Literature DB >> 7959781

Assignment of a human melanoma associated gene MG50 (D2S448) to chromosome 2p25.3 by fluorescence in situ hybridization.

S R Weiler1, S M Taylor, R J Deans, J Kan-Mitchell, M S Mitchell, J M Trent.   

Abstract

Entities:  

Mesh：

Substances：

Year:  1994        PMID： 7959781     DOI： 10.1006/geno.1994.1374

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


× No keyword cloud information.
  2 in total

1.  Homozygous mutations in PXDN cause congenital cataract, corneal opacity, and developmental glaucoma.

Authors:  Kamron Khan; Adam Rudkin; David A Parry; Kathryn P Burdon; Martin McKibbin; Clare V Logan; Zakia I A Abdelhamed; James S Muecke; Narcis Fernandez-Fuentes; Kate J Laurie; Mike Shires; Rhys Fogarty; Ian M Carr; James A Poulter; Joanne E Morgan; Moin D Mohamed; Hussain Jafri; Yasmin Raashid; Ngy Meng; Horm Piseth; Carmel Toomes; Robert J Casson; Graham R Taylor; Michael Hammerton; Eamonn Sheridan; Colin A Johnson; Chris F Inglehearn; Jamie E Craig; Manir Ali
Journal:  Am J Hum Genet       Date:  2011-09-09       Impact factor: 11.025

2.  Identification and characterization of VPO1, a new animal heme-containing peroxidase.

Authors:  Guangjie Cheng; John C Salerno; Zehong Cao; Patrick J Pagano; J David Lambeth
Journal:  Free Radic Biol Med       Date:  2008-09-23       Impact factor: 7.376
  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.