| LOR | long open reading frame; lorazepam; loricrin; loss of righting reflex |
|---|---|
| LORF | long open reading frame |
| ORF | open reading frame |
| orf | open reading frame |
| RT | radiologic technologist; radiotelemetry; radiotherapy; radium therapy; rapid tranquilization; reacti... |
| AAMI | Age-Associated Memory Impairment |
|---|---|
| CVI | Cortical visual impairment |
| HI | Hearing impairment |
| MCI | Mild Cognitive Impairment |
| NFI | Nerve-function impairment |
| mental impairment | A disorder characterised by the display of an intellectual defect, as manifested by diminished cognitive, interpersonal, social, and vocational effectiveness and quantitatively evaluated by psychological examination and assessment. (05 Mar 2000) |
|---|---|
| physician impairment | The physician's inability to practice medicine with reasonable skill and safety to the patient due to the physician's disability. Common causes include alcohol and drug abuse, mental illness, physical disability, and senility. (12 Dec 1998) |
| hearing impairment | Hearing loss A reduction in the ability to perceive sound; may range from slight to complete deafness. See: deafness, threshold shift. (05 Mar 2000) |
| professional impairment | The inability of a health professional to provide proper professional care of patients due to his or her physical and/or mental disability. (12 Dec 1998) |
| hepatic function impairment | The impaired ability of the liver to fulfill its role in metabolism. (27 Sep 1997) |
| impairment | A physical or mental defect at the level of a body system or organ. The official WHO definition is: any loss or abnormality of psychological, physiological or anatomical structure or function. (05 Mar 2000) |
| albumin Reading | Types of human serum albumin, distinguished by characteristic mobility patterns on electrophoresis; each type is due to a mutation of a gene controlling albumin synthesis; the mutant genes are codominant with the normal gene for albumin A, and the group forms a system of genetic polymorphism; types include: albumin b (slow), found occasionally in persons of European ancestry; albumin Ghent (fast), found first at Ghent, Belgium; albumin Mexico (slow), found in Indians of Mexico and the southwestern United States; albumin Naskapi (fast), found in the Naskapi and other Indians of northern North America; and albumin Reading (fast), found first at Reading, England. (05 Mar 2000) |
| blocked reading frame | A sequence of DNA that cannot be translated into a viable protein; usually due to the interruption by one or more termination codons. Synonym: closed reading frame. (05 Mar 2000) |
| reading frame | One of the three possible ways of reading a nucleotide sequence. As the genetic code is read in nonoverlapping triplets (codons) there are three possible ways of translating a sequence of nucleotides into a protein, each with a different starting point. For example: given the nucleotide sequence: AGCAGCAGC, the three reading frames are: AGC AGC AGC, GCA GCA, CAG CAG. (18 Nov 1997) |
| reading frame, open | An open reading frame in DNA has no termination codon, no signal to stop reading the nucleotide sequence, and so may be translated into protein. (12 Dec 1998) |
| reading frames | The sequence of codons by which translation may occur. A segment of mRNA 5'auccga3' could be translated in three reading frames, 5'auc.. Or 5'ucc.. Or 5'ccg.., depending on the location of the start codon. (12 Dec 1998) |
| reading-frameshift mutation | <molecular biology> A type of mutation that results from insertion or deletion of a single nucleotide into, or from, an open reading frame in the normal DNA sequence. Normally, the genetic code is read in the wrong frame, three nucleotides at a time, and the entire sequence downstream of the mutation, is translated into a polypeptide with a garbled amino acid sequence from the mutated codon onwards. These mutations may be induced by certain types of mutagens or may occur spontaneously and usually result in the generation, downstream, of nonsense, chain termination codons. Synonym: addition mutation, addition-deletion mutation, deletion mutation, reading-frameshift mutation. (21 Jun 2000) |
| mind-reading | The knowledge or communication by one person with the mental processes of another through channels other than known physical or perceptual processes. (12 Dec 1998) |
| closed reading frame | A sequence of DNA that cannot be translated into a viable protein; usually due to the interruption by one or more termination codons. Synonym: closed reading frame. (05 Mar 2000) |
| open reading frame | <molecular biology> A reading frame in a sequence of nucleotides in DNA that contains no termination codons and so can potentially translate as a polypeptide chain. (18 Nov 1997) |
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
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제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|