Published in Arch Microbiol on May 05, 1975
Identification of blue-green algal nitrogen fixation genes by using heterologous DNA hybridization probes. Proc Natl Acad Sci U S A (1980) 2.77
Developmental regulation and spatial pattern of expression of the structural genes for nitrogenase in the cyanobacterium Anabaena. EMBO J (1990) 2.76
Use of a transposon with luciferase as a reporter to identify environmentally responsive genes in a cyanobacterium. Proc Natl Acad Sci U S A (1991) 2.64
Isolation and complementation of mutants of Anabaena sp. strain PCC 7120 unable to grow aerobically on dinitrogen. J Bacteriol (1988) 2.49
The patA gene product, which contains a region similar to CheY of Escherichia coli, controls heterocyst pattern formation in the cyanobacterium Anabaena 7120. Proc Natl Acad Sci U S A (1992) 2.34
Regulation of cellular differentiation in filamentous cyanobacteria in free-living and plant-associated symbiotic growth states. Microbiol Mol Biol Rev (2002) 2.25
Isolation and preliminary characterization of auxotrophs of a filamentous Cyanobacterium. J Bacteriol (1977) 2.10
Biochemical genetics of nitrogen fixation. Microbiol Rev (1980) 1.81
A gene encoding a protein related to eukaryotic protein kinases from the filamentous heterocystous cyanobacterium Anabaena PCC 7120. Proc Natl Acad Sci U S A (1993) 1.56
Trichodesmium--a widespread marine cyanobacterium with unusual nitrogen fixation properties. FEMS Microbiol Rev (2012) 1.20
The patB gene product, required for growth of the cyanobacterium Anabaena sp. strain PCC 7120 under nitrogen-limiting conditions, contains ferredoxin and helix-turn-helix domains. J Bacteriol (1993) 1.19
Heterocyst differentiation in the cyanobacterium Mastigocladus laminosus. J Bacteriol (1984) 1.18
A third genetic locus required for the formation of heterocysts in Anabaena sp. strain PCC 7120. J Bacteriol (1994) 1.18
Tn5 mutagenesis of Anabaena sp. strain PCC 7120: isolation of a new mutant unable to grow without combined nitrogen. J Bacteriol (1989) 1.03
Mutations in genes patA and patL of Anabaena sp. strain PCC 7120 result in similar phenotypes, and the proteins encoded by those genes may interact. J Bacteriol (2011) 0.79
Effect of nitrogen starvation on the morphology and ultrastructure of the cyanobacterium Mastigocladus laminosus. J Bacteriol (1985) 0.75
Pituitary-adrenal and autonomic responses to stress in women after sexual and physical abuse in childhood. JAMA (2000) 7.21
Perspectives on the basic reproductive ratio. J R Soc Interface (2005) 5.34
The epic project: developing national evidence-based guidelines for preventing healthcare associated infections. Phase I: Guidelines for preventing hospital-acquired infections. Department of Health (England). J Hosp Infect (2001) 4.95
Value-based pathology: a cost-benefit analysis of the examination of routine and nonroutine tonsil and adenoid specimens. Am J Clin Pathol (1997) 4.51
An adjustable fetal weight standard. Ultrasound Obstet Gynecol (1995) 3.70
Selective inhibition of receptor-coupled phospholipase C-dependent processes in human platelets and polymorphonuclear neutrophils. J Pharmacol Exp Ther (1990) 3.55
Usher syndrome 1D and nonsyndromic autosomal recessive deafness DFNB12 are caused by allelic mutations of the novel cadherin-like gene CDH23. Am J Hum Genet (2000) 3.48
The benefits and harms of breast cancer screening: an independent review. Br J Cancer (2013) 3.43
Protein products of the bithorax complex in Drosophila. Cell (1984) 3.40
Nonsyndromic hearing impairment: unparalleled heterogeneity. Am J Hum Genet (1997) 2.82
The gut: a central organ after surgical stress. Surgery (1988) 2.76
Insulin receptor phosphorylation, insulin receptor substrate-1 phosphorylation, and phosphatidylinositol 3-kinase activity are decreased in intact skeletal muscle strips from obese subjects. J Clin Invest (1995) 2.66
Estimating the date of confinement: ultrasonographic biometry versus certain menstrual dates. Am J Obstet Gynecol (1996) 2.64
Carrier rates in the midwestern United States for GJB2 mutations causing inherited deafness. JAMA (1999) 2.56
Mutations in the human alpha-tectorin gene cause autosomal dominant non-syndromic hearing impairment. Nat Genet (1998) 2.52
Distribution of Ultrabithorax proteins in Drosophila. EMBO J (1985) 2.49
Mutations in the novel protocadherin PCDH15 cause Usher syndrome type 1F. Hum Mol Genet (2001) 2.48
Update of Clostridium difficile infection due to PCR ribotype 027 in Europe, 2008. Euro Surveill (2008) 2.43
Congenital cytomegalovirus infection. N Engl J Med (1977) 2.35
Transfer RNA as a cofactor coupling amino acid synthesis with that of protein. Proc Natl Acad Sci U S A (1968) 2.31
Interventions to improve antibiotic prescribing practices for hospital inpatients. Cochrane Database Syst Rev (2005) 2.25
Viral gastroenteritis increases the reports of Clostridium difficile infection. J Hosp Infect (2007) 2.23
Global expression changes of constitutive and hormonally regulated genes during endometrial neoplastic transformation. Gynecol Oncol (2001) 2.20
The function of PS integrins during Drosophila embryogenesis. Cell (1989) 2.19
The Drosophila PS2 antigen is an invertebrate integrin that, like the fibronectin receptor, becomes localized to muscle attachments. Cell (1987) 2.18
Broadband observations of the naked-eye gamma-ray burst GRB 080319B. Nature (2008) 2.16
Phyllotaxis and the fibonacci series. Science (1977) 2.14
A re-examination of risk estimates from the NIOSH Occupational Noise and Hearing Survey (ONHS) J Acoust Soc Am (1997) 2.09
Congenital cytomegalovirus infection: diagnostic and prognostic significance of the detection of specific immunoglobulin M antibodies in cord serum. Pediatrics (1982) 2.07
Oral challenge tests for urticaria--an ethical dilemma. Br J Dermatol (1994) 1.98
The RNA code and protein synthesis. Cold Spring Harb Symp Quant Biol (1966) 1.96
Pattern formation in the blue-green alga, Anabaena. I. Basic mechanisms. J Cell Sci (1973) 1.92
Metabolic imaging of malignant pleural mesothelioma with fluorodeoxyglucose positron emission tomography. Chest (1998) 1.91
Camptodactyly and simialr atraumatic flexion deformities of the proximal interphalangeal joints of the fingers. A study of thirty-one cases. J Bone Joint Surg Am (1968) 1.89
Mutations in COL11A2 cause non-syndromic hearing loss (DFNA13). Nat Genet (1999) 1.82
Eye signs in craniopharyngioma. Br J Ophthalmol (1975) 1.80
Sustained endotoxemia leads to marked down-regulation of early steps in the insulin-signaling cascade. Crit Care Med (2001) 1.78
Pattern formation in the blue-green alga Anabaena. II. Controlled proheterocyst regression. J Cell Sci (1973) 1.78
Recurrent meningitis and Mondini dysplasia. Arch Otolaryngol Head Neck Surg (1990) 1.77
Pendred syndrome, DFNB4, and PDS/SLC26A4 identification of eight novel mutations and possible genotype-phenotype correlations. Hum Mutat (2001) 1.77
Genomic structure and identification of novel mutations in usherin, the gene responsible for Usher syndrome type IIa. Am J Hum Genet (2000) 1.76
Glutamine metabolism by the intestinal tract. JPEN J Parenter Enteral Nutr (1985) 1.71
Teratogenicity of 2-ethoxyethanol by dermal application. Drug Chem Toxicol (1982) 1.70
Localization of the Usher syndrome type ID gene (Ush1D) to chromosome 10. Hum Mol Genet (1996) 1.69
Biochemical changes in the collagen of the palmar fascia in patients with Dupuytren's disease. J Bone Joint Surg Am (1981) 1.69
Clinical and metabolic efficacy of glutamine-supplemented parenteral nutrition after bone marrow transplantation. A randomized, double-blind, controlled study. Ann Intern Med (1992) 1.68
Mutations in the transcriptional activator EYA4 cause late-onset deafness at the DFNA10 locus. Hum Mol Genet (2001) 1.68
Challenge test battery in chronic urticaria. Br J Dermatol (1976) 1.67
Prognostic value of FDG PET imaging in malignant pleural mesothelioma. J Nucl Med (1999) 1.67
Localization of Usher syndrome type II to chromosome 1q. Genomics (1990) 1.67
A single dose of endotoxin increases intestinal permeability in healthy humans. Arch Surg (1988) 1.66
The distribution of PS integrins, laminin A and F-actin during key stages in Drosophila wing development. Development (1993) 1.66
Bioregulation of lysosomal enzyme secretion from human neutrophils: roles of guanosine 3':5'-monophosphate and calcium in stimulus-secretion coupling. Proc Natl Acad Sci U S A (1975) 1.65
Developmentally regulated alternative splicing of Drosophila integrin PS2 alpha transcripts. Cell (1989) 1.64
Nonsyndromic hearing impairment is associated with a mutation in DFNA5. Nat Genet (1998) 1.63
Why retrobulbar anaesthesia? Br J Ophthalmol (1988) 1.63
A common founder for the 35delG GJB2 gene mutation in connexin 26 hearing impairment. J Med Genet (2001) 1.61
Related cell-surface antigens expressed with positional specificity in Drosophila imaginal discs. Proc Natl Acad Sci U S A (1984) 1.60
Ten per cent polarized optical emission from GRB 090102. Nature (2009) 1.58
Highly polarized light from stable ordered magnetic fields in GRB 120308A. Nature (2013) 1.57
Performance of a whole-body PET scanner using curve-plate NaI(Tl) detectors. J Nucl Med (2001) 1.56
Update of Clostridium difficile-associated disease due to PCR ribotype 027 in Europe. Euro Surveill (2007) 1.55
Giant-cell tumors of the bones of the hand. J Hand Surg Am (1980) 1.55
Mutations in the KCNQ4 gene are responsible for autosomal dominant deafness in four DFNA2 families. Hum Mol Genet (1999) 1.54
Increased intestinal permeability associated with infection in burn patients. Arch Surg (1988) 1.53
Abnormal movement of the arytenoid region during exercise presenting as exercise-induced asthma in an adolescent athlete. Chest (1994) 1.52
Setting up a quality assurance program in endoscopy. Endoscopy (2003) 1.51
ROR gamma: the third member of ROR/RZR orphan receptor subfamily that is highly expressed in skeletal muscle. Biochem Biophys Res Commun (1994) 1.48
Allometric scaling in comparative biology: problems of concept and method. Am J Physiol (1984) 1.48
Is macrosomia associated with poor glycaemic control in diabetic pregnancy? Diabet Med (1996) 1.48
The Lang lecture 1986. The enigma of primary open-angle glaucoma. Trans Ophthalmol Soc U K (1986) 1.48
[ The family physician's sentinel function studied with reference to referrals and referral cards]. Ned Tijdschr Geneeskd (1996) 1.47
Endobronchial tumors in children: an uncommon clinical entity. Ann Otol Rhinol Laryngol (2001) 1.45
Pyrazoline bisphosphonate esters as novel antiinflammatory and antiarthritic agents. J Med Chem (1993) 1.45
Evidence that the Abdominal-B r element function is conferred by a trans-regulatory homeoprotein. EMBO J (1988) 1.43
Management of congenital buccopharyngeal membrane. Cleft Palate Craniofac J (1997) 1.39
Study finds sleeping pills overprescribed. Science (1979) 1.39
Insulin-like growth factor-I receptor internalization regulates signaling via the Shc/mitogen-activated protein kinase pathway, but not the insulin receptor substrate-1 pathway. J Biol Chem (1998) 1.37
Linkage of a gene for dominant non-syndromic deafness to chromosome 19. Hum Mol Genet (1995) 1.36
A position-specific cell surface antigen in the drosophila wing imaginal disc. Cell (1981) 1.35
Effect of schizophrenia on frontotemporal activity during word encoding and recognition: a PET cerebral blood flow study. Am J Psychiatry (2001) 1.35
Rethinking allometry. J Theor Biol (1980) 1.34
Gamma-glutamyl phosphate attached to glutamine-specific tRNA. A precursor of glutaminyl-tRNA in Bacillus subtilis. Eur J Biochem (1969) 1.34
Distinct biologically active receptors for insulin, insulin-like growth factor I, and insulin-like growth factor II in cultured skeletal muscle cells. J Biol Chem (1985) 1.33
Two frequent missense mutations in Pendred syndrome. Hum Mol Genet (1998) 1.31
Phorbol myristate acetate-induced release of granule enzymes from human neutrophils: inhibition by the calcium antagonist, 8-(N,N-diethylamino)-octyl 3,4,5-trimethoxybenzoate hydrochloride. Biochem Biophys Res Commun (1979) 1.31
Functional differences of the PDS gene product are associated with phenotypic variation in patients with Pendred syndrome and non-syndromic hearing loss (DFNB4). Hum Mol Genet (2000) 1.30
Infection with cytomegalovirus during pregnancy: specific IgM antibodies as a marker of recent primary infection. J Infect Dis (1982) 1.30
Genetic heterogeneity of Usher syndrome: analysis of 151 families with Usher type I. Am J Hum Genet (2000) 1.29
Dual time point fluorine-18 fluorodeoxyglucose positron emission tomography: a potential method to differentiate malignancy from inflammation and normal tissue in the head and neck. Eur J Nucl Med (1999) 1.28
Excretion of cytomegalovirus in mothers: observations after delivery of congenitally infected and normal infants. J Infect Dis (1982) 1.27
Pediatric otolaryngologists' knowledge and understanding of genetic testing for deafness. Arch Otolaryngol Head Neck Surg (2001) 1.26
Laryngomalacia and its treatment. Laryngoscope (1999) 1.26
Use of isolated nuclei in the indirect fluorescent-antibody test for human cytomegalovirus infection: comparison with microneutralization, anticomplement, and conventional indirect fluorescent-antibody assays. J Clin Microbiol (1978) 1.25