Influence of heredity on human sensitivity to environmental chemicals (Q40549871)

21 September 2017

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title

Influence of heredity on human sensitivity to environmental chemicals (English)

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21 September 2017

Weber WW

1

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21 September 2017

1 January 1995

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Environmental and Molecular Mutagenesis

21 September 2017

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21 September 2017

25 Suppl 26

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21 September 2017

102-114

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A randomized trial of vitamin A and vitamin E supplementation for retinitis pigmentosa

21 September 2017

1 reference

https://api.crossref.org/works/10.1002%2FEM.2850250614

An enzyme from rat liver catalysing conjugations with glutathione

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FEM.2850250614

Nomenclature for human glutathione transferases

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FEM.2850250614

Glucocorticoid-remediable aldosteronism in a large kindred: clinical spectrum and diagnosis using a characteristic biochemical phenotype

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FEM.2850250614

The trans-stilbene oxide-active glutathione transferase in human mononuclear leucocytes is identical with the hepatic glutathione transferase mu

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FEM.2850250614

Genetic polymorphism of trimethylamine N-oxidation

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FEM.2850250614

7 January 2021

Trinucleotide repeat expansions and human genetic disease

1 reference

https://api.crossref.org/works/10.1002%2FEM.2850250614

7 January 2021

Tamoxifen withdrawal response. Report of a case

1 reference

https://api.crossref.org/works/10.1002%2FEM.2850250614

7 January 2021

Genetic risk and carcinogen exposure: a common inherited defect of the carcinogen-metabolism gene glutathione S-transferase M1 (GSTM1) that increases susceptibility to bladder cancer

1 reference

https://api.crossref.org/works/10.1002%2FEM.2850250614

7 January 2021

Hereditary aspects of malignant hyperthermia

1 reference

https://api.crossref.org/works/10.1002%2FEM.2850250614

7 January 2021

Genetic heterogeneity of the human glutathione transferases: a complex of gene families

1 reference

https://api.crossref.org/works/10.1002%2FEM.2850250614

7 January 2021

Cardiac arrest in a young woman with the long QT syndrome and concomitant astemizole ingestion

1 reference

https://api.crossref.org/works/10.1002%2FEM.2850250614

7 January 2021

Role of N-acetyltransferase phenotypes in bladder carcinogenesis: a pharmacogenetic epidemiological approach to bladder cancer

1 reference

https://api.crossref.org/works/10.1002%2FEM.2850250614

7 January 2021

Rearrangements of the retinoic acid receptor alpha and promyelocytic leukemia zinc finger genes resulting from t(11;17)(q23;q21) in a patient with acute promyelocytic leukemia

1 reference

https://api.crossref.org/works/10.1002%2FEM.2850250614

7 January 2021

The molecular basis of leukemia

1 reference

https://api.crossref.org/works/10.1002%2FEM.2850250614

7 January 2021

Cystic fibrosis: molecular biology and therapeutic implications

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https://api.crossref.org/works/10.1002%2FEM.2850250614

7 January 2021

Altered chloride ion channel kinetics associated with the ΔF508 cystic fibrosis mutation

1 reference

https://api.crossref.org/works/10.1002%2FEM.2850250614

7 January 2021

Anaesthetic deaths in a family

1 reference

https://api.crossref.org/works/10.1002%2FEM.2850250614

7 January 2021

The PML-RARα fusion mRNA generated by the t(15;17) translocation in acute promyelocytic leukemia encodes a functionally altered RAR

1 reference

https://api.crossref.org/works/10.1002%2FEM.2850250614

7 January 2021

Chloride Conductance Expressed by ΔF508 and Other Mutant CFTRs In Xenopus Oocytes

1 reference

https://api.crossref.org/works/10.1002%2FEM.2850250614

7 January 2021

Heterozygous missense mutation in the rhodopsin gene as a cause of congenital stationary night blindness

1 reference

https://api.crossref.org/works/10.1002%2FEM.2850250614

7 January 2021

Identification of a Mutation in Porcine Ryanodine Receptor Associated with Malignant Hyperthermia

1 reference

https://api.crossref.org/works/10.1002%2FEM.2850250614

7 January 2021

A substitution of cysteine for arginine 614 in the ryanodine receptor is potentially causative of human malignant hyperthermia

1 reference

https://api.crossref.org/works/10.1002%2FEM.2850250614

7 January 2021

Decoding at the ribosomal A site: antibiotics, misreading and energy of aminoacyl-tRNA binding.

1 reference

https://api.crossref.org/works/10.1002%2FEM.2850250614

7 January 2021

Genetic aspects of antibiotic induced deafness: mitochondrial inheritance

1 reference

https://api.crossref.org/works/10.1002%2FEM.2850250614

7 January 2021

The molecular basis of the human serum paraoxonase activity polymorphism.

1 reference

https://api.crossref.org/works/10.1002%2FEM.2850250614

7 January 2021

Two long QT syndrome loci map to chromosomes 3 and 7 with evidence for further heterogeneity

1 reference

https://api.crossref.org/works/10.1002%2FEM.2850250614

7 January 2021

Chromosomal translocation t(15;17) in human acute promyelocytic leukemia fuses RARα with a novel putative transcription factor, PML

1 reference

https://api.crossref.org/works/10.1002%2FEM.2850250614

7 January 2021

Parathion poisoning from contaminated barley

1 reference

https://api.crossref.org/works/10.1002%2FEM.2850250614

7 January 2021

Linkage of a cardiac arrhythmia, the long QT syndrome, and the Harvey ras-1 gene

1 reference

https://api.crossref.org/works/10.1002%2FEM.2850250614

7 January 2021

Increased risk of lung cancer in Japanese smokers with class mu glutathione S-transferase gene deficiency

1 reference

https://api.crossref.org/works/10.1002%2FEM.2850250614

7 January 2021

Constitutive activity of receptors coupled to guanine nucleotide regulatory proteins

1 reference

https://api.crossref.org/works/10.1002%2FEM.2850250614

7 January 2021

Evidence for genetic heterogeneity in malignant hyperthermia susceptibility

1 reference

https://api.crossref.org/works/10.1002%2FEM.2850250614

7 January 2021

A chimaeric llβ-hydroxylase/aldosterone synthase gene causes glucocorticoid-remediable aldosteronism and human hypertension

1 reference

https://api.crossref.org/works/10.1002%2FEM.2850250614

7 January 2021

Hereditary hypertension caused by chimaeric gene duplications and ectopic expression of aldosterone synthase

1 reference

https://api.crossref.org/works/10.1002%2FEM.2850250614

7 January 2021

Glutathione S-transferase μ in human lymphocyte and liver: role in modulating formation of carcinogen-derived DNA adducts

1 reference

https://api.crossref.org/works/10.1002%2FEM.2850250614

7 January 2021

Malignant hyperthermia

1 reference

https://api.crossref.org/works/10.1002%2FEM.2850250614

7 January 2021

Ryanodine receptor gene is a candidate for predisposition to malignant hyperthermia.

1 reference

https://api.crossref.org/works/10.1002%2FEM.2850250614

7 January 2021

A mutation of the glucocorticoid receptor in primary cortisol resistance

1 reference

https://api.crossref.org/works/10.1002%2FEM.2850250614

7 January 2021

Retinal genetics: a nullifying effect for rhodopsin

1 reference

https://api.crossref.org/works/10.1002%2FEM.2850250614

7 January 2021

Androgen resistance caused by mutations in the androgen receptor gene.

1 reference

https://api.crossref.org/works/10.1002%2FEM.2850250614

7 January 2021

The long-QT syndrome Genetic considerations

1 reference

https://api.crossref.org/works/10.1002%2FEM.2850250614

7 January 2021

To Be2+ or not to Be2+: immunogenetics and occupational exposure

1 reference

https://api.crossref.org/works/10.1002%2FEM.2850250614

7 January 2021

Androgen receptor gene mutations in human prostate cancer

1 reference

https://api.crossref.org/works/10.1002%2FEM.2850250614

7 January 2021

Somatic mutations in the thyrotropin receptor gene cause hyperfunctioning thyroid adenomas

1 reference

https://api.crossref.org/works/10.1002%2FEM.2850250614

7 January 2021

Biochemical characterization of a pedigree with mitochondrially inherited deafness

1 reference

https://api.crossref.org/works/10.1002%2FEM.2850250614

7 January 2021

Mitochondrial ribosomal RNA mutation associated with both antibiotic-induced and non-syndromic deafness

1 reference

https://api.crossref.org/works/10.1002%2FEM.2850250614

7 January 2021

The role of the human acetylation polymorphism in the metabolic activation of the food carcinogen 2-amino-3-methylimidazo[4,5-f]quinoline (IQ)

1 reference

https://api.crossref.org/works/10.1002%2FEM.2850250614

7 January 2021

Rhodopsin mutation G90D and a molecular mechanism for congenital night blindness

1 reference

https://api.crossref.org/works/10.1002%2FEM.2850250614

7 January 2021

HLA-DPB1 glutamate 69: a genetic marker of beryllium disease

1 reference

https://api.crossref.org/works/10.1002%2FEM.2850250614

7 January 2021

Constitutively active mutants of rhodopsin

1 reference

https://api.crossref.org/works/10.1002%2FEM.2850250614

7 January 2021

Flutamide withdrawal syndrome: its impact on clinical trials in hormone-refractory prostate cancer

1 reference

https://api.crossref.org/works/10.1002%2FEM.2850250614

7 January 2021

Microsatellite mutation (CAG24-->18) in the androgen receptor gene in human prostate cancer

1 reference

https://api.crossref.org/works/10.1002%2FEM.2850250614

7 January 2021

A glutathione transferase in human leukocytes as a marker for the susceptibility to lung cancer

1 reference

https://api.crossref.org/works/10.1002%2FEM.2850250614

7 January 2021

Isoenzyme(s) of glutathione transferase (class Mu) as a marker for the susceptibility to lung cancer: a follow up study

1 reference

https://api.crossref.org/works/10.1002%2FEM.2850250614

7 January 2021

A constitutively activating mutation of the luteinizing hormone receptor in familial male precocious puberty

1 reference

https://api.crossref.org/works/10.1002%2FEM.2850250614

7 January 2021

Estrogen resistance caused by a mutation in the estrogen-receptor gene in a man

1 reference

https://api.crossref.org/works/10.1002%2FEM.2850250614

7 January 2021

Parathion poisoning; increasing frequency in Finland

1 reference

https://api.crossref.org/works/10.1002%2FEM.2850250614

7 January 2021

Structural heterogeneity of Caucasian N-acetyltransferase at the NAT1 gene locus

1 reference

https://api.crossref.org/works/10.1002%2FEM.2850250614

7 January 2021

A mutation in the ligand binding domain of the androgen receptor of human LNCaP cells affects steroid binding characteristics and response to anti-androgens

1 reference

https://api.crossref.org/works/10.1002%2FEM.2850250614

7 January 2021

Anti-androgens and the mutated androgen receptor of LNCaP cells: differential effects on binding affinity, heat-shock protein interaction, and transcription activation

1 reference

https://api.crossref.org/works/10.1002%2FEM.2850250614

7 January 2021

Mitochondrial genetics: a paradigm for aging and degenerative diseases?

1 reference

https://api.crossref.org/works/10.1002%2FEM.2850250614

7 January 2021

Differentiation Therapy of Acute Promyelocytic Leukemia with Tretinoin (All-trans-Retinoic Acid)

1 reference

https://api.crossref.org/works/10.1002%2FEM.2850250614

7 January 2021

Individual variability in p-aminobenzoic acid N-acetylation by human N-acetyltransferase (NAT1) of peripheral blood

1 reference

https://api.crossref.org/works/10.1002%2FEM.2850250614

7 January 2021

Relationship between the GSTM1 genetic polymorphism and susceptibility to bladder, breast and colon cancer

1 reference

https://api.crossref.org/works/10.1002%2FEM.2850250614

7 January 2021

Identifiers

DOI

10.1002/EM.2850250614

1 reference

21 September 2017

1 reference

PubMed ID

7789356