Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Aaron Abbott"'
Autor:
Aaron Abbott
Since its foundation in 1948 as an environmental Stainless Steel Utensils, Cothas has grown into a major coffee Stainless Steel Utensils and producer. Cothas source the best coffee beans from the best places in Karnataka and surrounding areas of Indi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2659::6e21486e2748f768dbf507b5963a59de
https://zenodo.org/record/4963727
https://zenodo.org/record/4963727
Autor:
B. Paul Wordsworth, Gordon W. Duff, Andrei Calin, Owen Beynon, Aaron Abbott, Anne Marie Sims, A. M. Crane, Linda A. Bradbury, Ibi Herzberg, Heather J. Cordell, Andrew E. Timms, Lon R. Cardon, Matthew A. Brown, Mark R.E. Coyne
Ankylosing spondylitis (AS) is a common and highly heritable inflammatory arthropathy. Although the gene HLA-B27 is almost essential for the inheritance of the condition, it alone is not sufficient to explain the pattern of familial recurrence of the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f7ea5a91180a015f6cc2d73742819a86
https://doi.org/10.1086/424695
https://doi.org/10.1086/424695
Autor:
Aaron Abbott, Daniel E. Weeks, Richard Mott, Gabrielle Barnby, Andrew J. Morris, Nuala Sykes, Janine A. Lamb, Anthony J. Bailey, Anthony P. Monaco
Publikováno v:
The American Journal of Human Genetics. 76(6):950-966
Autism is a highly heritable neurodevelopmental disorder whose underlying genetic causes have yet to be identified. To date, there have been eight genome screens for autism, two of which identified a putative susceptibility locus on chromosome 16p. I
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e5e9518ba0525ebecea86761d136f755
Autor:
Jiannis Ragoussis, Hsiao P.J. Voon, Stephen Taylor, Karen M. Lower, Guilherme Martins Santos, Ian Dunham, Marco De Gobbi, Richard J. Gibbons, Aaron Abbott, David Garrick, Douglas R. Higgs, Helena Ayyub, Vip Viprakasit, Jim R. Hughes, Andrew J. Morris, Joe Cross, Daniela Rhodes, Marco A. Marra, Martin J. Law, Matthew Mitson, Steven P. Wilder, Steven J.M. Jones
SummaryATRX is an X-linked gene of the SWI/SNF family, mutations in which cause syndromal mental retardation and downregulation of α-globin expression. Here we show that ATRX binds to tandem repeat (TR) sequences in both telomeres and euchromatin. G
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7be0aa2c582e40d54e261fbddaf8a730
http://hdl.handle.net/2318/89805
http://hdl.handle.net/2318/89805
Autor:
M Paolucci, Jeremy R. Parr, I Ragoussis, Annemarie Poustka, Kim S. Beyer, Axel Benner, Anthony P. Monaco, Sabine M. Klauck, Anthony J. Bailey, Aaron Abbott, Enzo Bonora, Janine A. Lamb
Publikováno v:
Molecular psychiatry. 8(10)
Genetic studies indicate that chromosome 7q is likely to contain an autism susceptibility locus (AUTS1). We have followed a positional candidate gene approach to identify relevant gene(s) and report here the analysis of reelin (RELN), a gene located
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f5728195df5d7fc4443555849eb4f9ec
https://pubmed.ncbi.nlm.nih.gov/14515139
https://pubmed.ncbi.nlm.nih.gov/14515139
Autor:
Stephen D. Jackson, Aaron Abbott
Publikováno v:
Comparative Biochemistry and Physiology Part A: Molecular & Integrative Physiology. 153:S198
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c4f62e01f0115af9b67ffe3e5cd236af
https://doi.org/10.1016/j.cbpa.2009.04.446
https://doi.org/10.1016/j.cbpa.2009.04.446