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E L Smith

Showing results (331-340 of 359) with videos related to

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Human Molecular Genetics|March 24, 2017
Amelogenesis imperfecta caused by N-terminal enamelin point mutations in mice and men is driven by endoplasmic reticulum stressSteven J Brookes, Martin J Barron, Claire E L Smith, et al.
Geohealth|November 5, 2024
Updated Smoke Exposure Estimate for Indonesian Peatland Fires Using a Network of Low-Cost PM<sub>2.5</sub> Sensors and a Regional Air Quality ModelAilish M Graham, Dominick V Spracklen, James B McQuaid, et al.
Archives of Biochemistry and Biophysics|February 1, 1991
Ethanol increases cytochromes P450IIE, IIB1/2, and IIIA in cultured rat hepatocytesJ F Sinclair, J McCaffrey, P R Sinclair, et al.
Clinical Genetics|February 14, 2020
New missense variants in RELT causing hypomineralised amelogenesis imperfectaGeorgios Nikolopoulos, Claire E L Smith, Steven J Brookes, et al.
CNS Spectrums|December 2, 2004
Effects of LY354740, a novel glutamatergic metabotropic agonist, on nonhuman primate hypothalamic-pituitary-adrenal axis and noradrenergic functionJ D Coplan, S J Mathew, E L Smith, et al.
Journal of Dental Research|March 26, 2019
Phenotype and Variant Spectrum in the LAMB3 Form of Amelogenesis ImperfectaC E L Smith, J A Poulter, S J Brookes, et al.
Molecular Genetics & Genomic Medicine|January 8, 2016
A distinctive oral phenotype points to FAM20A mutations not identified by Sanger sequencingJames A Poulter, Claire E L Smith, Gina Murrillo, et al.
Human Molecular Genetics|March 14, 2020
A missense variant in specificity protein 6 (SP6) is associated with amelogenesis imperfectaClaire E L Smith, Laura L E Whitehouse, James A Poulter, et al.
Frontiers in Psychology|July 24, 2019
Positive Effects of Nature on Cognitive Performance Across Multiple Experiments: Test Order but Not Affect Modulates the Cognitive EffectsCecilia U D Stenfors, Stephen C Van Hedger, Kathryn E Schertz, et al.
European Journal of Human Genetics : EJHG|June 16, 2016
Spectrum of PEX1 and PEX6 variants in Heimler syndromeClaire E L Smith, James A Poulter, Alex V Levin, et al.
Pageof 36

Showing results (331-340 of 359) with videos related to

Sort By:
Pageof 36
Human Molecular Genetics|March 24, 2017
Amelogenesis imperfecta caused by N-terminal enamelin point mutations in mice and men is driven by endoplasmic reticulum stressSteven J Brookes, Martin J Barron, Claire E L Smith, et al.
Geohealth|November 5, 2024
Updated Smoke Exposure Estimate for Indonesian Peatland Fires Using a Network of Low-Cost PM<sub>2.5</sub> Sensors and a Regional Air Quality ModelAilish M Graham, Dominick V Spracklen, James B McQuaid, et al.
Archives of Biochemistry and Biophysics|February 1, 1991
Ethanol increases cytochromes P450IIE, IIB1/2, and IIIA in cultured rat hepatocytesJ F Sinclair, J McCaffrey, P R Sinclair, et al.
Clinical Genetics|February 14, 2020
New missense variants in RELT causing hypomineralised amelogenesis imperfectaGeorgios Nikolopoulos, Claire E L Smith, Steven J Brookes, et al.
CNS Spectrums|December 2, 2004
Effects of LY354740, a novel glutamatergic metabotropic agonist, on nonhuman primate hypothalamic-pituitary-adrenal axis and noradrenergic functionJ D Coplan, S J Mathew, E L Smith, et al.
Journal of Dental Research|March 26, 2019
Phenotype and Variant Spectrum in the LAMB3 Form of Amelogenesis ImperfectaC E L Smith, J A Poulter, S J Brookes, et al.
Molecular Genetics & Genomic Medicine|January 8, 2016
A distinctive oral phenotype points to FAM20A mutations not identified by Sanger sequencingJames A Poulter, Claire E L Smith, Gina Murrillo, et al.
Human Molecular Genetics|March 14, 2020
A missense variant in specificity protein 6 (SP6) is associated with amelogenesis imperfectaClaire E L Smith, Laura L E Whitehouse, James A Poulter, et al.
Frontiers in Psychology|July 24, 2019
Positive Effects of Nature on Cognitive Performance Across Multiple Experiments: Test Order but Not Affect Modulates the Cognitive EffectsCecilia U D Stenfors, Stephen C Van Hedger, Kathryn E Schertz, et al.
European Journal of Human Genetics : EJHG|June 16, 2016
Spectrum of PEX1 and PEX6 variants in Heimler syndromeClaire E L Smith, James A Poulter, Alex V Levin, et al.
Pageof 36