Major histocompatibility complex-conferred resistance to Theiler's virus-induced demyelinating disease is inherited as a dominant trait in B10 congenic mice.

Por Patick, A K, Pease, L R, David, C S, Rodriguez, M
Publicado em 1990

Unusual mutation clusters provide insight into class I gene conversion mechanisms.

Por Pease, L R, Horton, R M, Pullen, J K, Yun, T J
Publicado em 1993

Spontaneous H-2 mutants provide evidence that a copy mechanism analogous to gene conversion generates polymorphism in the major histocompatibility complex.

Por Pease, L R, Schulze, D H, Pfaffenbach, G M, Nathenson, S G
Publicado em 1983

The immune system preferentially clears Theiler's virus from the gray matter of the central nervous system.

Por Njenga, M K, Asakura, K, Hunter, S F, Wettstein, P, Pease, L R, Rodriguez, M
Publicado em 1997

Comparison of the cloned H-2Kbm1 variant gene with the H-2Kb gene shows a cluster of seven nucleotide differences.

Por Schulze, D H, Pease, L R, Geier, S S, Reyes, A A, Sarmiento, L A, Wallace, R B, Nathenson, S G
Publicado em 1983

Chromosome 14 contains determinants that regulate susceptibility to Theiler's virus-induced demyelination in the mouse.

Por Bureau, J F, Drescher, K M, Pease, L R, Vikoren, T, Delcroix, M, Zoecklein, L, Brahic, M, Rodriguez, M
Publicado em 1998

Positive selection of transgenic receptor-bearing thymocytes by Kb antigen is altered by Kb mutations that involve peptide binding.

Por Sha, W C, Nelson, C A, Newberry, R D, Pullen, J K, Pease, L R, Russell, J H, Loh, D Y
Publicado em 1990

Acidic polyamino acids inhibit human eosinophil granule major basic protein toxicity. Evidence of a functional role for ProMBP.

Por Barker, R L, Gundel, R H, Gleich, G J, Checkel, J L, Loegering, D A, Pease, L R, Hamann, K J
Publicado em 1991

Immunomodulation using the recombinant monoclonal human B7-DC cross-linking antibody rHIgM12

Por Van Keulen, V P, Ciric, B, Radhakrishnan, S, Heckman, K L, Mitsunaga, Y, Iijima, K, Kita, H, Rodriguez, M, Pease, L R
Publicado em 2006

Interaction between Kb and Q4 gene sequences generates the Kbm6 mutation.

Por Geliebter, J, Zeff, R A, Schulze, D H, Pease, L R, Weiss, E H, Mellor, A L, Flavell, R A, Nathenson, S G
Publicado em 1986