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Janna E Hutz

Showing results (1-10 of 8) with videos related to

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Plos One|September 28, 2011
Genomewide analysis of inherited variation associated with phosphorylation of PI3K/AKT/mTOR signaling proteinsJanna E Hutz, W Aaron Manning, Michael A Province, et al.
Genetic Epidemiology|July 10, 2008
CANDID: a flexible method for prioritizing candidate genes for complex human traitsJanna E Hutz, Aldi T Kraja, Howard L McLeod, et al.
Chromosome Research : an International Journal on the Molecular, Supramolecular and Evolutionary Aspects of Chromosome Biology|January 11, 2008
Tpp1/Acd maintains genomic stability through a complex role in telomere protectionTobias Else, Brian K Theisen, Yipin Wu, et al.
Molecular Genetics and Metabolism|March 1, 2006
IMAGe association and congenital adrenal hypoplasia: no disease-causing mutations found in the ACD geneJanna E Hutz, Andrea S Krause, John C Achermann, et al.
Human Molecular Genetics|November 13, 2004
Urogenital and caudal dysgenesis in adrenocortical dysplasia (acd) mice is caused by a splicing mutation in a novel telomeric regulatorCatherine E Keegan, Janna E Hutz, Tobias Else, et al.
Journal of Biomolecular Screening|December 4, 2012
The multidimensional perturbation value: a single metric to measure similarity and activity of treatments in high-throughput multidimensional screensJanna E Hutz, Thomas Nelson, Hua Wu, et al.
Clinical Endocrinology|May 1, 2007
Novel polymorphisms and lack of mutations in the ACD gene in patients with ACTH resistance syndromesCatherine E Keegan, Janna E Hutz, Andrea S Krause, et al.
Chemmedchem|February 1, 2021
E7766, a Macrocycle-Bridged Stimulator of Interferon Genes (STING) Agonist with Potent Pan-Genotypic ActivityDae-Shik Kim, Atsushi Endo, Francis G Fang, et al.
Pageof 1

Showing results (1-10 of 8) with videos related to

Sort By:
Pageof 1
Plos One|September 28, 2011
Genomewide analysis of inherited variation associated with phosphorylation of PI3K/AKT/mTOR signaling proteinsJanna E Hutz, W Aaron Manning, Michael A Province, et al.
Genetic Epidemiology|July 10, 2008
CANDID: a flexible method for prioritizing candidate genes for complex human traitsJanna E Hutz, Aldi T Kraja, Howard L McLeod, et al.
Chromosome Research : an International Journal on the Molecular, Supramolecular and Evolutionary Aspects of Chromosome Biology|January 11, 2008
Tpp1/Acd maintains genomic stability through a complex role in telomere protectionTobias Else, Brian K Theisen, Yipin Wu, et al.
Molecular Genetics and Metabolism|March 1, 2006
IMAGe association and congenital adrenal hypoplasia: no disease-causing mutations found in the ACD geneJanna E Hutz, Andrea S Krause, John C Achermann, et al.
Human Molecular Genetics|November 13, 2004
Urogenital and caudal dysgenesis in adrenocortical dysplasia (acd) mice is caused by a splicing mutation in a novel telomeric regulatorCatherine E Keegan, Janna E Hutz, Tobias Else, et al.
Journal of Biomolecular Screening|December 4, 2012
The multidimensional perturbation value: a single metric to measure similarity and activity of treatments in high-throughput multidimensional screensJanna E Hutz, Thomas Nelson, Hua Wu, et al.
Clinical Endocrinology|May 1, 2007
Novel polymorphisms and lack of mutations in the ACD gene in patients with ACTH resistance syndromesCatherine E Keegan, Janna E Hutz, Andrea S Krause, et al.
Chemmedchem|February 1, 2021
E7766, a Macrocycle-Bridged Stimulator of Interferon Genes (STING) Agonist with Potent Pan-Genotypic ActivityDae-Shik Kim, Atsushi Endo, Francis G Fang, et al.
Pageof 1