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Results 101-110 of 110 (Search time: 0.005 seconds).
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Issue Date
Title
Author(s)
1996
Assignment of the Human GRB14 Gene to Chromosome 2q22-q24 By Fluorescence in Situ Hybridization
Baker, E.
;
Sutherland, G.
;
Sutherland, R.
;
Daly, R.
1998
The human dead ringer/bright homolog, DRIL1: cDNA cloning, gene structure, and mapping to D19S886, a marker on 19p13.3 that is strictly linked to the Peutz-Jeghers Syndrome.
Kortschak, R.
;
Reimann, H.
;
Zimmer, M.
;
Eyre, H.
;
Saint, R.
;
Jenne, D.
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.
2001
TTYH2, a human homologue of the Drosophila melanogaster gene tweety, is located on 17q24 and upregulated in renal cell carcinoma
Rae, F.
;
Hooper, J.
;
Eyre, H.
;
Sutherland, G.
;
Nicol, D.
;
Clements, J.
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.
2014
A randomized, controlled trial of negative pressure wound therapy of pressure ulcers via a novel polyurethane foam
Wagstaff, M.
;
Driver, S.
;
Coghlan, P.
;
Greenwood, J.
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.
1997
Chromosomal localisation of the human P2y6 purinoceptor gene and phylogenetic analysis of the P2y purinoceptor family
Somers, G.
;
Hammet, F.
;
Woollatt, E.
;
Richards, R.
;
Southey, M.
;
Venter, D.
2002
Complementation of a yeast CYC3 deficiency identifies an X-linked mammalian activator of apocytochrome c
Schwarz, Q.
;
Cox, T.
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
27
Sutherland, G.
23
Gecz, J.
16
Mulley, J.
15
et al.
10
Baker, E.
9
Berkovic, S.
9
Eyre, H.
9
Scheffer, I.
8
Gedeon, A.
7
Haan, E.
.
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Subject
70
Female
65
Amino Acid Sequence
56
Base Sequence
51
Animals
37
Pedigree
33
Mutation
28
Mice
28
Sequence Homology, Amino Acid
27
Chromosome Mapping
19
Adult
.
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Date issued
21
2010 - 2015
44
2000 - 2009
45
1995 - 1999