Literature DB >> 25599669

Molecular cytogenetic analysis of telomere rearrangements.

Christa Lese Martin1, David H Ledbetter1.   

Abstract

Genomic imbalances involving the telomeric regions of human chromosomes, which contain the highest gene concentration in the genome, are proposed to have severe phenotypic consequences. For this reason, it is important to identify telomere rearrangements and assess their contribution to human pathology. This unit describes the structure and function of human telomeres and outlines several methodologies that can be employed to study these unique regions of human chromosomes. It is a revision of the original version of the unit published in 2000, now including an introductory section describing advances in the discipline that have taken place since the original publication.
Copyright © 2015 John Wiley & Sons, Inc.

Entities:  

Keywords:  chromosomal microarray; copy number variants; telomere

Mesh:

Substances:

Year:  2015        PMID: 25599669      PMCID: PMC4410364          DOI: 10.1002/0471142905.hg0811s84

Source DB:  PubMed          Journal:  Curr Protoc Hum Genet        ISSN: 1934-8258


  75 in total

1.  The clinical utility of enhanced subtelomeric coverage in array CGH.

Authors:  Blake C Ballif; Scott G Sulpizio; Richard M Lloyd; Sara L Minier; Aaron Theisen; Bassem A Bejjani; Lisa G Shaffer
Journal:  Am J Med Genet A       Date:  2007-08-15       Impact factor: 2.802

2.  Use of Affymetrix mapping arrays in the diagnosis of gene copy number variation.

Authors:  Allen D Delaney; Hong Qian; Jan M Friedman; Marco A Marra
Journal:  Curr Protoc Hum Genet       Date:  2008-10

3.  Multicolor Fluorescence In Situ Hybridization (FISH) approaches for simultaneous analysis of the entire human genome.

Authors:  C Lee; W Rens; F Yang
Journal:  Curr Protoc Hum Genet       Date:  2001-05

4.  Diagnosis of cryptic chromosomal syndromes by fluorescence in situ hybridization (FISH).

Authors:  Catherine D Kashork; Aaron Theisen; Lisa G Shaffer
Journal:  Curr Protoc Hum Genet       Date:  2010-10

Review 5.  Consensus statement: chromosomal microarray is a first-tier clinical diagnostic test for individuals with developmental disabilities or congenital anomalies.

Authors:  David T Miller; Margaret P Adam; Swaroop Aradhya; Leslie G Biesecker; Arthur R Brothman; Nigel P Carter; Deanna M Church; John A Crolla; Evan E Eichler; Charles J Epstein; W Andrew Faucett; Lars Feuk; Jan M Friedman; Ada Hamosh; Laird Jackson; Erin B Kaminsky; Klaas Kok; Ian D Krantz; Robert M Kuhn; Charles Lee; James M Ostell; Carla Rosenberg; Stephen W Scherer; Nancy B Spinner; Dimitri J Stavropoulos; James H Tepperberg; Erik C Thorland; Joris R Vermeesch; Darrel J Waggoner; Michael S Watson; Christa Lese Martin; David H Ledbetter
Journal:  Am J Hum Genet       Date:  2010-05-14       Impact factor: 11.025

Review 6.  The evolution of molecular ruler analysis for characterizing telomere imbalances: from fluorescence in situ hybridization to array comparative genomic hybridization.

Authors:  Christa Lese Martin; Zafar Nawaz; Erin L Baldwin; Elijah J Wallace; April N Justice; David H Ledbetter
Journal:  Genet Med       Date:  2007-09       Impact factor: 8.822

7.  Identification of chromosome abnormalities in subtelomeric regions by microarray analysis: a study of 5,380 cases.

Authors:  Lina Shao; Chad A Shaw; Xin-Yan Lu; Trilochan Sahoo; Carlos A Bacino; Seema R Lalani; Pawel Stankiewicz; Svetlana A Yatsenko; Yinfeng Li; Sarah Neill; Amber N Pursley; A Craig Chinault; Ankita Patel; Arthur L Beaudet; James R Lupski; Sau W Cheung
Journal:  Am J Med Genet A       Date:  2008-09-01       Impact factor: 2.802

Review 8.  Cryptic telomere imbalance: a 15-year update.

Authors:  David H Ledbetter; Christa Lese Martin
Journal:  Am J Med Genet C Semin Med Genet       Date:  2007-11-15       Impact factor: 3.908

9.  Whole-genome array-CGH identifies novel contiguous gene deletions and duplications associated with developmental delay, mental retardation, and dysmorphic features.

Authors:  Swaroop Aradhya; Melanie A Manning; Alessandra Splendore; Athena M Cherry
Journal:  Am J Med Genet A       Date:  2007-07-01       Impact factor: 2.802

10.  Enhanced detection of clinically relevant genomic imbalances using a targeted plus whole genome oligonucleotide microarray.

Authors:  Erin L Baldwin; Ji-Yun Lee; Douglas M Blake; Brian P Bunke; Chad R Alexander; Amy L Kogan; David H Ledbetter; Christa L Martin
Journal:  Genet Med       Date:  2008-06       Impact factor: 8.822

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