检索结果 - Sarah Edkins

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  1. 1
    Role of bile salts in fat malabsorption of premature infants

    Role of bile salts in fat malabsorption of premature infants 由 E Signer, G. M. Murphy, Sarah Edkins, C. M. Anderson

    出版 1974
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  2. 2
    The Gene for Cherubism Maps to Chromosome 4p16.3

    The Gene for Cherubism Maps to Chromosome 4p16.3 由 Jonathan Mangion, Nazneen Rahman, Sarah Edkins, Rita Barfoot, Trang Thi Thu Nguyen, Ásgeir Sigurðsson, John Townend, David Fitzpatrick, Adrienne M. Flanagan, Michael R. Stratton

    出版 1999
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  3. 3
    LKB1/KRAS mutant lung cancers constitute a genetic subset of NSCLC with increased sensitivity to MAPK and mTOR signalling inhibition

    LKB1/KRAS mutant lung cancers constitute a genetic subset of NSCLC with increased sensitivity to MAPK and mTOR signalling inhibition 由 Claire Mahoney, Bhudipa Choudhury, Helen Davies, Sarah Edkins, Chris Greenman, Gijs van Haaften, Tatiana Mironenko, Thomas Santarius, Claire Stevens, Michael R. Stratton, P. Andrew Futreal

    出版 2009
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  4. 4
    The V617F JAK2 mutation is uncommon in cancers and in myeloid malignancies other than the classic myeloproliferative disorders

    The V617F JAK2 mutation is uncommon in cancers and in myeloid malignancies other than the classic myeloproliferative disorders 由 Linda M. Scott, Peter J. Campbell, E. Joanna Baxter, Tony Todd, Philip Stephens, Sarah Edkins, Richard Wooster, Michael R. Stratton, P. Andrew Futreal, Anthony R. Green

    出版 2005
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  5. 5
    PICNIC: an algorithm to predict absolute allelic copy number variation with microarray cancer data

    PICNIC: an algorithm to predict absolute allelic copy number variation with microarray cancer data 由 Chris Greenman, Graham R. Bignell, Adam P. Butler, Sarah Edkins, Jonathan Hinton, David Beare, S. Swamy, Thomas Santarius, Lina Chen, Sara Widaa, P. Andrew Futreal, Michael R. Stratton

    出版 2009
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  6. 6
    Mutations in the <i>RSK2(RPS6KA3)</i> gene cause Coffin–Lowry syndrome and nonsyndromic X‐linked mental retardation

    Mutations in the <i>RSK2(RPS6KA3)</i> gene cause Coffin–Lowry syndrome and nonsyndromic X‐linked mental retardation 由 Michael Field, Patrick Tarpey, J Boyle, Sarah Edkins, Judith Goodship, Ying Luo, Jennifer A. Moon, Jon W. Teague, MR Stratton, PA Futreal, Richard Wooster, FL Raymond, Gillian Turner

    出版 2006
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  7. 7
    <i>GLO1</i>—A novel amplified gene in human cancer

    <i>GLO1</i>—A novel amplified gene in human cancer 由 Thomas Santarius, Graham R. Bignell, Chris Greenman, Sara Widaa, Lina Chen, Claire Mahoney, Adam P. Butler, Sarah Edkins, Sahar Waris, Paul J. Thornalley, P. Andrew Futreal, Michael R. Stratton

    出版 2010
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  8. 8
    Identification and characterization of two novel JARID1C mutations: suggestion of an emerging genotype–phenotype correlation

    Identification and characterization of two novel JARID1C mutations: suggestion of an emerging genotype–phenotype correlation 由 Sinitdhorn Rujirabanjerd, John W. Nelson, Patrick Tarpey, Anna Hackett, Sarah Edkins, F. Lucy Raymond, Charles E. Schwartz, Gillian Turner, Shigeki Iwase, Yang Shi, P. Andrew Futreal, Michael R. Stratton, Jozef Gécz

    出版 2009
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  9. 9
    Oligosaccharyltransferase-Subunit Mutations in Nonsyndromic Mental Retardation

    Oligosaccharyltransferase-Subunit Mutations in Nonsyndromic Mental Retardation 由 Florence Molinari, François Foulquier, Patrick Tarpey, Willy Morelle, Sarah Boissel, Jon W. Teague, Sarah Edkins, P. Andrew Futreal, Michael R. Stratton, Gillian Turner, Gert Matthijs, Jozef Gécz, Arnold Münnich, Laurence Colleaux

    出版 2008
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  10. 10
    Erratum: Identification and characterization of two novel JARID1C mutations: suggestion of an emerging genotype-phenotype correlation

    Erratum: Identification and characterization of two novel JARID1C mutations: suggestion of an emerging genotype-phenotype correlation 由 Sinitdhorn Rujirabanjerd, John W. Nelson, Patrick Tarpey, Anna Hackett, Sarah Edkins, F. Lucy Raymond, Charles E. Schwartz, Gillian Turner, Shigeki Iwase, Yang Shi, P. Andrew Futreal, Michael R. Stratton, Jozef Gécz

    出版 2012
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  11. 11
    A survey of homozygous deletions in human cancer genomes

    A survey of homozygous deletions in human cancer genomes 由 Charles Cox, Graham R. Bignell, Chris Greenman, Arne Stabenau, William Warren, Philip Stephens, Helen Davies, Stephen M. Watt, Jon W. Teague, Sarah Edkins, Ewan Birney, Douglas F. Easton, Richard Wooster, P. Andrew Futreal, Michael R. Stratton

    出版 2005
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  12. 12
    A Gene for Lymphedema-Distichiasis Maps to 16q24.3

    A Gene for Lymphedema-Distichiasis Maps to 16q24.3 由 Jonathan Mangion, Nazneen Rahman, Sahar Mansour, Glen Brice, Jane L. Rosbotham, Anne H. Child, Victoria A. Murday, Peter Mortimer, Rita Barfoot, A Sigurdsson, Sarah Edkins, M. Sarfarazi, K G Burnand, Alison Evans, T. O. NUNAN, Michael R. Stratton, Steve Jeffery

    出版 1999
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  13. 13
    Gata2 as a Crucial Regulator of Stem Cells in Adult Hematopoiesis and Acute Myeloid Leukemia

    Gata2 as a Crucial Regulator of Stem Cells in Adult Hematopoiesis and Acute Myeloid Leukemia 由 Juan Bautista Menendez-Gonzalez, Milica Vukovic, Ali Abdelfattah, Lubaid Saleh, Alhomidi Almotiri, Leigh-anne Thomas, Aloña Agirre‐Lizaso, Aleksandra Azevedo, Ana Catarina Menezes, Giusy Tornillo, Sarah Edkins, Kay Kong, Peter Giles, Fernando Anjos‐Afonso, Alex Tonks, Ashleigh S. Boyd, Kamil R. Kranc, Neil P. Rodrigues

    出版 2019
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  14. 14
    The Gene for Juvenile Hyaline Fibromatosis Maps to Chromosome 4q21

    The Gene for Juvenile Hyaline Fibromatosis Maps to Chromosome 4q21 由 Nazneen Rahman, Melanie Dunstan, M. Dawn Teare, Sandra Hanks, Sarah Edkins, Jaime Hughes, Graham R. Bignell, Grazia M.S. Mancini, Wim J. Kleijer, Mary Ellen Campbell, Gökhan Keser, Carol M. Black, Nigel Williams, Laura Arbour, Matthew L. Warman, Andrea Superti‐Furga, P. Andrew Futreal, F. Michael Pope

    出版 2002
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  15. 15
    The original Lujan syndrome family has a novel missense mutation (p.N1007S) in the MED12 gene

    The original Lujan syndrome family has a novel missense mutation (p.N1007S) in the MED12 gene 由 C E Schwartz, Patrick Tarpey, Herbert A. Lubs, Alain Verloès, Melanie May, Hiba Risheg, Michael J. Friez, PA Futreal, Sarah Edkins, J. Teague, Sylvain Briault, Cindy Skinner, Astrid Bauer‐Carlin, R J Simensen, Sumy Joseph, Julie R. Jones, Jozef Gécz, Michael R. Stratton, F. Lucy Raymond, R.E. Stevenson

    出版 2007
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  16. 16
    Zeb1 modulates hematopoietic stem cell fates required for suppressing acute myeloid leukemia

    Zeb1 modulates hematopoietic stem cell fates required for suppressing acute myeloid leukemia 由 Alhomidi Almotiri, Hamed Alzahrani, Juan Bautista Menendez-Gonzalez, Ali Abdelfattah, Badi Alotaibi, Lubaid Saleh, Adelle Greene, M. Georgiou, Alex Gibbs, Amani Alsayari, Sarab Taha, Leigh-anne Thomas, Dhruv Shah, Sarah Edkins, Peter Giles, Marc P. Stemmler, Simone Brabletz, Thomas Brabletz, Ashleigh S. Boyd, Florian A. Siebzehnrübl, Neil P. Rodrigues

    出版 2020
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  17. 17
    Recurrent KRAS codon 146 mutations in human colorectal cancer

    Recurrent KRAS codon 146 mutations in human colorectal cancer 由 Sarah Edkins, Sarah O’Meara, Adrian G. Parker, Claire Stevens, Marcelo Reis, Siân Jones, Chris Greenman, Helen Davies, Gillian L. Dalgliesh, Simon Forbes, Chris Hunter, Raffaella Smith, Philip Stephens, Peter Goldstraw, Andrew G. Nicholson, Tsun Leung Chan, Victor E. Velculescu, Siu Tsan Yuen, Suet Yi Leung, Michael R. Stratton, P. Andrew Futreal

    出版 2006
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  18. 18
    Signatures of mutation and selection in the cancer genome

    Signatures of mutation and selection in the cancer genome 由 Graham R. Bignell, Chris Greenman, Helen Davies, Adam P. Butler, Sarah Edkins, J. M. Andrews, Gemma Buck, Lina Chen, David Beare, Calli Latimer, Sara Widaa, Jonathon Hinton, Ciara Fahey, Beiyuan Fu, Sajani Swamy, Gillian L. Dalgliesh, Bin Tean Teh, Panos Deloukas, Fengtang Yang, Peter J. Campbell, P. Andrew Futreal, Michael R. Stratton

    出版 2010
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  19. 19
    Identification of somatically acquired rearrangements in cancer using genome-wide massively parallel paired-end sequencing

    Identification of somatically acquired rearrangements in cancer using genome-wide massively parallel paired-end sequencing 由 Peter J. Campbell, Philip J. Stephens, Erin Pleasance, Sarah O’Meara, Heng Li, Thomas Santarius, Lucy Stebbings, Catherine Leroy, Sarah Edkins, Claire Hardy, Jon W. Teague, Andrew Menzies, Ian Goodhead, Daniel J. Turner, Christopher Clee, Michael A. Quail, Antony V. Cox, Clive Brown, Richard Durbin, Matthew E. Hurles, Paul A. Edwards, Graham R. Bignell, Michael R. Stratton, P. Andrew Futreal

    出版 2008
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  20. 20
    SLC9A6 Mutations Cause X-Linked Mental Retardation, Microcephaly, Epilepsy, and Ataxia, a Phenotype Mimicking Angelman Syndrome

    SLC9A6 Mutations Cause X-Linked Mental Retardation, Microcephaly, Epilepsy, and Ataxia, a Phenotype Mimicking Angelman Syndrome 由 Gregor D. Gilfillan, Kaja Kristine Selmer, Ingrid Roxrud, Raffaella Smith, Mårten Kyllerman, Kristin Eiklid, Mette Kroken, Morten Mattingsdal, Thore Egeland, Harald Stenmark, Hans Sjöholm, Andrés Server, Lena Samuelsson, Arnold L. Christianson, Patrick Tarpey, Annabel Whibley, Michael R. Stratton, P. Andrew Futreal, Jon W. Teague, Sarah Edkins, Jozef Gécz, Gillian Turner, F. Lucy Raymond, Charles E. Schwartz, Roger E. Stevenson, Dag E. Undlien, Petter Strømme

    出版 2008
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