• Added genes are often accompanied by promoter and terminator regions as well as a selectable marker gene. (wikipedia.org)
  • These domestication traits likely consisted of a few major genes controlling dramatic changes in crop physiology, as is suggested by genetic studies comparing maize to its ancestor teosinte (Doebley et al. (springer.com)
  • The team first optimized this plasmid for bacteria-to-yeast conjugation by deleting 55 genes or small genetic regions to create four streamlined plasmids: M1-M4, with two clones each. (eurekalert.org)
  • Type 1 diabetes is characterized by the destruction of the insulin-secreting β-cells of the islets of Langerhans, by the production of little or no insulin, and, in most cases, by immune-mediated pathogenetic mechanisms highlighted by the presence of islet cell autoantibodies and by an altered frequency of immune-regulating genes in the HLA region. (diabetesjournals.org)
  • So far, most successful genetic engineering of plants has relied on inserting one or a few genes that supply simple, yet useful, properties. (istudy.pk)
  • Scientists have exploited this genetic transfer in order to get genes with desired properties into plant cells. (istudy.pk)
  • Analysis of drug resistance genes showed that all isolates harbored the inhA promoter mutation -15C→T ( 6 ). (cdc.gov)
  • The concept of genes as carriers of phenotypic information was introduced in the early 19th century by Gregor Mendel, who later demonstrated the properties of genetic inheritance in peas. (addgene.org)
  • This also leads us to the question of genetic changes that are outside of the coding region of protein-coding genes. (biomedcentral.com)
  • However, only sporadic knowledge existed till now regarding the regulatory regions of genes that might affect the expression of genes implicated in genetic diseases. (biomedcentral.com)
  • A recent publication has identified ~2.9 million DNase I hypersensitive sites (DHSs), markers of regulatory DNA in the human genome, based on the coexpression patterns of the regions and known promoters of all human protein-coding genes [ 16 ]. (biomedcentral.com)
  • It is believed that the occurrence of leukemia is the result of genetic and epigenetic changes in protooncogene and tumor suppressor genes [ 8 ]. (hindawi.com)
  • My thesis research focuses on five candidate sex determining genes: cyp19a1 (aromatase), Forkhead box protein L2, R-spondin1, Doublesex mab3-related transcription factor 1, and Sex-determining Region on Y chromosome-box 9. (utexas.edu)
  • The first three genes are markers of ovarian differentiation while the latter two genes are markers of testicular differentiation. (utexas.edu)
  • Importantly, it is shown that mutations affecting the isocitrate dehydrogenase (IDH) 1 and 2 genes, one of the most frequent genetic alterations in gliomas, lead to genome-wide DNA hypermethylation and the consequent IE dysfunction. (biomedcentral.com)
  • This pathway describes progression of a serrated precursor lesion, often followed by the onset of epigenetic instability involving promoter methylation and silencing of key tumour suppressor genes, and accounts for 15%-20% of sporadic colorectal cancer [ 1 , 2 ]. (hindawi.com)
  • These variations in genetic structure produce corresponding variations in the proteins that are encoded in the genes that are the blueprints for these proteins. (joessciencescorner.net)
  • Given this overall view, genetic research in regards to breast cancer is guided by an investigation of the genes that encode the structure of the enzymes involved in estrogen production. (joessciencescorner.net)
  • Highly polymorphic regions (such as HLA genes) are not represented either due to difficulty with designing primers because of the lack of constant regions flanking the variants. (tripod.com)
  • To reduce the risk of analyzing cell line- pathway can be divided into distinct stages based on the specific features, we used several representative cell lines for recombination status of the Ig genes and on the expression each of four major stages in B cell development: pro-B, pre-B, pattern of surface markers and the presence of intracellular proteins [1- 6]. (lu.se)
  • 11 genes and promoter regions. (msdmanuals.com)
  • Antimicrobial resistance occurs through different mechanisms, which include spontaneous (natural) genetic mutations and horizontal transfer of resistant genes through deoxyribonucleic acid (DNA). (who.int)
  • Therefore variations in the expression of these genes due to heritable genetic polymorphisms might modulate the process of carcinogenesis by altering the exposure levels of tobacco derived carcinogens. (bvsalud.org)
  • Our findings suggest that certain OPN gene polymorphisms may be used as molecular markers for the susceptibility and severity of OA. (biomedcentral.com)
  • We carried out a case-control study to clarify whether the abovementioned genetic polymorphisms in the OPN gene are associated with the susceptibility and severity of OA in a Chinese cohort. (biomedcentral.com)
  • Such patients probably have the same disease process as patients with type 1 diabetes in that they have similar HLA genetic susceptibility as well as autoantibodies to islet antigens, low insulin secretion, and a higher rate of progression to insulin dependency. (diabetesjournals.org)
  • There is evidence that, although incidence is almost always associated with environmental factors such as smoking or occupational exposure, susceptibility has a genetic component with early onset lung cancer following Mendelian inheritance. (bmj.com)
  • Many chromosomal regions have shown linkage to bipolar disorder, but meta-analyses of microsatellite marker-based linkage studies have not provided consistent findings of susceptibility regions. (medscape.com)
  • The Cancer Genetic Markers of Susceptibility genome-wide association study (GWAS) originally identified a single nucleotide polymorphism (SNP) rs11249433 at 1p11.2 associated with breast cancer risk. (johnshopkins.edu)
  • Fine-mapping analysis of the 1p11.2 breast cancer susceptibility locus confirms this region to be limited to risk to cancers that are ER-positive. (johnshopkins.edu)
  • Distinct germline genetic susceptibility profiles identified for common non-Hodgkin lymphoma subtypes. (who.int)
  • Although alcohol, tobacco, and human papillomavirus (HPV) are major risk factors for HNC, only a small fraction of high-risk individuals developed HNC implying a crucial role of genetic susceptibility in the disease. (who.int)
  • Carcinogenesis is a multistep process and individual risk to development of cancer depends not only on environmental factors or extrinsic exposure to carcinogens but also on genetic susceptibility of an individual. (bvsalud.org)
  • Factors that influence the tobacco exposed individuals developing a malignancy may thus include a combination of total tobacco exposure and genetic susceptibility of the individual 12 . (bvsalud.org)
  • Polymorphic genotypes of these enzymes may serve as genetic biomarkers for susceptibility to certain malignancies and therefore may help predict individual cancer risk 8 . (bvsalud.org)
  • in addition, they indicated recurrent mutations in the promoter region of telomerase (TERT) that reactivates the gene. (medscape.com)
  • The mutations that contributed to this increased efficiency were found to be in the promoter region of the conjugative gene traJ . (eurekalert.org)
  • Evidence of clonality was found within the 10 isolates because all exhibited identical genetic profiles defined by different molecular epidemiology methods ( 2 , 3 ) and mutations involved in drug resistance ( Figure ). (cdc.gov)
  • [ 14 , 15 ] Nevertheless, mechanisms behind therapeutic agents used in patients with the disorder have lent support to the possible role of a few different genetic pathways and mutations. (medscape.com)
  • Genetic factors such as the BRCA1 and BRCA2 genetic mutations and family history of the disease pointing to genetic factors that are poorly understood. (joessciencescorner.net)
  • Some of the recently discovered genetic risk factors, such as factor V Leiden and prothrombin G20210A mutations, are quite common in the population. (intechopen.com)
  • Over 95% of RIF-resistant M. tuberculosi s strains have mutations within the RIF resistance-determining region (RRDR) of the rpoB gene, and several molecular genetic tests to detect RRDR mutations have been developed. (msdmanuals.com)
  • In addition, the majority of diffuse astrocytomas (about 60%) carry TP53 mutations, which constitute a prognostic marker for shorter survival. (who.int)
  • IDH1/2 mutations are the histological classification and avoids the TeT2 pRomoteR methylation in low- most significant predictor of favourable ambiguity inherent to the diagnosis of gRade diffuse gliomas lacking idh1/2 outcome of glioblastoma patients. (who.int)
  • mutations high frequency of IDH1/2 mutations in oligodendrogliomas, astrocytomas and in alteRations in the RB1 pathway in The TET2 gene encodes the -KG- secondary glioblastomas derived thereof low-gRade diffuse gliomas lacking dependent enzyme that catalyses suggests that these tumours share a common genetic alteRations the conversion of 5-methylcytosine to common progenitor cell population. (who.int)
  • analyzed DNA methylation in the KIAA0319 promoter region to investigate whether epigenetic markers of language lateralization could be identified in nonneuronal tissue [ 7 ]. (biomedcentral.com)
  • Although these are histologically indistinguishable, they present distinct genetic and epigenetic signatures that allow their identification. (biomedcentral.com)
  • Sex differences at the genetic/epigenetic level in early development. (ubc.ca)
  • The association of genetic polymorphisms in CYP1A2, UGT1A4, and ABCB1 with autonomic nervous system dysfunction in schizophrenia patients treated with olanzapine. (nih.gov)
  • Further analysis with phylogenetic markers assigned MDR-TBEG to the principal genetic group 2, the Euro-American lineage of M. tuberculosis and its West African sublineage, on the basis of polymorphisms in codons kat G463 and gyr A95, the 7-bp pks15/1 deletion, and RD174 ( 7 , 8 ), respectively. (cdc.gov)
  • C, one of IL-6 functional polymorphisms in the promoter region, has been reported as influencing IL-6 gene transcription and has been associated with elevated CRP levels. (ijbls.org)
  • The polymorphism is in linkage disequilibrium with other MAOA and MAOB gene markers and displays significant variations in allele frequencies across ethnic groups. (nih.gov)
  • The polymorphism has been shown to affect the transcriptional activity of the MAOA gene promoter by gene fusion and transfection experiments involving three different cell types. (nih.gov)
  • This promoter region polymorphism may be useful as both a functional and an anonymous genetic marker for MAOA. (nih.gov)
  • For second task, Brain Tumor Radiogenomic Classification, participants build models that use mpMRI imaging to predict MGMT (O[6]-methylguanine-DNA methyltransferase) promoter methylation status. (rsna.org)
  • Promoter aberrant methylation status of ADRA1A is associated with hepatocellular carcinoma. (nih.gov)
  • Pharmacogenetic studies have been also performed in order to evaluate the role of host genetic variants in the prediction of recurrence risk and response to adjuvant treatment with FLs and OXA. (frontiersin.org)
  • This is becoming ever more evident as less single nucleotide variants are found to be associated with genetic diseases that affect the protein sequence than found in regulatory regions [ 15 ]. (biomedcentral.com)
  • Genetic variants of HIF1? (cdc.gov)
  • Objective 4: Phenotypic and genetic characterization of extra-intestinal pathogenic Escherichia coli (ExPEC) isolated from poultry and produce. (usda.gov)
  • Combined promoters, so-called stacked promoters, allowed, after detailed characterization of the genetic context, prediction of the resulting expression strength. (rwth-aachen.de)
  • In this context, there is a need for new predictive markers, beyond the tumor stage, to select what patients will benefit from an adjuvant treatment and to better tailor treatment schemes and schedules. (frontiersin.org)
  • [ 6 ] A majority of these tumors will exhibit polysomy of the epidermal growth factor receptor ( EGFR ) genetic locus on chromosome 7 in subsets of tumor cells. (medscape.com)
  • In the first task, Brain Tumor Segmentation, participants build models that produce detailed segmentations of brain tumor sub-regions that correspond to those created by neuroradiologists. (rsna.org)
  • research shows that about 90% of the blood system of malignant tumors with at least the height of single gene methylation is closely related since this is a reversible process of genetic modification can be through to handle to restore the normal expression of gene methylation, to achieve the purpose of prevention and treatment of tumor [ 10 ]. (hindawi.com)
  • Exposure to a tumor promoter will evoke an altered response pattern wherein initiated cells, but not the normal population, are stimulated to grow. (bvsalud.org)
  • The signal to expand clonally can be provided either by direct stimulation of the initiated cell, or as an indirect result of the effects of the tumor promoter on the adjacent normal cells. (bvsalud.org)
  • Our aim was to integrate our previously reported clinical-genetic prognostic score with new immunogenetic markers of 5-year disease-free survival (DFS) to evaluate the recurrence risk stratification before fluoropyrimidine (FL)-based adjuvant therapy. (frontiersin.org)
  • Furthermore, the introduction of novel prognostic markers may also promote exclusively new treatment possibilities, and there is an obvious need to identify markers that could be used as selection criteria for novel therapies. (biomedcentral.com)
  • These findings suggest that markers of inflammation could serve as prognostic indicators and potentially lead to immune-based therapies to prevent developmental delays in at-risk children. (cdc.gov)
  • This study utilised genetic and clinical data ( n = 1034) collected as part of the International Consortium on Lithium Genetics (ConLi + Gen) project. (cambridge.org)
  • 4, 5 The process involves use of many evenly spaced polymorphic DNA markers to create landmarks across each chromosome. (bmj.com)
  • It might have an important polymorphic association at the promoter regions of several MMPs such as MMP-1 (-1607 1G/2G), MMP-2 (-1306 C/T), MMP-3 (-1171 5A/6A), MMP-9 (-1562 C/T) and TIMP-2 (-418 G/C or C/C). Tissue inhibitors of metalloproteinases (TIMPs) are naturally occurring inhibitors of MMPs, which inhibit the activity of MMPs and control the breakdown of ECM. (biomedcentral.com)
  • Recruitment of modified histone proteins, H3K4me3 and H3K27me3, at the aromatase promoter is FPT-specific during gonad determination. (utexas.edu)
  • This book chapter will comment on fluorescent reporter proteins and nanocrystals' applicability as fluorescent markers. (intechopen.com)
  • In a meta-analysis of more than 8000 European-ancestry subjects significant association with schizophrenia was observed in a region of linkage disequilibrium on chromosome 6p22.1, a region that has been commonly implicated in schizophrenia for a long time [ 4 ]. (biomedcentral.com)
  • Like initiation, conversion requires genetic alterations in which cellular growth is further deregulated and thus proceeds uncontrolled 5,29 . (bvsalud.org)
  • Previously, classical genetic studies involving cross breeding of mouse strains with differing susceptibilities have identified chromosomal areas associated with predisposition to developing spontaneous and chemically induced lung adenomas. (bmj.com)
  • The presence of this uncommon mutation, Ile561Val, outside the rifampin resistance-determining region supports the hypothesis that the MDR isolates are clonal in origin. (cdc.gov)
  • This latter pathway involves the previously well-defined series of genetic aberrations such as APC mutation and chromosomal instability and accounts for the majority of colorectal cancer [ 12 ]. (hindawi.com)
  • To have a functional consequence, a mutation does not have to be in the coding region. (tripod.com)
  • Environmental carcinogens and certain other endogenous factor (genetic alteration and mutation) interacting in a complex manner can give rise to development of cancer. (bvsalud.org)
  • Mutation in the cellular machinery controlling growth or differentiation is an example of the type of genetic change that occurs in initiation 5 . (bvsalud.org)
  • There are clinical challenges related to adjuvant treatment in colorectal cancer (CRC) and novel molecular markers are needed for better risk stratification of patients. (frontiersin.org)
  • A meta-analysis of original data from 11 previous linkage studies in 1067 bipolar disorder families yielded significant findings in chromosomal regions 6q for bipolar I and 8q for bipolar I/II, as well as suggestive findings at chromosomal regions 9p and 20p for bipolar I. (medscape.com)
  • Etiology of mood disorders is unclear, although a genetic component has been strongly suggested by family and twin studies. (medscape.com)
  • Dr Heidi Mattock and use genetic data to identify the etiology of human canceRs. (who.int)
  • The finding that a TIGR/MYOC mt.1(+) determination provided a strong marker for glaucoma progression, above and beyond the other baseline risk factors, suggests a clinical utility in testing for this promoter genotype. (nih.gov)
  • All regions of the country showed high levels of genotype diversity, suggesting a low level of transmission of M. tuberculosis strains in previously treated patients. (who.int)
  • Our transgenic parasite lines have been designed so that we can target DNA damage for repair analysis to var gene coding regions or drug selectable markers driven by var gene promoters. (grantome.com)
  • A major variant of myocilin (MYOC) [TIGR/MYOC mt.1 (-1000 C/G)], present in the gene's promoter, is found to be associated with more rapid progression of the glaucoma disease state. (nih.gov)
  • When a genetic association is found, it is very tempting to speculate that the associated variant may be a good biomarker (usually because of the small P value accompanying the association). (tripod.com)
  • Association of functional variant in GDF1 promoter with risk of congenital heart disease and its regulation by Nkx2.5. (cdc.gov)
  • Alleles with 3.5 or 4 copies of the repeat sequence are transcribed 2-10 times more efficiently than those with 3 or 5 copies of the repeat, suggesting an optimal length for the regulatory region. (nih.gov)
  • We suggest GABBR1, GABA receptor B1 implicated in schizophrenia based on a HERV-W LTR in the regulatory region of GABBR1. (biomedcentral.com)
  • Hypermethylation in the promoter region of the ADRA1A gene is associated with opioid use disorder in Han Chinese. (nih.gov)
  • These inconsistencies can be explained in part by heterogeneity between studies, possibly due to the different criteria for phenotypic assessment, age, sample size, population genetic background, and environmental factors. (biomedcentral.com)
  • Response to lithium in patients with bipolar disorder is associated with clinical and transdiagnostic genetic factors. (cambridge.org)
  • Venous thrombosis is a multifactorial disease frequently related to the interaction of genetic and environmental risk factors. (intechopen.com)
  • Genetic sequencing may be a better way of characterizing gliomas than classic histopathology. (medscape.com)
  • So, as new evolutionary optima have been set by environmental changes (e.g., domestication, management practices, biotic or abiotic pressures) or major shifts in genetic background, plant breeders have selected better-adapted genotypes while pursuing faster genetic gains through technological innovations and scientific breakthroughs. (springer.com)
  • The integration of IFNG -rs1861494 in our previous clinical genetic multiparametric score of DFS improved the patients' risk stratification (Log-rank P = 0.0026 in the pooled population). (frontiersin.org)
  • We aimed to determine if clinical and biological markers of inflammation in the first year of life predict cognitive, language, and motor outcomes in children living in an urban slum in Bangladesh. (cdc.gov)
  • Febrile illness was used as a clinical marker of inflammation and elevated concentrations of inflammation-related cytokines (IL-1β, IL-6, TNF-α, IL-4, IL-10) in sera collected from a subset of the cohort (N = 127) at 6 months of age were used as biomarkers of inflammation. (cdc.gov)
  • Clinical and biological markers of inflammation in the first year of life were significantly associated with poor neurodevelopmental outcomes. (cdc.gov)
  • RIF resistance is used as a surrogate marker for MDR TB, because 95% of the strains resistant to RIF are also resistant to INH. (msdmanuals.com)
  • In the process called quantitative trait loci (QTL) mapping, attempts are made to find significant correlations between marker alleles and the phenotypic variation, or disease state. (bmj.com)
  • To fine-map this locus, we genotyped 92 SNPs in a 900kb region (120,505,799-121,481,132) flanking rs11249433 in 45,276 breast cancer cases and 48,998 controls of European, Asian and African ancestry from 50 studies in the Breast Cancer Association Consortium. (johnshopkins.edu)
  • Genetic heterogeneity and locus heterogeneity are used interchangeably in practice but this requires attention. (tripod.com)
  • Integration of Large-Scale Genomic Data Sources With Evolutionary History Reveals Novel Genetic Loci for Congenital Heart Disease. (cdc.gov)
  • Comparative chloroplast genomics as well as detailed characterizations of individual chloroplast genomes serve as the basis for functional genomic studies [ 20 ] and can direct attempts at chloroplast transformation for genetic engineering [ 21 ]. (biomedcentral.com)
  • Over the last decade, numerous findings regarding the distinct molecular and genetic profiles of GBM have led to the emergence of several therapeutic approaches. (biomedcentral.com)
  • Genetic Diversity and Streptomycin Sensitivity in Xanthomonas axonopodis pv. (mdpi.com)
  • Chapter 3 identifies the gonad-specific promoter and the temperature-dependent DNA methylation signatures of the aromatase gene during gonadal differentiation. (utexas.edu)
  • It is known that genetic variation accounts for 20-80% of the total variation in reading skills, and the genetic variations discovered thus far only explain the "tip of the iceberg" of estimated heritability [ 1 , 2 ]. (biomedcentral.com)
  • This proposal will further the understanding of antigenic variation in malaria by integrating the study of the parasite mechanisms for DNA recombination and repair and the genetic analysis of field isolates. (grantome.com)
  • To date, the species and cultivars that make up the AA genome clade have provided most of the genetic variation and resources that have led to the success of domesticated rice 4 , while other genome clades have contributed relatively little to domestication. (nature.com)
  • Given long-range effects of genetic variation, this assumption may not be right unless documented experimentally. (tripod.com)
  • Test each promoter in mice and measure the activity in retinal cells using a fluorescent marker to determine which promoter is best. (fightforsight.org.uk)
  • Lewy bodies which are intraneuronal aggregates composed mainly of misfolded alpha synuclein (a-syn) protein is a pathological hallmark seen in both sporadic and genetic forms of PD. (lu.se)
  • Although genetic similarity reflected geographical separation, the density of SNVs also correlated with our previous report on variations in salinity tolerance. (nature.com)
  • The study of copy number variations in the regions of PRKAB2 and PPM1K among congenital heart defects patients. (cdc.gov)
  • The order of these 4 nucleotides makes up the genetic code and provides the instructions to make every protein within an organism. (addgene.org)
  • The methylation level of the GRHL2 promoter region in acute leukemia patients and cell lines was significantly higher than the normal control group, and we found the elevated mRNA and protein levels of GRHL2 in acute leukemia cell lines after the use of the demethylation drug arsenic trioxide and 5-azacitidine. (hindawi.com)
  • Molecular genetic methods were implemented into the screening examinations for thrombophilic disorders in the 1990's along with the first discoveries of coagulation inhibitors (AT, protein C and protein S). The discovery of the molecular cause of activated protein C (APC) resistance by Bertina in 1994 greatly expanded their utilization. (intechopen.com)
  • Using proteomics and causal mediation analysis, we examined 155 circulating protein markers in 624 cases and 624 matched controls in a case-control study nested within the European Prospective Investigation into Cancer and Nutrition (EPIC). (who.int)
  • TPD1-like Gene as a Suitable Marker for Early Sex Determination in Date Palm (Phoenix dactylifera L. (mdpi.com)
  • Genetic determination of RIF resistance is now commonly available in developed countries and is becoming increasingly available in the developing world. (msdmanuals.com)
  • Genetic testing and molecular biomarkers 2019 8 23 (9): 601-609. (cdc.gov)
  • The goal of this project is to use omic technologies (proteomic, genomic, and transcriptomics methods) and bioinformatics in a systems approach to understand how pathogens become resistant to food-related stresses, to determine their pathogenicity, and to identify markers for detection and typing. (usda.gov)
  • A review outlined a long genomic region to be associated with the disease, encompassing 25 Mb of the 6p genomic region in question [ 14 ]. (biomedcentral.com)
  • Due to the complicated nature of the region on chr1p11.2:120,300,000-120,505,798, that lies near the centromere and contains seven duplicated genomic segments, we restricted analyses to 429 SNPs excluding the duplicated regions (42 genotyped and 387 imputed). (johnshopkins.edu)
  • Clinically, OPN in plasma and synovial fluid (SF) has been reported to be related to progressive joint damage in knee OA, suggesting that OPN may serve as a biochemical marker for determining disease severity [ 18 ]. (biomedcentral.com)
  • Diabetes which has been described as an inflammatory disease has provided avenues for investigations on inflammatory markers that might be associated to its development. (ijbls.org)
  • The cumulative genetic risk score (CGS) of 13 SNPs in KIAA0319 was calculated. (biomedcentral.com)
  • To identify and test a 'promoter' - a short stretch of DNA (genetic material) - that could target and deliver treatment to the over-active cells in the retina. (fightforsight.org.uk)
  • Mycobacterium tuberculosis isolates from previously treated patients ( n = 88) from all regions of Syrian Arab Republic were characterized in terms of antibiotic sensitivity and genotyping using double-repetitive- element polymerase chain reaction (DRE-PCR) method for the proximity of the repetitive DNA elements IS 6110 (a mobile genetic element) and PGRS. (who.int)
  • Here we analyzed these regulatory regions of the human genome for the presence of the long terminal region (LTR) of the human endogenous virus type W (HERV-W) as this type of HERV was identified in patients with recent-onset schizophrenia [ 7 ]. (biomedcentral.com)
  • When used with other PRS and biological markers in the future this approach may help inform which patients are most likely to respond to lithium treatment. (cambridge.org)
  • In addition to being speedy, genetic DST should also be accurate, and, to be useful in resource-poor countries where most MDR TB patients reside, should be simple to use and cost-effective. (msdmanuals.com)
  • Patients with Hunter syndrome are distinguished from patients with other MPSs because of the male dominant pattern due to the X-linked recessive genetic transmission. (medscape.com)
  • A library was constructed with single nucleotide exchanges, which reveals that the -35 and -10 regions are crucial for efficient promoter activity. (rwth-aachen.de)
  • J:208882 FANTOM Consortium and the RIKEN PMI and CLST (DGT) and others, A promoter-level mammalian expression atlas. (jax.org)
  • FPT) suppresses expression of ovarian markers while increasing expression of testicular markers. (utexas.edu)
  • MPT) increases expression of ovarian markers while testicular markers are suppressed. (utexas.edu)
  • We constructed and characterized several sigma-70 factor dependent synthetic promoters and combinations for heterologous gene expression. (rwth-aachen.de)
  • With well-characterized promoters and landing pads, fine tuning of gene expression can be conducted on two levels, promoter and integration site. (rwth-aachen.de)
  • 31 Genetic inheritance was first discovered by Gregor Mendel in 1865, following experiments crossing peas. (wikipedia.org)
  • Useful markers associated with molecular aggressiveness might have a role in prognostication of malignancies and to better recognize patient groups that need more antagonistic treatment options. (biomedcentral.com)
  • Genetic engineering techniques allow the modification of animal and plant genomes. (wikipedia.org)
  • oxidation modification of the genetic material may also participate in the progression of benign to malignant neoplasms. (bvsalud.org)
  • Region from 2016 to 2020. (who.int)
  • Plasmids are small genetic structures that are independent from the chromosomes and can replicate on their own. (eurekalert.org)