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Journal articles on the topic 'Rana japonica'

Author: Grafiati

Published: 4 June 2025

Last updated: 15 July 2025

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1

Ogushi, Yuji, Azumi Tsuzuki, Megumi Sato, et al. "The water-absorption region of ventral skin of several semiterrestrial and aquatic anuran amphibians identified by aquaporins." American Journal of Physiology-Regulatory, Integrative and Comparative Physiology 299, no. 5 (2010): R1150—R1162. http://dx.doi.org/10.1152/ajpregu.00320.2010.

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Regions of specialization for water absorption across the skin of Bufonid and Ranid anurans were identified by immunohistochemistry and Western blot analysis, using antibodies raised against arginine vasotocin (AVT)-stimulated aquaporins (AQPs) that are specific to absorbing regions of Hyla japonica . In Bufo marinus , labeling for Hyla urinary bladder-type AQP (AQP-h2), which is also localized in the urinary bladder, occurred in the ventral surface of the hindlimb, pelvic, and pectoral regions. AQP-h2 was not detected in any skin regions of Rana catesbeiana , Rana japonica , or Rana nigromacu

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2

Sharbel, Timothy F., and David M. Green. "Allozyme relationships of some frogs (genus Rana) from Yunnan, China." Amphibia-Reptilia 10, no. 3 (1989): 267–75. http://dx.doi.org/10.1163/156853889x00421.

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AbstractThe genetic relationships of four species of frogs, genus Rana, from Yunnan, China, were investigated using starch gel electrophoresis of isozymes. Rana chaochiaoensis, R. pleuraden, R. phrynoides and R. limnocharis, representing four different species groups, were compared to each other and to representative species from other parts of Asia: R. amurensis from eastern Siberia, R. japonica from Japan, and R. nigromaculata from Korea. Twenty-four isozyme loci were reliably detected and scored, of which all but one were variable. R. chaochiaoensis, R. japonica and R. amurensis, all member

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3

Fujishiro, Naoji, and Hiroshi Kawata. "Twitch potentiation of frog (Rana japonica) skeletal muscle by antipyrine." Comparative Biochemistry and Physiology Part C: Comparative Pharmacology 92, no. 1 (1989): 61–65. http://dx.doi.org/10.1016/0742-8413(89)90203-x.

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4

Sumida, M., and M. Nishioka. "Genetic linkage groups in the Japanese brown frog (Rana japonica." Journal of Heredity 91, no. 1 (2000): 1–7. http://dx.doi.org/10.1093/jhered/91.1.1.

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5

Igawa, Takeshi, Teruhiko Takahara, Quintin Lau, and Shohei Komaki. "An application of PCR-RFLP species identification assay for environmental DNA detection." PeerJ 7 (October 3, 2019): e7597. http://dx.doi.org/10.7717/peerj.7597.

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Recent advancement of environmental DNA (eDNA) methods for surveying species in aquatic ecosystems has been used for various organisms and contributed to monitoring and conservation of species and environments. Amphibians are one of the promising taxa which could be monitored efficiently by applying quantitative PCR (qPCR) or next generation sequencing to eDNA. However, the cost of eDNA detection using these approaches can be quite high and requires instruments that are not usually installed in ecology laboratories. For aiding researchers in starting eDNA studies of amphibians, especially thos

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6

Wang, Yan-Mei, Chi-Ying Zhang, Si-Te Luo, Guo-Hua Ding, and Fen Qiao. "Characterization and Comparison of the Two Mitochondrial Genomes in the Genus Rana." Genes 14, no. 9 (2023): 1786. http://dx.doi.org/10.3390/genes14091786.

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The mitochondrial genome (mitogenome) possesses several invaluable attributes, including limited recombination, maternal inheritance, a fast evolutionary rate, compact size, and relatively conserved gene arrangement, all of which make it particularly useful for applications in phylogenetic reconstruction, population genetics, and evolutionary research. In this study, we aimed to determine the complete mitogenomes of two morphologically similar Rana species (Rana hanluica and Rana longicrus) using next-generation sequencing. The entire circular mitogenome was successfully identified, with a len

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7

Sumida, Masayuki. "Incipient Intraspecific Isolating Mechanisms in the Japanese Brown Frog Rana japonica." Journal of Herpetology 30, no. 3 (1996): 333. http://dx.doi.org/10.2307/1565170.

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8

Wan, Han, Zhi-Tong Lyu, Shuo Qi, Jian Zhao, Pi-Peng Li, and Ying-Yong Wang. "A new species of the Rana japonica group (Anura, Ranidae, Rana) from China, with a taxonomic proposal for the R. johnsi group." ZooKeys 942 (June 18, 2020): 141–58. http://dx.doi.org/10.3897/zookeys.942.46928.

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Rana jiulingensissp. nov., a new species from Hunan and Jiangxi, southeastern China, is described. The new species is assigned to the R. japonica group. The clade comprising R. jiulingensissp. nov. and R. dabieshanensis from Anhui is the sister taxon of R. omeimontis from Sichuan. Rana jiulingensissp. nov. can be distinguished by the significant divergences in the 16S and COI genes, and the combination of following morphological characters: body size medium, SVL 48.3–57.8 mm in adult males and 48.2–57.5 mm in adult females; dorsolateral fold straight; digits without circummarginal grooves; dor

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9

Wan, Han, Zhi-Tong Lyu, Shuo Qi, Jian Zhao, Pi-Peng Li, and Ying-Yong Wang. "A new species of the Rana japonica group (Anura, Ranidae, Rana) from China, with a taxonomic proposal for the R. johnsi group." ZooKeys 942 (June 18, 2020): 141–58. https://doi.org/10.3897/zookeys.942.46928.

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Rana jiulingensis sp. nov., a new species from Hunan and Jiangxi, southeastern China, is described. The new species is assigned to the R. japonica group. The clade comprising R. jiulingensis sp. nov. and R. dabieshanensis from Anhui is the sister taxon of R. omeimontis from Sichuan. Rana jiulingensis sp. nov. can be distinguished by the significant divergences in the 16S and COI genes, and the combination of following morphological characters: body size medium, SVL 48.3–57.8 mm in adult males and 48.2–57.5 mm in adult females; dorsolateral fold straight; digits without circummarginal grooves;

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10

IIZUKA, KOJI. "Constitutive Heterochromatin and Nucleolus Organizer Regions in Japanese Brown Frogs, Rana japonica and Rana ornativentris." Japanese journal of herpetology 13, no. 1 (1989): 15–20. http://dx.doi.org/10.5358/hsj1972.13.1_15.

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11

Nath, Aniket, and Kunal Roy. "Chemometric modeling of acute toxicity of diverse aromatic compounds against Rana japonica." Toxicology in Vitro 83 (September 2022): 105427. http://dx.doi.org/10.1016/j.tiv.2022.105427.

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12

Kamiya, Yuji, Fumitaka Oyama, Rieko Oyama, et al. "Amino Acid Sequence of a Lectin from Japanese Frog (Rana japonica) Eggs1." Journal of Biochemistry 108, no. 1 (1990): 139–43. http://dx.doi.org/10.1093/oxfordjournals.jbchem.a123153.

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13

Hirai, Toshiaki, and Masafumi Matsui. "Feeding Relationships between Hyla japonica and Rana nigromaculata in Rice Fields of Japan." Journal of Herpetology 36, no. 4 (2002): 662–67. http://dx.doi.org/10.1670/0022-1511(2002)036[0662:frbhja]2.0.co;2.

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14

OGATA, Mitsuaki, and Hiroshi SICHIRI. "Genetic Assessment of Reinforcement of the Japanese Brown Frog（Rana japonica）." Japanese Journal of Zoo and Wildlife Medicine 24, no. 1 (2019): 1–7. http://dx.doi.org/10.5686/jjzwm.24.1.

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15

Huang, Hong, Xiaodong Wang, Wenhua Ou, Jinsong Zhao, Yun Shao, and Liansheng Wang. "Acute toxicity of benzene derivatives to the tadpoles (Rana japonica) and QSAR analyses." Chemosphere 53, no. 8 (2003): 963–70. http://dx.doi.org/10.1016/s0045-6535(03)00715-x.

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16

Gagliardi, S. R., and T. W. Schultz. "Regression Comparisons of Aquatic Toxicity of Benzene Derivatives: Tetrahymena pyriformis and Rana japonica." Bulletin of Environmental Contamination and Toxicology 74, no. 2 (2005): 256–62. http://dx.doi.org/10.1007/s00128-004-0578-7.

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17

Suzuki, Kazuo T., Naoro Itoh, Kazuhiro Ohta, and Hiroyuki Sunaga. "Amphibian metallothionein. Induction in the frogs Rana japonica, R. nigromaculata and Rhacophorus schlegeii." Comparative Biochemistry and Physiology Part C: Comparative Pharmacology 83, no. 2 (1986): 253–59. http://dx.doi.org/10.1016/0742-8413(86)90119-2.

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18

TANIGUCHI, Kazumi, Yoshinori TOSHIMA, Toru R. SAITO, and Kazuyuki TANIGUCHI. "Development of the Bowman's and Jacobson's Glands in the Japanese Reddish Frog, Rana japonica." Journal of Veterinary Medical Science 58, no. 1 (1996): 17–22. http://dx.doi.org/10.1292/jvms.58.17.

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19

Shirane, Terukiyo. "A new, early, morphological indication of sex differentiation in anura,Rana japonica andR. nigromaculata." Journal of Experimental Zoology 240, no. 1 (1986): 113–18. http://dx.doi.org/10.1002/jez.1402400114.

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20

Sato, Iwao, Kiyoshi Konishi, Masataka Sunohara, and Akiko Mikami. "Enzyme activities and morphology of Japanese brown frog (Rana japonica) mitochondria in the tibialis anterior muscle during hibernation and active life." Canadian Journal of Zoology 79, no. 7 (2001): 1316–21. http://dx.doi.org/10.1139/z01-083.

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Enzyme activities in the respiratory chain, as well as the structure and numbers of mitochondria of the tibialis anterior muscle, during hibernation were compared with those of normally active muscle in the Japanese brown frog (Rana japonica). Morphological examination using an electron microscope showed that during hibernation, mitochondria were larger and longer and had clearly distinguishable outer and inner membranes with developed cristae. A significantly greater number of glycogen granules was found in the tibialis anterior muscle of hibernating frogs. The average cross-sectional area (C

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21

Iwai, Noriko, Takashi Kagaya, and Okochi Isamu. "CHOICE OF OVIPOSITION SITE BY RANA JAPONICA: ROLE OF THE DEVELOPMENTAL STAGE OF CONSPECIFIC EGGS." Herpetologica 63, no. 1 (2007): 31–34. http://dx.doi.org/10.1655/0018-0831(2007)63[31:coosbr]2.0.co;2.

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22

Osawa, Satoshi, and Takehiko Katsuno. "The grassland on levees is the habitat of Rana japonica in the terrace paddy field." JOURNAL OF RURAL PLANNING ASSOCIATION 26 (2007): 221–26. http://dx.doi.org/10.2750/arp.26.221.

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23

Takesue, Yoshiki, та Sachiko Takesue. "Purification and characterization of α-glucosidase complex from the intestine of the frog, Rana japonica". Biochimica et Biophysica Acta (BBA) - Protein Structure and Molecular Enzymology 1296, № 2 (1996): 152–58. http://dx.doi.org/10.1016/0167-4838(96)00063-5.

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24

Wang, X., Y. Dong, S. Xu, L. Wang, and S. Han. "Quantitative Structure-Activity Relationships for the Toxicity to the Tadpole Rana japonica of Selected Phenols." Bulletin of Environmental Contamination and Toxicology 64, no. 6 (2000): 859–65. http://dx.doi.org/10.1007/s001280000082.

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25

Wang, X., Y. Dong, S. Xu, L. Wang, and S. Han. "Quantitative Structure-Activity Relationships for the Toxicity to the Tadpole Rana japonica of Selected Phenols." Bulletin of Environmental Contamination and Toxicology 64, no. 6 (2000): 859–65. http://dx.doi.org/10.1007/s0012800082.

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26

TANIGUCHI, Kazumi, Yoshinori TOSHIMA, Toru R. SAITO, and Kazuyuki TANIGUCHI. "Development of the Olfactory Epithelium and Vomeronasal Organ in the Japanese Reddish Frog, Rana japonica." Journal of Veterinary Medical Science 58, no. 1 (1996): 7–15. http://dx.doi.org/10.1292/jvms.58.7.

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27

Gerda, B. A., E. A. Skverchinskaya, A. Yu Andreeva, A. A. Volkova, S. P. Gambaryan, and I. V. Mindukshev. "Comparative Analysis of the Osmotic Fragility of Erythrocytes Across Various Taxa of Vertebrates." Žurnal èvolûcionnoj biohimii i fiziologii 60, no. 5 (2024): 460–82. https://doi.org/10.31857/s0044452924050029.

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The osmotic fragility of erythrocytes serves as a crucial parameter indicating the cells' ability to endure variations in the osmotic environment. Disorders in this attribute are often correlated with a spectrum of pathologies, encompassing hemolytic anemias, malignant tumors, and cardiovascular dysfunctions. Notably, osmotic fragility exhibits variability across different animal species and closely intertwines with their respective ecosystems. A methodology for assessing osmotic fragility has been devised utilizing a laser particle analyzer, facilitating the real-time monitoring of cell conce

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28

OSAWA, SATOSHI, and TAKEHIKO KATSUNO. "Dispersal of Brown Frogs Rana japonica and R. ornativentris in the Forests of the Tama Hills." Current herpetology 20, no. 1 (2001): 1–10. http://dx.doi.org/10.5358/hsj.20.1.

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29

Sumida, Masayuki. "Mitochondrial DNA differentiation in the Japanese brown frog Rana japonica as revealed by restriction endonuclease analysis." Genes & Genetic Systems 72, no. 2 (1997): 79–90. http://dx.doi.org/10.1266/ggs.72.79.

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30

KOIZUMI, NORIYUKI, KEIJI WATABE, ATSUSHI MORI, and TAKESHI TAKEMURA. "Isolation and characterization of 19 polymorphic microsatellite DNA markers in the Japanese brown frog (Rana japonica)." Molecular Ecology Resources 9, no. 1 (2009): 248–50. http://dx.doi.org/10.1111/j.1755-0998.2008.02429.x.

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31

FUJINO, Masako, Sumiko FUJINO, and Masahiro FUJINO. "Effects of phenylglyoxal, dihydropyridine, and ouabain on the single cardiac muscle fibers of frog, Rana japonica." Folia Pharmacologica Japonica 106, supplement (1995): 82–86. http://dx.doi.org/10.1254/fpj.106.supplement_82.

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32

Isaacson, Todd, AnaMaria Soto, Shawichi Iwamuro, Floyd C. Knoop, and J. Michael Conlon. "Antimicrobial peptides with atypical structural features from the skin of the Japanese brown frog Rana japonica." Peptides 23, no. 3 (2002): 419–25. http://dx.doi.org/10.1016/s0196-9781(01)00634-9.

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33

NATUHARA, Yosihiro, and Megumi KANBARA. "Habitat Suitability and Network for the Japanese Brown Frog, Rana japonica Gunther in the Southern Osaka." Journal of the Japanese Institute of Landscape Architecture 64, no. 5 (2000): 617–20. http://dx.doi.org/10.5632/jila.64.617.

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34

Lau, Quintin, Takeshi Igawa, Tiffany A. Kosch, and Yoko Satta. "Selective constraint acting on TLR2 and TLR4 genes of Japanese Rana frogs." PeerJ 6 (May 25, 2018): e4842. http://dx.doi.org/10.7717/peerj.4842.

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Toll-like receptors (TLRs) are an important component of innate immunity, the first line of pathogen defence. One of the major roles of TLRs includes recognition of pathogen-associated molecular patterns. Amphibians are currently facing population declines and even extinction due to chytridiomycosis caused by the Batrachochytrium dendrobatidis (Bd) fungus. Evidence from other vertebrates shows that TLR2 and TLR4 are involved in innate immunity against various fungi. Such genes therefore may play a functional role in amphibian-chytridiomycosis dynamics. Frogs from East Asia appear to be toleran

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35

Sumida, Masayuki, and Mitsuaki Ogata. "Intraspecific Differentiation in the Japanese Brown Frog Rana japonica Inferred from Mitochondrial DNA Sequences of the CytochromebGene." Zoological Science 15, no. 6 (1998): 989–1000. http://dx.doi.org/10.2108/zsj.15.989.

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36

Ishii, Yoshiki, and Teizo Tsuchiya. "Prolonged Relaxation after Stimulation of the Clasping Muscle of Male Frog,Rana japonica, during the Breeding Season." Zoological Science 27, no. 7 (2010): 595–601. http://dx.doi.org/10.2108/zsj.27.595.

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37

KATANO, Junya, Satoshi OSAWA, and Takehiko KATSUNO. "Characteristics of habitat use by Japanese brown frog, Rana japonica at non-breeding season in Yato-space." JOURNAL OF RURAL PLANNING ASSOCIATION 20 (2001): 127–32. http://dx.doi.org/10.2750/arp.20.20-suppl_127.

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38

Roy, Kunal, and Gopinath Ghosh. "QSTR with extended topochemical atom (ETA) indices. VI. Acute toxicity of benzene derivatives to tadpoles (Rana japonica)." Journal of Molecular Modeling 12, no. 3 (2005): 306–16. http://dx.doi.org/10.1007/s00894-005-0033-7.

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39

Kotani, Tomoya, Noriyuki Yoshida, Koichi Mita, and Masakane Yamashita. "Requirement of cyclin B2, but not cyclin B1, for bipolar spindle formation in frog (Rana japonica) oocytes." Molecular Reproduction and Development 59, no. 2 (2001): 199–208. http://dx.doi.org/10.1002/mrd.1023.

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40

BRIGITTE, PLANADE, BAIN ODILE, LENA JEAN-PAUL, and JOLY PIERRE. "Gyrinicola chabadamsoni n. sp. and G. tba (Dinnik 1933) (Nematoda, Oxyuroidea) from tadpoles of the hybridogenetic complex Rana lessonae-esculenta (Amphibia, Ranoidea)." Zootaxa 1764, no. 1 (2008): 25. http://dx.doi.org/10.11646/zootaxa.1764.1.3.

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Two morphological types of the viviparous oxyurid nematode Gyrinicola were recovered from waterfrog tadpoles in France (Ain department, Rhône-Alpes region) and assigned to two species: G. tba (Dinnik 1930), redescribed, and G. chabadamsoni n. sp. Gyrinicola tba is close to G. batrachiensis (Walton 1929) and G. chabaudi Araujo and Artigas 1982 in that the female possesses a long tail and few cuticular buccal flaps. The new species, type host Rana kl. esculenta, is distinct by several characters: in females, by the 12 cuticular buccal flaps with internal crests, short caudal filament, short ovar

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41

MARUNOUCHI, JUNSUKE, TAMOTSU KUSANO, and HIROAKI UEDA. "Validity of Back-calculation Methods of Body Size from Phalangeal Bones. An Assesment Using Data for Rana japonica." Current herpetology 19, no. 2 (2000): 81–89. http://dx.doi.org/10.5358/hsj.19.81.

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42

YASUTOMI, MASUMI. "Migration of Epidermal Melanophores to the Dermis Through the Basement Membrane During Metamorphosis in the Frog, Rana japonica." Pigment Cell Research 1, no. 3 (1987): 181–87. http://dx.doi.org/10.1111/j.1600-0749.1987.tb00411.x.

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43

Wang, Xiaodong, Yuying Dong, Liansheng Wang, and Shuokui Han. "Acute toxicity of substituted phenols to Rana japonica tadpoles and mechanism-based quantitative structure–activity relationship (QSAR) study." Chemosphere 44, no. 3 (2001): 447–55. http://dx.doi.org/10.1016/s0045-6535(00)00198-3.

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44

Matsushima, Noe, and Masakado Kawata. "The choice of oviposition site and the effects of density and oviposition timing on survivorship in Rana japonica." Ecological Research 20, no. 1 (2004): 81–86. http://dx.doi.org/10.1007/s11284-004-0010-0.

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45

Watabe, Keiji, Yutaro Senga, Atsushi Mori, Noriyuki Koizumi, Takeshi Takemura, and Kazuya Nishida. "Population model of Rana japonica crossing agricultural concrete canals: evaluating population conservation by improving the migration routes of frogs." Paddy and Water Environment 10, no. 3 (2012): 223–29. http://dx.doi.org/10.1007/s10333-012-0313-7.

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46

Saitoh, Yasunori, Yuji Ogushi, Yuki Shibata, Reiko Okada, Shigeyasu Tanaka, and Masakazu Suzuki. "Novel Vasotocin-Regulated Aquaporins Expressed in the Ventral Skin of Semiaquatic Anuran Amphibians: Evolution of Cutaneous Water-Absorbing Mechanisms." Endocrinology 155, no. 6 (2014): 2166–77. http://dx.doi.org/10.1210/en.2013-1928.

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Until now, it was believed that only one form of arginine vasotocin (AVT)-regulated aquaporin (AQP) existed to control water absorption from the ventral skin of semiaquatic anuran amphibians, eg, AQP-rj3(a) in Rana japonica. In the present study, we have identified a novel form of ventral skin-type AQP, AQP-rj3b, in R. japonica by cDNA cloning. The oocyte swelling assay confirmed that AQP-rj3b can facilitate water permeability. Both AQP-rj3a and AQP-rj3b were expressed abundantly in the ventral hindlimb skin and weakly in the ventral pelvic skin. For the hindlimb skin, water permeability was i

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47

Marunouchi, Junsuke, Tamotsu Kusano, and Hiroaki Ueda. "Fluctuation in Abundance and Age Structure of a Breeding Population of the Japanese Brown Frog, Rana japonica Günther (Amphibia, Anura)." Zoological Science 19, no. 3 (2002): 343–50. http://dx.doi.org/10.2108/zsj.19.343.

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48

Kidera, Noriko, Taku Kadoya, Hiroya Yamano, et al. "Hydrological effects of paddy improvement and abandonment on amphibian populations; long-term trends of the Japanese brown frog, Rana japonica." Biological Conservation 219 (March 2018): 96–104. http://dx.doi.org/10.1016/j.biocon.2018.01.007.

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49

Ihara, Jin, Noriyuki Yoshida, Toyomi Tanaka, Koichi Mita, and Masakane Yamashita. "Either cyclin B1 or B2 is necessary and sufficient for inducing germinal vesicle breakdown during frog (Rana japonica) oocyte maturation." Molecular Reproduction and Development 50, no. 4 (1998): 499–509. http://dx.doi.org/10.1002/(sici)1098-2795(199808)50:4<499::aid-mrd14>3.0.co;2-y.

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50

Koyama, Takumi, and Shawichi Iwamuro. "Molecular Cloning of a cDNA Encoding Atypical Antimicrobial and Cytotoxic Brevinin-1Ja from the Skin of the Japanese Brown Frog, Rana japonica." Zoological Science 25, no. 5 (2008): 487–91. http://dx.doi.org/10.2108/zsj.25.487.

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