Publications by authors named "Andrea Leitch"

25Publications

SET nuclear oncogene associates with microcephalin/MCPH1 and regulates chromosome condensation.

J Biol Chem 2011 Jun 22;286(24):21393-400. Epub 2011 Apr 22.

Department of Experimental Radiation Oncology, The University of Texas M.D. Anderson Cancer Center, Houston, Texas 77030, USA.

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http://dx.doi.org/10.1074/jbc.M110.208793DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3122199PMC
June 2011

Mutations in ORC1, encoding the largest subunit of the origin recognition complex, cause microcephalic primordial dwarfism resembling Meier-Gorlin syndrome.

Nat Genet 2011 Feb 27;43(4):350-5. Epub 2011 Feb 27.

Medical Research Council (MRC) Human Genetics Unit (HGU), Institute for Genetics and Molecular Medicine, Western General Hospital, Edinburgh, UK.

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http://dx.doi.org/10.1038/ng.776DOI Listing
February 2011

Nucleic acid-mediated inflammatory diseases.

Bioessays 2008 Sep;30(9):833-42

MRC Human Genetics Unit, Western General Hospital, Edinburgh EH42XU, UK.

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http://dx.doi.org/10.1002/bies.20808DOI Listing
September 2008

Clinical and molecular phenotype of Aicardi-Goutieres syndrome.

Authors:
Gillian Rice Teresa Patrick Rekha Parmar Claire F Taylor Alec Aeby Jean Aicardi Rafael Artuch Simon Attard Montalto Carlos A Bacino Bruno Barroso Peter Baxter Willam S Benko Carsten Bergmann Enrico Bertini Roberta Biancheri Edward M Blair Nenad Blau David T Bonthron Tracy Briggs Louise A Brueton Han G Brunner Christopher J Burke Ian M Carr Daniel R Carvalho Kate E Chandler Hans-Jurgen Christen Peter C Corry Frances M Cowan Helen Cox Stefano D'Arrigo John Dean Corinne De Laet Claudine De Praeter Catherine Dery Colin D Ferrie Kim Flintoff Suzanna G M Frints Angels Garcia-Cazorla Blanca Gener Cyril Goizet Francoise Goutieres Andrew J Green Agnes Guet Ben C J Hamel Bruce E Hayward Arvid Heiberg Raoul C Hennekam Marie Husson Andrew P Jackson Rasieka Jayatunga Yong-Hui Jiang Sarina G Kant Amy Kao Mary D King Helen M Kingston Joerg Klepper Marjo S van der Knaap Andrew J Kornberg Dieter Kotzot Wilfried Kratzer Didier Lacombe Lieven Lagae Pierre Georges Landrieu Giovanni Lanzi Andrea Leitch Ming J Lim John H Livingston Charles M Lourenco E G Hermione Lyall Sally A Lynch Michael J Lyons Daphna Marom John P McClure Robert McWilliam Serge B Melancon Leena D Mewasingh Marie-Laure Moutard Ken K Nischal John R Ostergaard Julie Prendiville Magnhild Rasmussen R Curtis Rogers Dominique Roland Elisabeth M Rosser Kevin Rostasy Agathe Roubertie Amparo Sanchis Raphael Schiffmann Sabine Scholl-Burgi Sunita Seal Stavit A Shalev C Sierra Corcoles Gyan P Sinha Doriette Soler Ronen Spiegel John B P Stephenson Uta Tacke Tiong Yang Tan Marianne Till John L Tolmie Pam Tomlin Federica Vagnarelli Enza Maria Valente Rudy N A Van Coster Nathalie Van der Aa Adeline Vanderver Johannes S H Vles Thomas Voit Evangeline Wassmer Bernhard Weschke Margo L Whiteford Michel A A Willemsen Andreas Zankl Sameer M Zuberi Simona Orcesi Elisa Fazzi Pierre Lebon Yanick J Crow

Am J Hum Genet 2007 Oct 4;81(4):713-25. Epub 2007 Sep 4.

Leeds Institute of Molecular Medicine, St James's University Hospital, Leeds, LS9 7TF, UK.

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http://dx.doi.org/10.1086/521373DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2227922PMC
October 2007

Stat3 is required for the development of skin cancer.

J Clin Invest 2004 Sep;114(5):619-22

Memorial Sloan Kettering Cancer Center, New York, New York, USA.

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http://dx.doi.org/10.1172/JCI22800DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC514594PMC
September 2004

Requirement of matrix metalloproteinase-9 for the transformation of human mammary epithelial cells by Stat3-C.

Proc Natl Acad Sci U S A 2004 Jul 12;101(29):10602-7. Epub 2004 Jul 12.

Laboratory of Molecular Cell Biology, The Rockefeller University, New York, NY 10021, USA.

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http://dx.doi.org/10.1073/pnas.0404100101DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC489981PMC
July 2004

Genetic interactions between the Wilms' tumor 1 gene and the p53 gene.

Cancer Res 2002 Nov;62(22):6615-20

Central Hematologie Laboratory, University Medical Centre St. Radboud, 6500 HB, Nijmegen, the Netherlands.

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November 2002

Heterozygosity for p53 promotes microsatellite instability and tumorigenesis on a Msh2 deficient background.

Oncogene 2002 Sep;21(41):6299-306

Department of Pathology, University Medical School, Teviot Place, Edinburgh EH8 9AG, UK.

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http://dx.doi.org/10.1038/sj.onc.1205727DOI Listing
September 2002