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C Murray

Showing results (1331-1340 of 1,465) with videos related to

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Molecular Genetics & Genomic Medicine|April 1, 2017
The prevalence, penetrance, and expressivity of etiologic <i>IRF6</i> variants in orofacial clefts patients from sub-Saharan AfricaLord Jephthah Joojo Gowans, Tamara D Busch, Peter A Mossey, et al.
Acta Neuropathologica Communications|March 25, 2022
Neutrophil-vascular interactions drive myeloperoxidase accumulation in the brain in Alzheimer's diseaseLeon C D Smyth, Helen C Murray, Madison Hill, et al.
Pediatric Research|August 21, 2012
No observed association for mitochondrial SNPs with preterm delivery and related outcomesBrandon W Alleman, Solveig Myking, Kelli K Ryckman, et al.
Plos Genetics|September 21, 2011
Genome-wide association study identifies four loci associated with eruption of permanent teethFrank Geller, Bjarke Feenstra, Hao Zhang, et al.
Molecular Cancer Therapeutics|November 4, 2025
Discovery and characterisation of VPRBP/DCAF1 kinase inhibitor analogues as microtubular destabilising agents with potent anti-myeloma activityOlivia Susanto, Emily Gruber, Cheng Mun Wun, et al.
Human Molecular Genetics|October 31, 2025
Haploinsufficiency of GRHL2 is associated with orofacial clefting in humansSarah W Curtis, Cinderella Yang, Alba Sanchis-Juan, et al.
American Journal of Human Genetics|October 7, 2025
Distinguishing syndromic and nonsyndromic cleft palate through analysis of protein-altering de novo variants in 818 triosKelsey R Robinson, Sarah W Curtis, Justin E Paschall, et al.
Stem Cells (Dayton, Ohio)|May 16, 2018
Loss of Angiotensin-Converting Enzyme 2 Exacerbates Diabetic Retinopathy by Promoting Bone Marrow DysfunctionYaqian Duan, Eleni Beli, Sergio Li Calzi, et al.
Epigenetics|August 8, 2015
Exploring the associations between microRNA expression profiles and environmental pollutants in human placenta from the National Children's Study (NCS)Qian Li, Maya A Kappil, An Li, et al.
Nature Genetics|October 7, 2008
Disruption of an AP-2alpha binding site in an IRF6 enhancer is associated with cleft lipFedik Rahimov, Mary L Marazita, Axel Visel, et al.
Pageof 147

Showing results (1331-1340 of 1,465) with videos related to

Sort By:
Pageof 147
Molecular Genetics & Genomic Medicine|April 1, 2017
The prevalence, penetrance, and expressivity of etiologic <i>IRF6</i> variants in orofacial clefts patients from sub-Saharan AfricaLord Jephthah Joojo Gowans, Tamara D Busch, Peter A Mossey, et al.
Acta Neuropathologica Communications|March 25, 2022
Neutrophil-vascular interactions drive myeloperoxidase accumulation in the brain in Alzheimer's diseaseLeon C D Smyth, Helen C Murray, Madison Hill, et al.
Pediatric Research|August 21, 2012
No observed association for mitochondrial SNPs with preterm delivery and related outcomesBrandon W Alleman, Solveig Myking, Kelli K Ryckman, et al.
Plos Genetics|September 21, 2011
Genome-wide association study identifies four loci associated with eruption of permanent teethFrank Geller, Bjarke Feenstra, Hao Zhang, et al.
Molecular Cancer Therapeutics|November 4, 2025
Discovery and characterisation of VPRBP/DCAF1 kinase inhibitor analogues as microtubular destabilising agents with potent anti-myeloma activityOlivia Susanto, Emily Gruber, Cheng Mun Wun, et al.
Human Molecular Genetics|October 31, 2025
Haploinsufficiency of GRHL2 is associated with orofacial clefting in humansSarah W Curtis, Cinderella Yang, Alba Sanchis-Juan, et al.
American Journal of Human Genetics|October 7, 2025
Distinguishing syndromic and nonsyndromic cleft palate through analysis of protein-altering de novo variants in 818 triosKelsey R Robinson, Sarah W Curtis, Justin E Paschall, et al.
Stem Cells (Dayton, Ohio)|May 16, 2018
Loss of Angiotensin-Converting Enzyme 2 Exacerbates Diabetic Retinopathy by Promoting Bone Marrow DysfunctionYaqian Duan, Eleni Beli, Sergio Li Calzi, et al.
Epigenetics|August 8, 2015
Exploring the associations between microRNA expression profiles and environmental pollutants in human placenta from the National Children's Study (NCS)Qian Li, Maya A Kappil, An Li, et al.
Nature Genetics|October 7, 2008
Disruption of an AP-2alpha binding site in an IRF6 enhancer is associated with cleft lipFedik Rahimov, Mary L Marazita, Axel Visel, et al.
Pageof 147