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Wyszukujesz frazę ""Taylor, GR"" wg kryterium: Autor

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Wyświetlanie 1-20 z 62
Tytuł:
High-Throughput Amplicon-Based Copy Number Detection of 11 Genes in Formalin-Fixed Paraffin-Embedded Ovarian Tumour Samples by MLPA-Seq.
Autorzy:
Kondrashova O; Department of Pathology, University of Melbourne, Melbourne, VIC, Australia.
Love CJ; Department of Pathology, University of Melbourne, Melbourne, VIC, Australia.
Lunke S; Department of Pathology, University of Melbourne, Melbourne, VIC, Australia.
Hsu AL; Department of Pathology, University of Melbourne, Melbourne, VIC, Australia.
Waring PM; Department of Pathology, University of Melbourne, Melbourne, VIC, Australia.
Taylor GR; Department of Pathology, University of Melbourne, Melbourne, VIC, Australia.
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Corporate Authors:
Australian Ovarian Cancer Study (AOCS) Group
Źródło:
PloS one [PLoS One] 2015 Nov 16; Vol. 10 (11), pp. e0143006. Date of Electronic Publication: 2015 Nov 16 (Print Publication: 2015).
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, Non-P.H.S.
MeSH Terms:
Gene Dosage*
Genes, Neoplasm*
Paraffin Embedding*
Tissue Fixation*
High-Throughput Nucleotide Sequencing/*methods
Multiplex Polymerase Chain Reaction/*methods
Ovarian Neoplasms/*genetics
BRCA1 Protein/genetics ; BRCA1 Protein/metabolism ; BRCA2 Protein/genetics ; BRCA2 Protein/metabolism ; Cyclin E/genetics ; Cyclin E/metabolism ; DNA Copy Number Variations/genetics ; Female ; Formaldehyde/chemistry ; Humans ; Limit of Detection ; Oncogene Proteins/genetics ; Oncogene Proteins/metabolism ; Receptor, ErbB-2/genetics ; Receptor, ErbB-2/metabolism ; Reproducibility of Results ; Sensitivity and Specificity
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknieSzczegóły
Tytuł:
A feasibility study testing four hypotheses with phase II outcomes in advanced colorectal cancer (MRC FOCUS3): a model for randomised controlled trials in the era of personalised medicine?
Autorzy:
Maughan TS; CRUK/MRC Oxford Institute for Radiation Oncology, University of Oxford, Oxford OX3 7DQ, UK.
Meade AM; MRC Clinical Trials Unit at UCL, Institute of Clinical Trials and Methodology, London WC2B 6NH, UK.
Adams RA; Cardiff University and Velindre Cancer Centre, Cardiff, UK.
Richman SD; Leeds Institute of Cancer and Pathology, University of Leeds, Leeds LS9 7TF, UK.
Butler R; University Hospital of Wales, Cardiff CF14 4XW, UK.
Fisher D; MRC Clinical Trials Unit at UCL, Institute of Clinical Trials and Methodology, London WC2B 6NH, UK.
Wilson RH; Centre for Cancer Research and Cell Biology, Queen's University Belfast, Belfast BT9 7AE, UK.
Jasani B; Institute of Cancer and Genetics, Cardiff University, Cardiff CF14 4XN, UK.
Taylor GR; Leeds Institute of Cancer and Pathology, University of Leeds, Leeds LS9 7TF, UK.
Williams GT; Institute of Cancer and Genetics, Cardiff University, Cardiff CF14 4XN, UK.
Sampson JR; Institute of Cancer and Genetics, Cardiff University, Cardiff CF14 4XN, UK.
Seymour MT; St James's Institute of Oncology, University of Leeds, Leeds LS9 7TF, UK.
Nichols LL; MRC Clinical Trials Unit at UCL, Institute of Clinical Trials and Methodology, London WC2B 6NH, UK.
Kenny SL; MRC Clinical Trials Unit at UCL, Institute of Clinical Trials and Methodology, London WC2B 6NH, UK.
Nelson A; Wales Cancer Trials Unit, Cardiff University, Cardiff CF14 4YS, UK.
Sampson CM; Wales Cancer Trials Unit, Cardiff University, Cardiff CF14 4YS, UK.
Hodgkinson E; Sheffield Teaching Hospitals NHS Foundation Trust, Sheffield S5 7AU, UK.
Bridgewater JA; UCL Cancer Institute, London WC1E 6BT, UK.
Furniss DL; Sheffield Teaching Hospitals NHS Foundation Trust, Sheffield S5 7AU, UK.
Roy R; Department of Oncology, Castle Hill Hospital, East Riding of Yorkshire HU16 5JQ, UK.
Pope MJ; MRC Clinical Trials Unit at UCL, Institute of Clinical Trials and Methodology, London WC2B 6NH, UK.
Pope JK; MRC Clinical Trials Unit at UCL, Institute of Clinical Trials and Methodology, London WC2B 6NH, UK.
Parmar M; MRC Clinical Trials Unit at UCL, Institute of Clinical Trials and Methodology, London WC2B 6NH, UK.
Quirke P; Leeds Institute of Cancer and Pathology, University of Leeds, Leeds LS9 7TF, UK.
Kaplan R; MRC Clinical Trials Unit at UCL, Institute of Clinical Trials and Methodology, London WC2B 6NH, UK.
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Źródło:
British journal of cancer [Br J Cancer] 2014 Apr 29; Vol. 110 (9), pp. 2178-86. Date of Electronic Publication: 2014 Apr 17.
Typ publikacji:
Clinical Trial, Phase II; Journal Article; Randomized Controlled Trial; Research Support, Non-U.S. Gov't
MeSH Terms:
Precision Medicine*
Colorectal Neoplasms/*drug therapy
Colorectal Neoplasms/*genetics
Proto-Oncogene Proteins/*genetics
Proto-Oncogene Proteins B-raf/*genetics
ras Proteins/*genetics
Aged ; Aged, 80 and over ; Biomarkers, Tumor/analysis ; Colorectal Neoplasms/mortality ; DNA Mutational Analysis ; Disease-Free Survival ; Feasibility Studies ; Female ; Humans ; Male ; Middle Aged ; Proto-Oncogene Proteins p21(ras) ; Treatment Outcome
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknieSzczegóły
Tytuł:
Mutations in NMNAT1 cause Leber congenital amaurosis and identify a new disease pathway for retinal degeneration.
Autorzy:
Koenekoop RK; McGill Ocular Genetics Laboratory, McGill University Health Centre, Montreal, Quebec, Canada.
Wang H
Majewski J
Wang X
Lopez I
Ren H
Chen Y
Li Y
Fishman GA
Genead M
Schwartzentruber J
Solanki N
Traboulsi EI
Cheng J
Logan CV
McKibbin M
Hayward BE
Parry DA
Johnson CA
Nageeb M
Poulter JA
Mohamed MD
Jafri H
Rashid Y
Taylor GR
Keser V
Mardon G
Xu H
Inglehearn CF
Fu Q
Toomes C
Chen R
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Corporate Authors:
Finding of Rare Disease Genes (FORGE) Canada Consortium
Źródło:
Nature genetics [Nat Genet] 2012 Sep; Vol. 44 (9), pp. 1035-9. Date of Electronic Publication: 2012 Jul 29.
Typ publikacji:
Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
MeSH Terms:
Mutation*/physiology
Leber Congenital Amaurosis/*genetics
Nicotinamide-Nucleotide Adenylyltransferase/*genetics
Retinal Degeneration/*genetics
Adolescent ; Adult ; Child ; Cohort Studies ; Family ; Female ; Genetic Predisposition to Disease ; HeLa Cells ; Humans ; Leber Congenital Amaurosis/complications ; Male ; Middle Aged ; Nicotinamide-Nucleotide Adenylyltransferase/physiology ; Pedigree ; Retinal Degeneration/complications ; Signal Transduction/genetics ; Young Adult
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknieSzczegóły
Tytuł:
Mutations in MEGF10, a regulator of satellite cell myogenesis, cause early onset myopathy, areflexia, respiratory distress and dysphagia (EMARDD).
Autorzy:
Logan CV; Leeds Institute of Molecular Medicine, The University of Leeds, UK.
Lucke B
Pottinger C
Abdelhamed ZA
Parry DA
Szymanska K
Diggle CP
van Riesen A
Morgan JE
Markham G
Ellis I
Manzur AY
Markham AF
Shires M
Helliwell T
Scoto M
Hübner C
Bonthron DT
Taylor GR
Sheridan E
Muntoni F
Carr IM
Schuelke M
Johnson CA
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Źródło:
Nature genetics [Nat Genet] 2011 Nov 20; Vol. 43 (12), pp. 1189-92. Date of Electronic Publication: 2011 Nov 20.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Abnormalities, Multiple/*genetics
Deglutition Disorders/*genetics
Membrane Proteins/*genetics
Muscular Diseases/*genetics
Respiratory Distress Syndrome, Newborn/*genetics
Satellite Cells, Skeletal Muscle/*metabolism
Adolescent ; Child ; Child, Preschool ; Consanguinity ; Deltoid Muscle/pathology ; Female ; Frameshift Mutation ; Genetic Association Studies ; Heredity ; Humans ; INDEL Mutation ; Infant ; Infant, Newborn ; Male ; Muscle Development/genetics ; Mutation, Missense ; Pedigree ; Sequence Analysis, DNA
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknieSzczegóły
Tytuł:
Clarity and claims in variation/mutation databasing.
Autorzy:
Dalgleish R
Oetting WS
Auerbach AD
Beckmann JS
Cambon-Thomsen A
Devereau A
Greenblatt MS
Patrinos GP
Taylor GR
Vihinen M
Brookes AJ
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Źródło:
Nature biotechnology [Nat Biotechnol] 2011 Sep 08; Vol. 29 (9), pp. 790-2; author reply 792-4. Date of Electronic Publication: 2011 Sep 08.
Typ publikacji:
Letter; Comment
MeSH Terms:
Database Management Systems*
Databases, Nucleic Acid*
DNA/*genetics
Humans
Opinia redakcyjna
Pełny tekst  Link otwiera się w nowym oknieSzczegóły
Tytuł:
Rheumatoid forefoot reconstruction: first metatarsophalangeal joint fusion combined with weil's metatarsal osteotomies of the lesser rays.
Autorzy:
Bolland BJ
Sauvé PS
Taylor GR
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Źródło:
Journal of Foot & Ankle Surgery; Mar2008, Vol. 47 Issue 2, p80-88, 9p
Czasopismo naukowe
Szczegóły
Tytuł:
Complex pediatric elbow injury: an uncommon case.
Autorzy:
Sharma H; Department of Trauma and Orthopaedics, Victoria Infirmary, Glasgow, G42 9TY, UK. />Ayer R
Taylor GR
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Źródło:
BMC musculoskeletal disorders [BMC Musculoskelet Disord] 2005 Mar 09; Vol. 6, pp. 13. Date of Electronic Publication: 2005 Mar 09.
Typ publikacji:
Case Reports; Journal Article
MeSH Terms:
Bone Wires*
Elbow Injuries*
Fracture Fixation, Internal/*methods
Fractures, Bone/*surgery
Joint Dislocations/*therapy
Child ; Elbow Joint/diagnostic imaging ; Fractures, Bone/diagnostic imaging ; Humans ; Joint Dislocations/diagnostic imaging ; Male ; Radiography
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknieSzczegóły
Tytuł:
Investigations on a clinically and functionally unusual and novel germline p53 mutation.
Autorzy:
Rutherford J; Richard Dimbleby Department Cancer Research, Guy's, King's and St Thomas' School of Medicine, St Thomas' Hospital, London SE1 7EH, UK.
Chu CE
Duddy PM
Charlton RS
Chumas P
Taylor GR
Lu X
Barnes DM
Camplejohn RS
Pokaż więcej
Źródło:
British journal of cancer [Br J Cancer] 2002 May 20; Vol. 86 (10), pp. 1592-6.
Typ publikacji:
Case Reports; Journal Article
MeSH Terms:
Codon, Nonsense*
Frameshift Mutation*
Genes, p53*
Germ-Line Mutation*
Mutagenesis, Insertional*
Bone Neoplasms/*genetics
Choroid Plexus Neoplasms/*genetics
Neoplasm Proteins/*physiology
Neoplasms, Second Primary/*genetics
Osteosarcoma/*genetics
Papilloma/*genetics
Tumor Suppressor Protein p53/*physiology
Adult ; Alleles ; Amino Acid Substitution ; Apoptosis ; Base Sequence ; Bone Neoplasms/pathology ; DNA Mutational Analysis ; DNA, Neoplasm/genetics ; Exons/genetics ; Female ; Genetic Predisposition to Disease ; Humans ; Lymphocytes/pathology ; Lymphocytes/radiation effects ; Molecular Sequence Data ; Neoplasm Proteins/chemistry ; Neoplasm Proteins/deficiency ; Osteosarcoma/pathology ; Pedigree ; Recombinant Fusion Proteins/physiology ; Saccharomyces cerevisiae/genetics ; Transcriptional Activation ; Transfection ; Tumor Cells, Cultured/pathology ; Tumor Stem Cell Assay ; Tumor Suppressor Protein p53/chemistry ; Tumor Suppressor Protein p53/deficiency
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknieSzczegóły
Wyświetlanie 1-20 z 62

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