Carrier Proteins/Genetics

Last changed on Wed, 12/31/1969 - 17:00

A 122.5-kilobase deletion of the P gene underlies the high prevalence of oculocutaneous albinism type 2 in the Navajo population.

Digital Heritage
Community
UNM Health Sciences Library and Informatics Center
Category
Miscellaneous

Analysis of slc19a2, on 1q23.3 encoding a thiamine transporter as a candidate gene for type 2 diabetes mellitus in Pima Indians.

Digital Heritage
Community
UNM Health Sciences Library and Informatics Center
Category
Miscellaneous

Linkage of tuberculosis to chromosome 2q35 loci, including NRAMP1, in a large aboriginal Canadian family.

Digital Heritage
Community
UNM Health Sciences Library and Informatics Center
Category
Miscellaneous

An amino acid substitution in the human intestinal fatty acid binding protein is associated with increased fatty acid binding, increased fat oxidation, and insulin resistance.

Digital Heritage
Community
UNM Health Sciences Library and Informatics Center
Category
Miscellaneous

Association between uncoupling protein polymorphisms (UCP2-UCP3) and energy metabolism/obesity in Pima Indians.

Digital Heritage
Community
UNM Health Sciences Library and Informatics Center
Category
Miscellaneous

Structure and sequence variation at the human leptin receptor gene in lean and obese Pima Indians.

Digital Heritage
Community
UNM Health Sciences Library and Informatics Center
Category
Miscellaneous