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Results 1-10 of 19 (Search time: 0.003 seconds).
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Issue Date
Title
Author(s)
2001
An orphaned mammalian b-globin gene of ancient evolutionary origin
Wheeler, D.
;
Hope, R.
;
Cooper, S.
;
Dolman, G.
;
Webb, G.
;
Bottema, C.
;
Gooley, A.
;
Goodman, M.
;
Holland, R.
2001
The protein tyrosine phosphatase TCPTP suppresses the tumorigenicity of glioblastoma cells expressing a mutant epidermal growth factor receptor
Klingler-Hoffmann, M.
;
Fodero-Tavoletti, M.
;
Mishima, K.
;
Narita, Y.
;
Cavenee, W.
;
Furnari, F.
;
Huang, H.
;
Tiganis, T.
2001
Simple, directional cDNA cloning for in situ transcript hybridization screens
Tamme, R.
;
Mills, K.
;
Rainbird, B.
;
Nornes, S.
;
Lardelli, M.
2001
Phylogenetic analysis of the Monocotylidae (Monogenea) inferred from 28S rDNA sequences
Chisholm, L.
;
Morgan, J.
;
Adlard, R.
;
Whittington, I.
2001
Gene structure, alternative splicing, and chromosomal localization of pro-apoptotic Bcl-2 relative Bim
Bouillet, P.
;
Zhang, L.
;
Huang, D.
;
Webb, G.
;
Bottema, C.
;
Shore, P.
;
Eyre, H.
;
Sutherland, G.
;
Adams, J.
2001
Fcα/μ receptor is a single gene-family member closely related to polymeric immunoglobulin receptor encoded on Chromosome 1
Shimizu, Y.
;
Honda, S.
;
Yotsumoto, K.
;
Tahara-Hanaoka, S.
;
Eyre, H.
;
Sutherland, G.
;
Endo, Y.
;
Shibuya, K.
;
Koyama, A.
;
Nakauchi, H.
;
Shibuya, A.
2001
A molecular analysis of dietary diversity for three archaic Native Americans
Poinar, H.
;
Kuch, M.
;
Sobolik, K.
;
Barnes, I.
;
Stankiewicz, A.
;
Kuder, T.
;
Spaulding, W.
;
Bryant, V.
;
Cooper, A.
;
Paabo, S.
2001
A recurrent RNA-splicing mutation in the SEDL gene causes X-linked spondyloepiphyseal dysplasia tarda
Tiller, G.
;
Hannig, V.
;
Dozier, D.
;
Carrel, L.
;
Trevarthen, K.
;
Wilcox, W.
;
Mundlos, S.
;
Haines, J.
;
Gedeon, A.
;
Gecz, J.
2001
Glycosidase active site mutations in human a-L-iduronidase
Brooks, D.
;
Fabrega, S.
;
Hein, L.
;
Parkinson, E.
;
Durand, P.
;
Yogalingam, G.
;
Matte, U.
;
Giugliani, R.
;
Dasvarma, A.
;
Eslahpazire, J.
;
Henrissat, B.
;
Mornon, J.
;
Hopwood, J.
;
Lehn, P.
2001
A novel missense mutation in lysosomal sulfamidase is the basis of MPS III A in a spontaneous mouse mutant
Bhattacharyya, R.
;
Gliddon, B.
;
Beccari, T.
;
Hopwood, J.
;
Stanley, P.
Discover
Author
4
Sutherland, G.
2
Bottema, C.
2
Cooper, A.
2
Eyre, H.
2
Hopwood, J.
2
Webb, G.
1
Adams, J.
1
Adlard, R.
1
Ashman, L.
1
Baker, E.
.
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Subject
14
Humans
13
Molecular Sequence Data
8
Amino Acid Sequence
8
Mice
6
DNA Primers
5
Cloning, Molecular
4
Cell Line
4
Mutation
4
Phylogeny
4
Sequence Homology, Amino Acid
.
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