| ¿µ¹® | visual field test | ÇÑ±Û | ½Ã¾ß°Ë»ç |
|---|---|---|---|
| ¼³¸í | ´«À» ÇѰ÷¿¡ °íÁ¤½ÃŲ ä, °üÂûÇÒ ¼ö ÀÖ´Â ÁÖº¯°ø°£À» ½Ã¾ß¶ó ÇÑ´Ù. ½Ã¾ß¸¦ °Ë»çÇÏ´Â °¡Àå °£´ÜÇÑ ¹æ¹ýÀº ´ë¸é°Ë»ç(confronting test)ÀÌ´Ù. À̰ÍÀº Çǰ˻çÀÚÀÇ ´«À» °Ë»çÀÚÀÇ ´«¿¡ ¸ÂÃß¾î º¸µµ·Ï ÇÏ¿© ´«À» °íÁ¤½ÃŲä, °Ë»çÀÚ°¡ ¼Õ°¡¶ô³¡À» À§ÂÊ, ¾Æ·¡ÂÊ, ¿ÞÂÊ, ¿À¸¥ÂÊ, ±×¸®°í ºñ½ºµëÈ÷ °æ»çÁø °÷ µîÀ¸·Î ¿Å°Üº¸¾Æ Çǰ˻çÀÚ°¡ °üÂûÇÒ ¼ö ÀÖ´ÂÁö ¿©ºÎ¸¦ Á¤ÇÏ´Â °Ë»ç¹ýÀÌ´Ù. À̺¸´Ù Á¤È®ÇÑ °Ë»ç¹ýÀº ÀÚµ¿½Ä ÄÄÇ»Åͽþ߰˻ç¹ýÀÌ ÀÖ´Ù. ´ë°³, ´«ÀÚüÀÇ ÀÌ»óÀÌ À־ ½Ã¾ß°Ë»ç¿¡¼ ÀÌ»óÀÌ ³ª¿ÀÁö¸¸, ÀÌ¿Ü ³úÀÇ ÀÌ»óÀ¸·Î ½Ã°¢ÀÇ Çü¼º°æ·Î¿¡ ÀÌ»óÀÌ À־ ¿ª½Ã ÀÌ»ó¼Ò°ßÀ» º¸ÀδÙ. |
||
| ¿µ¹® | electrophoresis | ÇÑ±Û | Àü±âÀ̵¿ |
|---|---|---|---|
| ¼³¸í | Àü±â¿îµ¿Àû Çö»óÀÇ Çϳª·Î¼ ÀüÀå¿¡¼ ¾ç±ØÀ̳ª À½±ØÀ¸·Î ÇâÇÏ´Â ÀÔÀÚÀÇ ¿îµ¿À» ÀÌ¿ëÇÏ¿© ¹°ÁúÀÇ ºÐ¼®À̳ª Á¤·®¿¡ ÀÌ¿ëÇÏ´Â ¹æ¹ý. ¿ë¾× ¼Ó¿¡¼ Àü±Ø¿¡ Àü¾ÐÀ» °¡ÇÏ¸é ±× ÀÔÀÚ°¡ À½¼º Àü±â¸¦ ¶ì°í ÀÖÀ¸¸é ¾ç±ØÀ¸·Î, ±×¸®°í ¾ç¼º Àü±â¸¦ ¶ì°í ÀÖÀ¸¸é À½±ØÀ¸·Î Àü±âÀÇ ÈûÀ» ¹Þ¾Æ¼ À̵¿ÀÌ µÈ´Ù. À̵¿ÇÏ´Â ¸ð¾çµµ ÀÔÀÚÀÇ Çüųª Å©±â¿¡ µû¶ó ´Ù¸£¹Ç·Î ´Ü¹éÁúÀÇ ºÐ¼®¿¡ ÀÌ¿ëµÉ ¼ö°¡ ÀÖ´Ù. À̵¿¼Óµµ´Â ÀÔÀÚÀÚüÀÇ ÀüÇÏ ¹× Å©±â, ºÐÀÚ±¸Á¶¸¦ ºñ·ÔÇÏ¿© ¿ë¸ÅÀÇ Á¾·ù, ÁöÁöü ¹°Áú°úÀÇ »óÈ£ÀÛ¿ë, ¿Âµµ µî¿¡ ÀÇÇØ ¿µÇâÀ» ¹Þ°Ô µÈ´Ù. Àü±âÀ̵¿Àº À̵¿µµÀÇ Â÷ÀÌ¿¡ ÀÇÇØ¼ ¹°ÁúÀÇ ºÐ¸®, Á¤Á¦, È®ÀÎ, ¼øµµÀÇ °ËÁ¤ µîÀ» ½ÃÇàÇÏ´Â °ÍÀÌ´Ù. |
||
| FIGE | field inversion gel electrophoresis |
|---|---|
| AGE | acrylamide gel; acute gastroenteritis; advanced glycation end product; agarose gel electrophoresis; ... |
| OFAGE | orthogonal field alternation gel electrophoresis |
| PFG | peak flow gauge; pulsed-field gel electrophoresis |
| PFGE | pulsed field gel electrophoresis |
| FIGE | Field inversion gel electrophoresis |
|---|---|
| STIR | Inversion Time Inversion Recovery |
| STIR | Short-inversion time inversion-recovery |
| OFAGE | Orthogonal field alternation gel electrophoresis |
| PFGE | Pulse Field Gel Electrophoresis |
| pulsed-field gel electrophoresis | Gel electrophoresis in which, after electrophoretic migration has begun, the current is briefly stopped and reapplied in a different orientation; allows for the purification of long DNA molecules. Synonym: pulsed-field gel electrophoresis. (05 Mar 2000) |
|---|---|
| pulse-field gel electrophoresis | Gel electrophoresis in which, after electrophoretic migration has begun, the current is briefly stopped and reapplied in a different orientation; allows for the purification of long DNA molecules. Synonym: pulsed-field gel electrophoresis. (05 Mar 2000) |
| electrophoresis, gel, pulsed-field | Electrophoresis in which the direction of the electric field is changed periodically. This technique is similar to other electrophoretic methods normally used to separate double-stranded DNA molecules ranging in size up to tens of thousands of base-pairs. However, by alternating the electric field direction one is able to separate DNA molecules up to several million base-pairs in length. (12 Dec 1998) |
| agarose gel electrophoresis | <procedure> A type of electrophoresis that uses a matrix of highly purified agar to separate large nucleotides in size. (06 May 1997) |
| gel electrophoresis | <molecular biology> Electrophoresis using a gel supporting phase. Usually applied to systems where the gel is based on polyacrylamide. See: electrophoresis. (05 May 1997) |
| polyacrylamide gel electrophoresis | Analytical and separative technique in which molecules, particularly proteins, are separated by their different electrophoretic mobilities in a hydrated gel. The gel suppresses convective mixing of the fluid phase through which the electrophoresis takes place and contributes molecular sieving. Commonly carried out in the presence of the anionic detergent sodium dodecylsulphate (SDS). SDS denatures proteins so that noncovalently associating sub unit polypeptides migrate independently and by binding to the proteins confers a net negative charge roughly proportional to the chain weight. See: SDS PAGE. (21 Jun 1999) |
| electrophoresis, agar gel | Electrophoresis in which agar or agarose gel is used as the diffusion medium. (12 Dec 1998) |
| electrophoresis, gel, two-dimensional | Electrophoresis in which a second perpendicular electrophoretic transport is performed on the separate components resulting from the first electrophoresis. This technique is usually performed on polyacrylamide gels. (12 Dec 1998) |
| electrophoresis, polyacrylamide gel | Electrophoresis in which a polyacrylamide gel is used as the diffusion medium. (12 Dec 1998) |
| electrophoresis, starch gel | Electrophoresis in which a starch gel (a mixture of amylose and amylopectin) is used as the diffusion medium. (12 Dec 1998) |
| two dimensional gel electrophoresis | <technique> A high resolution separation technique in which protein samples are separated by isoelectric focussing in one dimension and then laid on an SDS gel for size determined separation in the second dimension. Can resolve hundreds of components on a single gel. (18 Nov 1997) |
| pulse field electrophoresis | <investigation> A method used for high resolution electrophoretic separation of very large (megabase) fragments of DNA. Electric fields 100 |
| paracentric inversion | A basic type of chromosome rearrangement. A segment that does not include the centromere (and so is paracentric) has been snipped out of a chromosome, turned through 180 degrees (inverted), and inserted right back into its original location in chromosome. (12 Dec 1998) |
| visceral inversion | A transposition of the viscera, e.g., the liver developing on the left side or the heart on the right. Synonym: visceral inversion. (05 Mar 2000) |
| pericentric inversion | <cell biology, genetics> Chromosomal inversion in which the region that is inverted includes the kinetochore. (18 Nov 1997) |
Á¦Ç°¸í |
ÆÇ¸Å»ç |
º¸ÇèÄÚµå | ¼ººÐ/ÇÔ·® | ±¸ºÐ/º¸Çè±Þ¿© |
|---|
Á¦Ç°¸í |
ÆÇ¸Å»ç |
º¸ÇèÄÚµå | ¼ººÐ/ÇÔ·® | ±¸ºÐ/º¸Çè±Þ¿© |
|---|