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T Morgan

Showing results (1161-1170 of 1,193) with videos related to

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Journal of Medical Genetics|November 3, 2022
In-depth characterisation of a cohort of individuals with missense and loss-of-function variants disrupting <i>FOXP2</i>Lottie D Morison, Elisabeth Meffert, Miriam Stampfer, et al.
Toxicologic Pathology|August 22, 2002
Application of cDNA microarray technology to in vitro toxicology and the selection of genes for a real-time RT-PCR-based screen for oxidative stress in Hep-G2 cellsKevin T Morgan, Hong Ni, H Roger Brown, et al.
Biology Letters|December 26, 2014
Statistical ecology comes of ageOlivier Gimenez, Stephen T Buckland, Byron J T Morgan, et al.
Molecular Ecology|November 25, 2003
Phylogeography of Biomphalaria glabrata and B. pfeifferi, important intermediate hosts of Schistosoma mansoni in the New and Old World tropicsR J Dejong, J A T Morgan, W D Wilson, et al.
Journal of Virology|September 13, 2008
Multiple virus lineages sharing recent common ancestry were associated with a Large Rift Valley fever outbreak among livestock in Kenya during 2006-2007Brian H Bird, Jane W K Githinji, Joseph M Macharia, et al.
Human Molecular Genetics|August 13, 2003
A genomic rearrangement resulting in a tandem duplication is associated with split hand-split foot malformation 3 (SHFM3) at 10q24Xavier J de Mollerat, Fiorella Gurrieri, Chad T Morgan, et al.
The Ocular Surface|October 16, 2024
Meibomian gland lipid alterations and ocular surface sequela in Awat2 knockout murine model of meibomian gland dysfunction and evaporative dry eye diseaseErin A Hisey, Sydni Wong, Sangwan Park, et al.
Elife|April 17, 2024
Ketamine induces multiple individually distinct whole-brain functional connectivity signaturesFlora Moujaes, Jie Lisa Ji, Masih Rahmati, et al.
Molecular Psychiatry|September 18, 2022
Genetic aetiologies for childhood speech disorder: novel pathways co-expressed during brain developmentAntony Kaspi, Michael S Hildebrand, Victoria E Jackson, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 20, 2026
Rare heterozygous de novo variants in RAPGEF2 are associated with a neurodevelopmental disorderAli H Bereshneh, Kirkland A Wilson, Xueyang Pan, et al.
Pageof 120

Showing results (1161-1170 of 1,193) with videos related to

Sort By:
Pageof 120
Journal of Medical Genetics|November 3, 2022
In-depth characterisation of a cohort of individuals with missense and loss-of-function variants disrupting <i>FOXP2</i>Lottie D Morison, Elisabeth Meffert, Miriam Stampfer, et al.
Toxicologic Pathology|August 22, 2002
Application of cDNA microarray technology to in vitro toxicology and the selection of genes for a real-time RT-PCR-based screen for oxidative stress in Hep-G2 cellsKevin T Morgan, Hong Ni, H Roger Brown, et al.
Biology Letters|December 26, 2014
Statistical ecology comes of ageOlivier Gimenez, Stephen T Buckland, Byron J T Morgan, et al.
Molecular Ecology|November 25, 2003
Phylogeography of Biomphalaria glabrata and B. pfeifferi, important intermediate hosts of Schistosoma mansoni in the New and Old World tropicsR J Dejong, J A T Morgan, W D Wilson, et al.
Journal of Virology|September 13, 2008
Multiple virus lineages sharing recent common ancestry were associated with a Large Rift Valley fever outbreak among livestock in Kenya during 2006-2007Brian H Bird, Jane W K Githinji, Joseph M Macharia, et al.
Human Molecular Genetics|August 13, 2003
A genomic rearrangement resulting in a tandem duplication is associated with split hand-split foot malformation 3 (SHFM3) at 10q24Xavier J de Mollerat, Fiorella Gurrieri, Chad T Morgan, et al.
The Ocular Surface|October 16, 2024
Meibomian gland lipid alterations and ocular surface sequela in Awat2 knockout murine model of meibomian gland dysfunction and evaporative dry eye diseaseErin A Hisey, Sydni Wong, Sangwan Park, et al.
Elife|April 17, 2024
Ketamine induces multiple individually distinct whole-brain functional connectivity signaturesFlora Moujaes, Jie Lisa Ji, Masih Rahmati, et al.
Molecular Psychiatry|September 18, 2022
Genetic aetiologies for childhood speech disorder: novel pathways co-expressed during brain developmentAntony Kaspi, Michael S Hildebrand, Victoria E Jackson, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 20, 2026
Rare heterozygous de novo variants in RAPGEF2 are associated with a neurodevelopmental disorderAli H Bereshneh, Kirkland A Wilson, Xueyang Pan, et al.
Pageof 120