Identification of the imprinted KLF14 transcription factor undergoing human-specific accelerated evolution.
Imprinted genes are expressed in a parent-of-origin manner and are located in clusters throughout the genome. Aberrations in the expression of imprinted genes on human Chromosome 7 have been suggested to play a role in the etiologies of Russell-Silver Syndrome and autism. We describe the imprinting...
Main Authors: | Layla Parker-Katiraee, Andrew R Carson, Takahiro Yamada, Philippe Arnaud, Robert Feil, Sayeda N Abu-Amero, Gudrun E Moore, Masahiro Kaneda, George H Perry, Anne C Stone, Charles Lee, Makiko Meguro-Horike, Hiroyuki Sasaki, Keiko Kobayashi, Kazuhiko Nakabayashi, Stephen W Scherer |
---|---|
Format: | Article |
Language: | English |
Published: |
Public Library of Science (PLoS)
2007-05-01
|
Series: | PLoS Genetics |
Online Access: | http://europepmc.org/articles/PMC1865561?pdf=render |
Similar Items
-
Preferential Allelic Expression of Genetic Information on Human Chromosome 7
by: Katiraee, Layla
Published: (2008) -
Preferential Allelic Expression of Genetic Information on Human Chromosome 7
by: Katiraee, Layla
Published: (2008) -
Molecular characterization of cytoplasmic genetic elements in a diseased isolate of Ophiostoma novo-ulmi
by: Abu-Amero, Sayeda Nasreen
Published: (1996) -
The Partial Role of KLF4 and KLF5 in Gastrointestinal Tumors
by: Jun-Chen Li, et al.
Published: (2021-01-01) -
ROLES OF KRÜPPEL LIKE FACTORS KLF1, KLF2, AND KLF4 IN EMBRYONIC BETA-GLOBIN GENE EXPRESSION
by: Alhashem, Yousef
Published: (2009)