particularly interesting that this gene in plants has been known, but never isolated.
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| 19398 |
Method for Improving Cuphea Oil Seed Production by Eliminating Premature Pod Shattering
Cuphea is a tropically grown flowering plant which is known as a rich source of medium-chain fatty acids having high commercial value. However, this plant is not commercially utilized in large-scale agriculture due to its characteristic, sequential maturation and release of oil seeds from the seed pods, which precludes mechanized harvesting. Cuphea is generally harvested by hand at present. Technology which would allow the cultivation and harvesting of Cuphea using modern agricultural methods and equipment would have the potential to create a new, high-value, oil-seed crop of major industrial importance.
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| 19374 |
Selective Control of Lignin Biosynthesis in Transgenic Plants
Researchers from UC San Diego have found a key gene that plays a central role in regulating lignin accumulation within plant cells. Specifically, mutants of this gene produce excess lignins in "ectopic" positions, while transgene constructs incorporating a constitutive promotor nearly abolish lignin biosynthesis. Furthermore, this patented technology details how certain cells that would normally become lignified show a complete absence of lignin in double mutants for this and a related gene, suggesting that these two genes act redundantly to positively regulate lignin production. These results suggest that these genes can be used to regulate lignification of plant cells.Specifically, the technology provides a method of reducing lignification in a vascular plant by ectopically expressing a nucleic acid molecule encoding an AGL8-like gene product in the plant, whereby lignification is reduced due to ectopic expression of the nucleic acid molecule.
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| 18679 |
Dna Recombination In Eukaryotic Cells By The Bacteriophage Phic31 Recombination
System
This invention provides methods for obtaining specific and stable integration of nucleic acids into eukaryotic cells. The method is an alternative to the widely used CRE-LOX method. The invention makes use of site-specific recombination systems that use prokaryotic recombinase polypeptides, such as the phiC31 recombinase, that can mediate recombination between the recombination sites, but not between hybrid recombination sites that are formed upon the recombination. Thus, the recombination is irreversible in the absence of additional factors. Eukaryotic cells that contain the recombinase polypeptides, or genes that encode the recombinases, are also provided. See also: MGG Molecular Genetics and Genomics. August, 2001. 265(6):1031-1038. Thomason, L. C.; Calendar, R.; Ow, D. W. Gene insertion and replacement in Schizosaccharomyces pombe mediated by the Streptomyces bacteriophagevariant phiC31 site-specific recombination system. Abstract: The site-specific recombination system used by the Streptomyces bacteriophage variant phiC31 was tested in the fission yeast Schizosaccharomyces pombe. A target strain with the phage attachment site attP inserted at the leu1 locus was co-transformed with one plasmid containing the bacterial attachment site attB linked to a ura4+ marker, and a second plasmid expressing the variant phiC31 integrase gene. High-efficiency transformation to the Ura+ phenotype occurred when the integrase gene was expressed. Southern analysis revealed that the attB-ura4+ plasmid integrated into the chromosomal attP site. Sequence analysis showed that the attBXattP recombination was precise. In another approach, DNA with a ura4+ marker flanked by two attB sites in direct orientation was used to transform S. pombe cells bearing an attP duplication. The variant phiC31 integrase catalyzed two reciprocal cross-overs, resulting in a precise gene replacement. The site-specific insertions are stable, as no excision (the reverse reaction) was observed on maintenance of the integrase gene in the integrant lines. The irreversibility of the variant phiC31 site-specific recombination system sets it apart from other systems currently used in eukaryotic cells, which reverse readily. Deployment of the variant phiC31 recombination provides new opportunities for directing transgene Y and chromosome rearrangements in eukaryotic systems.
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| 18570 |
Pathogen Resistance In Plants Using Cdna-n/intron Constructs
N genes were shown to require partial alternative processing of the third intron, which produces a truncated N protein, to provide full viral resistance. Insertion of a complete cDNA or truncated construct alone did not provide resistance in transgenic plants. Researchers at UC Berkeley have developed constructs comprising (1) a cDNA molecule corresponding to the tobacco N gene, and (2) at least a portion of the third intron of the N gene. Transgenic plants with this construct result in the required, partial, alternative processing to result in virus resistance.
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| 18565 |
Gene That Modulates Plant Reproductive Development
Shoot architecture and flowering time in angiosperms depend on the balanced expression of a large number of flowering time and flower meristem identity genes. Loss-of-function mutations in the Arabidopsis EMBRYONIC FLOWER (EMF) genes cause Arabidopsis to eliminate rosette shoot growth and transform the apical meristem from indeterminate to determinate growth by producing a single terminal flower on all nodes. Alteration of EMF1 expression in transgenic plants caused progressive changes in flowering time, shoot determinacy, and inflorescence architecture. EMF1 may belong to a new class of proteins that function as transcriptional regulators of phase transition during shoot development.
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| 18543 |
Resolution Of Complex Integration Patterns To Obtain
Single Copy Transgenes
Researchers at UC Berkeley have developed a method for producing a transgenic cell having a stably integrated, single copy of a transgene. The method, which resolves complicated gene insertions into a single copy, involves introducing into a cell the desired transgene flanked on each end by a recombination site. The recombination sites are oriented such that contact with a recombinase would not result in deletion of the polynucleotide sequence from the construct. When the multiple, tandem copies of the introduced polynucleotide locus are reacted with a recombinase, the multiple, tandem copies are resolved to a single copy. A different set of recombination sites can flank a marker gene to allow its deletion from the genome. The final single copy transgene includes unique recombinaiton target sites that can facilitate re-introduction of new DNA into the same chromosomal site through site-specific integration. References: V Srivastava & et al. 1999. Single-copy transgenic wheat generated through the resolution of complex integration patterns. PNAS. 96:11117-21. CD Day & et al. 2000. Transgene integration into the same chromosome location can produce alleles that express at a predictable level, or alleles that are differentially silenced. Genes & Dev. 14:2869-80
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| 18512 |
Cereal Transformation Of Using Cultured Organogenic Tissue
A novel transformation method for transforming many commercial genotypes of cereals has been developed. The method incolves using meristematic tissues which include vegetative shoot meristems and young leaf bases as initial explants and the induction of a direct organogenesis pathway for in vitro proliferation and plant regeneration. Use of this pathway results in less impact and destabilizaton of the methylation state of the genomic DNa during invitro growth and reduces the impact of somaclonal variation and instability of transgene expression. References; S. Zhang, et al. 1999. Genetic transformation of commercial cultivars of oat (Avena sativa L.) and barley (Hordeum vulgare L.) using in vitro shoot meristem cultures derived from germinated seedlings. Plant Cell Reports. 18:959-66. S. Zhang, et al., 1998. Expression of CDC2Zm an dknotted 1 during in=vitro axillary shoot meristem proliferation and adventitious shoot meristem formation in maize (Zea mays L.) and barley (Hordeum vulgare L.). Planta. 204:542-9
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| 18423 |
Methods For The Transformation Of Monocots Using Green Embryogenic Callus
Investigators at the University of California, Berkeley have developed improved compositions and methods for the transformation of monocots from embryogenic callus. Such methods include, for example, use of an intermediate incubation medium after callus induction to increase the competence of the transformed cells for regeneration; dim light conditions during early phases of selection; use of green callus tissue as a target for microprojectile bombardment; and media with optimized levels of phytohormones and copper concentrations.
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| 18317 |
Compositions And Methods For Plant Pathogen Resistance
Researchers at the University of California at Berkeley have identified a plant resistance gene family, the members of which encode plant resistance polypeptides having P-Loop and LRR structural motifs. This resistance gene class includes Prf, RPS2, RPM1, N, and L6 and represents a large fraction of known plant disease resistance genes. The invention further involves transgenic plants and transformed host cells that express these DNAs and exhibit enhanced disease resistance to plant pathogens. For example, when expressed in transgenic plants, Prf confers Fenthion sensitivity and resistance to a wide variety of phytopathogens, including not only Pseudomonas syringae, but also unrelated pathogens such as Xanthomonas campestris.
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| 17201 |
Identification Of A Novel Plant Gene That Regulates Cell-to-cell Transport
Plant cells are encased in cell walls that form the skeleton of plants, enabling and stabilizing growth. As the individual plant cells are separated by the cell wall and cannot directly touch, plants have evolved cytoplasmic bridges called plasmodesmata that connect the cytoplasm of adjacent cells and allow intercellular movement of large molecules. Researchers at UCB have identified a gene that modifies the plasmodesmata aperture and is modulates the movement of molecules from cell-to-cell. Control of aperture size and activity is critical for viral disease susceptibility or control since viral genomes are spread cell-to-cell through the plasmodesmata.
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| 17130 |
Genes Regulated In Response To Light
Light is a critical environmental factor for plants. It provides not only the energy for plant growth but also key informational signals that plants use to adapt and optimize growth morphology, fruiting, and formation of storage organs. The invention provides a method to identify nucleotide sequences regulated in response to light. The invention also provides a variety of expression vectors useful for developing constructs to test and further develop the identified genes. Using these methods, a large collection of genes have been identified that respond early and late to light stimulation. This collection of light regulated genes will be useful to investigate light regulated processes within plants or organisms. The genes can also be used to produce plants with improved or altered light regulated gene expression.
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| 17068 |
A Universal, Light-switchable Gene Promoter System
Synopsis: This invention consists of an artificial promoter system that can be fused upstream of any desired gene, enabling reversible and light-switchable induction or repression of gene expression in any suitable host cell. New data to be filed in a provisional patent application demonstrates optimized expression conditions and a "switching off" mechanism in addition to the "switching on" mechanism.
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| 17021 |
A Novel Stress-tolerance Protein
Drought, cold, and salinity are environmental factors that can limit crop productivity worldwide. in response to these stresses, plants mount a number of defense reactions that increase the tolerance to the stress. Scientists at UC Berkeley have recently isolated a plant gene encoding a novel protein which functions as a signaling molecule in the stress signal transduction pathway. Expression of this gene is strongly regulated by stress signals including drought, cold, and wounding.
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| 16955 |
Genetic Functions Required For Gene Silencing In Maize
Hollick, Jay B.; Chandler, Vicki L. Genetic factors required to maintain repression of a paramutagenic maize pl1 allele. Genetics. January, 2001. 157(1):369-378. Abstract: A genetic screen identified two novel gene functions required to maintain mitotically and meiotically heritable gene silencing associated with paramutation of the maize purple plant 1 (pl1) locus. Paramutation at pl1 leads to heritable alterations of pl1 gene regulation; the Pl-Rhoades (Pl-Rh) allele, which typically confers strong pigmentation to juvenile and adult plant structures, changes to a lower expression state termed Pl'-mahogany (Pl'). Paramutation spontaneously occurs at low frequencies in Pl-Rh homozygotes but always occurs when Pl-Rh is heterozygous with Pl'. We identified four mutations that caused increased Pl' pigment levels. Allelism tests revealed that three mutations identified two new maize loci, required to maintain repression 1 (rmr1) and rmr2 and that the other mutation represents a new allele of the previously described mediator of paramutation 1 (mop1) locus. RNA levels from Pl' are elevated in rmr mutants and genetic tests demonstrate that Pl' can heritably change back to Pl-Rh in rmr mutant individuals at variable frequencies. Pigment levels controlled by two pl1 alleles that do not participate in paramutation are unaffected rmr mutants. These results suggest that RMR functions are intimately involved in maintaining the repressed expression state of paramutant Pl' alleles. Despite strong effects on Pl' repression, rmr mutant plants have no gross developmental abnormalities even after several generations of inbreeding, implying that RMR1 and RMR2 functions are not generally required for developmental homeostasis. also see: Dorweiler, Jane E.; Carey, Charles C.; Kubo, Kenneth M.; Hollick, Jay B.; Kermicle, Jerry L.; Chandler, Vicki L. mediator of paramutation1 is required for establishment and maintenance of paramutation at multiple maize loci. Plant Cell. November, 2000. 12(11):2101-2118. Abstract: Paramutation is the directed, heritable alteration of the expression of one allele when heterozygous with another allele. Here, the isolation and characterization of a mutation affecting paramutation, mediator of paramutation1-1 (mop1-1), are described. Experiments demonstrate that the wild-type gene Mop1 is required for establishment and maintenance of the paramutant state. The mop1-1 mutation affects paramutation at the multiple loci tested but has no effect on alleles that do not participate in paramutation. The mutation does not alter the amounts of actin and ubiquitin transcripts, which suggests that the mop1 gene does not encode a global repressor. Maize plants homozygous for mop1-1 can have pleiotropic developmental defects, suggesting that mop1-1 may affect more genes than just the known paramutant ones. The mop1-1 mutation does not alter the extent of DNA methylation in rDNA and centromeric repeats. The observation that mop1 affects paramutation at multiple loci, despite major differences between these loci in their gene structure, correlations with DNA methylation, and stability of the paramutant state, suggests that a common mechanism underlies paramutation. A protein-based epigenetic model for paramutation is discussed.
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| 11438 |
Cucumber Mosaic Virus Inducible Viral Amplicon (CMViva) Expression System
A Chemically Inducible Cucumber Mosaic Virus Amplicon Expression System for Production of Recombinant Proteins in Plant-Based Systems
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| 11432 |
Biological Activity of Constitutively Active YX Alleles of Phytochrome in Plants
Light-Independent Phytochrome Signaling
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| 11409 |
Method for Creating Transgenic Pigs
Altering chimeric pigs' DNA for the purpose of creating transgenic and knockout pigs
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| 11283 |
Transgenic Plants with Increased Tolerance for Stress and Pathogens
Transgenic Plants with Increased Tolerance for Stress and Pathogens
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| 11216 |
Plant Transformation System
Biologically-Safe Plant-Transformation System for Producing Transgenic Crop Plants
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| 11208 |
Strong Promoter with Activity Analogous to the 35S Promoter
Novel Strong Promoter for Use in Conjunction with or Replacement of the 35S Promoter
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| 11178 |
Astrocyte-Specific BAFF and GFP Double Transgenic Mice
Researchers at the University of California, Davis have developed transgenic mouse models that constitutively express B cell Activating Factor (BAFF) in the Tumor Necrosis Factor (TNF) family, and Green Fluorescent Protein (GFP) under the control of Glial Fibrillary Acidic Protein (GFAP) promoter in astrocytes.
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