Results 161 to 170 of about 10,798 (215)

Non-canonical sex chromosome evolution revealed by extreme heterogeneity in homomorphic Y chromosome differentiation in the common frog

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Rana temporaria Linneaus 1758

2023
Common Frog Rana temporaria Linneaus 1758 Distribution (Figure 5). Included records from Artportalen (N=2000): a ubiquitous species for which all reported records have been included.Any rare confusion with Rana arvalis would not change the overall picture of distribution or abundance.
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Cerebellar afferents in the frogs, Rana esculenta and Rana temporaria

Cell and Tissue Research, 1984
Afferents to the cerebellum in frogs (Rana esculenta, Rana temporaria) were studied by use of retrograde transport of horseradish peroxidase. Following injections restricted to the molecular layer of the cerebellum cell labelling was found in the contralateral inferior olive and the ventral portion of the caudal medullary raphe.
B G, Grover, U, Grüsser-Cornehls
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Temperature and immobility reaction in Rana temporaria

Behavioural Processes, 1982
Experiments were conducted on two groups of Rana temporaria acclimatized to 7°C and to 14°C. Two hours prior to the experiments the animals were divided into six groups of 40 subjects each and placed in containers at temperatures of 5°, 10°, 15°, 20°, 25° and 30°C.
B, Dabrowska, S, Manikowski
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Toxicity of tetrachlorwinfos to Rana temporaria l.

Comparative Biochemistry and Physiology Part C: Comparative Pharmacology, 1993
1. Changes in the erythrocyte system of frogs poisoned with tetrachlorwinfos depend on the sex of the animals and the dose of pesticide applied. They are a result of the pathomorphological changes due to translocation of fluids from the tissues to the circulation and swelling of the blood cells. 2. Changes in the leucocyte system of frogs are caused by
K, Gromysz-Kałkowska, E, Szubartowska
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Rhodanese (thiosulfate:cyanide sulfurtransferase) from frog Rana temporaria

Journal of Chromatography B: Biomedical Sciences and Applications, 2000
The molecular mass of rhodanese from the mitochondrial fraction of frog Rana temporaria liver, equaling 8.7 kDa, was determined by high-performance size exclusion chromatography (HP-SEC). The considerable difference in molecular weight and the lack of common antigenic determinants between frog liver rhodanese and bovine rhodanese suggest the occurrence
M, Wróbel, J, Czubak
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Retinoscopic and neurophysiological refractometry in rana temporaria

Pfl�gers Archiv European Journal of Physiology, 1972
If frogs are measured by objective refractometry one finds a hyperopia of 6 D to 9 D. Therefore we investigated the neurophysiological state of refraction of the immobilized rana temporaria using the technique of extracellular recording. In the superficial neuropil the neural activity of 32 recorded neurons showed no dependence on the state of ...
E A, Moser, H, Krueger
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Albinism inRana temporaria

Journal of Genetics, 1949
White frog spawn gave rise to black-eyed white tadpoles, which later darkened, and developed into normal frogs. The latter produced normal tadpoles, some of which developed into albino adults. The facts can be explained if albinism is recessive, but the dominant allelomorphic gene found in normal frogs produces enough pigment in the eggs of ...
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The Common Frog Rana temporaria

1991
The oocytes, embryos, and larvae of Rana temporaria have long been traditional subjects of diverse experimental embryological studies. Experimental embryologists have often used the embryos of R. temporaria for studies concerning the mechanisms of development. In the first half of this century experiments were carried out on eggs collected from natural
N. V. Dabagyan, L. A. Sleptsova
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MHC zygosity in the frog, Rana temporaria

Immunogenetics, 1984
The major histocompatibility complex (MHC) zygosity of the field-collected frogs, Rana temporaria, was detected by progeny testing. Groups of sibling tadpoles were grafted with intrafamilial tail-tip allografts and the ratio of rapidly rejected allografts to slowly rejected ones was estimated.
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