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Genetic protection from the inflammatory disease type 1 diabetes in humansand animal models
IMMUNITY
Haplotype tagging for the identification of common disease genes
NATURE GENETICS
Conditional linkage disequilibrium analysis of a complex disease superlocus, IDDM1 in the HLA region, reveals the presence of independent modifying gene effects influencing the type 1 diabetes risk encoded by the major HLA-DQB1,-DRB1 disease loci
HUMAN MOLECULAR GENETICS
A correlation between the relative predisposition of MHC class II alleles to type 1 diabetes and the structure of their proteins
HUMAN MOLECULAR GENETICS
The murine type 1 diabetes loci, Idd1, Idd3, Idd5, Idd9, and idd17/10/18, do not control thymic CD4(-)CD8(-)/TCR alpha beta(+) deficiency in the nonobese diabetic mouse
MAMMALIAN GENOME
The sequence and gene characterization of a 400-kb candidate region for IDDM4 on chromosome 11q13
GENOMICS
The prescribing of acid suppressants prior to the endoscopic diagnosis of Barrett's oesophagus and oesophagitis
ALIMENTARY PHARMACOLOGY & THERAPEUTICS
Human genetics - Tackling common disease
NATURE
Statistical modeling of interlocus interactions in a complex disease: Rejection of the multiplicative model of epistasis in type 1 diabetes
GENETICS
Low frequency of HLA DRB1*03-DQB1*02 and DQB1*0302 haplotypes in Romania is consistent with the country's low incidence of Type I diabetes
DIABETOLOGIA
The HLA-DPB1-associated component of the IDDM1 and its relationship to themajor loci HLA-DQB1,-DQA1, and-DRB1
DIABETES
Mapping by genetic interaction - High-resolution congenic mapping of the type 1 diabetes loci Idd10 and Idd18 in the NOD mouse
DIABETES
Suggestive evidence for association of human chromosome 18q12-q21 and its orthologue on rat and mouse chromosome 18 with several autoimmune diseases
DIABETES
Seven regions of the genome show evidence of linkage to type 1 diabetes ina consensus analysis of 767 multiplex families
AMERICAN JOURNAL OF HUMAN GENETICS
Taphonomy
PALAEOBIOLOGY II
Crystal structure of 1-(phthalimidoethyl)-1,2-dicarba-closo-dodecaborane, C12H19B10NO2
ZEITSCHRIFT FUR KRISTALLOGRAPHIE-NEW CRYSTAL STRUCTURES
Crystal structure of 1-(phthalimidomethyl)-1,2-dicarba-closo-dodecaborane,C11H17B10NO2
ZEITSCHRIFT FUR KRISTALLOGRAPHIE-NEW CRYSTAL STRUCTURES
Congenic mapping of the type 1 diabetes locus, ldd3, to a 780-kb region ofmouse chromosome 3: Identification of a candidate segment of ancestral DNAby haplotype mapping
GENOME RESEARCH
Evaluation of single nucleotide polymorphism typing with invader on PCR amplicons and its automation
GENOME RESEARCH
The NOD Idd9 genetic interval influences the pathogenicity of insulitis and contains molecular variants of Cd30, Tnfr2, and Cd137
IMMUNITY
The genetically isolated populations of Finland and Sardinia may not be a panacea for linkage disequilibrium mapping of common disease genes
NATURE GENETICS
Evidence for Early Bronze Age tin ore processing
MATERIALS CHARACTERIZATION
Differential glycosylation of interleukin 2, the molecular basis for the NOD Idd3 type 1 diabetes gene?
CYTOKINE
Evaluation of fine mapping strategies for a multifactorial disease locus: systematic linkage and association analysis of IDDM1 in the HLA region on chromosome 6p21
HUMAN MOLECULAR GENETICS
Influence of allele lineage on the role of the insulin minisatellite in susceptibility to type 1 diabetes
HUMAN MOLECULAR GENETICS
Major factors influencing linkage disequilibrium by analysis of different chromosome regions in distinct populations: demography chromosome recombination frequency and selection
HUMAN MOLECULAR GENETICS
The inter-regional distribution of HLA class II haplotypes indicates the suitability of the Sardinian population for case-control association studiesin complex diseases
HUMAN MOLECULAR GENETICS
Confirmation of the DRB1-DQB1 loci as the major component of IDDM1 in the isolated founder population of Sardinia
HUMAN MOLECULAR GENETICS
Strategies in complex disease mapping
CURRENT OPINION IN GENETICS & DEVELOPMENT
Response to open access endoscopy findings by general practitioners guidelines need education for implementation
SCOTTISH MEDICAL JOURNAL
Determinants of the quantity of hepatitis C virus RNA
JOURNAL OF INFECTIOUS DISEASES
Expression of the Type I diabetes-associated gene LRP5 in macrophages, vitamin A system cells, and the islets of Langerhans suggests multiple potential roles in diabetes
JOURNAL OF HISTOCHEMISTRY & CYTOCHEMISTRY
Analysis of the mouse CD30 gene - A candidate for the NOD mouse type 1 diabetes locus Idd9.2
DIABETES
NOD Idd5 locus controls insulitis and diabetes and overlaps the orthologous CTLA4/IDDM12 and NRAMP1 loci in humans
DIABETES
Adaptation of the extended transmission/disequilibrium test to distinguishdisease associations of multiple loci: the Conditional Extended Transmission/Disequilibrium Test
ANNALS OF HUMAN GENETICS
Conditional ETDT analysis of the Human Leukocyte Antigen region in type 1 diabetes
ANNALS OF HUMAN GENETICS
Unbiased application of the transmission/disequilibrium test to multilocushaplotypes
AMERICAN JOURNAL OF HUMAN GENETICS
Transmission-ratio distortion at Xp11.4-p21.1 in type 1 diabetes
AMERICAN JOURNAL OF HUMAN GENETICS
HLA class II typing of whole genome amplified mouth swab DNA
TISSUE ANTIGENS
Transmission ratio distortion at the INS-IGF2 VNTR
NATURE GENETICS
The insulin gene VNTR, type 2 diabetes and birth weight
NATURE GENETICS
INS VNTR allelic variation and dynamic insulin secretion in healthy adult non-diabetic Caucasian subjects
DIABETIC MEDICINE
From genome to aetiology in a multifactorial disease, type 1 diabetes
BIOESSAYS
Interpretation of results from genetic studies of multifactorial diseases
LANCET
The predisposition to type 1 diabetes linked to the human leukocyte antigen complex includes at least one non-class II gene
AMERICAN JOURNAL OF HUMAN GENETICS
Creep behavior of Si3N4-whisker-reinforced Si3N4-matrix composites using an in situ dynamic beam profiling method
JOURNAL OF THE AMERICAN CERAMIC SOCIETY
A SEARCH FOR TYPE-1 DIABETES SUSCEPTIBILITY GENES IN FAMILIES FROM THE UNITED-KINGDOM
Nature genetics
A MALE-FEMALE BIAS IN TYPE-1 DIABETES AND LINKAGE TO CHROMOSOME XP INMHC HLA-DR3-POSITIVE PATIENTS
Nature genetics
ASSOCIATION OF THE INS VNTR WITH SIZE AT BIRTH
Nature genetics
TRANSMISSION OF HAPLOTYPES OF MICROSATELLITE MARKERS RATHER THAN SINGLE MARKER ALLELES IN THE MAPPING OF A PUTATIVE TYPE-1 DIABETES SUSCEPTIBILITY GENE (IDDM6)
Human molecular genetics
LOCALIZATION OF 2 INSULIN-DEPENDENT DIABETES (IDD) GENES TO THE IDD10REGION ON MOUSE-CHROMOSOME-3
Mammalian genome
CLONING OF A NOVEL MEMBER OF THE LOW-DENSITY-LIPOPROTEIN RECEPTOR FAMILY
Gene
NEW GENETIC-LOCI THAT CONTROL SUSCEPTIBILITY AND SYMPTOMS OF EXPERIMENTAL ALLERGIC ENCEPHALOMYELITIS IN INBRED MICE
The Journal of immunology (1950)
DIVERGENCE BETWEEN GENETIC-DETERMINANTS OF IGF2 TRANSCRIPTION LEVELS IN LEUKOCYTES AND OF IDDM2-ENCODED SUSCEPTIBILITY TO TYPE-1 DIABETES
The Journal of clinical endocrinology and metabolism
MAPPING MULTIPLE LINKED QUANTITATIVE TRAIT LOCI IN NONOBESE DIABETIC MICE USING A STEPWISE REGRESSION STRATEGY
Genetical Research
INSULIN VNTR AND HLA DRB1 DQB1 LOCI AFFECT AGE OF PRESENTATION OF AUTOIMMUNE DIABETES IN ADULTS/
Diabetologia
ALLELIC VARIATION AT THE INS VNTR LOCUS IS ASSOCIATED WITH CHANGES INTHE PATTERN OF PULSATILE INSULIN RELEASE
Diabetologia
INVESTIGATION OF LINKAGE OF CHROMOSOME-8 TO TYPE-1 DIABETES - MULTIPOINT ANALYSIS AND EXCLUSION MAPPING OF HUMAN-CHROMOSOME-8 IN 593 AFFECTED SIB-PAIR FAMILIES FROM THE UK AND US
Diabetes
ASSOCIATION OF APOLIPOPROTEIN EPSILON-2 ALLELE WITH DIABETIC NEPHROPATHY IN CAUCASIAN SUBJECTS WITH IDDM
Diabetes
GENETIC-ANALYSIS OF CHROMOSOME-2 IN TYPE-1 DIABETES - ANALYSIS OF PUTATIVE LOCI IDDM7, IDDM12, AND IDDM13 AND CANDIDATE GENES NRAMP1 AND IA-2 AND THE INTERLEUKIN-1 GENE-CLUSTER
Diabetes
THE HLA LINKED PREDISPOSITION TO DEVELOP TYPE-1 DIABETES INCLUDES A GENE LOCATED TELOMERIC TO THE HLA CLASS-II REGION
Diabetes
ISOLATION AND CHARACTERIZATION OF LRP6, A NOVEL MEMBER OF THE LOW-DENSITY-LIPOPROTEIN RECEPTOR GENE FAMILY
Biochemical and biophysical research communications (Print)
FINE MAPPING OF THE DIABETES-SUSCEPTIBILITY LOCUS, IDDM4, ON CHROMOSOME 11Q13
American journal of human genetics
AN ACCELERATED TEST METHOD FOR DETERMINING NEAR-THRESHOLD STRESS INTENSITY VALUES IN HSLA STEELS
Fatigue & fracture of engineering materials & structures
DEVELOPMENT OF A PROTOTYPE LASER PROCESSING SYSTEM FOR SHAPING ADVANCED CERAMIC MATERIALS
Journal of manufacturing science and engineering
PANNING FOR GOLD - GENOMEWIDE SCANNING IN TYPE-1 DIABETES (REPRINTED FROM HUMAN MOLECULAR-GENETICS, VOL 5, PG 1443-1448, 1996)
Diabetes reviews
INSULIN VNTR ALLELE-SPECIFIC EFFECT IN TYPE-1 DIABETES DEPENDS ON IDENTITY OF UNTRANSMITTED PATERNAL ALLELE
Nature genetics
INSULIN EXPRESSION IN HUMAN THYMUS IS MODULATED BY INS VNTR ALLELES AT THE IDDM2 LOCUS
Nature genetics
FRAMEWORK YAC CONTIG ANCHORED INTO A 3.2-MB HIGH-RESOLUTION PHYSICAL MAP IN PROXIMAL 11Q13
Genomics
GENETICS OF TYPE-1 DIABETES
Pathologie et biologie
INDIVIDUALS FROM MULTIPLEX INSULIN-DEPENDENT DIABETES-MELLITUS FAMILIES EXPRESS HIGHER LEVELS OF TCRBV2S1 THAN CONTROLS
Biochemical Society transactions
ASSOCIATION OF INSULIN GENE VNTR POLYMORPHISM WITH POLYCYSTIC-OVARY-SYNDROME - REPLY
Lancet
LINKAGE AND ASSOCIATION OF INSULIN GENE VNTR REGULATORY POLYMORPHISM WITH POLYCYSTIC-OVARY-SYNDROME
Lancet
CRACK CLOSURE EFFECTS ON FATIGUE-CRACK GROWTH THRESHOLDS AND REMAINING LIFE IN AN HSLA STEEL
Journal of pressure vessel technology
LATE JURASSIC SOFT-BODIED WOOD EPIBIONTS PRESERVED BY BIOIMMURATION
Lethaia
CONGENIC MAPPING OF THE INSULIN-DEPENDENT DIABETES (IDD) GENE, IDD10,LOCALIZES 2 GENE MEDIATING THE IDD10 EFFECT AND ELIMINATES THE CANDIDATE FCGR1
The Journal of immunology
A BIOIMMURED CTENOSTOME BRYOZOAN FROM THE EARLY CRETACEOUS OF THE CRIMEA AND THE NEW GENUS SIMPLICIDIUM
Geobios
MAPPING OF THE IDDM LOCUS IDD3 TO A 0.35-CM INTERVAL CONTAINING THE INTERLEUKIN-2 GENE
Diabetes
PLASMA VIRAL LOAD AND CD4(-1 INFECTION() LYMPHOCYTES AS PROGNOSTIC MARKERS OF HIV)
Annals of internal medicine
LINKAGE OF CHROMOSOME-6 AND TYPE-1 DIABETES
DNA sequence
SATURATION MULTIPOINT LINKAGE MAPPING OF CHROMOSOME 6Q IN TYPE-1 DIABETES
Human molecular genetics
THE CTLA-4 GENE REGION OF CHROMOSOME 2Q33 IS LINKED TO, AND ASSOCIATED WITH, TYPE-1 DIABETES
Human molecular genetics
PANNING FOR GOLD - GENOME-WIDE SCANNING FOR LINKAGE IN TYPE-1 DIABETES
Human molecular genetics
IDDM2-VNTR-ENCODED SUSCEPTIBILITY TO TYPE-1 DIABETES - DOMINANT PROTECTION AND PARENTAL TRANSMISSION OF ALLELES OF THE INSULIN GENE-LINKED MINISATELLITE LOCUS
Journal of autoimmunity
MAPPING OF IDDM7, A DIABETES SUSCEPTIBILITY GENE ON CHROMOSOME-2
Cytogenetics and cell genetics
GENETIC-ANALYSIS OF AUTOIMMUNE-DISEASE
Cell
HUMAN TYPE-1 DIABETES AND THE INSULIN GENE - PRINCIPLES OF MAPPING POLYGENES
Annual review of genetics
PROGNOSIS IN HIV-1 INFECTION PREDICTED BY THE QUANTITY OF VIRUS IN PLASMA
Science
MATERNAL VIRAL LOAD, ZIDOVUDINE TREATMENT, AND THE RISK OF TRANSMISSION OF HUMAN-IMMUNODEFICIENCY-VIRUS TYPE-1 FROM MOTHER-TO-INFANT
The New England journal of medicine
HUMAN-GENETICS - TRANSCRIBING DIABETES
Nature
GENETICS OF INSULIN-DEPENDENT DIABETES - NONMAJOR HISTOCOMPATIBILITY GENES
Hormone and Metabolic Research
EXAMINATION OF 2 GENETIC POLYMORPHISMS WITHIN THE RENIN-ANGIOTENSIN SYSTEM - NO EVIDENCE FOR AN ASSOCIATION WITH NEPHROPATHY IN IDDM
Diabetologia
CTLA-4 GENE POLYMORPHISM CONFERS SUSCEPTIBILITY TO IDDM INDEPENDENTLYFROM GENETIC AND IMMUNE DISEASE MARKERS
Diabetologia
CTLA-4 REGION PREDISPOSES TO IDDM AND GRAVES-DISEASE
Diabetologia
RAPID AND PRECISE QUANTIFICATION OF HIV-1 RNA IN PLASMA USING A BRANCHED DNA SIGNAL AMPLIFICATION ASSAY
Journal of acquired immune deficiency syndromes and human retrovirology
TOWARDS FULLY AUTOMATED GENOME-WIDE POLYMORPHISM SCREENING
Nature genetics
SUSCEPTIBILITY TO HUMAN TYPE-1 DIABETES AT IDDM2 IS DETERMINED BY TANDEM REPEAT VARIATION AT THE INSULIN GENE MINISATELLITE LOCUS
Nature genetics
LINKAGE DISEQUILIBRIUM MAPPING OF A TYPE-1 DIABETES SUSCEPTIBILITY GENE (IDDM7) TO CHROMOSOME 2Q31-Q33
Nature genetics
INSULIN EXPRESSION - IS VNTR ALLELE-698 REALLY ANOMALOUS - REPLY
Nature genetics
MUTATION OF THE GLUCAGON RECEPTOR GENE AND DIABETES-MELLITUS IN THE UK - ASSOCIATION OR FOUNDER EFFECT
Human molecular genetics