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1 - 25 of 29 results for author:"Gardiner K."Drop in Literature Citations

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Synaptojanin 1-linked phosphoinositide dyshomeostasis and cognitive deficits in mouse models of Down's syndrome.

Voronov S.V., Frere S.G., Giovedi S., Pollina E.A., Borel C., Zhang H., Schmidt C., Akeson E.C., Wenk M.R., Cimasoni L. et al.

Proc. Natl. Acad. Sci. U.S.A. 105:9415-9420(2008) · Mapped (1)

Editing of the serotonin 2C receptor pre-mRNA: Effects of the Morris Water Maze.

Du Y., Stasko M., Costa A.C., Davisson M.T., Gardiner K.J.

Gene 391:186-197(2007) · Mapped (6)

A-to-I pre-mRNA editing of the serotonin 2C receptor: comparisons among inbred mouse strains.

Du Y., Davisson M.T., Kafadar K., Gardiner K.

Gene 382:39-46(2006) · Mapped (9)

Alternative splicing of mammalian Intersectin 1: domain associations and tissue specificities.

Tsyba L., Skrypkina I., Rynditch A., Nikolaienko O., Ferenets G., Fortna A., Gardiner K.

Genomics 84:106-113(2004) · UniProtKB (6)

New forms of gene transcripts in human and mouse intersectin.

Skripkina I.A., Tsyba L.A., Slavov D., Gardiner K., Ryndich A.V.

Ukr. Biokhim. Zh. 74:33-43(2002) · UniProtKB (5)

Phylogenetic comparison of the pre-mRNA adenosine deaminase ADAR2 genes and transcripts: conservation and diversity in editing site sequence and alternative splicing patterns.

Slavov D., Gardiner K.

Gene 299:83-94(2002) · UniProtKB (3) · Mapped (4)

Annotation of human chromosome 21 for relevance to Down syndrome: gene structure and expression analysis.

Gardiner K., Slavov D., Bechtel L., Davisson M.

Genomics 79:833-843(2002) · UniProtKB (15) · Mapped (1)

Evolutionary breakpoints on human chromosome 21.

Davisson M.T., Bechtel L.J., Akeson E.C., Fortna A., Slavov D., Gardiner K.

Genomics 78:99-106(2001) · Mapped (36)

Ts65Dn -- localization of the translocation breakpoint and trisomic gene content in a mouse model for Down syndrome.

Akeson E.C., Lambert J.P., Narayanswami S., Gardiner K., Bechtel L.J., Davisson M.T.

Cytogenet. Cell Genet. 93:270-276(2001) · Mapped (21)

Comparative analysis of the DRADA A-to-I RNA editing gene from mammals, pufferfish and zebrafish.

Slavov D., Crnogorac-Jurcevic T., Clark M., Gardiner K.

Gene 250:53-60(2000) · UniProtKB (3)

Comparative analysis of the RED1 and RED2 A-to-I RNA editing genes from mammals, pufferfish and zebrafish.

Slavov D., Clark M., Gardiner K.

Gene 250:41-51(2000) · UniProtKB (5) · Mapped (2)

The DNA sequence of human chromosome 21.

Hattori M., Fujiyama A., Taylor T.D., Watanabe H., Yada T., Park H.-S., Toyoda A., Ishii K., Totoki Y., Choi D.-K. et al.

Nature 405:311-319(2000) · UniProtKB (506)

Criteria for gene identification and features of genome organization: analysis of 6.5 Mb of DNA sequence from human chromosome 21.

Slavov D., Hattori M., Sakaki Y., Rosenthal A., Shimizu N., Minoshima S., Kudoh J., Yaspo M.-L., Ramser J., Reinhardt R. et al.

Gene 247:215-232(2000) · UniProtKB (5)

Human phosphoribosylformylglycinamide amidotransferase (FGARAT): regional mapping, complete coding sequence, isolation of a functional genomic clone, and DNA sequence analysis.

Patterson D., Bleskan J., Gardiner K., Bowersox J.

Gene 239:381-391(1999) · UniProtKB (1)

Haploinsufficiency of CBFA2 causes familial thrombocytopenia with propensity to develop acute myelogenous leukaemia.

Song W.-J., Sullivan M.G., Legare R.D., Hutchings S., Tan X., Kufrin D., Ratajczak J., Resende I.C., Haworth C., Hock R. et al.

Nat. Genet. 23:166-175(1999) · UniProtKB (1)

Comparative genomic analysis of the interferon/interleukin-10 receptor gene cluster.

Reboul J., Gardiner K., Monneron D., Uze G., Lutfalla G.

Genome Res. 9:242-250(1999) · UniProtKB (10)

Structures, sequence characteristics, and synteny relationships of the transcription factor E4TF1, the splicing factor U2AF35 and the cystathionine beta synthetase genes from Fugu rubripes.

Tassone F., Villard L., Clancy K., Gardiner K.

Gene 226:211-223(1999) · UniProtKB (3)

Molecular cloning of a human cDNA IGSF3 encoding an immunoglobulin-like membrane protein: expression and mapping to chromosome band 1p13.

Saupe S., Roizes G., Peter M., Boyle S., Gardiner K., De Sario A.

Genomics 52:305-311(1998) · UniProtKB (1)

Analysis of pufferfish homologues of the AT-rich human APP gene.

Villard L., Tassone F., Crnogorac-Jurcevic T., Clancy K., Gardiner K.

Gene 210:17-24(1998) · UniProtKB (5)

Map location, genomic organization and expression patterns of the human RED1 RNA editase.

Villard L., Tassone F., Haymowicz M., Welborn R., Gardiner K.

Somat. Cell Mol. Genet. 23:135-145(1997) · UniProtKB (1)

Activation of a novel gene in 3q21 and identification of intergenic fusion transcripts with ecotropic viral insertion site I in leukemia.

Pekarsky Y., Rynditch A., Wieser R., Fonatsch C., Gardiner K.

Cancer Res. 57:3914-3919(1997) · UniProtKB (1)

Of messages and meaning.

Gardiner K., Brookes A., Mural R.

Trends Genet. 13:92-93(1997) · Mapped (1)

Molecular genetic characterization and comparative mapping of the human PCP4 gene.

Cabin D.E., Gardiner K., Reeves R.H.

Somat. Cell Mol. Genet. 22:167-175(1996) · UniProtKB (1) · Mapped (10)

The human myosin light chain kinase (MLCK) from hippocampus: cloning, sequencing, expression, and localization to 3qcen-q21.

Potier M.-C., Chelot E., Pekarsky Y., Gardiner K., Rossier J., Turnell W.G.

Genomics 29:562-570(1995) · UniProtKB (1)

GART, SON, IFNAR, and CRF2-4 genes cluster on human chromosome 21 and mouse chromosome 16.

Cheng S., Lutfalla G., Uze G., Chumakov I.M., Gardiner K.

Mamm. Genome 4:338-342(1993) · Mapped (24)

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