About: THE SITES OF NUCLEOLUS FORMATION IN HUMAN PACHYTENE CHROMOSOMES

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scientific article published on 01 January 1964

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) artigo científico (publicado na 1964) (pt) article scientifique publié en 1964 (fr) наукова стаття, опублікована в січні 1964 (uk) im Jahr 1964 veröffentlichter wissenschaftlicher Artikel (de) artikull shkencor i botuar më 01 janar 1964 (sq) scientific article published on 01 January 1964 (en) artículu científicu espublizáu en xineru de 1964 (ast)
publication date	wds:Q76908001-8C9EAEF5-F6CE-4CD9-A329-9D104866B654
publication date	1964-01-01 00:00:00Z (xsd:dateTime)
rdfs:label	THE SITES OF NUCLEOLUS FORMATION IN HUMAN PACHYTENE CHROMOSOMES (en) THE SITES OF NUCLEOLUS FORMATION IN HUMAN PACHYTENE CHROMOSOMES (nl) THE SITES OF NUCLEOLUS FORMATION IN HUMAN PACHYTENE CHROMOSOMES (sq)
skos:prefLabel	THE SITES OF NUCLEOLUS FORMATION IN HUMAN PACHYTENE CHROMOSOMES (en) THE SITES OF NUCLEOLUS FORMATION IN HUMAN PACHYTENE CHROMOSOMES (nl) THE SITES OF NUCLEOLUS FORMATION IN HUMAN PACHYTENE CHROMOSOMES (sq)
name	THE SITES OF NUCLEOLUS FORMATION IN HUMAN PACHYTENE CHROMOSOMES (en) THE SITES OF NUCLEOLUS FORMATION IN HUMAN PACHYTENE CHROMOSOMES (nl) THE SITES OF NUCLEOLUS FORMATION IN HUMAN PACHYTENE CHROMOSOMES (sq)
author	wds:Q76908001-D138CC02-22EB-4B06-849C-D74AF55E57C8
author	Malcolm Ferguson-Smith
title	wds:Q76908001-C671254A-7429-4C53-A04F-7A37FA7BEDDC
title	THE SITES OF NUCLEOLUS FORMATION IN HUMAN PACHYTENE CHROMOSOMES (en)
page(s)	wds:Q76908001-C3298B90-1E92-4A7C-A143-77B86088BCDE
page(s)	124-134
instance of	wds:Q76908001-C188A3E0-B663-4385-9059-2F4FCD787761
instance of	scholarly article
PubMed ID	wds:Q76908001-EF535402-00F6-4941-B828-22C4124E6182
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/14190611
PubMed ID	14190611
published in	wds:Q76908001-210EFEDC-4F21-4356-9AE2-E57E11EFA9E0
published in	Cytogenetics
volume	wds:Q76908001-919B7A4D-7750-42CB-8152-1FD76E95B310
volume	3
DOI	wds:Q76908001-87582371-65C0-451A-94DF-CBAF79F6981C
DOI	http://dx.doi.org/10.1159/000129803
DOI	10.1159/000129803
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q76908001
is cites work of	Ribosomal DNA Connectives between Human Acrocentric Chromosomes Differential Staining of Nucleolus Organisers in Mammalian Chromosomes Relationships between satellite association and the occurence of non-disjunction in man Pachytene analysis in a human reciprocal (10;11) translocation The behavior of the XY pair in mammals. Spontaneous fragility of an abnormally wide secondary constriction region in a human chromosome no. 9. The association of the nucleolus and the short arm of acrocentric chromosomes with the XY pair in human spermatocytes: its possible role in facilitating sex-chromosome acrocentric translocations Nucleolus organizer regions and nucleoli Differences in the satellite association pattern in the human population Nucleolar organizer region variants as a risk factor for Down syndrome Atypical acrocentric chromosomes in Negro and Caucasian Mongols The three-dimensional reconstruction of the XY chromosomal pair in human spermatocytes Satellite DNA loss and nucleolar organiser activity in an individual with a de novo chromosome 13,14 translocation Structural variability of human chromosome 9 in relation to its evolution. Frequency of satellite association of human chromosomes is correlated with amount of Ag-staining of the nucleolus organizer region Regulation of rRNA gene expression in a human familial 14p+ marker chromosome Nucleolar RNA synthesis of meiotic prophase spermatocytes in the human testis Selective suppression of the transcription of ribosomal genes in mouse-human hybrid cells Structural basis for Robertsonian translocations in man: association of ribosomal genes in the nucleolar fibrillar center in meiotic spermatocytes and oocytes On the number of ribosomal RNA genes in man Chromosomal constitution of nucleolus-associated chromatin in man The ultrastructure of the nuclei and the behaviour of the sex chromosomes of human spermatogonia The ultrastructure of the human sex vesicle Association of ribosomal genes in the fibrillar center of the nucleolus: a factor influencing translocation and nondisjunction in the human meiotic oocyte Nucleolar structures in chromosome and SC preparations from human oocytes at first meiotic prophase Satellite association in human metaphases. A comparative study of normal individuals, patients with Down syndrome and their parents [The significance of association of satellited chromosomes] Quantitative studies on the arrangement of human metaphase chromosomes. IV. The association frequency of human acrocentric marker chromosomes Frequency of satellite association in individuals with structural abnormalities of nucleolus organiser region Persistence of nucleoli in short term and long term cell cultures and in direct bone marrow preparations in mammalian materials Satellite associations of D group chromosomes in translocation carriers Satellite association. A possible cause of chromosome aberrations The nucleolus, virus infection, and trisomy in man. Acrocentric associations in mongol populations. In vitro alteration of association patterns of human acrocentric chromosomes Ribosomal cistrons and acrocentric chromosomes in man. The role of non-disjunction in aneuploidy in man an overview Meiotic analysis of XX/XY and neo-XX/XY sex chromosomes in Phyllostomidae by cross-species chromosome painting revealing a common chromosome 15-XY rearrangement in Stenodermatinae. Nucleoli and chromosomes: their relationships during the meiotic prophase of the human fetal oocyte Chromosomes and Cancer Nucleolar organizing regions of human chromosomes Cytogenetics, distribution and phenotypic effects of a translocation in Swedish cattle Mitotic and meiotic studies of a familial reciprocal translocation between autosomes 15 and 18 in man Structural and functional aspects of nucleolar organizer regions (NORs) of human chromosomes. Distribution of human chromosomes on the metaphase plate using banding techniques. Biochemical and cytogenetic studies on the nucleolus organizing regions (NOR) of man. II. A family with the 15/21 translocation Satellite association frequency and number of nucleoli depend on cell cycle duration and NOR-activity. Studies on first, second, and third mitoses of lymphocyte cultures Silver staining of human acrocentrics in metaphase does not reflect an induced inhibition in NOR activity Nuclear architecture of human pachytene spermatocytes: quantitative analysis of associations between nucleolar and XY bivalents Identification of pachytene bivalents in human male meiosis using G-banding technique The Influence of Neonatal Orchiopexy Upon the Testis in Persistent Müllerian Duct Syndrome Frequency of satelliting of the human chromosomes 21 and 22 and the identity of the mongol chromosome [Cytological aspect and intranuclear localization of the heterochromatic segments of C9 chromosomes in man]. [Satellite associations in autosomal and gonosomal chromosome abnormalities and in hypothyreosis] New BAGE (B melanoma antigen) genes mapping to the juxtacentromeric regions of human chromosomes 13 and 21 have a cancer/testis expression profile. Para-nucleolar Position of the Human Y Chromosome in Interphase Nuclei Complete autosomal chromomere maps of human early and mid/late pachytene spermatocytes THE KARYOTYPE OF THE MOUSE, WITH IDENTIFICATION OF A TRANSLOCATION. Quasi-linkage: a confounding factor in linkage analysis of complex diseases? Silver staining and nucleolar patterns in human heteroploid and measles-carrier cells [The establishment of polarity and bilateral symmetry in the oocytes of Gryllus domesticus L.]

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