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Novel visual system homeobox 1 gene mutations in Turkish patients
Novel visual system homeobox 1 gene mutations in Turkish patients

... 0.964/probably damaging 0.986/probably damaging ...
manual K. lactis Protein Expression Kit E1000S
manual K. lactis Protein Expression Kit E1000S

... are significantly pure, that do not require difficult lysis of yeast cells to isolate, and that may have desired post-translational modifications (e.g. glycosylation) that cytosolic proteins do not. Protein secretion using pKLAC2 is achieved by generating a fusion between the protein of interest and ...
Mouse mutants and phenotypes - Case Transgenic And Targeting
Mouse mutants and phenotypes - Case Transgenic And Targeting

... of interest, with the number of, and links to, corresponding entries at the respective sites. If you are interested in IKMC products, follow the ‘Details’ link in the ‘IKMC Knockout Attempts’ column. This brings you to a page that lists all IKMC knockout attempts for your gene of interest (Fig. 1 bo ...
Part 2 - Laboratory of Aquaculture & Artemia Reference Center
Part 2 - Laboratory of Aquaculture & Artemia Reference Center

... population genomics etc. Artemia shows well developed gene regulatory system for its survival even under extreme conditions. Artemia seems to be a promising system for stress response studies as observed in our laboratory since it shows a swift adaptation to harsh environments. A variety of Heat sho ...
region of the Bacillus subtilis chromosome containing genes
region of the Bacillus subtilis chromosome containing genes

... YseE show, respectively, homology to two integral membrane proteins, namely LacF and LacG. However, no ORF was found with homology to LacK, a membraneperipheral ATP binding protein. The product of the abfA gene shows very high homology with the a-L-arabinofuranosidase gene from Streptomyces lividans ...
as a PDF
as a PDF

... hypertranscription in somatic cells, presumably through the recruitment of histone acetylation factors [31,32], it does not associate specifically with the X chromosome in male germ cells. Furthermore, H4 acetylation at lysine 16, which is thought to be a reliable marker for active transcription, was ...
Lack of Ketone Body Response Associated with Hyperglycaemia
Lack of Ketone Body Response Associated with Hyperglycaemia

... hypoglycaemia. Post-operatively all infants developed diabetes mellitus (DM) requiring insulin. Their DM proved extremely difficult to control with each infant developing marked hyperglycaemia (laboratory blood glucose >26mmoV1). At the time of the hyperglycaemia blood was taken for measurement of f ...
Summary 121 Summary The Hox genes form a subset of the
Summary 121 Summary The Hox genes form a subset of the

... to have arisen by tandem duplication of a single gene, followed, in vertebrates, by duplication of the cluster itself. As a consequence, Hox genes occupying the same relative position along the 5' to 3' chromosomal coordinate, named paralogous genes, share more similarities in sequence, expression p ...
Title: Genes in the Postgenomic Era Authors: Paul E. Griffiths and
Title: Genes in the Postgenomic Era Authors: Paul E. Griffiths and

... be capable of autocatalysis (self-replication) in order to explain heredity. It must be capable of heterocatalysis – producing something different in structure from itself – in order to explain the manifestation of genetic differences in different phenotypes. Finally, it must be mutable – able to c ...
synthesis Gene Cluster of Streptomyces clavuligerus
synthesis Gene Cluster of Streptomyces clavuligerus

... with ten known ArgD proteins showed the presence of domains conserved in ACOAT’s and OAT’s, but the amino acid similarity of the ORF4-encoded protein is higher to ACOATs of B. subtilis and E. coli than to the corresponding OAT proteins. This observation is consistent with the amination of N-acetylgl ...
SET2 - CBSE
SET2 - CBSE

... Ans. Fossils are remains/ hard parts of life forms, found in sedimentary rocks, some of them appear similar to modern organisms /some represent extinct organisms, study of fossils in different sedimentary layers indicates the geological period in which they existed (provides palaentological evidence ...
Recombinant DNA Technology
Recombinant DNA Technology

... They can alter the genes of bacteria to cause them to produce a desired human protein product. 2. Once a gene is sequenced, it can be used in recombinant DNA techniques. Sequencing is a technique used to determine the order of genetic information in DNA. For example the sequence of a gene might begi ...
DNA sequence and chromatin structure
DNA sequence and chromatin structure

... Method 2 16 maps ...
Börjeson–Forssman–Lehmann syndrome: defining
Börjeson–Forssman–Lehmann syndrome: defining

... Mutations in the zinc finger protein ZIC3 are associated with visceral heterotaxy or situs abnormalities [23]. F9 is the well known coagulation factor IX associated with hemophilia B. MCF2, also called DBL, is an oncogene, where no clinical condition could be attributed yet to the loss of the MCF2 g ...
Molecular and Clinical Markers for the Diagnosis and Treatment of
Molecular and Clinical Markers for the Diagnosis and Treatment of

... • Type 2A, 2B and 2M variants with decreased platelet-dependent function Autosomal dominant • Can be caused mainly by missense mutations (small deletions or frameshift mutations also) ...
Coffee, B, Zhang, F, Warren, ST and Reines, D: Acetylated histones are associated with the FMR1 gene in normal but not fragile X syndrome cells. Nature Genetics 22:98-101 (1999).
Coffee, B, Zhang, F, Warren, ST and Reines, D: Acetylated histones are associated with the FMR1 gene in normal but not fragile X syndrome cells. Nature Genetics 22:98-101 (1999).

... drug-induced increases in histone acetylation are ineffective in activating transcription from some promoters such as the P1 promoter of c-myc (ref. 25), the herpes simplex virus thymidine kinase promoter26 and certain methylated genes in tumour cells27. A survey of human genes by differential displ ...
Gene expression patterns in human placenta
Gene expression patterns in human placenta

... complement inhibitor, Crry, which is similar to MCP and CD55. Deletion of Crry leads to death in utero, with C3 deposited on the placenta and marked invasion of inflammatory cells into the placenta (27). Also, the amnion compared with the chorion is remarkably nonimmunogenic: the amniotic membrane t ...
Unusual mutations in high functioning fragile X males
Unusual mutations in high functioning fragile X males

... expression of the premutated gene both at the RNA and the protein level.'0 1 The full mutation may occur at germ cell proliferation or in an early transitional stage of embryogenesis.'7-'9 The substrate is a maternally inherited premutation and the product is usually a mosaic pattern of full mutatio ...
document
document

... • Depending on the disease a small letter (Alleles) can be good or bad genes. In our disease it is bad. • Example: In order to have Galactosemia you need two bad genes, or two small Alleles, or recessive(aa) genes. Having two of the same genes (aa) is called a homozygous pair. To be a carrier you ne ...
Tutorial - Ensembl
Tutorial - Ensembl

... the live-site, search for ‘human EPO gene’ and click on the Ensembl gene identifier (ENSG0000130427)- this will link you to the ‘GeneView’ page for the Erythropoeitin precursor. Please note that since this tutorial was constructed updates may have been made, so to emulate this tutorial exactly, plea ...
Micro Array Explorer MAExplorer
Micro Array Explorer MAExplorer

... • The 2-class division allows using sets of replicates for computing better gene expression estimates and allows using t-Tests etc. to determine statistical significance • The ordered N-list of samples is used to represent an ordered timeseries, development stages, drug-dose response, etc. • [In MAE ...
Heterogeneous lengths of copy number mutations
Heterogeneous lengths of copy number mutations

... range of ~100 bp to several Mbs demonstrating an altered (or non-neutral) dosage status.5 They are typically introduced in the genome by recombination-based or replication-based mechanisms. The detection of CN variations is clinically important because they can provide the genetic background of huma ...
reported several instances of so-called " complex genes ", whose
reported several instances of so-called " complex genes ", whose

... two different pairs of M- and R-genes makes these cases distinct, and, at the same time, invalidates the view that their occurrence is a matter of chance. One is led to the conclusion that linkage, in the usual sense, is not involved here at all, but, rather, that two complex gene molecules exist: t ...
Immunome database for marsupials and monotremes Open Access
Immunome database for marsupials and monotremes Open Access

... Genome sequencing has generated huge amounts of genomic data. This has expedited the identification of genes in these species. Despite the availability of genome assemblies, only the most phylogenetically conserved immune genes have been identified using automated gene annotation pipelines. Genes in ...
open access - Max-Planck-Institut für Pflanzenzüchtungsforschung
open access - Max-Planck-Institut für Pflanzenzüchtungsforschung

... during domestication, genome-wide comparison of expression between domesticated and multiple wild species is lacking. One of the most heavily studied domestication events is that of tomato. Tomato is a member of a complex of 13 interfertile species that occupy a wide range of habitats in South Amer ...
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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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