Published in Am J Hum Genet on September 01, 1969
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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
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Systematic reviews of bed rest and advice to stay active for acute low back pain. Br J Gen Pract (1997) 1.91
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Transformation of human breast epithelial cells by c-Ha-ras oncogene. Mol Carcinog (1991) 1.87
Evidence of association of the ecNOS gene polymorphism with plasma NO metabolite levels in humans. Biochem Biophys Res Commun (1998) 1.86
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Adverse and beneficial secondary effects of mass treatment with azithromycin to eliminate blindness due to trachoma in Nepal. Clin Infect Dis (2002) 1.84
Brief report: severe infectious mononucleosis-like syndrome and primary human herpesvirus 6 infection in an adult. N Engl J Med (1993) 1.84
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Osteotropic agents regulate the expression of osteoclast differentiation factor and osteoprotegerin in osteoblastic stromal cells. Endocrinology (1998) 1.75
Safety of the new quinolones in pregnancy. Obstet Gynecol (1994) 1.75
A combination of osteoclast differentiation factor and macrophage-colony stimulating factor is sufficient for both human and mouse osteoclast formation in vitro. Endocrinology (1998) 1.75
A region of proto-dbl essential for its transforming activity shows sequence similarity to a yeast cell cycle gene, CDC24, and the human breakpoint cluster gene, bcr. New Biol (1991) 1.74
Cervical Chlamydia trachomatis infection in university women: relationship to history, contraception, ectopy, and cervicitis. Am J Obstet Gynecol (1985) 1.74
Crystal structure of the lambda repressor C-terminal domain provides a model for cooperative operator binding. Cell (2000) 1.73
Primary structure of heat-stable enterotoxin produced by Yersinia enterocolitica. Biochem Biophys Res Commun (1984) 1.72
SLC26A4/PDS genotype-phenotype correlation in hearing loss with enlargement of the vestibular aqueduct (EVA): evidence that Pendred syndrome and non-syndromic EVA are distinct clinical and genetic entities. J Med Genet (2005) 1.71
Apolipoprotein E Sendai (arginine 145-->proline): a new variant associated with lipoprotein glomerulopathy. J Am Soc Nephrol (1997) 1.71
Cloning and characterization of a nonmuscle myosin heavy chain cDNA. Proc Natl Acad Sci U S A (1985) 1.69
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Immunological evidence that plants use both HDEL and KDEL for targeting proteins to the endoplasmic reticulum. J Cell Sci (1992) 1.69
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Predicting zygosity in Norwegian twin pairs born 1915-1960. Clin Genet (1983) 1.68
Genetic models for the analysis of data from the families of identical twins. Genetics (1976) 1.67
Treatment of refractory Wegener's granulomatosis with humanized monoclonal antibodies. QJM (1996) 1.66
Primary structure and biological activity of a novel human neurotrophic factor. Neuron (1990) 1.65
Brain-derived neurotrophic factor rescues spinal motor neurons from axotomy-induced cell death. Nature (1993) 1.64
A brief screening tool for knee pain in primary care. 1. Validity and reliability. Rheumatology (Oxford) (2001) 1.64
CEA-related cell adhesion molecule 1: a potent angiogenic factor and a major effector of vascular endothelial growth factor. Mol Cell (2000) 1.63
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Occult biochemical pregnancy: fact or fiction? Br J Obstet Gynaecol (1988) 1.62
A new method for imaging perfusion and contrast extraction fraction: input functions derived from reference tissues. J Magn Reson Imaging (1998) 1.62
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Pycnodysostosis, with a familial chromosome anomaly. Am J Med (1966) 1.60
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Subcutaneous crystal-storing histiocytosis associated with lymphoplasmacytic lymphoma (immunocytoma) Pathol Res Pract (1996) 1.57
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Multidisciplinary predialysis programs: quantification and limitations of their impact on patient outcomes in two Canadian settings. Am J Kidney Dis (1997) 1.55