Browsing "Paediatrics publications" by Author Baker, E.

Jump to: 0-9 A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
or enter first few letters:  
Showing results 29 to 48 of 52 < previous   next >
PreviewIssue DateTitleAuthor(s)
1997Localisation of a 10q breakpoint within the PAX2 gene in a patient with a de novo t(10;13) translocation and optic nerve coloboma-renal diseaseNarahara, K.; Baker, E.; Ito, S.; Yokoyama, Y.; Yu, S.; Hewitt, D.; Sutherland, G.; Eccles, M.; Richards, R.
1995Localisation of the adenosine A1 receptor subtype gene (ADORA1) to chromosome 1q32.1Townsend-Nicholson, A.; Baker, E.; Schofield, P.; Sutherland, G.
1995Localisation of the adenosine A2b receptor subtype (ADORA2B) to chromosome 17p11.2-p12 by FISH and PCR screening of somatic cell hybridsTownsend-Nicholson, A.; Baker, E.; Sutherland, G.; Schofield, P.
1995Localization of the gene encoding the human heat shock cognate protein, HSP73 to chromosome 11Tavaria, M.; Gabriele, T.; Anderson, R.; Mirault, M.E.; Baker, E.; Sutherland, G.; Kola, I.
1995Localization of the gene for human 11b hydroxysteroid dehydrogenase type 2 enzyme to chromosome 16q22Krozowski, Z.; Baker, E.; Obeyesekere, V.; Callen, D.
1996Molecular Characterization of a Nonneuronal Human Unc18 HomologZiegler, S.; Mortrud, M.; Swartz, A.; Baker, E.; Sutherland, G.; Burmeister, M.; Mulligan, J.
1998Molecular characterization, pharmacological properties and chromosomal localization of the human GALR2 galanin receptorFathi, Z.; Battaglino, P.; Iben, L.; Li, H.; Baker, E.; Zhang, D.; McGovern, R.; Mahle, C.; Sutherland, G.; Iismaa, T.; Dickinson, K.; Antal Zimanyi, I.
1999Myeloid DAP12-associating lectin (MDL)-1 is a cell surface receptor involved in the activation of myeloid cellsBaker, E.; Sutherland, G.; Phillips, J.; Lanier, L.
1995Natural killer cell receptor for HLA-B allotypes, NKB1 map position 19q13.4Baker, E.; D'Andrea, A.; Phillips, J.; Sutherland, G.; Lanier, L.
2008Overexpression and altered glycosylation of MUC1 in malignant mesotheliomaCreaney, J.; Segal, A.; Sterrett, G.; Platten, M.; Baker, E.; Murch, A.; Nowak, A.; Robinson, B.; Millward, M.
2000Peek-a-boo fragile sites? Not reallySutherland, G.; Baker, E.
2002Sequencing, transcript identification, and quantitative gene expression profiling in the breast cancer loss of heterozygosity region 16q24.3 reveal three potential tumor-suppressor genesPowell, J.; Gardner, A.; Bais, A.; Hinze, S.; Baker, E.; Whitmore, S.; Crawford, J.; Kochetkova, M.; Spendlove, H.; Doggett, N.; Sutherland, G.; Callen, D.; Kremmidiotis, G.
2002Study of 250 children with idiopathic mental retardation reveals nine cryptic and diverse subtelomeric chromosome anomaliesBaker, E.; Hinton, L.; Callen, D.; Altree, M.; Dobbie, A.; Eyre, H.; Sutherland, G.; Thompson, E.; Thompson, P.; Woollatt, E.; Haan, E.
1995The brn-2 gene regulates the melanocytic phenotype and tumorigenic potential of human melanoma cellsAngus, J.; Thompson, F.; Murphy, K.; Baker, E.; Sutherland, G.; Parsons, P.; Sturm, R.
2000The clinical significance of fragile sites on human chromosomesSutherland, G.; Baker, E.
1995The closely linked genes encoding the myeloid nuclear differentation antigen (MNDA) and IFI16 exhibit contrasting haemopoietic expressionDawson, M.; Trapani, J.; Briggs, R.; Nicholl, J.; Sutherland, G.; Baker, E.
1995The genes encoding the myeloid nuclear differentiation antigen (MNDA) and IFI 16 are closely linked on human chromosome 1q22 but exhibit contrasting expression in haemopoietic cell lnesDawson, M.; Trapani, J.; Briggs, R.; Nicholl, J.; Sutherland, G.; Baker, E.
1996The human glycine receptor β subunit: primary structure, functional characterisation and chromosomal localisation of the human and murine genesHandford, C.; Lynch, J.; Baker, E.; Webb, G.; Ford, J.; Sutherland, G.; Schofield, P.
1995The human OTF1 locus which overlaps the CD3Z gene is located at 1q22>q23Sturm, R.; Eyre, H.; Baker, E.; Sutherland, G.
2005The Hunter-McAlpine syndrome results from duplication 5q35-qterHunter, A.; DuPont, B.; McLaughlin, M.; Hinton, L.; Baker, E.; Ades, L.; Haan, E.; Schwartz, C.