Published in In Vitro on March 21, 1973
Inactivation of viruses in serum with binary ethyleneimine. J Clin Microbiol (1976) 1.13
Method for reproducible large-volume production and purification of Rauscher murine leukemia virus. Appl Environ Microbiol (1976) 1.08
Smaller fleas ... ad infinitum: therapeutic bacteriophage redux. Proc Natl Acad Sci U S A (1996) 1.05
Use of electron microscopy for detection of viral and other microbial contaminants in bovine sera. J Clin Microbiol (1975) 1.04
Methods for the detection of viruses in bovine serum. J Clin Microbiol (1975) 1.03
New insights into the possible role of bacteriophages in host defense and disease. Med Immunol (2003) 0.93
What are the limitations on the wider therapeutic use of phage? Bacteriophage (2013) 0.91
Endotoxins in commercial vaccines. Appl Environ Microbiol (1978) 0.91
Persistence of bacteriophages in experimentally infected cell cultures. Appl Microbiol (1974) 0.82
Destruction of bacterial viruses in serum by heat and radiation under conditions that sustain the ability of serum to support growth of cells in suspended culture. J Clin Microbiol (1979) 0.80
Elimination of bacteriophages from tissue culture serum by affinity chromatography. J Clin Microbiol (1976) 0.77
Ultrasensitive stain for proteins in polyacrylamide gels shows regional variation in cerebrospinal fluid proteins. Science (1981) 23.67
Complementary DNA sequencing: expressed sequence tags and human genome project. Science (1991) 19.42
A highly sensitive silver stain for detecting proteins and peptides in polyacrylamide gels. Anal Biochem (1979) 4.77
Mutations in the connexin 26 gene (GJB2) among Ashkenazi Jews with nonsyndromic recessive deafness. N Engl J Med (1998) 4.34
Trace polypeptides in cellular extracts and human body fluids detected by two-dimensional electrophoresis and a highly sensitive silver stain. Proc Natl Acad Sci U S A (1979) 4.11
Reduced plasma dehydroepiandrosterone concentrations in Alzheimer's disease. Lancet (1989) 3.69
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
Mutations of the protocadherin gene PCDH15 cause Usher syndrome type 1F. Am J Hum Genet (2001) 3.42
Correction of deafness in shaker-2 mice by an unconventional myosin in a BAC transgene. Science (1998) 3.39
Gel protein stains: silver stain. Methods Enzymol (1984) 3.18
Association of unconventional myosin MYO15 mutations with human nonsyndromic deafness DFNB3. Science (1998) 3.00
Mutations in the gene encoding tight junction claudin-14 cause autosomal recessive deafness DFNB29. Cell (2001) 2.90
Methods for increasing the resolution of two-dimensional protein electrophoresis. Anal Biochem (1988) 2.78
Mutation in transcription factor POU4F3 associated with inherited progressive hearing loss in humans. Science (1998) 2.42
A rapid sensitive silver stain for polypeptides in polyacrylamide gels. Anal Biochem (1981) 2.42
Silver staining methods for polyacrylamide gel electrophoresis. Methods Enzymol (1983) 2.36
Affinity generation of single-stranded DNA for dideoxy sequencing following the polymerase chain reaction. Anal Biochem (1989) 2.29
Bacterial virus gene expression in human cells. Nature (1971) 2.04
Characterization of the human and mouse unconventional myosin XV genes responsible for hereditary deafness DFNB3 and shaker 2. Genomics (1999) 1.97
Fate of bacteriophage lambda in non-immune germ-free mice. Nature (1973) 1.96
Waardenburg syndrome (WS) type I is caused by defects at multiple loci, one of which is near ALPP on chromosome 2: first report of the WS consortium. Am J Hum Genet (1992) 1.94
CDH23 mutation and phenotype heterogeneity: a profile of 107 diverse families with Usher syndrome and nonsyndromic deafness. Am J Hum Genet (2002) 1.86
A mutation in PDS causes non-syndromic recessive deafness. Nat Genet (1998) 1.79
The cheetah is depauperate in genetic variation. Science (1983) 1.75
Novel mutations of MYO15A associated with profound deafness in consanguineous families and moderately severe hearing loss in a patient with Smith-Magenis syndrome. Hum Genet (2001) 1.66
Maternal transmission in Huntington's disease. Lancet (1983) 1.64
A simple sequence repeat polymorphism at the human growth hormone locus. Nucleic Acids Res (1991) 1.60
Immunologic reactions and hepatitis B vaccine. Ann Intern Med (2001) 1.55
OTOF encodes multiple long and short isoforms: genetic evidence that the long ones underlie recessive deafness DFNB9. Am J Hum Genet (2000) 1.52
Bacteriophage K1-5 encodes two different tail fiber proteins, allowing it to infect and replicate on both K1 and K5 strains of Escherichia coli. J Virol (2001) 1.50
Mutations of ESPN cause autosomal recessive deafness and vestibular dysfunction. J Med Genet (2004) 1.48
A significant dose-dependent relationship between mercury exposure from dental amalgams and kidney integrity biomarkers: a further assessment of the Casa Pia children's dental amalgam trial. Hum Exp Toxicol (2012) 1.47
Tetranucleotide repeat polymorphism at the human coagulation factor XIII A subunit gene (F13A1). Nucleic Acids Res (1991) 1.46
Gel-staining techniques. Methods Enzymol (1990) 1.39
Development of polyacrylamide gels that improve the separation of proteins and their detection by silver staining. Anal Biochem (1988) 1.38
Dethiobiotin synthesis from 7,8-diaminolargonic acid in cell-free extracts of a biotin auxotroph of Escherichia coli K-12. J Biol Chem (1969) 1.36
The purification and properties of dethiobiotin synthetase. J Biol Chem (1970) 1.35
Genetic homogeneity and phenotypic variability among Ashkenazi Jews with Usher syndrome type III. J Med Genet (2003) 1.34
The motor and tail regions of myosin XV are critical for normal structure and function of auditory and vestibular hair cells. Hum Mol Genet (2000) 1.29
Identities, frequencies and origins of TMC1 mutations causing DFNB7/B11 deafness in Pakistan. Clin Genet (2007) 1.26
Apparent digenic inheritance of Waardenburg syndrome type 2 (WS2) and autosomal recessive ocular albinism (AROA). Hum Mol Genet (1997) 1.24
A frameshift mutation in the HuP2 paired domain of the probable human homolog of murine Pax-3 is responsible for Waardenburg syndrome type 1 in an Indonesian family. Hum Mol Genet (1992) 1.23
Dominant modifier DFNM1 suppresses recessive deafness DFNB26. Nat Genet (2000) 1.22
Tetranucleotide repeat polymorphism at the human beta-actin related pseudogene H-beta-Ac-psi-2 (ACTBP2). Nucleic Acids Res (1992) 1.22
A novel mutation at the DFNA36 hearing loss locus reveals a critical function and potential genotype-phenotype correlation for amino acid-572 of TMC1. Clin Genet (2007) 1.19
Anthrax vaccination and joint related adverse reactions in light of biological warfare scenarios. Clin Exp Rheumatol (2002) 1.19
Chromosomal distribution of 320 genes from a brain cDNA library. Nat Genet (1993) 1.19
Novel mutations of TMPRSS3 in four DFNB8/B10 families segregating congenital autosomal recessive deafness. J Med Genet (2001) 1.17
Novel association of hypertrophic cardiomyopathy, sensorineural deafness, and a mutation in unconventional myosin VI (MYO6). J Med Genet (2004) 1.16
Tetranucleotide repeat polymorphism at the human aromatase cytochrome P-450 gene (CYP19). Nucleic Acids Res (1991) 1.15
USH1H, a novel locus for type I Usher syndrome, maps to chromosome 15q22-23. Clin Genet (2008) 1.15
Missense mutation in the paired domain of PAX3 causes craniofacial-deafness-hand syndrome. Hum Mutat (1996) 1.12
Human lymphocyte polymorphisms detected by quantitative two-dimensional electrophoresis. Am J Hum Genet (1983) 1.11
A relationship between the hallucinogenic activity of drugs and their electronic configuration. Proc Natl Acad Sci U S A (1965) 1.10
Mandibular molars with five canals: report of two cases. J Am Dent Assoc (1987) 1.10
Use of image analysis to quantitate changes in form of mitochondrial DNA after x-irradiation. Appl Theor Electrophor (1989) 1.10
On the loss of uricolytic activity during primate evolution--I. Silencing of urate oxidase in a hominoid ancestor. Comp Biochem Physiol B (1985) 1.09
Dinucleotide repeat polymorphism at the int-2 proto-oncogene locus (INT2). Nucleic Acids Res (1990) 1.08
'Catalysts' for polyacrylamide gel polymerization and detection of proteins by silver staining. Appl Theor Electrophor (1988) 1.08
Escherichia coli gal operon proteins made after prophage lambda induction. J Bacteriol (1981) 1.08
Mutations of human TMHS cause recessively inherited non-syndromic hearing loss. J Med Genet (2006) 1.07
PAX3 gene structure, alternative splicing and evolution. Gene (1999) 1.06
Locus heterogeneity for Waardenburg syndrome is predictive of clinical subtypes. Am J Hum Genet (1994) 1.06
Mouse and hamster mutants as models for Waardenburg syndromes in humans. J Med Genet (1990) 1.02
Correlation between Waardenburg syndrome phenotype and genotype in a population of individuals with identified PAX3 mutations. Hum Genet (1998) 1.02
An intraspecific gene duplication polymorphism of the urate oxidase gene of Drosophila virilis: a genetic and molecular analysis. Mol Biol Evol (1993) 1.02
Mitochondrial DNA sequence analysis of human skeletal remains: identification of remains from the Vietnam War. J Forensic Sci (1993) 1.02
Tetranucleotide repeat polymorphism at the human myelin basic protein gene (MBP). Hum Mol Genet (1992) 1.01
Identities and frequencies of mutations of the otoferlin gene (OTOF) causing DFNB9 deafness in Pakistan. Clin Genet (2009) 1.01
Chromosomal assignment of 46 brain cDNAs. Genomics (1992) 1.01
Synthesis of desthiobiotin from 7,8-diaminopelargonic acid in biotin auxotrophs of Escherichia coli K-12. J Bacteriol (1969) 1.00
Rubella vaccine and arthritic adverse reactions: an analysis of the Vaccine Adverse Events Reporting System (VAERS) database from 1991 through 1998. Clin Exp Rheumatol (2002) 0.99
Abnormal proteins in the cerebrospinal fluid of patients with Creutzfeldt-Jakob disease. N Engl J Med (1986) 0.99
Arthritic reactions following hepatitis B vaccination: an analysis of the vaccine adverse events reporting system (VAERS) data from 1990 through 1997. Clin Exp Rheumatol (2001) 0.98
Molecular characterization of the Drosophila melanogaster urate oxidase gene, an ecdysone-repressible gene expressed only in the malpighian tubules. Mol Cell Biol (1990) 0.98
Waardenburg syndrome (WS): the analysis of a single family with a WS1 mutation showing linkage to RFLP markers on human chromosome 2q. Am J Hum Genet (1991) 0.97
Two-dimensional gel electrophoresis of cerebrospinal fluid proteins. Clin Chem (1980) 0.97
Tetranucleotide repeat polymorphism at the human c-fes/fps proto-oncogene (FES). Nucleic Acids Res (1991) 0.96
A new locus for late-onset, progressive, hereditary hearing loss DFNA20 maps to 17q25. Genomics (2000) 0.96
Distinctive audiometric profile associated with DFNB21 alleles of TECTA. J Med Genet (2003) 0.96
Escape synthesis of the biotin operon in induced lambda b-2 lysogens. J Mol Biol (1972) 0.95
Trinucleotide repeat polymorphism at the human pancreatic phospholipase A-2 gene (PLA2). Nucleic Acids Res (1990) 0.95
Protein variations associated with Lesch-Nyhan syndrome. Proc Natl Acad Sci U S A (1981) 0.95
Tetranucleotide repeat polymorphism at the human tyrosine hydroxylase gene (TH). Nucleic Acids Res (1991) 0.94
A comprehensive review of mercury provoked autism. Indian J Med Res (2008) 0.93
A silver stain for the rapid quantitative detection of proteins or nucleic acids on membranes or thin layer plates. Anal Biochem (1986) 0.93
Creutzfeldt-Jakob disease following pituitary-derived human growth hormone therapy: a new American case. Neurology (1988) 0.93
Analysis of short tandem repeat (STR) allele frequency distributions in a Balinese population. Hum Mol Genet (1995) 0.93
Effects of Pax3 modifier genes on craniofacial morphology, pigmentation, and viability: a murine model of Waardenburg syndrome variation. Genomics (1996) 0.93
Dinucleotide repeat polymorphism at the human CTLA4 gene. Nucleic Acids Res (1991) 0.92
Genetic analysis of bacteriophage lambda strains which transduce the genes for leucine biosynthesis. Mol Gen Genet (1973) 0.92
Lymphocyte proteins in Huntington's disease: quantitative analysis by use of two-dimensional electrophoresis and computerized densitometry. Clin Chem (1982) 0.92
Cloning of a Drosophila melanogaster adenine phosphoribosyltransferase structural gene and deduced amino acid sequence of the enzyme. Gene (1987) 0.91
Endotoxins in commercial vaccines. Appl Environ Microbiol (1978) 0.91
Dinucleotide repeat polymorphism at the human interleukin 9 gene. Nucleic Acids Res (1991) 0.91
A physical map of the mouse shaker-2 region contains many of the genes commonly deleted in Smith-Magenis syndrome (del17p11.2p11.2). Genomics (1999) 0.91
Autosomal recessive nonsyndromic neurosensory deafness at DFNB1 not associated with the compound-heterozygous GJB2 (connexin 26) genotype M34T/167delT. Am J Hum Genet (2000) 0.90