Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 4 de 4
Filter
Add more filters










Database
Publication year range
1.
Neurosci Lett ; 289(3): 157-60, 2000 Aug 11.
Article in English | MEDLINE | ID: mdl-10961653

ABSTRACT

Amyotrophic lateral sclerosis (ALS) is a progressive fatal disorder, which results from the degeneration of motor neurons in the brain and spinal cord. Approximately 20% of the inherited autosomal dominant cases are due to mutations within the gene coding for Cu/Zn superoxide dismutase 1 (SOD1), a cytosolic homodimeric enzyme that catalyzes the dismutation of toxic superoxide anion. We investigated the presence of SOD1 gene mutations and activity alterations in two unrelated families of ALS patients from Elba, an island of central Italy. No mutation in SOD1 exon 1 to 5 and no activity alteration were observed in all members of the two analyzed ALS families (FALS). These data show an apparent heterogeneous distribution of ALS patients with SOD1 gene mutations among different populations and suggest that another genetic locus could be involved in the disease.


Subject(s)
Amyotrophic Lateral Sclerosis/genetics , Mutation/genetics , Superoxide Dismutase/genetics , DNA Mutational Analysis/statistics & numerical data , Exons/genetics , Female , Humans , Italy , Male , Middle Aged , Pedigree , Superoxide Dismutase-1
2.
Neurosci Lett ; 285(2): 83-6, 2000 May 12.
Article in English | MEDLINE | ID: mdl-10793232

ABSTRACT

We investigated the segregation of the copper chaperone for the superoxide dismutase (CCS) gene in two Italian families with amyotrophic lateral sclerosis lacking the mutations in superoxide dismutase 1 gene. We analyzed a total of 56 individuals; six people were affected. Diagnoses were made using the El Escorial criteria. The results of our study provide no evidence of a linkage between markers flanking the CCS gene and familial amyotrophic lateral sclerosis (FALS) in these FALS kindreds.


Subject(s)
Amyotrophic Lateral Sclerosis/genetics , Genetic Linkage/genetics , Molecular Chaperones/genetics , Superoxide Dismutase/genetics , Adult , Amyotrophic Lateral Sclerosis/enzymology , Female , Humans , Italy , Male , Middle Aged , Pedigree , Superoxide Dismutase-1
3.
Phytochemistry ; 29(1): 31-3, 1990.
Article in English | MEDLINE | ID: mdl-1367419

ABSTRACT

The use of a DNA alkylating agent, which induces poly(ADP-ribose) formation, has been employed to study the incorporation of [adenine 14C]NAD into pea root meristem nuclei, which is a prerequisite for poly(ADP-ribose) synthesis. The incorporation of [adenine 14C]NAD is significantly reduced when the poly(ADP-ribose)polymerase inhibitors, 7-methylxanthine and 3-methoxybenzamide are present and this incorporation is augmented when the DNA alkylating agent methyl methanesulfonate is added. Such information supports the hypothesis that poly(ADP-ribose) may be involved in the cell cycle regulation of pea root meristem nuclei.


Subject(s)
Benzamides/pharmacology , Cell Nucleus/metabolism , Fabaceae/metabolism , NAD/metabolism , Nucleoside Diphosphate Sugars/biosynthesis , Plants, Medicinal , Poly Adenosine Diphosphate Ribose/biosynthesis , Xanthines/pharmacology , Adenine/metabolism , Alkaloids/pharmacology , Carbon Radioisotopes , Cell Nucleus/drug effects , DNA Damage , Fabaceae/genetics , Fabaceae/ultrastructure , Methyl Methanesulfonate/pharmacology , Poly(ADP-ribose) Polymerase Inhibitors
SELECTION OF CITATIONS
SEARCH DETAIL
...