UB Paderborn / Katalog / Suche / in CDI

Sortiert nach

Einfacher Volltextzugriff von (fast) überall

Installieren Sie die LibKey Nomad-Browsererweiterung und erhalten Sie von vielen Webseiten einfachen Zugriff auf lizenzierte Volltexte oder Open Access Publikationen. Mehr erfahren...

Temporal changes in the frequencies of HLA genotypes in patients with Type 1 diabetes: indication of an increased environmental pressure?

Diabetologia, 2003-03, Vol.46 (3), p.420-425

2003

Volltextzugriff (PDF)

The association of the HLA‐A24:02, B39:01 and B39:06 alleles with type 1 diabetes is restricted to specific HLA‐DR/DQ haplotypes in Finns

HLA, 2017-04, Vol.89 (4), p.215-224

2017

Volltextzugriff (PDF)

The HLA-B39 allele increases type 1 diabetes risk conferred by HLA-DRB104:04-DQB103:02 and HLA-DRB108-DQB104 class II haplotypes

Human immunology, 2014-01, Vol.75 (1), p.65-70

2014

Volltextzugriff (PDF)

interferon-induced helicase IFIH1 Ala946Thr polymorphism is associated with type 1 diabetes in both the high-incidence Finnish and the medium-incidence Hungarian populations

Diabetologia, 2010, Vol.53 (1), p.98-102

2010

Volltextzugriff (PDF)

Type 1 diabetes is insulin −2221 MspI and CTLA-4 +49 A/G polymorphism dependent

European journal of clinical investigation, 2004-08, Vol.34 (8), p.543-548

2004

Volltextzugriff (PDF)

The effect of HLA class II, insulin and CTLA4 gene regions on the development of humoral beta cell autoimmunity

Diabetologia, 2005-09, Vol.48 (9), p.1766-1775

2005

Volltextzugriff (PDF)

GIMAP GTPase family genes: potential modifiers in autoimmune diabetes, asthma, and allergy

The Journal of immunology (1950), 2015-06, Vol.194 (12), p.5885-5894

2015

Volltextzugriff (PDF)

Evidence for linkage to and association with type 1 diabetes at the 3q21 region in the Finnish population

Genes and immunity, 2006-01, Vol.7 (1), p.69-72

2006

Volltextzugriff (PDF)

Transient but not permanent neonatal diabetes mellitus is associated with paternal uniparental isodisomy of chromosome 6

Pediatrics (Evanston), 2000-01, Vol.105 (1 Pt 1), p.49-52

2000

Volltextzugriff (PDF)

The HLA-B∗ 39 allele increases type 1 diabetes risk conferred by HLA-DRB1∗ 04:04-DQB1∗ 03:02 and HLA-DRB1∗ 08-DQB1∗ 04 class II haplotypes

Human immunology, 2014-01, Vol.75 (1), p.65-70

2014

Volltextzugriff (PDF)

CD86 gene polymorphisms: no association with Type I diabetes among Finnish subjects

Diabetologia, 2002-07, Vol.45 (7), p.1041-1042

2002

Volltextzugriff (PDF)

Association of tumour necrosis factor a, b and c microsatellite polymorphisms with clinical disease activity and induction of remission in early rheumatoid arthritis

Clinical and experimental rheumatology, 2006-11, Vol.24 (6), p.636

2006

Volltextzugriff (PDF)

Associations of polymorphisms in non-HLA loci with autoantibodies at the diagnosis of type 1 diabetes: INS and IKZF4 associate with insulin autoantibodies

Pediatric diabetes, 2013-11, Vol.14 (7), p.490-496

2013

Volltextzugriff (PDF)

Non-class II HLA gene associated with type 1 diabetes maps to the 240-kb region near HLA-B

Diabetes (New York, N.Y.), 2000-12, Vol.49 (12), p.2217-2221

2000

Volltextzugriff (PDF)

The genetic locus for free sialic acid storage disease maps to the long arm of chromosome 6

American journal of human genetics, 1994-06, Vol.54 (6), p.1042-1049

1994

Volltextzugriff (PDF)

Transmission disequilibrium analysis of 31 type 1 diabetes susceptibility loci in Finnish families

Tissue antigens, 2013-07, Vol.82 (1), p.35-42

2013

Volltextzugriff (PDF)

Linkage Disequilibrium Utilized to Establish a Refined Genetic Position of the Salla Disease Locus on 6q14-q15

Genomics (San Diego, Calif.), 1995-05, Vol.27 (2), p.286-292

1995

Volltextzugriff (PDF)

Characterisation of rapid progressors to type 1 diabetes among children with HLA-conferred disease susceptibility

Diabetologia, 2017-07, Vol.60 (7), p.1284-1293

2017

Volltextzugriff (PDF)

HLA DR-DQ-encoded genetic determinants of childhood-onset type 1 diabetes in Finland: An analysis of 622 nuclear families

Tissue antigens, 2003-08, Vol.62 (2), p.162-169

2003

Volltextzugriff (PDF)

Two insulin gene single nucleotide polymorphisms associated with type 1 diabetes risk in the Finnish and Swedish populations

Disease markers, 2007, Vol.23 (3), p.139-145

2007

Volltextzugriff (PDF)

Intercellular adhesion molecule-1 (ICAM-1) K469E polymorphism: no association with type 1 diabetes among Finns

Tissue antigens, 2000-06, Vol.55 (6), p.568-570

2000

Volltextzugriff (PDF)

A linkage analysis of the CTLA4 gene region in Finnish patients with type 1 diabetes

European journal of immunogenetics, 2003-08, Vol.30 (4), p.289-293

2003

Volltextzugriff (PDF)

The human leukocyte antigen genotype has a modest effect on the insulin gene polymorphism-associated susceptibility to type 1 diabetes in the Finnish population

Tissue antigens, 2004-01, Vol.63 (1), p.72-74

2004

Volltextzugriff (PDF)

Association of CTLA4 but not ICOS polymorphisms with type 1 diabetes in two populations with different disease rates

Human immunology, 2009-07, Vol.70 (7), p.536-539

2009

Volltextzugriff (PDF)

Vitamin D receptor polymorphisms: no association with type 1 diabetes in the Finnish population

European journal of endocrinology, 2003-12, Vol.149 (6), p.591-596

2003

Volltextzugriff (PDF)

1 – 25 von 224

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(105)
Mit Volltextzugriff
(200)

Publikationsform

Sprache

Erscheinungsjahr

n.n

Thema

Science & Technology
(94)
Life Sciences & Biomedicine
(87)
Humans
(56)
Female
(33)
Male
(33)
Biological And Medical Sciences
(27)
Clinical Trials As Topic - Standards
(27)
Editorial Policies
(27)
Registries
(23)
Diabetes Mellitus, Type 1 - Genetics
(20)
Medical Sciences
(20)
General & Internal Medicine
(18)
Medicine, General & Internal
(18)
Periodicals As Topic - Standards
(18)
Finland
(17)
Type 1 Diabetes
(15)
Clinical Trials
(14)
Geography
(14)
International Relations
(14)
Child
(13)

15 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Temporal changes in the frequencies of HLA genotypes in patients with Type 1 diabetes: indication of an increased environmental pressure?

The association of the HLA‐A24:02, B39:01 and B39:06 alleles with type 1 diabetes is restricted to specific HLA‐DR/DQ haplotypes in Finns

The HLA-B39 allele increases type 1 diabetes risk conferred by HLA-DRB104:04-DQB103:02 and HLA-DRB108-DQB104 class II haplotypes

interferon-induced helicase IFIH1 Ala946Thr polymorphism is associated with type 1 diabetes in both the high-incidence Finnish and the medium-incidence Hungarian populations

Type 1 diabetes is insulin −2221 MspI and CTLA-4 +49 A/G polymorphism dependent

The effect of HLA class II, insulin and CTLA4 gene regions on the development of humoral beta cell autoimmunity

GIMAP GTPase family genes: potential modifiers in autoimmune diabetes, asthma, and allergy

Evidence for linkage to and association with type 1 diabetes at the 3q21 region in the Finnish population

Transient but not permanent neonatal diabetes mellitus is associated with paternal uniparental isodisomy of chromosome 6

The HLA-B∗ 39 allele increases type 1 diabetes risk conferred by HLA-DRB1∗ 04:04-DQB1∗ 03:02 and HLA-DRB1∗ 08-DQB1∗ 04 class II haplotypes

CD86 gene polymorphisms: no association with Type I diabetes among Finnish subjects

Association of tumour necrosis factor a, b and c microsatellite polymorphisms with clinical disease activity and induction of remission in early rheumatoid arthritis

Associations of polymorphisms in non-HLA loci with autoantibodies at the diagnosis of type 1 diabetes: INS and IKZF4 associate with insulin autoantibodies

Non-class II HLA gene associated with type 1 diabetes maps to the 240-kb region near HLA-B

The genetic locus for free sialic acid storage disease maps to the long arm of chromosome 6

Transmission disequilibrium analysis of 31 type 1 diabetes susceptibility loci in Finnish families

Linkage Disequilibrium Utilized to Establish a Refined Genetic Position of the Salla Disease Locus on 6q14-q15

Characterisation of rapid progressors to type 1 diabetes among children with HLA-conferred disease susceptibility

HLA DR-DQ-encoded genetic determinants of childhood-onset type 1 diabetes in Finland: An analysis of 622 nuclear families

Two insulin gene single nucleotide polymorphisms associated with type 1 diabetes risk in the Finnish and Swedish populations

Intercellular adhesion molecule-1 (ICAM-1) K469E polymorphism: no association with type 1 diabetes among Finns

A linkage analysis of the CTLA4 gene region in Finnish patients with type 1 diabetes

The human leukocyte antigen genotype has a modest effect on the insulin gene polymorphism-associated susceptibility to type 1 diabetes in the Finnish population

Association of CTLA4 but not ICOS polymorphisms with type 1 diabetes in two populations with different disease rates

Vitamin D receptor polymorphisms: no association with type 1 diabetes in the Finnish population

Suchergebnisse filtern