Literature DB >> 8825632

Chromosomal localization of six human forkhead genes, freac-1 (FKHL5), -3 (FKHL7), -4 (FKHL8), -5 (FKHL9), -6 (FKHL10), and -8 (FKHL12).

C Larsson1, M Hellqvist, S Pierrou, I White, S Enerbäck, P Carlsson.   

Abstract

The forkhead family of transcription factors has been shown to be involved in the regulation of embryonic development in organisms from Drosophila to humans. Genes encoding forkhead proteins are also emerging as a new class of oncogenes with relevance for human cancer. We have used a combination of fluorescence in situ hybridization and somatic cell hybrids to map the chromosomal localizations of five previously cloned human forkhead genes, freac-1, -3, -4, -5, and -6. (HGMW-approved symbols FKHL5, FKHL7, FKHL8, FKHL9 and FKHL10). We also report the sequence and the chromosomal position of a novel human forkhead gene, freac-8 (FKHL12). The freac genes have been localized to the following positions: freac-1, 16q24; freac-3, 6p25; freac-4, 5q12-q13; freac-5, 9 pericen; freac-6, 5q34, and freac-8, 1p32.

Entities:  

Mesh:

Substances:

Year:  1995        PMID: 8825632     DOI: 10.1006/geno.1995.1266

Source DB:  PubMed          Journal:  Genomics        ISSN: 0888-7543            Impact factor:   5.736


  12 in total

1.  Analyses of the effects that disease-causing missense mutations have on the structure and function of the winged-helix protein FOXC1.

Authors:  R A Saleem; S Banerjee-Basu; F B Berry; A D Baxevanis; M A Walter
Journal:  Am J Hum Genet       Date:  2001-03       Impact factor: 11.025

2.  The evolutionary origin of human subtelomeric homologies--or where the ends begin.

Authors:  Christa Lese Martin; Andrew Wong; Alyssa Gross; June Chung; Judy A Fantes; David H Ledbetter
Journal:  Am J Hum Genet       Date:  2002-03-01       Impact factor: 11.025

3.  Gene content and function of the ancestral chromosome fusion site in human chromosome 2q13-2q14.1 and paralogous regions.

Authors:  Yuxin Fan; Tera Newman; Elena Linardopoulou; Barbara J Trask
Journal:  Genome Res       Date:  2002-11       Impact factor: 9.043

4.  A forkhead gene, FoxE3, is essential for lens epithelial proliferation and closure of the lens vesicle.

Authors:  A Blixt; M Mahlapuu; M Aitola; M Pelto-Huikko; S Enerbäck; P Carlsson
Journal:  Genes Dev       Date:  2000-01-15       Impact factor: 11.361

Review 5.  Glaucoma genetics.

Authors:  Pratap Challa
Journal:  Int Ophthalmol Clin       Date:  2008

6.  Mutations of the forkhead/winged-helix gene, FKHL7, in patients with Axenfeld-Rieger anomaly.

Authors:  A J Mears; T Jordan; F Mirzayans; S Dubois; T Kume; M Parlee; R Ritch; B Koop; W L Kuo; C Collins; J Marshall; D B Gould; W Pearce; P Carlsson; S Enerbäck; J Morissette; S Bhattacharya; B Hogan; V Raymond; M A Walter
Journal:  Am J Hum Genet       Date:  1998-11       Impact factor: 11.025

7.  Autosomal dominant iridogoniodysgenesis anomaly maps to 6p25.

Authors:  A J Mears; F Mirzayans; D B Gould; W G Pearce; M A Walter
Journal:  Am J Hum Genet       Date:  1996-12       Impact factor: 11.025

8.  A mutation in the FOXE3 gene causes congenital primary aphakia in an autosomal recessive consanguineous Pakistani family.

Authors:  Iram Anjum; Hans Eiberg; Shahid Mahmood Baig; Niels Tommerup; Lars Hansen
Journal:  Mol Vis       Date:  2010-03-30       Impact factor: 2.367

9.  Dedicator of cytokinesis 8 is disrupted in two patients with mental retardation and developmental disabilities.

Authors:  Bradley L Griggs; Sydney Ladd; Robert A Saul; Barbara R DuPont; Anand K Srivastava
Journal:  Genomics       Date:  2007-12-03       Impact factor: 5.736

10.  A Family with Axenfeld-Rieger Syndrome: Report of the Clinical and Genetic Findings.

Authors:  Hee Jung Yang; You Kyung Lee; Choun-Ki Joo; Jung Il Moon; Jee Won Mok; Myoung Hee Park
Journal:  Korean J Ophthalmol       Date:  2015-07-21
View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.