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Living Things
Living Things

... Mutations Mutations can cause a cell to produce an incorrect protein during protein synthesis. As a result, the organism’s trait, or phenotype, may be different from what it normally would have been. ...
Genetics of mammalian meiosis: regulation, dynamics and impact
Genetics of mammalian meiosis: regulation, dynamics and impact

... stood in Saccharomyces cerevisiae, in which genetic and molecular studies have led to a relatively comprehen­ sive understanding of the transcriptional regulation of genes involved in meiosis 7. The ‘master regulator’ of yeast meiosis is meiosis­inducing protein 1 (Ime1), which, by interacting with ...
IFN
IFN

... state = lupus Lovgren T, Eloranta ML, Bave U, Alm GV, Ronnblom L. Induction of interferon-alpha production in plasmacytoid dendritic cells by immune complexes containing nucleic acid released by necrotic or late apoptotic cells and lupus IgG. Arthritis Rheum 2004; 50 ...
Cover Letter
Cover Letter

... /note=33294 is selected for better Z-score and final score CDS complement (33667 - 34023) /note=Glimmers and GeneMark both agree with 34023. 34023 is selected because of better scores. CDS complement (34044 - 35870) /note=According to Phage DB, the function should be DNA Polymerase I. DNA primase/po ...
Jeopardy
Jeopardy

... DOMINATE OR RECESSIVE TRAIT DEPENDS ON THE TRAITS IN THAT POPULATION ...
Origin and specification of type II sensory neurons in
Origin and specification of type II sensory neurons in

... labelled cells within the postulated sensory organ lineages, since many precursor cells had already completed their last Sphase (i.e. last possibility for BrdU incorporation) at the time of exposure. A likely pattern of SOP division was inferred from the patterns of BrdU-labelled cells (Bodmer et al ...
Saccharomyces Genome Database.
Saccharomyces Genome Database.

... These databases include those that provide specifics about yeast genes (such as descriptions of gene products, sequences, intron/exon boundaries, promoters, and tRNAs), those that provide a framework for classifying gene products, and those that provide information about homologs of yeast genes in o ...
[ 19] Saccharomyces Genome Database - SGD-Wiki
[ 19] Saccharomyces Genome Database - SGD-Wiki

PowerPoint-Präsentation
PowerPoint-Präsentation

... Figure S6. Analyses of the primary RpoN regulon in P. aeruginosa A The PseudoCAP annotation (Winsor et al, 2005) was used to categorize the members of the primary RpoN regulon and the enrichment of specific gene classes is displayed. Strong and moderate over-represented classes are highlighted in d ...
Jeopardy
Jeopardy

... FREQUENCY OF A DOMINATE OR RECESSIVE TRAIT ...
Case report - HAL
Case report - HAL

... surrounding non-tumor liver was normal. A somatic mutation of HNF1 (787 C>T) leading to an amino acid substitution (R263S) was found in the adenoma sample. The mutation appeared homozygous at the RNA level. Moreover, genotyping of 3 polymorphisms in the HNF1 gene comparing the non-tumor and tumor ...
Regulation and Flexibility of Genomic Imprinting
Regulation and Flexibility of Genomic Imprinting

... ranging from the regulation of pigmentation, protein storage, transcriptional regulation, chromatin modification, and cytoskeletal function to mRNA regulation (Table 1). For instance, five recently described potentially imprinted genes, for which only transcripts from one parental allele were detect ...
MicroRNAs: key participants in gene regulatory networks
MicroRNAs: key participants in gene regulatory networks

... for miR165 encoded HD-Zip transcription factors. The potential complementary sites might explain the ectopic expression previously described for mutations in these genes. It seemed that complementarity to miR165 was required for confining these mRNA’s accumulation to the proper cell types [33]. Ta ...
Somatic Cell Gene Mutations in Humans
Somatic Cell Gene Mutations in Humans

... Somatic cell gene mutations arising in vivo in humans provide biomarkers for genotoxicity. Four assays, each measuring changes in a different "recorder" gene, are available for detecting mutations of the hemoglobin (Hb) and glycophorin A (gpa) genes in red blood cells and the hypoxanthine-guanine ph ...
Gene mapping - Australian Mathematical Sciences Institute
Gene mapping - Australian Mathematical Sciences Institute

... of the other allele, called recessive, is masked. It is possible to have co-dominant alleles. In this case neither allele is dominant nor recessive with respect to the other allele. We will see an example of this with blood types later in these notes. ...
THE ROLE OF THE ret PROTO-ONCOGENE IN HUMAN DISEASE
THE ROLE OF THE ret PROTO-ONCOGENE IN HUMAN DISEASE

... Papillary thyroid carcinoma is the most common malignant tumor developed in the thyroid gland. In 1990, Grieco et a1. 6 ) reported that rearrangement of ret was detected in approximately 30% of human papillary thyroid carcinomas in which ret was fused to unrelated gene sequences just before its tyro ...
PHAR2811 Dale`s lecture 7 The Transcriptome Definitions: Genome
PHAR2811 Dale`s lecture 7 The Transcriptome Definitions: Genome

... • The 3’ end of the tRNAs all have a CCA, some of which are attached after cleavage (some have the sequence encoded in the DNA). The attachment is done by a special enzyme. • The CCA is important as this is where the amino acid is attached. • Several of the bases e.g. pseudouracils in tRNA molecules ...
Slides PPT
Slides PPT

... • Some of the subunits are unique to each polymerase • All have 2 large subunits (>140 kD) similar in sequence to the b and b’ subunits of bacterial RNA polymerase (fundamental catalytic site between the 2 faces conserved throughout life) ...
genetics - Your Heading Goes Here
genetics - Your Heading Goes Here

... sister chromatids centromere B. Describe what major events occur during the G1, S, and G2 of interphase. Distinguish between mitosis and cytokinesis C. Discuss the structure and function of the mitotic spindle and its related parts centrosome centriole aster kinetochore D. List the phases of mitosis ...
What is the Molecular Clock? Components of the Molecular Clock
What is the Molecular Clock? Components of the Molecular Clock

... in a series of negative feedback loops. These transcription factors bind to DNA regions called promoters, which are DNA sequences found near a gene. The binding of a transcription factor to a promoter may turn the gene on or off, thereby controlling production of proteins. In some cases, a heterodim ...
KAT6A Syndrome - Rarechromo.org
KAT6A Syndrome - Rarechromo.org

... infections, all of which commonly occur in childhood but may occur more frequently in some children with KAT6A syndrome. There are several reasons why this may be the case. Children with KAT6A syndrome often vomit when they are younger and this can lead to chest infections if material from the stoma ...
KAT6A Syndrome - Rarechromo.org
KAT6A Syndrome - Rarechromo.org

... infections, all of which commonly occur in childhood but may occur more frequently in some children with KAT6A syndrome. There are several reasons why this may be the case. Children with KAT6A syndrome often vomit when they are younger and this can lead to chest infections if material from the stoma ...
Molecular approaches for bacterial azoreductases
Molecular approaches for bacterial azoreductases

... Azo dyes are the dominant types of synthetic dyes, widely used in textiles, foods, leather, printing, tattooing, cosmetics, and pharmaceutical industries. Many microorganisms are able to decolorize azo dyes, and there is increasing interest in biological waste treatment methods. Bacterial azoreducta ...
Mutations affecting development of the zebrafish retina
Mutations affecting development of the zebrafish retina

... In wild-type zebrafish pigmentation appears at 24 hpf both in the pigmented epithelium and melanophores. The mutants oko meduzy (ome)m98, glass onion (glo)m117 and nagie oko (nok)m227 exhibit an eye specific pigmentation defect (Table 1). The eye phenotype of these mutations becomes visible shortly ...
Ch. 13 Meiosis - HobbsAPBiology
Ch. 13 Meiosis - HobbsAPBiology

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NEDD9

Neural precursor cell expressed developmentally down-regulated protein 9 (NEDD-9) is a protein that in humans is encoded by the NEDD9 gene. NEDD-9 is also known as enhancer of filamentation 1 (EF1), CRK-associated substrate-related protein (CAS-L), and Cas scaffolding protein family member 2 (CASS2). An important paralog of this gene is BCAR1.
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