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sequence /se·quence/ (se´kwens)
1. a connected series of events or things. 2. in dysmorphology, a pattern of multiple anomalies derived from a single prior anomaly or mechanical factor. 3. in molecular biology, DNA having a particular nucleotide pattern or occurring in a particular region of the genome. amniotic band sequence early rupture of the amnion with formation of strands of amnion that may adhere to or compress parts of the fetus, resulting in a wide variety of deformities. gene sequence the ordered arrangement of nucleotides into codons along the stretch of DNA to be transcribed. oligohydramnios sequence a group of anomalies, usually fatal shortly after birth, caused by compression of the fetus secondary to oligohydramnios, which may result from renal agenesis or other urinary tract defects or from leakage of amniotic fluid; infants have characteristic flattened facies (Potter facies), skeletal abnormalities, and often hypoplasia of the lungs.
sequence [sē′kwəns] Etymology: L, sequi, to follow an order of arrangement of objects or events, as the sequence of peptides in a protein molecule. sequence, n the order of occurrence or performance. sequence planning,
n a method of identifying all the various dental treatments that a patient will need and putting those treatments in the most logical and effective order. sequence the order in which monomers occur in polymeric molecules; the order of amino acids in a polypeptide chain or of nucleotides in nucleic acid. autonomously replicating sequence usually plasmids that replicate independently of chromosomal DNA. coding s's sections of DNA which code for the amino acids of a protein. consensus sequence a sequence of nucleotides that is always present in a large set of independently determined sequences. See also box. enhancer sequence in DNA transcription, an upstream cis-acting DNA sequence that enhances expression of a particular gene and forms part of a complex array of upstream sequences that control gene expression. expressed s's in eukaryotic pre-messenger RNA the noncoding sequences, also called intervening sequences or introns, are removed in the nucleus; the mRNA is transported to the cytoplasm where the exons are translated to a protein. intervening sequence see intron. palindromic sequence see palindrome. signal sequence a collection of hydrophobic amino acid residues at the amino terminus of secretory or integrated membrane proteins that direct the protein to cell membranes, particularly endoplasmic reticulum where the proteins are modified, e.g. glycosylated, and the signal sequence is removed prior to secretion or integration of the protein into the lumen of the endoplasmic reticulum. temporal sequence
in protein synthesis, is from the amino to the carboxyl end. sequence Pediatrics Anomalad An array of multiple congenital anomalies resulting from an early single 1º defect of morphogenesis that unleashes a 'cascade' of 2º and 3º defects; a sequence is also defined as a set
of clinicopathologic consequences of the aberrant formation of one or more early embryologic structures. See Dysmorphology.
Sequence types
Malformation Incorrect formation of tissues
Deformation Abnormal forces acting on normal tissues
Disruption Breakdown of normal tissue
Note: The Pierre-Robin sequence is caused by 1º mandibular hypoplasia, which results in a tongue that is too small for the oral cavity and which drops back–glossoptosis, blocking closure of the posterior palatal shelf, resulting in a high
arched U-shaped cleft palate Examples of sequences include athyroidotic hypothyroidism sequence, DiGeorge sequence, early urethral obstruction sequence, bladder exstrophy sequence, cloacal extrophy sequence, holoprosencephaly sequence, jugular
lymphatic obstruction sequence, Kartagener syndrome/sequence, Klippel-Feil sequence, laterality sequence, meningomyelocele, anencephaly, iniencephaly sequence, occult spinal dysraphism sequence, oligohydramnios sequence, Rokitansky sequence,
septo-optic dysplasia–de Morsier sequence, sirenomelia sequence
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