Autor: "Mero IL" - OpacWWW

Skocz do pozycji: 1.

Tytuł:: Analysis of immune-related loci identifies 48 new susceptibility variants for multiple sclerosis.
Autorzy:: Beecham AH
Patsopoulos NA
Xifara DK
Davis MF
Kemppinen A
Cotsapas C
Shah TS
Spencer C
Booth D
Goris A
Oturai A
Saarela J
Fontaine B
Hemmer B
Martin C
Zipp F
D'Alfonso S
Martinelli-Boneschi F
Taylor B
Harbo HF
Kockum I
Hillert J
Olsson T
Ban M
Oksenberg JR
Hintzen R
Barcellos LF
Agliardi C
Alfredsson L
Alizadeh M
Anderson C
Andrews R
Søndergaard HB
Baker A
Band G
Baranzini SE
Barizzone N
Barrett J
Bellenguez C
Bergamaschi L
Bernardinelli L
Berthele A
Biberacher V
Binder TM
Blackburn H
Bomfim IL
Brambilla P
Broadley S
Brochet B
Brundin L
Buck D
Butzkueven H
Caillier SJ
Camu W
Carpentier W
Cavalla P
Celius EG
Coman I
Comi G
Corrado L
Cosemans L
Cournu-Rebeix I
Cree BA
Cusi D
Damotte V
Defer G
Delgado SR
Deloukas P
di Sapio A
Dilthey AT
Donnelly P
Dubois B
Duddy M
Edkins S
Elovaara I
Esposito F
Evangelou N
Fiddes B
Field J
Franke A
Freeman C
Frohlich IY
Galimberti D
Gieger C
Gourraud PA
Graetz C
Graham A
Grummel V
Guaschino C
Hadjixenofontos A
Hakonarson H
Halfpenny C
Hall G
Hall P
Hamsten A
Harley J
Harrower T
Hawkins C
Hellenthal G
Hillier C
Hobart J
Hoshi M
Hunt SE
Jagodic M
Jelčić I
Jochim A
Kendall B
Kermode A
Kilpatrick T
Koivisto K
Konidari I
Korn T
Kronsbein H
Langford C
Larsson M
Lathrop M
Lebrun-Frenay C
Lechner-Scott J
Lee MH
Leone MA
Leppä V
Liberatore G
Lie BA
Lill CM
Lindén M
Link J
Luessi F
Lycke J
Macciardi F
Männistö S
Manrique CP
Martin R
Martinelli V
Mason D
Mazibrada G
McCabe C
Mero IL
Mescheriakova J
Moutsianas L
Myhr KM
Nagels G
Nicholas R
Nilsson P
Piehl F
Pirinen M
Price SE
Quach H
Reunanen M
Robberecht W
Robertson NP
Rodegher M
Rog D
Salvetti M
Schnetz-Boutaud NC
Sellebjerg F
Selter RC
Schaefer C
Shaunak S
Shen L
Shields S
Siffrin V
Slee M
Sorensen PS
Sorosina M
Sospedra M
Spurkland A
Strange A
Sundqvist E
Thijs V
Thorpe J
Ticca A
Tienari P
van Duijn C
Visser EM
Vucic S
Westerlind H
Wiley JS
Wilkins A
Wilson JF
Winkelmann J
Zajicek J
Zindler E
Haines JL
Pericak-Vance MA
Ivinson AJ
Stewart G
Hafler D
Hauser SL
Compston A
McVean G
De Jager P
Sawcer SJ
McCauley JL; Pokaż więcej
Corporate Authors:: International Multiple Sclerosis Genetics Consortium (IMSGC); 1] John P. Hussman Institute for Human Genomics, University of Miami, Miller School of Medicine, Miami, Florida, USA. [2].
Wellcome Trust Case Control Consortium 2 (WTCCC2)
International IBD Genetics Consortium (IIBDGC)
Źródło:: Nature genetics [Nat Genet] 2013 Nov; Vol. 45 (11), pp. 1353-60. Date of Electronic Publication: 2013 Sep 29.
Typ publikacji:: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
MeSH Terms:: Multiple Sclerosis/*genetics
Multiple Sclerosis/*immunology
Chromosome Mapping ; Gene Frequency ; Genetic Loci ; Genetic Predisposition to Disease ; Genetic Variation ; Genome-Wide Association Study ; Genotype ; Humans ; Polymorphism, Single Nucleotide ; White People/genetics

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Skocz do pozycji: 2.

Tytuł:: Association of genetic markers with CSF oligoclonal bands in multiple sclerosis patients.
Autorzy:: Leone MA; MS Centre, SCDU Neurology, AOU Maggiore della Carità, Novara, Italy. />Barizzone N
Esposito F
Lucenti A
Harbo HF
Goris A
Kockum I
Oturai AB
Celius EG
Mero IL
Dubois B
Olsson T
Søndergaard HB
Cusi D
Lupoli S
Andreassen BK
Myhr KM
Guerini FR
Comi G
Martinelli-Boneschi F
D'Alfonso S; Pokaż więcej
Corporate Authors:: International Multiple Sclerosis Genetics Consortium
Wellcome Trust Case Control Consortium 2
PROGEMUS Group
PROGRESSO Group
Źródło:: PloS one [PLoS One] 2013 Jun 13; Vol. 8 (6), pp. e64408. Date of Electronic Publication: 2013 Jun 13 (Print Publication: 2013).
Typ publikacji:: Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:: Genome-Wide Association Study*
Multiple Sclerosis/*cerebrospinal fluid
Multiple Sclerosis/*genetics
Oligoclonal Bands/*cerebrospinal fluid
Adult ; Female ; Genetic Markers ; HLA-DRB1 Chains/genetics ; Humans ; Male ; Meta-Analysis as Topic ; Middle Aged ; Polymorphism, Single Nucleotide ; Young Adult

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Skocz do pozycji: 3.

Tytuł:: Associations between APOE genotypes and disease susceptibility, joint damage and lipid levels in patients with rheumatoid arthritis.
Autorzy:: Maehlen MT; Department of Medical Genetics, University of Oslo and Oslo University Hospital, Ullevål, Oslo, Norway. />Provan SA
de Rooy DP
van der Helm-van Mil AH
Krabben A
Saxne T
Lindqvist E
Semb AG
Uhlig T
van der Heijde D
Mero IL
Olsen IC
Kvien TK
Lie BA; Pokaż więcej
Źródło:: PloS one [PLoS One] 2013 Apr 17; Vol. 8 (4), pp. e60970. Date of Electronic Publication: 2013 Apr 17 (Print Publication: 2013).
Typ publikacji:: Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:: Genetic Association Studies*
Genetic Predisposition to Disease*
Apolipoproteins E/*genetics
Arthritis, Rheumatoid/*blood
Arthritis, Rheumatoid/*genetics
Joints/*pathology
Lipids/*blood
Acute-Phase Reaction/blood ; Acute-Phase Reaction/complications ; Acute-Phase Reaction/genetics ; Arthritis, Rheumatoid/complications ; Arthritis, Rheumatoid/diagnostic imaging ; Arthrography ; Blood Sedimentation ; C-Reactive Protein/metabolism ; Cardiovascular Diseases/blood ; Cardiovascular Diseases/complications ; Cardiovascular Diseases/genetics ; Case-Control Studies ; Demography ; Disease Progression ; Female ; Humans ; Longitudinal Studies ; Male ; Meta-Analysis as Topic ; Middle Aged ; Norway

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Skocz do pozycji: 4.

Tytuł:: Multiple sclerosis-associated single-nucleotide polymorphisms in CLEC16A correlate with reduced SOCS1 and DEXI expression in the thymus.
Autorzy:: Leikfoss IS; Department of Neurology, Oslo University Hospital, Oslo, Norway.
Mero IL
Dahle MK
Lie BA
Harbo HF
Spurkland A
Berge T; Pokaż więcej
Źródło:: Genes and immunity [Genes Immun] 2013 Jan; Vol. 14 (1), pp. 62-6. Date of Electronic Publication: 2012 Nov 15.
Typ publikacji:: Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:: Polymorphism, Single Nucleotide*
DNA-Binding Proteins/*metabolism
Lectins, C-Type/*genetics
Membrane Proteins/*metabolism
Monosaccharide Transport Proteins/*genetics
Multiple Sclerosis/*genetics
Suppressor of Cytokine Signaling Proteins/*metabolism
Thymus Gland/*metabolism
Case-Control Studies ; Child ; DNA-Binding Proteins/genetics ; Down-Regulation ; Genetic Predisposition to Disease ; Humans ; Membrane Proteins/genetics ; Suppressor of Cytokine Signaling 1 Protein ; Suppressor of Cytokine Signaling Proteins/genetics

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Skocz do pozycji: 5.

Tytuł:: Oligoclonal band status in Scandinavian multiple sclerosis patients is associated with specific genetic risk alleles.
Autorzy:: Mero IL; Department of Neurology, Oslo University Hospital, Ullevål, and Department of Medical Genetics, University of Oslo, Oslo, Norway.
Gustavsen MW
Sæther HS
Flåm ST
Berg-Hansen P
Søndergaard HB
Jensen PE
Berge T
Bjølgerud A
Muggerud A
Aarseth JH
Myhr KM
Celius EG
Sellebjerg F
Hillert J
Alfredsson L
Olsson T
Oturai AB
Kockum I
Lie BA
Andreassen BK
Harbo HF; Pokaż więcej
Corporate Authors:: International Multiple Sclerosis Genetics Consortium
Źródło:: PloS one [PLoS One] 2013; Vol. 8 (3), pp. e58352. Date of Electronic Publication: 2013 Mar 05.
Typ publikacji:: Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:: Genome-Wide Association Study*
Multiple Sclerosis/*epidemiology
Multiple Sclerosis/*genetics
Oligoclonal Bands/*genetics
Adult ; Alleles ; Case-Control Studies ; Denmark ; Female ; Gene Frequency ; Genotype ; HLA-DRB1 Chains/genetics ; Humans ; Male ; Multiple Sclerosis/cerebrospinal fluid ; Norway ; Oligoclonal Bands/cerebrospinal fluid ; Polymorphism, Single Nucleotide ; Sweden

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Skocz do pozycji: 6.

Tytuł:: From genes to characteristics of multiple sclerosis.
Autorzy:: Harbo HF; Department of Neurology, Oslo University Hospital, Oslo, Norway. />Mero IL; Pokaż więcej
Źródło:: Acta neurologica Scandinavica. Supplementum [Acta Neurol Scand Suppl] 2012 (195), pp. 76-83.
Typ publikacji:: Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:: Genetic Predisposition to Disease*
Multiple Sclerosis/*genetics
Multiple Sclerosis/*therapy
Biological Specimen Banks ; Central Nervous System/physiopathology ; Demyelinating Diseases/genetics ; Demyelinating Diseases/immunology ; Humans ; Multiple Sclerosis/immunology ; Risk Factors ; Treatment Outcome

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Skocz do pozycji: 7.

Tytuł:: Alterations in KLRB1 gene expression and a Scandinavian multiple sclerosis association study of the KLRB1 SNP rs4763655.
Autorzy:: Søndergaard HB; Department of Neurology, Danish Multiple Sclerosis Center, University Hospital Rigshospitalet, Copenhagen, Denmark. />Sellebjerg F
Hillert J
Olsson T
Kockum I
Lindén M
Mero IL
Myhr KM
Celius EG
Harbo HF
Christensen JR
Börnsen L
Sørensen PS
Oturai AB; Pokaż więcej
Źródło:: European journal of human genetics : EJHG [Eur J Hum Genet] 2011 Oct; Vol. 19 (10), pp. 1100-3. Date of Electronic Publication: 2011 May 25.
Typ publikacji:: Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:: Gene Expression Regulation*
Genetic Predisposition to Disease*
Multiple Sclerosis/*genetics
NK Cell Lectin-Like Receptor Subfamily B/*genetics
NK Cell Lectin-Like Receptor Subfamily B/*metabolism
Case-Control Studies ; Female ; Gene Frequency ; Genome-Wide Association Study ; Humans ; Male ; Multiple Sclerosis/epidemiology ; Polymorphism, Single Nucleotide ; Scandinavian and Nordic Countries/epidemiology

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Skocz do pozycji: 8.

Tytuł:: Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis.
Autorzy:: Sawcer S
Hellenthal G
Pirinen M
Spencer CC
Patsopoulos NA
Moutsianas L
Dilthey A
Su Z
Freeman C
Hunt SE
Edkins S
Gray E
Booth DR
Potter SC
Goris A
Band G
Oturai AB
Strange A
Saarela J
Bellenguez C
Fontaine B
Gillman M
Hemmer B
Gwilliam R
Zipp F
Jayakumar A
Martin R
Leslie S
Hawkins S
Giannoulatou E
D'alfonso S
Blackburn H
Martinelli Boneschi F
Liddle J
Harbo HF
Perez ML
Spurkland A
Waller MJ
Mycko MP
Ricketts M
Comabella M
Hammond N
Kockum I
McCann OT
Ban M
Whittaker P
Kemppinen A
Weston P
Hawkins C
Widaa S
Zajicek J
Dronov S
Robertson N
Bumpstead SJ
Barcellos LF
Ravindrarajah R
Abraham R
Alfredsson L
Ardlie K
Aubin C
Baker A
Baker K
Baranzini SE
Bergamaschi L
Bergamaschi R
Bernstein A
Berthele A
Boggild M
Bradfield JP
Brassat D
Broadley SA
Buck D
Butzkueven H
Capra R
Carroll WM
Cavalla P
Celius EG
Cepok S
Chiavacci R
Clerget-Darpoux F
Clysters K
Comi G
Cossburn M
Cournu-Rebeix I
Cox MB
Cozen W
Cree BA
Cross AH
Cusi D
Daly MJ
Davis E
de Bakker PI
Debouverie M
D'hooghe MB
Dixon K
Dobosi R
Dubois B
Ellinghaus D
Elovaara I
Esposito F
Fontenille C
Foote S
Franke A
Galimberti D
Ghezzi A
Glessner J
Gomez R
Gout O
Graham C
Grant SF
Guerini FR
Hakonarson H
Hall P
Hamsten A
Hartung HP
Heard RN
Heath S
Hobart J
Hoshi M
Infante-Duarte C
Ingram G
Ingram W
Islam T
Jagodic M
Kabesch M
Kermode AG
Kilpatrick TJ
Kim C
Klopp N
Koivisto K
Larsson M
Lathrop M
Lechner-Scott JS
Leone MA
Leppä V
Liljedahl U
Bomfim IL
Lincoln RR
Link J
Liu J
Lorentzen AR
Lupoli S
Macciardi F
Mack T
Marriott M
Martinelli V
Mason D
McCauley JL
Mentch F
Mero IL
Mihalova T
Montalban X
Mottershead J
Myhr KM
Naldi P
Ollier W
Page A
Palotie A
Pelletier J
Piccio L
Pickersgill T
Piehl F
Pobywajlo S
Quach HL
Ramsay PP
Reunanen M
Reynolds R
Rioux JD
Rodegher M
Roesner S
Rubio JP
Rückert IM
Salvetti M
Salvi E
Santaniello A
Schaefer CA
Schreiber S
Schulze C
Scott RJ
Sellebjerg F
Selmaj KW
Sexton D
Shen L
Simms-Acuna B
Skidmore S
Sleiman PM
Smestad C
Sørensen PS
Søndergaard HB
Stankovich J
Strange RC
Sulonen AM
Sundqvist E
Syvänen AC
Taddeo F
Taylor B
Blackwell JM
Tienari P
Bramon E
Tourbah A
Brown MA
Tronczynska E
Casas JP
Tubridy N
Corvin A
Vickery J
Jankowski J
Villoslada P
Markus HS
Wang K
Mathew CG
Wason J
Palmer CN
Wichmann HE
Plomin R
Willoughby E
Rautanen A
Winkelmann J
Wittig M
Trembath RC
Yaouanq J
Viswanathan AC
Zhang H
Wood NW
Zuvich R
Deloukas P
Langford C
Duncanson A
Oksenberg JR
Pericak-Vance MA
Haines JL
Olsson T
Hillert J
Ivinson AJ
De Jager PL
Peltonen L
Stewart GJ
Hafler DA
Hauser SL
McVean G
Donnelly P
Compston A; Pokaż więcej
Corporate Authors:: International Multiple Sclerosis Genetics Consortium
Wellcome Trust Case Control Consortium 2
Źródło:: Nature [Nature] 2011 Aug 10; Vol. 476 (7359), pp. 214-9. Date of Electronic Publication: 2011 Aug 10.
Typ publikacji:: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
MeSH Terms:: Genetic Predisposition to Disease/*genetics
Immunity, Cellular/*immunology
Multiple Sclerosis/*genetics
Multiple Sclerosis/*immunology
Alleles ; Cell Differentiation/immunology ; Europe/ethnology ; Genome, Human/genetics ; Genome-Wide Association Study ; HLA-A Antigens/genetics ; HLA-DR Antigens/genetics ; HLA-DRB1 Chains ; Humans ; Immunity, Cellular/genetics ; Major Histocompatibility Complex/genetics ; Polymorphism, Single Nucleotide/genetics ; Sample Size ; T-Lymphocytes, Helper-Inducer/cytology ; T-Lymphocytes, Helper-Inducer/immunology

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Skocz do pozycji: 9.

Tytuł:: Exploring the CLEC16A gene reveals a MS-associated variant with correlation to the relative expression of CLEC16A isoforms in thymus.
Autorzy:: Mero IL; Department of Neurology, Oslo University Hospital, Oslo, Norway. />Ban M
Lorentzen ÅR
Smestad C
Celius EG
Sæther H
Saeedi H
Viken MK
Skinningsrud B
Undlien DE
Aarseth J
Myhr KM
Granum S
Spurkland A
Sawcer S
Compston A
Lie BA
Harbo HF; Pokaż więcej
Źródło:: Genes and immunity [Genes Immun] 2011 Apr; Vol. 12 (3), pp. 191-8. Date of Electronic Publication: 2010 Dec 23.
Typ publikacji:: Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:: Gene Expression Regulation*
Genetic Predisposition to Disease/*genetics
Lectins, C-Type/*genetics
Monosaccharide Transport Proteins/*genetics
Multiple Sclerosis/*genetics
Thymus Gland/*metabolism
Adult ; Alleles ; Female ; Gene Expression Profiling ; Gene Frequency ; Genome-Wide Association Study ; Genotype ; Humans ; Male ; Middle Aged ; Polymorphism, Single Nucleotide/genetics ; Protein Isoforms/genetics ; Young Adult

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Skocz do pozycji: 10.

Tytuł:: A rare variant of the TYK2 gene is confirmed to be associated with multiple sclerosis.
Autorzy:: Mero IL; Department of Neurology, Oslo University Hospital, Ullevål, N-0407 Oslo, Norway. />Lorentzen AR
Ban M
Smestad C
Celius EG
Aarseth JH
Myhr KM
Link J
Hillert J
Olsson T
Kockum I
Masterman T
Oturai AB
Søndergaard HB
Sellebjerg F
Saarela J
Kemppinen A
Elovaara I
Spurkland A
Dudbridge F
Lie BA
Harbo HF; Pokaż więcej
Źródło:: European journal of human genetics : EJHG [Eur J Hum Genet] 2010 Apr; Vol. 18 (4), pp. 502-4. Date of Electronic Publication: 2009 Nov 04.
Typ publikacji:: Comparative Study; Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:: Multiple Sclerosis/*genetics
Polymorphism, Single Nucleotide/*genetics
TYK2 Kinase/*genetics
Case-Control Studies ; Gene Frequency ; Genetic Predisposition to Disease ; Genome-Wide Association Study ; Genotype ; Humans

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