Published in Biochem J on September 01, 1975
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Hormonal stimulation of hepatic ornithine decarboxylase. Biochem Biophys Res Commun (1971) 1.33
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The effects of testosterone, 5 -dihydrotestosterone and adenosine 3',5'-monophosphate on cell proliferation and differentiation in rat prostate. Biochim Biophys Acta (1973) 1.24
Imbalance in ornithine metabolism in hepatomas of different growth rates as expressed in formation of putrescine, spermidine, and spermine. Cancer Res (1972) 1.23
Effect of cyclic nucleotides on the induction of ornithine decarboxylase in BHK cells by serum and insulin. Cell (1974) 1.03
A reappraisal of the effects of adenosine 3':5'-cyclic monophosphate on the function and morphology of the rat prostate gland. Biochem J (1973) 1.02
An evaluation of radioiodine-labeled 5-iodo-2'-deoxyuridine as a tracer for measuring cell loss from solid tumors. Cell Tissue Kinet (1971) 1.01
Reutilization of thymidine and iododeoxyuridine by mouse mammary carcinoma strain MTG-B 1 . Proc Soc Exp Biol Med (1973) 0.95
3H-5-iodo-2'-deoxyuridine toxicity. Problems in cell proliferation studies. Cell Tissue Kinet (1974) 0.91
Differences in proliferative activity of rat and human prostate in culture. Br J Cancer (1975) 0.90
Growth and lactogenic hormone stimulation of ornithine decarboxylase in neonatal rat brain. Endocrinology (1974) 0.87
Some properties of guinea pig brain glutamate decarboxylase and its inhibition by the convulsant allylglycine (2-amino-4-pentenoic acid). J Neurochem (1974) 0.80
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Occurrence of cancer in Asians and non-Asians. J Epidemiol Community Health (1984) 2.36
Initial effect of injury on ketone bodies and other blood metabolites. Lancet (1975) 2.27
A prescribing incentive scheme for non-fundholding general practices: an observational study. BMJ (1996) 2.09
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Genomic insight into the amino acid relations of the pea aphid, Acyrthosiphon pisum, with its symbiotic bacterium Buchnera aphidicola. Insect Mol Biol (2010) 1.92
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The synthesis of 4-methylumbelliferyl alpha-ketoside of N-acetylneuraminic acid and its use in a fluorometric assay for neuraminidase. Anal Biochem (1980) 1.78
Single strand interruptions in DNA and the effects of caffeine in Chinese hamster cells irradiated with ultraviolet light. Biochem Biophys Res Commun (1969) 1.77
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Characteristics of elderly people misplaced in hospitals and homes. Public Health (1983) 1.68
NADP-linked 17-beta- and 20-alpha-steroid reductase activity in the rabbit uterus. J Endocrinol (1969) 1.64
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Familial tandem duplication of bands q31.1 to q32.3 on chromosome 4 with mild phenotypic effect. Am J Med Genet (1997) 1.54
Analysing stages of care in hospital stay for fractured neck of femur. Lancet (1984) 1.52
Complex chromosome rearrangements. Report of a new case and literature review. Clin Genet (1980) 1.51
Mucolipidosis III (pseudo-Hurler polydystrophy): Clinical and laboratory studies in a series of 12 patients. Johns Hopkins Med J (1975) 1.48
Health education for ethnic minorities--current provision and future directions. Health Educ J (1988) 1.46
Syndromes due to chromosomal abnormalities: partial trisomy 22, interstitial deletion of the long arm of 13, and trisomy 8. Johns Hopkins Med J (1979) 1.45
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Ashkenazi-Jewish and non-Jewish adult GM2 gangliosidosis patients share a common genetic defect. Am J Hum Genet (1990) 1.40
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Excision repair (dimer excision, strand breakage and repair replication) in primary cultures of eukaryotic (bovine) cells. Exp Cell Res (1972) 1.31
Mannosidosis: deficiency of a specific alpha-mannosidase component in cultured fibroblasts. Clin Chim Acta (1975) 1.29
Deposition of scar tissue in the central nervous system. Acta Neurochir Suppl (Wien) (1983) 1.26
Clinical governance: a statutory duty for quality improvement. J Epidemiol Community Health (1998) 1.26
The elderly in residential care: mortality in relation to functional capacity. J Epidemiol Community Health (1980) 1.26
Increased levels of sialic acid associated with a sialidase deficiency in I-cell disease (mucolipidosis II) fibroblasts. Biochem Biophys Res Commun (1976) 1.26
Polyamine biosynthesis and accumulation during the G1 to S phase transition. J Cell Physiol (1977) 1.26
Cryptic terminal rearrangement of chromosome 22q13.32 detected by FISH in two unrelated patients. J Med Genet (1997) 1.24
Biological damage from intranuclear tritium: DNA strand breaks and their repair. Science (1972) 1.24
Oxygens in DNA are main targets for ethylnitrosourea in normal and xeroderma pigmentosum fibroblasts and fetal rat brain cells. Nature (1978) 1.23
Influenza A(H1N1)pdm09 in England, 2009 to 2011: a greater burden of severe illness in the year after the pandemic than in the pandemic year. Euro Surveill (2012) 1.23
Genetic complementation after fusion of Tay-Sachs and Sandhoff cells. Nature (1974) 1.22
High-resolution microscopic methods for the analysis of cellular movements in Drosophila embryos. Methods Cell Biol (1994) 1.17
Evidence for removal at different rates of O-ethyl pyrimidines and ethylphosphotriesters in two human fibroblast cell lines. Nucleic Acids Res (1979) 1.14
Infantile form of sialic acid storage disorder: clinical, ultrastructural, and biochemical studies in two siblings. Eur J Pediatr (1982) 1.13
Trisomy 9 mosaicism with multiple congenital anomalies. J Med Genet (1973) 1.13
Nonuniform deficiency of hexosaminidase A in tissues and fluids of two unrelated individuals. Pediatr Res (1982) 1.13
Apical spectrin is essential for epithelial morphogenesis but not apicobasal polarity in Drosophila. J Cell Biol (1999) 1.13
Sialidase (alpha-n-acetyl neuraminidase) deficiency: the enzyme defect in an adult with macular cherry-red spots and myoclonus without dementia. Clin Genet (1978) 1.13
Prenatal diagnosis of hemoglobinopathies by restriction endonuclease analysis: pregnancies at risk for sickle cell anemia and S--O Arab disease. Johns Hopkins Med J (1979) 1.12
Developmental abnormalities associated with a ring chromosome 6. J Med Genet (1973) 1.11
Characterization of a supercoil-dependent S1 sensitive site 5' to the Drosophila melanogaster hsp 26 gene. Nucleic Acids Res (1986) 1.10
Defective lysosomal egress of free sialic acid (N-acetylneuraminic acid) in fibroblasts of patients with infantile free sialic acid storage disease. J Biol Chem (1989) 1.10
Mortality due to pandemic (H1N1) 2009 influenza in England: a comparison of the first and second waves. Epidemiol Infect (2011) 1.10
Two anonymous DNA segments distinguish the Wilms' tumor and aniridia loci. Science (1988) 1.10
Familial isolated aniridia associated with a translocation involving chromosomes 11 and 22 [t(11;22)(p13;q12.2)]. Hum Genet (1986) 1.09
Mucolipidosis 3 (Pseudo-Hurler polydystrophy): multiple lysosomal enzyme abnormalities in serum and cultured fibroblast cells. Pediatr Res (1973) 1.08
Heat shock stimulates polyamine oxidation by two distinct mechanisms in mammalian cell cultures. Int J Radiat Oncol Biol Phys (1989) 1.03
Malunited fractures of the forearm in children. J Bone Joint Surg Br (1982) 1.03
Genomic evidence for complementary purine metabolism in the pea aphid, Acyrthosiphon pisum, and its symbiotic bacterium Buchnera aphidicola. Insect Mol Biol (2010) 1.03
Sialic acid metabolism in sialuria fibroblasts. J Biol Chem (1991) 1.02
Replication of type 2 herpes simplex virus in human endocervical tissue in organ culture. Br J Exp Pathol (1976) 1.02
Morphological responses of prostatic carcinoma to testosterone in organ culture. Br J Cancer (1972) 1.01
Rugby football injuries to the cervical spine. Br Med J (Clin Res Ed) (1983) 0.99
New approaches to the diagnosis and treatment of inborn errors or urea synthesis. Pediatrics (1981) 0.99
Hyperprolinaemia in patients with deletion (22)(q11.2) syndrome. J Inherit Metab Dis (2000) 0.99
C-group chromosome abnormality (? 10p-). Occurrence in a child with multiple malformations. Am J Dis Child (1970) 0.98
Uptake and interconversion of oestrone and oestradiol in rabbit uterus. Biochem J (1970) 0.98
Xeroderma pigmentosum variants have a slow recovery of DNA synthesis after irradiation with ultraviolet light. Biochim Biophys Acta (1979) 0.98
The use of topical thrombin to reduce wound haematoma in patients receiving low-dose heparin. Curr Med Res Opin (1981) 0.98
A mutation common in non-Jewish Tay-Sachs disease: frequency and RNA studies. Hum Mutat (1992) 0.98
Identification of the alpha-aminoadipic semialdehyde dehydrogenase-phosphopantetheinyl transferase gene, the human ortholog of the yeast LYS5 gene. Mol Genet Metab (2001) 0.98
Clinical, cytogenetic, and fluorescence in situ hybridization findings in two cases of "complete ring" syndrome. Am J Med Genet (1999) 0.97
Survival and functional capacity: three year follow up of an elderly population in hospitals and homes. J Epidemiol Community Health (1983) 0.97
Hyperpipecolic acidemia associated with hepatomegaly, mental retardation, optic nerve dysplasia and progressive neurological disease. Clin Genet (1975) 0.97
Metaplasia in endocervical tissue maintained in organ culture--an experimental model. J Obstet Gynaecol Br Commonw (1973) 0.96
Primate hemoglobins: Some sequences and some proposals concerning the character of evolution and mutation. Biochem Genet (1971) 0.96
Sister chromatid exchange in xeroderma pigmentosum cells that are defective in DNA excision repair or post-replication repair. Genetics (1975) 0.96
Molecular basis of hexosaminidase A deficiency and pseudodeficiency in the Berks County Pennsylvania Dutch. Hum Mutat (1992) 0.95
Impact of premature stop codons on mRNA levels in infantile Sandhoff disease. Hum Mol Genet (1994) 0.95
Morphological changes of benign prostatic hyperplasia in culture. Br J Cancer (1973) 0.94
Regional hip blockade in osteoarthrosis. Effects on pain perception. Anaesthesia (1982) 0.94
Topical thrombin and control of wound haematoma. Lancet (1977) 0.94
Six novel deleterious and three neutral mutations in the gene encoding the alpha-subunit of hexosaminidase A in non-Jewish individuals. Am J Hum Genet (1992) 0.94
Occurrence of a presumptive C-B translocation carrier [46,XY,t (? Cp-; Bp+)] in a family of D-G translocation carriers [45,D-,G-,t (DqGq)+]. J Med Genet (1969) 0.94
Effects of oestrone and oestradiol on rat and rabbit uterus in organ culture. Biochem J (1969) 0.94
Rapid diagnosis of sensitivity to ultraviolet light in fibroblasts from dermatologic disorders, with particular reference to xeroderma pigmentosum. J Invest Dermatol (1988) 0.93
Specific regulation by steroid hormones of the amount of type I cyclic AMP-dependent protein kinase holoenzyme. Proc Natl Acad Sci U S A (1978) 0.93
Effects of diethyldithiocarbamate and endogenous polyamine content on cellular responses to hydrogen peroxide cytotoxicity. Biochem J (1989) 0.93
A new R-banding technique in clinical cytogenetics. Hum Genet (1980) 0.92
Molecular cytogenetic evaluation in a patient with a translocation (3;21) associated with blepharophimosis, ptosis, epicanthus inversus syndrome (BPES). Genomics (2000) 0.92
Mucolipidosis 3 (pseudo-Hurler polydystrophy): cytological and ultrastructural observations of cultured fibroblast cells. Clin Genet (1973) 0.92
Cytomegalovirus infection after autologous bone marrow transplantation with comparison to infection after allogeneic bone marrow transplantation. Blood (1988) 0.92