Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Andrew Fortna"'
Autor:
Andrew Fortna, Young Kim, Erik MacLaren, Kriste Marshall, Gretchen Hahn, Lynne Meltesen, Matthew Brenton, Raquel Hink, Sonya Burgers, Tina Hernandez-Boussard, Anis Karimpour-Fard, Deborah Glueck, Loris McGavran, Rebecca Berry, Jonathan Pollack, James M Sikela
Publikováno v:
PLoS Biology, Vol 2, Iss 7, p E207 (2004)
Given that gene duplication is a major driving force of evolutionary change and the key mechanism underlying the emergence of new genes and biological processes, this study sought to use a novel genome-wide approach to identify genes that have underg
Externí odkaz:
https://doaj.org/article/899b049c6a78430ea3a2c33859010d2f
Publikováno v:
Gene. 318:137-147
With an incidence of approximately 1 in 700 live births, Down syndrome (DS) remains the most common genetic cause of mental retardation. The phenotype is assumed to be due to overexpression of some number of the >300 genes encoded by human chromosome
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::059b57331d48deab35fb5e19f0793210
https://doi.org/10.1016/s0378-1119(03)00769-8
https://doi.org/10.1016/s0378-1119(03)00769-8
Autor:
Andrew Fortna, K. Gardiner
Publikováno v:
Trends in Genetics. 17:158-164
The wealth of information from various genome sequencing projects provides the biologist with a new perspective from which to analyze, and design experiments with, mammalian systems. The complexity of the information, however, requires new software t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::35218e39810cb1a8d39b93ef564dc150
https://doi.org/10.1016/s0168-9525(01)02229-6
https://doi.org/10.1016/s0168-9525(01)02229-6
Autor:
Young Ho Kim, Rebecca Berry, Gretchen Hahn, Andrew Fortna, Kriste E Marshall, Raquel Hink, Matthew D. Brenton, Erik J. MacLaren, Deborah H. Glueck, Tina Hernandez-Boussard, Lynne Meltesen, James M. Sikela, Loris McGavran, Sonya Burgers, Jonathan R. Pollack, Anis Karimpour-Fard
Publikováno v:
PLoS Biology, Vol 2, Iss 7, p E207 (2004)
Given that gene duplication is a major driving force of evolutionary change and the key mechanism underlying the emergence of new genes and biological processes, this study sought to use a novel genome-wide approach to identify genes that have underg
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9bb4998c56962370cee44093892254e8
https://doaj.org/article/899b049c6a78430ea3a2c33859010d2f
https://doaj.org/article/899b049c6a78430ea3a2c33859010d2f
Autor:
Lyudmyla Tsyba, Alla Rynditch, Ganna Ferenets, Oleksii Nikolaienko, Andrew Fortna, Katheleen Gardiner, Inessa Skrypkina
Publikováno v:
Genomics. 84(1)
The Intersectin 1 (ITSN1) protein functions in clathrin-mediated endocytosis and in MAP kinase signaling. The complex domain structure comprises two EH and five SH3 domains in the short isoform, plus RhoGEF, pleckstrin, and putative calcium-interacti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4754ec08634f82613c2f8ebe53dcfdb9
https://pubmed.ncbi.nlm.nih.gov/15203208
https://pubmed.ncbi.nlm.nih.gov/15203208
Autor:
Andrew Fortna, Muriel T. Davisson, D. Slavov, Ellen C. Akeson, Lar J. Bechtel, Katheleen Gardiner
Publikováno v:
Genomics. 78(1-2)
Segments of the long arm of human chromosome 21 are conserved, centromere to telomere, in mouse chromosomes 16, 17, and 10. There have been 28 genes identified in human chromosome 21 between TMPRSS2, whose orthologue is the most distal gene mapped to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9400717658e268fa323f8b296276df31
https://pubmed.ncbi.nlm.nih.gov/11707078
https://pubmed.ncbi.nlm.nih.gov/11707078