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Jennifer Schleit

Showing results (1-10 of 29) with videos related to

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FEBS Letters|July 26, 2012
Yeast as a model to understand the interaction between genotype and the response to calorie restrictionJennifer Schleit, Brian M Wasko, Matt Kaeberlein
Biochemical and Biophysical Research Communications|May 11, 2010
Analysis of nucleic acid binding by a recombinant translin-trax complexMatthew Lluis, Warren Hoe, Jennifer Schleit, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 16, 2018
First, do no harm: direct-to-consumer genetic testingJennifer Schleit, Lorraine V Naylor, Fuki M Hisama
Plos One|December 2, 2011
The MDT-15 subunit of mediator interacts with dietary restriction to modulate longevity and fluoranthene toxicity in Caenorhabditis elegansJennifer Schleit, Valerie Z Wall, Marissa Simko, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|December 17, 2017
LMX1B-Associated Nephropathy With Type III Collagen Deposition in the Glomerular and Tubular Basement MembranesNicole K Andeen, Jennifer Schleit, Christopher D Blosser, et al.
Human Mutation|May 13, 2015
Molecular Outcome, Prediction, and Clinical Consequences of Splice Variants in COL1A1, Which Encodes the proα1(I) Chains of Type I ProcollagenJennifer Schleit, Samuel S Bailey, Thao Tran, et al.
European Journal of Human Genetics : EJHG|June 25, 2020
Diphthamide-deficiency syndrome: a novel human developmental disorder and ribosomopathyHarmen Hawer, Bryce A Mendelsohn, Klaus Mayer, et al.
Neuromuscular Disorders : NMD|May 22, 2018
Neutral lipid storage disease with myopathy: Further phenotypic characterization of a rare PNPLA2 variantCaitlin S Latimer, Jennifer Schleit, Adam Reynolds, et al.
Molecular Genetics & Genomic Medicine|November 6, 2018
CTC1 mutations in a Brazilian family with progeroid features and recurrent bone fracturesForough Sargolzaeiaval, Jiaming Zhang, Jennifer Schleit, et al.
American Journal of Medical Genetics. Part A|March 3, 2023
Novel filamin C (FLNC) variant causes a severe form of familial mixed hypertrophic-restrictive cardiomyopathyNathalie Gaudreault, Louis-Jacques Ruel, Cyndi Henry, et al.
Pageof 3

Showing results (1-10 of 29) with videos related to

Sort By:
Pageof 3
FEBS Letters|July 26, 2012
Yeast as a model to understand the interaction between genotype and the response to calorie restrictionJennifer Schleit, Brian M Wasko, Matt Kaeberlein
Biochemical and Biophysical Research Communications|May 11, 2010
Analysis of nucleic acid binding by a recombinant translin-trax complexMatthew Lluis, Warren Hoe, Jennifer Schleit, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 16, 2018
First, do no harm: direct-to-consumer genetic testingJennifer Schleit, Lorraine V Naylor, Fuki M Hisama
Plos One|December 2, 2011
The MDT-15 subunit of mediator interacts with dietary restriction to modulate longevity and fluoranthene toxicity in Caenorhabditis elegansJennifer Schleit, Valerie Z Wall, Marissa Simko, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|December 17, 2017
LMX1B-Associated Nephropathy With Type III Collagen Deposition in the Glomerular and Tubular Basement MembranesNicole K Andeen, Jennifer Schleit, Christopher D Blosser, et al.
Human Mutation|May 13, 2015
Molecular Outcome, Prediction, and Clinical Consequences of Splice Variants in COL1A1, Which Encodes the proα1(I) Chains of Type I ProcollagenJennifer Schleit, Samuel S Bailey, Thao Tran, et al.
European Journal of Human Genetics : EJHG|June 25, 2020
Diphthamide-deficiency syndrome: a novel human developmental disorder and ribosomopathyHarmen Hawer, Bryce A Mendelsohn, Klaus Mayer, et al.
Neuromuscular Disorders : NMD|May 22, 2018
Neutral lipid storage disease with myopathy: Further phenotypic characterization of a rare PNPLA2 variantCaitlin S Latimer, Jennifer Schleit, Adam Reynolds, et al.
Molecular Genetics & Genomic Medicine|November 6, 2018
CTC1 mutations in a Brazilian family with progeroid features and recurrent bone fracturesForough Sargolzaeiaval, Jiaming Zhang, Jennifer Schleit, et al.
American Journal of Medical Genetics. Part A|March 3, 2023
Novel filamin C (FLNC) variant causes a severe form of familial mixed hypertrophic-restrictive cardiomyopathyNathalie Gaudreault, Louis-Jacques Ruel, Cyndi Henry, et al.
Pageof 3