Published in Proc Natl Acad Sci U S A on May 01, 1992
PCR-based immortalization and screening of hierarchical pools of cDNAs. Nucleic Acids Res (1994) 0.94
Design factors that influence PCR amplification success of cross-species primers among 1147 mammalian primer pairs. BMC Genomics (2006) 0.88
Comparative genomics and host resistance against infectious diseases. Emerg Infect Dis (1999) 0.87
DNA sequencing with chain-terminating inhibitors. Proc Natl Acad Sci U S A (1977) 790.54
Complementary DNA sequencing: expressed sequence tags and human genome project. Science (1991) 19.42
A common language for physical mapping of the human genome. Science (1989) 17.36
Altering the genome by homologous recombination. Science (1989) 12.73
Alu polymerase chain reaction: a method for rapid isolation of human-specific sequences from complex DNA sources. Proc Natl Acad Sci U S A (1989) 8.68
A novel, rapid method for the isolation of terminal sequences from yeast artificial chromosome (YAC) clones. Nucleic Acids Res (1990) 8.52
Evidence for higher rates of nucleotide substitution in rodents than in man. Proc Natl Acad Sci U S A (1985) 8.18
Systematic screening of yeast artificial-chromosome libraries by use of the polymerase chain reaction. Proc Natl Acad Sci U S A (1990) 6.20
OSP: a computer program for choosing PCR and DNA sequencing primers. PCR Methods Appl (1991) 4.72
Molecular phylogeny of Rodentia, Lagomorpha, Primates, Artiodactyla, and Carnivora and molecular clocks. Proc Natl Acad Sci U S A (1990) 3.23
Characterization of a murine gene expressed from the inactive X chromosome. Nature (1991) 3.21
Construction and characterization of a yeast artificial chromosome library containing seven haploid human genome equivalents. Proc Natl Acad Sci U S A (1990) 3.09
Construction of yeast artificial chromosome libraries with large inserts using fractionation by pulsed-field gel electrophoresis. Nucleic Acids Res (1989) 2.90
Yeast artificial chromosome libraries containing large inserts from mouse and human DNA. Proc Natl Acad Sci U S A (1991) 2.89
The major human erythroid DNA-binding protein (GF-1): primary sequence and localization of the gene to the X chromosome. Proc Natl Acad Sci U S A (1990) 2.68
The pattern of mammalian evolution and the relative rate of molecular evolution. Genetics (1990) 2.61
The molecular clock may be an episodic clock. Proc Natl Acad Sci U S A (1984) 2.23
Maps of linkage and synteny homologies between mouse and man. Trends Genet (1989) 1.79
The William Allan memorial award address: X-chromosome inactivation and the location and expression of X-linked genes. Am J Hum Genet (1988) 1.71
Biochemical characterization of the 94- and 78-kilodalton glucose-regulated proteins in hamster fibroblasts. J Biol Chem (1984) 1.54
The gene for autosomal dominant spinocerebellar ataxia (SCA1) maps telomeric to the HLA complex and is closely linked to the D6S89 locus in three large kindreds. Am J Hum Genet (1991) 1.53
Duplication of the gamma-globin gene mediated by L1 long interspersed repetitive elements in an early ancestor of simian primates. Proc Natl Acad Sci U S A (1991) 1.48
Yeast artificial chromosomes containing human Xq24-Xq28 DNA: library construction and representation of probe sequences. Genomics (1990) 1.35
Yeast artificial chromosome-based genome mapping: some lessons from Xq24-q28. Genomics (1991) 1.21
Molecular history of gene conversions in the primate fetal gamma-globin genes. Nucleotide sequences from the common gibbon, Hylobates lar. J Biol Chem (1990) 1.14
A protocol for DNA fragment extraction from polyacrylamide gels. Biotechniques (1990) 1.07
A wild-type DNA ligase I gene is expressed in Bloom's syndrome cells. Proc Natl Acad Sci U S A (1991) 1.04
Identifying genes within the genome: new ways for finding the needle in a haystack. Bioessays (1991) 0.87
AMINO ACID INCORPORATION INTO PROTEINS BY ESCHERICHIA COLI RIBOSOMES. Proc Natl Acad Sci U S A (1960) 11.02
Mapping of DNA instability at the fragile X to a trinucleotide repeat sequence p(CCG)n. Science (1991) 5.99
Juxtaposed regions of extensive and minimal linkage disequilibrium in human Xq25 and Xq28. Nat Genet (2000) 5.65
Isolation of single-copy human genes from a library of yeast artificial chromosome clones. Science (1989) 5.29
Microsatellite diversity and the demographic history of modern humans. Proc Natl Acad Sci U S A (1997) 4.96
Mutations in GPC3, a glypican gene, cause the Simpson-Golabi-Behmel overgrowth syndrome. Nat Genet (1996) 4.62
Fragile X genotype characterized by an unstable region of DNA. Science (1991) 4.33
Structure and organization of ribosomal DNA. Biochimie (1991) 4.31
The putative forkhead transcription factor FOXL2 is mutated in blepharophimosis/ptosis/epicanthus inversus syndrome. Nat Genet (2001) 4.15
Potentiation of rifampicin and 5-fluorocytosine as antifungal antibiotics by amphotericin B (yeast-membrane permeability-ribosomal RNA-eukaryotic cell-synergism). Proc Natl Acad Sci U S A (1972) 4.09
X-linked anhidrotic (hypohidrotic) ectodermal dysplasia is caused by mutation in a novel transmembrane protein. Nat Genet (1996) 3.90
Isolation of human glucose-6-phosphate dehydrogenase (G6PD) cDNA clones: primary structure of the protein and unusual 5' non-coding region. Nucleic Acids Res (1986) 3.86
PROTEIN SYNTHESIS IN ERYTHROID CELLS, I. RETICULOCYTE RIBOSOMES ACTIVE IN STIMULATING AMINO ACID INCORPORATION. Proc Natl Acad Sci U S A (1962) 3.81
Direct selection: a method for the isolation of cDNAs encoded by large genomic regions. Proc Natl Acad Sci U S A (1991) 3.66
Genomic rearrangement in NEMO impairs NF-kappaB activation and is a cause of incontinentia pigmenti. The International Incontinentia Pigmenti (IP) Consortium. Nature (2000) 3.61
Biosynthetic precursors of 30S and 50S ribosomal particles in Escherichia coli. Biochemistry (1968) 3.43
Mechanism and regulation of bacterial ribosomal RNA processing. Annu Rev Microbiol (1990) 3.37
A gene (RPGR) with homology to the RCC1 guanine nucleotide exchange factor is mutated in X-linked retinitis pigmentosa (RP3). Nat Genet (1996) 3.31
Polyribosome metabolism in Escherichia coli. I. Extraction of polyribosomes and ribosomal subunits from fragile, growing Escherichia coli. J Mol Biol (1966) 3.29
Patterns of polymorphism and linkage disequilibrium for cystic fibrosis. Genomics (1987) 3.03
Mutational hot spot within a new RPGR exon in X-linked retinitis pigmentosa. Nat Genet (2000) 2.82
Nucleolytic processing of ribonucleic acid transcripts in procaryotes. Microbiol Rev (1986) 2.70
Mutations of the Down-regulated in adenoma (DRA) gene cause congenital chloride diarrhoea. Nat Genet (1996) 2.70
Locations and contexts of sequences that hybridize to poly(dG-dT).(dC-dA) in mammalian ribosomal DNAs and two X-linked genes. Nucleic Acids Res (1988) 2.64
Structural analysis of the X-linked gene encoding human glucose 6-phosphate dehydrogenase. EMBO J (1986) 2.64
X-linked situs abnormalities result from mutations in ZIC3. Nat Genet (1997) 2.62
Binding of adenosine 3':5'-cyclic phosphate to G factor of Escherichia coli, and its effects on GTPase, RNase V, and protein synthesis. Proc Natl Acad Sci U S A (1970) 2.49
Human Xq24-Xq28: approaches to mapping with yeast artificial chromosomes. Am J Hum Genet (1990) 2.45
Selection of sucrose-dependent Escherichia coli to obtain envelope mutants and fragile cultures. Science (1966) 2.43
Diverse point mutations in the human glucose-6-phosphate dehydrogenase gene cause enzyme deficiency and mild or severe hemolytic anemia. Proc Natl Acad Sci U S A (1988) 2.33
Amphotericin B potentiation of rifampicin as an antifungal agent against the yeast phase of Histoplasma capsulatum. Science (1972) 2.31
Genome-wide association scan for five major dimensions of personality. Mol Psychiatry (2008) 2.29
Pathological consequences of sequence duplications in the human genome. Genome Res (1998) 2.26
Potentiation of the antifungal effects of antibiotics by amphotericin B. Antimicrob Agents Chemother (1972) 2.24
Multiple ribosomal RNA cleavage pathways in mammalian cells. Nucleic Acids Res (1981) 2.17
Synthesis of a large precursor to ribosomal RNA in a mutant of Escherichia coli. Proc Natl Acad Sci U S A (1973) 2.14
X chromosome map at 75-kb STS resolution, revealing extremes of recombination and GC content. Genome Res (1997) 2.06
Multiple pathogenic and benign genomic rearrangements occur at a 35 kb duplication involving the NEMO and LAGE2 genes. Hum Mol Genet (2001) 2.00
Dominantly inherited hyperinsulinism caused by a mutation in the sulfonylurea receptor type 1. J Clin Invest (2000) 1.97
Meta-analysis of genome-wide association studies for personality. Mol Psychiatry (2010) 1.96
RNase III cleavage is obligate for maturation but not for function of Escherichia coli pre-23S rRNA. Proc Natl Acad Sci U S A (1984) 1.96
Interaction of plasma proteins and lipoproteins with amphotericin B. J Infect Dis (1984) 1.93
Synthesis and breakdown of ribonucleic acid in Escherichia coli starving for nitrogen. Biochim Biophys Acta (1966) 1.86
Genetic control of serum IgE levels and asthma: linkage and linkage disequilibrium studies in an isolated population. Hum Mol Genet (1997) 1.82
Coresistance to neomycin and kanamycin by mutations in an Escherichia coli locus that affects ribosomes. J Bacteriol (1968) 1.80
The formation and stabilization of 30S and 50S ribosome couples in Escherichia coli. Proc Natl Acad Sci U S A (1967) 1.79
Irreversible block of the mycelial-to-yeast phase transition of Histoplasma capsulatum. Science (1986) 1.78
Data mining applied to linkage disequilibrium mapping. Am J Hum Genet (2000) 1.78
The Tabby phenotype is caused by mutation in a mouse homologue of the EDA gene that reveals novel mouse and human exons and encodes a protein (ectodysplasin-A) with collagenous domains. Proc Natl Acad Sci U S A (1997) 1.77
Location of the initial cleavage sites in mouse pre-rRNA. Mol Cell Biol (1983) 1.77
Loss of dispensable endonuclease activity in relief of polarity by suA. Nat New Biol (1971) 1.76
Specific methylation pattern at the 3' end of the human housekeeping gene for glucose 6-phosphate dehydrogenase. EMBO J (1984) 1.75
Mechanism of action of streptomycin in E. coli: interruption of the ribosome cycle at the initiation of protein synthesis. Proc Natl Acad Sci U S A (1968) 1.72
High neuroticism and low conscientiousness are associated with interleukin-6. Psychol Med (2009) 1.71
Classification of polyene antibiotics according to chemical structure and biological effects. Antimicrob Agents Chemother (1979) 1.69
cDNA sequences of human glucose 6-phosphate dehydrogenase cloned in pBR322. Nature (1981) 1.69
Arrhythmic disorder mapped to chromosome 1q42-q43 causes malignant polymorphic ventricular tachycardia in structurally normal hearts. J Am Coll Cardiol (1999) 1.68
Yeast artificial chromosomes with 200- to 800-kilobase inserts of human DNA containing HLA, V kappa, 5S, and Xq24-Xq28 sequences. Proc Natl Acad Sci U S A (1989) 1.66
S1 nuclease mapping analysis of ribosomal RNA processing in wild type and processing deficient Escherichia coli. J Biol Chem (1983) 1.66
Long-range sequence analysis in Xq28: thirteen known and six candidate genes in 219.4 kb of high GC DNA between the RCP/GCP and G6PD loci. Hum Mol Genet (1996) 1.65
Involvement of oxidative damage in erythrocyte lysis induced by amphotericin B. Antimicrob Agents Chemother (1985) 1.62
Mammalian male and female germ cells express a germ cell-specific Y-Box protein, MSY2. Biol Reprod (1998) 1.60
Characterization of the binding of amphotericin B to Saccharomyces cerevisiae and relationship to the antifungal effects. Antimicrob Agents Chemother (1974) 1.60
Mapping of five new putative anion transporter genes in human and characterization of SLC26A6, a candidate gene for pancreatic anion exchanger. Genomics (2000) 1.57
Polyribosome metabolism in Escherichia coli treated with chloramphenicol, neomycin, spectinomycin or tetracycline. J Mol Biol (1969) 1.55
Myotilin, a novel sarcomeric protein with two Ig-like domains, is encoded by a candidate gene for limb-girdle muscular dystrophy. Hum Mol Genet (1999) 1.55
Coregulation of processing and translation: mature 5' termini of Escherichia coli 23S ribosomal RNA form in polysomes. Proc Natl Acad Sci U S A (1988) 1.54
Turnover of protein in Escherichia coli starving for nitrogen. Biochim Biophys Acta (1966) 1.52
Synergistic effect of amphotericin B and 1,3-bis(2-chloroethyl)-1-nitrosourea against a transplantable AKR leukemia. Cancer Res (1974) 1.52
Differential dimer activities of the transcription factor Oct-1 by DNA-induced interface swapping. Mol Cell (2001) 1.50
The human HPRT gene on a yeast artificial chromosome is functional when transferred to mouse cells by cell fusion. Genomics (1991) 1.49
Downregulated in adenoma gene encodes a chloride transporter defective in congenital chloride diarrhea. Am J Physiol (1999) 1.47
Fine mapping of the congenital chloride diarrhea gene by linkage disequilibrium. Am J Hum Genet (1995) 1.46
RNA metabolism during morphogenesis in Histoplasma capsulatum. J Gen Microbiol (1974) 1.45
Patterns of matrix metalloproteinase and TIMP-1 expression in chronic and normally healing human cutaneous wounds. Br J Dermatol (1996) 1.44
Regulation of dimorphism in the pathogenic fungus Histoplasma capsulatum. Nature (1977) 1.44
DYX1C1 functions in neuronal migration in developing neocortex. Neuroscience (2006) 1.42
Longins: a new evolutionary conserved VAMP family sharing a novel SNARE domain. Trends Biochem Sci (2001) 1.41
Mutants in Escherichia coli ribosomes: a new selection. Proc Natl Acad Sci U S A (1969) 1.40
Frequent silencing of the GPC3 gene in ovarian cancer cell lines. Cancer Res (1999) 1.40
Saccharomyces cerevisiae: sorbitol-dependent fragile mutants. Biochem Biophys Res Commun (1974) 1.39
Phenylketonuria screening registry as a resource for population genetic studies. J Med Genet (2005) 1.38
Distinct expression profiles of stromelysin-2 (MMP-10), collagenase-3 (MMP-13), macrophage metalloelastase (MMP-12), and tissue inhibitor of metalloproteinases-3 (TIMP-3) in intestinal ulcerations. Am J Pathol (1998) 1.38
Coupling of rates of transcription, translation, and messenger ribonucleic acid degradation in streptomycin-dependent mutants of Escherichia coli. J Bacteriol (1976) 1.37
A susceptibility locus for asthma-related traits on chromosome 7 revealed by genome-wide scan in a founder population. Nat Genet (2001) 1.36
Yeast artificial chromosomes containing human Xq24-Xq28 DNA: library construction and representation of probe sequences. Genomics (1990) 1.35
A genome scan for developmental dyslexia confirms linkage to chromosome 2p11 and suggests a new locus on 7q32. J Med Genet (2003) 1.35
Finnish hereditary amyloidosis is caused by a single nucleotide substitution in the gelsolin gene. FEBS Lett (1990) 1.35