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Showing results (371-380 of 456) with videos related to

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Prenatal Diagnosis|February 27, 2024
Noninvasive single-cell-based prenatal genetic testing: A proof of concept clinical studyMichelle Bellair, Elisabete Amaral, Mason Ouren, et al.
American Journal of Medical Genetics. Part A|September 25, 2004
A mixed epigenetic/genetic model for oligogenic inheritance of autism with a limited role for UBE3AYong-Hui Jiang, Trilochan Sahoo, Ron C Michaelis, et al.
Journal of Inherited Metabolic Disease|May 27, 2016
Erratum to: Untargeted metabolomic analysis for the clinical screening of inborn errors of metabolismMarcus J Miller, Adam D Kennedy, Andrea D Eckhart, et al.
Elife|January 3, 2023
Antisense oligonucleotide therapy rescues disturbed brain rhythms and sleep in juvenile and adult mouse models of Angelman syndromeDongwon Lee, Wu Chen, Heet Naresh Kaku, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 27, 1999
Administration of helper-dependent adenoviral vectors and sequential delivery of different vector serotype for long-term liver-directed gene transfer in baboonsN Morral, W O'Neal, K Rice, et al.
Elife|October 15, 2024
Correction: Antisense oligonucleotide therapy rescues disturbed brain rhythms and sleep in juvenile and adult mouse models of Angelman syndromeDongwon Lee, Wu Chen, Heet Naresh Kaku, et al.
BMC Biology|June 22, 2018
Comparative analysis of single-stranded DNA donors to generate conditional null mouse allelesDenise G Lanza, Angelina Gaspero, Isabel Lorenzo, et al.
Journal of Inherited Metabolic Disease|April 16, 2015
Untargeted metabolomic analysis for the clinical screening of inborn errors of metabolismMarcus J Miller, Adam D Kennedy, Andrea D Eckhart, et al.
Prenatal Diagnosis|October 21, 2016
Genome-wide copy number analysis on DNA from fetal cells isolated from the blood of pregnant womenSteen Kølvraa, Ripudaman Singh, Elizabeth A Normand, et al.
Nature Genetics|November 10, 2009
A small recurrent deletion within 15q13.3 is associated with a range of neurodevelopmental phenotypesMarwan Shinawi, Christian P Schaaf, Samarth S Bhatt, et al.
Pageof 46

Showing results (371-380 of 456) with videos related to

Sort By:
Pageof 46
Prenatal Diagnosis|February 27, 2024
Noninvasive single-cell-based prenatal genetic testing: A proof of concept clinical studyMichelle Bellair, Elisabete Amaral, Mason Ouren, et al.
American Journal of Medical Genetics. Part A|September 25, 2004
A mixed epigenetic/genetic model for oligogenic inheritance of autism with a limited role for UBE3AYong-Hui Jiang, Trilochan Sahoo, Ron C Michaelis, et al.
Journal of Inherited Metabolic Disease|May 27, 2016
Erratum to: Untargeted metabolomic analysis for the clinical screening of inborn errors of metabolismMarcus J Miller, Adam D Kennedy, Andrea D Eckhart, et al.
Elife|January 3, 2023
Antisense oligonucleotide therapy rescues disturbed brain rhythms and sleep in juvenile and adult mouse models of Angelman syndromeDongwon Lee, Wu Chen, Heet Naresh Kaku, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 27, 1999
Administration of helper-dependent adenoviral vectors and sequential delivery of different vector serotype for long-term liver-directed gene transfer in baboonsN Morral, W O'Neal, K Rice, et al.
Elife|October 15, 2024
Correction: Antisense oligonucleotide therapy rescues disturbed brain rhythms and sleep in juvenile and adult mouse models of Angelman syndromeDongwon Lee, Wu Chen, Heet Naresh Kaku, et al.
BMC Biology|June 22, 2018
Comparative analysis of single-stranded DNA donors to generate conditional null mouse allelesDenise G Lanza, Angelina Gaspero, Isabel Lorenzo, et al.
Journal of Inherited Metabolic Disease|April 16, 2015
Untargeted metabolomic analysis for the clinical screening of inborn errors of metabolismMarcus J Miller, Adam D Kennedy, Andrea D Eckhart, et al.
Prenatal Diagnosis|October 21, 2016
Genome-wide copy number analysis on DNA from fetal cells isolated from the blood of pregnant womenSteen Kølvraa, Ripudaman Singh, Elizabeth A Normand, et al.
Nature Genetics|November 10, 2009
A small recurrent deletion within 15q13.3 is associated with a range of neurodevelopmental phenotypesMarwan Shinawi, Christian P Schaaf, Samarth S Bhatt, et al.
Pageof 46