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Results 1-10 of 18 (Search time: 0.002 seconds).
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Issue Date
Title
Author(s)
2006
Novel DNA binding by a basic helix-loop-helix protein - The role of the dioxin receptor PAS domain
Chapman-Smith, A.
;
Whitelaw, M.
2008
PU.1 and NFATc1 mediate osteoclastic induction of the mouse β₃ integrin promoter
Crotti, T.
;
Sharma, S.
;
Fleming, J.
;
Flannery, M.
;
Ostrowski, M.
;
Goldring, S.
;
McHugh, K.
2003
Nova regulates GABA(A) receptor gamma 2 alternative splicing via a distal downstream UCAU-rich intronic splicing enhancer
Dredge, B.
;
Darnell, R.
2006
Disruptions of the novel KIAA1202 gene are associated with X-linked mental retardation
Hagens, O.
;
Dubos, A.
;
Abidi, F.
;
Barbi, G.
;
Van Zutven, L.
;
Hoeltzenbein, M.
;
Tommerup, N.
;
Moraine, C.
;
Fryns, J.
;
Chelly, J.
;
van Bokhoven, H.
;
Gecz, J.
;
Dollfus, H.
;
Ropers, H.
;
Schwartz, C.
;
de Cassia Stocco dos Santos, R.
;
Kalscheuer, V.
;
Hanauer, A.
2000
Gene encoding the mouse sulphamidase: cDNA cloning, structure, and chromosomal mapping
Costanzi, E.
;
Beccari, T.
;
Stinchi, S.
;
Bibi, L.
;
Hopwood, J.
;
Orlacchio, A.
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.
2000
The Aspergillus nidulans creC gene involved in carbon catabolite represssion encodes a WD40 repeat protein
Todd, R.
;
Lockington, R.
;
Kelly, J.
2004
HLS5, a novel RBCC (ring finger, B box, coiled-coil) family member isolated from a hemopoietic lineage switch, is a candidate tumor suppressor
Lalonde, J.
;
Lim, R.
;
Ingley, E.
;
Tilbrook, P.
;
Thompson, M.
;
McCulloch, R.
;
Beaumont, J.
;
Wicking, C.
;
Eyre, H.
;
Sutherland, G.
;
Howe, K.
;
Solomon, E.
;
Williams, J.
;
Klinken, S.
2004
Mutations of CDKL5 cause a severe neurodevelopmental disorder with infantile spasms and mental retardation
Weaving, L.
;
Christodoulou, J.
;
Williamson, S.
;
Friend, K.
;
McKenzie, O.
;
Archer, H.
;
Evans, J.
;
Clarke, A.
;
Pelka, G.
;
Tam, P.
;
Watson, C.
;
Lahooti, H.
;
Ellaway, C.
;
Bennetts, B.
;
Leonard, H.
;
Gecz, J.
Discover
Author
4
Sutherland, G.
3
Eyre, H.
2
Gecz, J.
2
Paton, J.
2
Webb, G.
1
Abidi, F.
1
Adams, J.
1
Antonarakis, S.
1
Archer, H.
1
Barbi, G.
.
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Subject
18
Animals
11
Amino Acid Sequence
8
Sequence Homology, Amino Acid
5
Cell Line
4
Chromosome Mapping
4
DNA
4
DNA, Complementary
4
Exons
4
Introns
3
Base Pairing
.
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Date issued
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2006
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2004
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2003
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2001
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2000