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Dive into the research topics where Gerassimos N. Pagoulatos is active.

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Featured researches published by Gerassimos N. Pagoulatos.


FEBS Letters | 1994

The hsc70 gene which is slightly induced by heat is the main virus inducible member of the hsp70 gene family

Ioannis Sainis; Charalambos Angelidis; Gerassimos N. Pagoulatos; Ioannis Lazaridis

We have found that SV40 infection of CV1 cells induces the synthesis of a 72 kDa protein that upon molecular cloning was shown to be the product of the hsc70 gene. The above gene product was found to be mainly virus inducible, in contrast to the hsp70 gene product which was mainly heat inducible. The two genes were found to be cell cycle regulated in a distinctively different manner.


American Journal of Medical Genetics | 1999

Fragile X premutations and (TA)n estrogen receptor polymorphism in women with ovarian dysfunction.

Maria Syrrou; Ioannis Georgiou; Philippos C. Patsalis; Ioanna Bouba; George Adonakis; Gerassimos N. Pagoulatos

We studied five groups of women with ovarian dysfunction for the CGG expansion in FMR1 and a (TA)n polymorphism in the estrogen receptor gene: a) poor responders to ovarian stimulation as part of in vitro fertilization (n = 13); b) women with familial premature ovarian failure (POF) (n = 7); c) sporadic cases with POF (n = 16); d) FRAXA premutation carriers with POF (n = 7); and e) FRAXA premutation carriers without POF (n = 9). FRAXA premutation was found in one woman with familial POF. A significant association of familial POF and FRAXA premutation carriers with POF having low copy of the (TA)n polymorphism as compared to controls was observed. Our preliminary data suggest a potential role of the estrogen receptor in POF, and it may influence the variable age of menopause of the FRAXA premutation carriers.


Genetic Epidemiology | 1998

FRAXA and FRAXE prevalence in patients with nonspecific mental retardation in the Hellenic population

Maria Syrrou; Ioannis Georgiou; Maria Grigoriadou; Michael B. Petersen; Sofia Kitsiou; Gerassimos N. Pagoulatos; Philippos C. Patsalis

Mutations at FRAXA and FRAXE loci are due to expansions of a CGG trinucleotide repeat and are characterized by mental retardation. Here we report a pilot screening survey by means of cytogenetic and molecular methods of 433 unrelated retarded individuals and their parents of Hellenic origin coming from various parts of Greece and Cyprus. The purpose of the study was to estimate the frequency of FRAXA mutation in individuals with nonspecific mental retardation without family history and phenotypic stigmata in the Hellenic population. Five FRAXA‐positive children (1.15%) were identified, of whom four were found to carry a full mutation and one a premutation. Furthermore we present preliminary data on a screening of FRAXE mutation frequency. We screened 257 male patients with nonspecific mental retardation, finding none positive for FRAXE mutation. Genet. Epidemiol. 15:103–109,1998.


FEBS Letters | 1988

Variable expression of SV40 large T antigen in CV1 cell clones

Demetrios P. Matthopoulos; Gerassimos N. Pagoulatos

Using immunofluorescence and immunoadsorption, CV1 cell clones MA2, V4, USA3, TR7 and P3 infected with SV40 were found to express variably SV40 large T antigen. The monoclonal antibody used was Pab 419. The results indicate that P3 cells express T antigen to a considerable level as early as 10 h post‐infection, while that of TR7 and USA3 cells is minute as judged from their positive nuclei. MA2 and V4 cells did not show any positive nuclei over this period of infection. At 20 h post‐infection MA2, V4 and USA3 cells developed a considerable amount of fluorescence in their nuclei while TR7 and P3 cells produced high values. By immunoadsorption of cell extracts for the same periods of infection, similar results were obtained on the electrophoretograms. We also relate these findings with those from induction of heat‐shock proteins by SV40 infection.


The Journal of Neuroscience | 2003

Heat Shock Protein 70 Chaperone Overexpression Ameliorates Phenotypes of the Spinal and Bulbar Muscular Atrophy Transgenic Mouse Model by Reducing Nuclear-Localized Mutant Androgen Receptor Protein

Hiroaki Adachi; Masahisa Katsuno; Makoto Minamiyama; Chen Sang; Gerassimos N. Pagoulatos; Charalampos Angelidis; Moriaki Kusakabe; Atsushi Yoshiki; Yasushi Kobayashi; Manabu Doyu; Gen Sobue


FEBS Journal | 1991

Constitutive expression of heat‐shock protein 70 in mammalian cells confers thermoresistance

Charalampos Angelidis; Ioannis Lazaridis; Gerassimos N. Pagoulatos


FEBS Journal | 1999

Aggregation of hsp70 and hsc70 in vivo is distinct and temperature‐dependent and their chaperone function is directly related to non‐aggregated forms

Charalampos Angelidis; Ioannis Lazaridis; Gerassimos N. Pagoulatos


American Journal of Medical Genetics | 1999

Molecular screening of fragile X (FRAXA) and FRAXE mental retardation syndromes in the Hellenic population of Greece and Cyprus: incidence, genetic variation, and stability.

Philippos C. Patsalis; Carolina Sismani; Joe A. Hettinger; I. Boumba; Ioannis Georgiou; G. Stylianidou; V. Anastasiadou; R. Koukoulli; Gerassimos N. Pagoulatos; Maria Syrrou


American Journal of Medical Genetics | 1996

Evidence for high-risk haplotypes and (CGG)n expansion in fragile X syndrome in the Hellenic population of Greece and Cyprus.

Maria Syrrou; Philippos C. Patsalis; Ioannis Georgiou; Michael I. Hadjimarcou; C. D. Constantinou-Deltas; Gerassimos N. Pagoulatos


FEBS Journal | 1988

Specific inhibition of simian virus 40 protein synthesis by heat and arsenite treatment

Charalampos Angelidis; Ioannis Lazaridis; Gerassimos N. Pagoulatos

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Philippos C. Patsalis

The Cyprus Institute of Neurology and Genetics

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