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Showing results (661-670 of 703) with videos related to

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Gastroenterology|September 6, 2006
Intraepithelial gammadelta+ lymphocytes maintain the integrity of intestinal epithelial tight junctions in response to infectionJane E Dalton, Sheena M Cruickshank, Charlotte E Egan, et al.
Human Brain Mapping|November 15, 2005
Human attachment security is mediated by the amygdala: evidence from combined fMRI and psychophysiological measuresErwin Lemche, Vincent P Giampietro, Simon A Surguladze, et al.
Neurobiology of Disease|October 5, 2023
Time- and region-dependent blood-brain barrier impairment in a rat model of organophosphate-induced status epilepticusPedro N Bernardino, Brad A Hobson, Sydney L Huddleston, et al.
Microvascular Research|April 10, 2021
Assessment of the conjunctival microcirculation in adult patients with cyanotic congenital heart disease compared to healthy controlsPaul F Brennan, Min Jing, Andrew J McNeil, et al.
Archives of General Psychiatry|September 8, 2004
Attenuation of the neural response to sad faces in major depression by antidepressant treatment: a prospective, event-related functional magnetic resonance imaging studyCynthia H Y Fu, Steven C R Williams, Anthony J Cleare, et al.
American Journal of Physiology. Renal Physiology|November 27, 2009
CLC-5 and KIF3B interact to facilitate CLC-5 plasma membrane expression, endocytosis, and microtubular transport: relevance to pathophysiology of Dent's diseaseAnita A C Reed, Nellie Y Loh, Sara Terryn, et al.
Endocrine Connections|January 22, 2020
Studies of mice deleted for Sox3 and uc482: relevance to X-linked hypoparathyroidismKatie U Gaynor, Irina V Grigorieva, Samantha M Mirczuk, et al.
Human Molecular Genetics|March 2, 2010
Identification and characterization of novel parathyroid-specific transcription factor Glial Cells Missing Homolog B (GCMB) mutations in eight families with autosomal recessive hypoparathyroidismMichael R Bowl, Samantha M Mirczuk, Irina V Grigorieva, et al.
The Journal of Clinical Investigation|September 17, 2005
MMP13 mutation causes spondyloepimetaphyseal dysplasia, Missouri type (SEMD(MO)Ann M Kennedy, Masaki Inada, Stephen M Krane, et al.
Scientific Data|February 24, 2026
Global daily CO<sub>2</sub> emissions from 1970 to 2024Tao Li, Lixing Wang, Zihan Qiu, et al.
Pageof 71

Showing results (661-670 of 703) with videos related to

Sort By:
Pageof 71
Gastroenterology|September 6, 2006
Intraepithelial gammadelta+ lymphocytes maintain the integrity of intestinal epithelial tight junctions in response to infectionJane E Dalton, Sheena M Cruickshank, Charlotte E Egan, et al.
Human Brain Mapping|November 15, 2005
Human attachment security is mediated by the amygdala: evidence from combined fMRI and psychophysiological measuresErwin Lemche, Vincent P Giampietro, Simon A Surguladze, et al.
Neurobiology of Disease|October 5, 2023
Time- and region-dependent blood-brain barrier impairment in a rat model of organophosphate-induced status epilepticusPedro N Bernardino, Brad A Hobson, Sydney L Huddleston, et al.
Microvascular Research|April 10, 2021
Assessment of the conjunctival microcirculation in adult patients with cyanotic congenital heart disease compared to healthy controlsPaul F Brennan, Min Jing, Andrew J McNeil, et al.
Archives of General Psychiatry|September 8, 2004
Attenuation of the neural response to sad faces in major depression by antidepressant treatment: a prospective, event-related functional magnetic resonance imaging studyCynthia H Y Fu, Steven C R Williams, Anthony J Cleare, et al.
American Journal of Physiology. Renal Physiology|November 27, 2009
CLC-5 and KIF3B interact to facilitate CLC-5 plasma membrane expression, endocytosis, and microtubular transport: relevance to pathophysiology of Dent's diseaseAnita A C Reed, Nellie Y Loh, Sara Terryn, et al.
Endocrine Connections|January 22, 2020
Studies of mice deleted for Sox3 and uc482: relevance to X-linked hypoparathyroidismKatie U Gaynor, Irina V Grigorieva, Samantha M Mirczuk, et al.
Human Molecular Genetics|March 2, 2010
Identification and characterization of novel parathyroid-specific transcription factor Glial Cells Missing Homolog B (GCMB) mutations in eight families with autosomal recessive hypoparathyroidismMichael R Bowl, Samantha M Mirczuk, Irina V Grigorieva, et al.
The Journal of Clinical Investigation|September 17, 2005
MMP13 mutation causes spondyloepimetaphyseal dysplasia, Missouri type (SEMD(MO)Ann M Kennedy, Masaki Inada, Stephen M Krane, et al.
Scientific Data|February 24, 2026
Global daily CO<sub>2</sub> emissions from 1970 to 2024Tao Li, Lixing Wang, Zihan Qiu, et al.
Pageof 71