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C Murray

Showing results (1191-1200 of 1,465) with videos related to

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Genetic Epidemiology|September 25, 2018
Inferring disease risk genes from sequencing data in multiplex pedigrees through sharing of rare variantsAlexandre Bureau, Ferdouse Begum, Margaret A Taub, et al.
BMC Pediatrics|November 28, 2012
Oral cleft prevention program (OCPP)George L Wehby, Norman Goco, Danilo Moretti-Ferreira, et al.
Journal of Medicinal Chemistry|February 24, 2015
2-Aryl-3-methyloctahydrophenanthrene-2,3,7-triols as potent dissociated glucocorticoid receptor agonistsYves A Chantigny, John C Murray, Edward F Kleinman, et al.
Genetic Epidemiology|June 15, 2021
FAT4 identified as a potential modifier of orofacial cleft lateralitySarah W Curtis, Daniel Chang, Miranda R Sun, et al.
Journal of Alzheimer'S Disease : JAD|February 6, 2023
PSA-NCAM Regulatory Gene Expression Changes in the Alzheimer's Disease Entorhinal Cortex Revealed with Multiplexed in situ HybridizationBlake Highet, James A Wiseman, Hannah Mein, et al.
Neurobiology of Disease|February 5, 2025
Elucidating cortical neurovascular involvement in Huntington's disease using human brain tissue microarraysAdelie Y S Tan, Lance C M G Martinez, Helen C Murray, et al.
G3 (Bethesda, Md.)|June 10, 2023
An allelic series of spontaneous Rorb mutant mice exhibit a gait phenotype, changes in retina morphology and behavior, and gene expression signatures associated with the unfolded protein responseGeorge C Murray, Jason A Bubier, Oraya J Zinder, et al.
Plos Genetics|February 10, 2011
Mapping a new spontaneous preterm birth susceptibility gene, IGF1R, using linkage, haplotype sharing, and association analysisRitva Haataja, Minna K Karjalainen, Aino Luukkonen, et al.
AJOB Empirical Bioethics|January 18, 2024
Parents and Provider Perspectives on the Return of Genomic Findings for Cleft Families in AfricaAbimbola M Oladayo, Sydney Prochaska, Tamara Busch, et al.
Blood|April 15, 1997
CD6-depleted allogeneic bone marrow transplantation for acute leukemia in first complete remissionR J Soiffer, D Fairclough, M Robertson, et al.
Pageof 147

Showing results (1191-1200 of 1,465) with videos related to

Sort By:
Pageof 147
Genetic Epidemiology|September 25, 2018
Inferring disease risk genes from sequencing data in multiplex pedigrees through sharing of rare variantsAlexandre Bureau, Ferdouse Begum, Margaret A Taub, et al.
BMC Pediatrics|November 28, 2012
Oral cleft prevention program (OCPP)George L Wehby, Norman Goco, Danilo Moretti-Ferreira, et al.
Journal of Medicinal Chemistry|February 24, 2015
2-Aryl-3-methyloctahydrophenanthrene-2,3,7-triols as potent dissociated glucocorticoid receptor agonistsYves A Chantigny, John C Murray, Edward F Kleinman, et al.
Genetic Epidemiology|June 15, 2021
FAT4 identified as a potential modifier of orofacial cleft lateralitySarah W Curtis, Daniel Chang, Miranda R Sun, et al.
Journal of Alzheimer'S Disease : JAD|February 6, 2023
PSA-NCAM Regulatory Gene Expression Changes in the Alzheimer's Disease Entorhinal Cortex Revealed with Multiplexed in situ HybridizationBlake Highet, James A Wiseman, Hannah Mein, et al.
Neurobiology of Disease|February 5, 2025
Elucidating cortical neurovascular involvement in Huntington's disease using human brain tissue microarraysAdelie Y S Tan, Lance C M G Martinez, Helen C Murray, et al.
G3 (Bethesda, Md.)|June 10, 2023
An allelic series of spontaneous Rorb mutant mice exhibit a gait phenotype, changes in retina morphology and behavior, and gene expression signatures associated with the unfolded protein responseGeorge C Murray, Jason A Bubier, Oraya J Zinder, et al.
Plos Genetics|February 10, 2011
Mapping a new spontaneous preterm birth susceptibility gene, IGF1R, using linkage, haplotype sharing, and association analysisRitva Haataja, Minna K Karjalainen, Aino Luukkonen, et al.
AJOB Empirical Bioethics|January 18, 2024
Parents and Provider Perspectives on the Return of Genomic Findings for Cleft Families in AfricaAbimbola M Oladayo, Sydney Prochaska, Tamara Busch, et al.
Blood|April 15, 1997
CD6-depleted allogeneic bone marrow transplantation for acute leukemia in first complete remissionR J Soiffer, D Fairclough, M Robertson, et al.
Pageof 147