Synteny
Genes, Mitochondrial
Chromosome Mapping
Evolution, Molecular
Gene Rearrangement
Genome
DNA, Mitochondrial
Chromosome Inversion
Molecular Sequence Data
Genetic Linkage
Chromosomes, Bacterial
Sequence Analysis, DNA
Operon
Gene Duplication
Base Sequence
Annelida
RNA, Transfer
Genes
Conserved Sequence
Arthropods
Multigene Family
Transduction, Genetic
Species Specificity
Chromosomes, Artificial, Bacterial
Recombination, Genetic
RNA, Transfer, Asn
Methanobacteriales
Sequence Inversion
Escherichia coli
Pseudogenes
DNA, Intergenic
RNA, Transfer, Cys
Models, Genetic
Open Reading Frames
Contig Mapping
Sequence Homology, Nucleic Acid
Chromosomes
Physical Chromosome Mapping
Codon
Sequence Alignment
Cloning, Molecular
Pactamycin
Formiminoglutamic Acid
DNA Transposable Elements
Isopoda
Mutation
Amino Acid Sequence
Radiation Hybrid Mapping
Genetic Markers
Vertebrates
Chromosome Walking
Repetitive Sequences, Nucleic Acid
Cosmids
RNA, Ribosomal
Restriction Mapping
Chromosomes, Plant
Biological Evolution
Crosses, Genetic
RNA, Transfer, Glu
Chlorophyta
Algorithms
Nucleic Acid Conformation
Plasmids
Gene Transfer, Horizontal
Expressed Sequence Tags
Saccharomyces
Computational Biology
Genes, Regulator
Anticodon
Mollusca
Salmonella typhimurium
Angiosperms
Molecular Sequence Annotation
Genetic Complementation Test
Songbirds
Likelihood Functions
Genetic Code
DNA Restriction Enzymes
X Chromosome
Software
Chromosomes, Artificial, Yeast
Nucleic Acid Hybridization
Gene Deletion
Eukaryota
Polyploidy
Chromosomes, Fungal
Introns
Oryza sativa
Transcription, Genetic
Sex Chromosomes
Localization of psoriasis-susceptibility locus PSORS1 to a 60-kb interval telomeric to HLA-C. (1/1933)
Recent genome scans have established the presence of a major psoriasis-susceptibility locus in the human leukocyte antigen (HLA) complex on chromosome 6p21.3. To narrow the interval for candidate gene testing, we performed a linkage-disequilibrium analysis of 339 families, with the use of 62 physically mapped microsatellite markers spanning the major histocompatibility complex (MHC). As detected by use of the transmission/disequilibrium test (TDT), individual markers yielded significant linkage disequilibrium across most of the MHC. However, the strongest evidence for marker-trait disequilibrium was found in an approximately 300-kb region extending from the MICA gene to the corneodesmosin gene. Maximum-likelihood haplotypes were constructed across the entire MHC in the original sample and across a 1.2-Mb region of the central MHC in an expanded sample containing 139 additional families. Short (two- to five-marker) haplotypes were subjected to the TDT using a "moving-window" strategy that reduced the variability of TDT P values relative to the single-locus results. Furthermore, the expanded sample yielded a sharp peak of evidence for linkage disequilibrium that spanned approximately 170 kb and that was centered 100 kb telomeric to HLA-C. The 1.2-Mb interval was further dissected by means of recombinant ancestral haplotype analysis. This analysis identified risk haplotype 1 (RH1), which is a 60-kb fragment of ancestral haplotype 57.1, on all identifiable HLA risk haplotypes. One of these haplotypes exhibits significant linkage disequilibrium with psoriasis but does not carry Cw6, which is the HLA allele most strongly associated with the disease. These results demonstrate that RH1 is highly likely to carry the disease allele at PSORS1, and they exclude HLA-C and corneodesmosin with a high degree of confidence. (+info)Soggy, a spermatocyte-specific gene, lies 3.8 kb upstream of and antipodal to TEAD-2, a transcription factor expressed at the beginning of mouse development. (2/1933)
Investigation of the regulatory region of mTEAD-2, a gene expressed at the beginning of mouse pre-implantation development, led to the surprising discovery of another gene only 3.8 kb upstream of mTEAD-2. Here we show that this new gene is a single copy, testis-specific gene called SOGGY: (mSgy) that produces a single, dominant mRNA approximately 1.3 kb in length. It is transcribed in the direction opposite to mTEAD-2, thus placing the regulatory elements of these two genes in close proximity. mSgy contains three methionine codons that could potentially act as translation start sites, but most mSGY protein synthesis in vitro was initiated from the first Met codon to produce a full-length protein, suggesting that mSGY normally consists of 230 amino acids (26.7 kDa). Transcription began at a cluster of nucleotides approximately 150 bp upstream of the first Met codon using a TATA-less promoter contained within the first 0.9 kb upstream. The activity of this promoter was repressed by upstream sequences between -0.9 and -2.5 kb in cells that did not express mSgy, but this repression was relieved in cells that did express mSgy. mSgy mRNA was detected in embryos only after day 15 and in adult tissues only in the developing spermatocytes of seminiferous tubules, suggesting that mSgy is a spermatocyte-specific gene. Since mTEAD-2 and mSgy were not expressed in the same cells, the mSgy/mTEAD-2 locus provides a unique paradigm for differential regulation of gene expression during mammalian development. (+info)Automatic detection of conserved gene clusters in multiple genomes by graph comparison and P-quasi grouping. (3/1933)
We previously reported two graph algorithms for analysis of genomic information: a graph comparison algorithm to detect locally similar regions called correlated clusters and an algorithm to find a graph feature called P-quasi complete linkage. Based on these algorithms we have developed an automatic procedure to detect conserved gene clusters and align orthologous gene orders in multiple genomes. In the first step, the graph comparison is applied to pairwise genome comparisons, where the genome is considered as a one-dimensionally connected graph with genes as its nodes, and correlated clusters of genes that share sequence similarities are identified. In the next step, the P-quasi complete linkage analysis is applied to grouping of related clusters and conserved gene clusters in multiple genomes are identified. In the last step, orthologous relations of genes are established among each conserved cluster. We analyzed 17 completely sequenced microbial genomes and obtained 2313 clusters when the completeness parameter P: was 40%. About one quarter contained at least two genes that appeared in the metabolic and regulatory pathways in the KEGG database. This collection of conserved gene clusters is used to refine and augment ortholog group tables in KEGG and also to define ortholog identifiers as an extension of EC numbers. (+info)High-resolution transcript map of the region spanning D12S1629 and D12S312 at chromosome 12q13: triple A syndrome-linked region. (4/1933)
For those searching for human disease-causing genes, information on the position of genes with respect to genetic markers is essential. The physical map composed of ESTs and genetic markers provides the positional information of these markers as well as the starting point of gene identification in the form of genomic clones containing exons. To facilitate the effort of identification of genes in the region spanning D12S1629 and D12S312, we constructed a high-resolution transcript map with PAC/BAC/cosmid clones. The strategy for the construction of such a map involved utilization of STSs for the screening of the large insert bacterial chromosome libraries and a chromosome 12-specific cosmid library by hybridization. The contig was constructed based on the STS contents of the clones. The resulting high-resolution transcript map of the region between P273P14/SP6 and D12S312 spans 4.4 cM from 66.8 to 71.2 cM of the Genethon genetic map and represents approximately 2.4 Mb. It was composed of 81 BAC, 45 PAC, and 91 cosmid clones with a minimal tiling path consisting of 16 BAC and 4 PAC clones. These clones are being used to sequence this part of chromosome 12. We determined the order of 135 STSs including 74 genes and ESTs in the map. Among these, 115 STSs were unambiguously ordered, resulting in one ordered marker per 21 kb. The order of keratin type II locus genes was determined. This map would greatly enhance the positional cloning effort of the responsible genes for those diseases that are linked to this region, including male germ cell tumor as well as palmoplantar keratoderma, Bothnian-type, and triple A syndrome. This transcript map was localized at human chromosome 12q13. (+info)Developmentally regulated excision of a 28-base-pair sequence from the Paramecium genome requires flanking DNA. (5/1933)
The micronuclear DNA of Paramecium tetraurelia is estimated to contain over 50,000 short DNA elements that are precisely removed during the formation of the transcriptionally active macronucleus. Each internal eliminated sequence (IES) is bounded by 5'-TA-3' dinucleotide repeats, a feature common to some classes of DNA transposons. We have developed an in vivo assay to analyze these highly efficient and precise DNA excision events. The microinjection of a cloned IES into mating cells results in accurately spliced products, and the transformed cells maintain the injected DNA as extrachromosomal molecules. A series of deletions flanking one side of a 28-bp IES were constructed and analyzed with the in vivo assay. Whereas 72 bp of DNA flanking the eliminated region is sufficient for excision, lengths of 31 and 18 bp result in reduced excision and removal of all wild-type sequences adjacent to the TA results in complete failure of excision. In contrast, nucleotide mutations within the middle of the 28-bp IES do not prevent excision. The results are consistent with a functional role for perfect inverted repeats flanking the IES. (+info)Genomic organization and the promoter region of the round-spotted pufferfish (Tetraodon fluviatilis) CDC37 gene. (6/1933)
The CDC37 gene was isolated from a round-spotted pufferfish genomic library and characterized. This gene is composed of nine exons spanning 3.5 kb. Exon 1 contains the 5'-untranslated region and exon 2 contains the putative translation initiation site. By 5'-RACE (rapid amplication of cDNA ends) and sequence analysis, we deduced the promoter region for the CDC37 gene and found that it does not contain typical TATA or CCAAT box. The 1.8 kb DNA fragment upstream of the putative transcription initiation site contains numerous potential binding sites for transcription factors including CREB, E2A, Ets-1, GATA, NF-IL6 and PEA3. When this DNA fragment was placed upstream of the chloramphenicol acetyltransferase (CAT) reporter gene and transfected into a carp CF cell line, it could drive the synthesis of CAT enzyme four times more efficiently than the promoterless pCAT-Basic did. In addition, the CDC37 gene is linked to the TYK2 gene in a tail-to-head manner with a small intergenic region of 292 bp. (+info)Diversity in organization and the origin of gene orders in the mitochondrial DNA molecules of the genus Saccharomyces. (7/1933)
Sequencing of the Saccharomyces cerevisiae nuclear and mitochondrial genomes provided a new background for studies on the evolution of the genomes. In this study, mitochondrial genomes of a number of Saccharomyces yeasts were mapped by restriction enzyme analysis, the orders of the genes were determined, and two of the genes were sequenced. The genome organization, i.e., the size, presence of intergenic sequences, and gene order, as well as polymorphism within the coding regions, indicate that Saccharomyces mtDNA molecules are dynamic structures and have undergone numerous changes during their evolution. Since the separation and sexual isolation of different yeast lineages, the coding parts have been accumulating point mutations, presumably in a linear manner with the passage of time. However, the accumulation of other changes may not have been a simple function of time. Larger mtDNA molecules belonging to Saccharomyces sensu stricto yeasts have acquired extensive intergenic sequences, including guanosine-cytosine-rich clusters, and apparently have rearranged the gene order at higher rates than smaller mtDNAs belonging to the Saccharomyces sensu lato yeasts. While within the sensu stricto group transposition has been a predominant mechanism for the creation of novel gene orders, the sensu lato yeasts could have used both transposition- and inversion-based mechanisms. (+info)Nucleotide variation at the yellow gene region is not reduced in Drosophila subobscura: a study in relation to chromosomal polymorphism. (8/1933)
In contrast to Drosophila melanogaster and Drosophila simulans, the yellow (y) gene region of Drosophila subobscura is not located in a region with a strong reduction in recombination. In addition, this gene maps very close to the breakpoints of different inversions that segregate as polymorphic in natural populations of D. subobscura. Therefore, levels of variation at the y gene region in this species relative to those found in D. melanogaster and D. simulans may be affected not only by the change in the recombinational environment, but also by the presence of inversion polymorphism. To further investigate these aspects, an approximately 5.4-kb region of the A (=X) chromosome including the y gene was sequenced in 25 lines of D. subobscura and in the closely related species Drosophila madeirensis and Drosophila guanche. The D. subobscura lines studied differed in their A-chromosomal arrangements, A(st), A(2), and A(1). Unlike in D. melanogaster and D. simulans, levels of variation at the y gene region of D. subobscura are not reduced relative to those found at other genomic regions in the same species (rp49, Acp70A, and Acph-1). This result supports the effect of the change in the recombinational environment of a particular gene on the level of neutral variation. In addition, nucleotide variation is affected by chromosomal polymorphism. A strong genetic differentiation is detected between the A(1) arrangement and either A(st) or A(2), but not between A(st) and A(2). This result is consistent with the location of the y gene relative to the breakpoints of inversions A(1) and A(2). In addition, the pattern of nucleotide polymorphism in A(st)+A(2) and A(1) seems to point out that variation at the y gene region within these chromosomal classes is in the phase transient to equilibrium. The estimated ages of these arrangements assuming a star genealogy indicate that their origin cannot predate the D. madeirensis split. Therefore, the present results are consistent with a chromosomal phylogeny where Am(1), which is an arrangement present in D. madeirensis but absent in current populations of D. subobscura, would be the ancestral arrangement. (+info)Inversions are classified based on their location along the chromosome:
* Interstitial inversion: A segment of DNA is reversed within a larger gene or group of genes.
* Pericentric inversion: A segment of DNA is reversed near the centromere, the region of the chromosome where the sister chromatids are most closely attached.
Chromosome inversions can be detected through cytogenetic analysis, which allows visualization of the chromosomes and their structure. They can also be identified using molecular genetic techniques such as PCR (polymerase chain reaction) or array comparative genomic hybridization (aCGH).
Chromosome inversions are relatively rare in the general population, but they have been associated with various developmental disorders and an increased risk of certain diseases. For example, individuals with an inversion on chromosome 8p have an increased risk of developing cancer, while those with an inversion on chromosome 9q have a higher risk of developing neurological disorders.
Inversions can be inherited from one or both parents, and they can also occur spontaneously as a result of errors during DNA replication or repair. In some cases, inversions may be associated with other genetic abnormalities, such as translocations or deletions.
Overall, chromosome inversions are an important aspect of human genetics and can provide valuable insights into the mechanisms underlying developmental disorders and disease susceptibility.
Polyploidy is a condition where an organism has more than two sets of chromosomes, which are the thread-like structures that carry genetic information. It can occur in both plants and animals, although it is relatively rare in most species. In humans, polyploidy is extremely rare and usually occurs as a result of errors during cell division or abnormal fertilization.
In medicine, polyploidy is often used to describe certain types of cancer, such as breast cancer or colon cancer, that have extra sets of chromosomes. This can lead to the development of more aggressive and difficult-to-treat tumors.
However, not all cases of polyploidy are cancerous. Some individuals with Down syndrome, for example, have an extra copy of chromosome 21, which is a non-cancerous form of polyploidy. Additionally, some people may be born with extra copies of certain genes or chromosomal regions due to errors during embryonic development, which can lead to various health problems but are not cancerous.
Overall, the term "polyploidy" in medicine is used to describe any condition where an organism has more than two sets of chromosomes, regardless of whether it is cancerous or non-cancerous.
Gene orders
Eugene Forsey
Eugene Bullard
Seth Eugene Meek
Eugene Morse
Eugene Whelan
Gene Long
Gene regulatory network
Eugene Reimer
Eugene Kingman
Genes, Brain and Behavior
Eugene Levy
Eugene Gendlin
Eugene McCarthy
Gene cluster
Gene Sherman (art specialist)
White Light (Gene Clark album)
Pope Eugene IV
Larry Gene Bell
John Eugene
Gene cassette
Eugene M. Landrum
Gene therapy of the human retina
Gene Kelly
MAX (gene)
Alfred Eugene Bradley
Gene Keyes
Eugene Wong
Gene expression profiling
Gene therapy
David F. Swensen
Socialist Sunday School
Turquoise cichlid
Ariosa v. Sequenom
Benji (1974 film)
Phyllanthaceae
List of North Queensland United FC players
Uridine monophosphate synthase
Tetsuya Kakihara
2008 UEFA Champions League Final
Brooks (surname)
Phage display
Thomas de Littleton
February 1909
Matthew Bourne
G1 phase
Occupation of the Malheur National Wildlife Refuge
Mr. Majestyk
Prostaglandin-endoperoxide synthase 2
Pirates of the Caribbean: Dead Men Tell No Tales
American cockroach
Internal combustion engine cooling
Stealing Time
Hurricane Inez
Military Order of the Loyal Legion of the United States
Health realization
El Paso, Texas
Norovirus
April 1918
Blue Sky Studios
Can I order multiple variable regions in my gBlocks™ Gene Fragment? |IDT
Client Note: Kroger's Long-Lasting Avocados, Anonymous Gene Sequencing, Amazon's EV Truck Order, And More - CB Insights Research
Video: Gene Clark & Carla Olsen "Gypsy Rider" - Americana UK
The State of Squamate Genomics: Past, Present, and Future of Genome Research in the Most Speciose Terrestrial Vertebrate Order....
You searched for Gene J. Koprowski | Page 3 of 12 | LinuxInsider
Fhod1 formin homology 2 domain containing 1 [Mus musculus (house mouse)] - Gene - NCBI
Animals | Special Issue : Farm Animal Gene Exploration
Association of AFF3 Gene Polymorphism rs10865035 with Rheumatoid Arthritis: A Population-Based Case-Control Study on a...
'Dr Kildare'Richard Chamberlain with his 1963Chevrolet Corvette1964 © 1978 Gene Trindl - Image 9448 0025
| Most iconic images...
Where to Order Meal Kits for Carryout and Delivery in Chicago - Eater Chicago
Gene Simmons Talks About Michael Jackson - Sleaze Roxx
Evolution of gene order in the genomes of two related yeast species. | Laboratoire de Biologie Computationnelle et Quantitative
Vertex Sphere (Encore Sphere) Contacts | Find Reviews, Order Replacements | Lens.com
Gene Set Network Enrichment (Network Miner) · babelomics/babelomics Wiki · GitHub
Batikwalla located in Eugene, Oregon. Freestyle and Handmade Batik Artwork on Yoga Wear, Organic Cotton Hoodies and Hemp Dresses
Thomas A Easton Books In Order - Books In Order
Rotor-Gene Q
Browsing by Subject "Genes, Recessive"
Sketches and notes from the period when Gene Summers worked in the Office of Mies van der Rohe - Gene Summers fonds | CCA
Gene Polymorphisms in Gingivitis | IntechOpen
Info Sorting Types for Gene Sorter
DeCS - Termos Novos
About Panda Express at SR 200 & Gene Lasserre Blvd | Panda Express
gene-discuss (date)
Gordon Strong, 'Brewing Better Beer' on Amazon pre-order & in WorldCat
Gene Regulation
Ecology by Eugene P Odum - Paperback - from Bonita (SKU: 0030047714.G)
C. F. Martin and His Guitars, 1796-1873 (H. Eugene and Lillian Youngs Lehman Series) Hardcover ...
Chromosome1
- The BCKDHA gene is found on chromosome 19 . (medlineplus.gov)
Loci3
- After the development of DNA chips whole genomes of species, it has been more effective and feasible to find major candidate genes or loci using the genome-wide association study, even some traits have very low heritabilities. (mdpi.com)
- Different genome-wide association and candidate gene studies have shown the role of several genetic variants in multiple loci/genes with ethnical and geographical variations. (hindawi.com)
- We demonstrated that histone H3 Lys-4 was trimethylated at the promoter regions of many loci, among which only a fraction, including cell-cycle-related genes, were transcriptionally up-regulated. (jbc.org)
Genomic3
- Here, we introduce and define squamates (Order Squamata) and review the history and promise of genomic investigations into the patterns and processes governing squamate evolution, given recent technological advances in DNA sequencing , genome assembly, and evolutionary analysis . (bvsalud.org)
- To assign the function of genes before the genomic era, the target genes were individually explored through molecular biological techniques and populational genetics. (mdpi.com)
- This Special Issue "Farm Animal Genes" invites your manuscripts that discuss the function of genes in any kind of livestock animals using the recent advanced molecular genetic technologies, and/or using the whole genomic and transcriptomic NGS data. (mdpi.com)
Genome5
- The State of Squamate Genomics: Past, Present, and Future of Genome Research in the Most Speciose Terrestrial Vertebrate Order. (bvsalud.org)
- uvarum genome, 35 different synteny breakpoints between neighboring genes and two cases of local gene inversion were characterized in detail. (upmc.fr)
- Shigella strains harboring PMQR genes were identified earlier this year following whole genome sequencing of isolates from a multistate outbreak of multidrug-resistant Shigella flexneri infections predominantly affecting adult men, many of whom identify as men who have sex with men, according to epidemiologic data collected by CDC's Shigella program as part of outbreak response. (cdc.gov)
- The complete collection of gene, which is called genome , is a set of instructions for constructing human being. (who.int)
- It is estimated that the entire human genome consists of 50,000 to 100,00 genes. (who.int)
20231
- Genes (Basel);14(7)2023 07 01. (bvsalud.org)
Producing bacteria1
- Y. enterocolitica bacteria contain the urease gene cluster that enables them to hydrolyze urea, however, though this test may yield positive results, Y. enterocolitica is not the only organism that can perform this process, and further testing would be required in order to rule out the presence of other urease producing bacteria. (cdc.gov)
Taxonomy1
- Taxonomy of the order Mononegavirales: update 2017. (cdc.gov)
Species6
- Evolution of gene order in the genomes of two related yeast species. (upmc.fr)
- Changes in gene order between the genomes of two related yeast species, Saccharomyces cerevisiae and Saccharomyces bayanus var. (upmc.fr)
- We show that evolution of gene order in the genomes of these two yeast species is driven mainly by gene duplication onto different chromosomes followed by differential loss of the repeated copies. (upmc.fr)
- DOI: 10.1006/ young could help clarify AIV epide- species of the order Anura. (cdc.gov)
- Some of these genes have been shown to be conserved across a wide range of species. (cdc.gov)
- Rising fluoroquinolone MIC values among Shigella isolates may be related to the emergence of plasmid-mediated quinolone resistance (PMQR) genes in Shigella species in the United States. (cdc.gov)
Strains2
- Three strains of C diphtheriae are recognized, in decreasing order of virulence: gravis, intermedius, and mitis. (medscape.com)
- However, recent data from the Centers for Disease Control and Prevention (CDC) and state and local public health partners show that these strains often have a quinolone resistance gene that may lead to clinically significant reduced susceptibility to fluoroquinolone antibiotics. (cdc.gov)
Polymorphisms1
- The presence of genetic polymorphisms in HLA (human leukocyte antigen) and non-HLA genes contributes about 60% to the pathogenesis of RA. (hindawi.com)
Genomes2
- More recently, after the development of next-generation sequencing (NGS) technology, studies have not only focused on genomes, but also transcriptomes to identify the functional genes for target traits including the conventional economic traits and the brand new issues like disease resistance and immune response. (mdpi.com)
- While the transfer of already existing genes from one cell to another characterized an earlier phase of the field of biotechnology, synthetic biology involves the design, assembly, synthesis, or manufacture of new genomes, biological pathways, devices or organisms not found in nature. (cdc.gov)
Chronological order1
- For Appendix B , all personal identifiers were removed from the commentsreceived and placed in chronological order. (cdc.gov)
Functional2
- We also welcome submissions of prospective novel approaches to identify functional genes. (mdpi.com)
- The first era was the classical genetics where phenotypes of interest among family members are observed to identify segregation patterns of the "functional units" of genes or different forms of gene (alleles) and to lead to understanding of genetic mechanisms of particular phenotypes. (who.int)
Protein3
- The AFF3 (lymphoid nuclear protein related to the AF4 gene) is located at 2q11.2 position and encodes a protein of 1227 amino acids. (hindawi.com)
- The method detects gene sets (forming a protein-protein interaction subnetwork) that are consistently associated to high or low values in a ranked list of genes. (github.com)
- capsid protein gene sequence. (cdc.gov)
Sequence3
- Specifically, up to 18 consecutive N or K bases can be ordered, with a minimum of 125 bp of fixed, flanking sequence on either side of the variable bases. (idtdna.com)
- If you require a sequence outside of these design specifications, please contact [email protected] for evaluation. (idtdna.com)
- The expression of NF-kappa-B dependent genes was increased in HTE cells transfected with an NF-kappa-B consensus sequence and exposed to lipopolysaccharide for 4 or 16 hours or crocidolite for 16 hours. (cdc.gov)
Genetic3
- This study was designed to detect the association of a single-nucleotide polymorphism (SNP) rs10865035 in the AFF3 gene with the genetic background of rheumatoid arthritis (RA) in the Pakistani cohort. (hindawi.com)
- Genetic heritage of the Old Order Mennonites of southeastern Pennsylvania. (medlineplus.gov)
- In the nematode Caenorhabditis elegans, genetic studies resulted in the discovery of 15 genes that are essential for the apoptotic program. (cdc.gov)
Susceptibility2
- The AFF3 gene is not only important in the susceptibility to RA but also is a good candidate in the assessment of the therapeutic response in individuals [ 12 ]. (hindawi.com)
- Preliminary data suggest that all Shigella isolates with ciprofloxacin MICs in this range for which results are available harbor at least one quinolone resistance gene known to confer reduced susceptibility in enteric bacteria. (cdc.gov)
Parameter1
- The input for the Gene Set Network Enrichment Analysis (also known as NetworkMiner) is a list of genes, transcripts or proteins ordered according to a phenotypic parameter (as well as for Gene Set Enrichment Analysis or FatiScan). (github.com)
Expression5
- This gene is highly expressed in the lymphoid tissue and has been suggested to be involved in its development, while a lower level of expression has been reported in other tissues like the brain and lungs [ 1 , 10 - 12 ]. (hindawi.com)
- Asbestos induces nuclear factor kappa B (NF-kappa B) DNA-binding activity and NF-kappa B-dependent gene expression in tracheal epithelial cells. (cdc.gov)
- The effects of asbestos (1332214) on nuclear-factor-kappa-B (NF- kappa-B) DNA binding activity and NF-kappa-B dependent gene expression were examined. (cdc.gov)
- Transfection studies using the calcium phosphate coprecipitation technique were conducted in order to measure NF- kappa-B dependent gene expression. (cdc.gov)
- The authors conclude that asbestos induces NF-kappa-B DNA binding activity and NF-kappa-B dependent gene expression, both of which may be involved in the development of asbestos induced lung cancers. (cdc.gov)
Assembly1
- If grid execution is on & limit exceeded, number of array tasks for the final assembly step per gene segment. (cdc.gov)
Binds2
- This gene forms a nuclear factor that binds to DNA through its transcriptional activation domain. (hindawi.com)
- Binding of ferrous iron to the DtxR molecule forms a complex that binds to the tox gene operator and inhibits transcription. (medscape.com)
Resistance4
- Shigella isolates without a quinolone resistance gene typically have a ciprofloxacin MIC of ≤0.015 μg/mL. (cdc.gov)
- Fluoroquinolone resistance is of particular concern given that data from the National Antimicrobial Resistance Monitoring System indicate that many Shigella isolates with a quinolone resistance gene also are resistant to many other commonly used treatment agents, such as azithromycin, trimethoprim-sulfamethoxazole, amoxicillin-clavulanic acid, and ampicillin. (cdc.gov)
- Plasmid-mediated resistance genes are of particular concern because of their ability to spread between bacteria and their ability to promote chromosomal mutations conferring quinolone resistance, potentially resulting in rapid spread of fluoroquinolone resistance within or between populations of bacteria. (cdc.gov)
- Any patient with a Shigella infection could carry a strain harboring a quinolone resistance gene with a ciprofloxacin MIC of 0.12-1 μg/mL. (cdc.gov)
Results1
- We must now sustain these good results in order to spare everyone from suffering from leprosy. (who.int)
Conventional1
- Progress in this branch of synthetic biology has yielded remarkable therapeutic advances in gene therapy well beyond the achievements of conventional drugs and biologic agents. (cdc.gov)
Therapy1
- A second capability of synthetic biology involves the re-design of existing genes, cells or organisms for the purpose of gene therapy. (cdc.gov)
Design1
- 2. Re-Design Existing Genes. (cdc.gov)
Cases1
- PMQR genes have also been identified in sporadic cases of Shigella sonnei . (cdc.gov)
Account1
- Gene-discuss] Activate Your Account! (gnu.org)
Cells1
- Modification of existing genes in living animal and human cells is enabled by engineered nucleases such as meganucleases, zinc finger nucleases, transcription activator-like effector-based nucleases, and the CRISPR-Cas system. (cdc.gov)
Show1
- The identification of traces of anciently duplicated genes, called relics, show that the loss of duplicates is more frequently caused by the accumulation of numerous mutations in one of the two copies than by DNA deletion. (upmc.fr)
Made2
- This property of the AFF3 gene has made it a strong candidate for autoimmunity in the human cell [ 13 - 15 ]. (hindawi.com)
- This information is packaged in the form of genes made up of DNA. (who.int)
Browse1
- If you have decided to include a seed list of genes in your analysis, then browse it. (github.com)
Code1
- The genes that code for Shiga toxins are generally carried by bacteriophages, which are viruses that can infect bacteria. (cdc.gov)
Form1
- Two alpha subunits connect with two beta subunits, which are produced from the BCKDHB gene, to form a critical piece of the enzyme complex called the E1 component. (medlineplus.gov)
Multiple1
- Can I order multiple variable regions in my gBlocks™ Gene Fragment? (idtdna.com)
Analysis1
- Messenger RNA (mRNA) levels of c- myc, a gene regulated by NF-kappa-B, were determined via Northern blot analysis. (cdc.gov)
Copy2
- In addition, local gene inversions also would result from a mechanism of gene duplication, but in an inverted orientation, followed by loss of the original copy. (upmc.fr)
- Order your copy now. (concreteproducts.com)
Human1
- This working paper is prepared with the objective of providing brief accounts of development of human genetics and ELSI implications, and possible areas of debate in order to solicit future strategic directions and actions to be undertaken. (who.int)
Program1
- Tell the program whether you submit a list of proteins, transcripts or genes. (github.com)
Original1
- The material in this project series was likely kept in its original order by the archivist who first processed this fonds. (cca.qc.ca)
People1
- More than 80 mutations in the BCKDHA gene have been identified in people with maple syrup urine disease. (medlineplus.gov)
Position1
- In the Old Order Mennonite population, where maple syrup urine disease occurs frequently, the most common mutation replaces the amino acid tyrosine with the amino acid asparagine at position 438 (written as Tyr438Asn or Y438N). (medlineplus.gov)
Features1
- This weeks retro slot features the late great Gene Clark accompanied by Carla Olsen on a wonderful song from his last album So Rebellious A Lover . (americana-uk.com)