458 results on '"Remmers, Elaine F."'
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52. Meta-analysis of genome-wide association studies in celiac disease and rheumatoid arthritis identifies fourteen non-HLA shared loci
53. Contributors
54. A genetic linkage map of rat chromosome 20 derived from five F2 crosses
55. Familial mediterranean fever with a single MEFV mutation: Where is the second hit?
56. Genetic risk factors for rheumatoid arthritis differ in caucasian and Korean populations
57. The Chromosome 7q Region Association With Rheumatoid Arthritis in Females in a British Population Is Not Replicated in a North American Case–Control Series
58. Severe delayed hypersensitivity reactions to IL-1 and IL-6 inhibitors link to common HLA-DRB1*15 alleles.
59. Rheumatoid Arthritis, Systemic Lupus Erythematosus, and STAT4
60. The clinical continuum of cryopyrinopathies: Novel CIAS1 mutations in North American patients and a new cryopyrin model
61. 19 - Principles and techniques in molecular biology
62. Ten polymorphic DNA loci, including five in the rat MHC (RT1) region, form a single linkage group on rat chromosome 20
63. Mutational Analysis in Neonatal-Onset Multisystem Inflammatory Disease: Comment on the Articles by Frenkel et al and Saito et al
64. The functional −169T→C single-nucleotide polymorphism in FCRL3 is not associated with rheumatoid arthritis in white North Americans
65. Genetic map of seven polymorphic markers comprising a single linkage group on rat Chromosome 5
66. Four polymorphic markers on rat chromosome 12 form a single linkage group
67. Regulation of Anti–Cyclic Citrullinated Peptide Antibodies in Rheumatoid Arthritis: Contrasting Effects of HLA–DR3 and the Shared Epitope Alleles
68. Linkage map of seven polymorphic markers on rat Chromosome 18
69. Map of seven polymorphic markers on rat Chromosome 14: linkage conservation with human Chromosome 4
70. Genetic mapping of the athymic nude (RNU) locus in the rat to a region on Chromosome 10
71. The non–Major Histocompatibility Complex Quantitative Trait Locus Cia10 Contains a Major Arthritis Gene and Regulates Disease Severity, Pannus Formation, and Joint Damage
72. Genomic regions controlling corticosterone levels in rats
73. Application of interval haplotype analysis facilitates efficient mapping of the mutation causing osteopetrosis in tl rats
74. Identification of Two Novel Female-Specific Non–Major Histocompatibility Complex Loci Regulating Collagen-Induced Arthritis Severity and Chronicity, and Evidence of Epistasis
75. Polymorphisms of the tumor necrosis factor receptor type 1 locus among autoimmune susceptible and resistant inbred rat strains
76. De novo CIAS1 Mutations, Ctokine Activation, and Evidence for Genetic Heterogeneity in Patients With Neonatal-Onset Multisystem Inflammatory Disease (NOMID): A New Member of the Expanding Family of Pyrin-Associated Autoinflammatory Diseases
77. Modulation of Multiple Experimental Arthritis Models by Collagen-Induced Arthritis Quantitative Trait Loci Isolated in Congenic Rat Lines: Different Effects of Non–Major Histocompatibility Complex Quantitative Trait Loci in Males and Females
78. Evaluation of Quantitative Trait Loci Regulating Severity of Mycobacterial Adjuvant-Induced Arthritis in Monocongenic and Polycongenic Rats: Identification of a New Regulatory Locus on Rat Chromosome 10 and Evidence of Overlap With Rheumatoid Arthritis Susceptibility Loci
79. Genetic analysis of collagen-induced arthritis in rats: a polygenic model for rheumatoid arthritis predicts a common framework of cross-species inflammatory/autoimmune disease loci
80. A genetic linkage map of rat Chromosome 15 derived from five F2 crosses
81. IDENTIFICATION OF FOUR NEW QUANTITATIVE TRAIT LOCI REGULATING ARTHRITIS SEVERITY AND ONE NEW QUANTITATIVE TRAIT LOCUS REGULATING AUTOANTIBODY PRODUCTION IN RATS WITH COLLAGEN-INDUCED ARTHRITIS
82. Susceptibility to Autoimmune Disease and Drug Addiction in Inbred Rats: Are There Mechanistic Factors in Common Related to Abnormalities in Hypothalamic-Pituitary-Adrenal Axis and Stress Response Function?
83. HLAand autoantibodies define scleroderma subtypes and risk in African and European Americans and suggest a role for molecular mimicry
84. IDENTIFICATION OF A NEW NON-MAJOR HISTOCOMPATIBILITY COMPLEX GENETIC LOCUS ON CHROMOSOME 2 THAT CONTROLS DISEASE SEVERITY IN COLLAGEN-INDUCED ARTHRITIS IN RATS
85. Mutation of macrophage colony stimulating factor ( Csf1) causes osteopetrosis in the tl rat
86. Cyclooxygenase-1 and -2 Expression in Rheumatoid Synovial Tissues: Effects of Interleukin-1beta, Phorbol Ester, and Corticosteroids
87. Sequence‐Based Screening of Patients With Idiopathic Polyarteritis Nodosa, Granulomatosis With Polyangiitis, and Microscopic Polyangiitis for Deleterious Genetic Variants in ADA2.
88. Coexpression of Phosphotyrosine-containing Proteins, Platelet-derived Growth Factor-B, and Fibroblast Growth Factor-1 In Situ in Synovial Tissues of Patients With Rheumatoid Arthritis and Lewis Rats With Adjuvant or Streptococcal Cell Wall Arthritis
89. Deficiency of Complement 1r subcomponent in early-onset SLE: Role for disease-modifying alleles in a monogenic disease
90. An Integrated Genetic Linkage Map with 1137 Markers Constructed from Five F2 Crosses of Autoimmune Disease-Prone and -Resistant Inbred Rat Strains
91. Brief Report: Whole‐Exome Sequencing to Identify Rare Variants and Gene Networks That Increase Susceptibility to Scleroderma in African Americans
92. Mapping autoimmunity genes
93. Deficiency Of Complement 1R Subcomponent In Early-Onset Systemic Lupus Erythematosus: The Role Of Disease-Modifying Alleles In A Monogenic Disease
94. 12 - Principles and techniques in molecular biology
95. Aberrant tRNA processing causes an autoinflammatory syndrome responsive to TNF inhibitors
96. Three variants in the nicotinamide adenine dinucleotide phosphate oxidase complex are associated with HCV‐related liver damage
97. HLA-DRB1*11 and variants of the MHC class II locus are strong risk factors for systemic juvenile idiopathic arthritis
98. Cryopyrin-associated Periodic Syndrome Caused by a Myeloid-Restricted Somatic NLRP3 Mutation
99. Clinical and serological features of systemic sclerosis in a multicenter African American cohort: Analysis of the genome research in African American scleroderma patients clinical database.
100. Contributors
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