The DNA Double-Strand Break Repair Gene hMRE11 Is Mutated in Individuals with an Ataxia-Telangiectasia-like Disorder
Open Access
- 1 December 1999
- journal article
- research article
- Published by Elsevier BV in Cell
- Vol. 99 (6), 577-587
- https://doi.org/10.1016/s0092-8674(00)81547-0
Abstract
No abstract availableKeywords
This publication has 28 references indexed in Scilit:
- The Many Interfaces of Mre11Cell, 1998
- ATAXIA-TELANGIECTASIA AND THE NIJMEGEN BREAKAGE SYNDROME: Related Disorders But Genes ApartAnnual Review of Genetics, 1997
- TheRAD52epistasis group in mammalian double strand break repairSeminars in Immunology, 1997
- A gene transcribed from the bidirectional ATM promoter coding for a serine rich protein: amino acid sequence, structure and expression studiesHuman Molecular Genetics, 1996
- Ataxia without telangiectasia masquerading as benign hereditary choreaMovement Disorders, 1996
- Isolation and Characterization of the Human MRE11 HomologueGenomics, 1995
- Structural and functional similarities between the SbcCD proteins of Escherichia coli and the RAD50 and MRE11 (RAD32) recombination and repair proteins of yeastMolecular Microbiology, 1995
- A family showing no evidence of linkage between the ataxia telangiectasia gene and chromosome 11q22-23.Journal of Medical Genetics, 1993
- Hypersensitivity of cells from a new chromosomal-breakage syndrome to DNA-damaging agentsMutation Research - Reviews in Mutation Research, 1986
- X-Ray—Induced Breakage and Rejoining of Human Interphase ChromosomesScience, 1983