Informacja

Drogi użytkowniku, aplikacja do prawidłowego działania wymaga obsługi JavaScript. Proszę włącz obsługę JavaScript w Twojej przeglądarce.

Wyszukujesz frazę ""Hamby, SE"" wg kryterium: Autor


Wyświetlanie 1-7 z 7
Tytuł:
Novel loss of function mutation in NOTCH1 in a family with bicuspid aortic valve, ventricular septal defect, thoracic aortic aneurysm, and aortic valve stenosis.
Autorzy:
Debiec R; Department of Cardiovascular Sciences, University of Leicester, NIHR (National Institute for Health Research) Leicester Biomedical Research Centre, Glenfield Hospital, Leicester, UK.
Hamby SE; Department of Cardiovascular Sciences, University of Leicester, NIHR (National Institute for Health Research) Leicester Biomedical Research Centre, Glenfield Hospital, Leicester, UK.
Jones PD; Department of Cardiovascular Sciences, University of Leicester, NIHR (National Institute for Health Research) Leicester Biomedical Research Centre, Glenfield Hospital, Leicester, UK.
Coolman S; Department of Cardiovascular Sciences, University of Leicester, NIHR (National Institute for Health Research) Leicester Biomedical Research Centre, Glenfield Hospital, Leicester, UK.
Asiani M; Department of Cardiovascular Sciences, University of Leicester, NIHR (National Institute for Health Research) Leicester Biomedical Research Centre, Glenfield Hospital, Leicester, UK.
Kharodia S; Department of Cardiovascular Sciences, University of Leicester, NIHR (National Institute for Health Research) Leicester Biomedical Research Centre, Glenfield Hospital, Leicester, UK.
Skinner GJ; East Midlands Congenital Heart Centre, Glenfield Hospital, Leicester, UK.
Samani NJ; Department of Cardiovascular Sciences, University of Leicester, NIHR (National Institute for Health Research) Leicester Biomedical Research Centre, Glenfield Hospital, Leicester, UK.
Webb TR; Department of Cardiovascular Sciences, University of Leicester, NIHR (National Institute for Health Research) Leicester Biomedical Research Centre, Glenfield Hospital, Leicester, UK.
Bolger A; Department of Cardiovascular Sciences, University of Leicester, NIHR (National Institute for Health Research) Leicester Biomedical Research Centre, Glenfield Hospital, Leicester, UK.; East Midlands Congenital Heart Centre, Glenfield Hospital, Leicester, UK.
Pokaż więcej
Źródło:
Molecular genetics & genomic medicine [Mol Genet Genomic Med] 2020 Oct; Vol. 8 (10), pp. e1437. Date of Electronic Publication: 2020 Jul 27.
Typ publikacji:
Case Reports; Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Loss of Function Mutation*
Aortic Aneurysm, Thoracic/*genetics
Aortic Valve Stenosis/*genetics
Bicuspid Aortic Valve Disease/*genetics
Heart Septal Defects, Ventricular/*genetics
Receptor, Notch1/*genetics
Adult ; Aged ; Aortic Aneurysm, Thoracic/pathology ; Aortic Valve Stenosis/pathology ; Bicuspid Aortic Valve Disease/pathology ; Codon, Nonsense ; Female ; Heart Septal Defects, Ventricular/pathology ; Humans ; Male ; Middle Aged ; Pedigree ; Phenotype
Czasopismo naukowe
Tytuł:
Adult height and risk of 50 diseases: a combined epidemiological and genetic analysis.
Autorzy:
Lai FY; Department of Cardiovascular Sciences, University of Leicester, Leicester, UK.; NIHR Leicester Biomedical Research Centre, Glenfield Hospital, Leicester, UK.
Nath M; Department of Cardiovascular Sciences, University of Leicester, Leicester, UK.; NIHR Leicester Biomedical Research Centre, Glenfield Hospital, Leicester, UK.
Hamby SE; Department of Cardiovascular Sciences, University of Leicester, Leicester, UK.; NIHR Leicester Biomedical Research Centre, Glenfield Hospital, Leicester, UK.
Thompson JR; Department of Cardiovascular Sciences, University of Leicester, Leicester, UK.; Department of Health Sciences, University of Leicester, Leicester, UK.
Nelson CP; Department of Cardiovascular Sciences, University of Leicester, Leicester, UK.; NIHR Leicester Biomedical Research Centre, Glenfield Hospital, Leicester, UK.
Samani NJ; Department of Cardiovascular Sciences, University of Leicester, Leicester, UK. .; NIHR Leicester Biomedical Research Centre, Glenfield Hospital, Leicester, UK. .
Pokaż więcej
Źródło:
BMC medicine [BMC Med] 2018 Oct 25; Vol. 16 (1), pp. 187. Date of Electronic Publication: 2018 Oct 25.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Body Height/*genetics
Disease/*genetics
Genetic Testing/*methods
Mendelian Randomization Analysis/*methods
Adult ; Aged ; Disease/etiology ; Female ; Humans ; Male ; Middle Aged ; Risk Factors
Czasopismo naukowe
Tytuł:
Exploring the somatic NF1 mutational spectrum associated with NF1 cutaneous neurofibromas.
Autorzy:
Thomas L; Institute of Medical Genetics, School of Medicine, Cardiff University, Heath Park Way, Cardiff, UK.
Spurlock G
Eudall C
Thomas NS
Mort M
Hamby SE
Chuzhanova N
Brems H
Legius E
Cooper DN
Upadhyaya M
Pokaż więcej
Źródło:
European journal of human genetics : EJHG [Eur J Hum Genet] 2012 Apr; Vol. 20 (4), pp. 411-9. Date of Electronic Publication: 2011 Nov 23.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Genes, Neurofibromatosis 1*
Mutation*
Neurofibromatosis 1/*genetics
Skin Neoplasms/*genetics
Base Sequence ; Humans ; Molecular Sequence Data ; Sequence Analysis, DNA ; Tumor Cells, Cultured
Czasopismo naukowe
Tytuł:
Comparative analysis of genome sequences covering the seven cronobacter species.
Autorzy:
Joseph S; Pathogen Research Group, School of Science and Technology, Nottingham Trent University, Nottingham, United Kingdom.
Desai P
Ji Y
Cummings CA
Shih R
Degoricija L
Rico A
Brzoska P
Hamby SE
Masood N
Hariri S
Sonbol H
Chuzhanova N
McClelland M
Furtado MR
Forsythe SJ
Pokaż więcej
Źródło:
PloS one [PLoS One] 2012; Vol. 7 (11), pp. e49455. Date of Electronic Publication: 2012 Nov 16.
Typ publikacji:
Comparative Study; Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
MeSH Terms:
Evolution, Molecular*
Phylogeny*
Cronobacter/*genetics
Genome, Bacterial/*genetics
Bacterial Secretion Systems/genetics ; Base Sequence ; Cronobacter/pathogenicity ; Fimbriae, Bacterial/genetics ; Likelihood Functions ; Models, Genetic ; Molecular Sequence Data ; Multigene Family/genetics ; Sequence Analysis, DNA ; Species Specificity ; Virulence Factors/genetics
Czasopismo naukowe
Tytuł:
In Silico identification of pathogenic strains of Cronobacter from Biochemical data reveals association of inositol fermentation with pathogenicity.
Autorzy:
Hamby SE; School of Science and Technology, Nottingham Trent University, Nottingham, NG11 8NS, UK. stephen.hamby@ntu.ac.uk
Joseph S
Forsythe SJ
Chuzhanova N
Pokaż więcej
Źródło:
BMC microbiology [BMC Microbiol] 2011 Sep 20; Vol. 11, pp. 204. Date of Electronic Publication: 2011 Sep 20.
Typ publikacji:
Evaluation Study; Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Bacterial Typing Techniques/*methods
Computational Biology/*methods
Cronobacter/*chemistry
Cronobacter/*classification
Enterobacteriaceae Infections/*microbiology
Inositol/*metabolism
Bacterial Proteins/genetics ; Bacterial Proteins/metabolism ; Cronobacter/metabolism ; Cronobacter/pathogenicity ; Fermentation ; Food Microbiology ; Humans ; Molecular Sequence Data ; Virulence
Czasopismo naukowe
Tytuł:
Prediction of glycosylation sites using random forests.
Autorzy:
Hamby SE; School of Chemistry, University of Nottingham, University Park, Nottingham NG7 2RD, UK. />Hirst JD
Pokaż więcej
Źródło:
BMC bioinformatics [BMC Bioinformatics] 2008 Nov 27; Vol. 9, pp. 500. Date of Electronic Publication: 2008 Nov 27.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Algorithms*
Protein Processing, Post-Translational*
Proteins/*chemistry
Proteins/*metabolism
Databases, Protein ; Glycosylation
Czasopismo naukowe
    Wyświetlanie 1-7 z 7

    Ta witryna wykorzystuje pliki cookies do przechowywania informacji na Twoim komputerze. Pliki cookies stosujemy w celu świadczenia usług na najwyższym poziomie, w tym w sposób dostosowany do indywidualnych potrzeb. Korzystanie z witryny bez zmiany ustawień dotyczących cookies oznacza, że będą one zamieszczane w Twoim komputerze. W każdym momencie możesz dokonać zmiany ustawień dotyczących cookies