PubMed Health⌕ Search

Biomedical subjects

S Mitsui

Publications and source records attributed to S Mitsui.

At least 19 recordsLinked to original sources
PubMed1995

Mitochondrial presequences can induce aggregation of unfolded proteins.

We have studied the interactions between various synthetic peptides and two model unfolded proteins, reduced alpha-lactalbumin and reduced and carboxymethylated alpha-lactalbumin. We found that mitochondrial presequences could induce aggregation of the unfolded alpha-lactalbumins but not of the native alpha-lactalbumin. The presequence-induced aggregation of unfolded alpha-lactalbumin was dependent on electrostatic interactions and on the amphiphilicity of the presequences. Since positive charge and amphiphilicity are necessary for the targeting function of mitochondrial presequences, presequence-induced aggregation may be responsible for the instability of mitochondrial precursor proteins and may need to be inhibited by binding factors in the cytosol.

Amino Acid Sequence↗
PubMed1983

[Relationship between verbal information processing and CNV pattern: effects of the numbers of letter and word upon CNV components].

The present experiment was designed to examine the effects of the numbers of letter and word upon CNV components, by using a modified Sternberg's paradigm. The results indicated that CNV amplitude decreased and CNV rising time increased as a function of the numbers of letter and word. CNV resolution time increased with the number of word, while no increase in resolution time was observed with the number of letter. These findings were discussed in relation to recent information processing models.

Adolescent↗
PubMed1978

[Anterior pituitary function in patients with cerebrovascular diseases with special reference to TSH secretion in response to TRH administration (author's transl)].

TSH secretion in response to TRH was studied in patients with cerebrovascular diseases in order to elucidate the influence of cerebrovascular lesions on the hypothalamus-anterior pituitary function. Blood specimens were obtained before and at intervals of 10, 20, 30, 40, 60, 90 and 120 minutes after the intravenous administration of 500 microgram of TRH. Serum TSH was measured using the RIA method. In 20 normal subjects, the serum TSH level before TRH administration was 1.0 +/- 1.4 microunits/ml (MEAN +/- SD). Following the intravenous administration of TRH, serum TSH increased and reached the maximum level of 9.0 +/- 2.3 microunits/mil at 30 minutes and returned near to the original level at 120 minutes. The response was the same for both male & female patients. In 17 patients with cerebral hemorrhage, the response of serum TSH to TRH was variable, including the types of excess, delayed or low response besides the normal response. In severe cases, cases of acute phase and male patients, a marked variability in the response was observed. In 8 patients with cerebral infarction, a low response of serum TSH to TRH was observed in all cases. There was no difference of the response with regard to severity of the diseases, duration after onset or sex difference of the patients.

Adolescent↗