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Results 71-79 of 79 (Search time: 0.003 seconds).
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Issue Date
Title
Author(s)
1997
Structural organization of the mouse and human GALR1 Galanin receptor genes (Galnr and GALNR) and chromosomal localization of the mouse gene
Jacoby, A.
;
Webb, G.
;
Liu, M.
;
Kofler, B.
;
Hort, Y.
;
Fathi, Z.
;
Bottema, C.
;
Shine, J.
;
Iismaa, T.
1999
Identification, functional characterization, and chromosomal localization of USP15, a novel human ubiquitin-specific protease related to the UNP oncoprotein, and a systematic nomenclature for human ubiquitin-specific proteases
Baker, R.
;
Wang, X.W.
;
Woollatt, E.
;
White, J.
;
Sutherland, G.
1998
SOLH, a human homologue of the Drosophila melanogaster small optic lobes gene is a member of the Calpain and Zinc-Finger gene families and maps to human chromosome 16p13.3 near CATM (cataract with microphthalmia)
Kamei, M.
;
Webb, G.
;
Young, I.
;
Campbell, H.
2000
Human and mouse homologues of the Drosophila melanogaster tweety (tty) gene: A novel gene family encoding predicted transmembrane proteins
Campbell, H.
;
Kamei, M.
;
Claudianos, C.
;
Woollatt, E.
;
Sutherland, G.
;
Suzuki, Y.
;
Hida, M.
;
Sugano, S.
;
Young, I.
2001
Molecular and functional analyses of the human and mouse genes encoding AFG3L1, a mitochondrial metalloprotease homologous to the human spastic paraplegia protein
Kremmidiotis, G.
;
Gardner, A.
;
Settasatian, C.
;
Savoia, A.
;
Sutherland, G.
;
Callen, D.
2000
Solh, the mouse homologue of the Drosophila melanogaster small optic lobes gene: organization, chromosomal mapping, and localization of gene product to the olfactory bulb
Kamei, M.
;
Webb, G.
;
Heydon, K.
;
Hendry, I.
;
Young, I.
;
Campbell, H.
1995
Cloning and sequence analysis of caprine N-acetylglucosamine 6-sulfatase cDNA
Friderici, K.
;
Cavanagh, K.
;
Leipprandt, J.
;
Traviss, C.
;
Anson, D.
;
Hopwood, J.
;
Jones, M.
1994
Isolation and characterization of ovine IGFBP-4: protein purification and cDNA sequence
CARR, J.M.
;
GRANT, P.A.
;
FRANCIS, G.L.
;
OWENS, J.A.
;
WALLACE, J.C.
;
WALTON, P.E.
2009
Aire-Deficient C57BL/6 Mice Mimicking the Common Human 13-Base Pair Deletion Mutation Present with Only a Mild Autoimmune Phenotype
Hubert, F.
;
Kinkel, S.
;
Crewther, P.
;
Cannon, P.
;
Webster, K.
;
Link, M.
;
Uibo, R.
;
O'Bryan, M.
;
Meager, A.
;
Forehan, S.
;
Smyth, G.
;
Mittaz, L.
;
Antonarakis, S.
;
Peterson, P.
;
Heath, W.
;
Scott, H.
Discover
Author
12
Sutherland, G.
6
Kumar, S.
4
Baker, E.
4
Hopwood, J.
4
Kamei, M.
4
Saint, R.
4
Whitelaw, M.
3
Bagley, C.
3
Campbell, H.
3
Campbell, I.
.
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Subject
78
Molecular Sequence Data
56
Humans
40
Mice
35
Base Sequence
24
DNA, Complementary
18
Cloning, Molecular
17
Chromosome Mapping
17
Male
17
Sequence Alignment
14
Female
.
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Date issued
8
2010 - 2015
37
2000 - 2009
34
1994 - 1999