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David Francis

Showing results (141-150 of 176) with videos related to

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International Journal of Molecular Sciences|October 22, 2020
DNA Methylation at Birth Predicts Intellectual Functioning and Autism Features in Children with Fragile X SyndromeClaudine M Kraan, Emma K Baker, Marta Arpone, et al.
American Journal of Medical Genetics. Part A|September 21, 2021
Paternal retraction of a fragile X allele to normal size, showing normal function over two generationsEssra Bartlett, Alison D Archibald, David Francis, et al.
Clinical Chemistry|April 30, 2014
Early detection of fragile X syndrome: applications of a novel approach for improved quantitative methylation analysis in venous blood and newborn blood spotsYoshimi Inaba, Charles E Schwartz, Quang M Bui, et al.
Expert Reviews in Molecular Medicine|July 2, 2015
Detection of skewed X-chromosome inactivation in Fragile X syndrome and X chromosome aneuploidy using quantitative melt analysisDavid E Godler, Yoshimi Inaba, Charles E Schwartz, et al.
OTO Open|July 1, 2026
Voice Outcomes of Patients Intubated for Critical COVID Illness: A Multicenter StudyFrancesco F Caruana, Alexander Gelbard, David Francis, et al.
Human Mutation|September 9, 2020
Rapid exome sequencing and adjunct RNA studies confirm the pathogenicity of a novel homozygous ASNS splicing variant in a critically ill neonateLauren S Akesson, Adam Bournazos, Andrew Fennell, et al.
Frontiers in Genetics|November 29, 2018
The Spectrum of Neurological and White Matter Changes and Premutation Status Categories of Older Male Carriers of the <i>FMR1</i> Alleles Are Linked to Genetic (CGG and FMR1 mRNA) and Cellular Stress (AMPK) MarkersDanuta Z Loesch, Nicholas Trost, Minh Q Bui, et al.
Science Translational Medicine|January 5, 2018
Neoadjuvant oncolytic virotherapy before surgery sensitizes triple-negative breast cancer to immune checkpoint therapyMarie-Claude Bourgeois-Daigneault, Dominic Guy Roy, Amelia Sadie Aitken, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 30, 2018
FMR1 allele size distribution in 35,000 males and females: a comparison of developmental delay and general population cohortsClaudine M Kraan, Quang M Bui, Mike Field, et al.
Theranostics|September 15, 2020
<i>E. coli</i> nitroreductase NfsA is a reporter gene for non-invasive PET imaging in cancer gene therapy applicationsAlexandra Marie Mowday, Janine Naomi Copp, Sophie Philippa Syddall, et al.
Pageof 18

Showing results (141-150 of 176) with videos related to

Sort By:
Pageof 18
International Journal of Molecular Sciences|October 22, 2020
DNA Methylation at Birth Predicts Intellectual Functioning and Autism Features in Children with Fragile X SyndromeClaudine M Kraan, Emma K Baker, Marta Arpone, et al.
American Journal of Medical Genetics. Part A|September 21, 2021
Paternal retraction of a fragile X allele to normal size, showing normal function over two generationsEssra Bartlett, Alison D Archibald, David Francis, et al.
Clinical Chemistry|April 30, 2014
Early detection of fragile X syndrome: applications of a novel approach for improved quantitative methylation analysis in venous blood and newborn blood spotsYoshimi Inaba, Charles E Schwartz, Quang M Bui, et al.
Expert Reviews in Molecular Medicine|July 2, 2015
Detection of skewed X-chromosome inactivation in Fragile X syndrome and X chromosome aneuploidy using quantitative melt analysisDavid E Godler, Yoshimi Inaba, Charles E Schwartz, et al.
OTO Open|July 1, 2026
Voice Outcomes of Patients Intubated for Critical COVID Illness: A Multicenter StudyFrancesco F Caruana, Alexander Gelbard, David Francis, et al.
Human Mutation|September 9, 2020
Rapid exome sequencing and adjunct RNA studies confirm the pathogenicity of a novel homozygous ASNS splicing variant in a critically ill neonateLauren S Akesson, Adam Bournazos, Andrew Fennell, et al.
Frontiers in Genetics|November 29, 2018
The Spectrum of Neurological and White Matter Changes and Premutation Status Categories of Older Male Carriers of the <i>FMR1</i> Alleles Are Linked to Genetic (CGG and FMR1 mRNA) and Cellular Stress (AMPK) MarkersDanuta Z Loesch, Nicholas Trost, Minh Q Bui, et al.
Science Translational Medicine|January 5, 2018
Neoadjuvant oncolytic virotherapy before surgery sensitizes triple-negative breast cancer to immune checkpoint therapyMarie-Claude Bourgeois-Daigneault, Dominic Guy Roy, Amelia Sadie Aitken, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 30, 2018
FMR1 allele size distribution in 35,000 males and females: a comparison of developmental delay and general population cohortsClaudine M Kraan, Quang M Bui, Mike Field, et al.
Theranostics|September 15, 2020
<i>E. coli</i> nitroreductase NfsA is a reporter gene for non-invasive PET imaging in cancer gene therapy applicationsAlexandra Marie Mowday, Janine Naomi Copp, Sophie Philippa Syddall, et al.
Pageof 18