Analyze Diet

Cytogenetics and cell genetics.

Discontinued
Periodical
Genetics
Cytogenetics
Publisher:
Karger.. Basel : Karger
Frequency: Sixteen no. a year,
Country: Switzerland
Language: English
Start Year:1973 - 2001
ISSN:
0301-0171 (Print)
0301-0171 (Linking)
Impact Factor
1.7
NLM ID:0367735
(DNLM):C58880000(s)
(OCoLC):01787030
Coden:CGCGBR
LCCN:73644001
Classification:W1 CY755
Comparative FISH mapping of 32 loci reveals new homologous regions between donkey and horse karyotypes.
Cytogenetics and cell genetics    February 22, 2002   Volume 94, Issue 3-4 180-185 doi: 10.1159/000048812
Raudsepp T, Mariat D, Guérin G, Chowdhary BP.A total of 32 loci comprising specific genes, microsatellites and anonymous BAC clones from horse and cattle were mapped on donkey chromosomes. Of these, 13 markers were also mapped for the first time in the horse. This information, together with that previously available in donkey and horse updates the comparative status of the karyotypes of the two species. The findings of the present study for the first time show correlation between eleven equine acrocentric autosomes and the donkey chromosomes and in part enable detection of rearrangements between them. There are still 7-8 pairs of chromos...
Chromosome homologies between man and mountain zebra (Equus zebra hartmannae) and description of a new ancestral synteny involving sequences homologous to human chromosomes 4 and 8.
Cytogenetics and cell genetics    August 31, 2001   Volume 93, Issue 3-4 291-296 doi: 10.1159/000057000
Richard F, Messaoudi C, Lombard M, Dutrillaux B.Using human chromosome painting probes, we looked for homologies between human and mountain zebra (Equus zebra hartmannae, Equidae, Perissodactyla) karyotypes. Except for two very short segments, all euchromatic regions were found to have a human homologous chromosome segment. Conserved syntenies previously described in various mammalian orders were detected. Each synteny corresponded to a chromosomal region homologous to two parts of human chromosomes: HSA3 and HSA21, HSA7 and HSA16, HSA12 and HSA22, and HSA16 and HSA19. Chromosomal segments homologous to a part of HSA11 and HSA19p are found ...
Chromosomal distribution of the telomere sequence (TTAGGG)(n) in the Equidae.
Cytogenetics and cell genetics    July 28, 2001   Volume 93, Issue 1-2 127-130 doi: 10.1159/000056964
Lear TL.Telomeres are a class of repetitive DNA sequences that are located at chromosome termini and that act to stabilize the chromosome ends. The rapid karyotypic evolution of the genus Equus has given rise to ten taxa, all with different diploid chromosome numbers. Using fluorescence in situ hybridization (FISH) we localized the mammalian telomere sequence, (TTAGGG)(n), to the chromosomes of nine equid taxa. TTAGGG signal was located at chromosome termini in all species, however additional signal was seen at interstitial sites on some chromosomes in the Burchell's zebra, Equus quagga burchelli, the...
Isolation, characterization and FISH assignments of horse BAC clones containing type I and II markers.
Cytogenetics and cell genetics    April 18, 2001   Volume 92, Issue 1-2 144-148 doi: 10.1159/000056886
Mariat D, Oustry-Vaiman A, Cribiu EP, Raudsepp T, Chowdhary BP, Guérin G.In order to increase the number of markers on the horse cytogenetic map and expand the integration with the linkage map, an equine BAC library was screened for genes and for microsatellites. Eighty-nine intra-exon primers were designed from consensus gene sequences in documented species. After PCR screening, 38 clones containing identified genes were isolated and FISH mapped. These data allowed us to refine the available Zoo-FISH results, to define ten new conserved cytogenetic segments and expand two others, thus leading to the identification of a total of 26 conserved segments between horse ...
Assignment of the horse progesterone receptor (PGR) and estrogen receptor (ESR1) genes to horse chromosomes 7 and 31, respectively, by in situ hybridization.
Cytogenetics and cell genetics    October 9, 1998   Volume 82, Issue 1-2 110-111 doi: 10.1159/000015079
Lear TL, Adams MH, Sullivan ND, McDowell KJ, Bailey E.No abstract available
Susumu and Swiss horses.
Cytogenetics and cell genetics    July 25, 1998   Volume 80, Issue 1-4 20-22 doi: 10.1159/000014950
Klinger HP.No abstract available
Tandem 1;30 translocation: a new structural abnormality in the horse (Equus caballus).
Cytogenetics and cell genetics    January 1, 1996   Volume 72, Issue 2-3 162-163 doi: 10.1159/000134176
Long SE.A 1;30 tandem translocation was found in an 8-yr-old thoroughbred stallion referred because of reduced fertility. The diagnosis was confirmed by GTG and CBG staining. This is the first report of a tandem translocation in the horse.
Molecular cloning of an equine satellite-type DNA sequence and its chromosomal localization.
Cytogenetics and cell genetics    January 1, 1994   Volume 66, Issue 1 27-30 doi: 10.1159/000133657
Sakagami M, Hirota K, Awata T, Yasue H.We have molecularly cloned portions of equine satellite-type DNA and investigated the organization of the DNA sequence of the cloned segments. Sequence analysis and dot-blot analysis, using the cloned sequence (ES200) as a probe, indicate that the satellite-type DNA sequence consists mainly of 221-bp tandem repeats and represents 3.7-11% of the equine genome. Southern blot analysis further shows that (1) no sequences homologous to ES200 exist in the human, swine, and bovine genomes and that (2) the fragment pattern of the satellite-type DNA produced by ApaI cleavage shows a slight difference a...
Localization of the horse (Equus caballus) alpha-globin gene complex to chromosome 13 by fluorescence in situ hybridization.
Cytogenetics and cell genetics    January 1, 1993   Volume 62, Issue 2-3 136-138 doi: 10.1159/000133456
Oakenfull EA, Buckle VJ, Clegg JB.The alpha-globin gene complex in Equus caballus has been mapped by fluorescence in situ hybridization to the telomeric region of the long arm of chromosome 13. This is the first equine gene to be mapped to this chromosome.
Synaptonemal complex analysis of an autosomal trisomy in the horse.
Cytogenetics and cell genetics    January 1, 1992   Volume 61, Issue 3 202-207 doi: 10.1159/000133408
Power MM, Gustavsson I, Switoński M, Plöen L.Synaptonemal complex analysis by electron microscopy of a trisomy 28 in a male horse demonstrated a trivalent or a bivalent plus a univalent in primary spermatocytes. Two of the chromosomes making up the trivalent were, most often, completely paired with each other and only partially paired or associated with the third one. Half of the spermatocytes analysed demonstrated heterologous pairing or association between the free axis of the trivalent and the sex bivalent. The pairings remained, to a large extent, into diakinesis-metaphase I. In most pachytene cells one autosomal bivalent showed prox...
Identification of equine chromosomes in horse x mouse somatic cell hybrids.
Cytogenetics and cell genetics    January 1, 1992   Volume 61, Issue 1 58-60 doi: 10.1159/000133369
Lear TL, Trembicki KA, Ennis RB.Giemsa-11 (G-11) staining and in situ hybridization were used to identify the equine chromosome complement of horse x mouse somatic cell hybrids. The presence of horse chromosomes in somatic cell hybrids was determined by differential G-11 staining. The slides were then destained and hybridized with biotinylated total horse (Equus caballus) genomic DNA without suppression. Fluorescence detection permitted rapid confirmation of horse chromosomal DNA in the hybrid cells.
Conserved repetitive DNA sequences (Bkm) in normal equine males and sex-reversed females detected by in situ hybridization.
Cytogenetics and cell genetics    January 1, 1988   Volume 48, Issue 2 99-102 doi: 10.1159/000132599
Kent MG, Elliston KO, Shroeder W, Guise KS, Wachtel SS.In situ hybridization with a cloned banded krait sex-specific repetitive DNA probe (Bkm) indicates a high concentration of Bkm sequences on the horse Y chromosome in both normal XY males and XY sex-reversed females. Lesser, but still significant, concentrations of Bkm sequences were mapped to horse chromosomes 3, 4, and 30.
Equine half sibs with an unbalanced X;15 translocation or trisomy 28.
Cytogenetics and cell genetics    January 1, 1987   Volume 45, Issue 3-4 163-168 doi: 10.1159/000132448
Power MM.Two unrelated chromosome abnormalities were found in equine half sibs. The proposita, Case 1, which was short in stature and infertile, had a de novo unbalanced X;15 translocation involving loss of Xp. Replication studies indicated that the translocated X was preferentially late replicating and that this late replication spread variably into the autosomal segment. Case 2, a half brother of the proposita, was short in stature, had cryptorchidism, and was trisomic for chromosome 28. Cytogenetic analysis of the dam, the sire of Case 1, and two other phenotypically normal half sibs revealed normal...
XY sex-reversal syndrome in the domestic horse.
Cytogenetics and cell genetics    January 1, 1986   Volume 42, Issue 1-2 8-18 doi: 10.1159/000132243
Kent MG, Shoffner RN, Buoen L, Weber AF.The XY sex-reversal syndrome occurs when a phenotypic mare is born that has the karyotype of a stallion. The syndrome is manifested by both genotypic and phenotypic heterogeneity. The sex-reversed genetic condition occurs frequently within certain pedigrees where XY females have been found and can be readily detected by chromosome karyotyping. The phenotypic spectrum ranges from the feminine mare with a reproductive tract that is within normal limits to the greatly masculinized mare. Pedigree analysis suggests that there are two modes of inheritance: (1) an X-linked recessive or autosomal sex-...
Cytogenetic and DNA analyses of equine abortion.
Cytogenetics and cell genetics    January 1, 1982   Volume 34, Issue 3 204-214 doi: 10.1159/000131808
Haynes SE, Reisner AH.Although no major structural or numerical abnormalities were found in the karyotypes of 12 aborted equine fetuses, two unrelated abortuses each carried a large polymorphism for the amount of heterochromatin in chromosome 1. In both karyotypes this chromosome was shown to be larger than its homolog. To determine the nature of the extra DNA in these chromosomes, equine DNA was isolated and characterized by buoyant density analysis. Equine mainband DNA had a buoyant density in neutral CsCl of 1.699 g/cm3, while the highly repetitive (dG+dC)-rich fraction had a buoyant density of 1.715 g/cm3. A ra...
An examination of chromosomes in the stallion (Equus caballus) during meiosis.
Cytogenetics and cell genetics    January 1, 1980   Volume 26, Issue 1 7-13 doi: 10.1159/000131415
Scott IS, Long SE.Meiotic preparations were made from testicular material obtained after surgical castration of eight stallions (Equus caballus) with normal spermatogenesis. The material was examined after conventional Giemsa staining and C-banding. C-banding demonstrated that the Y chromosome at diakinesis associated with the short arm of the X chromosome. In 315 cells at diplotene or diakinesis, 56 (17.7%) had univalents and 51 (16.1%) of these involved the sex chromosomes. The overall mean chiasma number was 54.4 +/- 1.8 SD, and the mean calculated nondisjunction (ND) frequency was 3.4%. These results are di...
Chromosome banding studies of the Equidae.
Cytogenetics and cell genetics    January 1, 1978   Volume 20, Issue 1-6 332-350 
Ryder OA, Epel NC, Benirschke K.No abstract available
Meiosis in interspecific equine hybrids. II. The przewalski horse/domestic horse hybrid.
Cytogenetics and cell genetics    January 1, 1974   Volume 13, Issue 5 465-478 doi: 10.1159/000130300
Short RV, Chandley AC, Jones RC, Allen WR.No abstract available
Meiosis in interspecific equine hybrids. I. The male mule (Equus asinus X E. caballus) and hinny (E. caballus X E. asinus).
Cytogenetics and cell genetics    January 1, 1974   Volume 13, Issue 4 330-341 doi: 10.1159/000130284
Chandley AC, Jones RC, Dott HM, Allen WR, Short RV.No abstract available