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Andrea Leitch

Showing results (1-10 of 27) with videos related to

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The Journal of Clinical Investigation|September 3, 2004
Stat3 is required for the development of skin cancerLaura Pedranzini, Andrea Leitch, Jacqueline Bromberg
Bioessays : News and Reviews in Molecular, Cellular and Developmental Biology|August 12, 2008
Nucleic acid-mediated inflammatory diseasesRachel E Rigby, Andrea Leitch, Andrew P Jackson
Proceedings of the National Academy of Sciences of the United States of America|July 14, 2004
Requirement of matrix metalloproteinase-9 for the transformation of human mammary epithelial cells by Stat3-CTobias N Dechow, Laura Pedranzini, Andrea Leitch, et al.
The Journal of Biological Chemistry|April 26, 2011
SET nuclear oncogene associates with microcephalin/MCPH1 and regulates chromosome condensationJustin W Leung, Andrea Leitch, Jamie L Wood, et al.
Cancer Research|November 20, 2002
Genetic interactions between the Wilms' tumor 1 gene and the p53 geneAswin L Menke, Alan R Clarke, Andrea Leitch, et al.
Nature Genetics|March 2, 2011
Mutations in ORC1, encoding the largest subunit of the origin recognition complex, cause microcephalic primordial dwarfism resembling Meier-Gorlin syndromeLouise S Bicknell, Sarah Walker, Anna Klingseisen, et al.
The EMBO Journal|February 12, 2014
RNA:DNA hybrids are a novel molecular pattern sensed by TLR9Rachel E Rigby, Lauren M Webb, Karen J Mackenzie, et al.
Nature|July 25, 2017
cGAS surveillance of micronuclei links genome instability to innate immunityKaren J Mackenzie, Paula Carroll, Carol-Anne Martin, et al.
Genes & Development|October 16, 2020
PRIM1 deficiency causes a distinctive primordial dwarfism syndromeDavid A Parry, Lukas Tamayo-Orrego, Paula Carroll, et al.
Human Mutation|April 18, 2013
Synonymous mutations in RNASEH2A create cryptic splice sites impairing RNase H2 enzyme function in Aicardi-Goutières syndromeGillian I Rice, Martin A M Reijns, Stephanie R Coffin, et al.
Pageof 3

Showing results (1-10 of 27) with videos related to

Sort By:
Pageof 3
The Journal of Clinical Investigation|September 3, 2004
Stat3 is required for the development of skin cancerLaura Pedranzini, Andrea Leitch, Jacqueline Bromberg
Bioessays : News and Reviews in Molecular, Cellular and Developmental Biology|August 12, 2008
Nucleic acid-mediated inflammatory diseasesRachel E Rigby, Andrea Leitch, Andrew P Jackson
Proceedings of the National Academy of Sciences of the United States of America|July 14, 2004
Requirement of matrix metalloproteinase-9 for the transformation of human mammary epithelial cells by Stat3-CTobias N Dechow, Laura Pedranzini, Andrea Leitch, et al.
The Journal of Biological Chemistry|April 26, 2011
SET nuclear oncogene associates with microcephalin/MCPH1 and regulates chromosome condensationJustin W Leung, Andrea Leitch, Jamie L Wood, et al.
Cancer Research|November 20, 2002
Genetic interactions between the Wilms' tumor 1 gene and the p53 geneAswin L Menke, Alan R Clarke, Andrea Leitch, et al.
Nature Genetics|March 2, 2011
Mutations in ORC1, encoding the largest subunit of the origin recognition complex, cause microcephalic primordial dwarfism resembling Meier-Gorlin syndromeLouise S Bicknell, Sarah Walker, Anna Klingseisen, et al.
The EMBO Journal|February 12, 2014
RNA:DNA hybrids are a novel molecular pattern sensed by TLR9Rachel E Rigby, Lauren M Webb, Karen J Mackenzie, et al.
Nature|July 25, 2017
cGAS surveillance of micronuclei links genome instability to innate immunityKaren J Mackenzie, Paula Carroll, Carol-Anne Martin, et al.
Genes & Development|October 16, 2020
PRIM1 deficiency causes a distinctive primordial dwarfism syndromeDavid A Parry, Lukas Tamayo-Orrego, Paula Carroll, et al.
Human Mutation|April 18, 2013
Synonymous mutations in RNASEH2A create cryptic splice sites impairing RNase H2 enzyme function in Aicardi-Goutières syndromeGillian I Rice, Martin A M Reijns, Stephanie R Coffin, et al.
Pageof 3