Published in Enzyme on January 01, 1982
Purification of uroporphyrinogen decarboxylase from human erythrocytes. Immunochemical evidence for a single protein with decarboxylase activity in human erythrocytes and liver. Biochem J (1983) 1.11
Inhibition of uroporphyrinogen decarboxylase by halogenated biphenyls in chick hepatocyte cultures. Essential role for induction of cytochrome P-448. Biochem J (1984) 1.03
Modified uroporphyrinogen decarboxylase activity in a yeast mutant which mimics porphyria cutanea tarda. Biochem J (1984) 0.91
Uroporphyria produced in mice by 20-methylcholanthrene and 5-aminolaevulinic acid. Biochem J (1988) 0.89
Iron and the liver: acute effects of iron-loading on hepatic heme synthesis of rats. Role of decreased activity of 5-aminolevulinate dehydrase. J Clin Invest (1983) 0.83
Heterogeneity of familial porphyria cutanea tarda. J Med Genet (1988) 0.75
Economic stress, coercive family process, and developmental problems of adolescents. Child Dev (1994) 5.45
A family process model of economic hardship and adjustment of early adolescent boys. Child Dev (1992) 4.32
Pubertal transition, stressful life events, and the emergence of gender differences in adolescent depressive symptoms. Dev Psychol (2001) 3.79
Competence in early adult romantic relationships: a developmental perspective on family influences. J Pers Soc Psychol (2000) 2.87
Macrocyclic intermediates in the biosynthesis of porphyrins. Philos Trans R Soc Lond B Biol Sci (1976) 2.73
Are religious grandparents more involved grandparents? J Gerontol B Psychol Sci Soc Sci (1999) 2.36
Molecular epidemiology of erythropoietic protoporphyria in the U.K. Br J Dermatol (2010) 2.15
Couple resilience to economic pressure. J Pers Soc Psychol (1999) 2.09
Coming of age too early: pubertal influences on girls' vulnerability to psychological distress. Child Dev (1996) 2.08
Trial of strategy for reducing the use of laboratory tests. Br Med J (Clin Res Ed) (1986) 1.82
Erythropoietic protoporphyria in the U.K.: clinical features and effect on quality of life. Br J Dermatol (2006) 1.77
Increased frequency of the haemochromatosis Cys282Tyr mutation in sporadic porphyria cutanea tarda. Lancet (1997) 1.69
Pathways of economic influence on adolescent adjustment. Am J Community Psychol (1999) 1.69
A radiochemical method for the measurement of coproporphyrinogen oxidase and the utilization of substrates other than coproporphyrinogen III by the enzyme from rat liver. Biochem J (1978) 1.58
Continuities and consequences of interactional styles across the life course. J Pers (1989) 1.52
Linking family hardship to children's lives. Child Dev (1985) 1.52
ACP Best Practice No 165: front line tests for the investigation of suspected porphyria. J Clin Pathol (2001) 1.50
Parent-adolescent reciprocity in negative affect and its relation to early adult social development. Dev Psychol (2001) 1.49
The efficacy of a serum screening service for neural-tube defects: the South Wales experience. Lancet (1983) 1.49
Decreased activity of hepatic uroporphyrinogen decarboxylase in sporadic porphyria cutanea tarda. N Engl J Med (1978) 1.39
A MspI polymorphism for the human porphobilinogen deaminase gene. Nucleic Acids Res (1987) 1.37
Porphyrin metabolism in porphyria cutanea tarda. Semin Hematol (1977) 1.35
Can we afford screening for neural tube defects? The South Wales experience. Br Med J (Clin Res Ed) (1985) 1.34
A 50-year prospective study of the psychological sequelae of World War II combat. Am J Psychiatry (1995) 1.29
The porphyrias: a review. J Clin Pathol (1972) 1.28
Evidence that the coproporphyrinogen oxidase activity of rat liver is situated in the intermembrane space of mitochondria. Biochem J (1978) 1.26
Husband and wife differences in response to undesirable life events. J Health Soc Behav (1993) 1.24
Differentiation of porphyria cutanea tarda symptomatica from other types of porphyria by measurement of isocoproporphyrin in faeces. J Clin Pathol (1975) 1.24
The effect of the porphyrogenic compound, hexachlorobenzene, on the activity of hepatic uroporphyrinogen decarboxylase in the rat. Clin Sci Mol Med (1976) 1.24
The intergenerational transmission of health-risk behaviors: adolescent lifestyles and gender moderating effects. J Health Soc Behav (1999) 1.23
Investigation of the subcellular location of the tetrapyrrole-biosynthesis enzyme coproporphyrinogen oxidase in higher plants. Biochem J (1993) 1.18
DNA polymorphism of human porphobilinogen deaminase gene in acute intermittent porphyria. Lancet (1987) 1.17
Appearance and education in marriage mobility. Am Sociol Rev (1969) 1.16
Family history and the life course. J Fam Hist (1977) 1.15
Hepatoerythropoietic porphyria: a new uroporphyrinogen decarboxylase defect or homozygous porphyria cutanea tarda? Lancet (1981) 1.12
Immunoreactive uroporphyrinogen decarboxylase in the liver in porphyria cutanea tarda. Lancet (1985) 1.11
Purification of uroporphyrinogen decarboxylase from human erythrocytes. Immunochemical evidence for a single protein with decarboxylase activity in human erythrocytes and liver. Biochem J (1983) 1.11
Identification of two types of porphyria cutanea tarda by measurement of erythrocyte uroporphyrinogen decarboxylase. Clin Sci (Lond) (1980) 1.09
Worklives and longevity: insights from a life course perspective. J Health Soc Behav (1993) 1.09
The primary enzyme defect in hereditary coproporphyria. Lancet (1976) 1.08
Mutations in the hemochromatosis gene, porphyria cutanea tarda, and iron overload. Hepatology (1998) 1.04
Isocoproporphyrin: nuclear-magnetic-resonance-and mass-spectral methods for the determination of porphyrin structure. Biochem J (1973) 1.04
Immunoreactive uroporphyrinogen decarboxylase is unchanged in porphyria caused by TCDD and hexachlorobenzene. Biochem Biophys Res Commun (1982) 1.00
Intergenerational continuity of parental rejection and depressed affect. J Pers Soc Psychol (1992) 0.99
Factors determining the sequence of oxidative decarboxylation of the 2- and 4-propionate substituents of coproporphyrinogen III by coproporphyrinogen oxidase in rat liver. Biochem J (1978) 0.99
Decreased activity of uroporphyrinogen decarboxylase caused by 2,4,5,3',4'-pentabromobiphenyl in chick embryo hepatocyte cultures. Difference in activity in intact or homogenized cells. FEBS Lett (1983) 0.98
The metabolism of porphyrins of the isocoproporphyrin series. Enzyme (1974) 0.98
Acute intermittent porphyria caused by a C----T mutation that produces a stop codon in the porphobilinogen deaminase gene. Hum Genet (1990) 0.97
Immunoreactive uroporphyrinogen decarboxylase in porphyria cutanea tarda. Lancet (1983) 0.96
Economic hardship and marital relations in the 1930s. Am Sociol Rev (1983) 0.95
The porphyrias: clinical chemistry, diagnosis and methodology. Clin Haematol (1980) 0.94
Variegate porphyria in Western Europe: identification of PPOX gene mutations in 104 families, extent of allelic heterogeneity, and absence of correlation between phenotype and type of mutation. Am J Hum Genet (1999) 0.93
Late presentation of erythropoietic protoporphyria: case report and genetic analysis of family members. Br J Dermatol (2007) 0.93
Management of acute and cutaneous porphyrias. Int J Clin Pract (2002) 0.92
Enzymatic defects in porphyria: an overview. Semin Liver Dis (1982) 0.92
Matrilineal advantage in grandchild-grandparent relations. Gerontologist (2000) 0.92
Life satisfaction in old age: linking social psychology and history. Psychol Aging (1986) 0.92
Autosomal recessive erythropoietic protoporphyria in the United Kingdom: prevalence and relationship to liver disease. J Med Genet (2004) 0.91
Homozygous acute intermittent porphyria: compound heterozygosity for adjacent base transitions in the same codon of the porphobilinogen deaminase gene. Hum Genet (1992) 0.90
Uroporphyria produced in mice by 20-methylcholanthrene and 5-aminolaevulinic acid. Biochem J (1988) 0.89
Molecular characterization of homozygous variegate porphyria. Hum Mol Genet (1998) 0.89
Acute intermittent porphyria caused by an arginine to histidine substitution (R26H) in the cofactor-binding cleft of porphobilinogen deaminase. Hum Mol Genet (1993) 0.88
Homozygous variegate porphyria: a case report. Br J Dermatol (1990) 0.88
Detection of latent variegate porphyria by fluorescence emission spectroscopy of plasma. Br J Dermatol (1993) 0.88
Isolation of an hydroxylated porphyrin from urine and faeces of patients with cutaneous hepatic porphyria. Biochim Biophys Acta (1970) 0.88
Characterization of mutations in the CPO gene in British patients demonstrates absence of genotype-phenotype correlation and identifies relationship between hereditary coproporphyria and harderoporphyria. Am J Hum Genet (2001) 0.88
Adolescent paid labor and relationships with parents: early work-family linkages. Child Dev (1996) 0.87
Partial characterization and assignment of the gene for protoporphyrinogen oxidase and variegate porphyria to human chromosome 1q23. Hum Mol Genet (1995) 0.87
Comparison of complementary and genomic DNA sequencing for the detection of mutations in the HMBS gene in British patients with acute intermittent porphyria: identification of 25 novel mutations. Hum Genet (1999) 0.87
Linking occupational conditions to physical health through marital, social, and intrapersonal processes. J Health Soc Behav (1997) 0.87
Uroporphyrin accumulation produced by halogenated biphenyls in chick-embryo hepatocytes. Reversal of the accumulation by piperonyl butoxide. Biochem J (1986) 0.87
Measurement of 5-aminolevulinic acid synthase activity in whole and fractionated human bone marrow: effect of myeloid cell lysis by monoclonal antibody. Anal Biochem (1986) 0.86
Faecal 'X porphyrin' in the hepatic porphyrias. Enzyme (1974) 0.86
Molecular mechanisms of dominant expression in porphyria. J Inherit Metab Dis (2005) 0.86
Linkage disequilibrium between DNA polymorphisms within the porphobilinogen deaminase gene. Hum Genet (1990) 0.85
Is hepatoerythropoietic porphyria a homozygous form of porphyria cutanea tarda? Inheritance of uroporphyrinogen decarboxylase deficiency in a Spanish family. Br J Dermatol (1984) 0.85
Acute intermittent porphyria caused by defective splicing of porphobilinogen deaminase RNA: a synonymous codon mutation at -22 bp from the 5' splice site causes skipping of exon 3. J Med Genet (1996) 0.85
Late-onset erythropoietic porphyria caused by a chromosome 18q deletion in erythroid cells. J Invest Dermatol (2001) 0.85
A mutation (G281E) of the human uroporphyrinogen decarboxylase gene causes both hepatoerythropoietic porphyria and overt familial porphyria cutanea tarda: biochemical and genetic studies on Spanish patients. J Invest Dermatol (1995) 0.84
Hepatic heme synthesis in a new model of experimental hemochromatosis: studies in rats fed finely divided elemental iron. Hepatology (1988) 0.84
Separation of porphyrin methyl esters by two-dimensional thin-layer chromatography. J Chromatogr (1971) 0.84
The metabolism of coproporphyrinogen-III into protoporphyrin-IX. Int J Biochem (1978) 0.84
Homozygous variegate porphyria: a compound heterozygote with novel mutations in the protoporphyrinogen oxidase gene. Br J Dermatol (2001) 0.84
Co-inheritance of mutations in the uroporphyrinogen decarboxylase and hemochromatosis genes accelerates the onset of porphyria cutanea tarda. J Invest Dermatol (2000) 0.84
Uroporphyrinogen decarboxylase activity of human tissues [proceedings]. Biochem Soc Trans (1977) 0.83
The porphyrin excretion pattern of symptomatic porphyria. S Afr Med J (1971) 0.83
Iron and the liver: acute effects of iron-loading on hepatic heme synthesis of rats. Role of decreased activity of 5-aminolevulinate dehydrase. J Clin Invest (1983) 0.83
Homozygous variegate porphyria: two similar cases in unrelated families. J R Soc Med (1986) 0.83
Hepatoerythropoietic porphyria: a missense mutation in the UROD gene is associated with mild disease and an unusual porphyrin excretion pattern. Br J Dermatol (2004) 0.83
Uroporphyrinogen decarboxylase deficiency in hepatoerythropoietic porphyria: further evidence for genetic heterogeneity. Br J Dermatol (1990) 0.82
Marital timing in women's life patterns. J Fam Hist (1976) 0.82
Ferrochelatase activity in human lymphocytes: effect of storage on haem formation. Ann Clin Biochem (1990) 0.82
Variegate porphyria associated with hepatocellular carcinoma. Br J Dermatol (1989) 0.82
Linking economic hardship to adolescent aggression. J Youth Adolesc (1992) 0.81
5-Aminolaevulinic acid synthase activity in developing human erythroblasts. Br J Haematol (1988) 0.81
Evaluation of a new strategy for detection of thyroid dysfunction in the routine laboratory. Clin Chem (1988) 0.80
Alternative splicing and tissue-specific transcription of human and rodent ubiquitous 5-aminolevulinate synthase (ALAS1) genes. Biochim Biophys Acta (2001) 0.80
Uroporphyria produced in mice by iron and 5-aminolevulinic acid. Biochem Pharmacol (1991) 0.80
Plasma alkaline phosphatase activity and its relation to rickets in pre-term infants. Ann Clin Biochem (1986) 0.79