听力与言语-语言病理学

行为科学

医学伦理学

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  • Strand-specific fluorescence in situ hybridization: the CO-FISH family.

    abstract::The ability to prepare single-stranded chromosomal target DNA allows innovative uses of FISH technology for studies of chromosome organization. Standard FISH methodologies require functionally single-stranded DNAs in order to facilitate hybridization between the probe and the complementary chromosomal target sequence....

    journal_title:Cytogenetic and genome research

    pub_type: 杂志文章,评审

    doi:10.1159/000079565

    authors: Bailey SM,Goodwin EH,Cornforth MN

    更新日期:2004-01-01 00:00:00

  • The relationship between male infertility and increased levels of sperm disomy.

    abstract::Sperm chromosome abnormalities cut across a number of areas relevant to ICC XV. The association between increased levels of sperm aneuploidy (usually disomy) and male infertility has implications for the sessions on reproduction, sex chromosomes, aneuploidy and meiosis and was, to the best of our knowledge, first repo...

    journal_title:Cytogenetic and genome research

    pub_type: 杂志文章,评审

    doi:10.1159/000079575

    authors: Tempest HG,Griffin DK

    更新日期:2004-01-01 00:00:00

  • Mismatch repair proteins: key regulators of genetic recombination.

    abstract::Mismatch repair (MMR) systems are central to maintaining genome stability in prokaryotes and eukaryotes. MMR proteins play a fundamental role in avoiding mutations, primarily by removing misincorporation errors that occur during DNA replication. MMR proteins also act during genetic recombination in steps that include ...

    journal_title:Cytogenetic and genome research

    pub_type: 杂志文章,评审

    doi:10.1159/000080593

    authors: Surtees JA,Argueso JL,Alani E

    更新日期:2004-01-01 00:00:00

  • The mammalian mid-pachytene checkpoint: meiotic arrest in spermatocytes with a mutation in Atm alone or in combination with a Trp53 (p53) or Cdkn1a (p21/cip1) mutation.

    abstract::ATM, the protein product of the gene mutated in the human autosomal recessive disorder ataxia telangiectasia, is involved in detection of double strand breaks (DSBs) and is a key component of the damage surveillance network of cell cycle proteins. In somatic cells ATM phosphorylates many other proteins including p53, ...

    journal_title:Cytogenetic and genome research

    pub_type: 杂志文章

    doi:10.1159/000080603

    authors: Ashley T,Westphal C,Plug-de Maggio A,de Rooij DG

    更新日期:2004-01-01 00:00:00

  • The most common chromosome aberration detected by high-resolution comparative genomic hybridization in vulvar intraepithelial neoplasia is not seen in vulvar squamous cell carcinoma.

    abstract::We analyzed genetic changes in condylomas (four cases), vulvar intraepithelial neoplasia I-III (VIN I-III, eleven cases), and primary vulvar squamous cell carcinomas (VSCC, ten cases) by high-resolution comparative genomic hybridization (HR-CGH) and flowcytometry. All samples were also human papilloma virus (HPV)-geno...

    journal_title:Cytogenetic and genome research

    pub_type: 杂志文章

    doi:10.1159/000078559

    authors: Bryndorf T,Kirchhoff M,Larsen J,Andreasson B,Bjerregaard B,Westh H,Rose H,Lundsteen C

    更新日期:2004-01-01 00:00:00

  • Karyotypic evolution in the Galliformes: an examination of the process of karyotypic evolution by comparison of the molecular cytogenetic findings with the molecular phylogeny.

    abstract::To define the process of karyotypic evolution in the Galliformes on a molecular basis, we conducted genome-wide comparative chromosome painting for eight species, i.e. silver pheasant (Lophura nycthemera), Lady Amherst's pheasant (Chrysolophus amherstiae), ring-necked pheasant (Phasianus colchicus), turkey (Meleagris ...

    journal_title:Cytogenetic and genome research

    pub_type: 杂志文章

    doi:10.1159/000078570

    authors: Shibusawa M,Nishibori M,Nishida-Umehara C,Tsudzuki M,Masabanda J,Griffin DK,Matsuda Y

    更新日期:2004-01-01 00:00:00

  • Interspecies comparison of neuroglobin, cytoglobin and myoglobin: sequence evolution and candidate regulatory elements.

    abstract::Neuroglobin and cytoglobin are two novel members of the vertebrate globin family. Their physiological role is poorly understood, although both proteins bind oxygen reversibly and may be involved in cellular oxygen homeostasis. Here we investigate the selective constraints on coding and non-coding sequences of the neur...

    journal_title:Cytogenetic and genome research

    pub_type: 杂志文章

    doi:10.1159/000078011

    authors: Wystub S,Ebner B,Fuchs C,Weich B,Burmester T,Hankeln T

    更新日期:2004-01-01 00:00:00

  • Ultrastructural analysis of chromatin in meiosis I + II of rye (Secale cereale L.).

    abstract::Scanning electron microscopy (SEM) proves to be an appropriate technique for imaging chromatin organization in meiosis I and II of rye (Secale cereale) down to a resolution of a few nanometers. It could be shown for the first time that organization of basic structural elements (coiled and parallel fibers, chromomeres)...

    journal_title:Cytogenetic and genome research

    pub_type: 杂志文章

    doi:10.1159/000078021

    authors: Zoller JF,Hohmann U,Herrmann RG,Wanner G

    更新日期:2004-01-01 00:00:00

  • New mouse genetic models for human contraceptive development.

    abstract::Genetic strategies for the post-genomic sequence age will be designed to provide information about gene function in a myriad of physiological processes. Here an ENU mutagenesis program (http://reprogenomics.jax.org) is described that is generating a large resource of mutant mouse models of infertility; male and female...

    journal_title:Cytogenetic and genome research

    pub_type: 杂志文章

    doi:10.1159/000078192

    authors: Lessard C,Pendola JK,Hartford SA,Schimenti JC,Handel MA,Eppig JJ

    更新日期:2004-01-01 00:00:00

  • DNA methylation profiles of CpG islands for cellular differentiation and development in mammals.

    abstract::DNA methylation has been implicated in mammalian development. Transcription units contain CpG islands, but expression of CpG island associated genes in normal tissues was not believed to be controlled by DNA methylation. There are, however, numerous CpG islands containing tissue-dependent and differentially methylated...

    journal_title:Cytogenetic and genome research

    pub_type: 杂志文章

    doi:10.1159/000078205

    authors: Shiota K

    更新日期:2004-01-01 00:00:00

  • Long dsRNA and silent genes strike back:RNAi in mouse oocytes and early embryos.

    abstract::RNA interference (RNAi) refers to the selective degradation of mRNA induced by double-stranded RNA (dsRNA), first discovered in Caenorhabditis elegans. Homology-dependent silencing phenomena related to RNAi have been observed in many species from all eukaryotic kingdoms. RNAi and related mechanisms share several conse...

    journal_title:Cytogenetic and genome research

    pub_type: 杂志文章,评审

    doi:10.1159/000078215

    authors: Svoboda P

    更新日期:2004-01-01 00:00:00

  • Distribution and stability of supernumerary microchromosomes in natural populations of the Amazon molly, Poecilia formosa.

    abstract::In animals, supernumerary chromosomes and their evolution have mostly been studied in sexual reproducing species. In the present study, for the first time, the natural distribution and stability of supernumerary microchromosomes were investigated in the unisexual fish species Poecilia formosa. Natural habitats through...

    journal_title:Cytogenetic and genome research

    pub_type: 杂志文章

    doi:10.1159/000079286

    authors: Lamatsch DK,Nanda I,Schlupp I,Epplen JT,Schmid M,Schartl M

    更新日期:2004-01-01 00:00:00

  • B chromosomes in Brazilian rodents.

    abstract::B chromosomes are now known in eight Brazilian rodent species: Akodon montensis, Holochilus brasiliensis, Nectomys rattus, N. squamipes, Oligoryzomys flavescens, Oryzomys angouya, Proechimys sp. 2 and Trinomys iheringi. Typically these chromosomes are heterogeneous relative to size, morphology, banding patterns, prese...

    journal_title:Cytogenetic and genome research

    pub_type: 杂志文章,评审

    doi:10.1159/000079296

    authors: Silva MJ,Yonenaga-Yassuda Y

    更新日期:2004-01-01 00:00:00

  • Different numbers of rye B chromosomes induce identical compaction changes in distinct A chromosome domains.

    abstract::In rye each B chromosome (B) represents 5.5% of the diploid A genome. Rye Bs have several nuclear to whole plant effects although they seem to bear no genes except for the ones that lead to their maintenance within a population. In this context, and considering that rye Bs are enriched in repetitive non-coding regions...

    journal_title:Cytogenetic and genome research

    pub_type: 杂志文章

    doi:10.1159/000079306

    authors: Delgado M,Caperta A,Ribeiro T,Viegas W,Jones RN,Morais-Cecílio L

    更新日期:2004-01-01 00:00:00

  • The parasitic effects of rye B chromosomes might be beneficial in the long term.

    abstract::Rye B chromosomes (Bs) have strong parasitic effects on fertility. B carrying plants are less fertile than 0B ones, whereas the Bs have no significant effects on plant vigour. On the other hand, it has been reported that B transmission is under genetic control in such a way that H line plants transmit the Bs at high f...

    journal_title:Cytogenetic and genome research

    pub_type: 杂志文章

    doi:10.1159/000079316

    authors: González-Sánchez M,Chiavarino M,Jiménez G,Manzanero S,Rosato M,Puertas MJ

    更新日期:2004-01-01 00:00:00

  • LIM-kinase as a regulator of actin dynamics in spermatogenesis.

    abstract::We have identified LIM-kinase (LIMK1 and LIMK2), the only known catalytic protein among LIM-family molecules. Both LIMK1 and LIMK2 phosphorylate (inactivate) cofilin, an actin depolymerizing factor, and induce actin cytoskeleton reorganization. We as well as others concurrently demonstrated that LIMK activation was re...

    journal_title:Cytogenetic and genome research

    pub_type: 杂志文章,评审

    doi:10.1159/000076815

    authors: Takahashi H,Funakoshi H,Nakamura T

    更新日期:2003-01-01 00:00:00

  • Expression of peroxisomal proteins provides clear evidence for the presence of peroxisomes in the male germ cell line GC1spg.

    abstract::Peroxisomes are cell organelles that perform multiple functions in the metabolism of lipids and of reactive oxygen species. They are present in most eukaryotic cells. However, they are believed to be absent in spermatozoa and they have never been described in male germ cells. We have used the immortalized germ cell li...

    journal_title:Cytogenetic and genome research

    pub_type: 杂志文章

    doi:10.1159/000076825

    authors: Lüers GH,Schad A,Fahimi HD,Völkl A,Seitz J

    更新日期:2003-01-01 00:00:00

  • How common are common fragile sites in humans: interindividual variation in the distribution of aphidicolin-induced fragile sites.

    abstract::To obtain an estimate of the variation in common fragile sites (CFSs) among individuals, aphidicolin (APC)-induced chromosomal breakage data were analyzed for 20 karyotypically normal adult humans. As it is specifically designed to meet the analytical requirements for considering fragile sites as presence/absence char...

    journal_title:Cytogenetic and genome research

    pub_type: 杂志文章

    doi:10.1159/000073411

    authors: Denison SR,Simper RK,Greenbaum IF

    更新日期:2003-01-01 00:00:00

  • Chromosome banding in Amphibia. XXIX. The primitive XY/XX sex chromosomes of Hyla femoralis (Anura, Hylidae).

    abstract::The karyotype of the pine woods treefrog, Hyla femoralis, is characterized by primitive XY female/XX male sex chromosomes. The sole difference between the X and the Y is the presence of a nucleolus organizer region (NOR) in the X. Due to a deletion of the NOR in the Y, this chromosome is distinctly smaller than the X....

    journal_title:Cytogenetic and genome research

    pub_type: 杂志文章

    doi:10.1159/000073421

    authors: Schmid M,Steinlein C

    更新日期:2003-01-01 00:00:00

  • A 3.4-kbp transcript of ZNF331 is solely expressed in follicular thyroid adenomas.

    abstract::Translocations involving chromosomal region 19q13 are a frequent finding in follicular adenomas of the thyroid and might represent the most frequent type of structural aberration in human epithelial tumors. By positional cloning, a putative candidate gene, ZNF331 (formerly RITA) located close to the breakpoint was ide...

    journal_title:Cytogenetic and genome research

    pub_type: 杂志文章

    doi:10.1159/000074165

    authors: Meiboom M,Murua Escobar H,Pentimalli F,Fusco A,Belge G,Bullerdiek J

    更新日期:2003-01-01 00:00:00

  • The temporal and spatial pattern of histone H3 phosphorylation at serine 28 and serine 10 is similar in plants but differs between mono- and polycentric chromosomes.

    abstract::Immunolabeling using site-specific antibodies against phosphorylated histone H3 at serine 10 or serine 28 revealed in plants an almost similar temporal and spatial pattern of both post-translational modification sites at mitosis and meiosis. During the first meiotic division the entire chromosomes are highly H3 phosph...

    journal_title:Cytogenetic and genome research

    pub_type: 杂志文章

    doi:10.1159/000074175

    authors: Gernand D,Demidov D,Houben A

    更新日期:2003-01-01 00:00:00

  • Characterization of the first supernumerary tricentric ring chromosome 1 mosaicism by conventional and molecular cytogenetic techniques.

    abstract::We report on the conventional cytogenetic and fluorescence in situ hybridization (FISH) results obtained for a 3.5-year-old girl with developmental and language delay and a supernumerary ring chromosome mosaicism in 8% of T-lymphocytes analyzed. Using different conventional and molecular cytogenetic techniques as YAC ...

    journal_title:Cytogenetic and genome research

    pub_type: 杂志文章

    doi:10.1159/000076285

    authors: Tönnies H,Hennies HC,Spohr HL,Neitzel H

    更新日期:2003-01-01 00:00:00

  • A high-resolution comparative RH map of the telomeric end of bovine chromosome 2 with human chromosomes 1 and 2.

    abstract::High density livestock to human comparative maps are necessary for the implementation of comparative positional candidate gene cloning. We have constructed a high-density comparative radiation hybrid (RH) map of the telomeric end of bovine chromosome 2 (BTA2) using a 12,000-rad whole genome cattle-hamster radiation hy...

    journal_title:Cytogenetic and genome research

    pub_type: 杂志文章

    doi:10.1159/000076295

    authors: Liu Z,Womack JE,Antoniou E

    更新日期:2003-01-01 00:00:00

  • Comparative cytogenetic analysis on four tree frog species (Anura, Hylidae, Hylinae) from Brazil.

    abstract::A comparative cytogenetic analysis was carried out on four Hylinae tree frogs from Brazil ((Aparasphenodon brunoi, Corythomantis greeningi, Osteocephalus langsdorffii, and Scinax fuscovarius) using Giemsa staining, BrdU replication banding, Ag-NOR staining, C-banding, DAPI and CMA(3) fluorochrome staining, and fluores...

    journal_title:Cytogenetic and genome research

    pub_type: 杂志文章

    doi:10.1159/000076304

    authors: Kasahara S,Zampieri Silva AP,Gruber SL,Haddad CF

    更新日期:2003-01-01 00:00:00

  • Development of a linkage map and QTL scan for growth traits in North American bison.

    abstract::PCR protocols incorporating fluorescently labeled multiplexed primer combinations were developed to produce a linkage map for bison. Three hundred fifty eight microsatellite loci spanning all 29 autosomes were genotyped via 83 PCR multiplexes and nine individual amplifications. A total of 292 markers were integrated i...

    journal_title:Cytogenetic and genome research

    pub_type: 杂志文章

    doi:10.1159/000075726

    authors: Schnabel RD,Taylor JF,Derr JN

    更新日期:2003-01-01 00:00:00

  • Improving the comparative map of porcine chromosome 10 with respect to human chromosomes 1, 9 and 10.

    abstract::ZOO-FISH mapping shows human chromosomes 1, 9 and 10 share regions of homology with pig chromosome 10 (SSC10). A more refined comparative map of SSC10 has been developed to help identify positional candidate genes for QTL on SSC10 from human genome sequence. Genes from relevant chromosomal regions of the public human ...

    journal_title:Cytogenetic and genome research

    pub_type: 杂志文章

    doi:10.1159/000075736

    authors: Aldenhoven J,Chen Y,Backofen B,Moran C

    更新日期:2003-01-01 00:00:00

  • Equine genomics: galloping to new frontiers.

    abstract::Analysis of the horse genome is proceeding at a rapid pace. Within a short span of 6-7 years, approximately 1,500 markers have been mapped in horse, of which at least half are genes/ESTs. Health, performance and phenotypic characteristic are of major concern/interest to horse breeders and owners. Current efforts to an...

    journal_title:Cytogenetic and genome research

    pub_type: 杂志文章,评审

    doi:10.1159/000075746

    authors: Chowdhary BP,Bailey E

    更新日期:2003-01-01 00:00:00

  • Digging up the canine genome--a tale to wag about.

    abstract::There is incredible morphological and behavioral diversity among the hundreds of breeds of the domestic dog, CANIS FAMILIARIS. Many of these breeds have come into existence within the last few hundred years. While there are obvious phenotypic differences among breeds, there is marked interbreed genetic homogeneity. Th...

    journal_title:Cytogenetic and genome research

    pub_type: 杂志文章,评审

    doi:10.1159/000075756

    authors: Greer KA,Cargill EJ,Cox ML,Clark LA,Tsai KL,Credille KM,Dunstan RW,Venta PJ,Murphy KE

    更新日期:2003-01-01 00:00:00

  • Integration of chicken genomic resources to enable whole-genome sequencing.

    abstract::Different genomic resources in chicken were integrated through the Wageningen chicken BAC library. First, a BAC anchor map was created by screening this library with two sets of markers: microsatellite markers from the consensus linkage map and markers created from BAC end sequencing in chromosome walking experiments....

    journal_title:Cytogenetic and genome research

    pub_type: 杂志文章

    doi:10.1159/000075766

    authors: Aerts J,Crooijmans R,Cornelissen S,Hemmatian K,Veenendaal T,Jaadar A,van der Poel J,Fillon V,Vignal A,Groenen M

    更新日期:2003-01-01 00:00:00

  • WWOX, the common chromosomal fragile site, FRA16D, cancer gene.

    abstract::Gross chromosomal rearrangements and aneuploidy are among the most common somatic genomic abnormalities that occur during cancer initiation and progression, in particular in human solid tumor carcinogenesis. The loss of large chromosomal regions as consequence of gross rearrangements (e.g. deletions, monosomies, unbal...

    journal_title:Cytogenetic and genome research

    pub_type: 杂志文章

    doi:10.1159/000072844

    authors: Ludes-Meyers JH,Bednarek AK,Popescu NC,Bedford M,Aldaz CM

    更新日期:2003-01-01 00:00:00

  • Molecular characterization of three gonad cell lines.

    abstract::To facilitate the study of the regulation and downstream interactions of genes involved in gonad development it is important to have a suitable cell culture model. We therefore aimed to characterize molecularly three different mouse gonad cell lines. TM3 and TM4 cells were originally isolated from prepubertal mouse go...

    journal_title:Cytogenetic and genome research

    pub_type: 杂志文章

    doi:10.1159/000074344

    authors: Beverdam A,Wilhelm D,Koopman P

    更新日期:2003-01-01 00:00:00

  • Why is SCA12 different from other SCAs?

    abstract::Spinocerebellar ataxia type 12 (SCA12), now described in European-American and Asian (Indian) pedigrees, is unique among the SCAs from clinical, pathological, and molecular perspectives. Clinically, the distinguishing feature is early and prominent action tremor with variability in other signs. Pathologically, brain M...

    journal_title:Cytogenetic and genome research

    pub_type: 杂志文章,评审

    doi:10.1159/000072854

    authors: Holmes SE,O'Hearn E,Margolis RL

    更新日期:2003-01-01 00:00:00

  • Mechanisms of neuronal cell death in Huntington's disease.

    abstract::Huntington's disease (HD) is a genetically dominant neurodegenerative condition caused by an unique mutation in the disease gene huntingtin. Although the Huntington protein (Htt) is ubiquitously expressed, expansion of the polyglutamine tract in Htt leads to the progressive loss of specific neuronal subpopulations in ...

    journal_title:Cytogenetic and genome research

    pub_type: 杂志文章,评审

    doi:10.1159/000072864

    authors: Sawa A,Tomoda T,Bae BI

    更新日期:2003-01-01 00:00:00

  • Differential Dmrt1 transcripts in gonads of the protandrous black porgy, Acanthopagrus schlegeli.

    abstract::Black porgy, Acanthopagrus schlegeli Bleeker, is a marine protandrous hermaphrodite fish. A Dmrt1 cDNA was cloned and characterized and in order to study the process of sex change in this species, mRNA transcripts of Dmrt1 were monitored. Dmrt1 was specifically transcribed in testis and seminal vesicle in 2-year-old b...

    journal_title:Cytogenetic and genome research

    pub_type: 杂志文章

    doi:10.1159/000074354

    authors: He CL,Du JL,Wu GC,Lee YH,Sun LT,Chang CF

    更新日期:2003-01-01 00:00:00

  • Complete cDNA sequence, expression, alternative splicing, and genomic organization of the mouse Nfat5 gene.

    abstract::Members of the NFAT (nuclear factors of activated T cells) gene family have been investigated in numerous organisms, including man and mouse. All NFATs may be synthesized in several isoforms differing in amino or carboxy termini due to 5' and 3' alternative splicing of the corresponding mRNA. Recently, we mapped the m...

    journal_title:Cytogenetic and genome research

    pub_type: 杂志文章

    doi:10.1159/000066604

    authors: Dalski A,Hebinck A,Winking H,Butzmann U,Schwinger E,Zühlke Ch

    更新日期:2002-01-01 00:00:00

  • Identification and characterization of murine Brunol4, a new member of the elav/bruno family.

    abstract::RNA-binding proteins are involved in post-transcriptional processes like mRNA stabilization, post-transcriptional modification, and transport and have been suggested to play an important role in developmental gene regulation. We report here the cloning and characterization of Brunol4, a novel mouse cDNA closely relate...

    journal_title:Cytogenetic and genome research

    pub_type: 杂志文章

    doi:10.1159/000066619

    authors: Meins M,Schlickum S,Wilhelm C,Missbach J,Yadav S,Gläser B,Grzmil M,Burfeind P,Laccone F

    更新日期:2002-01-01 00:00:00

  • The genomic structure, chromosomal localization, and analysis of SIL as a candidate gene for holoprosencephaly.

    abstract::Holoprosencephaly (HPE) is the most common congenital malformation of the brain and face in humans. In this study we report the analysis of SIL (Sumacr;CL iumacr;nterrupting lumacr;ocus) as a candidate gene for HPE. Fluorescent in situ hybridization (FISH) analysis using a BAC 246e16 confirmed the assignment of SIL to...

    journal_title:Cytogenetic and genome research

    pub_type: 杂志文章

    doi:10.1159/000064057

    authors: Karkera JD,Izraeli S,Roessler E,Dutra A,Kirsch I,Muenke M

    更新日期:2002-01-01 00:00:00

  • Cloning, expression, and chromosomal localization of the mouse gene (Scgb3a1, alias Ugrp2) that encodes a member of the novel uteroglobin-related protein gene family.

    abstract::The mouse UGRP gene family consists of two genes, Ugrp1 and Ugrp2. In this study, the genomic structure and expression patterns of Ugrp2 and its alternative spliced form were characterized. The authentic Ugrp2 gene has three exons and two introns, similar to the Ugrp1 gene, which produces a secreted protein. The Ugrp2...

    journal_title:Cytogenetic and genome research

    pub_type: 杂志文章

    doi:10.1159/000064067

    authors: Niimi T,Copeland NG,Gilbert DJ,Jenkins NA,Srisodsai A,Zimonjic DB,Keck-Waggoner CL,Popescu NC,Kimura S

    更新日期:2002-01-01 00:00:00

  • Evolutionary aspects of the genomic organization of rat chromosome 10.

    abstract::Using FISH and RH mapping a chromosomal map of rat chromosome 10 (RNO10) was constructed. Our mapping data were complemented by other published data and the final map was compared to maps of mouse and human chromosomes. RNO10 contained segments homologous to mouse chromosomes (MMU) 11, 16 and 17, with evolutionary bre...

    journal_title:Cytogenetic and genome research

    pub_type: 杂志文章

    doi:10.1159/000063052

    authors: Behboudi A,Sjöstrand E,Gómez-Fabre P,Sjöling A,Taib Z,Klinga-Levan K,Ståhl F,Levan G

    更新日期:2002-01-01 00:00:00

  • Comparative molecular cytogenetic studies in the order Carnivora: mapping chromosomal rearrangements onto the phylogenetic tree.

    abstract::We have made a set of chromosome-specific painting probes for the American mink by degenerate oligonucleotide primed-PCR (DOP-PCR) amplification of flow-sorted chromosomes. The painting probes were used to delimit homologous chromosomal segments among human, red fox, dog, cat and eight species of the family Mustelidae...

    journal_title:Cytogenetic and genome research

    pub_type: 杂志文章

    doi:10.1159/000063032

    authors: Graphodatsky AS,Yang F,Perelman PL,O'Brien PC,Serdukova NA,Milne BS,Biltueva LS,Fu B,Vorobieva NV,Kawada SI,Robinson TJ,Ferguson-Smith MA

    更新日期:2002-01-01 00:00:00

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