Published in Hum Hered on January 01, 1980
Genetic distances between the Utah Mormons and related populations. Am J Hum Genet (1984) 1.79
Are the Basques a single and a unique population? Am J Hum Genet (1991) 1.03
A new rare variant of the glyoxalase I system of the red cell: GLO-Sicily. Am J Hum Genet (1983) 0.75
Extended lymph-node dissection for gastric cancer. N Engl J Med (1999) 7.43
Compilation of vertebrate-encoded transcription factors. Nucleic Acids Res (1992) 5.35
Expression of two T cell receptor alpha chains: dual receptor T cells. Science (1993) 3.54
A view of Neandertal genetic diversity. Nat Genet (2000) 3.31
Prelingual deafness: high prevalence of a 30delG mutation in the connexin 26 gene. Hum Mol Genet (1997) 3.26
Evidence that HIV-1 Rev directly promotes the nuclear export of unspliced RNA. EMBO J (1994) 3.02
The translational regulator CPEB1 provides a link between dcp1 bodies and stress granules. J Cell Sci (2005) 2.86
Septic shock, multiple organ failure, and disseminated intravascular coagulation. Compared patterns of antithrombin III, protein C, and protein S deficiencies. Chest (1992) 2.80
A human homologue of the Drosophila eyes absent gene underlies branchio-oto-renal (BOR) syndrome and identifies a novel gene family. Nat Genet (1997) 2.68
Concepts of trust among patients with serious illness. Soc Sci Med (2000) 2.65
A quantitative analysis of bleeding symptoms in type 1 von Willebrand disease: results from a multicenter European study (MCMDM-1 VWD). J Thromb Haemost (2006) 2.56
Tuberculosis treatment programmes in low-income countries. Lancet (1994) 2.31
Affinity differences for vitamin D metabolites associated with the genetic isoforms of the human serum carrier protein (DBP). Hum Genet (1993) 2.27
Regulation of pim and myb mRNA accumulation by interleukin 2 and interleukin 3 in murine hematopoietic cell lines. J Biol Chem (1988) 2.19
The impact of agricultural intensification and land-use change on the European arable flora. Proc Biol Sci (2011) 2.19
Targets for global tuberculosis control. Int J Tuberc Lung Dis (2006) 2.16
A novel deletion involving the connexin-30 gene, del(GJB6-d13s1854), found in trans with mutations in the GJB2 gene (connexin-26) in subjects with DFNB1 non-syndromic hearing impairment. J Med Genet (2005) 2.11
Isolation of cDNA and genomic clones encoding human pro-alpha 1 (III) collagen. Partial characterization of the 3' end region of the gene. J Biol Chem (1985) 2.09
Clinical features of the prevalent form of childhood deafness, DFNB1, due to a connexin-26 gene defect: implications for genetic counselling. Lancet (1999) 2.00
Compilation of human mtDNA control region sequences. Nucleic Acids Res (1998) 2.00
Assignment of the human pro alpha 2(I) collagen structural gene (COLIA2) to chromosome 7 by molecular hybridization. Am J Hum Genet (1982) 1.98
Neutrophil alkaline phosphatase in AIDS. Acta Haematol (1988) 1.94
Characterization of a set of X-linked sequences and of a panel of somatic cell hybrids useful for the regional mapping of the human X chromosome. Hum Genet (1986) 1.92
Pathological features and prenatal diagnosis in the newly recognised limb/pelvis-hypoplasia/aplasia syndrome. J Med Genet (1988) 1.82
Nosocomial Legionnaires' disease caused by aerosolized tap water from respiratory devices. J Infect Dis (1982) 1.81
Detailed von Willebrand factor multimer analysis in patients with von Willebrand disease in the European study, molecular and clinical markers for the diagnosis and management of type 1 von Willebrand disease (MCMDM-1VWD). J Thromb Haemost (2008) 1.81
Human type I procollagen genes are located on different chromosomes. Proc Natl Acad Sci U S A (1982) 1.78
Systematic screening for active tuberculosis: rationale, definitions and key considerations. Int J Tuberc Lung Dis (2013) 1.70
Treatment of severe von Willebrand disease with a high-purity von Willebrand factor concentrate (Wilfactin): a prospective study of 50 patients. J Thromb Haemost (2007) 1.69
In vivo kinetics of mRNA splicing and transport in mammalian cells. Mol Cell Biol (2002) 1.63
Connexin 26 gene linked to a dominant deafness. Nature (1998) 1.62
Clustering of mutations responsible for branchio-oto-renal (BOR) syndrome in the eyes absent homologous region (eyaHR) of EYA1. Hum Mol Genet (1997) 1.59
Ultrasonography of the hip in developmental hip dysplasia. J Bone Joint Surg Br (1998) 1.58
Cannabis arteritis revisited--ten new case reports. Angiology (2001) 1.58
Isolation and characterisation of a cDNA clone for human apolipoprotein CI and assignment of the gene to chromosome 19. Hum Genet (1985) 1.53
Long-term follow-up of non-seminomatous testicular cancer patients with mature teratoma or carcinoma at postchemotherapy surgery. EORTC Genitourinary Tract Cancer Cooperative Group (EORTC GU Group) Eur J Cancer (1991) 1.52
New model system for a one-dimensional electron liquid: self-organized atomic gold chains on Ge(001). Phys Rev Lett (2008) 1.49
Ecological correlates of achene mass variation in Chrysothamnus nauseosus (Asteraceae). Am J Bot (1997) 1.46
Clinical significance of translocation. Gut (1994) 1.44
An alpha-tectorin gene defect causes a newly identified autosomal recessive form of sensorineural pre-lingual non-syndromic deafness, DFNB21. Hum Mol Genet (1999) 1.44
Two infants with life-threatening diffuse neonatal hemangiomatosis treated with cyclophosphamide. Pediatr Blood Cancer (2006) 1.41
[The treatment of liver metastases of colorectal tumors using intra-arterial fluorouracil via hepatic artery, administered with a completely implantable access system and a portable infusion pump]. Ned Tijdschr Geneeskd (1993) 1.40
[Cannabis arteriopathy]. Presse Med (1999) 1.39
[Myopericarditis and atrial fibrillation disclosing leptospirosis septicemia]. Presse Med (1996) 1.38
Endemic and epidemic aspergillosis associated with in-hospital replication of Aspergillus organisms. J Infect Dis (1991) 1.38
Double-blind, placebo-controlled trial of antithrombin III concentrates in septic shock with disseminated intravascular coagulation. Chest (1993) 1.35
Viral transcription in human keratinocyte cell lines immortalized by human papillomavirus type-16. Virology (1991) 1.32
The genes coding for A alpha-, B beta-, and gamma-chains of fibrinogen map to 4q2. Am J Hum Genet (1984) 1.30
GW body disassembly triggered by siRNAs independently of their silencing activity. Nucleic Acids Res (2007) 1.29
A computer program for incidence density sampling of controls in case-control studies nested within occupational cohort studies. Am J Epidemiol (1989) 1.28
Prolonged retention of high concentrations of 5-fluorouracil in human and murine tumors as compared with plasma. Cancer Chemother Pharmacol (1993) 1.27
Mutation profile of all 49 exons of the human myosin VIIA gene, and haplotype analysis, in Usher 1B families from diverse origins. Am J Hum Genet (1997) 1.26
Nerve growth factor delivery by gene transfer induces differential outgrowth of sensory, motor, and noradrenergic neurites after adult spinal cord injury. Exp Neurol (1996) 1.26
Overwintering cost associated with resistance to transgenic cotton in the pink bollworm (Lepidoptera: Gelechiidae). J Econ Entomol (2001) 1.26
Organization of the human pro-alpha 2(I) collagen gene. J Biol Chem (1987) 1.24
Metabolism of vitamin A and its active metabolite all-trans-retinoic acid in small intestinal enterocytes. J Pharmacol Exp Ther (2000) 1.23
Cellular composition of milky spots in the human greater omentum: an immunochemical and ultrastructural study. Anat Rec (1995) 1.23
Human cellular fibronectin: comparison of the carboxyl-terminal portion with rat identifies primary structural domains separated by hypervariable regions. Biochemistry (1985) 1.23
Do "whiplash injuries" occur in low-speed rear impacts? Eur Spine J (1997) 1.22
Mutation analysis of TMC1 identifies four new mutations and suggests an additional deafness gene at loci DFNA36 and DFNB7/11. Clin Genet (2008) 1.21
Cloning and analysis of the 5' portion of the human type-III procollagen gene (COL3A1). Gene (1989) 1.21
Identification of a specific exon sequence that is a major determinant in the selection between a natural and a cryptic 5' splice site. Mol Cell Biol (1991) 1.21
The enzymatic antioxidant system in blood and glutathione status in human immunodeficiency virus (HIV)-infected patients: effects of supplementation with selenium or beta-carotene. Am J Clin Nutr (1996) 1.20
The structural gene for aldolase B (ALDB) maps to 9q13----32. Ann Hum Genet (1985) 1.19
A specific promoter of the sensory cells of the inner ear defined by transgenesis. Hum Mol Genet (2001) 1.19
Torsion of the gallbladder in children. J Pediatr Surg (1994) 1.17
Assignment of the gene for F-type phosphofructokinase to human chromosome 10 by somatic cell hybridization and specific immunoprecipitation. Ann Hum Genet (1980) 1.17
Prevalence and significance of Legionella pneumophila contamination of residential hot-tap water systems. J Infect Dis (1985) 1.14
Ehlers-Danlos syndrome type IV: cosegregation of the phenotype to a COL3A1 allele of type III procollagen. Hum Genet (1986) 1.14
Linkage analysis in families diagnosed with type 1 von Willebrand disease in the European study, molecular and clinical markers for the diagnosis and management of type 1 VWD. J Thromb Haemost (2006) 1.14
Group-specific component: evidence for two subtypes of the Gc1 gene. Science (1977) 1.13
Expression of 14 von Willebrand factor mutations identified in patients with type 1 von Willebrand disease from the MCMDM-1VWD study. J Thromb Haemost (2009) 1.13
Myosin VIIA gene: heterogeneity of the mutations responsible for Usher syndrome type IB. Hum Mol Genet (1997) 1.13
Outcome of acquired haemophilia in France: the prospective SACHA (Surveillance des Auto antiCorps au cours de l'Hémophilie Acquise) registry. Haemophilia (2013) 1.12
Novel short-acting A2A adenosine receptor agonists for coronary vasodilation: inverse relationship between affinity and duration of action of A2A agonists. J Pharmacol Exp Ther (2001) 1.12
Multicenter retrospective study on the utilization of FEIBA in France in patients with factor VIII and factor IX inhibitors. French FEIBA Study Group. Factor Eight Bypassing Activity. Thromb Haemost (1997) 1.12
Determination of the DNA sequence recognized by the bHLH-zip domain of the N-Myc protein. Nucleic Acids Res (1992) 1.11
Possible interaction between USH1B and USH3 gene products as implied by apparent digenic deafness inheritance. Am J Hum Genet (1999) 1.10
Treatment of thyroid associated ophthalmopathy with periocular injections of triamcinolone. Br J Ophthalmol (2004) 1.10
Enhanced tumour growth in the rat liver after selective elimination of Kupffer cells. Cancer Immunol Immunother (1993) 1.10
Further evidence for the dispersion of the human fibrillar collagen genes. Am J Hum Genet (1986) 1.09
Long-term outcome of patients with polymyositis/ dermatomyositis and anti-PM-Scl antibody. Br J Dermatol (2009) 1.07
In vivo cooperation between introns during pre-mRNA processing. Genes Dev (1993) 1.06
The mutants of the vitamin-D-binding protein: more than 120 variants of the GC/DBP system. Vox Sang (1988) 1.05
Surgical treatment of displaced supracondylar fractures of the humerus in children. Analysis of fifty-two cases followed for five to fifteen years. J Bone Joint Surg Am (1978) 1.05
Abnormal XY interchange between a novel isolated protein kinase gene, PRKY, and its homologue, PRKX, accounts for one third of all (Y+)XX males and (Y-)XY females. Hum Mol Genet (1997) 1.05
The pro alpha 2(V) collagen gene is evolutionarily related to the major fibrillar-forming collagens. Nucleic Acids Res (1987) 1.04
Programmatic approaches to screening for active tuberculosis. Int J Tuberc Lung Dis (2013) 1.04
HLA-A, B, C, DR antigens, Bf, C4 and glyoxalase I (GLO) polymorphisms in French Basques with insulin-dependent diabetes mellitus (IDDM). Tissue Antigens (1982) 1.04
Plasma vascular endothelial growth factor and its receptor Flt-1 in patients with hyperlipidemia and atherosclerosis and the effects of fluvastatin or fenofibrate. Am J Cardiol (2001) 1.04
Population distribution of the human vitamin D binding protein: anthropological considerations. Am J Phys Anthropol (1985) 1.03
Cryptococcus gattii meningoencephalitis in an immunocompetent person 13 months after exposure. Infection (2009) 1.03
Amplification of ColE1 related plasmids in recombinant cultures of Escherichia coli after IPTG induction. J Biotechnol (1998) 1.02
[Localization of the gene for human acid alpha-glucosidase (alpha-GLUa) on the 17q21 to 17qter by interspecific hybridization (author's transl)]. Hum Genet (1979) 1.02
Isolation and characterization of the human fibrillar collagen genes. Ann N Y Acad Sci (1985) 1.02
Self-renewal and differentiation of normal avian erythroid progenitor cells: regulatory roles of the TGF alpha/c-ErbB and SCF/c-kit receptors. Cell (1993) 1.01
Analysis of the promoter region and the N-propeptide domain of the human pro alpha 2(I) collagen gene. Nucleic Acids Res (1985) 1.01
Outbreak of JK diphtheroid infections associated with environmental contamination. J Clin Microbiol (1984) 1.01