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Results 801-810 of 825 (Search time: 0.002 seconds).
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PreviewIssue DateTitleAuthor(s)
1998SOLH, 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.
1996Detection of a megabase deletion in a patient with branchio-oto-renal syndrome (BOR) and tricho-rhino-phalangeal syndrome: implications for mapping and cloning the BOR geneGu, J.; Wagner, M.; Haan, E.; Wells, D.
2014A randomized, controlled trial of negative pressure wound therapy of pressure ulcers via a novel polyurethane foamWagstaff, M.; Driver, S.; Coghlan, P.; Greenwood, J.
2000Human and mouse homologues of the Drosophila melanogaster tweety (tty) gene: A novel gene family encoding predicted transmembrane proteinsCampbell, H.; Kamei, M.; Claudianos, C.; Woollatt, E.; Sutherland, G.; Suzuki, Y.; Hida, M.; Sugano, S.; Young, I.
1997Chromosomal localisation of the human P2y6 purinoceptor gene and phylogenetic analysis of the P2y purinoceptor familySomers, G.; Hammet, F.; Woollatt, E.; Richards, R.; Southey, M.; Venter, D.
1999The PISSLRE Gene: structure, exon skipping, and exclusion as tumor suppressor in breast cancerCrawford, J.; Ianzano, L.; Savino, M.; Whitmore, S.; Cleton-Jansen, A.M.; Settasatian, C.; d'Apolito, M.; Seshadri, R.; Pronk, J.; Auerbach, A.; Verlander, P.; Mathew, C.; Tipping, A.; Doggett, N.; Zelante, L.; Callen, D.; Savoia, A.
2001Molecular and functional analyses of the human and mouse genes encoding AFG3L1, a mitochondrial metalloprotease homologous to the human spastic paraplegia proteinKremmidiotis, G.; Gardner, A.; Settasatian, C.; Savoia, A.; Sutherland, G.; Callen, D.
2000Solh, the mouse homologue of the Drosophila melanogaster small optic lobes gene: organization, chromosomal mapping, and localization of gene product to the olfactory bulbKamei, M.; Webb, G.; Heydon, K.; Hendry, I.; Young, I.; Campbell, H.
2002Complementation of a yeast CYC3 deficiency identifies an X-linked mammalian activator of apocytochrome cSchwarz, Q.; Cox, T.
2002Identification of a mutation causing mucopolysaccharidosis type IIIA in New Zealand Huntaway dogsYogalingam, G.; Pollard, T.; Gliddon, B.; Jolly, R.; Hopwood, J.