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Danny E Miller

Showing results (21-30 of 112) with videos related to

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Proceedings of the National Academy of Sciences of the United States of America|November 19, 2014
Synaptonemal complex extension from clustered telomeres mediates full-length chromosome pairing in Schmidtea mediterraneaYoubin Xiang, Danny E Miller, Eric J Ross, et al.
American Journal of Medical Genetics. Part A|December 14, 2019
Catel-Manzke syndrome without Manzke dysostosisDanny E Miller, Penny Chow, Emily R Gallagher, et al.
Journal of the American Society for Mass Spectrometry|November 16, 2011
HDXFinder: automated analysis and data reporting of deuterium/hydrogen exchange mass spectrometryDanny E Miller, Charulata B Prasannan, Maria T Villar, et al.
Bioinformatics (Oxford, England)|June 17, 2026
needLR: Long-read structural variant annotation with population-scale frequency estimationJonas A Gustafson, Jiadong Lin, Miranda P G Zalusky, et al.
Emerging Topics in Life Sciences|October 31, 2023
Advances in the discovery and analyses of human tandem repeatsMark J P Chaisson, Arvis Sulovari, Paul N Valdmanis, et al.
Neoreviews|May 1, 2021
Case 2: Seizures in a NeonateDanny E Miller, Jason Wright, Randall A Bly, et al.
Genetics|January 31, 2014
Discovery of supernumerary B chromosomes in Drosophila melanogasterElisabeth Bauerly, Stacie E Hughes, Dana R Vietti, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|July 10, 2022
Targeted Long-Read Sequencing Identifies a Retrotransposon Insertion as a Cause of Altered GNAS Exon A/B Methylation in a Family With Autosomal Dominant Pseudohypoparathyroidism Type 1b (PHP1B)Danny E Miller, Patrick Hanna, Miranda Galey, et al.
Plos Genetics|April 13, 2023
Heterozygous inversion breakpoints suppress meiotic crossovers by altering recombination repair outcomesHaosheng Li, Erica Berent, Savannah Hadjipanteli, et al.
Seminars in Perinatology|July 2, 2025
Genetic and epigenetic contributors and mimickers of phenotypic hypoxic-ischemic encephalopathy (HIE)Ulrike Mietzsch, Janessa B Law, Basel Thayyil, et al.
Pageof 12

Showing results (21-30 of 112) with videos related to

Sort By:
Pageof 12
Proceedings of the National Academy of Sciences of the United States of America|November 19, 2014
Synaptonemal complex extension from clustered telomeres mediates full-length chromosome pairing in Schmidtea mediterraneaYoubin Xiang, Danny E Miller, Eric J Ross, et al.
American Journal of Medical Genetics. Part A|December 14, 2019
Catel-Manzke syndrome without Manzke dysostosisDanny E Miller, Penny Chow, Emily R Gallagher, et al.
Journal of the American Society for Mass Spectrometry|November 16, 2011
HDXFinder: automated analysis and data reporting of deuterium/hydrogen exchange mass spectrometryDanny E Miller, Charulata B Prasannan, Maria T Villar, et al.
Bioinformatics (Oxford, England)|June 17, 2026
needLR: Long-read structural variant annotation with population-scale frequency estimationJonas A Gustafson, Jiadong Lin, Miranda P G Zalusky, et al.
Emerging Topics in Life Sciences|October 31, 2023
Advances in the discovery and analyses of human tandem repeatsMark J P Chaisson, Arvis Sulovari, Paul N Valdmanis, et al.
Neoreviews|May 1, 2021
Case 2: Seizures in a NeonateDanny E Miller, Jason Wright, Randall A Bly, et al.
Genetics|January 31, 2014
Discovery of supernumerary B chromosomes in Drosophila melanogasterElisabeth Bauerly, Stacie E Hughes, Dana R Vietti, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|July 10, 2022
Targeted Long-Read Sequencing Identifies a Retrotransposon Insertion as a Cause of Altered GNAS Exon A/B Methylation in a Family With Autosomal Dominant Pseudohypoparathyroidism Type 1b (PHP1B)Danny E Miller, Patrick Hanna, Miranda Galey, et al.
Plos Genetics|April 13, 2023
Heterozygous inversion breakpoints suppress meiotic crossovers by altering recombination repair outcomesHaosheng Li, Erica Berent, Savannah Hadjipanteli, et al.
Seminars in Perinatology|July 2, 2025
Genetic and epigenetic contributors and mimickers of phenotypic hypoxic-ischemic encephalopathy (HIE)Ulrike Mietzsch, Janessa B Law, Basel Thayyil, et al.
Pageof 12