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Transcriptional profiling of wheat caryopsis development using
Transcriptional profiling of wheat caryopsis development using

... wheat caryopses was analyzed using cDNA arrays. Using a mixed model analysis of variance (ANOVA) method, 29% (2,237) of the genes on the array were identified to be differentially expressed at the 6 different time-points examined, which covers the developmental stages from coenocytic endosperm to ph ...
Gene Section SIL (SCL/TAL1 interrupting locus) Atlas of Genetics and Cytogenetics
Gene Section SIL (SCL/TAL1 interrupting locus) Atlas of Genetics and Cytogenetics

... holopresencephaly, randomized left/right asymmetry and marked apoptosis of the neural folds. Genetic evidence showed that SIL is required for the Sonic Hedgehog response pathway. SIL phosphorylation and interactions with PIN1 is required for maintenance of the mitotic checkpoint. ...
WebGestalt 2017 Manual
WebGestalt 2017 Manual

... (+61.2%), with at least 15% increase for each organism. Specially, the new version significantly increased the number of supported Affymetrix platforms from 68 to 101 (+48.5%), Agilent platforms from 18 to 25 (+38.9%) and Illumina platforms from 10 to 18 (+80.0%). These expansions fill the gap betwe ...
Biostat Jhsph Edu Hji Courses Genomics Sequencing Ppt
Biostat Jhsph Edu Hji Courses Genomics Sequencing Ppt

... and their assignment to one or more gene models is indicated in color. Sequence reads falling outside known or predicted regions are shown in gray. RNAFAR regions (clusters of reads that do not belong to any gene model in our reference set) are shown as dotted lines. They can either be assigned to n ...
Statistical analysis of DNA microarray data
Statistical analysis of DNA microarray data

... comparable GEO Samples and forms the basis of GEO's suite of data display and analysis tools. Samples within a GDS refer to the same Platform, that is, they share a common set of probe elements. Value measurements for each Sample within a GDS are assumed to be calculated in an equivalent manner, tha ...
Probing the evolution of appendage specialization by
Probing the evolution of appendage specialization by

... explanation is that there may be weak or transient PhUbx expression in Mxp/T1 that was previously overlooked. Careful examination of PhUbx expression in the anterior thorax found no evidence for such expression, beyond expression in posterior T1 in the neuroectoderm (21). In addition, this explanati ...
XistAR write up
XistAR write up

... to our understanding of X-inactivation via Xist thus far, these researchers found an additional novel piece of long non-coding RNA expressed from the inactivated X chromosome. They identified this lncRNA to be antisense of Xist, and that its expression is required for proper Xist functioning. Here, ...
Analysis of non‐polar deletion mutations in the genes of the spo0K
Analysis of non‐polar deletion mutations in the genes of the spo0K

... in many di¡erent organisms [5]. The Spo0K oligopeptide permease in B. subtilis can import oligopeptides from 3^5 amino acids with apparently little, if any, speci¢city, and is required for cells to utilize oligopeptides as a source of amino acids (for example, see [6,7]). The function of each of the ...
No Slide Title
No Slide Title

... Diagnose malignant tissue from normal one Drug effect study ...
Statistical analysis of DNA microarray data
Statistical analysis of DNA microarray data

... comparable GEO Samples and forms the basis of GEO's suite of data display and analysis tools. Samples within a GDS refer to the same Platform, that is, they share a common set of probe elements. Value measurements for each Sample within a GDS are assumed to be calculated in an equivalent manner, tha ...
Guidelines for Human Gene Nomenclature (1997)
Guidelines for Human Gene Nomenclature (1997)

... In one of the most thought-provoking talks for many participants, Carl Price (Rutgers) described the system of the Commission Plant Gene Nomenclature (CPGN) system. Angiosperms, with the ability and propensity for duplicating whole genomes, have widely differing numbers of members in different gene ...
Hemolytic anemias - Hemoglobinopathies
Hemolytic anemias - Hemoglobinopathies

... » Mild hypochromic, microcytic anemia » Patients are usually asymptomatic with symptoms occurring under stressful conditions such as pregnancy –  thalassemia may also be found in combination with any of the hemoglobinopathies (S, C, or E) leading to a mild to severe anemia depending upon the partic ...
Cluster analysis
Cluster analysis

... Current methods for classifying human malignancies rely on a variety of morphological, clinical, and molecular variables. In spite of recent progress, there are still uncertainties in diagnosis. Also, it is likely that the existing classes are heterogeneous. DNA microarrays may be used to characteri ...
Phytozome Tutorial from David Goodstein
Phytozome Tutorial from David Goodstein

... kinase or repeat !), so the results page presents an overview of the gene families that have  been found (Figure 7).  Results are ordered in decreasing family size.  Each row shows the  family size, which node it was found at (if you performed an “all nodes” search; otherwise  the node is simply the ...
Rate Asymmetry After Genome Duplication Causes Substantial
Rate Asymmetry After Genome Duplication Causes Substantial

... However, a previous study of gene pairs formed by WGD in the yeast Saccharomyces cerevisiae found conflicting topologies among neighbor-joining (NJ) trees drawn from different loci and suggested that this conflict was the result of ‘‘asynchronous functional divergence’’ of duplicated genes (Langkjae ...
The trp Operon
The trp Operon

... the flexible neck straw. Smooth the tape down as much as possible. Each colored straw segment represents a gene. Collectively, the structure formed when the pieces are taped to the longer straw now represents the trp operon. d. The RNA polymerase is represented by the segment of straw with the large ...
splice sites at the termini generating a novel intron from a dSpm
splice sites at the termini generating a novel intron from a dSpm

... term dSpm will be used here to designate the nonautonomous elements. The interaction of functions encoded in trans by En/Spm with dSpm elements has led to the genetic characterization of En/Spm-encoded functions (McClintock, 1961) and provided insights into the substrate requirements for transpositi ...
Notification of a Notifiable Low Risk Dealing
Notification of a Notifiable Low Risk Dealing

... The primary interest here is in the gene or genes under study and the function of these gene(s). Please list this information if known. Such details are not required about gene(s) commonly used as markers, for selection and/or any other routine procedures. However it is of interest to identify gener ...
View Full PDF - Biochemical Society Transactions
View Full PDF - Biochemical Society Transactions

... several mechanisms have been postulated to explain the beneficial effect associated with the symbiotic hydrogenase activity. Among them, hydrogenase reaction might protect nitrogenase from the detrimental effect of oxygen, prevent inhibition of the nitrogenase reaction by hydrogen or provide an addi ...
Extended Life-Span and Stress Resistance in Drosophila
Extended Life-Span and Stress Resistance in Drosophila

... • In vertebrates, the insulin receptor regulates glucose metabolism, while IGF-1R promotes growth. IGF-1R is activated by its ligand IGF-1, which is secreted in response to growth hormone. • While is has been demonstrated that the InR family of proteins regulate lifespan in invertebrates, it is not ...
Notification of a Notifiable Low Risk Dealing
Notification of a Notifiable Low Risk Dealing

... longer an available response (c) a dealing involving a replication defective vector derived from Human adenovirus or Adeno associated virus in a host mentioned in item 4 of Part 2 of Schedule 2, if the donor nucleic acid: (i) cannot restore replication competence to the vector; and (ii) does not: (A ...
Heritable Disorders of Connective Tissue: Research & Repository
Heritable Disorders of Connective Tissue: Research & Repository

... Schalkwijk et al., 2001 reported the 5 (of 151 screened) patients with an EDS syndrome with deficiency of Tenascin X protein– an extracellular matrix protein resulting from recessive mutations in the encoding XB gene. – hypermobile joints – hyperextensible skin – easy bruising – slow wound healing, ...
10 new
10 new

... it is bound to tryptophan. b. The trpR gene encodes the repressor; trpO is the operator; trpA encodes the enzyme tryptophan synthetase. A trpR2 repressor cannot bind tryptophan, a trpO2 operator cannot be bound by the repressor, and the enzyme encoded by a trpA2 mutant gene is completely inactive. D ...
A xylem-specific cellulose synthase gene from aspen (Populus
A xylem-specific cellulose synthase gene from aspen (Populus

... plants were bent to create tension stress for various time intervals (from 4 to 40 h). Surprisingly, tension stress rapidly induced phloem-speci®c GUS expression (Figure 5), but did not cause an apparent change in GUS expression in the developing xylem (Figure 5b). Thus under a normal developmental ...
Evolution of antifreeze glycoprotein gene from a trypsinogen gene in
Evolution of antifreeze glycoprotein gene from a trypsinogen gene in

... types of antifreeze proteins in various polar and subpolar fishes represents a remarkable example of cold adaptation, but how these unique proteins arose is unknown. We have found that the antifreeze glycoproteins (AFGPs) of the predominant Antarctic fish taxon, the notothenioids, evolved from a pan ...
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Epigenetics of diabetes Type 2

In recent years it has become apparent that the environment and underlying mechanisms affect gene expression and the genome outside of the central dogma of biology. It has been found that many Epigenetic mechanisms are involved in the regulation and expression of genes such as DNA methylation and chromatin remodeling. These epigenetic mechanisms are believed to be a contributing factor to pathological diseases such as Diabetes type II. An understanding of the epigenome of Diabetes patients may help to elucidate otherwise hidden causes of this disease.
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