Literature DB >> 954550

BrdU-33258 Hoechst analysis of DNA replication in human lymphocytes with supernumerary or structurally abnormal X chromosomes.

S A Latt, H F Willard, P S Gerald.   

Abstract

BrdU-33258 Hoechst techniques have been used to characterize DNA replication patterns in lymphocytes from hunam females with supernumerary or structurally abnormal X chromosomes. Fluorescence analysis permits identification of late replicating X chromosomes in a very high proportion of cells and affords a high resolution method for determining the interchange points of X-X and X-autosome translocations. Asynchrony among terminal replication patterns of multiple late replicating X chromosomes within an individual cell can occasionally be demonstrated. The arms of isochromosomes usually exhibit symmetrical fluorescence patterns, with replication terminating in bands Xq21 and Xq23 (predominant pattern) or in bands Xq25 and Xq27 (alternative pattern) in both arms. In the vast majority of lymphocytes containing a balanced X-13 or X-19 translocation, the normal X is late replicating. However, DNA synthesis in the translocation products occasionally appears somewhat delayed relative to that expected for an early replicating X, consistent with possible position effects on replication kinetics.

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Year:  1976        PMID: 954550     DOI: 10.1007/BF00292912

Source DB:  PubMed          Journal:  Chromosoma        ISSN: 0009-5915            Impact factor:   4.316


  53 in total

1.  Deletion mapping of the human X chromosome.

Authors:  A de la Chapelle; J Schröder; T Haahtela; P Aro
Journal:  Hereditas       Date:  1975       Impact factor: 3.271

2.  Variegated-type position effects in the mouse.

Authors:  L B RUSSELL; J W BANGHAM
Journal:  Genetics       Date:  1961-05       Impact factor: 4.562

3.  HUMAN SEX CHROMOSOME ABNORMALITIES IN RELATION TO DNA REPLICATION AND HETEROCHROMATINIZATION.

Authors:  M M Grumbach; A Morishima; J H Taylor
Journal:  Proc Natl Acad Sci U S A       Date:  1963-05       Impact factor: 11.205

4.  Microfluorometric analysis of deoxyribonucleic acid replication kinetics and sister chromatid exchanges in human chromosomes.

Authors:  S A Latt
Journal:  J Histochem Cytochem       Date:  1974-07       Impact factor: 2.479

5.  Microfluorometric detection of deoxyribonucleic acid replication in human metaphase chromosomes.

Authors:  S A Latt
Journal:  Proc Natl Acad Sci U S A       Date:  1973-12       Impact factor: 11.205

6.  Abnormal X chromosomes in man: origin, behavior and effects.

Authors:  E Therman; K Patau
Journal:  Humangenetik       Date:  1974

7.  Cytogenetics of fifty patients with primary amenorrhea.

Authors:  G E Sarto
Journal:  Am J Obstet Gynecol       Date:  1974-05-01       Impact factor: 8.661

Review 8.  X-autosome translocations in the mouse: total inactivation versus partial inactivation of the X chromosome.

Authors:  E M Eicher
Journal:  Adv Genet       Date:  1970       Impact factor: 1.944

9.  Isochromosome-X in man. I.

Authors:  A De la Chapelle; J Wennström; H Hortling; C H Ockey
Journal:  Hereditas       Date:  1966       Impact factor: 3.271

10.  [Late replication and X-autosome traslocation a case with banding patterns autoradiographic and B.U.D.R. studies (author's transl)].

Authors:  S Gilgenkrantz; G Mauuary; B Dutrillaux; G Masocco
Journal:  Humangenetik       Date:  1975
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  62 in total

1.  Evidence for a correlation between late replication and autosomal gene inactivation in a familial translocation t(X;21).

Authors:  J Couturier; B Dutrillaux; P Garber; O Raoul; M F Croquette; J C Fourlinnie; E Maillard
Journal:  Hum Genet       Date:  1979-07-18       Impact factor: 4.132

Review 2.  The critical region on the human Xq.

Authors:  E Therman; R Laxova; B Susman
Journal:  Hum Genet       Date:  1990-10       Impact factor: 4.132

3.  Sequential G- to R-banding for high resolution chromosome analysis.

Authors:  B Hirsch; R Mack; D Arthur
Journal:  Hum Genet       Date:  1987-05       Impact factor: 4.132

4.  Localization of the human angiogenin gene to chromosome band 14q11, proximal to the T cell receptor alpha/delta locus.

Authors:  S Weremowicz; E A Fox; C C Morton; B L Vallee
Journal:  Am J Hum Genet       Date:  1990-12       Impact factor: 11.025

5.  Relation between the SCE points and the DNA replication bands.

Authors:  J J Hoo; M I Parslow
Journal:  Chromosoma       Date:  1979-06-21       Impact factor: 4.316

6.  Absence of a single repeat from the coding region of the human involucrin gene leading to RFLP.

Authors:  M Simon; M Phillips; H Green; H Stroh; K Glatt; G Burns; S A Latt
Journal:  Am J Hum Genet       Date:  1989-12       Impact factor: 11.025

7.  The 35 kd pulmonary surfactant-associated protein is encoded on chromosome 10.

Authors:  G Bruns; H Stroh; G M Veldman; S A Latt; J Floros
Journal:  Hum Genet       Date:  1987-05       Impact factor: 4.132

8.  Symmetrical replication patterns and sex chromatin bodies formation of an idic(X)(p22.3::p22.3) chromosome.

Authors:  O Mutchinik; L Casas; L Ruz; R Lisker; O Lozano
Journal:  Hum Genet       Date:  1981       Impact factor: 4.132

9.  Isolation and sequence of a human apolipoprotein CII cDNA clone and its use to isolate and map to human chromosome 19 the gene for apolipoprotein CII.

Authors:  C L Jackson; G A Bruns; J L Breslow
Journal:  Proc Natl Acad Sci U S A       Date:  1984-05       Impact factor: 11.205

10.  Late replication in an X-autosome translocation in the mouse: correlation with genetic inactivation and evidence for selective effects during embryogenesis.

Authors:  C M Disteche; E M Eicher; S A Latt
Journal:  Proc Natl Acad Sci U S A       Date:  1979-10       Impact factor: 11.205

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