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Wyszukujesz frazę ""Tobin, Martin D."" wg kryterium: Autor


Tytuł:
Public health professionals' perceptions toward provision of health protection in England: a survey of expectations of Primary Care Trusts and Health Protection Units in the delivery of health protection.
Autorzy:
Cosford, Paul A.
O'Mahony, Mary
Angell, Emma
Bickler, Graham
Crawshaw, Shirley
Glencross, Janet
Horsley, Stephen S.
McCloskey, Brian
Puleston, Richard
Seare, Nichola
Tobin, Martin D.
Pokaż więcej
Źródło:
BMC Public Health. 2006, Vol. 6 Issue 1, p297-11. 11p.
Czasopismo naukowe
Tytuł:
Public health professionals' perceptions toward provision of health protection in England: a survey of expectations of Primary Care Trusts and Health Protection Units in the delivery of health protection
Autorzy:
Horsley Stephen S
Glencross Janet
Crawshaw Shirley
Bickler Graham
Angell Emma
O'Mahony Mary
Cosford Paul A
McCloskey Brian
Puleston Richard
Seare Nichola
Tobin Martin D
Pokaż więcej
Temat:
Public aspects of medicine
RA1-1270
Źródło:
BMC Public Health, Vol 6, Iss 1, p 297 (2006)
Opis pliku:
electronic resource
Relacje:
http://www.biomedcentral.com/1471-2458/6/297; https://doaj.org/toc/1471-2458
Dostęp URL:
https://doaj.org/article/54876ad5e95545adbc856cbfc3049738  Link otwiera się w nowym oknie
Czasopismo naukowe
Tytuł:
Association scan of 14,500 nonsynonymous SNPs in four diseases identifies autoimmunity variants.
Autorzy:
Burton PR
Clayton DG
Cardon LR
Craddock N
Deloukas P
Duncanson A
Kwiatkowski DP
McCarthy MI
Ouwehand WH
Samani NJ
Todd JA
Donnelly P
Barrett JC
Davison D
Easton D
Evans DM
Leung HT
Marchini JL
Morris AP
Spencer CC
Tobin MD
Attwood AP
Boorman JP
Cant B
Everson U
Hussey JM
Jolley JD
Knight AS
Koch K
Meech E
Nutland S
Prowse CV
Stevens HE
Taylor NC
Walters GR
Walker NM
Watkins NA
Winzer T
Jones RW
McArdle WL
Ring SM
Strachan DP
Pembrey M
Breen G
St Clair D
Caesar S
Gordon-Smith K
Jones L
Fraser C
Green EK
Grozeva D
Hamshere ML
Holmans PA
Jones IR
Kirov G
Moskivina V
Nikolov I
O'Donovan MC
Owen MJ
Collier DA
Elkin A
Farmer A
Williamson R
McGuffin P
Young AH
Ferrier IN
Ball SG
Balmforth AJ
Barrett JH
Bishop TD
Iles MM
Maqbool A
Yuldasheva N
Hall AS
Braund PS
Dixon RJ
Mangino M
Stevens S
Thompson JR
Bredin F
Tremelling M
Parkes M
Drummond H
Lees CW
Nimmo ER
Satsangi J
Fisher SA
Forbes A
Lewis CM
Onnie CM
Prescott NJ
Sanderson J
Matthew CG
Barbour J
Mohiuddin MK
Todhunter CE
Mansfield JC
Ahmad T
Cummings FR
Jewell DP
Webster J
Brown MJ
Lathrop MG
Connell J
Dominiczak A
Marcano CA
Burke B
Dobson R
Gungadoo J
Lee KL
Munroe PB
Newhouse SJ
Onipinla A
Wallace C
Xue M
Caulfield M
Farrall M
Barton A
Bruce IN
Donovan H
Eyre S
Gilbert PD
Hilder SL
Hinks AM
John SL
Potter C
Silman AJ
Symmons DP
Thomson W
Worthington J
Dunger DB
Widmer B
Frayling TM
Freathy RM
Lango H
Perry JR
Shields BM
Weedon MN
Hattersley AT
Hitman GA
Walker M
Elliott KS
Groves CJ
Lindgren CM
Rayner NW
Timpson NJ
Zeggini E
Newport M
Sirugo G
Lyons E
Vannberg F
Hill AV
Bradbury LA
Farrar C
Pointon JJ
Wordsworth P
Brown MA
Franklyn JA
Heward JM
Simmonds MJ
Gough SC
Seal S
Stratton MR
Rahman N
Ban M
Goris A
Sawcer SJ
Compston A
Conway D
Jallow M
Newport M
Sirugo G
Rockett KA
Bumpstead SJ
Chaney A
Downes K
Ghori MJ
Gwilliam R
Hunt SE
Inouye M
Keniry A
King E
McGinnis R
Potter S
Ravindrarajah R
Whittaker P
Widden C
Withers D
Cardin NJ
Davison D
Ferreira T
Pereira-Gale J
Hallgrimsdo'ttir IB
Howie BN
Su Z
Teo YY
Vukcevic D
Bentley D
Brown MA
Compston A
Farrall M
Hall AS
Hattersley AT
Hill AV
Parkes M
Pembrey M
Stratton MR
Mitchell SL
Newby PR
Brand OJ
Carr-Smith J
Pearce SH
McGinnis R
Keniry A
Deloukas P
Reveille JD
Zhou X
Sims AM
Dowling A
Taylor J
Doan T
Davis JC
Savage L
Ward MM
Learch TL
Weisman MH
Brown M
Pokaż więcej
Corporate Authors:
Wellcome Trust Case Control Consortium; Genetic Epidemiology Group, Department of Health Sciences, University of Leicester, Adrian Building, University Road, Leicester LE1 7RH, UK.
Australo-Anglo-American Spondylitis Consortium (TASC)
Biologics in RA Genetics and Genomics Study Syndicate (BRAGGS) Steering Committee
Breast Cancer Susceptibility Collaboration (UK)
Źródło:
Nature genetics [Nat Genet] 2007 Nov; Vol. 39 (11), pp. 1329-37. Date of Electronic Publication: 2007 Oct 21.
Typ publikacji:
Journal Article; Randomized Controlled Trial
MeSH Terms:
Autoimmunity/*genetics
Breast Neoplasms/*genetics
Multiple Sclerosis/*genetics
Polymorphism, Single Nucleotide/*genetics
Spondylitis, Ankylosing/*genetics
Thyroiditis, Autoimmune/*genetics
Aminopeptidases/genetics ; Breast Neoplasms/epidemiology ; Case-Control Studies ; Chromosome Mapping ; Genetics, Population ; Genotype ; Haplotypes/genetics ; Humans ; Linkage Disequilibrium ; Minor Histocompatibility Antigens ; Multiple Sclerosis/epidemiology ; North America/epidemiology ; Polymerase Chain Reaction ; Receptors, Immunologic/genetics ; Receptors, Interleukin/genetics ; Spondylitis, Ankylosing/epidemiology ; Thyroiditis, Autoimmune/epidemiology
Czasopismo naukowe
Tytuł:
The novel genetic variant predisposing to coronary artery disease in the region of the PSRC1 and CELSR2 genes on chromosome 1 associates with serum cholesterol
Autorzy:
Samani, Nilesh J.
Braund, Peter S.
Erdmann, Jeanette
Götz, Anika
Tomaszewski, Maciej
Linsel-Nitschke, Patrick
Hajat, Cother
Mangino, Massimo
Hengstenberg, Christian
Stark, Klaus
Ziegler, Andreas
Caulfield, Mark
Burton, Paul R.
Schunkert, Heribert
Tobin, Martin D.
Pokaż więcej
Źródło:
Journal of Molecular Medicine. November 2008 86(11):1233-1241
Czasopismo naukowe
Tytuł:
Genome-wide association study identifies eight loci associated with blood pressure.
Autorzy:
Newton-Cheh C; Center for Human Genetic Research, Massachusetts General Hospital, Boston, Massachusetts, USA. />Johnson T
Gateva V
Tobin MD
Bochud M
Coin L
Najjar SS
Zhao JH
Heath SC
Eyheramendy S
Papadakis K
Voight BF
Scott LJ
Zhang F
Farrall M
Tanaka T
Wallace C
Chambers JC
Khaw KT
Nilsson P
van der Harst P
Polidoro S
Grobbee DE
Onland-Moret NC
Bots ML
Wain LV
Elliott KS
Teumer A
Luan J
Lucas G
Kuusisto J
Burton PR
Hadley D
McArdle WL
Brown M
Dominiczak A
Newhouse SJ
Samani NJ
Webster J
Zeggini E
Beckmann JS
Bergmann S
Lim N
Song K
Vollenweider P
Waeber G
Waterworth DM
Yuan X
Groop L
Orho-Melander M
Allione A
Di Gregorio A
Guarrera S
Panico S
Ricceri F
Romanazzi V
Sacerdote C
Vineis P
Barroso I
Sandhu MS
Luben RN
Crawford GJ
Jousilahti P
Perola M
Boehnke M
Bonnycastle LL
Collins FS
Jackson AU
Mohlke KL
Stringham HM
Valle TT
Willer CJ
Bergman RN
Morken MA
Döring A
Gieger C
Illig T
Meitinger T
Org E
Pfeufer A
Wichmann HE
Kathiresan S
Marrugat J
O'Donnell CJ
Schwartz SM
Siscovick DS
Subirana I
Freimer NB
Hartikainen AL
McCarthy MI
O'Reilly PF
Peltonen L
Pouta A
de Jong PE
Snieder H
van Gilst WH
Clarke R
Goel A
Hamsten A
Peden JF
Seedorf U
Syvänen AC
Tognoni G
Lakatta EG
Sanna S
Scheet P
Schlessinger D
Scuteri A
Dörr M
Ernst F
Felix SB
Homuth G
Lorbeer R
Reffelmann T
Rettig R
Völker U
Galan P
Gut IG
Hercberg S
Lathrop GM
Zelenika D
Deloukas P
Soranzo N
Williams FM
Zhai G
Salomaa V
Laakso M
Elosua R
Forouhi NG
Völzke H
Uiterwaal CS
van der Schouw YT
Numans ME
Matullo G
Navis G
Berglund G
Bingham SA
Kooner JS
Connell JM
Bandinelli S
Ferrucci L
Watkins H
Spector TD
Tuomilehto J
Altshuler D
Strachan DP
Laan M
Meneton P
Wareham NJ
Uda M
Jarvelin MR
Mooser V
Melander O
Loos RJ
Elliott P
Abecasis GR
Caulfield M
Munroe PB
Pokaż więcej
Corporate Authors:
Wellcome Trust Case Control Consortium
Źródło:
Nature genetics [Nat Genet] 2009 Jun; Vol. 41 (6), pp. 666-76. Date of Electronic Publication: 2009 May 10.
Typ publikacji:
Journal Article; Research Support, N.I.H., Extramural; Research Support, N.I.H., Intramural; Research Support, Non-U.S. Gov't
MeSH Terms:
Genome-Wide Association Study*
Polymorphism, Single Nucleotide*
Blood Pressure/*genetics
Cardiovascular Diseases/*genetics
Adaptor Proteins, Signal Transducing ; Cardiovascular Diseases/physiopathology ; Chromosome Mapping ; Cytochrome P-450 CYP1A2/genetics ; DNA-Binding Proteins/genetics ; Diastole/genetics ; Europe ; Fibroblast Growth Factor 5/genetics ; Genetic Variation ; Humans ; India ; Intracellular Signaling Peptides and Proteins ; Methylenetetrahydrofolate Reductase (NADPH2)/genetics ; Open Reading Frames/genetics ; Phospholipase C delta/genetics ; Proteins/genetics ; Steroid 17-alpha-Hydroxylase/genetics ; Systole/genetics ; White People/genetics
Czasopismo naukowe
Tytuł:
Genome-wide association study identifies five loci associated with lung function.
Autorzy:
Repapi E; Departments of Health Sciences and Genetics, Adrian Building, University of Leicester, Leicester, UK.
Sayers I
Wain LV
Burton PR
Johnson T
Obeidat M
Zhao JH
Ramasamy A
Zhai G
Vitart V
Huffman JE
Igl W
Albrecht E
Deloukas P
Henderson J
Granell R
McArdle WL
Rudnicka AR
Barroso I
Loos RJ
Wareham NJ
Mustelin L
Rantanen T
Surakka I
Imboden M
Wichmann HE
Grkovic I
Jankovic S
Zgaga L
Hartikainen AL
Peltonen L
Gyllensten U
Johansson A
Zaboli G
Campbell H
Wild SH
Wilson JF
Gläser S
Homuth G
Völzke H
Mangino M
Soranzo N
Spector TD
Polasek O
Rudan I
Wright AF
Heliövaara M
Ripatti S
Pouta A
Naluai AT
Olin AC
Torén K
Cooper MN
James AL
Palmer LJ
Hingorani AD
Wannamethee SG
Whincup PH
Smith GD
Ebrahim S
McKeever TM
Pavord ID
MacLeod AK
Morris AD
Porteous DJ
Cooper C
Dennison E
Shaheen S
Karrasch S
Schnabel E
Schulz H
Grallert H
Bouatia-Naji N
Delplanque J
Froguel P
Blakey JD
Britton JR
Morris RW
Holloway JW
Lawlor DA
Hui J
Nyberg F
Jarvelin MR
Jackson C
Kähönen M
Kaprio J
Probst-Hensch NM
Koch B
Hayward C
Evans DM
Elliott P
Strachan DP
Hall IP
Tobin MD
Pokaż więcej
Corporate Authors:
Wellcome Trust Case Control Consortium
NSHD Respiratory Study Team
Źródło:
Nature genetics [Nat Genet] 2010 Jan; Vol. 42 (1), pp. 36-44. Date of Electronic Publication: 2009 Dec 13.
Typ publikacji:
Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
MeSH Terms:
Gene Expression Profiling*
Genome, Human/*genetics
Genome-Wide Association Study/*methods
Lung/*physiology
Female ; Forced Expiratory Volume ; Glutathione Transferase/genetics ; Humans ; Lung/metabolism ; Lung/physiopathology ; Male ; Meta-Analysis as Topic ; Microfilament Proteins/genetics ; Polymorphism, Single Nucleotide ; Pulmonary Disease, Chronic Obstructive/genetics ; Pulmonary Disease, Chronic Obstructive/physiopathology ; RNA, Messenger/genetics ; RNA, Messenger/metabolism ; Receptor for Advanced Glycation End Products ; Receptors, Immunologic/genetics ; Receptors, Serotonin, 5-HT4/genetics ; Respiratory Function Tests ; Spirometry ; Tensins ; Thrombospondins/genetics ; Vital Capacity
Czasopismo naukowe
Tytuł:
Common variants near TERC are associated with mean telomere length.
Autorzy:
Codd V; Department of Cardiovascular Sciences, University of Leicester, Glenfield Hospital, Leicester, UK.
Mangino M
van der Harst P
Braund PS
Kaiser M
Beveridge AJ
Rafelt S
Moore J
Nelson C
Soranzo N
Zhai G
Valdes AM
Blackburn H
Mateo Leach I
de Boer RA
Kimura M
Aviv A
Goodall AH
Ouwehand W
van Veldhuisen DJ
van Gilst WH
Navis G
Burton PR
Tobin MD
Hall AS
Thompson JR
Spector T
Samani NJ
Pokaż więcej
Corporate Authors:
Wellcome Trust Case Control Consortium
Źródło:
Nature genetics [Nat Genet] 2010 Mar; Vol. 42 (3), pp. 197-9. Date of Electronic Publication: 2010 Feb 07.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Polymorphism, Single Nucleotide*/physiology
RNA/*genetics
Telomerase/*genetics
Telomere/*genetics
Age Factors ; Aging/genetics ; Chromosomes, Human, Pair 3 ; Cohort Studies ; Gene Frequency ; Genome-Wide Association Study ; Humans ; Meta-Analysis as Topic ; Quantitative Trait Loci ; RNA/physiology ; Telomerase/physiology ; Telomere/metabolism ; Time Factors
Czasopismo naukowe
Tytuł:
Genome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controls.
Autorzy:
Craddock N
Hurles ME
Cardin N
Pearson RD
Plagnol V
Robson S
Vukcevic D
Barnes C
Conrad DF
Giannoulatou E
Holmes C
Marchini JL
Stirrups K
Tobin MD
Wain LV
Yau C
Aerts J
Ahmad T
Andrews TD
Arbury H
Attwood A
Auton A
Ball SG
Balmforth AJ
Barrett JC
Barroso I
Barton A
Bennett AJ
Bhaskar S
Blaszczyk K
Bowes J
Brand OJ
Braund PS
Bredin F
Breen G
Brown MJ
Bruce IN
Bull J
Burren OS
Burton J
Byrnes J
Caesar S
Clee CM
Coffey AJ
Connell JM
Cooper JD
Dominiczak AF
Downes K
Drummond HE
Dudakia D
Dunham A
Ebbs B
Eccles D
Edkins S
Edwards C
Elliot A
Emery P
Evans DM
Evans G
Eyre S
Farmer A
Ferrier IN
Feuk L
Fitzgerald T
Flynn E
Forbes A
Forty L
Franklyn JA
Freathy RM
Gibbs P
Gilbert P
Gokumen O
Gordon-Smith K
Gray E
Green E
Groves CJ
Grozeva D
Gwilliam R
Hall A
Hammond N
Hardy M
Harrison P
Hassanali N
Hebaishi H
Hines S
Hinks A
Hitman GA
Hocking L
Howard E
Howard P
Howson JM
Hughes D
Hunt S
Isaacs JD
Jain M
Jewell DP
Johnson T
Jolley JD
Jones IR
Jones LA
Kirov G
Langford CF
Lango-Allen H
Lathrop GM
Lee J
Lee KL
Lees C
Lewis K
Lindgren CM
Maisuria-Armer M
Maller J
Mansfield J
Martin P
Massey DC
McArdle WL
McGuffin P
McLay KE
Mentzer A
Mimmack ML
Morgan AE
Morris AP
Mowat C
Myers S
Newman W
Nimmo ER
O'Donovan MC
Onipinla A
Onyiah I
Ovington NR
Owen MJ
Palin K
Parnell K
Pernet D
Perry JR
Phillips A
Pinto D
Prescott NJ
Prokopenko I
Quail MA
Rafelt S
Rayner NW
Redon R
Reid DM
Renwick
Ring SM
Robertson N
Russell E
St Clair D
Sambrook JG
Sanderson JD
Schuilenburg H
Scott CE
Scott R
Seal S
Shaw-Hawkins S
Shields BM
Simmonds MJ
Smyth DJ
Somaskantharajah E
Spanova K
Steer S
Stephens J
Stevens HE
Stone MA
Su Z
Symmons DP
Thompson JR
Thomson W
Travers ME
Turnbull C
Valsesia A
Walker M
Walker NM
Wallace C
Warren-Perry M
Watkins NA
Webster J
Weedon MN
Wilson AG
Woodburn M
Wordsworth BP
Young AH
Zeggini E
Carter NP
Frayling TM
Lee C
McVean G
Munroe PB
Palotie A
Sawcer SJ
Scherer SW
Strachan DP
Tyler-Smith C
Brown MA
Burton PR
Caulfield MJ
Compston A
Farrall M
Gough SC
Hall AS
Hattersley AT
Hill AV
Mathew CG
Pembrey M
Satsangi J
Stratton MR
Worthington J
Deloukas P
Duncanson A
Kwiatkowski DP
McCarthy MI
Ouwehand W
Parkes M
Rahman N
Todd JA
Samani NJ
Donnelly P
Pokaż więcej
Corporate Authors:
Wellcome Trust Case Control Consortium
Źródło:
Nature [Nature] 2010 Apr 01; Vol. 464 (7289), pp. 713-20.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Disease*
Genome-Wide Association Study*
DNA Copy Number Variations/*genetics
Genetic Predisposition to Disease/*genetics
Arthritis, Rheumatoid/genetics ; Case-Control Studies ; Crohn Disease/genetics ; Diabetes Mellitus/genetics ; Gene Frequency/genetics ; Humans ; Nucleic Acid Hybridization ; Oligonucleotide Array Sequence Analysis ; Pilot Projects ; Polymorphism, Single Nucleotide/genetics ; Quality Control
Czasopismo naukowe

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