Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Galen W Heyne"'
Autor:
Galen W Heyne, Cal G Melberg, Padydeh Doroodchi, Kia F Parins, Henry W Kietzman, Joshua L Everson, Lydia J Ansen-Wilson, Robert J Lipinski
Publikováno v:
PLoS ONE, Vol 10, Iss 3, p e0120517 (2015)
The Hedgehog (Hh) signaling pathway mediates multiple spatiotemporally-specific aspects of brain and face development. Genetic and chemical disruptions of the pathway are known to result in an array of structural malformations, including holoprosence
Externí odkaz:
https://doaj.org/article/0d35fea9865541e895abcebe1dd8023e
Autor:
Joshua L. Everson, Sookhee Park, Miranda R. Sun, Hannah M. Chung, Michael D. Sheets, Robert J. Lipinski, Dustin M. Fink, Galen W. Heyne
Publikováno v:
Cellular Signalling. 44:1-9
Sonic Hedgehog (Shh) signaling plays key regulatory roles in embryonic development and postnatal homeostasis and repair. Modulation of the Shh pathway is known to cause malformations and malignancies associated with dysregulated tissue growth. Howeve
Autor:
Joshua L. Everson, Galen W. Heyne, Matthew T. McLaughlin, Robert J. Lipinski, Alexander A. Martin, Dustin M. Fink, Caden M. Ulschmid, Padydeh Doroodchi, Cal G. Melberg, Miranda R. Sun, Lydia J. Colopy, Kia F. Nelson
Publikováno v:
Environmental Health Perspectives
Background: Piperonyl butoxide (PBO) is a pesticide synergist used in residential, commercial, and agricultural settings. PBO was recently found to inhibit Sonic hedgehog (Shh) signaling, a key developmental regulatory pathway. Disruption of Shh sign
Autor:
Austin P Prichard, Callyssa M. Cronick, Kimberly P. Keil, Laura L. Hernandez, Chad M. Vezina, Galen W. Heyne, Jimena Laporta, Robert J. Lipinski, Thomas D. Crenshaw, Samantha R. Weaver
Publikováno v:
Molecular Endocrinology. 28:1866-1874
Calcium homeostasis during lactation is critical for maternal and neonatal health. We previously showed that nonneuronal/peripheral serotonin [5-hydroxytryptamine (5-HT)] causes the lactating mammary gland to synthesize and secrete PTHrP in an acute
Autor:
Caden M. Ulschmid, Galen W. Heyne, Joshua L. Everson, Lydia J. Ansen-Wilson, Padydeh Doroodchi, Robert J. Lipinski, Kia F. Parins, Dustin M. Fink, Cal G. Melberg
Publikováno v:
Disease Models & Mechanisms.
Holoprosencephaly (HPE) is a common and severe human developmental abnormality marked by malformations of the forebrain and face. Although several genetic mutations have been linked to HPE, phenotypic outcomes range dramatically, and most cases canno
Publikováno v:
Investigative ophthalmologyvisual science. 54(7)
PURPOSE To determine the effect of the nitric oxide donor, sodium nitroprusside (SNP), and the nitric oxide synthase (NOS) inhibitor, L-nitro-arginine-methylester (L-NAME), on IOP, mean arterial pressure (MAP), pupil diameter (PD), refraction (Rfx),
Autor:
Dustin M. Fink, Caden M. Ulschmid, Cal G. Melberg, Joshua L. Everson, Galen W. Heyne, Lydia J. Ansen-Wilson, Kia F. Parins, Robert J. Lipinski, Padydeh Doroodchi
Publikováno v:
Development. 143:e1.2-e1.2
Holoprosencephaly (HPE) is a common and severe human developmental abnormality marked by malformations of the forebrain and face. Although several genetic mutations have been linked to HPE, phenotypic outcomes range dramatically, and most cases canno
Autor:
Cal G. Melberg, Robert J. Lipinski, Padydeh Doroodchi, Joshua L. Everson, Kia F. Parins, Galen W. Heyne, Lydia J. Ansen-Wilson, Henry W. Kietzman
Publikováno v:
PLoS ONE, Vol 10, Iss 3, p e0120517 (2015)
PLoS ONE
PLoS ONE
The Hedgehog (Hh) signaling pathway mediates multiple spatiotemporally-specific aspects of brain and face development. Genetic and chemical disruptions of the pathway are known to result in an array of structural malformations, including holoprosence
Autor:
Galen W. Heyne, Joshua L. Everson, Lydia J. Ansen-Wilson, Cal G. Melberg, Dustin M. Fink, Kia F. Parins, Padydeh Doroodchi, Caden M. Ulschmid, Robert J. Lipinski
Publikováno v:
Disease Models & Mechanisms, Vol 9, Iss 11, Pp 1307-1315 (2016)
Holoprosencephaly (HPE) is a common and severe human developmental abnormality marked by malformations of the forebrain and face. Although several genetic mutations have been linked to HPE, phenotypic outcomes range dramatically, and most cases canno
Externí odkaz:
https://doaj.org/article/5a807d1f7f5f49e4b86b88fa9ece4960