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1.
Summary Somatic chromosome complements of the Indian burrowing toad,Uperodon globulosum, have been described for the first time. The 2n number is 26 (NF=52) in both the sexes. No heteromorphism in relation to sex chromosome pair has been recorded. Deviations from 2n number (2n=10–28) have been noticed in the cells of different specimens. The result has been compared withU. systoma.Acknowledgment. Sincere thanks are due to Prof. P. K. Ghosh, Hooghly Mohsin College and to Dr A. K. Roy of the same college for encouragement. Thanks are due to Mr Bipul Kumar Das for his help during collection of specimen.  相似文献   

2.
Summary In chromosome preparations from swine lymphocyte cultures, quadriradial figures and homolog associations were seen only of chromosome 10 and at a low frequency. The frequency of quadriradial figures was substantially increased by mitomycin C treatment, whereby 26.2% of the quadriradials were formed from the same chromosome pair with the number 10.  相似文献   

3.
Summary Karyotypic races of the common shrew which differed with respect to the combinations of chromosome arms in certain 2-armed autosomes were distinguished in Poland. Two eastern races with the arm combinationik, and one western race with the arm combinationhi in the third pair of autosomes were established. In the contact area of these chromosomal forms, the fourth karyotypic race with the arm combinationhk was found.I wish to express my gratitude to my wife, A.M. Wójcik, M. Sc., for her help in catching the animals and making chromosome preparations. I must also offer my thanks to Dr J. Zima for giving me access to his as yet unpublished data, and to Prof. Z. Pucek and Dr S. Fedyk for reading the first draft of this paper.  相似文献   

4.
GTG chromosomic banding of a male and a female Lophocebus albigena is reported. The chromosome number of the karyotypes is 2 n = 42, characterized by a pair of marked chromosomes and a mediocentric Y chromosome, similar to that of the Lophocebus aterimus.  相似文献   

5.
Summary The autosomal karyotypes of all subspecies studied ofCitellus citellus from Bulgaria do not differ. The X chromosome, by contrast, is different in 1 of the subspecies where it seems to have undergone a pericentric inversion.The authors wish to express their sincere thanks to Prof. Ts. Peshev (Sofia University, Department of Zoology) for providing and identifying the subspecies and also to D. Todorova for her skilful technical help.  相似文献   

6.
Exposure to 9.4 GHz pulsed microwaves at low power densities for 1 h/day during 2 weeks induces in adult male Balb/c mice disturbances in meiosis, consisting in an increase of translocations and the appearance of cells with several chromosome pair remaining univalents at MI.  相似文献   

7.
Summary Meiosis in a plant with 2n=12+2 pseudo-isochromosomes was studied. The pseudo-isochromosomes were compensating for the loss of the 3rd chromosome pair of the normal diploid complement.Acknowledgments. The authors are thankful to Dr J. Sybenga, for his helpful suggestions. The first 2 authors are thankful to the University Grants Commission, New Delhi, for financial assistance.  相似文献   

8.
Summary 2 new species of the anuran genusXenopus have been found in western Uganda:X. ruwenzoriensis sp.n. with the hexaploid chromosome number of 108 in the Semliki Valley, west of the Ruwenzori, andX. species nova with the tetraploid chromosome number of 72 in and near lake Bunyoni.This work has been made possible by a grant from the Georges and Antoine Claraz Foundation and the permission and help the Uganda Fisheries Department gave us to carry out the field work.  相似文献   

9.
Summary The C and G chromosome banding patterns and the AgAS positive sites (NOR regions) of cultured lung cells of the Eastern mole (Scalopus aquaticus) are presented. A distinctive secondary constriction is found on a pair of autosomes instead of on the X-chromosome as previously believed. The presence of a heterochromatic heteromorphism is noted and a large amount of constitutive heterochromatin is present in the karyotype.  相似文献   

10.
Down's syndrome (DS), the most frequent of congenital birth defects, results from the trisomy of chromosome 21 in all cells of affected patients. This disease is characterized by developmental anomalies, mental retardation and features of rapid aging, particularly in the brain, where the occurrence of Alzheimer's disease is observed in trisomy 21 patients over the age of 35. Copper-zinc superoxide dismutase (CuZnSOD) is one of the proteins encoded by chromosome 21 (21q22.1). As a consequence of gene dosage excess, CuZnSOD activity is increased by 50% in all DS tissues. This work reports the SOD activity of a population of DS patients with complete trisomy 21, partial trisomy 21, translocations and mosaicism, in order to confirm the gene dosage effect of SOD on the clinical features of DS, and to help to establish which is the critical region of chromosome 21 in DS. CuZnSOD was measured in red blood cells using the Minami and Yoshikawa method. In the population with complete trisomy 21, SOD activity was increased by 42%; in the population with partial trisomy 21, translocations and mosaicism, SOD activity was normal. In the population diagnosed as DS, but not karyotyped, SOD activity was increased by 28%. No differences between sexes or among ages were found. We conclude that the 21q22.1 segment is not the critical region responsible for DS, as we have found normal SOD activity in patients with the clinical features of DS.  相似文献   

11.
12.
Summary The enzymes which were extracted by autodigestion from the microsomal fractions of the pig kidney, liver and submaxillary gland and from the serum showed an immunochemical identity by a double immunodiffusion test. But the kidney enzyme had a different pI-value from the pI-values of the enzymes of other organs.This investigation was supported by a grant from the Ministry of Education, Japan to K. M. F. We would like to thank Dr Toshiharu Nagatsu (Department of Life Chemistry, Graduate School at Nagatsuta, Tokyo Institute of Technology, Yokohama, Japan) for helpful suggestions, Mr Moritoshi Sato (Matsumoto Meat Inspection Station, Matsumoto, Japan) for their generous supply of pig organs and Ajinomoto Co. Inc., Tokyo, Japan, for the gift of Gly-Pro-p-nitroanilide tosylate. Technical assistance of Miss K. Yanagisawa is gratefully acknowledged.  相似文献   

13.
Summary The 2 n=10 complement ofPasseromyia heterochaeta Villeneuve consists of 4 pairs of metacentric chromosomes and 1 pair of dots. The evolutionary implications of 2 n=10 in the tribe Phaoniini (Fam. Muscidae) are discussed.Acknowledgments. Thank are due to Dr Adrian C. Pont of British Museum (Natural Histoty), London for identifying our speciens through the courtesy of Dr Rokuro Kano, Dean Faculty of Medicine, Tokyo Medical and Dental University Tokyo, Japan. We also thank Dr U.S. Srivastava, Professor and Head, Dept. of Zoology, Univ. of Allahabad for providing the necessary laboratory faclities.  相似文献   

14.
Summary The C-banding and silver staining of the chromosomes of the knifefishApteronotus albifrons (2n=24), demonstrated the presence of constitutive heterochromatin in the centromeric region of every chromosome, except pair 4, where the entire long arm was darkly stained, the silver stain positive nucleolus organizer region (NOR) being embedded in it.The authors are grateful to Dr Sen Pathak (University of Texas System Cancer Center at Houston, Texas, USA) and Dr Yatiyo Yassuda (Universidade de São Paulo, São Paulo, Brasil) for their suggestions. This study was supported in part by grants of the Conselho Nacional de Desenvolvimento Cientifico e Tecnológico (CNPq).  相似文献   

15.
Summary A primitive representative of the Caudata endemic to Japan,Hynobius abei Sato (Caudata: Hynobiidae) has 2n=56 chromosomes, with 9 large, 4 medium and 15 small-sized homologous pairs. The morphology of the large-sized chromosomes is similar to that of the knownHynobius species, but the presence of a pair of acrocentrics in the medium-sized group and 5 pairs of biarmed chromosomes in the small-sized group characterized the karyotype ofH. abei.We thank A. Itoi, S. Segawa, K. Ban, T. Hikida and O. Murakami for their assistance in collecting specimens.  相似文献   

16.
Summary An in vitro dose effect curve of dicentric chromosome aberrations in human cord blood lymphocytes has been obtained for 250-kV X-rays. This is compared with a curve prepared in an identical manner using blood from adults. The comparison shows a marginally higher dicentric yield in blood of newborns at doses above about 250 rads.Acknowledgment. We wish to thank Miss P. Orledge of the John Radcliffe Hospital, Oxford, for samples of cord blood, Mr M.J. Corp of the MRC Radiobiology Unit, Harwell, for irradiating the samples and Mr A.A. Edwards of NRPB, for help with statistics. The work was partly supported by Euratom Contract No. 171-76-1 BIO UK.  相似文献   

17.
J M Wójcik 《Experientia》1986,42(8):960-962
Karyotypic races of the common shrew which differed with respect to the combinations of chromosome arms in certain 2-armed autosomes were distinguished in Poland. Two eastern races with the arm combination ik, and one western race with the arm combination hi in the third pair of autosomes were established. In the contact area of these chromosomal forms, the fourth karyotypic race with the arm combination hk was found.  相似文献   

18.
Summary Male Swiss Albino mice were injected i.p. with an As2O3 solution (0; 4; 8 and 12 mg As/kg) and sacrificed 12, 24, 36 and 48 h after injection. Neither chromatid nor chromosome aberrations were observed in bone marrow cells and spermatogonia.Acknowledgments. We thank Mr L. De Langhe for skillfull technical help. We acknowledge this work was supported by a grant of the Ministery of Public Health.  相似文献   

19.
Summary Exposure to 9.4 GHz pulsed microwaves at low power densities for 1 h/day during 2 weeks induces in adult male Balb/c mice disturbances in meiosis, consisting in an increase of translocations and the appearance of cells with several chromosome pair remaining univalents at MI.Acknowledgments. Grant No. 30121/120/53674 of the Centre International des Etudiants et Stagiaires to E. Manikowska and grant No. 78-1017/DRED of the Direction des Recherches et Etudes Techniques du Ministère de Défense to B. Servantie accorded by the French Government are gratefully acknowledged. The authors express their thanks to Miss M.R. Morazzani for her technical assistance.  相似文献   

20.
Summary The chromosomes of the fowl were studied with the aid ofMakino's andNishimura's water pretreatment squash technique, modified byMatthey, in embryonic spleen and gonads of both sexes. The number of chromosomes was found to be about 78; the numerical variations are to be ascribed to technical difficulties, caused by the extremely small size of the microchromosomes, rather than to an unchromosomelike behaviour of the latter, as was supposed byNewcomer andBrant. As to the exact number of chromosomes, we consider its determination beyond the possibilities of cytology. The 5th largest pair of the male, represented by a single element in the female, could be identified as the sex chromosome pair, in accordance with the findings ofYamashina. The digamety might be of theZ-O orZ-W type.  相似文献   

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