Travels through Sweden, Finland, and Lapland, to the North Cape, in the years 1798 and 1799 : by Joseph Acerbi. In two volumes. Illustrated with seventeen elegant engravings. Vol. I[-II].

Vol. I: Portrait of Joseph Acerbi. Painted by P. Violet, engr. by P. W. Tomkins.

Reizen door Zweeden en Finland, tot aan de uiterste grenzen van Lapland, in de jaaren 1798 en 1799 : door Joseph Acerbi. Uit het engelsch. ... Eerste deel[-vierde en laatste deel].

Digital reproduction, The National Library of Finland, Centre for Preservation and Digitisation, Mikkeli

Reizen door Zweeden en Finland, tot aan de uiterste grenzen van Lapland, in de jaaren 1798 en 1799 : door Joseph Acerbi. Uit het engelsch. ... Eerste deel[-vierde en laatste deel].

Digital reproduction, The National Library of Finland, Centre for Preservation and Digitisation, Mikkeli

Entretiens. 1, Livre I (2 éd.) / Épictète ; texte établi et trad. par Joseph Souilhé

[Entretiens (grec ancien-français). 1975]

Vägledare för allmänheten inom städerna Haparanda och Torneå samt Tornedalen m. fl. orter

kuv., 13 x 22 cm

Darwinin Lajien synty (1859) ensimmäistä kertaa suomeksi

Kirjallisuusarvostelu

Pseudobrânquia do guaru Poecilia reticulata (Peter, 1859): análise estrutural, morfométrica e histoquímica para detecção de glicoconjugados

A morfologia, os parâmetros citomorfométricos e os glicoconjugados presentes na pseudobrânquia de guaru, Poecilia reticulata Peter, 1859 (Cyprinodontiformes: Poeciliidae), foram investigados por microscopia de luz acoplada ao sistema de captura e análise de imagens, juntamente por histoquímica com lectinas. A anatomia microscópica indicou que P. reticulata possui pseudobrânquia glandular formada por dois lóbulos, a qual se localiza abaixo do epitélio faringiano. O órgão é constituído por parênquima vascularizado e rico em células pseudobranquiais. Esse tipo celular exibe estado citofisiológico ativo, com abundante sistema de biomembranas e ausência de óstio na superfície apical,que por sua vez é encontrado nas células ricas em mitocôndrias das holobrânquias. Assim, indica-se que as células da pseudobrânquia se distinguem das células das holobrânquias em relação à morfologia, histoquímica e fisiologia. Em decorrência dessas características intrínsecas, a pseudobrânquia de alevinos do guaru pode desempenhar funções não respiratórias nas fases iniciais do desenvolvimento. Além disso, a caracterização da pseudobrânquia do guaru possibilitará estudos futuros sobre o efeito de poluentes aquáticos em espécies biomonitoras, como P. reticulata.

Fionnula Hunt : a reflection

julkaisumaa: 372 IE IRL Irlanti

Brühler Schlosskonzerte : "Psiche" von Johann Joseph Fux

Lavataltiointi Brühler Schlosskonzerte -festivaaleilta 1978.

Molecular characteristics of Machado-Joseph disease mutation in 25 newly described Brazilian families

Machado-Joseph disease (MJD) is a form of autosomal dominant spinocerebellar ataxia first described in North-American patients originating from the Portuguese islands of the Azores. Clinically this disorder is characterized by late onset progressive ataxia with associated features, such as: ophthalmoplegia, pyramidal and extrapyramidal signs and distal muscular atrophies. The causative mutation is an expansion of a CAG repeat in the coding region of the MJD1 gene. We have identified 25 unrelated families segregating the MJD mutation during a large collaborative study of spinocerebellar ataxias in Brazil. In the present study a total of 62 family members were genotyped for the CAG repeat in the MJD1 gene, as well as 63 non-MJD individuals (126 normal chromosomes), used as normal controls. We observed a wide gap between the size range of the normal and expanded CAG repeats: the normal allele had from 12 to 33 CAGs (mean = 23 CAGs), whereas the expanded alleles ranged from 66 to 78 CAGs (mean = 71.5 CAGs). There were no differences in CAG tract length according to gender of affected individuals or transmitting parent. We observed a significant negative correlation between age at onset of the disease and length of the CAG tract in the expended allele (r = -0.6, P = 0.00006); however, the size of the expanded CAG repeat could explain only about 40% of the variability in age at onset (r2 = 0.4). There was instability of the expanded CAG tract during transmission from parent to offspring, both expansions and contractions were observed; however, there was an overall tendency for expansion, with a mean increase of +2.4 CAGs. The tendency for expansion appeared to the greater in paternal (mean increase of +3.5 CAGs) than in maternal transmissions (mean increase of +1.3 CAGs). Anticipation was observed in all transmissions in which ages at onset for parent and offspring were known; however, anticipation was not always associated with an increase in the expanded CAG repeat length. Our results indicate that the molecular diagnosis of MJD can be confirmed or excluded in all suspected individuals, since alleles of intermediary size were not observed.

Suomen suuriruhtinanmaan kartta vuonna 1859 /

1 kartta kahdessa osassa :, vär. ;, 48 x 39,6 cm, lehti 56,3 x 45,3 cm

Plan af Helsingfors år 1859

Kartan esitystekniikka: maastokartta

Karta öfver Helsingfors omgifningar upptagande delar af Helsinge, Sibbo, Esbo och Kyrkslätt m. fl. socknar

Mittakaava laskettu janamittakaavasta