26 relations: Alternative splicing, Anemia, Angiotensin II receptor type 1, Chromosome 17, Cochlea, Conductive hearing loss, Cytoplasm, Diamond–Blackfan anemia, Drosophila melanogaster, Eukaryotic large ribosomal subunit (60S), Eukaryotic small ribosomal subunit (40S), Eustachian tube, Exon, Gene, Gestation, Locus (genetics), Middle ear, Organelle, Ossification, Otitis media, Phenotype, Prenatal development, Protein, Pseudogene, Ribosome, Zygosity.
Alternative splicing, or differential splicing, is a regulated process during gene expression that results in a single gene coding for multiple proteins.
Anemia is a decrease in the total amount of red blood cells (RBCs) or hemoglobin in the blood, or a lowered ability of the blood to carry oxygen.
Angiotensin II receptor type 1 or AT1 receptor is the best characterized angiotensin receptor.
Chromosome 17 is one of the 23 pairs of chromosomes in humans.
The cochlea is the part of the inner ear involved in hearing.
Conductive hearing loss occurs when there is a problem conducting sound waves anywhere along the route through the outer ear, tympanic membrane (eardrum), or middle ear (ossicles).
In cell biology, the cytoplasm is the material within a living cell, excluding the cell nucleus.
Diamond–Blackfan anemia (DBA) is a congenital erythroid aplasia that usually presents in infancy.
Drosophila melanogaster is a species of fly (the taxonomic order Diptera) in the family Drosophilidae.
Ribosomal particles are denoted according to their sedimentation coefficients in Svedberg units.
The eukaryotic small ribosomal subunit (40S) is the smaller subunit of the eukaryotic 80S ribosomes, with the other major component being the large ribosomal subunit (60S).
The Eustachian tube, also known as the auditory tube or pharyngotympanic tube, is a tube that links the nasopharynx to the middle ear.
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 biology, a gene is a sequence of DNA or RNA that codes for a molecule that has a function.
Gestation is the carrying of an embryo or fetus inside viviparous animals.
A locus (plural loci) in genetics is a fixed position on a chromosome, like the position of a gene or a marker (genetic marker).
The middle ear is the portion of the ear internal to the eardrum, and external to the oval window of the inner ear.
In cell biology, an organelle is a specialized subunit within a cell that has a specific function, in which their function is vital for the cell to live.
Ossification (or osteogenesis) in bone remodeling is the process of laying down new bone material by cells called osteoblasts.
Otitis media is a group of inflammatory diseases of the middle ear.
A phenotype is the composite of an organism's observable characteristics or traits, such as its morphology, development, biochemical or physiological properties, behavior, and products of behavior (such as a bird's nest).
Prenatal development is the process in which an embryo and later fetus develops during gestation.
Proteins are large biomolecules, or macromolecules, consisting of one or more long chains of amino acid residues.
Pseudogenes are segments of DNA that are related to real genes.
The ribosome is a complex molecular machine, found within all living cells, that serves as the site of biological protein synthesis (translation).
Zygosity is the degree of similarity of the alleles for a trait in an organism.