Publications by authors named "Diane Gleeson"

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High-throughput genotyping of high-homology mutant mouse strains by next-generation sequencing.
Diane Gleeson, Debarati Sethi, Radka Platte, Jonathan Burvill, Daniel Barrett

Methods· July 2021

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FBXO7 sensitivity of phenotypic traits elucidated by a hypomorphic allele.
Carmen Ballesteros Reviriego, Simon Clare, Mark J Arends, Emma L Cambridge, Agnieszka Swiatkowska, Diane Gleeson

PLoS One· November 2019

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The mouse line: lessons from the Deciphering the Mechanisms of Developmental Disorders program.
Lukas F Reissig, Anna Nele Herdina, Julia Rose, Barbara Maurer-Gesek, Jenna L Lane, Diane Gleeson

Biol Open· August 2019

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Direct-Acting Oral Anticoagulants and Warfarin-Associated Intracerebral Hemorrhage Protocol Reduces Timing of Door to Correction Interventions.
Rosemary C Olivier, Diane Gleeson, Claudia Skinner, Marysol Cacciata, Mary Wickman

J Neurosci Nurs· April 2019

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Mammalian Hbs1L deficiency causes congenital anomalies and developmental delay associated with Pelota depletion and 80S monosome accumulation.
Amy E O'Connell, Maxim V Gerashchenko, Marie-Francoise O'Donohue, Samantha M Rosen, Eric Huntzinger, Diane Gleeson

PLoS Genet· February 2019

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Placentation defects are highly prevalent in embryonic lethal mouse mutants.
Vicente Perez-Garcia, Elena Fineberg, Robert Wilson, Alexander Murray, Cecilia Icoresi Mazzeo, Diane Gleeson

Nature· March 2018

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Genome-wide in vivo screen identifies novel host regulators of metastatic colonization.
Louise van der Weyden, Mark J Arends, Andrew D Campbell, Tobias Bald, Hannah Wardle-Jones, Diane Gleeson

Nature· January 2017

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Alkaline ceramidase 1 is essential for mammalian skin homeostasis and regulating whole-body energy expenditure.
Kifayathullah Liakath-Ali, Valerie E Vancollie, Christopher J Lelliott, Anneliese O Speak, David Lafont, Diane Gleeson

J Pathol· July 2016

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Blastocyst genotyping for quality control of mouse mutant archives: an ethical and economical approach.
Ferdinando Scavizzi, Edward Ryder, Stuart Newman, Marcello Raspa, Diane Gleeson

Transgenic Res· October 2015

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Rapid conversion of EUCOMM/KOMP-CSD alleles in mouse embryos using a cell-permeable Cre recombinase.
Edward Ryder, Brendan Doe, Diane Gleeson, Richard Houghton, Priya Dalvi

Transgenic Res· February 2014

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Molecular characterization of mutant mouse strains generated from the EUCOMM/KOMP-CSD ES cell resource.
Edward Ryder, Diane Gleeson, Debarati Sethi, Sapna Vyas, Evelina Miklejewska

Mamm Genome· August 2013

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Genomic analysis of a novel spontaneous albino C57BL/6N mouse strain.
Edward Ryder, Kim Wong, Diane Gleeson, Thomas M Keane, Debarati Sethi

Genesis· July 2013

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Mutations in SLC29A3, encoding an equilibrative nucleoside transporter ENT3, cause a familial histiocytosis syndrome (Faisalabad histiocytosis) and familial Rosai-Dorfman disease.
Neil V Morgan, Mark R Morris, Hakan Cangul, Diane Gleeson, Anna Straatman-Iwanowska

PLoS Genet· February 2010

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