Literature DB >> 9973272

Fragile sites-cytogenetic similarity with molecular diversity.

G R Sutherland1, R I Richards.   

Abstract

Mesh：

Year:  1999        PMID： 9973272      PMCID： PMC1377744          DOI： 10.1086/302267

Source DB:  PubMed          Journal:  Am J Hum Genet        ISSN： 0002-9297            Impact factor:   11.025


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  33 in total

1.  Selection in blood cells from female carriers of the fragile X syndrome: inverse correlation between age and proportion of active X chromosomes carrying the full mutation.

Authors:  F Rousseau; D Heitz; I Oberlé; J L Mandel
Journal:  J Med Genet       Date:  1991-12       Impact factor: 6.318

2.  The fragile site (16) (q22). I. Induction by AT-specific DNA-ligands and population frequency.

Authors:  M Schmid; W Feichtinger; A Jessberger; J Köhler; R Lange
Journal:  Hum Genet       Date:  1986-09       Impact factor: 4.132

3.  Molecular basis of p(CCG)n repeat instability at the FRA16A fragile site locus.

Authors:  J K Nancarrow; K Holman; M Mangelsdorf; T Hori; M Denton; G R Sutherland; R I Richards
Journal:  Hum Mol Genet       Date:  1995-03       Impact factor: 6.150

4.  Simple repeat DNA is not replicated simply.

Authors:  R I Richards; G R Sutherland
Journal:  Nat Genet       Date:  1994-02       Impact factor: 38.330

5.  Complex gene conversion events in germline mutation at human minisatellites.

Authors:  A J Jeffreys; K Tamaki; A MacLeod; D G Monckton; D L Neil; J A Armour
Journal:  Nat Genet       Date:  1994-02       Impact factor: 38.330

6.  Precursor arrays for triplet repeat expansion at the fragile X locus.

Authors:  M C Hirst; P K Grewal; K E Davies
Journal:  Hum Mol Genet       Date:  1994-09       Impact factor: 6.150

7.  Implications of FRA16A structure for the mechanism of chromosomal fragile site genesis.

Authors:  J K Nancarrow; E Kremer; K Holman; H Eyre; N A Doggett; D Le Paslier; D F Callen; G R Sutherland; R I Richards
Journal:  Science       Date:  1994-06-24       Impact factor: 47.728

8.  The most common fragile site in man is 3p14.

Authors:  D F Smeets; J M Scheres; T W Hustinx
Journal:  Hum Genet       Date:  1986-03       Impact factor: 4.132

9.  Evidence of founder chromosomes in fragile X syndrome.

Authors:  R I Richards; K Holman; K Friend; E Kremer; D Hillen; A Staples; W T Brown; P Goonewardena; J Tarleton; C Schwartz
Journal:  Nat Genet       Date:  1992-07       Impact factor: 38.330

10.  Association of a chromosome deletion syndrome with a fragile site within the proto-oncogene CBL2.

Authors:  C Jones; L Penny; T Mattina; S Yu; E Baker; L Voullaire; W Y Langdon; G R Sutherland; R I Richards; A Tunnacliffe
Journal:  Nature       Date:  1995-07-13       Impact factor: 49.962
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  9 in total

1.  Replication delay along FRA7H, a common fragile site on human chromosome 7, leads to chromosomal instability.

Authors:  A Hellman; A Rahat; S W Scherer; A Darvasi; L C Tsui; B Kerem
Journal:  Mol Cell Biol       Date:  2000-06       Impact factor: 4.272

2.  A common breakpoint on 11q23 in carriers of the constitutional t(11;22) translocation.

Authors:  L Edelmann; E Spiteri; N McCain; R Goldberg; R K Pandita; S Duong; J Fox; D Blumenthal; S R Lalani; L G Shaffer; B E Morrow
Journal:  Am J Hum Genet       Date:  1999-12       Impact factor: 11.025

3.  Fragile sites in human and Macaca fascicularis chromosomes are breakpoints in chromosome evolution.

Authors:  A Ruiz-Herrera; M Ponsà; F García; J Egozcue; M García
Journal:  Chromosome Res       Date:  2002       Impact factor: 5.239

4.  Cancer-specific chromosome alterations in the constitutive fragile region FRA3B.

Authors:  K Mimori; T Druck; H Inoue; H Alder; L Berk; M Mori; K Huebner; C M Croce
Journal:  Proc Natl Acad Sci U S A       Date:  1999-06-22       Impact factor: 11.205

5.  Fluorescent in-situ hybridization of cattle and sheep chromosomes with cloned human fragile-X DNA.

Authors:  Ahmad Ali; P D Thomsen; M E Babar
Journal:  Mol Biol Rep       Date:  2008-03-14       Impact factor: 2.316

6.  Replication inhibitors modulate instability of an expanded trinucleotide repeat at the myotonic dystrophy type 1 disease locus in human cells.

Authors:  Zhi Yang; Rachel Lau; Julien L Marcadier; David Chitayat; Christopher E Pearson
Journal:  Am J Hum Genet       Date:  2003-10-21       Impact factor: 11.025

7.  Is mammalian chromosomal evolution driven by regions of genome fragility?

Authors:  Aurora Ruiz-Herrera; Jose Castresana; Terence J Robinson
Journal:  Genome Biol       Date:  2006       Impact factor: 13.583

8.  Chromosomal instability in Afrotheria: fragile sites, evolutionary breakpoints and phylogenetic inference from genome sequence assemblies.

Authors:  Aurora Ruiz-Herrera; Terence J Robinson
Journal:  BMC Evol Biol       Date:  2007-10-24       Impact factor: 3.260

9.  Association between Genomic Instability and Evolutionary Chromosomal Rearrangements in Neotropical Primates.

Authors:  Fiona Puntieri; Nancy B Andrioli; Mariela Nieves
Journal:  Genome Biol Evol       Date:  2018-07-01       Impact factor: 3.416
  9 in total

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