يعرض 1 - 10 نتائج من 15 نتيجة بحث عن '"Kelly Halliday"', وقت الاستعلام: 1.12s تنقيح النتائج
  1. 1
    Supplementary Information from A Hypermutation Phenotype and Somatic MSH6 Mutations in Recurrent Human Malignant Gliomas after Alkylator Chemotherapy

    المؤلفون: Richard Wooster, P. Andrew Futreal, Michael R. Stratton, David N. Louis, Tracy T. Batchelor, Wolf Mueller, Kymberly K. Levine, Jennifer E. Roy, Gregory Riggins, Douglas F. Easton, Andy Yates, Sara Widaa, Sofie West, Jennifer Varian, Calli Tofts, Helen Solomon, Alexandra Small, Rebecca Shepherd, David Richardson, Keiran Raine, Robert Petty, Janet Perry, Andrew Menzies, Richard Lugg, Ross Laman, Vivienne Kosmidou, David Jones, Andy Jenkinson, Jonathon Hinton, Katy Hills, Rachel Harrison, Kelly Halliday, Kristian Gray, Matthew Gorton, Simon Forbes, Ed Dicks, Jennifer Cole, Jody Clements, Adam Butler, Gemma Buck, Lisa Brackenbury, Syd Barthorpe, Tim Avis, Adrian Parker, Sarah O'Meara, Helen Davies, Graham Bignell, Sarah Edkins, Chris Greenman, Jon Teague, Claire Stevens, Philip Stephens, Daniel P. Cahill, Raffaella Smith, Chris Hunter

    URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::96d0e7301459a6795af7b4fc360e50d5
    https://doi.org/10.1158/0008-5472.22366754.v1

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  2. 2
    Supplementary Glioma Genes from A Hypermutation Phenotype and Somatic MSH6 Mutations in Recurrent Human Malignant Gliomas after Alkylator Chemotherapy

    المؤلفون: Richard Wooster, P. Andrew Futreal, Michael R. Stratton, David N. Louis, Tracy T. Batchelor, Wolf Mueller, Kymberly K. Levine, Jennifer E. Roy, Gregory Riggins, Douglas F. Easton, Andy Yates, Sara Widaa, Sofie West, Jennifer Varian, Calli Tofts, Helen Solomon, Alexandra Small, Rebecca Shepherd, David Richardson, Keiran Raine, Robert Petty, Janet Perry, Andrew Menzies, Richard Lugg, Ross Laman, Vivienne Kosmidou, David Jones, Andy Jenkinson, Jonathon Hinton, Katy Hills, Rachel Harrison, Kelly Halliday, Kristian Gray, Matthew Gorton, Simon Forbes, Ed Dicks, Jennifer Cole, Jody Clements, Adam Butler, Gemma Buck, Lisa Brackenbury, Syd Barthorpe, Tim Avis, Adrian Parker, Sarah O'Meara, Helen Davies, Graham Bignell, Sarah Edkins, Chris Greenman, Jon Teague, Claire Stevens, Philip Stephens, Daniel P. Cahill, Raffaella Smith, Chris Hunter

    URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::843c39d3c59a93addd968798398f0edf
    https://doi.org/10.1158/0008-5472.22366757

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  3. 3
    Supplementary Glioma Gene Mutations from A Hypermutation Phenotype and Somatic MSH6 Mutations in Recurrent Human Malignant Gliomas after Alkylator Chemotherapy

    المؤلفون: Richard Wooster, P. Andrew Futreal, Michael R. Stratton, David N. Louis, Tracy T. Batchelor, Wolf Mueller, Kymberly K. Levine, Jennifer E. Roy, Gregory Riggins, Douglas F. Easton, Andy Yates, Sara Widaa, Sofie West, Jennifer Varian, Calli Tofts, Helen Solomon, Alexandra Small, Rebecca Shepherd, David Richardson, Keiran Raine, Robert Petty, Janet Perry, Andrew Menzies, Richard Lugg, Ross Laman, Vivienne Kosmidou, David Jones, Andy Jenkinson, Jonathon Hinton, Katy Hills, Rachel Harrison, Kelly Halliday, Kristian Gray, Matthew Gorton, Simon Forbes, Ed Dicks, Jennifer Cole, Jody Clements, Adam Butler, Gemma Buck, Lisa Brackenbury, Syd Barthorpe, Tim Avis, Adrian Parker, Sarah O'Meara, Helen Davies, Graham Bignell, Sarah Edkins, Chris Greenman, Jon Teague, Claire Stevens, Philip Stephens, Daniel P. Cahill, Raffaella Smith, Chris Hunter

    URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4ae2ab66f6628c677ca985204a900e72
    https://doi.org/10.1158/0008-5472.22366760.v1

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  4. 4
    Data from A Hypermutation Phenotype and Somatic MSH6 Mutations in Recurrent Human Malignant Gliomas after Alkylator Chemotherapy

    المؤلفون: Richard Wooster, P. Andrew Futreal, Michael R. Stratton, David N. Louis, Tracy T. Batchelor, Wolf Mueller, Kymberly K. Levine, Jennifer E. Roy, Gregory Riggins, Douglas F. Easton, Andy Yates, Sara Widaa, Sofie West, Jennifer Varian, Calli Tofts, Helen Solomon, Alexandra Small, Rebecca Shepherd, David Richardson, Keiran Raine, Robert Petty, Janet Perry, Andrew Menzies, Richard Lugg, Ross Laman, Vivienne Kosmidou, David Jones, Andy Jenkinson, Jonathon Hinton, Katy Hills, Rachel Harrison, Kelly Halliday, Kristian Gray, Matthew Gorton, Simon Forbes, Ed Dicks, Jennifer Cole, Jody Clements, Adam Butler, Gemma Buck, Lisa Brackenbury, Syd Barthorpe, Tim Avis, Adrian Parker, Sarah O'Meara, Helen Davies, Graham Bignell, Sarah Edkins, Chris Greenman, Jon Teague, Claire Stevens, Philip Stephens, Daniel P. Cahill, Raffaella Smith, Chris Hunter

    URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::588bec3d7e4554e771f3e1702e327bb2
    https://doi.org/10.1158/0008-5472.c.6495272.v1

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  5. 5
    Mutations in the BRWD3 Gene Cause X-Linked Mental Retardation Associated with Macrocephaly

    المؤلفون: Kelly Halliday, F. Lucy Raymond, Kristian Gray, Sofie West, Rebecca Shepherd, Sara Widaa, Syd Barthorpe, P. Andrew Futreal, Gillian Turner, H. E. Hughes, Claire Stevens, Alexandra Small, Mark A. Corbett, Andrew M. Jenkinson, Gemma Buck, Roger E. Stevenson, Sarah O’Meara, Raffaella Smith, Marie Shaw, Jozef Gecz, David S. Richardson, Andrew Menzies, Calli Tofts, Janet Perry, Uma Mallya, Jennifer Varian, Michael R. Stratton, John C. Mulley, Tatiana Mironenko, David T. Jones, Michael Partington, Patrick S. Tarpey, Ed Dicks, Richard Wooster, Martin Bobrow, Jenny Moon, Jennifer Cole, Sarah Edkins, Charles E. Schwartz, Ying Luo, Keiran Raine, Katy Hills, Adam Butler, Michael Field, Jon W. Teague, Kathryn Friend

    المصدر: The American Journal of Human Genetics. 81(2):367-374

    مصطلحات موضوعية: Male, Biology, medicine.disease_cause, Report, Intellectual disability, medicine, Genetics, Humans, Abnormalities, Multiple, Genetics(clinical), Gene, Genetics (clinical), X chromosome, Mutation, Macrocephaly, medicine.disease, Phenotype, Bromodomain, Pedigree, Developmental disorder, Mental Retardation, X-Linked, medicine.symptom, Head, Sequence Alignment, Transcription Factors

    URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fe8a751d98f32479c99f003601ddfbd4

    View record from ScienceDirect
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  6. 6
    X-linked protocadherin 19 mutations cause female-limited epilepsy and cognitive impairment

    المؤلفون: Lucianne Vandeleur, Amos D. Korczyn, Michael R. Stratton, Andrew M. Jenkinson, Samantha J. Turner, Gemma Buck, Raffaella Smith, Tatiana Mironenko, David T. Jones, Syd Barthorpe, Adam Butler, Samuel F. Berkovic, Ingrid E. Scheffer, Mark A. Corbett, Zaid Afawi, Sarah O’Meara, Leanne M. Dibbens, Kelly Halliday, Paul Q. Thomas, Andrew Menzies, Daniel H. Geschwind, Jozef Gecz, Marta A. Bayly, John Teague, Tally Lerman-Sagie, Paul Wray, James F. Gusella, Shane McKee, John C. Mulley, Sofie West, Christopher P. Derry, Eric Haan, Hyung Goo Kim, Dorit Lev, Rebecca Shepherd, Aziz Mazarib, Calli Tofts, Rebecca Lee, Mark Madison, Marie Shaw, Edwina Sutton, Jennifer Cole, Sarah Edkins, Grant R. Sutherland, Claire Stevens, Cheryl Shoubridge, Jamee M. Bomar, Jennifer Varian, Miriam Y. Neufeld, Stephen G Ryan, Ed Dicks, Patrick S. Tarpey, Kim Hynes, Sara Widaa, P. Andrew Futreal, Sara Kivity, Kathryn Friend

    المساهمون: Dibbens, Leanne M, Tarpey, Patrick S, Hynes, Kim, Bayly, Marta A, Gecz, Jozef

    مصطلحات موضوعية: Male, medicine.medical_specialty, Mutation, Missense, Protocadherin, Gene mutation, Biology, medicine.disease_cause, Epilepsy, Genomic Imprinting, Mice, Basic Science, Genes, X-Linked, Genetics, medicine, Missense mutation, Animals, Humans, RNA, Messenger, Gene, X chromosome, In Situ Hybridization, Skin, Mutation, Chromosomes, Human, X, Reverse Transcriptase Polymerase Chain Reaction, Brain, Gene Expression Regulation, Developmental, Fibroblasts, medicine.disease, Cadherins, Protocadherins, Pedigree, Phenotype, Codon, Nonsense, Case-Control Studies, Mental Retardation, X-Linked, Medical genetics, Female, Cognition Disorders

    URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::31979957e8a81d88068cf27150e29bef
    https://hdl.handle.net/1959.8/128633

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  7. 7
    Patterns of somatic mutation in human cancer genomes

    المؤلفون: David N. Louis, Syd Barthorpe, Peter J. Campbell, Richard Wooster, Claire Stevens, Douglas F. Easton, Daniel P. Cahill, Ewan Birney, Keiran Raine, Simon A. Forbes, Gurpreet Bhamra, Jon Hinton, Michael R. Stratton, Tim Avis, Barbara L. Weber, Andy Menzies, Bhudipa Choudhury, Yoke Eng Chiew, Andrew D. Yates, Georgia Chenevix-Trench, Imre Vastrik, Gillian L. Dalgliesh, Andrew G. Nicholson, Alexandra Small, Ed Dicks, Janet Perry, Anthony R. Green, Sarah O’Meara, Raffaella Smith, Rachel Harrison, Bin Tean Teh, Sofie West, Tony Webb, Adam Butler, Sara Widaa, Gemma Buck, Rebecca Shepherd, Jennifer Cole, Sarah Edkins, Jennifer Varian, Peter Goldstraw, Andy Jenkinson, Jon W. Teague, Helen Davies, Sok Kean Khoo, Kris Gray, Suet Yi Leung, Calli Tofts, Dave Richardson, Christopher Greenman, P. Andrew Futreal, Tatiana Mironenko, Jody Clements, David T. Jones, Anna deFazio, Katy Hills, Kelly Halliday, Min-Han Tan, Siu Tsan Yuen, Philip J. Stephens, Christopher I. Hunter, Francis Brasseur, Leendert H. J. Looijenga, Mel Greaves, Esther Schmidt, Graham R. Bignell

    مصطلحات موضوعية: DNA Mutational Analysis, Molecular Sequence Data, Genomics, Biology, medicine.disease_cause, Genome, Article, Germline mutation, Neoplasms, medicine, Humans, Amino Acid Sequence, Genetics, Mutation, Multidisciplinary, Genome, Human, Cancer, medicine.disease, Neoplasm Proteins, Kataegis, Human genome, Carcinogenesis, Protein Kinases, Genes, Neoplasm

    URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8181b6b39035a77f21373fb15d405e3d
    https://europepmc.org/articles/PMC2712719/

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  8. 8
    Mutations in CUL4B, Which Encodes a Ubiquitin E3 Ligase Subunit, Cause an X-linked Mental Retardation Syndrome Associated with Aggressive Outbursts, Seizures, Relative Macrocephaly, Central Obesity, Hypogonadism, Pes Cavus, and Tremor

    المؤلفون: Patrick S. Tarpey, Richard Wooster, Tatiana Mironenko, David T. Jones, Michael R. Stratton, Jackie Boyle, Claire Stevens, Sarah F. Smithson, Janet Perry, Alexandra Small, Kelly Halliday, Sara Widaa, Syd Barthorpe, Jennifer Varian, David S. Richardson, Anand Srivastava, Lucianne Vandeleur, Sarah O’Meara, Jozef Gecz, Charles E. Schwartz, Jenny Moon, Jennifer Cole, Ed Dicks, Tim Avis, Sarah Edkins, Susan E. Holder, Andrew Menzies, Roger E. Stevenson, Gillian Turner, Andrew M. Jenkinson, Ying Luo, Douglas F. Easton, F. Lucy Raymond, Jill Clayton-Smith, Jane A. Hurst, Gemma Buck, Jayson Rodriguez, Rachel Harrison, Keiran Raine, Marie Shaw, Rebecca Shepherd, Katy Hills, Calli Tofts, Uma Mallya, Bronwyn Kerr, Adam Butler, Jon W. Teague, Rachel Slaugh, Sofie West, P. Andrew Futreal, Martin Bobrow, Michael Partington, Kristian Gray

    مصطلحات موضوعية: Foot Deformities, Male, medicine.medical_specialty, Pes cavus, Ubiquitin-Protein Ligases, Molecular Sequence Data, Poison control, Short stature, 03 medical and health sciences, 0302 clinical medicine, Seizures, Internal medicine, Report, Tremor, Genetics, medicine, Missense mutation, Humans, Genetics(clinical), Abnormalities, Multiple, Amino Acid Sequence, Obesity, Child, Genetics (clinical), 030304 developmental biology, 0303 health sciences, biology, business.industry, Hypogonadism, Macrocephaly, medicine.disease, Cullin Proteins, Ubiquitin ligase, Aggression, Protein Subunits, Endocrinology, Child, Preschool, Mutation, biology.protein, Mental Retardation, X-Linked, Intention tremor, CUL4B, medicine.symptom, business, Head, 030217 neurology & neurosurgery

    URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::02448979caa304c89b5488e2b60debc7
    https://europepmc.org/articles/PMC1785336/

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  9. 9
    Mutations in UPF3B, a member of the nonsense-mediated mRNA decay complex, cause syndromic and nonsyndromic mental retardation

    المؤلفون: Syd Barthorpe, Mark A. Corbett, George Hoganson, Doug A. Brooks, John Teague, Richard Wooster, Claire Stevens, Charles E. Schwartz, Janet Perry, Jennifer Varian, Jennifer Cole, Sarah Edkins, P. Andrew Futreal, John P. Warner, Jayson Rodriguez, David S. Richardson, Anand Srivastava, Paul Q. Thomas, Jenny Moon, Gillian Turner, F. Lucy Raymond, Cheryl Shoubridge, Michael R. Stratton, Duane W Superneau, Andrew Menzies, Patrick S. Tarpey, Adam Butler, Lam Son Nguyen, Raffaella Smith, Martin Bobrow, Sofie West, Pauline Pearson, Tracy Sanderson, Sarah O’Meara, Katy Hills, Emma J. Parkinson-Lawrence, Jozef Gecz, Andrew M. Jenkinson, Rebecca Shepherd, Gemma Buck, Alison Gardner, Kelly Halliday, Josep Parnau, Anna Hackett, Keiran Raine, Richard J. Simensen, Sara Widaa, Cindy Skinner, Calli Tofts, Mary Porteous, Roger E. Stevenson, Tatiana Mironenko, Shambhu Bhat, David T. Jones, Lucianne Vandeleur, Ed Dicks, Yin Luo

    المساهمون: Tarpey, Patrick, Raymond, F Lucy, Nguyen, Lam, Rodriguez, Jayson, Hackett, Anna, Vandeleur, Lucianne, Smith, Raffaella, Shoubridge, Cheryl, Edkins, Sarah, Stevens, Claire, O'Meara, Sarah, Tofts, Calli, Barthorpe, Syd, Buck, Gemma, Cole, Jennifer, Halliday, Kelly, Hills, Katy

    مصطلحات موضوعية: Male, RNA Stability, DNA Mutational Analysis, Immunoblotting, Molecular Sequence Data, Nonsense-mediated decay, RNA-binding protein, Biology, medicine.disease_cause, Article, Genetics, medicine, Humans, Missense mutation, Amino Acid Sequence, RNA, Messenger, Gene, X chromosome, Cell Line, Transformed, Family Health, Mutation, Messenger RNA, Sequence Homology, Amino Acid, Reverse Transcriptase Polymerase Chain Reaction, Gene Expression Profiling, RNA-Binding Proteins, Syndrome, Phenotype, Pedigree, Codon, Nonsense, Mental Retardation, X-Linked, Female

    URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b2fbdc66e723f0bfd983aba61027bf26
    https://hdl.handle.net/1959.8/48618

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  10. 10
    Mutation analysis of 24 known cancer genes in the NCI-60 cell line set

    المؤلفون: Andy Jenkinson, Janet Perry, Jennifer Varian, Michael R. Stratton, Tony Webb, Claire Stevens, Tim Avis, Alex Small, Lisa Brackenbury, Kristian Gray, David S. Richardson, Kelly Halliday, Thomas Santarius, Ogechi Ikediobi, Graham R. Bignell, Syd Barthorpe, Keiran Raine, Calli Tofts, Andrew Menzies, Jennifer Cole, Sarah Edkins, Rachel Harrison, Sarah O’Meara, Raffaella Smith, Jody Clements, Helen Davies, Rebecca Shepherd, Helen Solomon, Tatiana Mironenko, Adrian Parker, David T. Jones, John N. Weinstein, Christopher I. Hunter, Katy Hills, William C. Reinhold, P. Andrew Futreal, Vivienne Kosmidou, Jonathan Hinton, Adam Butler, Jon W. Teague, Andrew D. Yates, Philip J. Stephens, Gemma Buck, Richard Lugg, Ed Dicks, Simon A. Forbes, Richard Wooster, Sara Widaa, Sofie West

    المصدر: Molecular cancer therapeutics. 5(11)

    مصطلحات موضوعية: Neuroblastoma RAS viral oncogene homolog, Cancer Research, Sequence analysis, DNA Mutational Analysis, medicine.disease_cause, Article, Cell Line, Tumor, medicine, PTEN, Humans, HRAS, Genetics, Mutation, biology, Gene Expression Profiling, Homozygote, Cancer, Exons, medicine.disease, Oncology, biology.protein, KRAS, RNA Splice Sites, Carcinogenesis, Gene Deletion, Genes, Neoplasm

    URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7a23ce5956c82521e5c3c6ccd4840927
    https://pubmed.ncbi.nlm.nih.gov/17088437

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