Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Matthew Cadman"'
Autor:
Paul Denny, Shoumo Bhattacharya, Andy Greenfield, Patrick M. Nolan, Jiannis Ragoussis, Gimara Duncan, Kulvinder Kaur, Andrea Hardy, Richard McKeone, Ramya Chandrasekara, Matthew Cadman, Steve D.M. Brown, Anju Paudyal, Jennifer R. Davies, Jürgen E. Schneider, Michael J. Depew, Paul T. Sharpe, Ruth M. Arkell, Nikos Tripodis, Ghazala Mirza, Debora Bogani, Heather Haines, Catherine Willoughby, Guido E Pieles
Publikováno v:
Proceedings of the National Academy of Sciences. 102:12477-12482
Monosomy of the human chromosome 6p terminal region results in a variety of congenital malformations that include brain, craniofacial, and organogenesis abnormalities. To examine the genetic basis of these phenotypes, we have carried out an unbiased
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::56a4b03b9fcf7fb97228753106e22043
https://doi.org/10.1073/pnas.0500584102
https://doi.org/10.1073/pnas.0500584102
Autor:
Marc Botcherby, Joseph Weekes, Paul Denny, John M. Hancock, James G. R. Gilbert, Sandrine Peyrefitte, Laurens G. Wilming, Jane Rogers, Steve D.M. Brown, Ruth M. Arkell, Ann-Marie Mallon, Jennifer L. Ashurst, Matthew Cadman, Lucy Matthews, Richard McKeone, Mark A. Strivens, Christopher A. Sellick, R. Duncan Campbell, Simon G. Gregory
Publikováno v:
Genome Research. 14:1888-1901
The Del(13)Svea36H mutation (referred to hereafter as Del36H) is a microscopically visible deletion of ∼20% of mouse chromosome 13 (Arkell et al. 2001). Mice that are heterozygous for Del36H display a phenotype that varies with genetic background a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::616405a28e5324baac5d36940ae87da9
https://doi.org/10.1101/gr.2478604
https://doi.org/10.1101/gr.2478604
Autor:
Jiannis Ragoussis, Phillip I. Bird, Dion Kaiserman, Ghazala Mirza, Richard McKeone, Jessica Cooley, Susan Knaggs, Anneliese Gillard, Paul Denny, Charaf Benarafa, Katrina L Scarff, Eileen Remold-O'Donnell, Matthew Cadman
Publikováno v:
Genomics. 79:349-362
Ov-serpins are intracellular proteinase inhibitors implicated in the regulation of tumor progression, inflammation, and cell death. The 13 human ov-serpin genes are clustered at 6p25 (3 genes) and 18q21 (10 genes), and share common structures. We sho
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cebd6b60ad5660b5b5aed288ec72eaaa
https://doi.org/10.1006/geno.2002.6716
https://doi.org/10.1006/geno.2002.6716
Autor:
Anne Southwell, Caroline Thaung, Colin V. Beechey, Ruth M. Arkell, Steve D.M. Brown, Paul Denny, Tracy Marsland, Matthew Cadman, Toni Clay, Jennifer Davies, Mark A. Strivens, Edward P. Evans
Publikováno v:
Mammalian Genome. 12:687-694
The Del(13)Svea36H deletion was recovered from a radiation mutagenesis experiment and represents a valuable resource for investigating gene content and function at this region of mouse Chromosome (Chr) 13 and human Chr 6p21.3-23 and 6p25. In this pap
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::05fff3f5fac511fb07c0965bede5d02f
https://doi.org/10.1007/s00335-001-2066-2
https://doi.org/10.1007/s00335-001-2066-2
Autor:
André Rosenthal, Mark E. Harrison, Mary F. Lyon, Steve D.M. Brown, Christopher Hayes, Gillian M. Morriss-Kay, Matthew Cadman, Edward P. Evans, Andreas Rump
Publikováno v:
Genomics. 78(3)
The mouse doublefoot (Dbf) mutant exhibits preaxial polydactyly in association with craniofacial defects. This mutation has previously been mapped to mouse chromosome 1. We have used a positional cloning strategy, coupled with a comparative sequencin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::19ba8d3c3befa1abfb8efd9f8985d26a
https://pubmed.ncbi.nlm.nih.gov/11735226
https://pubmed.ncbi.nlm.nih.gov/11735226
Autor:
Nigel P. Carter, Thomas J. Hudson, Wenjuan Ye, Mark S. Boguski, Bruce W. Birren, Gail Farino, Lincoln Stein, Olga Merport, Pamela Trickett, William F. Dietrich, Donna K. Slonim, Delphine Gray, Robert Nahf, Chad Nusbaum, Anne Southwell, Andrew R. Haynes, Robert G. Steen, Irina S. Zemsteva, Zeeshan Husain, Eric S. Lander, Tracy Marsland, Vardouhie Kouyoumjian, Mark T. Ross, Xiaoyun Wu, Matthew Cadman, Richard Devine, Victoria E. H. Wang, Christine Heuston, Yi Wu, Paul Denny, James Tam, Steve D.M. Brown, Andrew B. Castle, Dorothy F. Courtney, Alville Collymore, Joyce C. Miller, Mark A. Strivens, Mechele O. Anderson, Lloyd T. Horton, Katrina Harris, Yixun Xu, Wojciech Makalowski
Publikováno v:
Nature genetics. 22(4)
A physical map of the mouse genome is an essential tool for both positional cloning and genomic sequencing in this key model system for biomedical research. Indeed, the construction of a mouse physical map with markers spaced at an average interval o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::22dad6af9a1464415723a12e94d814df
https://pubmed.ncbi.nlm.nih.gov/10431246
https://pubmed.ncbi.nlm.nih.gov/10431246