Zobrazeno 1 - 10
of 32
pro vyhledávání: '"Sylvia L Anderson"'
Publikováno v:
Frontiers in Ecology and Evolution, Vol 10 (2022)
Long-distance pollen dispersal is critical for gene flow in plant populations, yet pollen dispersal patterns in urban habitats such as green roofs have not been extensively studied. Pollen dispersal patterns typically are assessed either by fitting n
Externí odkaz:
https://doaj.org/article/2c900212c64c430ea49b8f1b93ad1a22
Autor:
Chelsea L. Butcher, Berish Y. Rubin, Sylvia L. Anderson, Vijay K. Nandula, Micheal D. K. Owen, Randolph G. Gardner, J. D. Lewis
Publikováno v:
Applications in Plant Sciences, Vol 8, Iss 3, Pp n/a-n/a (2020)
Premise Pollen dispersal plays a critical role in gene flow of seed plants. Most often, pollen dispersal is measured using paternity assignment. However, this approach can be time‐consuming because it typically entails genotyping all pollen donors,
Externí odkaz:
https://doaj.org/article/af27cc5c220f4883b09b600cf6e32a27
Publikováno v:
Human Molecular Genetics. 31:3521-3538
Recent research on familial dysautonomia (FD) has focused on the development of therapeutics that facilitate the production of the correctly spliced, exon 20-containing, transcript in cells and individuals bearing the splice-altering, FD-causing muta
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::442991fdcf0769fdea410fbd0e27f8ec
https://doi.org/10.1093/hmg/ddac133
https://doi.org/10.1093/hmg/ddac133
Autor:
Randolph G. Gardner, Sylvia L. Anderson, Vijay K. Nandula, James D. Lewis, Chelsea L. Butcher, Berish Y. Rubin, Micheal D. K. Owen
Publikováno v:
Applications in Plant Sciences, Vol 8, Iss 3, Pp n/a-n/a (2020)
Applications in Plant Sciences
Applications in Plant Sciences
Premise Pollen dispersal plays a critical role in gene flow of seed plants. Most often, pollen dispersal is measured using paternity assignment. However, this approach can be time-consuming because it typically entails genotyping all pollen donors, r
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f855756111548a459f5251fcf48d2c39
https://doaj.org/article/af27cc5c220f4883b09b600cf6e32a27
https://doaj.org/article/af27cc5c220f4883b09b600cf6e32a27
Publikováno v:
American journal of botanyLITERATURE CITED. 107(11)
Premise Pollen dispersal, the main component of overall plant gene flow, generally decreases with increasing distance from the pollen source, but the pattern of this relationship may differ among sites. Although site-based differences in pollen dispe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::498d3081d266e6fc4918851d5db3b1e6
https://pubmed.ncbi.nlm.nih.gov/33108685
https://pubmed.ncbi.nlm.nih.gov/33108685
Autor:
Sylvia L. Anderson, Berish Y. Rubin
Publikováno v:
The Application of Clinical Genetics. 10:95-103
The successful completion of the Human Genome Project led to the discovery of the molecular basis of thousands of genetic disorders. The identification of the mutations that cause familial dysautonomia (FD), an autosomal recessive disorder that impac
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7559b5d9ed9112d6c5b267607d155838
https://doi.org/10.2147/tacg.s129638
https://doi.org/10.2147/tacg.s129638
Autor:
Nathan R. Treff, Anastasia Fedick, T.O. Carpenter, Sylvia L. Anderson, Josef Ekstein, Berish Y. Rubin, Chaim Jalas, K.F. Reid, D. Chirnomas
Publikováno v:
Clinical Genetics. 88:74-79
Osteopetrosis is a rare and heterogeneous genetic disorder characterized by dense bone mass that is a consequence of defective osteoclast function and/or development. Autosomal recessive osteopetrosis (ARO) is the most severe form and is often fatal
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4d7af4514aaf89bc54f9cd0e6081e4ce
https://doi.org/10.1111/cge.12448
https://doi.org/10.1111/cge.12448
Autor:
Chaim Jalas, Sylvia L. Anderson, Xie Xie, Alex Bulanov, Kristina Martimucci, Tova Laufer, Berish Y. Rubin, Josef Ekstein
Publikováno v:
Blood Cells, Molecules, and Diseases. 47:79-83
Congenital amegakaryocytic thrombocytopenia (MIM #604498) (CAMT) is a rare inherited disease presenting as severe thrombocytopenia in infancy. Untreated, many CAMT patients develop aplastic anemia within the first decade of life; the only effective t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ad685e6aff0e061d8e217a1e904e0b56
https://doi.org/10.1016/j.bcmd.2011.03.006
https://doi.org/10.1016/j.bcmd.2011.03.006
Publikováno v:
Antioxidants & Redox Signaling. 10:837-842
Familial dysautonomia (FD) is an inherited, fatal, neurodegenerative disorder manifested by autonomic/hypertensive crises and cardiac instability. Patients produce little IKAP, the gene product of the affected mutated gene, and have low levels of mon
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d61f620bf3c3a48081ecb1139d6364cf
https://doi.org/10.1089/ars.2007.1874
https://doi.org/10.1089/ars.2007.1874
Autor:
Berish Y. Rubin, Sylvia L. Anderson
Publikováno v:
Biochemical and Biophysical Research Communications. 336:150-156
Familial dysautonomia (FD), a recessive neurodegenerative disease, is caused by mutations in the IKBKAP gene that result in the production of nonfunctional IKAP protein. Manifestations of FD include autonomic crises characterized by hypertension, tac
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b954ca7fbec246cc10b58f07966cda48
https://doi.org/10.1016/j.bbrc.2005.08.054
https://doi.org/10.1016/j.bbrc.2005.08.054