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Susan M Hiatt

Showing results (1-10 of 42) with videos related to

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Methods (San Diego, Calif.)|July 1, 2008
Bimolecular fluorescence complementation (BiFC) analysis of protein interactions in Caenorhabditis elegansSusan M Hiatt, Y John Shyu, Holli M Duren, et al.
Nature Protocols|April 5, 2008
Visualization of protein interactions in living Caenorhabditis elegans using bimolecular fluorescence complementation analysisY John Shyu, Susan M Hiatt, Holli M Duren, et al.
Molecular Biology of the Cell|July 3, 2009
Caenorhabditis elegans FOS-1 and JUN-1 regulate plc-1 expression in the spermatheca to control ovulationSusan M Hiatt, Holli M Duren, Y John Shyu, et al.
Frontiers in Physiology|April 27, 2019
A YWHAZ Variant Associated With Cardiofaciocutaneous Syndrome Activates the RAF-ERK PathwayIvan K Popov, Susan M Hiatt, Sandra Whalen, et al.
HGG Advances|April 11, 2026
Heterozygous CECR2 Variants Support a Distinct Neurodevelopmental Syndrome with Features Overlapping Cat Eye SyndromeAnushree Acharya, Irma Järvelä, Andrea Hernandez, et al.
HGG Advances|May 3, 2021
Long-read genome sequencing for the molecular diagnosis of neurodevelopmental disordersSusan M Hiatt, James M J Lawlor, Lori H Handley, et al.
AJOB Empirical Bioethics|April 12, 2021
The Therapeutic Odyssey: Positioning Genomic Sequencing in the Search for a Child's Best Possible LifeJanet Elizabeth Childerhose, Carla Rich, Kelly M East, et al.
Neurology. Genetics|November 11, 2016
Germline and somatic mutations in the <i>MTOR</i> gene in focal cortical dysplasia and epilepsyRikke S Møller, Sarah Weckhuysen, Mathilde Chipaux, et al.
Biorxiv : the Preprint Server for Biology|January 30, 2023
Poison exon annotations improve the yield of clinically relevant variants in genomic diagnostic testingStephanie A Felker, James Mj Lawlor, Susan M Hiatt, et al.
American Journal of Human Genetics|March 19, 2019
Deleterious Variation in BRSK2 Associates with a Neurodevelopmental DisorderSusan M Hiatt, Michelle L Thompson, Jeremy W Prokop, et al.
Pageof 5

Showing results (1-10 of 42) with videos related to

Sort By:
Pageof 5
Methods (San Diego, Calif.)|July 1, 2008
Bimolecular fluorescence complementation (BiFC) analysis of protein interactions in Caenorhabditis elegansSusan M Hiatt, Y John Shyu, Holli M Duren, et al.
Nature Protocols|April 5, 2008
Visualization of protein interactions in living Caenorhabditis elegans using bimolecular fluorescence complementation analysisY John Shyu, Susan M Hiatt, Holli M Duren, et al.
Molecular Biology of the Cell|July 3, 2009
Caenorhabditis elegans FOS-1 and JUN-1 regulate plc-1 expression in the spermatheca to control ovulationSusan M Hiatt, Holli M Duren, Y John Shyu, et al.
Frontiers in Physiology|April 27, 2019
A YWHAZ Variant Associated With Cardiofaciocutaneous Syndrome Activates the RAF-ERK PathwayIvan K Popov, Susan M Hiatt, Sandra Whalen, et al.
HGG Advances|April 11, 2026
Heterozygous CECR2 Variants Support a Distinct Neurodevelopmental Syndrome with Features Overlapping Cat Eye SyndromeAnushree Acharya, Irma Järvelä, Andrea Hernandez, et al.
HGG Advances|May 3, 2021
Long-read genome sequencing for the molecular diagnosis of neurodevelopmental disordersSusan M Hiatt, James M J Lawlor, Lori H Handley, et al.
AJOB Empirical Bioethics|April 12, 2021
The Therapeutic Odyssey: Positioning Genomic Sequencing in the Search for a Child's Best Possible LifeJanet Elizabeth Childerhose, Carla Rich, Kelly M East, et al.
Neurology. Genetics|November 11, 2016
Germline and somatic mutations in the <i>MTOR</i> gene in focal cortical dysplasia and epilepsyRikke S Møller, Sarah Weckhuysen, Mathilde Chipaux, et al.
Biorxiv : the Preprint Server for Biology|January 30, 2023
Poison exon annotations improve the yield of clinically relevant variants in genomic diagnostic testingStephanie A Felker, James Mj Lawlor, Susan M Hiatt, et al.
American Journal of Human Genetics|March 19, 2019
Deleterious Variation in BRSK2 Associates with a Neurodevelopmental DisorderSusan M Hiatt, Michelle L Thompson, Jeremy W Prokop, et al.
Pageof 5