Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Gregory B Willer"'
Autor:
Kerry N Veth, Jason R Willer, Ross F Collery, Matthew P Gray, Gregory B Willer, Daniel S Wagner, Mary C Mullins, Ava J Udvadia, Richard S Smith, Simon W M John, Ronald G Gregg, Brian A Link
Publikováno v:
PLoS Genetics, Vol 7, Iss 2, p e1001310 (2011)
The glaucomas comprise a genetically complex group of retinal neuropathies that typically occur late in life and are characterized by progressive pathology of the optic nerve head and degeneration of retinal ganglion cells. In addition to age and fam
Externí odkaz:
https://doaj.org/article/38ba329e10954c9f95fdf5132f63c35f
Autor:
Yuanquan Song, Jason R Willer, Paul C Scherer, Jessica A Panzer, Amy Kugath, Emmanuel Skordalakes, Ronald G Gregg, Gregory B Willer, Rita J Balice-Gordon
Publikováno v:
PLoS ONE, Vol 5, Iss 10, p e13743 (2010)
Congenital disorder of glycosylation type IIc (CDG IIc) is characterized by mental retardation, slowed growth and severe immunodeficiency, attributed to the lack of fucosylated glycoproteins. While impaired Notch signaling has been implicated in some
Externí odkaz:
https://doaj.org/article/bf92e3045b0d493d91f711d1cbc89c42
Autor:
Jiwoon Lee, Kierann Smith, Ronald G. Gregg, Gregory B. Willer, Jeffrey M. Gross, Jason R. Willer
Publikováno v:
Developmental Biology. 319(1):10-22
In this study, we have characterized the ocular defects in the recessive zebrafish mutant blowout that presents with a variably penetrant coloboma phenotype. blowout mutants develop unilateral or bilateral colobomas and as a result, the retina and re
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::32f7a4e382b3b61e2d02016039abcc13
Autor:
David R. Hyde, D.V. Bosenko, Ronald G. Gregg, Elena V. Semina, Thomas S. Vihtelic, Gregory B. Willer, Kelly A Soules, Brian A. Link, Natalya C. Zinkevich
Publikováno v:
Developmental Biology. 299(1):63-77
We report phenotypic and genetic analyses of a recessive, larval lethal zebrafish mutant, bal(a69), characterized by severe eye defects and shortened body axis. The bal(a69) mutation was mapped to chromosome 24 near the laminin alpha 1 (lama1) gene.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f890321593f7295d62e5e3cf691056a6
Autor:
Jennifer L. Thomas, Ryan Thummel, Xixia Luo, Ronald G. Gregg, Aaron D. denDekker, Thomas S. Vihtelic, David R. Hyde, Taylor R. Murphy, Gregory B. Willer
Oculocutaneous albinism (OCA) is a group of genetically inherited conditions that result in pigmentation defects in the eyes, skin, and hair.1 The types of albinism have been divided into tryosinase-negative (no pigmentation) and those that produce v
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::729d221f64a9bfa94daf787edbfc5e04
https://europepmc.org/articles/PMC3109019/
https://europepmc.org/articles/PMC3109019/
Autor:
Ronald G. Gregg, Taylor R. Murphy, Vytas A. Bankaitis, David R. Hyde, Kristina E. Ile, Thomas S. Vihtelic, Corey T. Watson, Gregory B. Willer
The zebrafish lens opaque (lop) mutant was previously isolated in a genetic screen and shown to lack rod and cone photoreceptors and exhibit lens opacity, or cataract, at 7 days post-fertilization (dpf). In this manuscript, we provide four different
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::60c7ea83f21e1540a4fa3d183731c430
Publikováno v:
The Journal of neuroscience : the official journal of the Society for Neuroscience. 29(42)
Multiple molecular cues guide neuronal axons to their targets during development. Previous studiesin vitrohave shown that mechanical stimulation also can affect axon growth; however, whether mechanical force contributes to axon guidancein vivois unkn
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::574a3abec83d007b34738af45ae4f217
https://pubmed.ncbi.nlm.nih.gov/19846707
https://pubmed.ncbi.nlm.nih.gov/19846707
Publikováno v:
Genetics. 170(4)
The zebrafish perplexed mutation disrupts cell proliferation and differentiation during retinal development. In addition, growth and morphogenesis of the tectum, jaw, and pectoral fins are also affected. Positional cloning was used to identify a muta
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::23fadcea3ac7ab79940b53ac52110c32
https://pubmed.ncbi.nlm.nih.gov/15937129
https://pubmed.ncbi.nlm.nih.gov/15937129
Publikováno v:
Proceedings of the National Academy of Sciences of the United States of America. 100(11)
Zebrafish with the young (yng) mutation show a defect in retinal cell differentiation. Here we demonstrate that a mutation in a brahma-related gene ( brg1 ) is responsible for the yng phenotype. Brahma homologues function as essential subunits for SW
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b2d4ecde4a15a9686ec1aa004240c011
https://pubmed.ncbi.nlm.nih.gov/12748389
https://pubmed.ncbi.nlm.nih.gov/12748389
Autor:
Brian A. Link, Daniel S. Wagner, Kerry N. Veth, Jason R. Willer, Ross F Collery, Gregory B. Willer, Mary C. Mullins, Matthew P. Gray, Richard S. Smith, Ronald G. Gregg, Ava J. Udvadia, Simon W. M. John
Publikováno v:
PLoS Genetics
PLoS Genetics, Vol 7, Iss 2, p e1001310 (2011)
PLoS Genetics, Vol 7, Iss 2, p e1001310 (2011)
The glaucomas comprise a genetically complex group of retinal neuropathies that typically occur late in life and are characterized by progressive pathology of the optic nerve head and degeneration of retinal ganglion cells. In addition to age and fam
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1d5d3711e9e31c7ead36522b441fb29f
https://doi.org/10.1371/journal.pgen.1001310
https://doi.org/10.1371/journal.pgen.1001310