TY  - JOUR
A1  - Chung, W K
A1  - Power-Kehoe, L
A1  - Chua, M
A1  - Lee, R
A1  - Leibel, R L
T1  - Genomic structure of the human OB receptor and identification of two novel intronic microsatellites.
Y1  - 1996/12/01 
JF  - Genome Research 
JO  - Genome Research 
SP  - 1192 
EP  - 1199 
DO  - 10.1101/gr.6.12.1192 
VL  - 6 
IS  - 12 
UR  - http://genome.cshlp.org/content/6/12/1192.abstract 
N2  - Identification of the OB (leptin) receptor (OBR) as the gene that is defective in diabetes (Leprdb) mice and fatty (Leprfa) rats provides an important candidate gene for the study of the genetics of human obesity. We defined the boundaries of the 18 coding exons for the long form of OBR, and sequenced the immediately adjacent intronic regions. These sequences can be used to generate reagents for genetic analysis (e.g., direct sequencing, single-stranded conformational polymorphism analysis, etc.) of the possible role of OBR in the regulation of adiposity in humans. In addition, we have identified two highly polymorphic intronic microsatellites that can be scored with the polymerase chain reaction. 
ER  -