Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Program Projects (P01)
Project #
5P01GM022167-10
Application #
4693511
Study Section
Project Start
Project End
Budget Start
Budget End
Support Year
10
Fiscal Year
1985
Total Cost
Indirect Cost
Name
University of Minnesota Twin Cities
Department
Type
DUNS #
168559177
City
Minneapolis
State
MN
Country
United States
Zip Code
55455
Oetting, W S; King, R A (1999) Molecular basis of albinism: mutations and polymorphisms of pigmentation genes associated with albinism. Hum Mutat 13:99-115
Orlow, S J; Brilliant, M H (1999) The pink-eyed dilution locus controls the biogenesis of melanosomes and levels of melanosomal proteins in the eye. Exp Eye Res 68:147-54
Oetting, W S; Armstrong, C M; Ronan, S M et al. (1998) Multiplexed short tandem repeat polymorphisms of the Weber 8A set of markers using tailed primers and infrared fluorescence detection. Electrophoresis 19:3079-83
Sweet, H O; Brilliant, M H; Cook, S A et al. (1998) A new allelic series for the underwhite gene on mouse chromosome 15. J Hered 89:546-51
Wildenberg, S C; Fryer, J P; Gardner, J M et al. (1998) Identification of a novel transcript produced by the gene responsible for the Hermansky-Pudlak syndrome in Puerto Rico. J Invest Dermatol 110:777-81
Oetting, W S; Gardner, J M; Fryer, J P et al. (1998) Mutations of the human P gene associated with Type II oculocutaneous albinism (OCA2). Mutations in brief no. 205. Online. Hum Mutat 12:434
Oetting, W S; Fryer, J P; King, R A (1998) Mutations of the human tyrosinase gene associated with tyrosinase related oculocutaneous albinism (OCA1). Mutations in brief no. 204. Online. Hum Mutat 12:433-4
Lehman, A L; Nakatsu, Y; Ching, A et al. (1998) A very large protein with diverse functional motifs is deficient in rjs (runty, jerky, sterile) mice. Proc Natl Acad Sci U S A 95:9436-41
Gardner, J M; Wildenberg, S C; Keiper, N M et al. (1997) The mouse pale ear (ep) mutation is the homologue of human Hermansky-Pudlak syndrome. Proc Natl Acad Sci U S A 94:9238-43
Puri, N; Durbam-Pierre, D; Aquaron, R et al. (1997) Type 2 oculocutaneous albinism (OCA2) in Zimbabwe and Cameroon: distribution of the 2.7-kb deletion allele of the P gene. Hum Genet 100:651-6

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