Literature DB >> 9054929

Nonhomologous Robertsonian translocations form predominantly during female meiosis.

S L Page, L G Shaffer.   

Abstract

Mesh：

Year:  1997        PMID： 9054929     DOI： 10.1038/ng0397-231

Source DB:  PubMed          Journal:  Nat Genet        ISSN： 1061-4036            Impact factor:   38.330


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  21 in total

1.  A new molecular approach to investigate origin and formation of structural chromosome aberrations.

Authors:  B Röthlisberger; A Schinzel; D Kotzot
Journal:  Chromosome Res       Date:  2000       Impact factor: 5.239

Review 2.  Parental origin and timing of de novo Robertsonian translocation formation.

Authors:  Ruma Bandyopadhyay; Anita Heller; Cami Knox-DuBois; Christopher McCaskill; Sue Ann Berend; Scott L Page; Lisa G Shaffer
Journal:  Am J Hum Genet       Date:  2002-11-06       Impact factor: 11.025

3.  Translocation breakpoint mapping and sequence analysis in three monosomy 1p36 subjects with der(1)t(1;1)(p36;q44) suggest mechanisms for telomere capture in stabilizing de novo terminal rearrangements.

Authors:  Blake C Ballif; Keiko Wakui; Marzena Gajecka; Lisa G Shaffer
Journal:  Hum Genet       Date:  2003-10-25       Impact factor: 4.132

4.  Obligate short-arm exchange in de novo Robertsonian translocation formation influences placement of crossovers in chromosome 21 nondisjunction.

Authors:  Sue Ann Berend; Scott L Page; William Atkinson; Christopher McCaskill; Neil E Lamb; Stephanie L Sherman; Lisa G Shaffer
Journal:  Am J Hum Genet       Date:  2002-12-23       Impact factor: 11.025

Review 5.  The constitutional t(11;22): implications for a novel mechanism responsible for gross chromosomal rearrangements.

Authors:  H Kurahashi; H Inagaki; T Ohye; H Kogo; M Tsutsumi; T Kato; M Tong; B S Emanuel
Journal:  Clin Genet       Date:  2010-10       Impact factor: 4.438

6.  Paternal origin of the de novo constitutional t(11;22)(q23;q11).

Authors:  Tamae Ohye; Hidehito Inagaki; Hiroshi Kogo; Makiko Tsutsumi; Takema Kato; Maoqing Tong; Merryn V E Macville; Livija Medne; Elaine H Zackai; Beverly S Emanuel; Hiroki Kurahashi
Journal:  Eur J Hum Genet       Date:  2010-02-24       Impact factor: 4.246

7.  Characterization of a complex rearrangement with interstitial deletions and inversion on human chromosome 1.

Authors:  Marzena Gajecka; Caron D Glotzbach; Lisa G Shaffer
Journal:  Chromosome Res       Date:  2006-04-20       Impact factor: 5.239

8.  Unexpected complexity at breakpoint junctions in phenotypically normal individuals and mechanisms involved in generating balanced translocations t(1;22)(p36;q13).

Authors:  Marzena Gajecka; Andrew J Gentles; Albert Tsai; David Chitayat; Katherine L Mackay; Caron D Glotzbach; Michael R Lieber; Lisa G Shaffer
Journal:  Genome Res       Date:  2008-09-02       Impact factor: 9.043

9.  Recurrence risks for different pregnancy outcomes and meiotic segregation analysis of spermatozoa in carriers of t(1;11)(p36.22;q12.2).

Authors:  Alina Teresa Midro; Barbara Panasiuk; Beata Stasiewicz-Jarocka; Marta Olszewska; Ewa Wiland; Marta Myśliwiec; Maciej Kurpisz; Lisa G Shaffer; Marzena Gajecka
Journal:  J Hum Genet       Date:  2014-10-16       Impact factor: 3.172

10.  Further delineation of nonhomologous-based recombination and evidence for subtelomeric segmental duplications in 1p36 rearrangements.

Authors:  Carla S D'Angelo; Marzena Gajecka; Chong A Kim; Andrew J Gentles; Caron D Glotzbach; Lisa G Shaffer; Célia P Koiffmann
Journal:  Hum Genet       Date:  2009-03-07       Impact factor: 4.132
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