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34
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for author:"Callen D.F."
in Literature Citations
| Identification of ANKRD11 as a p53 coactivator. Neilsen P.M., Cheney K.M., Li C.W., Chen J.D., Cawrse J.E., Schulz R.B., Powell J.A., Kumar R., Callen D.F. J. Cell. Sci. 121:3541-3552(2008) · Mapped (38) |
| CBFA2T3-ZNF652 corepressor complex regulates transcription of the E-box gene HEB. Kumar R., Cheney K.M., McKirdy R., Neilsen P.M., Schulz R.B., Lee J., Cohen J., Booker G.W., Callen D.F. J. Biol. Chem. 283:19026-19038(2008) · Mapped (26) |
| ZNF652, a novel zinc finger protein, interacts with the putative breast tumor suppressor CBFA2T3 to repress transcription. Kumar R., Manning J., Spendlove H.E., Kremmidiotis G., McKirdy R., Lee J., Millband D.N., Cheney K.M., Stampfer M.R., Dwivedi P.P. et al. Mol. Cancer Res. 4:655-665(2006) · UniProtKB (2) · Mapped (3) |
| FBXO31 is the chromosome 16q24.3 senescence gene, a candidate breast tumor suppressor, and a component of an SCF complex. Kumar R., Neilsen P.M., Crawford J., McKirdy R., Lee J., Powell J.A., Saif Z., Martin J.M., Lombaerts M., Cornelisse C.J. et al. Cancer Res. 65:11304-11313(2005) · UniProtKB (1) · Mapped (1) |
| The sequence and analysis of duplication-rich human chromosome 16. Martin J., Han C., Gordon L.A., Terry A., Prabhakar S., She X., Xie G., Hellsten U., Chan Y.M., Altherr M. et al. Nature 432:988-994(2004) · UniProtKB (638) |
| CARD15/NOD2 risk alleles in the development of Crohn's disease in the Australian population. Cavanaugh J.A., Adams K.E., Quak E.J., Bryce M.E., O'Callaghan N.J., Rodgers H.J., Magarry G.R., Butler W.J., Eaden J.A., Roberts-Thomson I.C. et al. Ann. Hum. Genet. 67:35-41(2003) · Mapped (7) |
| CBFA2T3 (MTG16) is a putative breast tumor suppressor gene from the breast cancer loss of heterozygosity region at 16q24.3. Kochetkova M., McKenzie O.L.D., Bais A.J., Martin J.M., Secker G.A., Seshadri R., Powell J.A., Hinze S.J., Gardner A.E., Spendlove H.E. et al. |
| Molecular and functional analyses of the human and mouse genes encoding AFG3L1, a mitochondrial metalloprotease homologous to the human spastic paraplegia protein. Kremmidiotis G., Gardner A.E., Settasatian C., Savoia A., Sutherland G.R., Callen D.F. |
| Analysis of lymphoedema-distichiasis families for FOXC2 mutations reveals small insertions and deletions throughout the gene. Bell R., Brice G., Child A.H., Murday V.A., Mansour S., Sandy C.J., Collin J.R.O., Brady A.F., Callen D.F., Burnand K. et al. Hum. Genet. 108:546-551(2001) · UniProtKB (1) |
| C16orf5, a novel proline-rich gene at 16p13.3, is highly expressed in the brain. Bhalla K., Eyre H.J., Whitmore S.A., Sutherland G.R., Callen D.F. J. Hum. Genet. 44:383-387(1999) · UniProtKB (1) |
| Characterization of copine VII, a new member of the copine family, and its exclusion as a candidate in sporadic breast cancers with loss of heterozygosity at 16q24.3. Savino M., D'Apolito M., Centra M., van Beerendonk H.M., Cleton-Jansen A.-M., Whitmore S.A., Crawford J., Callen D.F., Zelante L., Savoia A. Genomics 61:219-226(1999) · UniProtKB (1) |
| Genomic structure and expression analysis of the spastic paraplegia gene, SPG7. Settasatian C., Whitmore S.A., Crawford J., Bilton R.L., Cleton-Jansen A.-M., Sutherland G.R., Callen D.F. Hum. Genet. 105:139-144(1999) · UniProtKB (1) |
| The PISSLRE gene: structure, exon skipping, and exclusion as tumor suppressor in breast cancer. Crawford J., Ianzano L., Savino M., Whitmore S., Cleton-Jansen A.-M., Settasatiani C., D'Apolito M., Seshadri R., Pronk J.C., Auerbach A.D. et al. Genomics 56:90-97(1999) · UniProtKB (1) |
| Construction of an approximately 700-kb transcript map around the familial Mediterranean fever locus on human chromosome 16p13.3. Centola M., Chen X., Sood R., Deng Z., Aksentijevich I., Blake T., Ricke D.O., Chen X., Wood G., Zaks N. et al. Genome Res. 8:1172-1191(1998) · UniProtKB (2) |
| Characterization and screening for mutations of the growth arrest-specific 11 (GAS11) and C16orf3 genes at 16q24.3 in breast cancer. Whitmore S.A., Settasatian C., Crawford J., Lower K.M., McCallum B., Seshadri R., Cornelisse C.J., Moerland E.W., Cleton-Jansen A.-M., Tipping A.J. et al. Genomics 52:325-331(1998) · UniProtKB (2) |
| Localization of human cadherin genes to chromosome regions exhibiting cancer-related loss of heterozygosity. Kremmidiotis G., Baker E., Crawford J., Eyre H.J., Nahmias J., Callen D.F. Genomics 49:467-471(1998) · UniProtKB (1) |
| A novel gene encoding an integral membrane protein is mutated in nephropathic cystinosis. Town M., Jean G., Cherqui S., Attard M., Forestier L., Whitmore S.A., Callen D.F., Gribouval O., Broyer M., Bates G.P. et al. |
| Comparative analysis of the phosphomannomutase genes PMM1, PMM2 and PMM2psi: the sequence variation in the processed pseudogene is a reflection of the mutations found in the functional gene. Schollen E., Pardon E., Heykants L., Renard J., Doggett N.A., Callen D.F., Cassiman J.J., Matthijs G. Hum. Mol. Genet. 7:157-164(1998) · UniProtKB (1) |
| Structure of the CLN3 gene and predicted structure, location and function of CLN3 protein. Mitchison H.M., Taschner P.E., Kremmidiotis G., Callen D.F., Doggett N.A., Lerner T.J., Janes R.B., Wallace B.A., Munroe P.B., O'Rawe A.M. et al. Neuropediatrics 28:12-14(1997) · Mapped (1) |
| Genomic structure and complete nucleotide sequence of the Batten disease gene, CLN3. Mitchison H.M., Munroe P.B., O'Rawe A.M., Taschner P.E.M., de Vos N., Kremmidiotis G., Lensink I., Munk A.C., D'Arigo K.L., Anderson J.W. et al. Genomics 40:346-350(1997) · UniProtKB (1) |
| Expression cloning of a cDNA for the major Fanconi anaemia gene, FAA. Lo Ten Foe J.R., Rooimans M.A., Bosnoyan-Collins L., Alon N., Wijker M., Parker L., Lightfoot J., Carreau M., Callen D.F., Savoia A. et al. Nat. Genet. 14:320-323(1996) · UniProtKB (1) |
| Molecular cloning, expression and chromosomal localization of a human gene encoding a 33 kDa putative metallopeptidase (PRSM1). Scott I.C., Halila R., Jenkins J.M., Mehan S., Apostolou S., Winqvist R., Callen D.F., Prockop D.J., Peltonen L., Kadler K.E. Gene 174:135-143(1996) · UniProtKB (1) |
| Molecular cloning of the cDNA and chromosome localization of the gene for human ubiquitin-conjugating enzyme 9. Wang Z.-Y., Qiu Q., Seufert W., Taguchi T., Testa J.R., Whitmore S.A., Callen D.F., Welsh D., Shenk T., Deuel T.F. J. Biol. Chem. 271:24811-24816(1996) · UniProtKB (1) · Mapped (1) |
| Genetic association of 11 beta-hydroxysteroid dehydrogenase type 2 (HSD11B2) flanking microsatellites with essential hypertension in blacks. Watson B. Jr., Bergman S.M., Myracle A., Callen D.F., Acton R.T., Warnock D.G. Hypertension 28:478-482(1996) · Mapped (1) |
| Smooth muscle myosin heavy chain locus (MYH11) maps to 16p13.13-p13.12 and establishes a new region of conserved synteny between human 16p and mouse 16. Deng Z., Liu P., Marlton P., Claxton D.F., Lane S., Callen D.F., Collins F.S., Siciliano M.J. Genomics 18:156-159(1993) · Mapped (3) |
