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K Moses

Showing results (151-160 of 246) with videos related to

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Journal of Medical Genetics|May 7, 2011
The 57 kb deletion in cystinosis patients extends into TRPV1 causing dysregulation of transcription in peripheral blood mononuclear cellsKaty A Freed, John Blangero, Tom Howard, et al.
Physiological Genomics|April 15, 2010
Serotonin (5-HT) receptor 5A sequence variants affect human plasma triglyceride levelsY Zhang, E M Smith, T M Baye, et al.
Neurobiology of Learning and Memory|January 9, 2023
Lesion-induced sprouting promotes neurophysiological integration of septal and entorhinal inputs to granule cells in the dentate gyrus of ratsMatthew A De Niear, Garrett R Smith, Mercedes L Robinson, et al.
The Journal of Endocrinology|July 1, 1997
The expression of parathyroid hormone-related protein mRNA and immunoreactive protein in human amnion and choriodecidua is increased at term compared with preterm gestationN E Curtis, P W Ho, R G King, et al.
The Australian & New Zealand Journal of Obstetrics & Gynaecology|January 10, 2009
The prevalence of inherited thrombophilic polymorphisms in an asymptomatic Australian antenatal populationJoanne M Said, Shaun P Brennecke, Eric K Moses, et al.
Casopis Lekaru Ceskych|August 27, 1981
[Crystepin CH. A multi-centre trial of an antihypertensive drug (author's transl)]O Mayer, V Cepelák, M Blazek, et al.
Journal of Clinical Lipidology|June 23, 2022
A variant in the fibronectin (FN1) gene, rs1250229-T, is associated with decreased risk of coronary artery disease in familial hypercholesterolaemiaMichael M Page, Katrina L Ellis, Dick C Chan, et al.
American Journal of Obstetrics and Gynecology|December 11, 2007
Genetic association of preeclampsia to the inflammatory response gene SEPS1Eric K Moses, Matthew P Johnson, Linda Tømmerdal, et al.
Clinical Genetics|October 2, 2019
A genetic risk score predicts coronary artery disease in familial hypercholesterolaemia: enhancing the precision of risk assessmentKatrina L Ellis, Amanda J Hooper, Jing Pang, et al.
Plos One|May 27, 2015
Genome-wide transcriptome directed pathway analysis of maternal pre-eclampsia susceptibility genesHannah E J Yong, Phillip E Melton, Matthew P Johnson, et al.
Pageof 25

Showing results (151-160 of 246) with videos related to

Sort By:
Pageof 25
Journal of Medical Genetics|May 7, 2011
The 57 kb deletion in cystinosis patients extends into TRPV1 causing dysregulation of transcription in peripheral blood mononuclear cellsKaty A Freed, John Blangero, Tom Howard, et al.
Physiological Genomics|April 15, 2010
Serotonin (5-HT) receptor 5A sequence variants affect human plasma triglyceride levelsY Zhang, E M Smith, T M Baye, et al.
Neurobiology of Learning and Memory|January 9, 2023
Lesion-induced sprouting promotes neurophysiological integration of septal and entorhinal inputs to granule cells in the dentate gyrus of ratsMatthew A De Niear, Garrett R Smith, Mercedes L Robinson, et al.
The Journal of Endocrinology|July 1, 1997
The expression of parathyroid hormone-related protein mRNA and immunoreactive protein in human amnion and choriodecidua is increased at term compared with preterm gestationN E Curtis, P W Ho, R G King, et al.
The Australian & New Zealand Journal of Obstetrics & Gynaecology|January 10, 2009
The prevalence of inherited thrombophilic polymorphisms in an asymptomatic Australian antenatal populationJoanne M Said, Shaun P Brennecke, Eric K Moses, et al.
Casopis Lekaru Ceskych|August 27, 1981
[Crystepin CH. A multi-centre trial of an antihypertensive drug (author's transl)]O Mayer, V Cepelák, M Blazek, et al.
Journal of Clinical Lipidology|June 23, 2022
A variant in the fibronectin (FN1) gene, rs1250229-T, is associated with decreased risk of coronary artery disease in familial hypercholesterolaemiaMichael M Page, Katrina L Ellis, Dick C Chan, et al.
American Journal of Obstetrics and Gynecology|December 11, 2007
Genetic association of preeclampsia to the inflammatory response gene SEPS1Eric K Moses, Matthew P Johnson, Linda Tømmerdal, et al.
Clinical Genetics|October 2, 2019
A genetic risk score predicts coronary artery disease in familial hypercholesterolaemia: enhancing the precision of risk assessmentKatrina L Ellis, Amanda J Hooper, Jing Pang, et al.
Plos One|May 27, 2015
Genome-wide transcriptome directed pathway analysis of maternal pre-eclampsia susceptibility genesHannah E J Yong, Phillip E Melton, Matthew P Johnson, et al.
Pageof 25