Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Melissa L. Eckert"'
Publikováno v:
Molecular Biology and Evolution. 28:249-256
The genotypic signature of spatially varying selection is ubiquitous across the Drosophila melanogaster genome. Spatially structured adaptive phenotypic differences are also commonly found, particularly along New World and Australian latitudinal grad
Publikováno v:
American Journal of Botany. 97:650-659
The density and dispersion of individuals, nonequilibrium demographics, and habitat fragmentation all affect the magnitude and extent of spatial genetic structure within forest tree populations. Here, we investigate the link between historical demogr
Autor:
Melissa L. Eckert, Andrew J. Eckert
Publikováno v:
Madroño. 54:117-125
Variation in size class distributions along elevation gradients can indicate localized spatial expansion by tree populations inhabiting mountaintops. We searched for this pattern in northern foxtail pine (Pinus balfouriana Grev. & Balf. ssp. balfouri
Publikováno v:
Genetics. 179(1)
Drosophila melanogaster shows clinal variation along latitudinal transects on multiple continents for several phenotypes, allozyme variants, sequence variants, and chromosome inversions. Previous investigation suggests that many such clines are due t
Autor:
Stef J.F. Letteboer, Kelly N. Owens, John B. Vincent, Sylvia E. C. van Beersum, Yangfan Liu, Michael O. Dorschner, Dana M. Knutzen, Melissa L. Eckert, Abdulrahman Alswaid, Cecilia B. Moens, Nine V A M Knoers, Friedhelm Hildebrandt, Nicholas T. Gorden, Edgar A. Otto, Dorus A. Mans, P. Rosenthal, Nicholas Katsanis, Phillip F. Chance, Edwin W. Rubel, Ronald Roepman, Abigail Hikida, Heleen H. Arts, Elaine H. Zackai, David W. Raible, Ian A. Glass, Dan Doherty, Meral Topçu, Karlien L.M. Coene, Frederico M. Farin, Erica E. Davis, Carolyn M. Hutter, Melissa A. Parisi, Sel Dibooglu, Hamit Özyürek, Theo K. Bammler
Publikováno v:
American Journal of Human Genetics, 83, 559-71
American Journal of Human Genetics, 83, 5, pp. 559-71
American Journal of Human Genetics, 83, 5, pp. 559-71
Roepman, Ronald/0000-0002-5178-8163; van Beersum, Sylvia E.C./0000-0002-4552-2908; Coene, Karlien/0000-0001-9873-1458; Dibooglu, Sel/0000-0002-3865-5868; Moens, Cecilia/0000-0002-1099-0728; Davis, Erica/0000-0002-2412-8397; Otto, Edgar/0000-0002-2387
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::26748fa4d6cbea87521f581b8df134de
http://hdl.handle.net/2066/70259
http://hdl.handle.net/2066/70259
Autor:
Charles L. White, Evan P. Gallagher, Michael J. Dabrowski, Terrance J. Kavanagh, Melissa L. Eckert, Jing Shao
Publikováno v:
Toxicological sciences : an official journal of the Society of Toxicology. 101(1)
The polybrominated diphenyl ethers (PBDEs) are a group of flame retardants whose residues have markedly increased in the environment and in human tissues during the last decade. Of the various congeners, BDE 47 (2,2',4,4'-tetrabromodiphenyl ether) is
Autor:
Ian A. Glass, Dennis W. W. Shaw, Craig L. Bennett, O. Giray, S. Aysun, Melissa A. Parisi, H. Ozyurek, E. Bakhsh, N. Dohayan, Dan Doherty, Phillip F. Chance, Melissa L. Eckert, Olafur S. Indridason, S. Al Shahwan, William B. Dobyns, A. Al Swaid
Background: Joubert syndrome (JS) is an autosomal recessive disorder characterised by hypotonia, ataxia, mental retardation, altered respiratory pattern, abnormal eye movements, and a brain malformation known as the molar tooth sign (MTS) on cranial
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3bdc247659b453bdbf0fb425db20f602
http://hdl.handle.net/11655/13768
http://hdl.handle.net/11655/13768
Autor:
Melissa A. Parisi, Ian A. Glass, Phillip F. Chance, Melissa L. Eckert, Craig L. Bennett, Huy M. Huynh
Publikováno v:
American journal of medical genetics. Part A. (2)
Joubert syndrome (JS) is a rare autosomal recessive malformation syndrome, involving dysgenesis of the cerebellar vermis with accompanying brainstem malformations (comprising the molar tooth sign). JS is characterized by hypotonia, developmental dela
Autor:
Melissa A. Parisi, William B. Dobyns, Melissa L. Eckert, Ian A. Glass, Phillip F. Chance, Allison A. Eddy, Joseph G. Gleeson, Craig L. Bennett, Ruth A. McDonald, Dennis W. W. Shaw
Publikováno v:
The American Journal of Human Genetics. (1):82-91
Joubert syndrome (JS) is an autosomal recessive multisystem disease characterized by cerebellar vermis hypoplasia with prominent superior cerebellar peduncles (the “molar tooth sign” [MTS] on axial magnetic resonance imaging), mental retardation,
Autor:
Jing Shao, Collin C. White, Michael J. Dabrowski, Terrance J. Kavanagh, Melissa L. Eckert, Evan P. Gallagher
Publikováno v:
Toxicological Sciences; Jan2008, Vol. 101 Issue 1, p81-81, 1p