93 relations: Addiction, Adenoviridae, Affymetrix, Apoptosis, Arabidopsis thaliana, AspicDB, Behavioral addiction, Biodiversity, Caenorhabditis elegans, Calcitonin, Calcitonin gene-related peptide, Cell migration, Cis-regulatory element, Complementary DNA, Consensus sequence, Coverage (genetics), Cross-link, DNA, DNA (cytosine-5)-methyltransferase 3A, DNA methylation, DNA methyltransferase, DNA microarray, Doublesex, Drosophila melanogaster, DSCAM, Endogeny (biology), Eukaryote, Exitron, Exon, Exon skipping, Exonic splicing enhancer, Exonic splicing silencer, Expressed sequence tag, Fas receptor, FOSB, Gene, Gene expression, Genetic disorder, Genome, Heterogeneous ribonucleoprotein particle, HIV, HIV/AIDS, Human genome, Human Genome Project, Hyaluronidase, Immunoprecipitation, Intrinsically disordered proteins, Intron, Isogenic human disease models, Messenger RNA, ..., MST1R, Mutation, Nematode, Nonsense-mediated decay, Nucleus accumbens, Oncogene, One gene–one enzyme hypothesis, Peptide, Phosphodiester bond, Phosphorylation, Polyadenylation, Polypyrimidine tract, Precursor mRNA, Primary transcript, Promoter (genetics), Protein, Protein isoform, Proteome, Pyrimidine, Reading frame, Reporter gene, Retrovirus, RNA-binding protein, RNA-Seq, SciVee, Serine/arginine-rich splicing factor 1, SnRNP, Spliceosome, SR protein, Stop codon, Thyroid, TIA1, Trans-acting, Transcription (biology), Transcription factor, Transcriptional regulation, Transcriptome instability, Transesterification, Translation (biology), Tumors of the hematopoietic and lymphoid tissues, U2, U2AF2, Zygosity. Expand index (43 more) » « Shrink index
Addiction is a brain disorder characterized by compulsive engagement in rewarding stimuli despite adverse consequences.
Adenoviruses (members of the family Adenoviridae) are medium-sized (90–100 nm), nonenveloped (without an outer lipid bilayer) viruses with an icosahedral nucleocapsid containing a double stranded DNA genome.
Affymetrix, Inc. was an American company that manufactured DNA microarrays; it was based in Santa Clara, California, United States.
Apoptosis (from Ancient Greek ἀπόπτωσις "falling off") is a process of programmed cell death that occurs in multicellular organisms.
Arabidopsis thaliana, the thale cress, mouse-ear cress or arabidopsis, is a small flowering plant native to Eurasia and Africa.
ASPicDB is a database of human protein variants generated by alternative splicing, a process by which the exons of the RNA produced by transcription of a gene are reconnected in multiple ways during RNA splicing.
Behavioral addiction is a form of addiction that involves a compulsion to engage in a rewarding non-drug-related behavior – sometimes called a natural reward – despite any negative consequences to the person's physical, mental, social or financial well-being.
Biodiversity, a portmanteau of biological (life) and diversity, generally refers to the variety and variability of life on Earth.
Caenorhabditis elegans is a free-living (not parasitic), transparent nematode (roundworm), about 1 mm in length, that lives in temperate soil environments.
Calcitonin (also known as thyrocalcitonin) is a 32-amino acid linear polypeptide hormone that is produced in humans primarily by the parafollicular cells (also known as C-cells) of the thyroid gland, and in many other animals in the ultimopharyngeal body.
Calcitonin gene-related peptide (CGRP) is a member of the calcitonin family of peptides, which in humans exists in two forms, α-CGRP and β-CGRP.
Cell migration is a central process in the development and maintenance of multicellular organisms.
Cis-regulatory elements (CREs) are regions of non-coding DNA which regulate the transcription of neighboring genes.
In genetics, complementary DNA (cDNA) is DNA synthesized from a single stranded RNA (e.g., messenger RNA (mRNA) or microRNA) template in a reaction catalyzed by the enzyme reverse transcriptase.
In molecular biology and bioinformatics, the consensus sequence (or canonical sequence) is the calculated order of most frequent residues, either nucleotide or amino acid, found at each position in a sequence alignment.
Coverage (or depth) in DNA sequencing is the number of unique reads that include a given nucleotide in the reconstructed sequence.
A cross-link is a bond that links one polymer chain to another.
Deoxyribonucleic acid (DNA) is a thread-like chain of nucleotides carrying the genetic instructions used in the growth, development, functioning and reproduction of all known living organisms and many viruses.
DNA (cytosine-5)-methyltransferase 3A is an enzyme that catalyzes the transfer of methyl groups to specific CpG structures in DNA, a process called DNA methylation.
DNA methylation is a process by which methyl groups are added to the DNA molecule.
In biochemistry, the DNA methyltransferase (DNA MTase) family of enzymes catalyze the transfer of a methyl group to DNA.
A DNA microarray (also commonly known as DNA chip or biochip) is a collection of microscopic DNA spots attached to a solid surface.
Doublesex (dsx) is a gene that is involved in the sex determination system of many insects including the fruit fly Drosophila melanogaster.
Drosophila melanogaster is a species of fly (the taxonomic order Diptera) in the family Drosophilidae.
DSCAM and Dscam are both abbreviations for Down syndrome cell adhesion molecule.
Endogenous substances and processes are those that originate from within an organism, tissue, or cell.
Eukaryotes are organisms whose cells have a nucleus enclosed within membranes, unlike Prokaryotes (Bacteria and other Archaea).
Exitrons (exonic introns) are produced through alternative splicing and have characteristics of both introns and exons, but are described as retained introns.
An exon is any part of a gene that will encode a part of the final mature RNA produced by that gene after introns have been removed by RNA splicing.
In molecular biology, exon skipping is a form of RNA splicing used to cause cells to “skip” over faulty or misaligned sections of genetic code, leading to a truncated but still functional protein despite the genetic mutation.
In molecular biology, an exonic splicing enhancer (ESE) is a DNA sequence motif consisting of 6 bases within an exon that directs, or enhances, accurate splicing of heterogeneous nuclear RNA (hnRNA) or pre-mRNA into messenger RNA (mRNA).
An exonic splicing silencer (ESS) is a short region (usually 4-18 nucleotides) of an exon and is a cis-regulatory element.
In genetics, an expressed sequence tag (EST) is a short sub-sequence of a cDNA sequence.
The first apoptosis signal receptor (Fas or FasR), also known as apoptosis antigen 1 (APO-1 or APT), cluster of differentiation 95 (CD95) or tumor necrosis factor receptor superfamily member 6 (TNFRSF6) is a protein that in humans is encoded by the FAS gene.
FBJ murine osteosarcoma viral oncogene homolog B, also known as Finkel-Biskis-Jinkins murine osteosarcoma viral oncogene homolog B, FOSB or FosB, is a protein that, in humans, is encoded by the FOSB gene.
In biology, a gene is a sequence of DNA or RNA that codes for a molecule that has a function.
Gene expression is the process by which information from a gene is used in the synthesis of a functional gene product.
A genetic disorder is a genetic problem caused by one or more abnormalities in the genome.
In the fields of molecular biology and genetics, a genome is the genetic material of an organism.
Heterogeneous nuclear ribonucleoproteins (hnRNPs) are complexes of RNA and protein present in the cell nucleus during gene transcription and subsequent post-transcriptional modification of the newly synthesized RNA (pre-mRNA).
The human immunodeficiency virus (HIV) is a lentivirus (a subgroup of retrovirus) that causes HIV infection and over time acquired immunodeficiency syndrome (AIDS).
Human immunodeficiency virus infection and acquired immune deficiency syndrome (HIV/AIDS) is a spectrum of conditions caused by infection with the human immunodeficiency virus (HIV).
The human genome is the complete set of nucleic acid sequences for humans, encoded as DNA within the 23 chromosome pairs in cell nuclei and in a small DNA molecule found within individual mitochondria.
The Human Genome Project (HGP) was an international scientific research project with the goal of determining the sequence of nucleotide base pairs that make up human DNA, and of identifying and mapping all of the genes of the human genome from both a physical and a functional standpoint.
Hyaluronidases are a family of enzymes that catalyse the degradation of hyaluronic acid (HA).
Immunoprecipitation (IP) is the technique of precipitating a protein antigen out of solution using an antibody that specifically binds to that particular protein.
An intrinsically disordered protein (IDP) is a protein that lacks a fixed or ordered three-dimensional structure.
An intron is any nucleotide sequence within a gene that is removed by RNA splicing during maturation of the final RNA product.
Isogenic human disease models are a family of cells that are selected or engineered to accurately model the genetics of a specific patient population, in vitro.
Messenger RNA (mRNA) is a large family of RNA molecules that convey genetic information from DNA to the ribosome, where they specify the amino acid sequence of the protein products of gene expression.
Macrophage-stimulating protein receptor is a protein that in humans is encoded by the MST1R gene.
In biology, a mutation is the permanent alteration of the nucleotide sequence of the genome of an organism, virus, or extrachromosomal DNA or other genetic elements.
The nematodes or roundworms constitute the phylum Nematoda (also called Nemathelminthes).
Nonsense-mediated mRNA decay (NMD) is a surveillance pathway that exists in all eukaryotes.
The nucleus accumbens (NAc or NAcc), also known as the accumbens nucleus, or formerly as the nucleus accumbens septi (Latin for nucleus adjacent to the septum) is a region in the basal forebrain rostral to the preoptic area of the hypothalamus.
An oncogene is a gene that has the potential to cause cancer.
The one gene–one enzyme hypothesis is the idea that genes act through the production of enzymes, with each gene responsible for producing a single enzyme that in turn affects a single step in a metabolic pathway.
Peptides (from Gr.: πεπτός, peptós "digested"; derived from πέσσειν, péssein "to digest") are short chains of amino acid monomers linked by peptide (amide) bonds.
A phosphodiester bond occurs when exactly two of the hydroxyl groups in phosphoric acid react with hydroxyl groups on other molecules to form two ester bonds.
In chemistry, phosphorylation of a molecule is the attachment of a phosphoryl group.
Polyadenylation is the addition of a poly(A) tail to a messenger RNA.
The polypyrimidine tract is a region of pre-messenger RNA (mRNA) that promotes the assembly of the spliceosome, the protein complex specialized for carrying out RNA splicing during the process of post-transcriptional modification.
Precursor mRNA (pre-mRNA) is an immature single strand of messenger ribonucleic acid (mRNA).
A primary transcript is the single-stranded ribonucleic acid (RNA) product synthesized by transcription of DNA, and processed to yield various mature RNA products such as mRNAs, tRNAs, and rRNAs.
In genetics, a promoter is a region of DNA that initiates transcription of a particular gene.
Proteins are large biomolecules, or macromolecules, consisting of one or more long chains of amino acid residues.
A protein isoform, or "protein variant" is a member of a set of highly similar proteins that originate from a single gene or gene family and are the result of genetic differences.
The proteome is the entire set of proteins that is, or can be, expressed by a genome, cell, tissue, or organism at a certain time.
Pyrimidine is an aromatic heterocyclic organic compound similar to pyridine.
In molecular biology, a reading frame is a way of dividing the sequence of nucleotides in a nucleic acid (DNA or RNA) molecule into a set of consecutive, non-overlapping triplets.
In molecular biology, a reporter gene (often simply reporter) is a gene that researchers attach to a regulatory sequence of another gene of interest in bacteria, cell culture, animals or plants.
A retrovirus is a single-stranded positive-sense RNA virus with a DNA intermediate and, as an obligate parasite, targets a host cell.
RNA-binding proteins (often abbreviated as RBPs) are proteins that bind to the double or single stranded RNA in cells and participate in forming ribonucleoprotein complexes.
RNA-Seq (RNA sequencing), also called whole transcriptome shotgun sequencing (WTSS), uses next-generation sequencing (NGS) to reveal the presence and quantity of RNA in a biological sample at a given moment.
SciVee was a science video sharing website where researchers could upload, view and share science video clips and connect them to scientific literature, posters and slides from 2007-2015.
Serine/arginine-rich splicing factor 1 (SRSF1) also known as alternative splicing factor 1 (ASF1), pre-mRNA-splicing factor SF2 (SF2) or ASF1/SF2 is a protein that in humans is encoded by the SFRS1 gene.
snRNPs (pronounced "snurps"), or small nuclear ribonucleoproteins, are RNA-protein complexes that combine with unmodified pre-mRNA and various other proteins to form a spliceosome, a large RNA-protein molecular complex upon which splicing of pre-mRNA occurs.
A spliceosome is a large and complex molecular machine found primarily within the splicing speckles of the cell nucleus of eukaryotic cells.
SR proteins are a conserved family of proteins involved in RNA splicing.
In the genetic code, a stop codon (or termination codon) is a nucleotide triplet within messenger RNA that signals a termination of translation into proteins.
The thyroid gland, or simply the thyroid, is an endocrine gland in the neck, consisting of two lobes connected by an isthmus.
TIA1 is a 3'UTR mRNA binding protein that can bind the 5'TOP sequence of 5'TOP mRNAs.
In the field of molecular biology, trans-acting (trans-regulatory, trans-regulation), in general, means "acting from a different molecule" (i.e., intermolecular).
Transcription is the first step of gene expression, in which a particular segment of DNA is copied into RNA (especially mRNA) by the enzyme RNA polymerase.
In molecular biology, a transcription factor (TF) (or sequence-specific DNA-binding factor) is a protein that controls the rate of transcription of genetic information from DNA to messenger RNA, by binding to a specific DNA sequence.
In molecular biology and genetics, transcriptional regulation is the means by which a cell regulates the conversion of DNA to RNA (transcription), thereby orchestrating gene activity.
Transcriptome instability is a genome-wide, pre-mRNA splicing-related characteristic of certain cancers.
In organic chemistry, transesterfication is the process of exchanging the organic group R″ of an ester with the organic group R′ of an alcohol.
In molecular biology and genetics, translation is the process in which ribosomes in the cytoplasm or ER synthesize proteins after the process of transcription of DNA to RNA in the cell's nucleus.
Tumors of the hematopoietic and lymphoid tissues or haematopoietic and lymphoid malignancies are tumors that affect the blood, bone marrow, lymph, and lymphatic system.
U2 are an Irish rock band from Dublin formed in 1976.
Splicing factor U2AF 65 kDa subunit is a protein that in humans is encoded by the U2AF2 gene.
Zygosity is the degree of similarity of the alleles for a trait in an organism.
Alternate mRNA splicing, Alternate splicing, Alternate transcriptional splice, Alternative splicings, Alternatively spliced, Differential splicing, Splice form, Splice isoform, Splice variant, Splice variant analysis, Splicing alteration, Transcript isoform, Transcript variant, Transcript variants.