Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Sofia Shirley"'
Autor:
Daniel Severin, Cristián Moreno, Trinh Tran, Christian Wesselborg, Sofia Shirley, Altagracia Contreras, Alfredo Kirkwood, Jorge Golowasch
Publikováno v:
Cell Reports, Vol 43, Iss 10, Pp 114744- (2024)
Summary: Capacitance of biological membranes is determined by the properties of the lipid portion of the membrane as well as the morphological features of a cell. In neurons, membrane capacitance is a determining factor of synaptic integration, actio
Externí odkaz:
https://doaj.org/article/446a0d5905b74e218d3d8f1f1e45abb9
Capacitance is a property of biological membranes determined by the properties of the lipid portion of the membrane, as well as morphological features of a cell. In neurons, membrane capacitance is a determining factor of synaptic integration, action
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0cad193a6f3d8143efadace31cd2f41c
https://doi.org/10.1101/2022.12.09.519806
https://doi.org/10.1101/2022.12.09.519806
Publikováno v:
Mammalian Genome
Recent linkage-based studies in humans suggest the presence of loci that affect either genome-wide recombination rates, utilization of recombination hotspots, or both. We have been interested in utilizing cytological methodology to directly assess re
Autor:
Annette E. Cockwell, Urvashi Surti, LuAnn Judis, Terry J. Hassold, Sofia Shirley, Lori Hoffner, Andrew Collins, E. Ricky Chan, Heather E. Hall, Patricia A. Jacobs
Publikováno v:
American Journal of Medical Genetics Part A. :2242-2248
Trisomy 13 is one of the most common trisomies in clinically recognized pregnancies and one of the few trisomies identified in liveborns, yet relatively little is known about the errors that lead to trisomy 13. Accordingly, we initiated studies to in
Autor:
Sofia Shirley, Lori Hoffner, Heather E. Hall, Eleanor Feingold, Urvashi Surti, Terry J. Hassold
Publikováno v:
American journal of medical genetics. Part A. (19)
Trisomy 22 is one of the most common trisomies in clinically recognized pregnancies, yet relatively little is known about the origin of nondisjunction for chromosome 22. Accordingly, we initiated studies to investigate the origin of the extra chromos
Publikováno v:
Biology of Reproduction. 81:173-173
Autor:
Matthew E. Johnson, Catherine A. VandeVoort, Jeffrey A. Bailey, Terry J. Hassold, Ross Rowsey, Sofia Shirley
Publikováno v:
Molecular Cytogenetics
Johnson, Matthew E; Rowsey, Ross A; Shirley, Sofia; VandeVoort, Catherine; Bailey, Jeffrey; & Hassold, Terry. (2013). A specific family of interspersed repeats (SINEs) facilitates meiotic synapsis in mammals. Molecular Cytogenetics, 6(1), 1. doi: http://dx.doi.org/10.1186/1755-8166-6-1. Retrieved from: http://www.escholarship.org/uc/item/50k8z758
Molecular Cytogenetics, Vol 6, Iss 1, p 1 (2013)
Johnson, Matthew E; Rowsey, Ross A; Shirley, Sofia; VandeVoort, Catherine; Bailey, Jeffrey; & Hassold, Terry. (2013). A specific family of interspersed repeats (SINEs) facilitates meiotic synapsis in mammals. Molecular Cytogenetics, 6(1), 1. doi: http://dx.doi.org/10.1186/1755-8166-6-1. Retrieved from: http://www.escholarship.org/uc/item/50k8z758
Molecular Cytogenetics, Vol 6, Iss 1, p 1 (2013)
Background Errors during meiosis that affect synapsis and recombination between homologous chromosomes contribute to aneuploidy and infertility in humans. Despite the clinical relevance of these defects, we know very little about the mechanisms by wh