Published in Thromb Haemost on April 30, 1982
Influence of blood specimen collection method on various preanalytical sample quality indicators. Indian J Clin Biochem (2008) 0.95
Influence of blood collection systems on coagulation tests. Turk J Haematol (2012) 0.75
Quantitative assessment of prevalence of pre-analytical variables and their effect on coagulation assay. Can intervention improve patient safety? Med J Armed Forces India (2017) 0.75
Positional cloning of the APECED gene. Nat Genet (1997) 5.47
Failure of the International Normalized Ratio to generate consistent results within a local medical community. Am J Clin Pathol (1993) 2.81
Opsonic requirements for staphylococcal phagocytosis. Heterogeneity among strains. Immunology (1977) 2.73
In vitro activity of cephalosporins against methicillin-resistant, coagulase-negative staphylococci. J Infect Dis (1978) 2.39
Highly sensitive thromboplastins do not improve INR precision. Am J Clin Pathol (1998) 2.03
Putative receptor binding sites on alphaviruses as visualized by cryoelectron microscopy. Proc Natl Acad Sci U S A (1995) 1.81
Experience of the Polycythemia Vera Study Group with essential thrombocythemia: a final report on diagnostic criteria, survival, and leukemic transition by treatment. Semin Hematol (1997) 1.78
Plaque color method for rapid isolation of novel recA mutants of Escherichia coli K-12: new classes of protease-constitutive recA mutants. J Bacteriol (1985) 1.74
Identification by molecular cloning of an autoantigen associated with Addison's disease as steroid 17 alpha-hydroxylase. Lancet (1992) 1.73
Isolation and initial characterization of a novel zinc finger gene, DNMT3L, on 21q22.3, related to the cytosine-5-methyltransferase 3 gene family. Genomics (2000) 1.70
Two subsets of epithelial cells in the thymic medulla. J Exp Med (1992) 1.59
Uptake and activity of rifapentine in human peritoneal macrophages and polymorphonuclear leukocytes. Eur J Clin Microbiol (1987) 1.55
RNA and protein expression of the murine autoimmune regulator gene (Aire) in normal, RelB-deficient and in NOD mouse. Eur J Immunol (2000) 1.55
NIH conference. Chronic fatigue syndrome research. Definition and medical outcome assessment. Ann Intern Med (1992) 1.50
Vitamin A teratogenicity and risk assessment in the macaque retinoid model. Reprod Toxicol (2000) 1.50
The autoimmune regulator protein has transcriptional transactivating properties and interacts with the common coactivator CREB-binding protein. J Biol Chem (2000) 1.49
Autoimmune regulator is expressed in the cells regulating immune tolerance in thymus medulla. Biochem Biophys Res Commun (1999) 1.48
Lipids of human leukocytes: relation to celltype. J Lipid Res (1967) 1.45
Correlation of 24-hour urinary protein quantification with spot urine protein:creatinine ratio in lupus nephritis. Lupus (2012) 1.42
Heart transplantation in patients with heparin-induced thrombocytopenia on the Novacor left ventricular assist system. J Heart Lung Transplant (1998) 1.39
Selecting T cell receptors with high affinity for self-MHC by decreasing the contribution of CD8. Science (1992) 1.38
[Mystery of the blue man: alkaptonuria]. Duodecim (1997) 1.37
A common mutation in Sardinian autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy patients. Hum Genet (1998) 1.30
Autoimmune regulator: from loss of function to autoimmunity. Genes Immun (2003) 1.21
Effects of the glucosidase inhibitors nojirimycin and deoxynojirimycin on the biosynthesis of membrane and secretory glycoproteins. EMBO J (1983) 1.20
Glycerol lysis time as a screening test for erythrocyte disorders. J Lab Clin Med (1974) 1.16
Genetic studies in neural tube defects. NTD Collaborative Group. Pediatr Neurosurg (2000) 1.15
Cooperative activation of transcription by autoimmune regulator AIRE and CBP. Biochem Biophys Res Commun (2005) 1.14
Mutation analyses of North American APS-1 patients. Hum Mutat (1999) 1.14
A randomized phase III trial comparing standard and high-dose pemetrexed as second-line treatment in patients with locally advanced or metastatic non-small-cell lung cancer. Ann Oncol (2008) 1.13
Hepatic vascular disease and portal hypertension in polycythemia vera and agnogenic myeloid metaplasia: a clinicopathological study of 145 patients examined at autopsy. Hepatology (1990) 1.11
Common mutations in autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy patients of different origins. Mol Endocrinol (1998) 1.11
Teaching peer review. JAMA (1973) 1.10
Pathologist review of the peripheral smear. A mandatory quality assurance activity? Clin Lab Med (1993) 1.10
Subcellular localization of the autoimmune regulator protein. characterization of nuclear targeting and transcriptional activation domain. J Biol Chem (2001) 1.08
From efficacy to safety: a Polycythemia Vera Study group report on hydroxyurea in patients with polycythemia vera. Semin Hematol (1997) 1.05
Benign reversible muscle cytochrome c oxidase deficiency: a second case. Neurology (1987) 1.04
Deficiency of the autoimmune regulator AIRE in thymomas is insufficient to elicit autoimmune polyendocrinopathy syndrome type 1 (APS-1). J Pathol (2007) 1.04
Successful amplification of DNA specific for Finnish Borrelia burgdorferi isolates in erythema chronicum migrans but not in circumscribed scleroderma lesions. J Invest Dermatol (1994) 1.04
Hemoglobin from a deep-sea hydrothermal-vent copepod. Biol Bull (2000) 1.03
Autoantibodies to cytochrome P450 enzymes P450scc, P450c17, and P450c21 in autoimmune polyglandular disease types I and II and in isolated Addison's disease. J Clin Endocrinol Metab (1994) 1.01
Adalimumab in clinical practice. Outcome in 70 rheumatoid arthritis patients, including comparison of patients with and without previous anti-TNF exposure. Rheumatology (Oxford) (2005) 1.01
Isolation and characterization of human B cell alloantigens. J Immunol (1976) 1.00
Studies of the bone marrow in polycythemia vera and the evolution of myelofibrosis and second hematologic malignancies. Semin Hematol (1986) 1.00
Evidence for linkage to psychosis and cerebral asymmetry (relative hand skill) on the X chromosome. Am J Med Genet (1998) 0.99
Nasopharyngeal perforation as a complication of nasogastric intubation. Ear Nose Throat J (1993) 0.98
The effects of various load paths and different loads on the load transfer characteristics of the wrist. J Hand Surg Am (1989) 0.98
Bioenergetic heterogeneity of human mitochondrial myopathies: phosphorus magnetic resonance spectroscopy study. Neurology (1987) 0.97
Hepatotoxicity of salicylates in monolayer cell cultures. Gastroenterology (1978) 0.96
Analysis of extended human leukocyte antigen haplotype association with Addison's disease in three populations. Eur J Endocrinol (2007) 0.96
Adult onset Still's disease and collapsing glomerulopathy: successful treatment with intravenous immunoglobulins and mycophenolate mofetil. Rheumatology (Oxford) (2004) 0.96
Isolation and initial characterization of the mouse Dnmt3l gene. Cytogenet Cell Genet (2001) 0.95
Identification of Her-2/Neu CTL epitopes using double transgenic mice expressing HLA-A2.1 and human CD.8. Hum Immunol (1997) 0.94
SAP30L interacts with members of the Sin3A corepressor complex and targets Sin3A to the nucleolus. Nucleic Acids Res (2006) 0.94
Intraoperative autologous blood donation preserves red cell mass but does not decrease postoperative bleeding. Ann Thorac Surg (1996) 0.94
Medial (hamate) facet of the lunate. J Hand Surg Am (1990) 0.94
The diagnostic significance of a prolonged erythrocytic glycerol lysis time (GLT50). Am J Clin Pathol (1978) 0.92
Benign cervical teratoma in the adult: report of a rare case with dense fibrosis involving adjacent vital structures. Otolaryngol Head Neck Surg (1996) 0.92
Isolation and characterization of the mouse Aire gene. Biochem Biophys Res Commun (1999) 0.91
Blocking of HLA and B lymphocyte alloantigens with F (ab')2 fragments of rabbit antibodies. J Immunol (1976) 0.90
Novel AIRE mutations and P450 cytochrome autoantibodies in Central and Eastern European patients with APECED. Hum Mutat (2001) 0.90
Clinical presentation and natural history of patients with essential thrombocythemia and the Philadelphia chromosome. Am J Hematol (1988) 0.90
Anti-cytokine autoantibodies preceding onset of autoimmune polyendocrine syndrome type I features in early childhood. J Clin Immunol (2013) 0.89
APECED mutations in the autoimmune regulator (AIRE) gene. Hum Mutat (2001) 0.89
A cytotoxic T lymphocyte antigen-4 (CTLA-4) gene polymorphism is associated with autoimmune Addison's disease in English patients. Clin Endocrinol (Oxf) (1998) 0.88
Infant botulism in the age of botulism immune globulin. Neurology (2005) 0.88
In vitro antistaphylococcal activity of teicoplanin and ciprofloxacin in peritoneal dialysis effluent. Eur J Clin Microbiol (1986) 0.88
Prolonged prothrombin time and activated partial thromboplastin time due to underfilled specimen tubes with 109 mmol/L (3.2%) citrate anticoagulant. Am J Clin Pathol (1998) 0.88
Patterns of serologic specificity of human gamma-G erythrocyte autoantibodies. Correlation of antibody specificity with complement-fixing behavior. J Immunol (1970) 0.87
Fracture-dislocation of the base of the fifth metacarpal associated with injury to the deep motor branch of the ulnar nerve: a case report. J Hand Surg Am (1986) 0.87
A phase II trial of high-dose bromodeoxyuridine with accelerated fractionation radiotherapy followed by procarbazine, lomustine, and vincristine for glioblastoma multiforme. Int J Radiat Oncol Biol Phys (1999) 0.87
A linkage study of schizophrenia to markers within Xp11 near the MAOB gene. Psychiatry Res (1997) 0.87
Mediastinal-width/chest-width ratio in blunt chest trauma: a reappraisal. AJR Am J Roentgenol (1984) 0.86
Soluble HLA antigens present in normal human serum. Tissue Antigens (1977) 0.86
Hypothetical review: thymic aberrations and type-I interferons; attempts to deduce autoimmunizing mechanisms from unexpected clues in monogenic and paraneoplastic syndromes. Clin Exp Immunol (2008) 0.86
Anti-cytokine autoantibodies suggest pathogenetic links with autoimmune regulator deficiency in humans and mice. Clin Exp Immunol (2013) 0.85
Autoimmune hemolytic anemia with predominance of IgA autoantibody. Transfusion (1982) 0.85
Multiple manifestations of renovascular hypertension. Am J Kidney Dis (1994) 0.85
Mutational analysis of the HGO gene in Finnish alkaptonuria patients. J Med Genet (1999) 0.84
Hereditary nonspherocytic hemolytic disease associated with an altered phospholipid composition of the erythrocytes. J Clin Invest (1968) 0.84
The bone marrow in polycythemia vera. Pathol Annu (1979) 0.84
Application of regularized Richardson-Lucy algorithm for deconvolution of confocal microscopy images. J Microsc (2011) 0.83
Neurofibroma involving the penis in a child. J Urol (1984) 0.83
Lipid patterns of leukocytes in health and disease. Semin Hematol (1972) 0.82
Glycerol lysis time of incubated erythrocytes in the diagnosis of hereditary spherocytosis. J Lab Clin Med (1974) 0.82
The absence of B-cell antigen B2 from leukaemia cells and lymphoblastoid cell lines. Lancet (1976) 0.81
Lipid patterns in human leukocytes maintained in long-term culture. J Lipid Res (1971) 0.81
Recombinant human thyroid stimulating hormone: development of a biotechnology product for detection of metastatic lesions of thyroid carcinoma. Biotechnology (N Y) (1993) 0.81
Elevated cerebrospinal fluid lactic acid levels in Creutzfeldt-Jakob disease. Int J Neurosci (1988) 0.80
Increased erythrocyte osmotic fragility in pregnancy. Am J Obstet Gynecol (1982) 0.80
Erythrocyte indexes with the electronic counter. N Engl J Med (1979) 0.80
A televised, self-help, cigarette smoking cessation intervention. Addict Behav (1990) 0.80
Cutaneous sarcoidosis with hypopigmentation and asthma. Rocky Mt Med J (1972) 0.80
Immunochemical characterization of a novel mitochondrially located protein encoded by a nuclear gene within the DFNB8/10 critical region on 21q22.3. Biochem Biophys Res Commun (1997) 0.80
Nonhuman primates: their role in assessing developmental effects of immunomodulatory agents. Hum Exp Toxicol (2000) 0.79
Biochemical comparison of HLA-DR molecules derived from autologous human T and B lymphoblasts. Eur J Immunol (1980) 0.79
Perinatal factors influencing the outcome of 501- to 1000-gm newborns. Clin Perinatol (1986) 0.79
Suppression of erythropoiesis by intrauterine transfusions in hemolytic disease of the newborn: use of erythropoietin to treat the late anemia. J Pediatr (1993) 0.79
3beta-hydroxysteroid dehydrogenase autoantibodies are rare in premature ovarian failure. J Clin Endocrinol Metab (2000) 0.78
Characterization of a novel gene, C21orf2, on human chromosome 21q22.3 and its exclusion as the APECED gene by mutation analysis. Genomics (1998) 0.78