Àá½Ã¸¸ ±â´Ù·Á ÁÖ¼¼¿ä. ·ÎµùÁßÀÔ´Ï´Ù.

±¸¼ø±¸°³¿­ ¹ß»ýÀÇ ºÐÀÚÀ¯ÀüÇÐ ¿¬±¸¸¦ À§ÇÑ À¯ÀüÀÚ Ç¥Àû/ÀûÁß »ýÁã¸ðµ¨ÀÇ ÀÌ¿ë

Gene Targeting Mouse Genetic Models for Cleft Lip and Palate

´ëÇѱ¸¼ø±¸°³¿­ÇÐȸÁö 2008³â 11±Ç 2È£ p.65 ~ 70
¹éÁø¾Æ,
¼Ò¼Ó »ó¼¼Á¤º¸
¹éÁø¾Æ ( Baek Jin-A ) - ÀüºÏ´ëÇб³ Ä¡°ú´ëÇÐ ±¸°­¾Ç¾È¸é¿Ü°úÇб³½Ç

Abstract


Cleft lip and/or palate are common birth defects in humans and the causes including multiple genetic and environmental factors are complex. Combinations of genetic, biochemical, and embryological approaches in the laboratory mice are used to investigate the molecular mechanisms underlying normal craniofacial development and the congenital craniofacial malformations including cleft lip and/or palate. Both forward and reverse genetic approaches are used. The forward genetic approach involves identification of causative genes and molecular pathways disrupted by uncharacterized mutations that cause craniofacial malformations including cleft lip and/or cleft palate. The reverse genetic approach involves generation and analyses of mice carrying null or conditional mutations using the Cre-loxP mediated gene targeting techniques.

Å°¿öµå

Gene targeting mouse model;Cre-loxP;Cleft lip and palate

¿ø¹® ¹× ¸µÅ©¾Æ¿ô Á¤º¸

  

µîÀçÀú³Î Á¤º¸

KCI