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Enhanced CD8+ cytolytic T cell responses in the peripheral circulation of patients with sarcoidosis and non-Löfgren's disease

Respiratory medicine, 2018-05, Vol.138, p.S38-S44

2018

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Distribution of T-Cell Subsets in BAL Fluid of Patients With Mild to Moderate COPD Depends on Current Smoking Status and Not Airway Obstruction

Chest, 2014-04, Vol.145 (4), p.711-722

2014

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T cell receptor-Vβ repertoires in lung and blood CD4+ and CD8+ T cells of pulmonary sarcoidosis patients

BMC pulmonary medicine, 2014-03, Vol.14 (1), p.50-50, Article 50

2014

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CD4+ Invariant T-Cell–Receptor+ Natural Killer T Cells in Bronchial Asthma

The New England journal of medicine, 2006-03, Vol.354 (11), p.1117-1129

2006

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A mutation in POLE predisposing to a multi-tumour phenotype

International journal of oncology, 2014-07, Vol.45 (1), p.77-81

2014

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Familial Dyslexia in a Large Swedish Family: A Whole Genome Linkage Scan

Behavior genetics, 2011, Vol.41 (1), p.43-49

2011

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Gender differences in the T-cell profiles of the airways in COPD patients associated with clinical phenotypes

International journal of chronic obstructive pulmonary disease, 2017-01, Vol.12, p.35-48

2017

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Identification of HLA-DR-bound peptides presented by human bronchoalveolar lavage cells in sarcoidosis

The Journal of clinical investigation, 2007-11, Vol.117 (11), p.3576-3582

2007

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No evidence of altered alveolar macrophage polarization, but reduced expression of TLR2, in bronchoalveolar lavage cells in sarcoidosis

Respiratory research, 2010-09, Vol.11 (1), p.121-121, Article 121

2010

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Hypoxia but not cigarette smoke modulates VEGF secretion from human T cells

Growth factors (Chur, Switzerland), 2009-12, Vol.27 (6), p.352-361

2009

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Autoimmune T cell responses to antigenic peptides presented by bronchoalveolar lavage cell HLA-DR molecules in sarcoidosis

Clinical immunology (Orlando, Fla.), 2009-12, Vol.133 (3), p.353-363

2009

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T-cell expansions with conserved T-cell receptor β chain motifs in the peripheral blood of HLA-DRB10401 positive patients with necrotizing vasculitis

Blood, 1998-11, Vol.92 (10), p.3737-3744

1998

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Risk of tuberculosis in a large sample of patients with coeliac disease – a nationwide cohort study

Alimentary pharmacology & therapeutics, 2011-03, Vol.33 (6), p.689-696

2011

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Altered expression of T cell immunoglobulin-mucin (TIM) molecules in bronchoalveolar lavage CD4+ T cells in sarcoidosis

Respiratory research, 2009-05, Vol.10 (1), p.42-42, Article 42

2009

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The V471A polymorphism in autophagy-related gene ATG7 modifies age at onset specifically in Italian Huntington disease patients

PloS one, 2013-07, Vol.8 (7), p.e68951-e68951

2013

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Periampullary adenomas and adenocarcinomas in familial adenomatous polyposis: Cumulative risks and APC gene mutations

Gastroenterology (New York, N.Y. 1943), 2001-11, Vol.121 (5), p.1127-1135

2001

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A large deletion disrupts the exon 3 transcription activation domain of the BRCA2 gene in a breast/ovarian cancer family

Cancer research (Chicago, Ill.), 1998-04, Vol.58 (7), p.1372-1375

1998

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A population study of apoE genotype at the age of 85: relation to dementia, cerebrovascular disease, and mortality

Journal of neurology, neurosurgery and psychiatry, 1998-01, Vol.64 (1), p.37-43

1998

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Collecting a set of psoriasis family material through a patient organisation; clinical characterisation and presence of additional disorders

BMC dermatology, 2005-10, Vol.5 (1), p.10-10, Article 10

2005

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Genome-wide linkage analysis of Scandinavian affected sib-pairs supports presence of susceptibility loci for celiac disease on chromosomes 5 and 11

European journal of human genetics : EJHG, 2001-12, Vol.9 (12), p.938-944

2001

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Novel Findings in Swedish Patients With MYH-Associated Polyposis: Mutation Detection and Clinical Characterization

Clinical gastroenterology and hepatology, 2006-04, Vol.4 (4), p.499-506

2006

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Mutations and sequence variation in the human myosin heavy chain IIa gene ( )

European journal of human genetics : EJHG, 2005-05, Vol.13 (5), p.617-622

2005

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Incidence of CSF abnormalities in siblings of multiple sclerosis patients and unrelated controls

Journal of neurology, 2000-08, Vol.247 (8), p.616-622

2000

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A population genetic study of psoriasis

British journal of dermatology (1951), 1994-07, Vol.131 (1), p.32-39

1994

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Utilizing Physiologically Based Pharmacokinetic Modeling to Inform Formulation and Clinical Development for a Compound with pH-Dependent Solubility

Journal of pharmaceutical sciences, 2015-04, Vol.104 (4), p.1522-1532

2015

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Enhanced CD8+ cytolytic T cell responses in the peripheral circulation of patients with sarcoidosis and non-Löfgren's disease

Distribution of T-Cell Subsets in BAL Fluid of Patients With Mild to Moderate COPD Depends on Current Smoking Status and Not Airway Obstruction

T cell receptor-Vβ repertoires in lung and blood CD4+ and CD8+ T cells of pulmonary sarcoidosis patients

CD4+ Invariant T-Cell–Receptor+ Natural Killer T Cells in Bronchial Asthma

A mutation in POLE predisposing to a multi-tumour phenotype

Familial Dyslexia in a Large Swedish Family: A Whole Genome Linkage Scan

Gender differences in the T-cell profiles of the airways in COPD patients associated with clinical phenotypes

Identification of HLA-DR-bound peptides presented by human bronchoalveolar lavage cells in sarcoidosis

No evidence of altered alveolar macrophage polarization, but reduced expression of TLR2, in bronchoalveolar lavage cells in sarcoidosis

Hypoxia but not cigarette smoke modulates VEGF secretion from human T cells

Autoimmune T cell responses to antigenic peptides presented by bronchoalveolar lavage cell HLA-DR molecules in sarcoidosis

T-cell expansions with conserved T-cell receptor β chain motifs in the peripheral blood of HLA-DRB10401 positive patients with necrotizing vasculitis

Risk of tuberculosis in a large sample of patients with coeliac disease – a nationwide cohort study

Altered expression of T cell immunoglobulin-mucin (TIM) molecules in bronchoalveolar lavage CD4+ T cells in sarcoidosis

The V471A polymorphism in autophagy-related gene ATG7 modifies age at onset specifically in Italian Huntington disease patients

Periampullary adenomas and adenocarcinomas in familial adenomatous polyposis: Cumulative risks and APC gene mutations

A large deletion disrupts the exon 3 transcription activation domain of the BRCA2 gene in a breast/ovarian cancer family

A population study of apoE genotype at the age of 85: relation to dementia, cerebrovascular disease, and mortality

Collecting a set of psoriasis family material through a patient organisation; clinical characterisation and presence of additional disorders

Genome-wide linkage analysis of Scandinavian affected sib-pairs supports presence of susceptibility loci for celiac disease on chromosomes 5 and 11

Novel Findings in Swedish Patients With MYH-Associated Polyposis: Mutation Detection and Clinical Characterization

Mutations and sequence variation in the human myosin heavy chain IIa gene ( )

Incidence of CSF abnormalities in siblings of multiple sclerosis patients and unrelated controls

A population genetic study of psoriasis

Utilizing Physiologically Based Pharmacokinetic Modeling to Inform Formulation and Clinical Development for a Compound with pH-Dependent Solubility

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