Published in J Antibiot (Tokyo) on March 01, 1969
A biomimetic domino reaction for the concise synthesis of capreomycidine and epicapreomycidine. Amino Acids (2012) 0.79
COSMIC 2005. Br J Cancer (2006) 5.07
Nmd3p is a Crm1p-dependent adapter protein for nuclear export of the large ribosomal subunit. J Cell Biol (2000) 3.36
Prevalence of fragile X syndrome. Am J Med Genet (1996) 3.19
Homogeneous Escherichia coli endonuclease IV. Characterization of an enzyme that recognizes oxidative damage in DNA. J Biol Chem (1988) 3.15
Yeast structural gene (APN1) for the major apurinic endonuclease: homology to Escherichia coli endonuclease IV. Proc Natl Acad Sci U S A (1990) 2.35
Uniparental paternal disomy in Angelman's syndrome. Lancet (1991) 2.26
The yeast antiviral proteins Ski2p, Ski3p, and Ski8p exist as a complex in vivo. RNA (2000) 2.13
NMD3 encodes an essential cytoplasmic protein required for stable 60S ribosomal subunits in Saccharomyces cerevisiae. Mol Cell Biol (1999) 2.08
Atheromatous macroembolism after balloon angioplasty of the superficial femoral artery. AJR Am J Roentgenol (1995) 2.02
Guidelines for reporting clinical features in cases with MECP2 mutations. Brain Dev (2001) 1.99
Population prevalence and estimated birth incidence and mortality rate for people with Prader-Willi syndrome in one UK Health Region. J Med Genet (2001) 1.94
Molecular and genetic analysis of the gene encoding the Saccharomyces cerevisiae strand exchange protein Sep1. Mol Cell Biol (1991) 1.92
The recovery of cognitive function after general anesthesia in elderly patients: a comparison of desflurane and sevoflurane. Anesth Analg (2001) 1.92
Saccharomyces cerevisiae RAI1 (YGL246c) is homologous to human DOM3Z and encodes a protein that binds the nuclear exoribonuclease Rat1p. Mol Cell Biol (2000) 1.82
Regulation and intracellular localization of Saccharomyces cerevisiae strand exchange protein 1 (Sep1/Xrn1/Kem1), a multifunctional exonuclease. Mol Cell Biol (1995) 1.74
Duplication of chromosome 15 in the region 15q11-13 in a patient with developmental delay and ataxia with similarities to Angelman syndrome. J Med Genet (1993) 1.54
Preparation and use of specifically purified antibodies for immunofluorescent labeling. Acta Histochem (1967) 1.45
The amino acid sequence of -crystallin (fraction II) from calf lens. Biochem J (1972) 1.43
Comparison of disposable and reusable laryngeal mask airways in spontaneously ventilating adult patients. Anaesth Intensive Care (2004) 1.42
Campylobacter pyloridis, urease, and gastric ulcers. Lancet (1986) 1.42
Potential magnitude of future vegetation change in eastern north america: comparisons with the past. Science (1991) 1.40
Nascent 60S ribosomal subunits enter the free pool bound by Nmd3p. RNA (2000) 1.40
Pathogenicity and interaction of three nematode species on six bermudagrasses. J Nematol (1970) 1.37
Ascorbic acid: a factor concentrated in human gastric juice. Clin Sci (Lond) (1989) 1.36
Children with the fragile X chromosome at schools for the mildly mentally retarded. Dev Med Child Neurol (1987) 1.29
Frequency and replication status of the fragile X, fra(X)(q27-28), in a pair of monozygotic twins of markedly differing intelligence. J Med Genet (1985) 1.29
Growth retardation in asthmatic children treated with inhaled beclomethasone dipropionate. Lancet (1988) 1.29
Prevalence of, and risk factors for, physical ill-health in people with Prader-Willi syndrome: a population-based study. Dev Med Child Neurol (2002) 1.27
Screening of newborn infants for cholestatic hepatobiliary disease with tandem mass spectrometry. BMJ (1999) 1.26
Isolation and study of rabbit antibodies specific for certain of the antigenic groups of human serum albumin. Biochem J (1964) 1.25
Is it possible to make a clinical diagnosis of the fragile X syndrome in a boy? Arch Dis Child (1985) 1.24
Mutational analysis of exoribonuclease I from Saccharomyces cerevisiae. Nucleic Acids Res (1998) 1.20
The course and outcome of psychiatric illness in people with Prader-Willi syndrome: implications for management and treatment. J Intellect Disabil Res (2007) 1.19
Prader-Willi syndrome, compulsive and ritualistic behaviours: the first population-based survey. Br J Psychiatry (2002) 1.14
Cytotoxicity of substituted alkyl-3,4-bis(4-methoxyphenyl)pyrrole-2-carboxylates in L1210 lymphoid leukemia cells. Arch Pharm (Weinheim) (1998) 1.13
Prevalence of fragile X syndrome. J Med Genet (1991) 1.13
Cognitive abilities and genotype in a population-based sample of people with Prader-Willi syndrome. J Intellect Disabil Res (2004) 1.12
Behavioural phenotypes associated with specific genetic disorders: evidence from a population-based study of people with Prader-Willi syndrome. Psychol Med (2003) 1.11
Effects of Rapeseed and Vetch as Green Manure Crops and Fallow on Nematodes and Soil-borne Pathogens. J Nematol (1992) 1.11
The mitochondrial trifunctional protein: centre of a beta-oxidation metabolon? Biochem Soc Trans (2000) 1.10
A method for the quantitation of conjugated bile acids in dried blood spots using electrospray ionization-mass spectrometry. Pediatr Res (1998) 1.09
Structural studies on bovine -crystallin. Biochem J (1971) 1.06
Prevalence of the fragile X anomaly amongst autistic twins and singletons. J Child Psychol Psychiatry (1993) 1.04
Crop Rotation and Nematicides for Management of Mixed Populations of Meloidogyne spp. on Tobacco. J Nematol (2001) 1.03
Screening for medium chain acyl-CoA dehydrogenase deficiency using electrospray ionisation tandem mass spectrometry. Arch Dis Child (1998) 1.03
Evidence for increased nitric oxide production in multiple sclerosis. J Neurol Neurosurg Psychiatry (1995) 1.03
Application of magnetic chromatography to the isolation of lysosomes from fibroblasts of patients with lysosomal storage disorders. FEBS Lett (1998) 1.03
Structural studies on calf lens gamma-crystallin fraction IV: a comparison of the cysteine-containing tryptic peptides with the corresponding amino acid sequence of gamma-crystallin fraction II. Exp Eye Res (1978) 0.99
Further evidence for dominant inheritance at the chromosome 15q11-13 locus in familial Angelman syndrome. Am J Med Genet (1992) 0.99
Developmental changes in the low molecular weight proteins of the bovine lens. Exp Eye Res (1973) 0.98
Seven-year discordance in age at onset in monozygotic twins with inherited prion disease (P102L). Neuropathol Appl Neurobiol (2009) 0.98
Maternal origin of deletion 15q11-13 in 25/25 cases of Angelman syndrome. Hum Genet (1992) 0.97
The phenomenology and diagnosis of psychiatric illness in people with Prader-Willi syndrome. Psychol Med (2008) 0.95
Phosphodiesterase 11 (PDE11) regulation of spermatozoa physiology. Int J Impot Res (2005) 0.95
A reinvestigation of thirty three fragile(X) families using probe StB12.3. Am J Med Genet (1992) 0.95
Twelve families with fragile X(q27). J Med Genet (1986) 0.94
Studies on the subunit structure of the adenosylcobalamin-dependent enzyme ethanolamine ammonia-lyase. FEBS Lett (1979) 0.93
The 'fragile' X chromosome in the Martin-Bell-Renpenning syndrome and in males with other forms of familial mental retardation. J Med Genet (1981) 0.93
Is skewed X inactivation responsible for symptoms in female carriers for adrenoleucodystrophy? J Med Genet (1993) 0.92
Typhoid ileal perforation in Nigerian children: an analysis of 106 operative cases. Pediatr Surg Int (2001) 0.92
Treatment of canine nasal aspergillosis with enilconazole. J Vet Intern Med (1993) 0.91
Effects of Planting Date, Small Grain Crop Destruction, Fallow, and Soil Temperature on the Management of Meloidogyne incognita. J Nematol (1990) 0.90
Maladaptive behaviour in Prader-Willi syndrome in adult life. J Intellect Disabil Res (1996) 0.90
Difference in methylation patterns within the D15S9 region of chromosome 15q11-13 in first cousins with Angelman syndrome and Prader-Willi syndrome. Am J Med Genet (1993) 0.90
Extracellular fluid volume expansion and third space sequestration at the site of small bowel anastomoses. Br J Surg (1983) 0.88
A spectrophotometric rapid kinetic study of reactions catalysed by coenzyme-B12-dependent ethanolamine ammonia-lyase. Eur J Biochem (1978) 0.88
Microbial inciters of acute asthma in urban Nigerian children. Thorax (1995) 0.87
Survival and development of Heliothis virescens (Lepidoptera: Noctuidae) larvae on isogenic tobacco lines with different levels of alkaloids. J Econ Entomol (2002) 0.87
The cytotoxicity and mode of action of 2,3,4-trisubstituted pyrroles and related derivatives in human Tmolt4 leukemia cells. Pharmazie (1999) 0.87
A comparison of three guinea-pig sensitization procedures for the detection of 19 reported human contact sensitizers. Contact Dermatitis (1981) 0.87
Low doses of repetitive ultraviolet A induce morphologic changes in human skin. J Invest Dermatol (1995) 0.87
Replication status of fragile X(q27.3) in 13 female heterozygotes. J Med Genet (1986) 0.87
Total dosage of chlorpromazine and ocular opacities. Am J Psychiatry (1967) 0.86
Identification of alpha(1)-antitrypsin variants in plasma with the use of proteomic technology. Clin Chem (2001) 0.86
Ovarian hormones modulate cocaine-induced locomotor and stereotypic activity. Ann N Y Acad Sci (2001) 0.86
Suitability of small grains as hosts of meloidogyne species. J Nematol (1989) 0.85
When theories collide: experts develop different models for carcinogenesis. J Natl Cancer Inst (2001) 0.85
Canine T-zone lymphoma: unique immunophenotypic features, outcome, and population characteristics. J Vet Intern Med (2014) 0.85
Molecular mechanisms in Angelman syndrome: a survey of 93 patients. J Med Genet (1993) 0.85
Giant omental cyst simulating ascites in a Nigerian child: case report and critique of clinical parameters and investigative modalities. Ann Trop Paediatr (2001) 0.85
Chloroquine-resistant Plasmodium falciparum malaria in Ilorin, Nigeria: prevalence and risk factors for treatment failure. Afr J Med Med Sci (2001) 0.85
Mutations in the MECP2 gene in a cohort of girls with Rett syndrome. J Med Genet (2000) 0.85
Violence and its injury consequences in American movies: a public health perspective. West J Med (2000) 0.85
On the existence of gamma-crystallin in the bird lens. Exp Eye Res (1977) 0.84
Condensation of ethyl diazoacetate with cobalt porphyrins. J Chem Soc Perkin 1 (1975) 0.84
Amino and carboxy terminal sequence of -crystallin, from haddock lens. Biochim Biophys Acta (1973) 0.84
Inhibition of mRNA turnover in yeast by an xrn1 mutation enhances the requirement for eIF4E binding to eIF4G and for proper capping of transcripts by Ceg1p. Genetics (2000) 0.84
The inactivation of the fragile X chromosome in female carriers of the Martin Bell syndrome as studied by two different methods. Clin Genet (1989) 0.84
X inactivation patterns in female monozygotic twins and their families. J Med Genet (1994) 0.84
Studies of the parathyroid hormone gene in normal subjects, and in subjects with primary hyperparathyroidism and familial benign hypercalcaemia. J Endocrinol (1987) 0.84
Coenzyme B-12-dependent reactions. Part IV. Observations on the purification of ethanolamine ammonia-lyase. Biochim Biophys Acta (1976) 0.83
Brain-water diffusion coefficients reflect the severity of inherited prion disease. Neurology (2010) 0.83
GM1-gangliosidosis in a cross-bred dog confirmed by detection of GM1-ganglioside using electrospray ionisation-tandem mass spectrometry. Acta Neuropathol (2000) 0.83
Distinct neuropsychological profiles correspond to distribution of cortical thinning in inherited prion disease caused by insertional mutation. J Neurol Neurosurg Psychiatry (2011) 0.83
Prenatal diagnosis of Martin-Bell syndrome associated with fragile site at Xq27-28. Lancet (1982) 0.82
Nutritional status in children. Lancet (2001) 0.82
Accelerated degradation of fenamiphos and its metabolites in soil previously treated with fenamiphos. J Nematol (1993) 0.82
Polyploidy and Environment in Arctic Alaska. Science (1965) 0.82