24
results
for author:"Brook J."
in Literature Citations
| Genetic variation in VEGF does not contribute significantly to the risk of congenital cardiovascular malformation. Griffin H.R., Hall D.H., Topf A., Eden J., Stuart A.G., Parsons J., Peart I., Deanfield J.E., O'Sullivan J., Babu-Narayan S.V. et al. PLoS ONE 4:e4978-e4978(2009) · Mapped (7) |
| Physical interaction between TBX5 and MEF2C is required for early heart development. Ghosh T.K., Song F.F., Packham E.A., Buxton S., Robinson T.E., Ronksley J., Self T., Bonser A.J., Brook J.D. Mol. Cell. Biol. 29:2205-2218(2009) · Mapped (1) |
| Muscleblind-like proteins: similarities and differences in normal and myotonic dystrophy muscle. Holt I., Jacquemin V., Fardaei M., Sewry C.A., Butler-Browne G.S., Furling D., Brook J.D., Morris G.E. Am. J. Pathol. 174:216-227(2009) · Mapped (16) |
| Defective mRNA in myotonic dystrophy accumulates at the periphery of nuclear splicing speckles. Holt I., Mittal S., Furling D., Butler-Browne G.S., Brook J.D., Morris G.E. Genes Cells 12:1035-1048(2007) · Mapped (5) |
| Flies deficient in Muscleblind protein model features of myotonic dystrophy with altered splice forms of Z-band associated transcripts. Machuca-Tzili L., Thorpe H., Robinson T.E., Sewry C., Brook J.D. Hum. Genet. 120:487-499(2006) · Mapped (6) |
| Mutation in myosin heavy chain 6 causes atrial septal defect. Ching Y.-H., Ghosh T.K., Cross S.J., Packham E.A., Honeyman L., Loughna S., Robinson T.E., Dearlove A.M., Ribas G., Bonser A.J. et al. |
| The DNA sequence and analysis of human chromosome 6. Mungall A.J., Palmer S.A., Sims S.K., Edwards C.A., Ashurst J.L., Wilming L., Jones M.C., Horton R., Hunt S.E., Scott C.E. et al. Nature 425:805-811(2003) · UniProtKB (1,570) |
| Three proteins, MBNL, MBLL and MBXL, co-localize in vivo with nuclear foci of expanded-repeat transcripts in DM1 and DM2 cells. Fardaei M., Rogers M.T., Thorpe H.M., Larkin K., Hamshere M.G., Harper P.S., Brook J.D. Hum. Mol. Genet. 11:805-814(2002) · UniProtKB (2) |
| Detection of a large TBX5 deletion in a family with Holt-Oram syndrome. Akrami S.M., Winter R.M., Brook J.D., Armour J.A. J. Med. Genet. 38:E44-E44(2001) · Mapped (5) |
| Characterization of the TBX5 binding site and analysis of mutations that cause Holt-Oram syndrome. Ghosh T.K., Packham E.A., Bonser A.J., Robinson T.E., Cross S.J., Brook J.D. Hum. Mol. Genet. 10:1983-1994(2001) · Mapped (6) |
| Virtual cloning and physical mapping of a human T-box gene, TBX4. Yi C.H., Russ A., Brook J.D. |
| Myotonic dystrophy is associated with a reduced level of RNA from the DMWD allele adjacent to the expanded repeat. Alwazzan M., Newman E., Hamshere M.G., Brook J.D. Hum. Mol. Genet. 8:1491-1497(1999) · Mapped (2) |
| Identification, mapping and phylogenomic analysis of four new human members of the T-box gene family: EOMES, TBX6, TBX18, and TBX19. Yi C.-H., Terrett J.A., Li Q.-Y., Ellington K., Packham E.A., Amstrong-Buisseret L., McClure P., Slingsby T., Brook J.D. Genomics 55:10-20(1999) · UniProtKB (4) |
| Six transcripts map within 200 kilobases of the myotonic dystrophy expanded repeat. Alwazzan M., Hamshere M.G., Lennon G.G., Brook J.D. Mamm. Genome 9:485-487(1998) · UniProtKB (2) |
| Holt-Oram syndrome is caused by mutations in TBX5, a member of the Brachyury (T) gene family. Li Q.Y., Newbury-Ecob R., Terrett J.A., Wilson D.I., Curtis A., Yi C.H., Bullen P.J., Strachan T., Robson S., Bonnet D. et al. |
| The amyloid precursor-like protein (APLP) gene maps to the long arm of human chromosome 19. Wasco W., Brook J.D., Tanzi R.E. Genomics 15:237-239(1993) · Mapped (4) |
| Cloning and sequencing of the Escherichia coli panB gene, which encodes ketopantoate hydroxymethyltransferase, and overexpression of the enzyme. Jones C.E., Brook J.M., Buck D., Abell C., Smith A.G. J. Bacteriol. 175:2125-2130(1993) · UniProtKB (2) |
| Increased plasma and lipoprotein lipid peroxidation in apo E-deficient mice. Hayek T., Oiknine J., Brook J.G., Aviram M. Biochem. Biophys. Res. Commun. 201:1567-1574(1994) · Mapped (9) |
| Genomic organization and transcriptional units at the myotonic dystrophy locus. Shaw D.J., McCurrach M., Rundle S.A., Harley H.G., Crow S.R., Sohn R., Thirion J.-P., Hamshere M.G., Buckler A.J., Harper P.S. et al. |
| Role of HDL apolipoprotein E in cellular cholesterol efflux: studies in apo E knockout transgenic mice. Hayek T., Oiknine J., Brook J.G., Aviram M. Biochem. Biophys. Res. Commun. 205:1072-1078(1994) · Mapped (9) |
| Mutations in SOX9, the gene responsible for Campomelic dysplasia and autosomal sex reversal. Kwok C., Weller P.A., Guioli S., Foster J.W., Mansour S., Zuffardi O., Punnett H.H., Dominguez-Steglich M.A., Brook J.D., Young I.D. et al. Am. J. Hum. Genet. 57:1028-1036(1995) · UniProtKB (1) |
| Close linkage of the human cytochrome P450IIA and P450IIB gene subfamilies: implications for the assignment of substrate specificity. Miles J.S., Bickmore W., Brook J.D., McLaren A.W., Meehan R., Wolf C.R. Nucleic Acids Res. 17:2907-2917(1989) · UniProtKB (1) |
| Physical and genetic characterization of the distal segment of the myotonic dystrophy area on 19q. Jansen G., de Jong P.J., Amemiya C., Aslanidis C., Shaw D.J., Harley H.G., Brook J.D., Fenwick R., Korneluk R.G., Tsilfidis C. Genomics 13:509-517(1992) · Mapped (1) |
| Molecular basis of myotonic dystrophy: expansion of a trinucleotide (CTG) repeat at the 3' end of a transcript encoding a protein kinase family member. Brook J.D., McCurrach M., Harley H.G., Buckler A.J., Church D., Aburatani H., Hunter K., Stanton V.P., Thirion J.-P., Hudson T. et al. Cell 68:799-808(1992) · UniProtKB (1) |
