The birth of a human-specific neural gene by incomplete duplication and gene fusion-Reference-Cited by-同舟云学术

The birth of a human-specific neural gene by incomplete duplication and gene fusion

Published:2017-03-09 Issue:1 Volume:18 Page:
ISSN:1474-760X
Container-title:Genome Biology
language:en
Short-container-title:Genome Biol

Author:

Dougherty Max L.,Nuttle Xander,Penn Osnat,Nelson Bradley J.,Huddleston John,Baker Carl,Harshman Lana,Duyzend Michael H.,Ventura Mario,Antonacci Francesca,Sandstrom Richard,Dennis Megan Y.,Eichler Evan E.

Funder

National Human Genome Research Institute

National Institute of Neurological Disorders and Stroke

Publisher

Springer Science and Business Media LLC

Link

http://link.springer.com/content/pdf/10.1186/s13059-017-1163-9.pdf

Reference74 articles.

1. Ohno S. Evolution by gene duplication. Berlin: New York, Springer-Verlag; 1970.

2. Marques-Bonet T, Kidd JM, Ventura M, Graves TA, Cheng Z, Hillier LW, et al. A burst of segmental duplications in the genome of the African great ape ancestor. Nature. 2009;457:877–81.

3. Sudmant PH, Huddleston J, Catacchio CR, Malig M, Hillier LW, Baker C, et al. Evolution and diversity of copy number variation in the great ape lineage. Genome Res. 2013;23:1373–82.

4. Lupski JR. Genomic disorders: structural features of the genome can lead to DNA rearrangements and human disease traits. Trends Genet. 1998;14:417–22.

5. Stankiewicz P, Shaw CJ, Withers M, Inoue K, Lupski JR. Serial segmental duplications during primate evolution result in complex human genome architecture. Genome Res. 2004;14:2209–20.

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