The knowledge base for public health strategies.

Por Russell, L B
Publicado em 1997

Balancing cost and quality: methods of evaluation.

Por Russell, L B
Publicado em 1986

How much does medical technology cost?

Por Russell, L. B.
Publicado em 1978

Providing medical care for the poor: a proposal.

Por Russell, L. B.
Publicado em 1990

Spontaneous mutations recovered as mosaics in the mouse specific-locus test

Por Russell, L. B., Russell, W. L.
Publicado em 1996

Murine fumarylacetoacetate hydrolase (Fah) gene is disrupted by a neonatally lethal albino deletion that defines the hepatocyte-specific developmental regulation 1 (hsdr-1) locus.

Por Klebig, M L, Russell, L B, Rinchik, E M
Publicado em 1992

Differential response of mouse male germ-cell stages to radiation-induced specific-locus and dominant mutations.

Por Russell, W L, Bangham, J W, Russell, L B
Publicado em 1998

X-linked lymphoreticular disease in the scurfy (sf) mutant mouse.

Por Godfrey, V. L., Wilkinson, J. E., Russell, L. B.
Publicado em 1991

Chlorambucil-induced mutations in mice recovered in homozygotes.

Por Flaherty, L, Messer, A, Russell, L B, Rinchik, E M
Publicado em 1992

Complementation Analyses for 45 Mutations Encompassing the Pink-Eyed Dilution (P) Locus of the Mouse

Por Russell, L. B., Montgomery, C. S., Cacheiro, NLA., Johnson, D. K.
Publicado em 1995

An extensive 3' regulatory region controls expression of Bmp5 in specific anatomical structures of the mouse embryo.

Por DiLeone, R J, Russell, L B, Kingsley, D M
Publicado em 1998

Fatal lymphoreticular disease in the scurfy (sf) mouse requires T cells that mature in a sf thymic environment: potential model for thymic education.

Por Godfrey, V L, Wilkinson, J E, Rinchik, E M, Russell, L B
Publicado em 1991

Molecular characterization of a region of DNA associated with mutations at the agouti locus in the mouse.

Por Bultman, S J, Russell, L B, Gutierrez-Espeleta, G A, Woychik, R P
Publicado em 1991

High frequency of mosaic mutants produced by N-ethyl-N-nitrosourea exposure of mouse zygotes.

Por Russell, L B, Bangham, J W, Stelzner, K F, Hunsicker, P R
Publicado em 1988

Genetic, cytogenetic, and molecular analyses of mutations induced by melphalan demonstrate high frequencies of heritable deletions and other rearrangements from exposure of postspe...

Por Russell, L B, Hunsicker, P R, Cacheiro, N L, Rinchik, E M
Publicado em 1992

Abnormal ornithine carbamoyltransferase in mice having the sparse-fur mutation.

Por DeMars, R, LeVan, S L, Trend, B L, Russell, L B
Publicado em 1976

Phenotypic consequences of deletion of the gamma 3, alpha 5, or beta 3 subunit of the type A gamma-aminobutyric acid receptor in mice.

Por Culiat, C T, Stubbs, L J, Montgomery, C S, Russell, L B, Rinchik, E M
Publicado em 1994

Characterization of a panel of somatic cell hybrids for regional mapping of the mouse X chromosome.

Por Avner, P, Arnaud, D, Amar, L, Cambrou, J, Winking, H, Russell, L B
Publicado em 1987

Three mouse models of human thalassemia.

Por Martinell, J, Whitney, J B, Popp, R A, Russell, L B, Anderson, W F
Publicado em 1981

Deletions in the alpha-globin gene complex in alpha-thalassemic mice.

Por Whitney, J B, Martinell, J, Popp, R A, Russell, L B, Anderson, W F
Publicado em 1981