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Emma L Duncan

Showing results (61-70 of 138) with videos related to

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Journal of Medical Genetics|April 13, 2016
Mutations in LTBP3 cause acromicric dysplasia and geleophysic dysplasiaAideen M McInerney-Leo, Carine Le Goff, Paul J Leo, et al.
JCI Insight|May 25, 2021
A KCNK16 mutation causing TALK-1 gain of function is associated with maturity-onset diabetes of the youngSarah M Graff, Stephanie R Johnson, Paul J Leo, et al.
BMC Musculoskeletal Disorders|March 29, 2014
The IFITM5 mutation c.-14C > T results in an elongated transcript expressed in human bone; and causes varying phenotypic severity of osteogenesis imperfecta type VSyndia Lazarus, Aideen M McInerney-Leo, Fiona A McKenzie, et al.
The European Respiratory Journal|April 4, 2024
Symptoms before and after COVID-19: a population and case-control study using prospective dataCarole H Sudre, Michela Antonelli, Nathan J Cheetham, et al.
Women and Birth : Journal of the Australian College of Midwives|March 2, 2024
Women's experiences of maternity care in the United Kingdom during the COVID-19 pandemic: A follow-up systematic review and qualitative evidence synthesisTisha Dasgupta, Gillian Horgan, Lili Peterson, et al.
International Journal of Molecular Sciences|February 10, 2024
The ATM Ser49Cys Variant Effects ATM Function as a Regulator of Oncogene-Induced SenescenceCaroline Atkinson, Aideen M McInerney-Leo, Martina Proctor, et al.
The Journal of Infection|January 12, 2025
Symptom evolution in individuals with ongoing symptomatic COVID-19 and post-COVID-19 syndrome after SARS-CoV-2 vaccination versus influenza vaccinationKhaled Rjoob, Michela Antonelli, Benjamin Murray, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|April 19, 2018
Mutations That Alter the Carboxy-Terminal-Propeptide Cleavage Site of the Chains of Type I Procollagen Are Associated With a Unique Osteogenesis Imperfecta PhenotypeTim Cundy, Michael Dray, John Delahunt, et al.
Calcified Tissue International|September 22, 2007
PTHR1 polymorphisms influence BMD variation through effects on the growing skeletonCarles Vilariño-Güell, Lisa J Miles, Emma L Duncan, et al.
Vaccines|April 27, 2024
Courage in Decision Making: A Mixed-Methods Study of COVID-19 Vaccine Uptake in Women of Reproductive Age in the U.KLaura A Magee, Julia R Brown, Vicky Bowyer, et al.
Pageof 14

Showing results (61-70 of 138) with videos related to

Sort By:
Pageof 14
Journal of Medical Genetics|April 13, 2016
Mutations in LTBP3 cause acromicric dysplasia and geleophysic dysplasiaAideen M McInerney-Leo, Carine Le Goff, Paul J Leo, et al.
JCI Insight|May 25, 2021
A KCNK16 mutation causing TALK-1 gain of function is associated with maturity-onset diabetes of the youngSarah M Graff, Stephanie R Johnson, Paul J Leo, et al.
BMC Musculoskeletal Disorders|March 29, 2014
The IFITM5 mutation c.-14C > T results in an elongated transcript expressed in human bone; and causes varying phenotypic severity of osteogenesis imperfecta type VSyndia Lazarus, Aideen M McInerney-Leo, Fiona A McKenzie, et al.
The European Respiratory Journal|April 4, 2024
Symptoms before and after COVID-19: a population and case-control study using prospective dataCarole H Sudre, Michela Antonelli, Nathan J Cheetham, et al.
Women and Birth : Journal of the Australian College of Midwives|March 2, 2024
Women's experiences of maternity care in the United Kingdom during the COVID-19 pandemic: A follow-up systematic review and qualitative evidence synthesisTisha Dasgupta, Gillian Horgan, Lili Peterson, et al.
International Journal of Molecular Sciences|February 10, 2024
The ATM Ser49Cys Variant Effects ATM Function as a Regulator of Oncogene-Induced SenescenceCaroline Atkinson, Aideen M McInerney-Leo, Martina Proctor, et al.
The Journal of Infection|January 12, 2025
Symptom evolution in individuals with ongoing symptomatic COVID-19 and post-COVID-19 syndrome after SARS-CoV-2 vaccination versus influenza vaccinationKhaled Rjoob, Michela Antonelli, Benjamin Murray, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|April 19, 2018
Mutations That Alter the Carboxy-Terminal-Propeptide Cleavage Site of the Chains of Type I Procollagen Are Associated With a Unique Osteogenesis Imperfecta PhenotypeTim Cundy, Michael Dray, John Delahunt, et al.
Calcified Tissue International|September 22, 2007
PTHR1 polymorphisms influence BMD variation through effects on the growing skeletonCarles Vilariño-Güell, Lisa J Miles, Emma L Duncan, et al.
Vaccines|April 27, 2024
Courage in Decision Making: A Mixed-Methods Study of COVID-19 Vaccine Uptake in Women of Reproductive Age in the U.KLaura A Magee, Julia R Brown, Vicky Bowyer, et al.
Pageof 14