Filtros de búsqueda

Lista de obras de Jukka Partanen

A cluster of missense mutations at Arg356 of human steroid 21-hydroxylase may impair redox partner interaction

artículo científico publicado en 1997

A collaborative European search for non-DQA1*05-DQB1*02 celiac disease loci on HLA-DR3 haplotypes: analysis of transmission from homozygous parents

scientific article published on 01 March 2003

A comparative study of HLA genes in HLA-B27 positive ankylosing spondylitis and HLA-B27 positive peripheral reactive arthritis

scientific article published on 01 June 1996

A new locus for coeliac disease mapped to chromosome 15 in a population isolate

A rare neutral polymorphism in 21-hydroxylase genes as HLA haplotype marker. Evidence for strong founder effect in the Finnish population

artículo científico publicado en 1995

AIRE mutations and human leukocyte antigen genotypes as determinants of the autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy phenotype

artículo científico publicado en 2002

Accuracy of Programs for the Determination of Human Leukocyte Antigen Alleles from Next-Generation Sequencing Data.

artículo científico publicado en 2017

Additional factor in some HLA DR3/DQ2 haplotypes confers a fourfold increased genetic risk of celiac disease

scientific article published on 01 April 2003

Alloimmunization against platelet antigens in renal transplant patients with acute vascular rejection

artículo científico publicado en 1997

An approach to mapping haplotype-specific recombination sites in human MHC class III.

artículo científico publicado en 1996

Antibodies against deamidated gliadin peptides in early-stage celiac disease

scientific article published on 01 September 2011

Antibodies to glutamic acid decarboxylase and insulin-dependent diabetes in patients with autoimmune polyendocrine syndrome type I.

artículo científico publicado en 1996

Association of HLA B27 with benign clinical course of nephropathia epidemica caused by Puumala hantavirus

artículo científico publicado en 1998

Association of IL-10 and IL-10Rbeta gene polymorphisms with graft-versus-host disease after haematopoietic stem cell transplantation from an HLA-identical sibling donor

artículo científico publicado en 2009

Association of chest radiography findings with host-related genetic factors in patients with nephropathia epidemica.

artículo científico publicado en 2007

Association of genetic variation in inducible costimulator gene with outcome of kidney transplantation.

artículo científico publicado en 2009

Association study ofFUT2(rs601338) with celiac disease and inflammatory bowel disease in the Finnish population

scientific article published on 18 October 2012

Autoimmunity to glutamic acid decarboxylase in patients with autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy (APECED)

scientific article published on 01 March 2000

Blood donors' preferences for blood donation for biomedical research.

artículo científico publicado en 2018

C4 null phenotypes among lupus erythematosus patients are predominantly the result of deletions covering C4 and closely linked 21-hydroxylase A genes.

artículo científico publicado en 1988

CD28/CTLA4 gene region on chromosome 2q33 confers genetic susceptibility to celiac disease. A linkage and family-based association study

article

CD80 (B7-1) and CD86 (B7-2) genes and genetic susceptibility to coeliac disease

artículo científico publicado en 2002

Candidate gene region 15q26 and genetic susceptibility to coeliac disease in Finnish families

artículo científico publicado en 2001

Candidate gene region 2q33 in European families with coeliac disease

artículo científico publicado en 2004

Celiac disease and HLA DQ in patients with IgA nephropathy

artículo científico publicado en 2002

Celiac disease and autoimmune endocrinologic disorders

scientific article published on 01 July 1999

Celiac disease and markers of celiac disease latency in patients with primary Sjögren's syndrome

artículo científico publicado en 1999

Celiac disease in patients with severe liver disease: gluten-free diet may reverse hepatic failure

artículo científico publicado en 2002

Celiac disease risk in the USA: high prevalence of antiendomysium antibodies in healthy blood donors

artículo científico publicado en 1998

Celiac disease without villous atrophy: revision of criteria called for

artículo científico publicado en 2001

Celiac disease, thyrotoxicosis, and autoimmune hepatitis in a child

artículo científico publicado en 2002

Celiac disease: from inflammation to atrophy: a long-term follow-up study

artículo científico publicado en 2005

Celiac patients predominantly inherit HLA-DPB1*0101 positive haplotype from HLA-DQ2 homozygous parent

artículo científico publicado en 1997

Characterization a novel HLA-B40 allele with serological Bw4 motif, HLA-B*4047, in the Finnish population and confirmation of B*270503 allele.

artículo científico publicado en 2004

Circulating T lymphocyte subsets in coeliac disease (CoD) patients and healthy family members

artículo científico publicado en 1998

Coeliac disease among healthy members of multiple case coeliac disease families

scientific article published on 01 February 2002

Collection of autologous blood for bone marrow donation: how useful is it?

artículo científico publicado en 2005

Complement activation and HLA-B27

artículo científico publicado en 1988

Concordance of dermatitis herpetiformis and celiac disease in monozygous twins

scientific article published on 01 December 2000

Conflicting HLA assignment by three different typing methods due to the apparent loss of heterozygosity in the MHC region.

artículo científico publicado en 2016

Cost-effective HLA typing with tagging SNPs predicts celiac disease risk haplotypes in the Finnish, Hungarian, and Italian populations

article

Cytokine gene polymorphisms and genetic association with coeliac disease in the Finnish population

artículo científico publicado en 2005

Cytokine gene polymorphisms and risks of acute rejection and delayed graft function after kidney transplantation

artículo científico publicado en 2004

DNA polymorphism unique for a complotype with deletion of HLA-linked C4B and 21-hydroxylase B genes causing congenital adrenal hyperplasia

artículo científico publicado en 1988

Determination of deletion sizes in the MHC-linked complement C4 and steroid 21-hydroxylase genes by pulsed-field gel electrophoresis

article

Diagnosing mild enteropathy celiac disease: a randomized, controlled clinical study

artículo científico publicado en 2008

Diagnosis of acute renal allograft rejection by analyzing whole blood mRNA expression of lymphocyte marker molecules

artículo científico publicado en 2007

Diagnostic significance of HLA-DQ typing in patients with previous coeliac disease diagnosis based on histology alone

artículo científico publicado en 2006

Distinct immunologic features of Finnish Sjögren's syndrome patients with HLA alleles DRB1*0301, DQA1*0501, and DQB1*0201. Alterations in circulating T cell receptor gamma/delta subsets

scientific article published on 01 October 1996

Domestic and foreign donor candidates result in differential probability of matching minor histocompatibility antigens--relevance of selection for hematopoietic stem cell transplantation.

artículo científico publicado en 2009

Donor Haplotype B of NK KIR Receptor Reduces the Relapse Risk in HLA-Identical Sibling Hematopoietic Stem Cell Transplantation of AML Patients

artículo científico publicado en 2014

Donor-recipient mismatch for common gene deletion polymorphisms in graft-versus-host disease

artículo científico publicado en 2009

Elevation of IgG antibodies against tissue transglutaminase as a diagnostic tool for coeliac disease in selective IgA deficiency

artículo científico publicado en 2003

Endomysial antibodies predict celiac disease irrespective of the titers or clinical presentation

artículo científico publicado en 2012

Endomysial antibody-negative coeliac disease: clinical characteristics and intestinal autoantibody deposits

artículo científico publicado en 2006

Expression of HSP-65 in jejunal epithelial cells in patients clinically suspected of coeliac disease

scientific article published on 01 October 1999

Extended HLA haplotypes in families with insulin-dependent diabetes mellitus in northern Finland

artículo científico publicado en 1988

FinDonor 10 000 study: a cohort to identify iron depletion and factors affecting it in Finnish blood donors

artículo científico publicado en 2019

Full likelihood analysis of genetic risk with variable age at onset disease--combining population-based registry data and demographic information

artículo científico publicado en 2009

Functional network reconstruction reveals somatic stemness genetic maps and dedifferentiation-like transcriptome reprogramming induced by GATA2.

artículo científico publicado en 2008

Gamete-level immunogenetic incompatibility in humans-towards deeper understanding of fertilization and infertility?

artículo científico publicado en 2020

Genetic association of coeliac disease susceptibility to polymorphisms in the ICOS gene on chromosome 2q33

article

Genetic background of type I protein C deficiency in Finland

artículo científico publicado en 2005

Genetic dissection between coeliac disease and dermatitis herpetiformis in sib pairs

artículo científico publicado en 2002

Genetic dissection between silent and clinically diagnosed symptomatic forms of coeliac disease in multiplex families

scientific article published on 01 December 2002

Genetic diversity of KIR natural killer cell markers in populations from France, Guadeloupe, Finland, Senegal and Réunion

artículo científico publicado en 2005

Genetic polymorphism H131R of Fcgamma receptor type IIA (FcgammaRIIA) in a healthy Finnish population and in patients with or without platelet-associated IgG.

artículo científico publicado en 1998

Genetic polymorphism in human platelet glycoprotein GP Ib/IX/V complex is enriched in GP V (CD42d).

artículo científico publicado en 1998

Genetic polymorphism of the human ICOS gene

artículo científico publicado en 2002

Genetic polymorphism related to monocyte-macrophage function is associated with graft-versus-host disease.

artículo científico publicado en 2017

Genetic structure of the novel low-frequency haplotype HLA-B49, SC01, DR4 and its contribution to insulin-dependent diabetes susceptibility

scientific article published on 01 January 1992

Genetic susceptibility to gluten sensitive enteropathy in Irish setter dogs is not linked to the major histocompatibility complex

artículo científico publicado en 1998

Genetic susceptibility to severe course of nephropathia epidemica caused by Puumala hantavirus.

artículo científico publicado en 1996

Genetic susceptibility to variant Creutzfeldt-Jakob disease

artículo científico publicado en 2003

Genetic variation in ICOS regulates mRNA levels of ICOS and splicing isoforms of CTLA4.

artículo científico publicado en 2006

Genome scan for predisposing loci for distal interphalangeal joint osteoarthritis: evidence for a locus on 2q.

artículo científico publicado en 1999

Genomewide linkage analysis of celiac disease in Finnish families

artículo científico publicado en 2001

Genomic prediction of relapse in recipients of allogeneic haematopoietic stem cell transplantation

scientific article published on 08 August 2018

Geographic distribution of cervical cancer-associated human leucocyte antigens and cervical cancer incidence in Finland

artículo científico publicado en 2007

Gliadin antibodies in older population and neurological and psychiatric disorders.

artículo científico publicado en 2012

Global gene expression profile of human cord blood-derived CD133+ cells

artículo científico publicado en 2005

Gluten-dependent small bowel mucosal transglutaminase 2-specific IgA deposits in overt and mild enteropathy coeliac disease

artículo científico publicado en 2008

Gluten-sensitive hypertransaminasemia in celiac disease: an infrequent and often subclinical finding

artículo científico publicado en 2011

Glycosylation pattern of anti-platelet IgG is stable during pregnancy and predicts clinical outcome in alloimmune thrombocytopenia

artículo científico publicado en 2016

Graft Immune Cell Composition Associates with Clinical Outcome of Allogeneic Hematopoietic Stem Cell Transplantation in Patients with AML

artículo científico publicado en 2016

HLA DQ and DP in Finnish families with celiac disease

artículo científico publicado en 1996

HLA antigens and complotypes in insulin-dependent diabetes mellitus

artículo científico publicado en 1986

HLA class II associated risk and protection against multiple sclerosis-a Finnish family study

artículo científico publicado en 2002

HLA types in celiac disease patients not carrying the DQA1*05-DQB1*02 (DQ2) heterodimer: results from the European Genetics Cluster on Celiac Disease

artículo científico publicado en 2003

HLA-DQ alleles and human papillomavirus DNA in adult-onset laryngeal papillomatosis

artículo científico publicado en 1999

HLA-DQ typing in the diagnosis of celiac disease

scientific article published on 01 March 2002

HLA-DQ2-negative celiac disease in Finland and Spain.

artículo científico publicado en 1998

HLA-DRB1, -DQB1 alleles in head and neck carcinoma patients

scientific article published on 01 March 2006

Haematopoietic stem cell transplantation induces severe dysbiosis in intestinal microbiota of paediatric ALL patients.

artículo científico publicado en 2017

Heme oxygenase 1 gene polymorphisms and outcome of renal transplantation

artículo científico publicado en 2007

Hidden genomic MHC disparity between HLA-matched sibling pairs in hematopoietic stem cell transplantation.

artículo científico publicado en 2018

High birth weight is associated with human leukocyte antigen (HLA) DRB1*13 in full-term infants

artículo científico publicado en 2004

High-producer allele of tumour necrosis factor-alpha is part of the susceptibility MHC haplotype in severe puumala virus-induced nephropathia epidemica

artículo científico publicado en 1998

Human leukocyte antigen-B8-DR3 is a more important risk factor for severe Puumala hantavirus infection than the tumor necrosis factor-alpha(-308) G/A polymorphism.

artículo científico publicado en 2002

Human leukocyte antigens B8-DRB1*03 in pediatric patients with nephropathia epidemica caused by Puumala hantavirus

artículo científico publicado en 2004

IgA-class autoantibodies against neuronal transglutaminase, TG6 in celiac disease: no evidence for gluten dependency

artículo científico publicado en 2011

Immunogenetic characteristics of patients with autoimmune gastritis

artículo científico publicado en 2010

Immunoglobulin A autoantibodies against transglutaminase 2 in the small intestinal mucosa predict forthcoming coeliac disease.

artículo científico publicado en 2006

Immunomonitoring of MSC-Treated GvHD Patients Reveals Only Moderate Potential for Response Prediction but Indicates Treatment Safety

artículo científico publicado en 2018

In vitro Treg expansion favors the full-length splicing isoform of CTLA4.

artículo científico publicado en 2016

Increased MHC Matching by C4 Gene Compatibility in Unrelated Donor Hematopoietic Stem Cell Transplantation

artículo científico publicado en 2018

Increased density of jejunal gammadelta+ T cells in patients having normal mucosa--marker of operative autoimmune mechanisms?

artículo científico publicado en 1999

Interaction with intestinal epithelial cells promotes an immunosuppressive phenotype in Lactobacillus casei

artículo científico publicado en 2013

Interspliced transcription chimeras: neglected pathological mechanism infiltrating gene accession queries?

artículo científico publicado en 2008

Intestinal transglutaminase 2 specific antibody deposits in non-responsive coeliac disease

artículo científico publicado en 2010

Intolerance to cereals is not specific for coeliac disease.

artículo científico publicado en 2000

Killer-cell immunoglobulin-like receptor gene profile predicts good molecular response to dasatinib therapy in chronic myeloid leukemia.

artículo científico publicado en 2012

Killer-cell immunoglobulin-like receptor ligand compatibility in the outcome of Finnish unrelated donor hematopoietic stem cell transplantation.

artículo científico publicado en 2007

Lack of association between thrombosis-associated and cytokine candidate gene polymorphisms and acute rejection or vascular complications after kidney transplantation

artículo científico publicado en 2007

Lectin from Erythrina cristagalli Supports Undifferentiated Growth and Differentiation of Human Pluripotent Stem Cells ⬇️

artículo científico publicado el 21 de diciembre de 2012

Low-medium resolution HLA-DQ2/DQ8 typing for coeliac disease predisposition analysis by colorimetric assay

scientific article published on 16 March 2012

Major histocompatibility complex (MHC)-linked microsatellite markers in a founder population

artículo científico publicado en 2000

Major histocompatibility complex class II and III in Addison's disease. MHC alleles do not predict autoantibody specificity and 21-hydroxylase gene polymorphism has no independent role in disease susceptibility

scientific article published on 01 October 1994

Medium-high resolution electrochemical genotyping of HLA-DQ2/DQ8 for detection of predisposition to coeliac disease

scientific article published on 15 March 2014

Minor histocompatibility antigens as determinants for graft-versus-host disease after allogeneic haematopoietic stem cell transplantation.

artículo científico publicado en 2013

Molecular characterization of two mutations in platelet glycoprotein (GP) Ib alpha in two Finnish Bernard-Soulier syndrome families

artículo científico publicado en 1999

Multicenter analyses demonstrate significant clinical effects of minor histocompatibility antigens on GvHD and GvL after HLA-matched related and unrelated hematopoietic stem cell transplantation

artículo científico publicado en 2013

Multiplex, fluorescent, solid-phase minisequencing for efficient screening of DNA sequence variation.

artículo científico publicado en 1996

Mutation-haplotype analysis of steroid 21-hydroxylase (CYP21) deficiency in Finland. Implications for the population history of defective alleles

artículo científico publicado en 1997

Myosin IXB gene region and gluten intolerance: linkage to coeliac disease and a putative dermatitis herpetiformis association

article

N-glycan structures and associated gene expression reflect the characteristic N-glycosylation pattern of human hematopoietic stem and progenitor cells.

artículo científico

Not all HLA DR3 DQ2 haplotypes confer equal susceptibility to coeliac disease: transmission analysis in families

scientific article published on 01 January 2002

Novel mutations in the human CYP21 gene

artículo científico publicado en 2001

Novel nonsense mutation (W302X) in the steroid 21-hydroxylase gene of a Finnish patient with the salt-wasting form of congenital adrenal hyperplasia

scientific article published on 01 January 1997

Patients with rheumatoid arthritis and gold-induced pneumonitis express two high-risk major histocompatibility complex patterns

scientific article published on 01 August 1987

Performance of a new rapid whole blood coeliac test in adult patients with low prevalence of endomysial antibodies.

artículo científico publicado en 2007

Persistent small bowel mucosal villous atrophy without symptoms in coeliac disease

artículo científico publicado en 2007

Persistently positive gliadin antibodies without transglutaminase antibodies in the elderly: Gluten intolerance beyond coeliac disease

artículo científico publicado en 2011

Platelet alloantigens HPA-1, -2, -3, -5 and -6b in Finns

scientific article published on 01 September 1995

Population-wide evaluation of disease manifestation in relation to molecular genotype in steroid 21-hydroxylase (CYP21) deficiency: good correlation in a well defined population

scientific article published on 01 October 1997

Protein S gene polymorphisms Pro626 and nt2698--no correlation to free protein S levels or protein S activities

scientific article published on 01 December 2005

Reappraisal of HLA in multiple sclerosis: close linkage in multiplex families

artículo científico publicado en 1993

Restriction fragment analysis of non-deleted complement C4 null genes suggests point mutations in C4A null alleles, but gene conversions in C4B null alleles

artículo científico publicado en 1989

Resurrection of gliadin antibodies in coeliac disease. Deamidated gliadin peptide antibody test provides additional diagnostic benefit

artículo científico publicado en 2007

Retrospective analysis of capillary hemoglobin recovery in nearly 1 200 000 blood donor returns

scientific article published on 08 June 2017

Secretion of celiac disease autoantibodies after in vitro gliadin challenge is dependent on small-bowel mucosal transglutaminase 2-specific IgA deposits

artículo científico publicado en 2008

Secretor genotype (FUT2 gene) is strongly associated with the composition of Bifidobacteria in the human intestine

artículo científico publicado en 2011

Serodiagnostic assays for celiac disease based on the open or closed conformation of the autoantigen, transglutaminase 2

artículo científico publicado en 2011

Single founder mutation (W380G) in type II protein C deficiency in Finland

scientific article published on 01 September 2000

Small-bowel mucosal transglutaminase 2-specific IgA deposits in coeliac disease without villous atrophy: a prospective and randomized clinical study.

artículo científico publicado en 2005

Steroid 21-hydroxylase gene polymorphism in Addison's disease patients

artículo científico publicado en 1995

Substitution of Ile-172 to Asn in the steroid 21-hydroxylase B (P450c21B) gene in a Finnish patient with the simple virilizing form of congenital adrenal hyperplasia

artículo científico publicado en 1991

Systematic screening for genetic polymorphism in human platelet glycoprotein Ibalpha

artículo científico publicado en 1996

T cell epitope-containing peptides of the major dog allergen Can f 1 as candidates for allergen immunotherapy

artículo científico publicado en 2005

T cell regeneration in pediatric allogeneic stem cell transplantation.

artículo científico publicado en 2007

TAP1 and TAP2 polymorphism in HLA-B27-positive subpopulations: no allelic differences in ankylosing spondylitis and reactive arthritis

scientific article published on 01 December 1995

TNF microsatellite alleles a2 and b3 are not primarily associated with celiac disease in the Finnish population

artículo científico publicado en 1998

Technical note: linkage disequilibrium and disease-associated CTLA4 gene polymorphisms

article

The DR4-DQ8 haplotype and a specific T cell receptor Vbeta T cell subset are associated with absence of allergy to Can f 1.

artículo científico publicado en 2005

The HLA-DRB4 gene does not explain genetic susceptibility in HLA-DQ2-negative celiac disease

scientific article published on 01 March 2000

The association between mannan-binding lectin gene alleles and celiac disease

scientific article published on 01 December 2003

The duodenal microbiota composition of adult celiac disease patients is associated with the clinical manifestation of the disease

artículo científico publicado en 2013

The impact of donor cytokine gene polymorphisms on the incidence of cytomegalovirus infection after kidney transplantation

artículo científico publicado en 2006

The natural history of an HLA haplotype and its recombinants.

artículo científico publicado en 1998

The prevalence of celiac disease among family members of celiac disease patients

scientific article published on 01 January 2004

The severity of acute Puumala hantavirus infection does not predict the long-term outcome of patients

artículo científico publicado en 2010

The shared CTLA4-ICOS risk locus in celiac disease, IgA deficiency and common variable immunodeficiency.

artículo científico publicado en 2008

Toll-like receptor gene polymorphisms confer susceptibility to graft-versus-host disease in allogenic hematopoietic stem cell transplantation.

artículo científico publicado en 2012

Tracing past population migrations: genealogy of steroid 21-hydroxylase (CYP21) gene mutations in Finland

artículo científico publicado en 1999

Transcriptional profiling reflects shared and unique characters for CD34+ and CD133+ cells

artículo científico publicado en 2006

Use of closely related affected individuals for the genetic study of complex diseases in founder populations.

artículo científico publicado en 2000

Variant Bernard-Soulier syndrome due to homozygous Asn45Ser mutation in the platelet glycoprotein (GP) IX in seven patients of five unrelated Finnish families.

artículo científico publicado en 1999

Villous tip intraepithelial lymphocytes as markers of early-stage coeliac disease

scientific article published on 01 May 2004

ss-cell autoantibodies, human leukocyte antigen II alleles, and type 1 diabetes in autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy

artículo científico publicado en 2000

Dominio Público Uruguay está sostenido por:

Acerca de Dominio Público Uruguay

Ayuda